retinitis pigmentosa 41
retinitis pigmentosa that has material basis in mutation in the PROM1 gene on chromosome 4p15
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retinitis pigmentosa 41
Summary
retinitis pigmentosa 41 is a rare disease[1].
Key Facts
- retinitis pigmentosa 41's instance of is recorded as rare disease[2].
- retinitis pigmentosa 41's instance of is recorded as class of disease[3].
- retinitis pigmentosa 41's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 41's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 41's subclass of is recorded as autosomal recessive disease[6].
- retinitis pigmentosa 41's MeSH descriptor ID is recorded as C567422[7].
- retinitis pigmentosa 41's OMIM ID is recorded as 612095[8].
- retinitis pigmentosa 41's Disease Ontology ID is recorded as DOID:0110376[9].
- retinitis pigmentosa 41's genetic association is recorded as PROM1[10].
- retinitis pigmentosa 41's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110376[11].
- retinitis pigmentosa 41's exact match is recorded as http://identifiers.org/doid/DOID:0110376[12].
- retinitis pigmentosa 41's UMLS CUI is recorded as C2677516[13].
- retinitis pigmentosa 41's ICD-10-CM is recorded as H35.5[14].
- retinitis pigmentosa 41's GARD rare disease ID is recorded as 10379[15].
- retinitis pigmentosa 41's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- retinitis pigmentosa 41's Mondo ID is recorded as MONDO_0012796[17].
- retinitis pigmentosa 41's UniProt disease ID is recorded as DI-00995[18].