FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term arthrogryposis multiplex congenita-4 ID (Ontology) DOID:0080980 (Human Disease)
Definition An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23.
Also Known As "Zain syndrome"
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 Genes
 arthrogryposis multiplex congenita-4       2
 for disease ribbon | arthrogryposis multiplex congenita-4       2
 model of | arthrogryposis multiplex congenita-4       2
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autosomal recessive disease__
physical disorder____________|
nervous system disease_______|
                             arthrogryposis multiplex congenita
                              |__arthrogryposis multiplex congenita-4  2 rec.
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Is a arthrogryposis multiplex congenita
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Synonyms
  • "Zain syndrome" EXACT
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MIM:618766