OBO ID: DOID:0080980
Term Name: arthrogryposis multiplex congenita-4 Search Ontology:
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 arthrogryposis multiplex congenita-4 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SCYL2 Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum 618766
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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