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add ORDO xref to cornea plana #7590

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11 changes: 7 additions & 4 deletions src/ontology/mondo-edit.obo
Original file line number Diff line number Diff line change
Expand Up @@ -9126,15 +9126,18 @@ property_value: seeAlso "https://rarediseases.info.nih.gov/diseases/12893/combin
[Term]
id: MONDO:0000733
name: cornea plana
def: "A rare developmental defect of the eye characterized by usually bilateral absence of the normal protrusion of the cornea from the sclera, the corneal curvature being the same as that of the adjacent sclera. Most patients develop hyperopia, hazy corneal limbus, and arcus lipoides at an early age. The condition may present as an autosomal dominant or an autosomal recessive form, with the latter showing more severe signs and symptoms (such as a round and opaque thickening located centrally in the cornea) and more frequent association with other ocular anomalies." [Orphanet:53691]
synonym: "congenital cornea plana" EXACT [Orphanet:53691]
synonym: "flat cornea" EXACT [DOID:0060287]
xref: DOID:0060287 {source="MONDO:equivalentTo"}
xref: HP:0007720 {source="DOID:0060287", source="MONDO:otherHierarchy"}
xref: ICD10CM:Q13.4 {source="DOID:0060287"}
xref: ICD10CM:Q13.4 {source="DOID:0060287", source="MONDO:equivalentTo", source="Orphanet:53691"}
xref: OMIMPS:121400 {source="MONDO:equivalentTo", source="https://orcid.org/0000-0002-6601-2165"}
xref: Orphanet:53691 {source="DOID:0060287"}
xref: Orphanet:53691 {source="DOID:0060287", source="MONDO:equivalentTo"}
xref: SCTID:204145006 {source="MONDO:equivalentTo"}
is_a: MONDO:0000942 {source="DOID:0060287"} ! corneal disorder
relationship: has_characteristic MONDO:0021152 {source="OMIMPS:121400"} ! inherited
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7573" xsd:anyURI

[Term]
id: MONDO:0000734
Expand Down Expand Up @@ -401580,14 +401583,14 @@ name: obsolete congenital cornea plana
subset: gard_rare {source="GARD:16657"}
subset: nord_rare {source="MONDO:NORD"}
xref: GARD:16657 {source="MONDO:obsoleteEquivalent", source="Orphanet:53691"}
xref: ICD10CM:Q13.4 {source="Orphanet:53691/attributed", source="Orphanet:53691/ntbt", source="Orphanet:53691"}
xref: Orphanet:53691 {source="MONDO:obsoleteEquivalent"}
property_value: IAO:0000231 OMO:0001000 {source="MONDO:excludeGrouping"}
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/4069" xsd:anyURI
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/5114" xsd:anyURI
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/6744" xsd:anyURI
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/6877" xsd:anyURI
property_value: IAO:0000233 "https://github.com/monarch-initiative/mondo/issues/7573" xsd:anyURI
is_obsolete: true
replaced_by: MONDO:0000733

[Term]
id: MONDO:0018889
Expand Down
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