Cardiomyopathy, dilated, 1w

Preferred Label : Cardiomyopathy, dilated, 1w;

Symbol : CMD1W;

CISMeF acronym : CMD1W;

Type : Phenotype, molecular basis known;

Prefixed ID : #611407;

Details

Origin ID

611407;

UMLS CUI

C1969639;

Automatic exact mappings (from CISMeF team)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
- VCL wt Allele [NCIt concept]
Broader ORDO disease(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- Dilated Cardiomyopathy-1W [NCIt concept]
- cardiomyopathy, dilated, 1w [MeSH concept]
- cardiomyopathy, dilated, 1w [MeSH Supplementary Concept]
- dilated cardiomyopathy 1W [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1W [DO Concept]
Genes related to phenotype
- Vinculin [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dilated cardiomyopathy [HPO term]
ORDO concept(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dilated Cardiomyopathy-1W [NCIt concept]
- cardiomyopathy, dilated, 1w [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1w [MeSH concept]
- dilated cardiomyopathy 1W [DO Concept]

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