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Summary Literature (3)
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,

Xenbase Genes : tnni2, tnnt3, mybpc1, fbn2, myh3, ecel1, piezo2, myh8, tpm2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019942 - distal arthrogryposis


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)