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Disease Ontology Browser
Duchenne muscular dystrophy (DOID:11723)
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 disease that has material basis in 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 (99)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
08/15/2017
MGI 6.10
The Jackson Laboratory