cone rod dystrophy 1 (autosomal dominant)

Preferred Label : cone rod dystrophy 1 (autosomal dominant);

Obsolete resource : true;

Approved symbol HGNC : CORD1;

Chromosome HGNC : 18q21.1-q21.3;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:2245;

UMLS CUI

C1413617;

Automatic exact mappings (from CISMeF team)
- Cone-rod dystrophy 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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