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DOID:0050646 - distal arthrogryposis
Disease Ontology Definition:A muscle tissue disease characterized by congenital joint contractures of hand and feet.
Synonyms: Arthrogryposis Multiplex Congenita, Freeman-Sheldon syndrome, Freeman-Sheldon syndrome variant, Sheldon-Hall syndrome,
Echinobase Genes
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Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
muscle tissue disease (is_a)