retinitis pigmentosa 50
retinitis pigmentosa that has material basis in mutation in the BEST1 gene on chromosome 11q13
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retinitis pigmentosa 50
Summary
retinitis pigmentosa 50 is a rare disease[1].
Key Facts
- retinitis pigmentosa 50's instance of is recorded as rare disease[2].
- retinitis pigmentosa 50's instance of is recorded as class of disease[3].
- retinitis pigmentosa 50's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 50's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 50's subclass of is recorded as autosomal recessive disease[6].
- retinitis pigmentosa 50's MeSH descriptor ID is recorded as C567712[7].
- retinitis pigmentosa 50's OMIM ID is recorded as 613194[8].
- retinitis pigmentosa 50's Disease Ontology ID is recorded as DOID:0110396[9].
- retinitis pigmentosa 50's genetic association is recorded as BEST1[10].
- retinitis pigmentosa 50's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110396[11].
- retinitis pigmentosa 50's exact match is recorded as http://identifiers.org/doid/DOID:0110396[12].
- retinitis pigmentosa 50's UMLS CUI is recorded as C2750789[13].
- retinitis pigmentosa 50's UMLS CUI is recorded as C2750788[14].
- retinitis pigmentosa 50's ICD-10-CM is recorded as H35.5[15].
- retinitis pigmentosa 50's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- retinitis pigmentosa 50's Mondo ID is recorded as MONDO_0013175[17].
- retinitis pigmentosa 50's UniProt disease ID is recorded as DI-01386[18].