Cardiomyopathy, dilated, 1p

Preferred Label : Cardiomyopathy, dilated, 1p;

Symbol : CMD1P;

CISMeF acronym : CMD1P;

Type : Phenotype, molecular basis known;

Prefixed ID : #609909;

Details

Origin ID

609909;

UMLS CUI

C1835928;

Automatic exact mappings (from CISMeF team)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
- phospholamban [ORDO Gene]
- phospholamban [HGNC gene]
Broader ORDO disease(s)
- Familial isolated dilated cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- Dilated Cardiomyopathy-1P [NCIt concept]
- cardiomyopathy, dilated, 1p [MeSH concept]
- cardiomyopathy, dilated, 1p [MeSH Supplementary Concept]
- dilated cardiomyopathy 1P [DO Concept]
DO Cross reference
- dilated cardiomyopathy 1P [DO Concept]
Genes related to phenotype
- Phospholamban [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Congestive heart failure [HPO term]
- Dilated cardiomyopathy [HPO term]
- Reduced systolic function [HPO term]
- Ventricular arrhythmia [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-1P [NCIt concept]
- cardiomyopathy, dilated, 1p [MeSH Supplementary Concept]
- cardiomyopathy, dilated, 1p [MeSH concept]
- dilated cardiomyopathy 1P [DO Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients