cone-rod dystrophy 12
cone-rod dystrophy that has material basis in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15
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cone-rod dystrophy 12
Summary
cone-rod dystrophy 12 is a rare disease[1].
Key Facts
- cone-rod dystrophy 12's instance of is recorded as rare disease[2].
- cone-rod dystrophy 12's instance of is recorded as class of disease[3].
- cone-rod dystrophy 12's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 12's MeSH descriptor ID is recorded as C567206[5].
- cone-rod dystrophy 12's OMIM ID is recorded as 612657[6].
- cone-rod dystrophy 12's Disease Ontology ID is recorded as DOID:0111019[7].
- cone-rod dystrophy 12's NCI Thesaurus ID is recorded as C212886[8].
- cone-rod dystrophy 12's genetic association is recorded as PROM1[9].
- cone-rod dystrophy 12's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111019[10].
- cone-rod dystrophy 12's exact match is recorded as http://identifiers.org/doid/DOID:0111019[11].
- cone-rod dystrophy 12's UMLS CUI is recorded as C2675210[12].
- cone-rod dystrophy 12's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- cone-rod dystrophy 12's Mondo ID is recorded as MONDO_0012983[14].
- cone-rod dystrophy 12's UniProt disease ID is recorded as DI-00326[15].