arthrogryposis multiplex congenita-4 Disease Ontology Browser

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Disease Ontology Browser

arthrogryposis multiplex congenita-4 (DOID:0080980)
Alliance: disease page
Synonyms: Zain syndrome
Alt IDs: OMIM:618766
Definition: An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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