Metadata | |
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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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