retinitis pigmentosa 39
retinitis pigmentosa that has material basis in mutation in the USH2A gene on chromosome 1q41
Press Enter · cited answer in seconds
0 sources
retinitis pigmentosa 39
Summary
retinitis pigmentosa 39 is a rare disease[1].
Key Facts
- retinitis pigmentosa 39's instance of is recorded as rare disease[2].
- retinitis pigmentosa 39's instance of is recorded as class of disease[3].
- retinitis pigmentosa 39's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 39's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 39's OMIM ID is recorded as 613809[6].
- retinitis pigmentosa 39's Disease Ontology ID is recorded as DOID:0110360[7].
- retinitis pigmentosa 39's genetic association is recorded as USH2A[8].
- retinitis pigmentosa 39's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110360[9].
- retinitis pigmentosa 39's exact match is recorded as http://identifiers.org/doid/DOID:0110360[10].
- retinitis pigmentosa 39's UMLS CUI is recorded as C3151138[11].
- retinitis pigmentosa 39's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 39's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 39's Mondo ID is recorded as MONDO_0013436[14].
- retinitis pigmentosa 39's UniProt disease ID is recorded as DI-00994[15].