Matches in Ubergraph for { <http://purl.obolibrary.org/obo/MONDO_0020207> ?p ?o ?g. }
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- MONDO_0020207 IAO_0000115 "OBSOLETE. Rare isolated myopia is a rare, genetic, refraction anomaly disorder characterized by non-syndromic severe myopia, which may be associated with cataract and vitreoretinal degeneration (retinal detachment) that may lead to blindness." @default.
- MONDO_0020207 IAO_0000233 "https://github.com/monarch-initiative/mondo/issues/254" @default.
- MONDO_0020207 IAO_0100001 "MONDO:0001384" @default.
- MONDO_0020207 normalizedInformationContent "100" @default.
- MONDO_0020207 referenceCount "1" @default.
- MONDO_0020207 hasDbXref "GARD:16859" @default.
- MONDO_0020207 hasDbXref "Orphanet:98619" @default.
- MONDO_0020207 hasDbXref "UMLS:C0027092" @default.
- MONDO_0020207 hasDbXref "UMLS:CN924920" @default.
- MONDO_0020207 id "MONDO:0020207" @default.
- MONDO_0020207 inSubset gard_rare @default.
- MONDO_0020207 inSubset nord_rare @default.
- MONDO_0020207 inSubset ordo_disease @default.
- MONDO_0020207 inSubset rare @default.
- MONDO_0020207 type Class @default.
- MONDO_0020207 isDefinedBy mondo.owl @default.
- MONDO_0020207 label "obsolete rare isolated myopia" @default.
- MONDO_0020207 subClassOf MONDO_0020207 @default.
- MONDO_0020207 subClassOf Thing @default.
- MONDO_0020207 deprecated "true" @default.
- MONDO_0020207 exactMatch CN924920 @default.
- MONDO_0020207 exactMatch Orphanet_98619 @default.