Cardiomyopathy, dilated, 1h

Preferred Label : Cardiomyopathy, dilated, 1h;

Symbol : CMD1H;

CISMeF acronym : CMD1H;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cardiomyopathy, dilated, with conduction defect;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of dilated cardiomyopathy, see CMD1A (115200).;

Prefixed ID : %604288;

Détails

Origin ID

604288;

UMLS CUI

C1858591;

Broader ORDO disease(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- cardiomyopathy, dilated, 1h [MeSH concept]
- dilated cardiomyopathy 1H [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1H [DO Concept]
ORDO concept(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cardiomyopathy, dilated, 1h [MeSH concept]
- dilated cardiomyopathy 1H [DO Concept]

Position du mot-clé dans l'(les) arborescence(s) :

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