retinitis pigmentosa 72
retinitis pigmentosa that has material basis in mutation in the ZNF408 gene on chromosome 11p11
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retinitis pigmentosa 72
Summary
retinitis pigmentosa 72 is a rare disease[1].
Key Facts
- retinitis pigmentosa 72's instance of is recorded as rare disease[2].
- retinitis pigmentosa 72's instance of is recorded as class of disease[3].
- retinitis pigmentosa 72's subclass of is recorded as retinitis pigmentosa[4].
- retinitis pigmentosa 72's subclass of is recorded as genetic disease[5].
- retinitis pigmentosa 72's subclass of is recorded as autosomal recessive disease[6].
- retinitis pigmentosa 72's OMIM ID is recorded as 616469[7].
- retinitis pigmentosa 72's Disease Ontology ID is recorded as DOID:0110395[8].
- retinitis pigmentosa 72's genetic association is recorded as ZNF408[9].
- retinitis pigmentosa 72's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110395[10].
- retinitis pigmentosa 72's exact match is recorded as http://identifiers.org/doid/DOID:0110395[11].
- retinitis pigmentosa 72's UMLS CUI is recorded as C4225315[12].
- retinitis pigmentosa 72's ICD-10-CM is recorded as H35.5[13].
- retinitis pigmentosa 72's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- retinitis pigmentosa 72's Mondo ID is recorded as MONDO_0014653[15].
- retinitis pigmentosa 72's UniProt disease ID is recorded as DI-04485[16].