retinitis pigmentosa 17
retinitis pigmentosa that has material basis in mutation in the CA4 gene on chromosome 17q23.1
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retinitis pigmentosa 17
Summary
retinitis pigmentosa 17 is a rare disease[1].
Key Facts
- retinitis pigmentosa 17's instance of is recorded as rare disease[2].
- retinitis pigmentosa 17's instance of is recorded as class of disease[3].
- retinitis pigmentosa 17's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 17's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 17's subclass of is recorded as autosomal dominant disease[6].
- retinitis pigmentosa 17's MeSH descriptor ID is recorded as C563437[7].
- retinitis pigmentosa 17's OMIM ID is recorded as 600852[8].
- retinitis pigmentosa 17's Disease Ontology ID is recorded as DOID:0110404[9].
- retinitis pigmentosa 17's genetic association is recorded as CA4[10].
- retinitis pigmentosa 17's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110404[11].
- retinitis pigmentosa 17's exact match is recorded as http://identifiers.org/doid/DOID:0110404[12].
- retinitis pigmentosa 17's UMLS CUI is recorded as C1833245[13].
- retinitis pigmentosa 17's ICD-10-CM is recorded as H35.5[14].
- retinitis pigmentosa 17's GARD rare disease ID is recorded as 10387[15].
- retinitis pigmentosa 17's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- retinitis pigmentosa 17's Mondo ID is recorded as MONDO_0010945[17].
- retinitis pigmentosa 17's UniProt disease ID is recorded as DI-00983[18].