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Metadata
ID	DOID:0080979
Name	arthrogryposis multiplex congenita-3
Definition	An arthrogryposis multiplex congenita that is characterized by decreased fetal movements, hypotonia, variable skeletal defects, including clubfoot and scoliosis, and delayed motor milestones with difficulty walking and that has_material_basis_in homozygous or compound heterozygous mutation in the SYNE1 gene on chromosome 6q25. https://pubmed.ncbi.nlm.nih.gov/27782104/
Xrefs	MIM:618484
Parent Relationships	is_a arthrogryposis multiplex congenita
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance