Term Name: | arthrogryposis multiplex congenita-4 |
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Synonyms: | Zain syndrome |
Definition: | An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23. |
Ontology: | Human Disease [DOID:0080980] ( DOID:0080980 ) |