arthrogryposis multiplex congenita-4

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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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Other Model Organisms: Alliance, 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)