Term Name: | arthrogryposis multiplex congenita-1 |
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Synonyms: | |
Definition: | An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the LGI4 gene on chromosome 19q13. |
Ontology: | Human Disease [DOID:0080978] ( DOID:0080978 ) |