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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: Freeman-Sheldon syndrome, Sheldon-Hall syndrome, Freeman-Sheldon syndrome variant, Arthrogryposis Multiplex Congenita
Xenbase Genes
:
tnni2,
tnnt3,
mybpc1,
fbn2,
myh3,
ecel1,
piezo2,
myh8,
tpm2
| MONDO:0019942 - distal arthrogryposis |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s):
muscle tissue disease (is_a)