Cardiomyopathy, dilated, 1g

Preferred Label : Cardiomyopathy, dilated, 1g;

Symbol : CMD1G;

CISMeF acronym : CMD1G;

Type : Phenotype, molecular basis known;

Prefixed ID : #604145;

Details

Origin ID

604145;

UMLS CUI

C1858763;

Automatic exact mappings (from CISMeF team)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
- TTN wt Allele [NCIt concept]
- symbol withdrawn CMD1G [HGNC gene]
Broader ORDO disease(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- cardiomyopathy, dilated, 1g [MeSH concept]
- cardiomyopathy, dilated, 1g [MeSH Supplementary Concept]
- dilated cardiomyopathy 1G [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1G [DO Concept]
Genes related to phenotype
- Titin [OMIM gene]
HPO term(s)
- Atrial fibrillation [HPO term]
- Atrioventricular block [HPO term]
- Autosomal dominant inheritance [HPO term]
- Congestive heart failure [HPO term]
- Dilated cardiomyopathy [HPO term]
- Premature atrial contractions [HPO term]
- Reduced ejection fraction [HPO term]
- Ventricular tachycardia [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-1G [NCIt concept]
- cardiomyopathy, dilated, 1g [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1g [MeSH concept]
- dilated cardiomyopathy 1G [DO Concept]

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