This is a listing of all the patterns hosted as part of this directory
This pattern is meant to be used for OMIM Mendelian diseases (ie unitary genetic diseases, as described in PMID:33417889), including children of OMIM phenotypic series (OMIMPS), which are represented as grouping classes in Mondo. Notes about the OMIMPS (see also OMIM_phenotypic_series.yaml): - every instance of the OMIMPS metaclass should be equivalent to (via annotated xref) to something in OMIMPS namespace - the OMIMPS will never have an asserted causative gene as logical axiom (and no single causative gene in text def) - the OMIMPS must never be equivalent to an OMIM:nnnnnn (often redundant with the above rule) - the OMIMPS must have an acronym synonym, e.g. HPE - the OMIMPS must have two or more subclasses (direct or indirect) that are equivalent to OMIMs and conform to this pattern - the subclasses should (not must) have a logical def that uses the PS as a genus - the OMIM subclasses must have acronym synonyms that are the parent syn + number, e.g. HPE1, HPE2 - the primary label for the children should also be parent + {"type"} + number - the first member will usually have the same number local ID as the PS Examples: holoprosencephaly 1, 3M syndrome 1
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disease_series_by_gene.yaml |
Name | OMIM_disease_series_by_gene |
Classes | MONDO:0000001, SO:0000704, |
Variables | disease (MONDO:0000001), gene (SO:0000704), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples |
This pattern is meant to be used for OMIM phenotypic series (OMIMPS), which are represented as grouping classes in Mondo. Note: - every instance of this metaclass should be equivalent to (via annotated xref) to something in OMIMPS namespace - it will never have an asserted causative gene as logical axiom (and no single causative gene in text def) - it must never be equivalent to an OMIM:nnnnnn (often redundant with the above rule) - it must have an acronym synonym, e.g. HPE - it must have two or more subclasses (direct or indirect) that are equivalent to OMIMs - the subclasses should (not must) have a logical def that uses the PS as a genus (see http://purl.obolibrary.org/obo/mondo/patterns/disease_series_by_gene.yaml) - the OMIM subclasses must have acronym synonyms that are the parent syn + number, e.g. HPE1, HPE2 - the primary label for the children should also be parent + {"type"} + number - the first member will usually have the same number local ID as the PS - the first member in OMIM usually has documentation that is pertinent to the parent PS - the members may(?) generally share high semantic similarity - All OMIMPS disease should have a has characteristic some inherited restricted, see http://purl.obolibrary.org/obo/mondo/sparql/omimps-should-be-inherited-violation.sparql Examples: holoprosencephaly OMIMPS:236100, '3-M syndrome'(http://purl.obolibrary.org/obo/MONDO_0007477) OMIMPS:236100.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml |
Name | OMIM_phenotypic_series |
Classes | MONDO:0000001, MONDO:0021152, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples |
Pattern for extending a etiology-generic disease class to an acquired form. Here acquired means that basis for the disease is acquired during the individuals lifetime. It need not exclude genetic etiology, but it excludes inherited.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/acquired.yaml |
Name | acquired |
Classes | MONDO:0021141, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0060779 | acquired Fanconi syndrome | MONDO:0001083 | Fanconi renotubular syndrome |
MONDO:0045023 | acquired adrenogenital syndrome | MONDO:0015898 | adrenogenital syndrome |
MONDO:0019846 | acquired central diabetes insipidus | MONDO:0015790 | central diabetes insipidus |
MONDO:0015130 | acquired chronic primary adrenal insufficiency | MONDO:0015129 | chronic primary adrenal insufficiency |
MONDO:0019193 | acquired generalized lipodystrophy | MONDO:0027766 | generalized lipodystrophy |
See full table here
This pattern is applied to diseases that are described as having an acute onset, i.e. the sudden appearance of disease manifestations over a short period of time. Examples: acute bronchiolitis, acute liver failure
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/acute.yaml |
Name | acute |
Classes | PATO:0000389, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0001930 | acute cholangitis | MONDO:0004789 | cholangitis |
MONDO:0020683 | acute disease | MONDO:0700096 | human disease or disorder |
MONDO:0004810 | acute ethmoiditis | MONDO:0005756 | ethmoid sinusitis |
MONDO:0001912 | acute frontal sinusitis | MONDO:0001121 | frontal sinusitis |
MONDO:0001080 | acute gonococcal cervicitis | MONDO:0021157 | gonococcal cervicitis |
See full table here
Adenocarcinoma is a common cancer characterized by the presence of malignant glandular cells. This is a design pattern for classes representing adenocarcinomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic disease has location relation, which generalized over primary and secondary sites. Examples: adenocarcinoma of cervix uteri, pituitary adenocarcinoma (disease)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/adenocarcinoma.yaml |
Name | adenocarcinoma disease has location X |
Classes | MONDO:0004970, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003853 | Bartholin gland adenocarcinoma | UBERON:0000460 | major vestibular gland |
MONDO:0003410 | Wolffian duct adenocarcinoma | UBERON:0003074 | mesonephric duct |
MONDO:0018351 | adenocarcinoma of penis | UBERON:0000989 | penis |
MONDO:0004173 | adenocarcinoma of skene gland origin | UBERON:0010145 | paraurethral gland |
MONDO:0002670 | ampulla of vater adenocarcinoma | UBERON:0004913 | hepatopancreatic ampulla |
See full table here
Adenomas are neoplasms arising from epithelium. This is a design pattern for classes representing adenomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic disease has location
relation, which is generalized over primary and secondary sites. Examples: pituitary gland adenoma, breast adenoma
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/adenoma.yaml |
Name | adenoma disease has location X |
Classes | MONDO:0004972, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003419 | Bartholin gland adenoma | UBERON:0000460 | major vestibular gland |
MONDO:0021301 | adenoma of nipple | UBERON:0002030 | nipple |
MONDO:0021303 | adenoma of small intestine | UBERON:0002108 | small intestine |
MONDO:0003924 | adrenal cortex adenoma | UBERON:0001235 | adrenal cortex |
MONDO:0006088 | appendix adenoma | UBERON:0001154 | vermiform appendix |
See full table here
An adenosquamous carcinoma is a carcinoma composed of malignant glandular cells and malignant squamous cells. This is a design pattern for classes representing adenosquamous carcinomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic 'disease has location' relation, which generalized over primary and secondary sites. Examples: adenosquamous breast carcinoma, [Bartholin gland adenosquamous carcinoma] (http://purl.obolibrary.org/obo/MONDO_0003555), gastric adenosquamous carcinoma
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/adenosquamous_carcinoma.yaml |
Name | adenosquamous carcinoma disease has location X |
Classes | MONDO:0006074, UBERON:0010000, |
Variables | location (UBERON:0010000), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003555 | Bartholin gland adenosquamous carcinoma | UBERON:0000460 | major vestibular gland |
MONDO:0003549 | adenosquamous bile duct carcinoma | UBERON:0002394 | bile duct |
MONDO:0003548 | adenosquamous breast carcinoma | UBERON:0000310 | breast |
MONDO:0003554 | adenosquamous colon carcinoma | UBERON:0001155 | colon |
MONDO:0004973 | adenosquamous lung carcinoma | UBERON:0002048 | lung |
See full table here
An instance of a disease that has an onset of signs or symptoms of disease between the age of 16 years or later (adult onset). Examples: adult brain stem neoplasm, adult-onset myasthenia gravis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/adult.yaml |
Name | adult |
Classes | HP:0003581, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0017723 | Sandhoff disease, adult form | MONDO:0010006 | Sandhoff disease |
MONDO:0060778 | adult Fanconi syndrome | MONDO:0001083 | Fanconi renotubular syndrome |
MONDO:0016091 | adult Krabbe disease | MONDO:0009499 | Krabbe disease |
MONDO:0100486 | adult acne | MONDO:0011438 | acne |
MONDO:0100130 | adult acute respiratory distress syndrome | MONDO:0006502 | acute respiratory distress syndrome |
See full table here
An etiological pattern that extends an etiology-generic disease to an allergic form (i.e. caused by pathological type I hypersensitivity reaction). The allergy.yaml pattern is to refine an existing disease by trigger. Examples: allergic respiratory disease, atopic eczema, allergic otitis media
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/allergic_form_of_disease.yaml |
Name | allergic_form_of_disease |
Classes | MONDO:0000001, GO:0016068, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0005271 | allergic disease | MONDO:0000001 | disease or disorder |
MONDO:0021202 | allergic otitis media | MONDO:0005441 | otitis media |
MONDO:0011786 | allergic rhinitis | MONDO:0003014 | rhinitis |
See full table here
Allergy classified according to allergic trigger. This pattern is to refine an existing disease by trigger, the allergic_form_of_disease.yaml pattern is for a generic disease. Examples: egg allergy, peach allergy, gluten allergy
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/allergy.yaml |
Name | allergy |
Classes | MONDO:0005271, owl:Thing, |
Variables | substance (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples |
An instance of a disease that is brought about or caused by autoimmunity. Examples: autoimmune cardiomyopathy, autoimmune pancreatitis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/autoimmune.yaml |
Name | autoimmune |
Classes | MONDO:0000001, HP:0002960, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0007179 | autoimmune disease | MONDO:0000001 | disease or disorder |
MONDO:0000587 | autoimmune disease of ear, nose and throat | MONDO:0024623 | otorhinolaryngologic disease |
MONDO:0018242 | autoimmune hypoparathyroidism | MONDO:0001220 | hypoparathyroidism |
MONDO:0022518 | autoimmune inner ear disease | MONDO:0002467 | inner ear disorder |
MONDO:0017979 | autoimmune lymphoproliferative syndrome | MONDO:0016537 | lymphoproliferative syndrome |
See full table here
An instance of an autoimmune disease that is described by inflammation in a specific anatomical entity. Example: autoimmune thyroid disease
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/autoimmune_inflammation.yaml |
Name | autoimmune_inflammation |
Classes | MONDO:0007179, UBERON:0000061, |
Variables | location (UBERON:0000061), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0005623 | autoimmune thyroid disease | UBERON:0002046 | thyroid gland |
See full table here
This pattern is applied to autosomal dominant forms of an inherited disease. Examples: autosomal dominant cerebellar ataxia, autosomal dominant osteopetrosis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/autosomal_dominant.yaml |
Name | autosomal_dominant |
Classes | HP:0000006, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0007086 | autosomal dominant Alport syndrome | MONDO:0018965 | Alport syndrome |
MONDO:0007524 | autosomal dominant Ehlers-Danlos syndrome, vascular type | MONDO:0017314 | Ehlers-Danlos syndrome, vascular type |
MONDO:0007478 | autosomal dominant Kenny-Caffey syndrome | MONDO:0016516 | Kenny-Caffey syndrome |
MONDO:0007779 | autosomal dominant Opitz G/BBB syndrome | MONDO:0017138 | Opitz G/BBB syndrome |
MONDO:0008389 | autosomal dominant Robinow syndrome | MONDO:0019978 | Robinow syndrome |
See full table here
This pattern is applied to autosomal recessive forms of an inherited disease. Examples: autosomal recessive brachyolmia, autosomal recessive sideroblastic anemia
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/autosomal_recessive.yaml |
Name | autosomal_recessive |
Classes | HP:0000007, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0008762 | autosomal recessive Alport syndrome | MONDO:0018965 | Alport syndrome |
MONDO:0002014 | autosomal recessive Ehlers-Danlos syndrome, vascular type | MONDO:0017314 | Ehlers-Danlos syndrome, vascular type |
MONDO:0009486 | autosomal recessive Kenny-Caffey syndrome | MONDO:0016516 | Kenny-Caffey syndrome |
MONDO:0009999 | autosomal recessive Robinow syndrome | MONDO:0019978 | Robinow syndrome |
MONDO:0016647 | autosomal recessive Stickler syndrome | MONDO:0019354 | Stickler syndrome |
See full table here
A pattern for generic groupings of diseases based around the molecular basis for the disease in terms of a GO molecular function or cellular process. For example: DNA repair or RAS signaling
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/basis_in_disruption_of_process.yaml |
Name | basis_in_disruption_of_process |
Classes | MONDO:0000001, BFO:0000015, |
Variables | process (BFO:0000015), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | process | process:label |
---|---|---|---|
MONDO:0012996 | AGAT deficiency | GO:0015068 | glycine amidinotransferase activity |
MONDO:0021190 | DNA repair disease | GO:0006281 | DNA repair |
MONDO:0018274 | GM3 synthase deficiency | GO:0047291 | lactosylceramide alpha-2,3-sialyltransferase activity |
MONDO:0021060 | RASopathy | GO:0007265 | Ras protein signal transduction |
MONDO:0005271 | allergic disease | GO:0016068 | type I hypersensitivity |
See full table here
This is a design pattern for classes representing benign neoplasms, extending a generic neoplasm class. For example, a benign adrenal gland pheochromocytoma, defined as being the benign form of the more general adrenal gland pheochromocytoma. TODO: encode alternate way of representing
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/benign.yaml |
Name | benign |
Classes | MONDO:0005070, PATO:0002096, |
Variables | neoplasm (MONDO:0005070), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | neoplasm | neoplasm:label |
---|---|---|---|
MONDO:0036990 | benign Leydig cell tumor | MONDO:0006266 | Leydig cell tumor |
MONDO:0020581 | benign PEComa | MONDO:0006359 | neoplasm with perivascular epithelioid cell differentiation |
MONDO:0006103 | benign adrenal gland pheochromocytoma | MONDO:0004974 | adrenal gland pheochromocytoma |
MONDO:0036781 | benign axillary neoplasm | MONDO:0036779 | axillary neoplasm |
MONDO:0002065 | benign breast adenomyoepithelioma | MONDO:0002066 | breast adenomyoepithelioma |
See full table here
Neoplasms are benign or malignant tissue growths resulting from uncontrolled cell proliferation cell types. This is a design pattern for classes representing benign neoplasms based on their location. See also: benign.yaml TODO: choose one over another
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/benign_neoplasm.yaml |
Name | benign_neoplasm |
Classes | MONDO:0005165, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0002193 | Bartholin gland benign neoplasm | UBERON:0000460 | major vestibular gland |
MONDO:0044764 | benign choroid plexus neoplasm | UBERON:0001886 | choroid plexus |
MONDO:0002278 | benign colon neoplasm | UBERON:0001155 | colon |
MONDO:0006105 | benign conjunctival neoplasm | UBERON:0001811 | conjunctiva |
MONDO:0000385 | benign digestive system neoplasm | UBERON:0005409 | alimentary part of gastrointestinal system |
See full table here
Cancers are malignant neoplasms arising from a variety of different cell types. This is a design pattern for classes representing cancers based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic 'disease has location' relation, which generalized over primary and secondary sites.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/cancer.yaml |
Name | cancer |
Classes | MONDO:0004992, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0000954 | Meckel diverticulum cancer | UBERON:0003705 | Meckel's diverticulum |
MONDO:0004685 | Waldeyer's ring cancer | UBERON:0001735 | tonsillar ring |
MONDO:0002817 | adrenal gland cancer | UBERON:0002369 | adrenal gland |
MONDO:0003606 | adrenal medulla cancer | UBERON:0001236 | adrenal medulla |
MONDO:0000919 | ampulla of vater cancer | UBERON:0004913 | hepatopancreatic ampulla |
See full table here
Carcinomas are malignant neoplasms arising from epithelial cells. This is a Design pattern for classes representing carcinomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic 'disease has location' relation, which generalized over primary and secondary sites.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/carcinoma.yaml |
Name | carcinoma |
Classes | MONDO:0004993, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003975 | Littre gland carcinoma | UBERON:0010186 | male urethral gland |
MONDO:0004965 | acinar cell carcinoma | CL:0000622 | acinar cell |
MONDO:0002814 | adrenal carcinoma | UBERON:0002369 | adrenal gland |
MONDO:0006639 | adrenal cortex carcinoma | UBERON:0001235 | adrenal cortex |
MONDO:0004202 | adrenal medulla carcinoma | UBERON:0001236 | adrenal medulla |
See full table here
This is a Design pattern for classes representing in situ carcinomas based on their location. Examples: breast carcinoma in situ, liver carcinoma in situ
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/carcinoma_in_situ.yaml |
Name | carcinoma_in_situ |
Classes | MONDO:0004647, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0004707 | anal canal carcinoma in situ | UBERON:0000159 | anal canal |
MONDO:0000374 | bile duct carcinoma in situ | UBERON:0002394 | bile duct |
MONDO:0004703 | bladder carcinoma in situ | UBERON:0001255 | urinary bladder |
MONDO:0004658 | breast carcinoma in situ | UBERON:0000310 | breast |
MONDO:0000375 | bronchus carcinoma in situ | UBERON:0002185 | bronchus |
See full table here
An instance of a disease that has an onset of signs or symptoms of disease between the age of 1 to 5 years (childhood onset). Examples: childhood astrocytic tumor, childhood malignant melanoma
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/childhood.yaml |
Name | childhood |
Classes | HP:0011463, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0044767 | childhood adrenal gland pheochromocytoma | MONDO:0004974 | adrenal gland pheochromocytoma |
MONDO:0022642 | childhood carcinoid tumor | MONDO:0005369 | carcinoid tumor |
MONDO:0004535 | childhood choriocarcinoma of the ovary | MONDO:0003507 | choriocarcinoma of ovary |
MONDO:0003788 | childhood embryonal testis carcinoma | MONDO:0006446 | testicular embryonal carcinoma |
MONDO:0004082 | childhood immature teratoma of ovary | MONDO:0018369 | immature ovarian teratoma |
See full table here
This pattern is meant to be used for chromosomal disorder which consists of the deletion of chromosomal region in which the chromosomal region is known. Note that to refer to a partial deletion of a chromosome when the region is not know (only the chromosome is known), the partial_chromosome_deletion pattern should be used.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/chromosomal_region_deletion.yaml |
Name | chromosomal_region_deletion |
Classes | MONDO:0000761, GO:0098687, |
Variables | chromosomal_region (GO:0098687), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosomal:region | chromosomal:region:label |
---|---|---|---|
MONDO:0018632 | 11q22.2q22.3 microdeletion syndrome | CHR:9606-chr11q22.2-q22.3 | 11q22.2-q22.3 (Human) |
MONDO:0017781 | 12p12.1 microdeletion syndrome | CHR:9606-chr12p12.1 | 12p12.1 (Human) |
MONDO:0019784 | 12q14 microdeletion syndrome | CHR:9606-chr12q14 | 12q14 (Human) |
MONDO:0017334 | 12q15q21.1 microdeletion syndrome | CHR:9606-chr12q15-q21.1 | 12q15-q21.1 (Human) |
MONDO:0018474 | 13q12.3 microdeletion syndrome | CHR:9606-chr13q12.3 | 13q12.3 (Human) |
See full table here
This pattern is meant to be used for chromosomal disorder which consists in the duplication of chromosomal region in which the chromosomal region is known. "Duplication" means an increase of copy number, and includes an extra copy (partial trisomy) and 2 extra copies (partial tetrasomy, also called triplication) of chromosomal region. Note that this pattern does not include the duplication of the entire chromosome (trisomy, tetrasomy, pentasomy).
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/chromosomal_region_duplication.yaml |
Name | chromosomal_region_duplication |
Classes | MONDO:0000762, GO:0098687, |
Variables | chromosomal_region (GO:0098687), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosomal:region | chromosomal:region:label |
---|---|---|---|
MONDO:0017180 | 10q22.3q23.3 microduplication syndrome | CHR:9606-chr10q22.3-q23.3 | 10q22.3-q23.3 (Human) |
MONDO:0017580 | 11p15.4 microduplication syndrome | CHR:9606-chr11p15.4 | 11p15.4 (Human) |
MONDO:0016835 | 14q11.2 microduplication syndrome | CHR:9606-chr14q11.2 | 14q11.2 (Human) |
MONDO:0012081 | 15q11q13 microduplication syndrome | CHR:9606-chr15q11-q13 | 15q11-q13 (Human) |
MONDO:0016834 | 16p11.2p12.2 microduplication syndrome | CHR:9606-chr16p11.2-p12.2 | 16p11.2-p12.2 (Human) |
See full table here
This pattern is meant to be used for chromosomal disorder defined by the chromosome affected.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/chromosome_type.yaml |
Name | chromosome_type |
Classes | MONDO:0019040, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosome | chromosome:label |
---|---|---|---|
MONDO:0700008 | chromosome 1 disorder | CHR:9606-chr1 | chromosome 1 (Human) |
MONDO:0700017 | chromosome 10 disorder | CHR:9606-chr10 | chromosome 10 (Human) |
MONDO:0700018 | chromosome 11 disorder | CHR:9606-chr11 | chromosome 11 (Human) |
MONDO:0700019 | chromosome 12 disorder | CHR:9606-chr12 | chromosome 12 (Human) |
MONDO:0700020 | chromosome 13 disorder | CHR:9606-chr13 | chromosome 13 (Human) |
See full table here
This pattern is applied to diseases that are described as having an chronic duration, i.e. a disease having a slow progressive course of indefinite duration. Examples: chronic bronchitis, chronic hepatitis B virus infection
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/chronic.yaml |
Name | chronic |
Classes | PATO:0001863, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0004924 | chronic canaliculitis | MONDO:0005631 | actinomycosis |
MONDO:0004786 | chronic cholangitis | MONDO:0004789 | cholangitis |
MONDO:0015574 | chronic cutaneous lupus erythematosus | MONDO:0005282 | cutaneous lupus erythematosus |
MONDO:0004806 | chronic eosinophilic pneumonia | MONDO:0005749 | eosinophilic pneumonia |
MONDO:0004757 | chronic ethmoidal sinusitis | MONDO:0005756 | ethmoid sinusitis |
See full table here
An instance of a disease in which the disease is present at birth, regardless of cause. Examples: congenital agammaglobulinemia, congenital nystagmus
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/congenital.yaml |
Name | congenital |
Classes | MONDO:0021140, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0001902 | congenital agammaglobulinemia | MONDO:0015977 | agammaglobulinemia |
MONDO:0017375 | congenital enterovirus infection | MONDO:0005747 | enterovirus infectious disease |
MONDO:0018612 | congenital hypothyroidism | MONDO:0005420 | hypothyroidism |
MONDO:0017361 | congenital rubella syndrome | MONDO:0004656 | rubella |
MONDO:0005714 | congenital syphilis | MONDO:0005976 | syphilis |
See full table here
This pattern is applied to a disease that is caused by an infectious agent. Examples: hepatitis C induced liver cirrhosis, rubella encephalitis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/consequence_of_infectious_disease.yaml |
Name | consequence_of_infectious_disease |
Classes | MONDO:0000001, MONDO:0005550, |
Variables | parent (MONDO:0000001), cause (MONDO:0005550), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | cause | cause:label | parent | parent:label |
---|---|---|---|---|---|
MONDO:0020689 | AIDS dementia complex | MONDO:0005109 | HIV infectious disease | MONDO:0001627 | dementia |
MONDO:0002812 | infectious otitis interna | MONDO:0005550 | infectious disease | MONDO:0002008 | labyrinthitis |
MONDO:0021673 | post-bacterial disorder | MONDO:0005113 | bacterial infectious disease | MONDO:0000001 | disease or disorder |
MONDO:0021669 | post-infectious disorder | MONDO:0005550 | infectious disease | MONDO:0000001 | disease or disorder |
MONDO:0021670 | post-infectious syndrome | MONDO:0005550 | infectious disease | MONDO:0002254 | syndromic disease |
See full table here
Dependence on a substance that specifies the environmental stimulus such as alcohol, cocaine, etc. Example: dependence on cocaine.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/dependence_on_substance.yaml |
Name | dependence_on_substance |
Classes | MONDO:0004938, CHEBI:24431, |
Variables | stimulus (CHEBI:24431), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, 0000-0002-7463-6306, |
Examples |
Diseases classified by a perturbation in an anatomical structure (such as a subcellular component, or an organ)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disease_by_dysfunctional_structure.yaml |
Name | disease_by_dysfunctional_structure |
Classes | MONDO:0000001, UBERON:0000061, |
Variables | structure (UBERON:0000061), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | structure | structure:label |
---|---|---|---|
MONDO:0004880 | bowel dysfunction | UBERON:0004907 | lower digestive tract |
MONDO:0001343 | impaired renal function disease | UBERON:0002113 | kidney |
See full table here
Diseases which have a phenotype as a major feature of the disease are included in this pattern, e.g. scurvy (MONDO:0009412) which has the major feature of low levels of vitamin C (HP:0100510).
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disease_has_major_feature.yaml |
Name | disease_has_phenotype |
Classes | MONDO:0005070, HP:0000118, |
Variables | disease (MONDO:0005070), phenotypic abnormality (HP:0000118), |
Contributors | 0000-0002-7463-6306, |
Examples |
This pattern is for grouping classes to group terms that are disease or disease-like. Sometimes we feel there is insufficient reason to group, and X and X-like are not connected via shared is-a but instead by shares-features-with. Children of this grouping class should be X and X-like disease. Examples: viral disease or post-viral disorder
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disease-or-disease-like.yaml |
Name | disease or disease-like |
Classes | MONDO:0000001, |
Variables | disease1 (MONDO:0000001), disease2 (MONDO:0000001), |
Contributors | 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease1 | disease1:label | disease2 | disease2:label |
---|---|---|---|---|---|
MONDO:0100318 | SARS-CoV-2-related disease | MONDO:0100096 | COVID-19 | MONDO:0100320 | post-COVID-19 disorder |
MONDO:0100318 | SARS-CoV-2-related disease | MONDO:0100320 | post-COVID-19 disorder | MONDO:0100096 | COVID-19 |
MONDO:0700003 | obstetric disorder | MONDO:0024575 | pregnancy disorder | MONDO:0044013 | puerperal disorder |
MONDO:0700003 | obstetric disorder | MONDO:0044013 | puerperal disorder | MONDO:0024575 | pregnancy disorder |
MONDO:0006964 | secondary hyperparathyroidism | MONDO:0001530 | secondary hyperparathyroidism of renal origin | MONDO:0001750 | non-renal secondary hyperparathyroidism |
See full table here
This pattern is for diseases that are caused by a single variation or mutation in a single gene, that have gene-based names, such as new disease terms that are requested by ClinGen, like MED12-related intellectual disability syndrome. See more details about disease naming in Mondo here. Examples: MED12-related intellectual disability syndrome, TTN-related myopathy, MYPN-related myopathy
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disease_series_by_gene.yaml |
Name | disease_series_by_gene |
Classes | MONDO:0000001, SO:0001217, |
Variables | disease (MONDO:0000001), gene (SO:0001217), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples |
This pattern is for diseases that are caused by a single mutation in a single gene, that have gene-based names, and are inherited by a specific mechanism, succh as autosomal dominant and autosomal recessive. Examples: Growth hormone insensitivity syndrome with immune dysregulation, Growth hormone insensitivity with immune dysregulation 1, autosomal recessive and Growth hormone insensitivity with immune dysregulation 2, autosomal dominant
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disease_series_by_gene.yaml |
Name | disease_series_by_gene_and_inheritance |
Classes | MONDO:0000001, SO:0000704, HP:0000005, |
Variables | disease (MONDO:0000001), gene (SO:0000704), mode_of_inheritance (HP:0000005), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, 0000-0002-7356-1779, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | gene | gene:label | mode:of:inheritance | mode:of:inheritance:label |
---|---|---|---|---|---|---|---|
MONDO:0007092 | amelogenesis imperfecta type 1B | MONDO:0019507 | amelogenesis imperfecta | http://identifiers.org/hgnc/3344 | ENAM | HP:0000006 | Autosomal dominant inheritance |
MONDO:0014865 | autosomal recessive severe congenital neutropenia due to CSF3R deficiency | MONDO:0018542 | severe congenital neutropenia | http://identifiers.org/hgnc/2439 | CSF3R | HP:0000007 | Autosomal recessive inheritance |
MONDO:0018487 | autosomal recessive severe congenital neutropenia due to CXCR2 deficiency | MONDO:0018542 | severe congenital neutropenia | http://identifiers.org/hgnc/6027 | CXCR2 | HP:0000007 | Autosomal recessive inheritance |
MONDO:0012930 | autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | MONDO:0018542 | severe congenital neutropenia | http://identifiers.org/hgnc/24861 | G6PC3 | HP:0000007 | Autosomal recessive inheritance |
MONDO:0014456 | autosomal recessive severe congenital neutropenia due to JAGN1 deficiency | MONDO:0018542 | severe congenital neutropenia | http://identifiers.org/hgnc/26926 | JAGN1 | HP:0000007 | Autosomal recessive inheritance |
See full table here
A disease that disrupts a process, like immune system function, or early development. Examples: type III hypersensitivity disease, type IV hypersensitivity disease, neural tube closure defect (55 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/disrupts_process.yaml |
Name | disease or disorder disease caused by disruption of X |
Classes | MONDO:0000001, owl:Thing, |
Variables | process (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | process | process:label |
---|---|---|---|
MONDO:0012996 | AGAT deficiency | GO:0015068 | glycine amidinotransferase activity |
MONDO:0021190 | DNA repair disease | GO:0006281 | DNA repair |
MONDO:0018274 | GM3 synthase deficiency | GO:0047291 | lactosylceramide alpha-2,3-sialyltransferase activity |
MONDO:0021060 | RASopathy | GO:0007265 | Ras protein signal transduction |
MONDO:0005271 | allergic disease | GO:0016068 | type I hypersensitivity |
See full table here
A disease that is caused by exposure to an environmental stimulus, like the sun or pesticides. Examples: carbon monoxide-induced parkinsonism, cocaine intoxication
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/environmental_stimulus.yaml |
Name | environmental_stimulus |
Classes | MONDO:0000001, BFO:0000040, |
Variables | disease (MONDO:0000001), stimulus (BFO:0000040), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | stimulus | stimulus:label |
---|---|---|---|---|---|
MONDO:0003969 | amphetamine abuse | MONDO:0002491 | substance abuse | CHEBI:2679 | amphetamine |
MONDO:0004599 | barbiturate abuse | MONDO:0002491 | substance abuse | CHEBI:29745 | barbiturate |
MONDO:0043523 | cadmium poisoning | MONDO:0029000 | poisoning | CHEBI:22977 | cadmium atom |
MONDO:0004456 | cocaine abuse | MONDO:0002491 | substance abuse | CHEBI:27958 | cocaine |
MONDO:0005186 | cocaine dependence | MONDO:0005303 | drug dependence | CHEBI:27958 | cocaine |
See full table here
A hemangioma (a benign vascular lesion characterized by the formation of capillary-sized or cavernous vascular channels) that is located in a specific anatomical site. Examples: skin hemangioma, breast hemangioma, gastric hemangioma (20 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/hemangioma.yaml |
Name | hemangioma disease has location X |
Classes | MONDO:0006500, UBERON:0001062, |
Variables | location (UBERON:0001062), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003126 | breast hemangioma | UBERON:0000310 | breast |
MONDO:0003241 | central nervous system hemangioma | UBERON:0001017 | central nervous system |
MONDO:0003948 | cerebral hemangioma | UBERON:0001893 | telencephalon |
MONDO:0002414 | gastric hemangioma | UBERON:0000945 | stomach |
MONDO:0021542 | hemangioma of choroid | UBERON:0001776 | optic choroid |
See full table here
Pattern for extending a etiology-generic disease class to a hereditary form. Here hereditary means that etiology is largely genetic, and that the disease is passed down or potentially able to be passed down via inheritance (i.e is germline).
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/hereditary.yaml |
Name | hereditary |
Classes | MONDO:0021152, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0003847 | Mendelian disease | MONDO:0700096 | human disease or disorder |
MONDO:0008734 | adrenocortical carcinoma, hereditary | MONDO:0006639 | adrenal cortex carcinoma |
MONDO:0013099 | combined pituitary hormone deficiencies, genetic form | MONDO:0005152 | hypopituitarism |
MONDO:0006536 | congenital generalized lipodystrophy | MONDO:0027766 | generalized lipodystrophy |
MONDO:0018827 | familial chilblain lupus | MONDO:0019557 | chilblain lupus |
See full table here
Some diseases are caused by diagnostic and therapeutic procedures undertaken on a patient, such as a hospital acquired infection like MRSA. Use this pattern to define the iatrogenic form of a disease. Examples: 'iatrogenic botulism', 'iatrogenic Creutzfeldt-Jakob disease'
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/iatrogenic.yaml |
Name | iatrogenic |
Classes | MONDO:0100426, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0016778 | iatrogenic botulism | MONDO:0005498 | botulism |
MONDO:0043543 | iatrogenic disease | MONDO:0700096 | human disease or disorder |
See full table here
This pattern is applied to diseases that are described as being idiopathic, i.e. having an uncertain or unknown cause. Examples: idiopathic aplastic anemia, idiopathic avascular necrosis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/idiopathic.yaml |
Name | idiopathic |
Classes | MONDO:0700005, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0015713 | idiopathic central precocious puberty | MONDO:0019165 | central precocious puberty |
MONDO:0700007 | idiopathic disease | MONDO:0700096 | human disease or disorder |
MONDO:0011895 | idiopathic hypereosinophilic syndrome | MONDO:0015691 | hypereosinophilic syndrome |
MONDO:0019554 | idiopathic localized lipodystrophy | MONDO:0019194 | localized lipodystrophy |
MONDO:0018170 | idiopathic nephrotic syndrome | MONDO:0005377 | nephrotic syndrome |
See full table here
An inherited metabolic disease that causes disruption of a process.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/inborn_metabolic.yaml |
Name | inborn_metabolic |
Classes | MONDO:0019052, BFO:0000015, |
Variables | process (BFO:0000015), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | process | process:label |
---|---|---|---|
MONDO:0009825 | 5-oxoprolinase deficiency | GO:0017168 | 5-oxoprolinase (ATP-hydrolyzing) activity |
MONDO:0005775 | G6PD deficiency | GO:0004345 | glucose-6-phosphate dehydrogenase activity |
MONDO:0007068 | adenylosuccinate lyase deficiency | GO:0070626 | (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity |
MONDO:0009665 | biotinidase deficiency | GO:0047708 | biotinidase activity |
MONDO:0015286 | congenital disorder of glycosylation | GO:0070085 | glycosylation |
See full table here
This pattern is used for inborn errors of metabolism that cause disruption of a specific biological process, such as enzyme activity or ion transport. Examples: '5-oxoprolinase deficiency (disease)', inborn disorder of methionine cycle and sulfur amino acid metabolism, inborn aminoacylase deficiency (51 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/inborn_metabolic_disrupts.yaml |
Name | inborn errors of metabolism disease caused by disruption of X |
Classes | MONDO:0019052, owl:Thing, |
Variables | process (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | process | process:label |
---|---|---|---|
MONDO:0009825 | 5-oxoprolinase deficiency | GO:0017168 | 5-oxoprolinase (ATP-hydrolyzing) activity |
MONDO:0005775 | G6PD deficiency | GO:0004345 | glucose-6-phosphate dehydrogenase activity |
MONDO:0007068 | adenylosuccinate lyase deficiency | GO:0070626 | (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity |
MONDO:0009665 | biotinidase deficiency | GO:0047708 | biotinidase activity |
MONDO:0015286 | congenital disorder of glycosylation | GO:0070085 | glycosylation |
See full table here
An instance of a disease that has an onset of signs or symptoms of disease within the first 12 months of life (infantile onset). Examples: infant botulism, infantile glycine encephalopathy
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/infantile.yaml |
Name | infantile |
Classes | HP:0003593, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0015804 | infant botulism | MONDO:0005498 | botulism |
MONDO:0016089 | infantile Krabbe disease | MONDO:0009499 | Krabbe disease |
MONDO:0017354 | infantile glycine encephalopathy | MONDO:0011612 | glycine encephalopathy |
MONDO:0019261 | infantile neuronal ceroid lipofuscinosis | MONDO:0016295 | neuronal ceroid lipofuscinosis |
MONDO:0019190 | juvenile polyposis of infancy | MONDO:0017380 | juvenile polyposis syndrome |
See full table here
Infectious diseases can be classified by the infectioos agent, such as bacteria, coronavirus, etc, that causes the disease. Examples: COVID-19, cholera
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/infectious_disease_by_agent.yaml |
Name | infectious_disease_by_agent |
Classes | MONDO:0000001, NCBITaxon:1, MONDO:0005550, |
Variables | agent (NCBITaxon:1), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | agent | agent:label |
---|---|---|---|
MONDO:0021747 | Acanthamoeba infectious disease | NCBITaxon:5754 | Acanthamoeba |
MONDO:0006635 | Acinetobacter infectious disease | NCBITaxon:469 | Acinetobacter |
MONDO:0006636 | Actinobacillus infectious disease | NCBITaxon:713 | Actinobacillus |
MONDO:0006921 | Actinomycetales infectious disease | NCBITaxon:2037 | Actinomycetales |
MONDO:0005117 | Aeromonas hydrophila infectious disease | NCBITaxon:644 | Aeromonas hydrophila |
See full table here
This combines the infectious disease by agent pattern and the inflammatory disease by site pattern. Examples: bacterial endocarditis (disease), fungal gastritis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/infectious_inflammation.yaml |
Name | infectious_inflammation |
Classes | MONDO:0000001, NCBITaxon:1, UBERON:0000061, MONDO:0005550, |
Variables | location (UBERON:0000061), agent (NCBITaxon:1), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples |
Inflammatory diseases can be classified by the location in which the pathological inflammatory process occurs. For inflammatory diseases caused by infection, this may be the site of infection. Examples: 'Achilles bursitis', blepharitis, epiglottitis
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/inflammatory_disease_by_site.yaml |
Name | inflammatory_disease_by_site |
Classes | MONDO:0000001, UBERON:0000061, |
Variables | location (UBERON:0000061), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0004551 | Meckel diverticulitis | UBERON:0003705 | Meckel's diverticulum |
MONDO:0019838 | adenohypophysitis | UBERON:0002196 | adenohypophysis |
MONDO:0000261 | adenoiditis | UBERON:0001732 | pharyngeal tonsil |
MONDO:0020710 | amnionitis | UBERON:0000305 | amnion |
MONDO:0006656 | aortitis | UBERON:0000947 | aorta |
See full table here
This pattern should be used for children of MONDO_0020573'inherited disease susceptibility', including OMIM phenotypic series (OMIMPS) for which the subclasses are susceptibilities. Note, this pattern should not have an asserted causative gene as logical axiom (and no single causative gene in text definition), in those cases, the susceptibility_by_gene pattern should be used instead. The children should have asserted causative genes in the text definitions and in the logical axioms. This pattern is a superclass of the susceptibility_by_gene pattern. Examples: 'microvascular complications of diabetes, susceptibility', 'epilepsy, idiopathic generalized', 'aspergillosis, susceptibility to'.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/inherited_susceptibility.yaml |
Name | inherited_susceptibility |
Classes | MONDO:0000001, MONDO:0020573, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0000093 | Schistosoma mansoni infection, susceptibility | MONDO:0044345 | Schistosoma mansoni infectious disease |
MONDO:0013562 | aspergillosis, susceptibility to | MONDO:0005657 | aspergillosis |
MONDO:0000162 | autoimmune thyroid disease, susceptibility to | MONDO:0005623 | autoimmune thyroid disease |
MONDO:0000108 | bacteremia, susceptibility | MONDO:0005229 | bacterial infectious disease with sepsis |
MONDO:0013713 | dengue virus, susceptibility to | MONDO:0005502 | dengue disease |
See full table here
Some diseases exist in both isolated and syndromic forms. For example, aniridia (MONDO_0019172 aniridia, MONDO_0020148'syndromic aniridia' and MONDO_0007119 'isolated aniridia'. Use this pattern to define the isolated form of a disease when a term exists for the isolated/syndromic-neutral version. In general, this pattern should be used in parallel with syndromic. E.g. if you make a term 'syndromic disease, you should also have 'isolated disease' [see pattern here(https://github.com/monarch-initiative/mondo/blob/master/src/patterns/dosdp-patterns/syndromic.yaml). Note that the isolated and syndromic forms will be inferred to be disjoint due to the GCI pattern. Examples: 'isolated aniridia', 'isolated dystonia', 'isolated focal palmoplantar keratoderma'
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/isolated.yaml |
Name | isolated |
Classes | MONDO:0021128, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0020075 | genetic non-syndromic obesity | MONDO:0019182 | inherited obesity |
MONDO:0017262 | inherited non-syndromic ichthyosis | MONDO:0015947 | inherited ichthyosis |
MONDO:0016462 | isolated agammaglobulinemia | MONDO:0015977 | agammaglobulinemia |
MONDO:0016553 | isolated congenital hypogonadotropic hypogonadism | MONDO:0015770 | congenital hypogonadotropic hypogonadism |
MONDO:0017667 | isolated diffuse palmoplantar keratoderma | MONDO:0017666 | diffuse palmoplantar keratoderma |
See full table here
An instance of a disease that has an onset of signs or symptoms of disease between the age of 5 and 15 years (juvenile onset). Examples: juvenile-onset Parkinson disease, 'juvenile idiopathic scoliosis'
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/juvenile.yaml |
Name | juvenile |
Classes | HP:0003621, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0020655 | juvenile ankylosing spondylitis | MONDO:0005306 | ankylosing spondylitis |
MONDO:0009066 | juvenile nephropathic cystinosis | MONDO:0100151 | nephropathic cystinosis |
MONDO:0019262 | juvenile neuronal ceroid lipofuscinosis | MONDO:0016295 | neuronal ceroid lipofuscinosis |
MONDO:0003741 | juvenile type testicular granulosa cell tumor | MONDO:0003395 | testicular granulosa cell tumor |
MONDO:0000828 | juvenile-onset Parkinson disease | MONDO:0005180 | Parkinson disease |
See full table here
This template is for disease which arises from the reactivation of a virus from a latent phase to a lytic phase. Examples: herpes zoster
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/latent_virus_reactivation_disease.yaml |
Name | latent_virus_reactivation_disease |
Classes | MONDO:0005108, NCBITaxon:10239, |
Variables | virus (NCBITaxon:10239), |
Contributors | 0000-0002-4142-7153, |
Examples |
A leiomyoma (a well-circumscribed benign smooth muscle neoplasm characterized by the presence of spindle cells with cigar-shaped nuclei, interlacing fascicles, and a whorled pattern) that is located in a specific anatomical entity. Examples: leiomyoma cutis, ureter leiomyoma, urethra leiomyoma (30 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/leiomyoma.yaml |
Name | leiomyoma disease has location X |
Classes | MONDO:0001572, UBERON:0001062, |
Variables | location (UBERON:0001062), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003292 | anus leiomyoma | UBERON:0001245 | anus |
MONDO:0003300 | appendix leiomyoma | UBERON:0001154 | vermiform appendix |
MONDO:0001634 | bladder leiomyoma | UBERON:0001255 | urinary bladder |
MONDO:0002057 | breast leiomyoma | UBERON:0000310 | breast |
MONDO:0003287 | central nervous system leiomyoma | UBERON:0001017 | central nervous system |
See full table here
An uncommon, aggressive malignant smooth muscle neoplasm, usually occurring in post-menopausal women that is characterized by a proliferation of neoplastic spindle cells that is located in a specific anatomical location. Examples: leiomyosarcoma of the cervix uteri, cutaneous leiomyosarcoma (disease), breast leiomyosarcoma (29 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/leiomyosarcoma.yaml |
Name | leiomyosarcoma disease has location X |
Classes | MONDO:0005058, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003358 | anus leiomyosarcoma | UBERON:0001245 | anus |
MONDO:0002624 | bone leiomyosarcoma | UBERON:0002481 | bone tissue |
MONDO:0003371 | breast leiomyosarcoma | UBERON:0000310 | breast |
MONDO:0003349 | central nervous system leiomyosarcoma | UBERON:0001017 | central nervous system |
MONDO:0003351 | colon leiomyosarcoma | UBERON:0001155 | colon |
See full table here
This pattern is applied to diseases that are described as having a lesion, where a localized pathological or traumatic structural change, damage, deformity, or discontinuity of tissue, organ, or body part is present. Examples: ulnar nerve lesion, peripheral nerve lesion
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/lesioned.yaml |
Name | lesioned |
Classes | PATO:0040025, UBERON:0001062, |
Variables | anatomical entity (UBERON:0001062), |
Contributors | 0000-0001-5208-3432, |
Examples |
A benign, usually painless, well-circumscribed lipomatous tumor composed of adipose tissue that is located in a specific anatomical location. Examples: skin lipoma, colorectal lipoma, tendon sheath lipoma (28 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/lipoma.yaml |
Name | lipoma disease has location X |
Classes | MONDO:0005106, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0000974 | axillary lipoma | UBERON:0009472 | axilla |
MONDO:0000970 | breast lipoma | UBERON:0000310 | breast |
MONDO:0003844 | central nervous system lipoma | UBERON:0001017 | central nervous system |
MONDO:0003843 | cerebral hemisphere lipoma | UBERON:0001869 | cerebral hemisphere |
MONDO:0000971 | chest wall lipoma | UBERON:0016435 | chest wall |
See full table here
A disease that is located in a specific anatomical site. Examples: 'abdominal cystic lymphangioma', 'articular cartilage disease', 'urethral disease'
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/location.yaml |
Name | location |
Classes | MONDO:0000001, UBERON:0001062, CL:0000000, |
Variables | disease (MONDO:0000001), location, |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | location | location:label |
---|---|---|---|---|---|
MONDO:0004120 | Bartholin gland small cell carcinoma | MONDO:0000402 | small cell carcinoma | UBERON:0000460 | major vestibular gland |
MONDO:0024283 | Demodex folliculitis | MONDO:0017280 | demodicidosis | UBERON:0002073 | hair follicle |
MONDO:0006576 | Ludwig's angina | MONDO:0005230 | cellulitis | UBERON:0003679 | mouth floor |
MONDO:0001858 | Tietze syndrome | MONDO:0002254 | syndromic disease | UBERON:0002293 | costochondral joint |
MONDO:0021726 | abdominal cystic lymphangioma | MONDO:0009761 | cystic hygroma | UBERON:0000916 | abdomen |
See full table here
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/location_top.yaml |
Name | location_top |
Classes | MONDO:0000001, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0020594 | abducens nerve disorder | UBERON:0001646 | abducens nerve |
MONDO:0002636 | accessory nerve disorder | UBERON:0002019 | accessory XI nerve |
MONDO:0002816 | adrenal cortex disorder | UBERON:0001235 | adrenal cortex |
MONDO:0005495 | adrenal gland disorder | UBERON:0002369 | adrenal gland |
MONDO:0003182 | anterior horn disorder | UBERON:0002257 | ventral horn of spinal cord |
See full table here
A malignant (clonal) proliferation of B- lymphocytes or T- lymphocytes which involves the lymph nodes, bone marrow and/or extranodal sites. This category includes Non-Hodgkin lymphomas and Hodgkin lymphomas. Examples: marginal zone lymphoma, ureteral lymphoma, colorectal lymphoma (37 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/lymphoma.yaml |
Name | lymphoma disease has location X |
Classes | MONDO:0005062, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0007650 | MALT lymphoma | UBERON:0001961 | mucosa-associated lymphoid tissue |
MONDO:0001888 | anus lymphoma | UBERON:0001245 | anus |
MONDO:0001237 | appendix lymphoma | UBERON:0001154 | vermiform appendix |
MONDO:0001381 | bladder lymphoma | UBERON:0001255 | urinary bladder |
MONDO:0003661 | breast lymphoma | UBERON:0000310 | breast |
See full table here
This is a design pattern for classes representing malignant neoplasms, extending a generic neoplasm class. Examples: malignant carotid body paraganglioma, malignant germ cell tumor
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/malignant.yaml |
Name | malignant |
Classes | MONDO:0005070, PATO:0002097, owl:Thing, |
Variables | neoplasm (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | neoplasm | neoplasm:label |
---|---|---|---|
MONDO:0004992 | cancer | MONDO:0005070 | neoplasm |
MONDO:0003113 | extragonadal germ cell cancer | MONDO:0018201 | extragonadal germ cell tumor |
MONDO:0003252 | granular cell cancer | MONDO:0006235 | granular cell tumor |
MONDO:0000377 | malignant Leydig cell tumor | MONDO:0006266 | Leydig cell tumor |
MONDO:0000378 | malignant Sertoli cell tumor | MONDO:0002696 | Sertoli cell tumor |
See full table here
Melanomas are malignant, usually aggressive tumor composed of atypical, neoplastic melanocytes. This is a design pattern for classes representing melanomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic 'disease has location' relation, which generalized over primary and secondary sites. Examples: cutaneous melanoma, malignant breast melanoma, malignant melanoma of the mucosa (22 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/melanoma.yaml |
Name | melanoma disease has location X |
Classes | MONDO:0005105, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0006081 | anal melanoma | UBERON:0001245 | anus |
MONDO:0005012 | cutaneous melanoma | UBERON:0000014 | zone of skin |
MONDO:0045070 | digestive system melanoma | UBERON:0001007 | digestive system |
MONDO:0001192 | esophageal melanoma | UBERON:0001043 | esophagus |
MONDO:0000928 | eyelid melanoma | UBERON:0001711 | eyelid |
See full table here
A meningioma is a slow growing tumor attached to the dura mater. This is a design pattern for classes representing meningiomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic 'disease has location' relation, which generalized over primary and secondary sites. Examples: skin meningioma, brain meningioma, choroid plexus meningioma (26 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/meningioma.yaml |
Name | meningioma disease has location X |
Classes | MONDO:0016642, UBERON:0001062, |
Variables | location (UBERON:0001062), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0002997 | anterior cranial fossa meningioma | UBERON:0003720 | anterior cranial fossa |
MONDO:0000642 | brain meningioma | UBERON:0000955 | brain |
MONDO:0002996 | cavernous sinus meningioma | UBERON:0003712 | cavernous sinus |
MONDO:0003860 | cerebellopontine angle meningioma | UBERON:0014908 | cerebellopontine angle |
MONDO:0004422 | cerebral falx meningioma | UBERON:0006059 | falx cerebri |
See full table here
Pattern for describing the severity of a disease, in this case, a mild form of the disease. Here mild means having a relatively minor degree of severity. This may correspond with specific genetic mutations (or homozygous or heterozygous forms). Examples: mild ichthyosis vulgaris
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/mild.yaml |
Name | mild |
Classes | HP:0012825, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0100474 | mild ichthyosis vulgaris | MONDO:0024304 | ichthyosis vulgaris |
See full table here
A disease that is classified as a mitochondrial subtype, due to a defect in a mitochondrial gene, such as MONDO:0100134 'mitochondrial complex I deficiency, mitochondrial type'.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/mitochondrial_subtype.yaml |
Name | mitochondriaal_subtype |
Classes | SO:0000088, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples |
This pattern is meant to be used for chromosomal disorder which consists of the absence of one chromosome from the normal diploid number. Note that the absence of chromosome refers to the entire chromosome, and not to part of a chromosome.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/monosomy.yaml |
Name | monosomy |
Classes | MONDO:0020639, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosome | chromosome:label |
---|---|---|---|
MONDO:0019891 | monosomy 22 | CHR:9606-chr22 | chromosome 22 (Human) |
MONDO:0020466 | monosomy X | CHR:9606-chrX | chromosome X (Human) |
MONDO:0700035 | monosomy chromosome 8 | CHR:9606-chr8 | chromosome 8 (Human) |
See full table here
Mucoepidermoid carcinomas are carcinomas morphologically characterized the presence of cuboidal mucous cells, goblet-like mucous cells, squamoid cells, cystic changes, and a fibrotic stromal formation. This is a design pattern for classes representing mucoepidermoid carcinomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized cancer. We use the generic 'disease has location' relation, which generalized over primary and secondary sites. Examples: cutaneous mucoepidermoid carcinoma, oral cavity mucoepidermoid carcinoma, mucoepidermoid breast carcinoma (18 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/mucoepidermoid_carcinoma.yaml |
Name | mucoepidermoid carcinoma disease has location X |
Classes | MONDO:0003036, UBERON:0001062, |
Variables | location (UBERON:0001062), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0000531 | bronchus mucoepidermoid carcinoma | UBERON:0002185 | bronchus |
MONDO:0003091 | cutaneous mucoepidermoid carcinoma | UBERON:0000014 | zone of skin |
MONDO:0003089 | extrahepatic bile duct mucoepidermoid carcinoma | UBERON:0003703 | extrahepatic bile duct |
MONDO:0006213 | floor of mouth mucoepidermoid carcinoma | UBERON:0003679 | mouth floor |
MONDO:0003092 | lacrimal gland mucoepidermoid carcinoma | UBERON:0001817 | lacrimal gland |
See full table here
Neoplasms are benign or malignant tissue growths resulting from uncontrolled cell proliferation cell types. This is a design pattern for classes representing neoplasms based on their location. This may be the site of origin, but it can also represent a secondary site for malignant neoplasms that have metastasized. We use the generic 'disease has location' relation, which generalized over primary and secondary sites. Note that tumor is typically a synonym for neoplasm, although this can be context dependent. For NETs, NCIT uses the nomenclature 'tumor' to indicate 'well differentiated, low or intermediate grade tumor'. This can also be called carcinoid, see https://www.cancer.org/cancer/gastrointestinal-carcinoid-tumor/about/what-is-gastrointestinal-carcinoid.html We attempt to spell this out in our labels.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/neoplasm.yaml |
Name | neoplasm |
Classes | MONDO:0005070, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0021114 | Bartholin gland neoplasm | UBERON:0000460 | major vestibular gland |
MONDO:0021082 | Meckel diverticulum neoplasm | UBERON:0003705 | Meckel's diverticulum |
MONDO:0001884 | abducens nerve neoplasm | UBERON:0001646 | abducens nerve |
MONDO:0036591 | adrenal cortex neoplasm | UBERON:0001235 | adrenal cortex |
MONDO:0021227 | adrenal gland neoplasm | UBERON:0002369 | adrenal gland |
See full table here
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/neoplasm_by_origin.yaml |
Name | neoplasm |
Classes | MONDO:0005070, owl:Thing, |
Variables | structure (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | structure | structure:label |
---|---|---|---|
MONDO:0015157 | human herpesvirus 8-related tumor | MONDO:0005187 | human herpesvirus 8 infection |
MONDO:0017341 | virus associated tumor | MONDO:0005108 | viral infectious disease |
See full table here
Note that tumor is typically a synonym for neoplasm, although this can be context dependent. For neuroendocrine tumors (NETs), NCIT uses the nomenclature 'tumor' to indicate 'well differentiated, low or intermediate grade tumor'. This can also be called carcinoid, see https://www.cancer.org/cancer/gastrointestinal-carcinoid-tumor/about/what-is-gastrointestinal-carcinoid.html. We attempt to spell this out in our labels. Examples: breast neuroendocrine neoplasm, digestive system neuroendocrine neoplasm, ovarian neuroendocrine neoplasm
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/neuroendocrine_neoplasm.yaml |
Name | neoendocrine_neoplasm |
Classes | MONDO:0019496, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003504 | anal canal neuroendocrine neoplasm | UBERON:0000159 | anal canal |
MONDO:0024501 | appendix neuroendocrine neoplasm | UBERON:0001154 | vermiform appendix |
MONDO:0002485 | breast neuroendocrine neoplasm | UBERON:0000310 | breast |
MONDO:0019963 | bronchial endocrine tumor | UBERON:0002185 | bronchus |
MONDO:0002882 | colon neuroendocrine neoplasm | UBERON:0001155 | colon |
See full table here
We follow NCIT in making carcinoid tumor a synonym for neuroendocrine neoplasm G1 (G1 NET). Examples: carcinoid tumor (disease)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/neuroendocrine_neoplasm_grade1.yaml |
Name | neoendocrine_neoplasm_grade1 |
Classes | MONDO:0019496, MONDO:0024491, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0006091 | appendix neuroendocrine tumor G1 | UBERON:0001154 | vermiform appendix |
MONDO:0006093 | ascending colon neuroendocrine tumor G1 | UBERON:0001156 | ascending colon |
MONDO:0006126 | cecum neuroendocrine tumor G1 | UBERON:0001153 | caecum |
MONDO:0006155 | colon neuroendocrine tumor G1 | UBERON:0001155 | colon |
MONDO:0006162 | colorectal neuroendocrine tumor G1 | UBERON:0012652 | colorectum |
See full table here
This pattern should be used for diseases affecting non-human animal which have a corresponding/an analog disease in human, AND the taxon affected is NOT known. Examples: leukemia, non-human animal, hepatitis, viral, animal
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/nonhuman_disease.yaml |
Name | nonhuman_disease |
Classes | MONDO:0005583, MONDO:0700096, |
Variables | human_disease (MONDO:0700096), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | human:disease | human:disease:label |
---|---|---|---|
MONDO:0700103 | nutritional deficiency disease, non-human animal | MONDO:0006873 | nutritional deficiency disease |
See full table here
This pattern should be used for diseases affecting non-human animal which have a corresponding/an analog disease in human AND the taxon affected is known. Examples: leukemia, feline
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/nonhuman_disease_taxon.yaml |
Name | nonhuman_disease_taxon |
Classes | MONDO:0005583, MONDO:0700096, NCBITaxon:1, |
Variables | human_disease (MONDO:0700096), taxon (NCBITaxon:1), |
Contributors | 0000-0002-4142-7153, |
Examples |
A disease that is classified as a nuclear subtype, due to a defect in a nuclear gene, such as MONDO:0009640 'mitochondrial complex I deficiency, nuclear type'.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/nuclear_subtype.yaml |
Name | nuclear_subtype |
Classes | SO:0000087, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples |
This pattern is meant to be used for chromosomal disorder which consists of the deletion of part of a chromosome in which only the chromosome which part is deleted is known (the chromosomal region is not known). Note that when the chromosomal region is known, the chromosomal_region_deletion pattern should be used. Also note that this pattern does not include the loss of the entire chromosome (monosomy).
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/partial_chromosomal_deletion.yaml |
Name | partial_chromosomal_deletion |
Classes | MONDO:0000761, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosome | chromosome:label |
---|---|---|---|
MONDO:0015607 | partial chromosome Y deletion | CHR:9606-chrY | chromosome Y (Human) |
MONDO:0016866 | partial deletion of chromosome 1 | CHR:9606-chr1 | chromosome 1 (Human) |
MONDO:0016875 | partial deletion of chromosome 10 | CHR:9606-chr10 | chromosome 10 (Human) |
MONDO:0016876 | partial deletion of chromosome 11 | CHR:9606-chr11 | chromosome 11 (Human) |
MONDO:0017277 | partial deletion of chromosome 12 | CHR:9606-chr12 | chromosome 12 (Human) |
See full table here
This pattern is meant to be used for chromosomal disorder which consists of the presence of three additional chromosomes of the same type from the normal diploid number. Note that the presence of additional chromosomes refers to the entire chromosome, and not to part of a chromosome.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/pentasomy.yaml |
Name | pentasomy |
Classes | MONDO:0700085, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples |
A disease that is caused by exposure to an environmental stimulus that causes poisoning. Examples: colchicine poisoning, cocaine intoxication
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/poisoning.yaml |
Name | poisoning |
Classes | MONDO:0029000, BFO:0000040, |
Variables | stimulus (BFO:0000040), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, 0000-0002-7463-6306, |
Examples | mondo |
defined:class | defined:class:label | stimulus | stimulus:label |
---|---|---|---|
MONDO:0043523 | cadmium poisoning | CHEBI:22977 | cadmium atom |
MONDO:0019544 | cocaine intoxication | CHEBI:27958 | cocaine |
MONDO:0017859 | colchicine poisoning | CHEBI:23359 | colchicine |
MONDO:0017863 | digitalis poisoning | CHEBI:4551 | digoxin |
MONDO:0017861 | ethylene glycol poisoning | CHEBI:30742 | ethylene glycol |
See full table here
This pattern is for diseases that are caused by a variation (or mutation) in a two or more genes. The relation disease has basis in dysfunction should be used for each gene that is affected. For digenic diseases, this would be twice, for polygenic diseases, it would be 3 or more. Examples: Usher syndrome, type 1D/F
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/polygenic_disorder.yaml |
Name | polygenic_disorder |
Classes | MONDO:0000001, SO:0001217, |
Variables | disease (MONDO:0000001), gene (SO:0001217), |
Contributors | 0000-0002-4142-7153, 0000-0001-5208-3432, |
Examples |
Post-infection disorder follows infection but is distinct from the infection itself and its usual manifestations. Examples: post-COVID-19 disorder
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/post_infectious_disease.yaml |
Name | post_infectious_disease |
Classes | MONDO:0000001, MONDO:0021669, MONDO:0005550, |
Variables | infectiousdisease (MONDO:0005550), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | infectiousdisease | infectiousdisease:label |
---|---|---|---|
MONDO:0021673 | post-bacterial disorder | MONDO:0005113 | bacterial infectious disease |
MONDO:0021669 | post-infectious disorder | MONDO:0005550 | infectious disease |
MONDO:0021674 | post-viral disorder | MONDO:0005108 | viral infectious disease |
See full table here
A design pattern for conditions such as post-herpetic neuralgia or postinfectious encephalitis, where the disease is secondary to the initial infection. TODO: write better guidelines on what constitutes a secondary disease vs primary. * We do not use this pattern for AIDS-HIV for example, instead representing this is using SubClassOf. * We draw a distinction between infectious and postinfectious encepahlitis. * we do not use this pattern for chickenpox, but we do for shingles
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/postinfectious_disease.yaml |
Name | postinfectious_disease |
Classes | MONDO:0000001, MONDO:0005550, NCBITaxon:1, |
Variables | disease (NCBITaxon:1), feature (MONDO:0005550), |
Contributors | 0000-0002-6601-2165, |
Examples |
An instance of a disease is associated with a pregnancy. Examples: pregnancy associated osteoporosis, hypertension, pregnancy-induced
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/pregnancy_form_of_disorder.yaml |
Name | pregnancy_form_of_disorder |
Classes | MONDO:0000001, MONDO:0024575, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0005406 | gestational diabetes | MONDO:0005015 | diabetes mellitus |
MONDO:0100194 | pregnancy associated osteoporosis | MONDO:0005298 | osteoporosis |
See full table here
Pattern for extending a disease class to a primary infectious form, a characteristic of an infectious disease in which the disease affects an immunologically normal host. Example: MONDO_0000308 'primary systemic mycosis'.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/primary_infectious.yaml |
Name | primary infectious |
Classes | MONDO:0045036, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0000314 | primary bacterial infectious disease | MONDO:0005113 | bacterial infectious disease |
MONDO:0000308 | primary systemic mycosis | MONDO:0000256 | systemic mycosis |
See full table here
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/rare.yaml |
Name | rare |
Classes | MONDO:0021136, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples |
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/rare_genetic.yaml |
Name | rare_genetic |
Classes | MONDO:0021150, MONDO:0021136, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples |
This pattern is used for a disease, where the cause of the disease is an exposure to an environmental stimulus (using ECTO exposure terms) or a medical action, such as a therapeutic treatment (using MAxO terms). Note that this pattern does not include infectious disease or classes that would include an organism, virus or viroid. Rather it includes exposures to chemicals (includng drugs), or mixtures. Examples: chemically-induced disorder, alcohol amnestic disorder, alcoholic polyneuropathy, chemotherapy-induced alopecia (26 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/realized_in_response_to_evironmental_exposure.yaml |
Name | disease realized in response to environmental exposure |
Classes | MONDO:0000001, ExO:0000002, |
Variables | disease (MONDO:0000001), exposure (ExO:0000002), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | exposure | exposure:label |
---|---|---|---|---|---|
MONDO:0060781 | Preeyasombat-Varavithya syndrome | MONDO:0001083 | Fanconi renotubular syndrome | ECTO:9000364 | exposure to tetracycline |
MONDO:0002046 | alcohol abuse | MONDO:0002491 | substance abuse | ECTO:0001082 | exposure to alcohol consumption |
MONDO:0021702 | alcohol amnestic disorder | MONDO:0001152 | amnestic disorder | ECTO:0001082 | exposure to alcohol consumption |
MONDO:0007079 | alcohol dependence | MONDO:0004938 | substance dependence | ECTO:0001082 | exposure to alcohol consumption |
MONDO:0021698 | alcohol-related disorders | MONDO:0002494 | substance-related disorder | ECTO:0001082 | exposure to alcohol consumption |
See full table here
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/refractory.yaml |
Name | refractory |
Classes | HP:0031375, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0004401 | testis refractory cancer | MONDO:0003510 | malignant testicular germ cell tumor |
MONDO:0005414 | treatment-refractory schizophrenia | MONDO:0005090 | schizophrenia |
See full table here
This is auto-generated. Add your description here Examples: rhabdomyosarcoma of the cervix uteri, breast rhabdomyosarcoma, testis rhabdomyosarcoma (15 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/rhabdomyosarcoma.yaml |
Name | rhabdomyosarcoma disease has location X |
Classes | MONDO:0005212, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0002864 | anus rhabdomyosarcoma | UBERON:0001245 | anus |
MONDO:0002859 | breast rhabdomyosarcoma | UBERON:0000310 | breast |
MONDO:0002850 | central nervous system rhabdomyosarcoma | UBERON:0001017 | central nervous system |
MONDO:0002577 | extrahepatic bile duct rhabdomyosarcoma | UBERON:0003703 | extrahepatic bile duct |
MONDO:0002856 | gallbladder rhabdomyosarcoma | UBERON:0002110 | gall bladder |
See full table here
This pattern is meant to be used for chromosomal disorder which consists of the presence of a ring chromosome. A ring chromosome is a chromosome whose arms have fused together to form a ring, often with the loss of the ends of the chromosome.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/ring_chromosome_anomaly.yaml |
Name | ring_chromosome_anomaly |
Classes | MONDO:0700091, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosome | chromosome:label |
---|---|---|---|
MONDO:0019926 | X small rings | CHR:9606-chrX | chromosome X (Human) |
MONDO:0015443 | chromosome 8-derived supernumerary ring/marker | CHR:9606-chr8 | chromosome 8 (Human) |
MONDO:0015430 | ring chromosome 1 | CHR:9606-chr1 | chromosome 1 (Human) |
MONDO:0015431 | ring chromosome 10 | CHR:9606-chr10 | chromosome 10 (Human) |
MONDO:0019906 | ring chromosome 11 | CHR:9606-chr11 | chromosome 11 (Human) |
See full table here
Sarcomas are malignant neoplasms arising from soft tissue or bone. This is a design pattern for classes representing sarcomas based on their location. This may be the site of origin, but it can also represent a secondary site for metastatized sarcma. We use the generic 'disease has location' relation, which generalized over primary and secondary sites.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/sarcoma.yaml |
Name | sarcoma |
Classes | MONDO:0005089, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0019480 | Langerhans cell sarcoma | CL:0000453 | Langerhans cell |
MONDO:0016982 | angiosarcoma | UBERON:0001981 | blood vessel |
MONDO:0002865 | anus sarcoma | UBERON:0001245 | anus |
MONDO:0002862 | bile duct sarcoma | UBERON:0002394 | bile duct |
MONDO:0001374 | bladder sarcoma | UBERON:0001255 | urinary bladder |
See full table here
Pattern for describing the severity of a disease, in this case, a severe form of the disease. Here severe means having a high degree of severity. This may correspond with specific genetic mutations (or homozygous or heterozygous forms). Examples: severe ichthyosis vulgaris
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/severe.yaml |
Name | severe |
Classes | HP:0012828, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0100475 | severe ichthyosis vulgaris | MONDO:0024304 | ichthyosis vulgaris |
See full table here
This is auto-generated. Add your description here Examples: cervical small cell carcinoma, pancreatic small cell neuroendocrine carcinoma, ureter small cell carcinoma (16 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/small_cell_carcinoma.yaml |
Name | small cell carcinoma disease has location X |
Classes | MONDO:0000402, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0004120 | Bartholin gland small cell carcinoma | UBERON:0000460 | major vestibular gland |
MONDO:0006142 | cervical small cell carcinoma | UBERON:0000002 | uterine cervix |
MONDO:0003978 | colon small cell neuroendocrine carcinoma | UBERON:0001155 | colon |
MONDO:0006197 | endometrial small cell carcinoma | UBERON:0001295 | endometrium |
MONDO:0004116 | esophageal small cell neuroendocrine carcinoma | UBERON:0001043 | esophagus |
See full table here
This is auto-generated. Add your description here Examples: disease of catalytic activity, disease of transporter activity, phagocytic cell dysfunction (49 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/X_disease_disrupts_X |
Name | X disease disrupts X |
Classes | owl:Thing, MONDO:0000001, |
Variables | disease (MONDO:0000001), process (owl:Thing), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | process | process:label |
---|---|---|---|---|---|
MONDO:0001531 | blood coagulation disease | MONDO:0000001 | disease or disorder | GO:0007596 | blood coagulation |
MONDO:0005557 | calcium metabolic disease | MONDO:0005066 | metabolic disease | GO:0055074 | calcium ion homeostasis |
MONDO:0045024 | cancer or benign tumor | MONDO:0700096 | human disease or disorder | GO:0008283 | cell population proliferation |
MONDO:0020779 | cartilage development disorder | MONDO:0000001 | disease or disorder | GO:0051216 | cartilage development |
MONDO:0019165 | central precocious puberty | MONDO:0000088 | precocious puberty | GO:0032274 | gonadotropin secretion |
See full table here
This is auto-generated. Add your description here Examples: collagenopathy type 2 alpha 1, hemoglobinopathy, blood platelet disease (2195 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/specific_disease_by_dysfunctional_structure.yaml |
Name | X disease has basis in dysfunction of X |
Classes | owl:Thing, MONDO:0000001, |
Variables | disease (MONDO:0000001), structure (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | structure | structure:label |
---|---|---|---|---|---|
MONDO:0002245 | blood platelet disease | MONDO:0000001 | disease or disorder | CL:0000233 | platelet |
MONDO:0004880 | bowel dysfunction | MONDO:0000001 | disease or disorder | UBERON:0004907 | lower digestive tract |
MONDO:0020144 | cerebrovascular dementia | MONDO:0001627 | dementia | UBERON:0008998 | vasculature of brain |
MONDO:0005308 | ciliopathy | MONDO:0000001 | disease or disorder | GO:0005929 | cilium |
MONDO:0004603 | collagenopathy | MONDO:0000001 | disease or disorder | GO:0005581 | collagen trimer |
See full table here
as for inflammatory_disease_by_site, but refining a specific disease
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/specific_infectious_disease_by_agent.yaml |
Name | specific_inflammatory_disease_by_site |
Classes | MONDO:0000001, NCBITaxon:1, |
Variables | disease (MONDO:0000001), agent (NCBITaxon:1), |
Contributors | 0000-0002-6601-2165, |
Examples |
TODO
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/specific_infectious_disease_by_location.yaml |
Name | specific_infectious_disease_by_location |
Classes | MONDO:0000001, UBERON:0000061, |
Variables | disease (MONDO:0000001), location (UBERON:0000061), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | location | location:label |
---|---|---|---|---|---|
MONDO:0004551 | Meckel diverticulitis | MONDO:0000001 | disease or disorder | UBERON:0003705 | Meckel's diverticulum |
MONDO:0019838 | adenohypophysitis | MONDO:0000001 | disease or disorder | UBERON:0002196 | adenohypophysis |
MONDO:0000261 | adenoiditis | MONDO:0000001 | disease or disorder | UBERON:0001732 | pharyngeal tonsil |
MONDO:0020710 | amnionitis | MONDO:0000001 | disease or disorder | UBERON:0000305 | amnion |
MONDO:0006656 | aortitis | MONDO:0000001 | disease or disorder | UBERON:0000947 | aorta |
See full table here
as for inflammatory_disease_by_site, but refining a specific disease
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/specific_inflammatory_disease_by_site.yaml |
Name | specific_inflammatory_disease_by_site |
Classes | MONDO:0000001, UBERON:0000061, |
Variables | disease (MONDO:0000001), location (UBERON:0000061), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | location | location:label |
---|---|---|---|---|---|
MONDO:0004551 | Meckel diverticulitis | MONDO:0000001 | disease or disorder | UBERON:0003705 | Meckel's diverticulum |
MONDO:0019838 | adenohypophysitis | MONDO:0000001 | disease or disorder | UBERON:0002196 | adenohypophysis |
MONDO:0000261 | adenoiditis | MONDO:0000001 | disease or disorder | UBERON:0001732 | pharyngeal tonsil |
MONDO:0020710 | amnionitis | MONDO:0000001 | disease or disorder | UBERON:0000305 | amnion |
MONDO:0006656 | aortitis | MONDO:0000001 | disease or disorder | UBERON:0000947 | aorta |
See full table here
This is auto-generated. Add your description here Examples: cervical squamous cell carcinoma, skin squamous cell carcinoma, ureter squamous cell carcinoma (63 total)
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/squamous_cell_carcinoma.yaml |
Name | squamous cell carcinoma disease has location X |
Classes | MONDO:0005096, owl:Thing, |
Variables | location (owl:Thing), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | location | location:label |
---|---|---|---|
MONDO:0003490 | ampulla of vater squamous cell carcinoma | UBERON:0004913 | hepatopancreatic ampulla |
MONDO:0004132 | anal canal squamous cell carcinoma | UBERON:0000159 | anal canal |
MONDO:0001470 | anal margin squamous cell carcinoma | UBERON:0012336 | perianal skin |
MONDO:0006082 | anal squamous cell carcinoma | UBERON:0001245 | anus |
MONDO:0004053 | bartholin gland squamous cell carcinoma | UBERON:0000460 | major vestibular gland |
See full table here
A substance abuse that specifies a specific environmental stimulus such as alcohol, cocaine, etc. Examples: alcohol abuse, cocaine abuse
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/substance_abuse.yaml |
Name | substance_abuse |
Classes | MONDO:0002491, BFO:0000040, |
Variables | stimulus (BFO:0000040), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, 0000-0002-7463-6306, |
Examples | mondo |
defined:class | defined:class:label | stimulus | stimulus:label |
---|---|---|---|
MONDO:0003969 | amphetamine abuse | CHEBI:2679 | amphetamine |
MONDO:0004599 | barbiturate abuse | CHEBI:29745 | barbiturate |
MONDO:0004456 | cocaine abuse | CHEBI:27958 | cocaine |
MONDO:0005912 | phencyclidine abuse | CHEBI:8058 | phencyclidine |
See full table here
This pattern should be used for terms in which a gene dysfunction causes a predisposition or susceptibility towards developing a specific disease. This pattern is a sub-pattern of inherited_susceptibility.yaml
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/susceptibility_by_gene.yaml |
Examples - autism, susceptibility to, X-linked 5, bulimia nervosa, susceptibility to, 2, nephrolithiasis susceptibility caused by SLC26A1' | |
Name | susceptibility_by_gene |
Classes | MONDO:0000001, MONDO:0020573, SO:0000704, |
Variables | gene (SO:0000704), disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label | gene | gene:label |
---|---|---|---|---|---|
MONDO:0012153 | Alzheimer disease 9 | MONDO:0015140 | early-onset autosomal dominant Alzheimer disease | http://identifiers.org/hgnc/37 | ABCA7 |
MONDO:0011896 | Parkinson disease 11, autosomal dominant, susceptibility to | MONDO:0008199 | late-onset Parkinson disease | http://identifiers.org/hgnc/11960 | GIGYF2 |
MONDO:0012466 | Parkinson disease 13, autosomal dominant, susceptibility to | MONDO:0005180 | Parkinson disease | http://identifiers.org/hgnc/14348 | HTRA2 |
MONDO:0013653 | Parkinson disease 18, autosomal dominant, susceptibility to | MONDO:0005180 | Parkinson disease | http://identifiers.org/hgnc/3296 | EIF4G1 |
MONDO:0013340 | Parkinson disease 5, autosomal dominant, susceptibility to | MONDO:0005180 | Parkinson disease | http://identifiers.org/hgnc/12513 | UCHL1 |
See full table here
Some diseases exist in both isolated and syndromic forms. For example, aniridia (MONDO_0019172 aniridia, MONDO_0020148'syndromic aniridia' and MONDO_0007119 'isolated aniridia'. Use this pattern to define the syndromic form of a disease when a term exists for the isolated/syndromic-neutral version. In general, this pattern should be used in parallel with isolated. E.g. if you make a term 'syndromic disease, you should also have 'isolated disease' [see pattern here(https://github.com/monarch-initiative/mondo/blob/master/src/patterns/dosdp-patterns/isolated.yaml). Note that the isolated and syndromic forms will be inferred to be disjoint due to the GCI pattern.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/syndromic.yaml |
Name | syndromic |
Classes | MONDO:0021127, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, 0000-0001-5208-3432, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0017263 | inherited ichthyosis syndromic form | MONDO:0015947 | inherited ichthyosis |
MONDO:0016463 | syndromic agammaglobulinemia | MONDO:0015977 | agammaglobulinemia |
MONDO:0002254 | syndromic disease | MONDO:0700096 | human disease or disorder |
MONDO:0015905 | syndromic dyslipidemia | MONDO:0002525 | inherited lipid metabolism disorder |
MONDO:0016565 | syndromic genetic obesity | MONDO:0019182 | inherited obesity |
See full table here
This pattern is meant to be used for chromosomal disorder which consists of the presence of two additional chromosomes of the same type from the normal diploid number. Note that the presence of additional chromosomes refers to the entire chromosome, and not to part of a chromosome.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/tetrasomy.yaml |
Name | tetrasomy |
Classes | MONDO:0030502, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosome | chromosome:label |
---|---|---|---|
MONDO:0019864 | tetrasomy 21 | CHR:9606-chr21 | chromosome 21 (Human) |
See full table here
This pattern is meant to be used for chromosomal disorder which consists of the presence of one additional chromosome from the normal diploid number. Note that the presence of additional chromosome refers to the entire chromosome, and not to part of a chromosome.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/trisomy.yaml |
Name | trisomy |
Classes | MONDO:0700065, GO:0005694, |
Variables | chromosome (GO:0005694), |
Contributors | 0000-0002-4142-7153, |
Examples | mondo |
defined:class | defined:class:label | chromosome | chromosome:label |
---|---|---|---|
MONDO:0022180 | chromosome 16 trisomy | CHR:9606-chr16 | chromosome 16 (Human) |
MONDO:0022757 | chromosome 20 trisomy | CHR:9606-chr20 | chromosome 20 (Human) |
MONDO:0043452 | chromosome 8, trisomy | CHR:9606-chr8 | chromosome 8 (Human) |
MONDO:0018068 | trisomy 13 | CHR:9606-chr13 | chromosome 13 (Human) |
MONDO:0018071 | trisomy 18 | CHR:9606-chr18 | chromosome 18 (Human) |
See full table here
An infectious disease where a pathogen is carried and transmitted by another organism that acts as disease vector. Examples: MONDO_0020601 'mosquito-borne viral encephalitis', MONDO_0017572 'tick-borne encephalitis'
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/vectorBorneDisease.yaml |
Name | vectorBorneDisease |
Classes | MONDO:0005550, OBI:0100026, |
Variables | infectious_disease (MONDO:0005550), vector (OBI:0100026), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | infectious:disease | infectious:disease:label | vector | vector:label |
---|---|---|---|---|---|
MONDO:0020731 | arbovirus infection | MONDO:0005108 | viral infectious disease | NCBITaxon:6943 | Amblyomma americanum |
MONDO:0001620 | louse-borne relapsing fever | MONDO:0019633 | relapsing fever | NCBITaxon:121225 | Pediculus humanus |
MONDO:0020601 | mosquito-borne viral encephalitis | MONDO:0006009 | viral encephalitis | NCBITaxon:7157 | Culicidae |
MONDO:0006941 | rat-bite fever | MONDO:0005113 | bacterial infectious disease | NCBITaxon:10114 | Rattus |
MONDO:0001621 | tick-borne relapsing fever | MONDO:0019633 | relapsing fever | NCBITaxon:6944 | Ixodes |
See full table here
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/x_linked.yaml |
Name | x_linked |
Classes | HP:0001417, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0010583 | Dyggve-Melchior-Clausen syndrome, X-linked | MONDO:0009130 | Dyggve-Melchior-Clausen disease |
MONDO:0010520 | X-linked Alport syndrome | MONDO:0018965 | Alport syndrome |
MONDO:0010586 | X-linked Ehlers-Danlos syndrome | MONDO:0020066 | Ehlers-Danlos syndrome |
MONDO:0010222 | X-linked Opitz G/BBB syndrome | MONDO:0017138 | Opitz G/BBB syndrome |
MONDO:0010556 | X-linked chondrodysplasia punctata | MONDO:0019701 | chondrodysplasia punctata |
See full table here
TBD.
Attribute | Info |
---|---|
IRI | http://purl.obolibrary.org/obo/mondo/patterns/y_linked.yaml |
Name | y_linked |
Classes | HP:0001450, MONDO:0000001, |
Variables | disease (MONDO:0000001), |
Contributors | 0000-0002-6601-2165, |
Examples | mondo |
defined:class | defined:class:label | disease | disease:label |
---|---|---|---|
MONDO:0000428 | Y-linked disease | MONDO:0000001 | disease or disorder |
MONDO:0010761 | retinitis pigmentosa Y-linked | MONDO:0019200 | retinitis pigmentosa |
See full table here