Search Ontology:
Human Disease

autosomal recessive limb-girdle muscular dystrophy type 2D

Term ID
DOID:0110278
Synonyms
  • Alpha-sarcoglycanopathy
  • DMDA2
  • Duchenne-like autosomal recessive muscular dystrophy type 2
  • LGMD2D
  • muscular dystrophy, limb-girdle, type 2D
  • primary adhalinopathy
Definition
An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the alpha-sarcoglycan gene (SGCA) on chromosome 17q. (2)
References
Ontology
Human Disease   ( DOID:0110278 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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