Search Ontology:
Human Disease

autosomal recessive limb-girdle muscular dystrophy type 2W

Term ID
DOID:0110288
Synonyms
  • LGMD2W
  • muscular dystrophy, limb-girdle, type 2W
Definition
An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in compound heterozygous mutation in the LIM zinc finger domain containing 2 gene (LIMS2) on chromosome 2q14. https://www.ncbi.nlm.nih.gov/pubmed/25589244
References
Ontology
Human Disease   ( DOID:0110288 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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