retinitis pigmentosa 23
retinitis pigmentosa that has material basis in mutation in the OFD1 gene on chromosome Xp22
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retinitis pigmentosa 23
Summary
retinitis pigmentosa 23 is a rare disease[1].
Key Facts
- retinitis pigmentosa 23's instance of is recorded as rare disease[2].
- retinitis pigmentosa 23's instance of is recorded as class of disease[3].
- retinitis pigmentosa 23's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 23's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 23's subclass of is recorded as X-linked recessive disease[6].
- retinitis pigmentosa 23's OMIM ID is recorded as 300424[7].
- retinitis pigmentosa 23's Disease Ontology ID is recorded as DOID:0110412[8].
- retinitis pigmentosa 23's genetic association is recorded as OFD1[9].
- retinitis pigmentosa 23's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110412[10].
- retinitis pigmentosa 23's exact match is recorded as http://identifiers.org/doid/DOID:0110412[11].
- retinitis pigmentosa 23's UMLS CUI is recorded as C1845542[12].
- retinitis pigmentosa 23's UMLS CUI is recorded as C1419610[13].
- retinitis pigmentosa 23's ICD-10-CM is recorded as H35.5[14].
- retinitis pigmentosa 23's GARD rare disease ID is recorded as 10391[15].
- retinitis pigmentosa 23's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- retinitis pigmentosa 23's Mondo ID is recorded as MONDO_0010320[17].
- retinitis pigmentosa 23's UniProt disease ID is recorded as DI-04060[18].