retinitis pigmentosa 46
retinitis pigmentosa that has material basis in mutation in the IDH3B on chromosome 20p13
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retinitis pigmentosa 46
Summary
retinitis pigmentosa 46 is a rare disease[1].
Key Facts
- retinitis pigmentosa 46's instance of is recorded as rare disease[2].
- retinitis pigmentosa 46's instance of is recorded as class of disease[3].
- retinitis pigmentosa 46's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 46's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 46's MeSH descriptor ID is recorded as C567249[6].
- retinitis pigmentosa 46's OMIM ID is recorded as 612572[7].
- retinitis pigmentosa 46's Disease Ontology ID is recorded as DOID:0110409[8].
- retinitis pigmentosa 46's genetic association is recorded as IDH3B[9].
- retinitis pigmentosa 46's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110409[10].
- retinitis pigmentosa 46's exact match is recorded as http://identifiers.org/doid/DOID:0110409[11].
- retinitis pigmentosa 46's UMLS CUI is recorded as C2675496[12].
- retinitis pigmentosa 46's ICD-10-CM is recorded as H35.5[13].
- retinitis pigmentosa 46's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- retinitis pigmentosa 46's Mondo ID is recorded as MONDO_0012943[15].
- retinitis pigmentosa 46's UniProt disease ID is recorded as DI-00996[16].