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Metadata
ID DOID:0080981
Name arthrogryposis multiplex congenita-5
Definition An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the TOR1A gene on chromosome 9q34.
https://pubmed.ncbi.nlm.nih.gov/29053766/
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MIM:618947

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is_a arthrogryposis multiplex congenita

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