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Summary Literature (0)
DOID:0080980 - arthrogryposis multiplex congenita-4

Disease Ontology Definition:An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23.

Synonyms: Zain syndrome,

Xenbase Genes :


OMIM:
OMIM:618766 - ARTHROGRYPOSIS MULTIPLEX CONGENITA 4, NEUROGENIC, WITH AGENESIS OF THE CORPUS CALLOSUM; AMC4

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): arthrogryposis multiplex congenita (is_a), autosomal recessive disease (is_a)