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Metadata
ID	DOID:0080978
Name	arthrogryposis multiplex congenita-1
Definition	An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the LGI4 gene on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/28318499/
Xrefs	MIM:617468
Parent Relationships	is_a arthrogryposis multiplex congenita
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance