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Metadata
ID	DOID:0080980
Name	arthrogryposis multiplex congenita-4
Definition	An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23. https://pubmed.ncbi.nlm.nih.gov/31960134/
Xrefs	MIM:618766
Synonyms	Zain syndrome [EXACT]
Parent Relationships	is_a arthrogryposis multiplex congenita
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance