Cardiomyopathy associated with myopathy and sudden death

Preferred Label : Cardiomyopathy associated with myopathy and sudden death;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %212130;

Details

Origin ID

212130;

UMLS CUI

C1859328;

Currated CISMeF NLP mapping
- cardiomyopathy associated with myopathy and sudden death [MeSH concept]
- cardiomyopathy associated with myopathy and sudden death [MeSH Supplementary Concept]
HPO term(s)
- Asymmetric septal hypertrophy [HPO term]
- Autosomal recessive inheritance [HPO term]
- Myopathy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cardiomyopathy associated with myopathy and sudden death [MeSH Supplementary Concept]
- cardiomyopathy associated with myopathy and sudden death [MeSH concept]

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