autosomal dominant Emery-Dreifuss muscular dystrophy

Preferred Label : autosomal dominant Emery-Dreifuss muscular dystrophy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0464070;

UMLS CUI

C0410190;

Currated CISMeF NLP mapping
- Autosomal dominant Emery-Dreifuss muscular dystrophy [ORDO Disease]
- Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) [SNOMED CT concept]
- Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) [SNOMED CT concept]
- Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant [NCIt concept]
- Emery-Dreifuss muscular dystrophy, autosomal dominant [ICD-11 More detail]
- Emery-dreifuss muscular dystrophy 2, autosomal dominant [OMIM Phenotype]
- autosomal dominant Emery-Dreifuss muscular dystrophy 2 [DO Concept]
Related record
- Autosomal Emery-Dreifuss Muscular Dystrophy [MeSH Descriptor]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal dominant Emery-Dreifuss muscular dystrophy [ORDO Disease]
- Autosomal dominant Emery-Dreifuss muscular dystrophy (disorder) [SNOMED CT concept]
- Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder) [SNOMED CT concept]
- Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant [NCIt concept]
- Emery-dreifuss muscular dystrophy 2, autosomal dominant [OMIM Phenotype]