cone-rod dystrophy 20
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the POC1B gene on chromosome 12q21
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cone-rod dystrophy 20
Summary
cone-rod dystrophy 20 is a rare disease[1].
Key Facts
- cone-rod dystrophy 20's instance of is recorded as rare disease[2].
- cone-rod dystrophy 20's instance of is recorded as class of disease[3].
- cone-rod dystrophy 20's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 20's OMIM ID is recorded as 615973[5].
- cone-rod dystrophy 20's Disease Ontology ID is recorded as DOID:0111026[6].
- cone-rod dystrophy 20's genetic association is recorded as POC1B[7].
- cone-rod dystrophy 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111026[8].
- cone-rod dystrophy 20's exact match is recorded as http://identifiers.org/doid/DOID:0111026[9].
- cone-rod dystrophy 20's UMLS CUI is recorded as C4014856[10].
- cone-rod dystrophy 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- cone-rod dystrophy 20's Mondo ID is recorded as MONDO_0014427[12].
- cone-rod dystrophy 20's UniProt disease ID is recorded as DI-04189[13].