Version: 8.0.0
Date: Tue Jan 28 2025
arthrogryposis multiplex congenita-1
DOID:0080978
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

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.
Synonyms
None
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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    Associated Alleles

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      Associated Models

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