retinitis pigmentosa 31
retinitis pigmentosa that has material basis in mutation in the TOPORS gene on chromosome 9p21
Press Enter · cited answer in seconds
0 sources
Summary
retinitis pigmentosa 31 is a rare disease[1].
Key Facts
- retinitis pigmentosa 31's instance of is recorded as rare disease[2].
- retinitis pigmentosa 31's instance of is recorded as class of disease[3].
- retinitis pigmentosa 31's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 31's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 31's MeSH descriptor ID is recorded as C563685[6].
- retinitis pigmentosa 31's OMIM ID is recorded as 609923[7].
- retinitis pigmentosa 31's Disease Ontology ID is recorded as DOID:0110391[8].
- retinitis pigmentosa 31's genetic association is recorded as TOPORS[9].
- retinitis pigmentosa 31's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110391[10].
- retinitis pigmentosa 31's exact match is recorded as http://identifiers.org/doid/DOID:0110391[11].
- retinitis pigmentosa 31's UMLS CUI is recorded as C1835923[12].
- retinitis pigmentosa 31's ICD-10-CM is recorded as H35.5[13].
- retinitis pigmentosa 31's GARD rare disease ID is recorded as 10396[14].
- retinitis pigmentosa 31's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- retinitis pigmentosa 31's Mondo ID is recorded as MONDO_0012367[16].
- retinitis pigmentosa 31's UniProt disease ID is recorded as DI-00991[17].