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Disease Ontology Browser
congenital muscular dystrophy (DOID:0050557)
Alliance: disease page
Alt IDs: OMIM:254100, ICD9CM:359.0, ORDO:97242, UMLS_CUI:C2937300
Definition: A muscular dystrophy that is characterized by diminished muscle tone (hypotonia), progressive muscle weakness and degeneration (atrophy), abnormally fixed joints, spinal rigidity, and delays in reaching motor milestones such as sitting or standing unassisted.

Disease References using Mouse Models (46)

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
MGI 6.13
The Jackson Laboratory