cardiomyopathy, dilated 1B (autosomal dominant)

Preferred Label : cardiomyopathy, dilated 1B (autosomal dominant);

Obsolete resource : true;

Approved symbol HGNC : CMD1B;

Alias symbols HGNC : FDC;

Chromosome HGNC : 9q13-q22;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:2102;

UMLS CUI

C1413520;

Automatic exact mappings (from CISMeF team)
- Cardiomyopathy, dilated, 1b [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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