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Disease Ontology Browser
arthrogryposis due to muscular dystrophy (DOID:0110631)
Alliance: disease page
Synonyms: congenital muscular dystrophy producing arthrogryposis
Alt IDs: OMIM:253900, ICD10CM:M62.8, ORDO:1155
Definition: A congenital muscular dystrophy characterized by nonprogressive myopathy resulting in an arthrogryposis syndrome.


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
11/14/2017
MGI 6.11
The Jackson Laboratory