Version: 8.0.0
Date: Tue Jan 28 2025
arthrogryposis multiplex congenita-4
DOID:0080980
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

arthrogryposis multiplex congenita-4

Definition
An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23.
Synonyms
  • Zain syndrome
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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