arthrogryposis multiplex congenita Disease Ontology Browser

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Disease Ontology Browser

arthrogryposis multiplex congenita (DOID:0080954)
Alliance: disease page
Alt IDs: OMIM:PS617468
Definition: A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth.

Disease References using Mouse Models (1)

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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