muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers

Preferred Label : muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers;

Origin ID

C563378;

UMLS CUI

C1832665;

Automatic exact mappings (from CISMeF team)
- Muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers [OMIM Phenotype]
MeSH term(s) associated for indexing
- heredodegenerative disorders, nervous system [MeSH Descriptor]
- muscular dystrophies [MeSH Descriptor]
Record concept(s)
- muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers [OMIM Phenotype]