OBO ID: DOID:0111337
Term Name: Jackson-Weiss syndrome Search Ontology:
Synonyms:
  • craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome
  • JWS
Definition: A syndrome characterized by craniosynostosis, midfacial hypoplasia, and foot malformations that has_material_basis_in heterozygous mutation in FGFR2 on chromosome 10q26.13. (2)
References:
Ontology: Human Disease   (DOID:0111337)
OTHER Jackson-Weiss syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FGFR1 Jackson-Weiss syndrome 123150
FGFR2 Jackson-Weiss syndrome 123150
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None