Search Ontology:
Human Disease

arthrogryposis multiplex congenita-4

Term ID
DOID:0080980
Synonyms
  • Zain syndrome
Definition
An arthrogryposis multiplex congenita that has_material_basis_in homozygous mutation in the SCYL2 gene on chromosome 12q23. https://pubmed.ncbi.nlm.nih.gov/31960134/
References
Ontology
Human Disease   ( DOID:0080980 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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