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Disease Ontology Browser
Duchenne muscular dystrophy (DOID:11723)
Alliance: disease page
Synonyms: Muscular dystrophy, Duchenne
Alt IDs: OMIM:310200, MESH:D020388, NCI:C75482, UMLS_CUI:C0013264
Definition: A muscular dystrophy that has_material_basis_in X-linked 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.

Disease References using Mouse Models (113)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
03/30/2021
MGI 6.16
The Jackson Laboratory