muscular dystrophy, congenital, type 1D

Preferred Label : muscular dystrophy, congenital, type 1D;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0564144;

UMLS CUI

C1837229;

Automatic exact mappings (from CISMeF team)
- muscular dystrophy-dystroglycanopathy type B6 [DO Concept]
Currated CISMeF NLP mapping
- Congenital muscular dystrophy type 1D [ORDO Disease]
- Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 6 [OMIM Phenotype]
Related record
- muscular dystrophy, congenital, type 1D [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital muscular dystrophy type 1D [ORDO Disease]
- Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 6 [OMIM Phenotype]