cone-rod dystrophy 16
cone-rod dystrophy that has material basis in homozygous or compound heterozygous mutation in the C8ORF37 gene on chromosome 8q22
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cone-rod dystrophy 16
Summary
cone-rod dystrophy 16 is a rare disease[1].
Key Facts
- cone-rod dystrophy 16's instance of is recorded as rare disease[2].
- cone-rod dystrophy 16's instance of is recorded as class of disease[3].
- cone-rod dystrophy 16's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 16's OMIM ID is recorded as 614500[5].
- cone-rod dystrophy 16's Disease Ontology ID is recorded as DOID:0111022[6].
- cone-rod dystrophy 16's genetic association is recorded as CFAP418[7].
- cone-rod dystrophy 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111022[8].
- cone-rod dystrophy 16's exact match is recorded as http://identifiers.org/doid/DOID:0111022[9].
- cone-rod dystrophy 16's UMLS CUI is recorded as C3281046[10].
- cone-rod dystrophy 16's UMLS CUI is recorded as C3281045[11].
- cone-rod dystrophy 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- cone-rod dystrophy 16's Mondo ID is recorded as MONDO_0013786[13].
- cone-rod dystrophy 16's UniProt disease ID is recorded as DI-03355[14].