Cardiomyopathy, dilated, 1z

Preferred Label : Cardiomyopathy, dilated, 1z;

Symbol : CMD1Z;

CISMeF acronym : CMD1Z;

Type : Phenotype, molecular basis known;

Prefixed ID : #611879;

Details

Origin ID

611879;

UMLS CUI

C2678475;

Automatic exact mappings (from CISMeF team)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Broader ORDO disease(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- cardiomyopathy, dilated, 1z [MeSH concept]
- cardiomyopathy, dilated, 1z [MeSH Supplementary Concept]
- dilated cardiomyopathy 1Z [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1Z [DO Concept]
Genes related to phenotype
- Troponin C, slow [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)
- cardiomyopathy, dilated, 1z [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1z [MeSH concept]
- dilated cardiomyopathy 1Z [DO Concept]

Keyword's position in hierarchy(ies) :

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