OBO ID: DOID:0111337 |
Term Name: | Jackson-Weiss syndrome | Search Ontology: | |
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Definition: | A syndrome characterized by craniosynostosis, midfacial hypoplasia, and foot malformations that has_material_basis_in heterozygous mutation in the FGFR2 gene on chromosome 10q26.13. (2) | ||
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Ontology: | Human Disease ( DOID:0111337 ) |
OTHER Jackson-Weiss syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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