Cardiomyopathy, dilated, 1m

Preferred Label : Cardiomyopathy, dilated, 1m;

Symbol : CMD1M;

CISMeF acronym : CMD1M;

Type : Phenotype, molecular basis known;

Prefixed ID : #607482;

Détails

Origin ID

607482;

UMLS CUI

C1843808;

Automatic exact mappings (from CISMeF team)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
- cysteine and glycine rich protein 3 [ORDO Gene]
- cysteine and glycine rich protein 3 [HGNC gene]
Broader ORDO disease(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- cardiomyopathy, dilated, 1M [MeSH concept]
- cardiomyopathy, dilated, 1M [MeSH Supplementary Concept]
- dilated cardiomyopathy 1M [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1M [DO Concept]
Genes related to phenotype
- Cysteine- and glycine-rich protein 3 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Dilated cardiomyopathy [HPO term]
- Endocardial fibroelastosis [HPO term]
- Impaired myocardial contractility [HPO term]
ORDO concept(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cardiomyopathy, dilated, 1M [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1M [MeSH concept]
- dilated cardiomyopathy 1M [DO Concept]

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