Cardiomyopathy, dilated, 1jj

Preferred Label : Cardiomyopathy, dilated, 1jj;

Symbol : CMD1JJ;

CISMeF acronym : CMD1JJ;

Type : Phenotype, molecular basis known;

Inheritance : Autosomal dominant;

Molecular basis : Caused by mutation in the alpha-4 laminin gene (LAMA4, 600133.0001);

Prefixed ID : #615235;

Details

Origin ID

615235;

UMLS CUI

C3808935;

Currated CISMeF NLP mapping
- dilated cardiomyopathy 1JJ [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1JJ [DO Concept]
Genes related to phenotype
- Laminin, alpha-4 [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 1JJ [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients