Search Ontology:
Human Disease

autosomal dominant limb-girdle muscular dystrophy type 3

Term ID
DOID:0110306
Synonyms
  • autosomal dominant limb-girdle muscular dystrophy type 1G
  • LGMD1G
  • muscular dystrophy limb-girdle type 1G
Definition
An autosomal dominant limb-girdle muscular dystrophy that has_material_basis_in heterozygous mutation in the HNRNPDL gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/24647604
References
Ontology
Human Disease   ( DOID:0110306 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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