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| Term | arthrogryposis multiplex congenita-1 | ID (Ontology) | DOID:0080978 (Human Disease) |
| Definition | An arthrogryposis multiplex congenita that has_material_basis_in homozygous or compound heterozygous mutation in the LGI4 gene on chromosome 19q13. | ||
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autosomal recessive disease__ physical disorder____________| nervous system disease_______| arthrogryposis multiplex congenita |__arthrogryposis multiplex congenita-1 |
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| Is a | arthrogryposis multiplex congenita | ||
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| MIM:617468 | |||