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Summary Literature (0)
DOID:0080954 - arthrogryposis multiplex congenita

Disease Ontology 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.

Synonyms:

Xenbase Genes : ergic1, lgi4



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), nervous system disease (is_a), physical disorder (is_a)