muscular dystrophy, duchenne Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A muscular dystrophy that has_material_basis_in X-linked disease caused by mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. (Human Disease Ontology, DOID_11723)
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5 genes associated with the disease muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
DMD dystrophin
HLA-A major histocompatibility complex, class I, A
HLA-B major histocompatibility complex, class I, B
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
SPP1 secreted phosphoprotein 1