retinitis pigmentosa 47
retinitis pigmentosa that has material basis in mutation in the SAG gene on chromosome 2q37
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retinitis pigmentosa 47
Summary
retinitis pigmentosa 47 is a rare disease[1].
Key Facts
- retinitis pigmentosa 47's instance of is recorded as rare disease[2].
- retinitis pigmentosa 47's instance of is recorded as class of disease[3].
- retinitis pigmentosa 47's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 47's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 47's OMIM ID is recorded as 613758[6].
- retinitis pigmentosa 47's Disease Ontology ID is recorded as DOID:0110369[7].
- retinitis pigmentosa 47's genetic association is recorded as SAG[8].
- retinitis pigmentosa 47's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110369[9].
- retinitis pigmentosa 47's exact match is recorded as http://identifiers.org/doid/DOID:0110369[10].
- retinitis pigmentosa 47's UMLS CUI is recorded as C3151061[11].
- retinitis pigmentosa 47's ICD-10-CM is recorded as H35.5[12].
- retinitis pigmentosa 47's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- retinitis pigmentosa 47's Mondo ID is recorded as MONDO_0013407[14].
- retinitis pigmentosa 47's UniProt disease ID is recorded as DI-03034[15].