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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/
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MIM:617468

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is_a arthrogryposis multiplex congenita

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