Muscular dystrophy, limb-girdle, autosomal recessive 28

Preferred Label : Muscular dystrophy, limb-girdle, autosomal recessive 28;

Symbol : LGMDR28;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Myopathy, limb-girdle, adult-onset; MYPLG;

Prefixed ID : #620375;

Details

Origin ID

620375;

UMLS CUI

C5830518;

Genes related to phenotype
- 3-hydroxy-3-methylglutaryl-coa reductase [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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