Muscular dystrophy, congenital, with cerebellar atrophy

Preferred Label : Muscular dystrophy, congenital, with cerebellar atrophy;

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 603323;

Details

Origin ID

603323;

UMLS CUI

C1864028;

Currated CISMeF NLP mapping
- muscular dystrophy, congenital, with cerebellar atrophy [MeSH concept]
- muscular dystrophy, congenital, with cerebellar atrophy [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- muscular dystrophy, congenital, with cerebellar atrophy [MeSH Supplementary Concept]
- muscular dystrophy, congenital, with cerebellar atrophy [MeSH concept]

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