[mass Obsolete] Entire list of mass obsoletion candidates

[nicolevasilevsky]

The Mondo development team is working on obsoleting the following terms as part of the mass obsoletion effort (from Sept - Nov 2023)

mondo_id	label
MONDO:0017447	congenital absence/hypoplasia of thumb
MONDO:0008347	idiopathic and/or familial pulmonary arterial hypertension
MONDO:0008406	autosomal recessive Emery-Dreifuss muscular dystrophy
MONDO:0013742	familial mesial temporal lobe epilepsy with febrile seizures
MONDO:0014753	autosomal recessive optic atrophy
MONDO:0015088	autosomal dominant pure spastic paraplegia
MONDO:0015089	autosomal recessive complex spastic paraplegia
MONDO:0015090	autosomal recessive pure spastic paraplegia
MONDO:0015135	primary immunodeficiency due to a genetic defect in innate immunity
MONDO:0015144	brain inflammatory disease
MONDO:0015145	neurovascular malformation
MONDO:0015179	intestinal disease due to vitamin absorption anomaly
MONDO:0015180	intestinal disease due to fat malabsorption
MONDO:0015207	non-syndromic esophageal malformation
MONDO:0015209	non-syndromic gastroduodenal malformation
MONDO:0015217	non-syndromic developmental defect of the eye
MONDO:0015219	non-syndromic central nervous system malformation
MONDO:0015221	non-syndromic respiratory or mediastinal malformation
MONDO:0015227	non-syndromic limb malformation
MONDO:0015330	overgrowth/obesity syndrome
MONDO:0015334	branchial arch or oral-acral syndrome
MONDO:0015359	autosomal dominant hereditary demyelinating motor and sensory neuropathy
MONDO:0015361	autosomal recessive hereditary demyelinating motor and sensory neuropathy
MONDO:0015365	autosomal dominant hereditary sensory and autonomic neuropathy
MONDO:0015366	autosomal recessive hereditary sensory and autonomic neuropathy
MONDO:0015368	neuro-ophthalmological disease
MONDO:0015385	external auditory canal aplasia/hypoplasia
MONDO:0015412	median facial cleft
MONDO:0015415	oblique facial cleft
MONDO:0015418	lateral facial cleft
MONDO:0015478	paramedian facial cleft
MONDO:0015482	otomandibular dysplasia
MONDO:0015485	primary hereditary glaucoma
MONDO:0015488	predominantly large-vessel vasculitis
MONDO:0015489	predominantly medium-vessel vasculitis
MONDO:0015490	predominantly small-vessel vasculitis
MONDO:0015499	paralytic facial malformation
MONDO:0015503	nose and cavum anomaly
MONDO:0015504	larynx anomaly
MONDO:0015505	tracheal anomaly
MONDO:0015586	benign familial mesial temporal lobe epilepsy
MONDO:0015591	limbic encephalitis associated with antibodies to cell membrane antigens
MONDO:0015619	non-syndromic urogenital tract malformation
MONDO:0015679	autosomal thrombocytopenia with normal platelets
MONDO:0015823	primary immunodeficiency due to a defect in adaptive immunity
MONDO:0015828	uterovaginal malformation
MONDO:0015829	non-syndromic uterovaginal malformation
MONDO:0015837	Unicervical bicornuate uterus
MONDO:0015902	major hypertriglyceridemia
MONDO:0015932	non-syndromic urogenital tract malformation of female
MONDO:0015933	non-syndromic urogenital tract malformation of male
MONDO:0016034	cleft lip with or without cleft palate
MONDO:0016109	autosomal recessive distal myopathy
MONDO:0016114	bulbospinal muscular atrophy of childhood
MONDO:0016115	bulbospinal muscular atrophy of adulthood
MONDO:0016149	qualitative or quantitative defects of merosin
MONDO:0016150	qualitative or quantitative defects of integrin alpha-7
MONDO:0016152	qualitative or quantitative defects of calpain
MONDO:0016154	qualitative or quantitative defects of myotubularin
MONDO:0016157	qualitative or quantitative defects of fukutin
MONDO:0016173	non-paraneoplastic sensory ganglionopathy
MONDO:0016174	paraneoplastic sensory ganglionopathy
MONDO:0016182	qualitative or quantitative defects of protein O-mannose beta1, 2N-acetylglucosaminyltransferase
MONDO:0016183	qualitative or quantitative defects of protein glycosyltransferase-like
MONDO:0016196	qualitative or quantitative defects of emerin
MONDO:0016200	qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
MONDO:0016201	qualitative or quantitative defects of myotilin
MONDO:0016221	temporomandibular joint anomaly
MONDO:0016224	autosomal dominant proximal spinal muscular atrophy
MONDO:0016229	hereditary vascular anomaly
MONDO:0016230	simple vascular malformation
MONDO:0016348	non-genetic cardiac rhythm disease
MONDO:0016355	semilobar holoprosencephaly
MONDO:0016361	isolated hereditary giant platelet disorder
MONDO:0016409	primary congenital hypothyroidism
MONDO:0016428	multiple sclerosis variant
MONDO:0016493	variant of Guillain-Barre syndrome
MONDO:0016494	regional variant of Guillain-Barre syndrome
MONDO:0016495	functional variant of Guillain-Barre syndrome
MONDO:0016518	isolated punctate palmoplantar keratoderma
MONDO:0016520	isolated Klippel-Feil syndrome
MONDO:0016536	autosomal recessive lymphoproliferative disease
MONDO:0016589	progressive cerebello-cerebral atrophy
MONDO:0016592	non-hereditary degenerative ataxia
MONDO:0016599	autosomal dominant secondary polycythemia
MONDO:0016647	autosomal recessive Stickler syndrome
MONDO:0016678	maternal disease-related embryofetopathy
MONDO:0016744	primary melanocytic tumor of central nervous system
MONDO:0016794	maternally-inherited mitochondrial myopathy
MONDO:0016797	multiple mitochondrial DNA deletion syndrome
MONDO:0016803	unspecified inborn mitochondrial disorder
MONDO:0016805	isolated oxidative phosphorylation complex disorder
MONDO:0016815	Leigh syndrome with leukodystrophy
MONDO:0016816	Leigh syndrome with nephrotic syndrome
MONDO:0017027	primary interstitial lung disease specific to adulthood
MONDO:0017036	Langerhans cell histiocytosis in childhood and adulthood
MONDO:0017059	neural tube closure defect
MONDO:0017090	midline cerebral malformation
MONDO:0017131	hereditary cardiac anomaly
MONDO:0017173	non-syndromic male infertility due to sperm motility disorder
MONDO:0017218	septopreoptic holoprosencephaly
MONDO:0017270	autosomal ichthyosis syndrome
MONDO:0017302	qualitative or quantitative defects of troponin
MONDO:0017421	non-syndromic terminal limb defects
MONDO:0017429	joint formation defects
MONDO:0017430	non-syndromic congenital joint dislocations
MONDO:0017431	non-syndromic limb overgrowth
MONDO:0017448	congenital absence/hypoplasia of fingers excluding thumb
MONDO:0017629	sodium channelopathy-related small fiber neuropathy
MONDO:0017651	primary myoclonus
MONDO:0017656	motor stereotypies
MONDO:0017676	marginal papular palmoplantar keratoderma
MONDO:0017709	disorder of lipid absorption and transport
MONDO:0017710	congenital systemic veins anomaly
MONDO:0017742	disorder of O-xylosylglycan synthesis
MONDO:0017743	disorder of O-N-acetylgalactosaminylglycan synthesis
MONDO:0017744	disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis
MONDO:0017745	disorder of O-mannosylglycan synthesis
MONDO:0017828	primary renal tubular acidosis
MONDO:0017912	X-linked pure spastic paraplegia
MONDO:0017914	pure or complex autosomal dominant spastic paraplegia
MONDO:0017915	pure or complex autosomal recessive spastic paraplegia
MONDO:0017916	pure or complex X-linked spastic paraplegia
MONDO:0017950	microcephalic primordial dwarfism
MONDO:0017954	pyogenic autoinflammatory syndrome
MONDO:0018112	isolated scaphocephaly
MONDO:0018113	isolated plagiocephaly
MONDO:0018144	congenital myasthenic syndromes with glycosylation defect
MONDO:0018185	congenital anomaly of the great veins
MONDO:0018191	tumor of testis and paratestis
MONDO:0018222	X-linked intellectual disability due to GRIA3 anomalies
MONDO:0018240	TRPV4-related bone disorder
MONDO:0018241	primary short bowel syndrome
MONDO:0018277	congenital muscular dystrophy with cerebellar involvement
MONDO:0018279	congenital muscular dystrophy without intellectual disability
MONDO:0018283	primary qualitative or quantitative defects of alpha-dystroglycan
MONDO:0018292	congenital disorder of glycosylation-related bone disorder
MONDO:0018318	disorder of asparagine metabolism
MONDO:0018329	persistent combined dystonia
MONDO:0018337	severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
MONDO:0018384	avascular necrosis of genetic origin
MONDO:0018385	osteochondrosis of genetic origin
MONDO:0018393	male infertility with azoospermia or oligozoospermia due to single gene mutation
MONDO:0018451	X-linked distal hereditary motor neuropathy
MONDO:0018529	qualitative or quantitative defects of Torsin-1A-interacting protein 1
MONDO:0018550	spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder
MONDO:0018575	microcephalic primordial dwarfism-insulin resistance syndrome
MONDO:0018579	disorder of ketone body transport
MONDO:0018580	PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
MONDO:0018640	secondary vasculitis
MONDO:0018731	lethal multiple congenital anomalies/dysmorphic syndrome
MONDO:0018743	immune-mediated acquired neuromuscular junction disease
MONDO:0018745	superficial pemphigus
MONDO:0018771	congenital anomaly of ventricular septum
MONDO:0018788	COL4A1 or COL4A2-related cerebral small vessel disease
MONDO:0018791	Moyomoya angiopathy
MONDO:0019044	tumor of hematopoietic and lymphoid tissues
MONDO:0019054	congenital limb malformation
MONDO:0019063	vascular anomaly
MONDO:0019138	bleeding diathesis due to a collagen receptor defect
MONDO:0019176	trichorhinophalangeal syndrome type I or III
MONDO:0019224	inborn disorder of gamma-aminobutyric acid metabolism
MONDO:0019227	inborn disorder of glycerol metabolism
MONDO:0019277	epidermal appendage anomaly
MONDO:0019286	sebaceous gland anomaly
MONDO:0019486	myoclonic epilepsy of infancy
MONDO:0019513	esophageal malformation
MONDO:0019541	non-infectious posterior uveitis
MONDO:0019599	primary lipodystrophy
MONDO:0019688	sulfation-related bone disorder
MONDO:0019689	perlecan-related bone disorder
MONDO:0019692	multiple epiphyseal dysplasia and pseudoachondroplasia
MONDO:0019693	multiple metaphyseal dysplasia
MONDO:0019697	mesomelic and rhizo-mesomelic dysplasia
MONDO:0019699	slender bone dysplasia
MONDO:0019712	patellar dysostosis
MONDO:0019713	non-syndromic limb reduction defect
MONDO:0019714	non-syndromic polydactyly, syndactyly and/or hyperphalangy
MONDO:0019718	lethal chondrodysplasia
MONDO:0019720	non-syndromic renal or urinary tract malformation
MONDO:0019724	secondary glomerular disease
MONDO:0019743	nephropathy secondary to a storage or other metabolic disease
MONDO:0019758	midline interhemispheric variant of holoprosencephaly
MONDO:0019831	congenital anomaly of the coronary sinus
MONDO:0019844	pituitary hormone deficiency secondary to storage disease
MONDO:0019998	gastroduodenal malformation
MONDO:0019999	intestinal malformation
MONDO:0020018	cranial malformation
MONDO:0020019	digestive tract malformation
MONDO:0020020	visceral malformation of the liver, biliary tract, pancreas or spleen
MONDO:0020069	chronic encephalitis
MONDO:0020081	macrophage or histiocytic tumor
MONDO:0020084	lymphoproliferative disease associated with primary immune disease
MONDO:0020093	autosomal dominant isolated diffuse palmoplantar keratoderma
MONDO:0020096	autosomal recessive isolated diffuse palmoplantar keratoderma
MONDO:0020130	malformation of the cerebellar vermis
MONDO:0020131	malformation of the cerebellar hemispheres
MONDO:0020133	posterior fossa malformation
MONDO:0020145	developmental defect of the eye
MONDO:0020146	major induction processes eye anomaly
MONDO:0020154	microblepharon-ablephara syndrome
MONDO:0020155	eyelid border anomaly
MONDO:0020160	secondary entropion
MONDO:0020162	secondary ectropion
MONDO:0020163	canthal anomaly
MONDO:0020164	epicanthal fold
MONDO:0020167	malposition of external canthus
MONDO:0020174	precancerous lesion of palpebral epidermis
MONDO:0020178	palpebral lentiginosis
MONDO:0020193	secretory apparatus of the lacrimal system anomaly
MONDO:0020195	excretory apparatus of the lacrimal system anomaly
MONDO:0020203	pigmented conjunctival lesion
MONDO:0020205	bulbar conjunctival dermoid or conjunctival dermolipoma
MONDO:0020216	secondary dysgenetic glaucoma
MONDO:0020235	lens size anomaly
MONDO:0020237	lens shape anomaly
MONDO:0020275	oculocutaneous or ocular albinism
MONDO:0020284	heart position anomaly
MONDO:0020285	transposition of the great arteries and conotruncal cardiac anomaly
MONDO:0020287	pulmonary artery or pulmonary branch anomaly
MONDO:0020339	X-linked complex spastic paraplegia
MONDO:0020345	presynaptic congenital myasthenic syndrome
MONDO:0020506	ovarioleukodystrophy
MONDO:0020524	primary parathyroid hyperplasia
MONDO:0020537	occupational allergic alveolitis
MONDO:0022397	retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene
MONDO:0022399	retinal ciliopathy due to mutation in the RPGR gene
MONDO:0022400	retinal ciliopathy due to mutation in the RPGRIP gene
MONDO:0022404	retinal ciliopathy due to mutation in Usher gene
MONDO:0022405	retinal ciliopathy due to mutation in nephronophthisis gene
MONDO:0022407	retinal ciliopathy due to mutation in Bardet-Biedl gene
MONDO:0022409	nephropathy-associated ciliopathy
MONDO:0024471	non-inflammatory vasculopathy
MONDO:0034024	kyphoscoliotic Ehlers-Danlos syndrome
MONDO:0034217	resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta
MONDO:0034669	non-syndromic preaxial polydactyly
MONDO:0034670	non-syndromic postaxial polydactyly
MONDO:0034671	non-syndromic complex polydactyly
MONDO:0034872	large granular lymphocyte leukemia
MONDO:0035002	isolated inherited retinal disorder
MONDO:0035014	primary orthostatic disorder
MONDO:0035075	secondary early-onset glaucoma of genetic origin
MONDO:0035162	PIK3CA-related overgrowth syndrome
MONDO:0035561	sporadic human prion disease
MONDO:0036042	KAT6B-related multiple congenital anomalies syndrome
MONDO:0044655	c12orf65-related combined oxidative phosphorylation defect
MONDO:0800084	primary bone dysplasia with increased bone density
MONDO:0800086	primary bone dysplasia with multiple joint dislocations
MONDO:0800087	type 11 collagen-related bone disorder
MONDO:0800089	primary bone dysplasia with disorganized development of skeletal components
MONDO:0800091	overgrowth or tall stature syndrome with skeletal involvement
MONDO:0017423	split hand or/and split foot malformation
MONDO:0015111	gastroesophageal disease
MONDO:0015130	acquired chronic primary adrenal insufficiency
MONDO:0015132	immunodeficiency predominantly affecting antibody production
MONDO:0015133	quantitative and/or qualitative congenital phagocyte defect
MONDO:0015141	disorder of medulla oblongata
MONDO:0015178	congenital intestinal transport defect
MONDO:0015208	syndromic esophageal malformation
MONDO:0015210	syndromic gastroduodenal malformation
MONDO:0015211	non-syndromic intestinal malformation
MONDO:0015212	syndromic intestinal malformation
MONDO:0015213	non-syndromic visceral malformation
MONDO:0015214	syndromic visceral malformation
MONDO:0015222	syndromic respiratory or mediastinal malformation
MONDO:0015310	syndromic optic nerve hypoplasia
MONDO:0015323	teratogenic Pierre Robin syndrome
MONDO:0015337	isolated craniosynostosis
MONDO:0015338	syndromic craniosynostosis
MONDO:0015470	familial isolated dilated cardiomyopathy
MONDO:0015497	hypoglossia/aglossia
MONDO:0015508	hereditary parenchymatous liver disease
MONDO:0015617	hereditary gastro-esophageal disease
MONDO:0015620	syndromic urogenital tract malformation
MONDO:0015668	hereditary dentin defect
MONDO:0015682	primary peritoneal tumor
MONDO:0015683	primary malignant peritoneal tumor
MONDO:0015765	congenital myopathy with cores
MONDO:0015777	adult hypothyroidism
MONDO:0015778	syndromic hypothyroidism
MONDO:0015817	aggressive primary cutaneous T-cell lymphoma
MONDO:0015818	aggressive primary cutaneous B-cell lymphoma
MONDO:0015822	acquired neutropenia
MONDO:0015846	syndromic uterovaginal malformation
MONDO:0015852	excess breast volume or number
MONDO:0015853	deficient breast volume or number
MONDO:0015860	anomaly of puberty or/and menstrual cycle
MONDO:0015915	cerebellar malformation
MONDO:0015921	ARX-related epileptic encephalopathy
MONDO:0015930	respiratory malformation
MONDO:0015950	inherited skin tumor
MONDO:0015961	hereditary head and neck malformation
MONDO:0015975	hyper-IgM syndrome with susceptibility to opportunistic infections
MONDO:0015976	hyper-IgM syndrome without susceptibility to opportunistic infections
MONDO:0016054	cerebral malformation
MONDO:0016072	anomaly of puberty or/and menstrual cycle of genetic origin
MONDO:0016116	generalized bulbospinal muscular atrophy
MONDO:0016121	congenital myotonia
MONDO:0016125	infectious, fungal or parasitic myopathy
MONDO:0016169	chronic acquired demyelinating polyneuropathy
MONDO:0016170	chronic polyradiculoneuropathy
MONDO:0016172	acquired sensory ganglionopathy
MONDO:0016179	acquired amyloid peripheral neuropathy
MONDO:0016352	idiopathic inherited hypercalciuria
MONDO:0016375	acquired peripheral movement disorder
MONDO:0016434	acquired dermis elastic tissue disorder
MONDO:0016524	congenital vascular bone syndrome
MONDO:0016565	syndromic genetic obesity
MONDO:0016579	dominant hypophosphatemia with nephrolithiasis or osteoporosis
MONDO:0016701	oligoastrocytic tumor
MONDO:0016708	embryonal tumor of neuroepithelial tissue
MONDO:0016721	pineal tumor of neuroepithelial tissue
MONDO:0016726	neuronal tumor
MONDO:0016738	primary germ cell tumor of central nervous system
MONDO:0016756	inherited nervous system cancer-predisposing syndrome
MONDO:0016899	Duchenne and Becker muscular dystrophy
MONDO:0016980	ATR-X-related syndrome
MONDO:0017049	hypomyelination neuropathy-arthrogryposis syndrome
MONDO:0017057	hereditary thrombocytopenia with normal platelets
MONDO:0017104	central nervous system cystic malformation
MONDO:0017114	global cerebellar malformation
MONDO:0017127	inherited soft tissue tumor
MONDO:0017128	inherited digestive tract tumor
MONDO:0017129	inherited cardiac tumor
MONDO:0017132	hereditary ATTR amyloidosis
MONDO:0017234	inherited prion disease
MONDO:0017240	acrodysostosis with multiple hormone resistance
MONDO:0017241	AP4-related intellectual disability and spastic paraplegia
MONDO:0017262	inherited non-syndromic ichthyosis
MONDO:0017263	inherited ichthyosis syndromic form
MONDO:0017397	constitutional dyserythropoietic anemia
MONDO:0017420	intercalary limb defects
MONDO:0017422	adactyly of hand
MONDO:0017428	congenital deformities of fingers
MONDO:0017581	familial infantile gigantism
MONDO:0017667	isolated diffuse palmoplantar keratoderma
MONDO:0017670	autosomal dominant diffuse mutilating palmoplantar keratoderma
MONDO:0017673	isolated focal palmoplantar keratoderma
MONDO:0017756	disorder of pterin metabolism
MONDO:0017891	inherited renal cancer-predisposing syndrome
MONDO:0017922	deafness-onychodystrophy syndrome
MONDO:0017955	granulomatous autoinflammatory syndrome
MONDO:0017961	46,XX disorder of gonadal development
MONDO:0017962	46,XX disorder of sex development induced by fetoplacental androgens excess
MONDO:0017963	46,XX disorder of sex development induced by endogenous maternal-derived androgen
MONDO:0017964	46,XX disorder of sex development induced by exogenous maternal-derived androgen
MONDO:0017966	46,XY disorder of gonadal development
MONDO:0017969	46,XY disorder of sex development of endocrine origin
MONDO:0017974	46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors
MONDO:0018114	isolated brachycephaly
MONDO:0018187	hereditary syndromic Pierre Robin syndrome
MONDO:0018188	hereditary intestinal polyposis
MONDO:0018239	aggrecan-related bone disorder
MONDO:0018246	homozygous 2p21 microdeletion syndrome
MONDO:0018262	fetal anticonvulsant syndrome
MONDO:0018340	hereditary isolated aplastic anemia
MONDO:0018454	dysostosis of genetic origin
MONDO:0018496	ARX-related encephalopathy-brain malformation spectrum
MONDO:0018532	adenocarcinoma of liver and intrahepatic biliary tract
MONDO:0018538	inherited digestive cancer-predisposing syndrome
MONDO:0018562	hereditary otorhinolaryngological malformation
MONDO:0018574	intellectual disability-expressive aphasia-facial dysmorphism syndrome
MONDO:0018701	congenital nemaline myopathy
MONDO:0018720	common cystic lymphatic malformation
MONDO:0018758	familial patent arterial duct
MONDO:0018779	hypercontractile muscle stiffness syndrome
MONDO:0018782	type 1 interferonopathy
MONDO:0018796	isolated constitutional thrombocytopenia
MONDO:0018831	HTRA1-related cerebral small vessel disease
MONDO:0018888	congenital cornea plana
MONDO:0018916	isolated anorectal malformation
MONDO:0019126	intractable diarrhea of infancy
MONDO:0019150	familial isolated restrictive cardiomyopathy
MONDO:0019213	cerebral organic aciduria
MONDO:0019271	acrokeratoderma
MONDO:0019281	isolated genetic hair shaft abnormality
MONDO:0019292	dermis elastic tissue disorder
MONDO:0019505	hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome
MONDO:0019520	syndromic lymphedema
MONDO:0019593	46,XX disorder of sex development induced by fetal androgens excess
MONDO:0019597	46,XY disorder of sex development due to isolated 17,20-lyase deficiency
MONDO:0019608	46,XX disorder of sex development induced by maternal-derived androgen
MONDO:0019619	duplication of the esophagus
MONDO:0019723	disease of glomerular basement membrane
MONDO:0019800	chronic hepatic porphyria
MONDO:0019816	anomaly of the tricuspid subvalvular apparatus
MONDO:0019822	arterial duct anomaly
MONDO:0019826	abnormal origin or aberrant course of coronary artery
MONDO:0019837	atrial appendage anomaly
MONDO:0020023	respiratory or mediastinal malformation
MONDO:0020039	46,XX disorder of sex development induced by androgens excess
MONDO:0020118	dense granule disease
MONDO:0020125	acquired neuromuscular junction disease
MONDO:0020132	cranial nerve and nuclear aplasia
MONDO:0020144	cerebrovascular dementia
MONDO:0020147	anophthalmia-microphthalmia syndrome
MONDO:0020148	syndromic aniridia
MONDO:0020156	syndromic ankyloblepharon
MONDO:0020157	syndromic palpebral coloboma
MONDO:0020158	eyelids malposition disorder
MONDO:0020165	syndromic epicanthus
MONDO:0020176	palpebral sebaceous gland tumor
MONDO:0020177	pigmented palpebral tumor
MONDO:0020180	palpebral piliary tumor
MONDO:0020181	mesenchymatous palpebral tumor
MONDO:0020194	congenital alacrima
MONDO:0020196	anomaly of the secretory and excretory apparatus of the lacrimal system
MONDO:0020197	EEC syndrome and related syndrome
MONDO:0020210	syndromic hyperopia
MONDO:0020211	syndromic keratoconus
MONDO:0020215	syndromic corneal dystrophy
MONDO:0020219	corneogoniodysgenesis
MONDO:0020238	inherited vitreous-retinal disease
MONDO:0020240	syndromic retinitis pigmentosa
MONDO:0020256	congenital trochlear nerve palsy
MONDO:0020286	aortic malformation
MONDO:0020288	atrioventricular valve anomaly
MONDO:0020293	ascending aorta anomaly
MONDO:0020294	atrial defect and interatrial communication
MONDO:0020343	alpha-crystallinopathy
MONDO:0020346	synaptic congenital myasthenic syndrome
MONDO:0020375	coralliform cataract
MONDO:0020392	discrete fixed membranous subaortic stenosis
MONDO:0021034	hereditary alopecia
MONDO:0025511	inherited neuroendocrine tumor
MONDO:0028618	gastroenteric neuroendocrine neoplasm
MONDO:0033947	hereditary angioedema with normal C1Inh
MONDO:0034661	syndromic biliary atresia
MONDO:0034901	ATP13A2-related parkinsonism
MONDO:0034954	syndromic vitreoretinopathy
MONDO:0035645	inherited gynecological cancer-predisposing syndrome
MONDO:0035682	fibrous dysplasia/McCune-Albright syndrome
MONDO:0035684	epidermolysis bullosa simplex without extracutaneous involvement
MONDO:0035685	epidermolysis bullosa simplex with extracutaneous involvement
MONDO:0035689	syndrome of reduced sensitivity to thyroid hormone
MONDO:0036192	EN1-related dorsoventral syndrome
MONDO:0038268	autoimmune neurological channelopathy
MONDO:0100189	apolipoprotein A-I deficiency
MONDO:0100343	antenatal Bartter syndrome
MONDO:0800075	dysostosis with predominant vertebral with and without costal involvement
MONDO:0800085	dysostosis with predominant craniofacial involvement
MONDO:0800090	ectrodactyly with and without other manifestations
MONDO:0800092	hereditary inflammatory or rheumatoid-like osteoarthropathy
MONDO:0800093	dysostosis with brachydactyly without extraskeletal manifestations
MONDO:0800094	dysostosis with brachydactyly with extraskeletal manifestations
MONDO:0800095	syndrome with synostosis or other joint formation defect
MONDO:0957001	hereditary mixed dermis disorder
MONDO:0957009	hereditary posterior fossa malformation
MONDO:0957024	hereditary 46,XX disorder of sex development
MONDO:0957025	hereditary 46,XY disorder of sex development
MONDO:0015509	hereditary biliary tract disease
MONDO:0015182	congenital enteropathy involving intestinal mucosa development
MONDO:0015360	autosomal dominant hereditary axonal motor and sensory neuropathy
MONDO:0018775	axonal hereditary motor and sensory neuropathy
MONDO:0016667	sickle cell disease associated with an other hemoglobin anomaly
MONDO:0017146	sickle cell disease and related diseases
MONDO:0016513	alpha-thalassemia-related diseases
MONDO:0017144	alpha-thalassemia and related diseases
MONDO:0017030	interstitial lung disease in childhood and adulthood
MONDO:0017031	primary interstitial lung disease in childhood and adulthood
MONDO:0017034	secondary interstitial lung disease in childhood and adulthood
MONDO:0017040	exposure-related interstitial lung disease
MONDO:0017760	disorder of other vitamins and cofactors metabolism and transport
MONDO:0015246	syndromic anorectal malformation
MONDO:0015979	hereditary predisposition to infections

[nicolevasilevsky]

@sabrinatoro this can be closed, yes?

[sabrinatoro]

yes, i think it can. Thank you!