Search Ontology:
Human Disease
Sweeney-Cox syndrome
- Term ID
- DOID:0080538
- Synonyms
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- Definition
- A syndrome that is characterized by striking facial dysostosis, including hypertelorism, deficiencies of the eyelids and facial bones, cleft palate/velopharyngeal insufficiency, and low-set cupped ears and has_material_basis_in heterozygous mutation in the TWIST1 gene on chromosome 7p21. https://www.ncbi.nlm.nih.gov/pubmed/28369379
- References
- Ontology
- Human Disease ( DOID:0080538 )
- is a type of
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Genes Involved
Zebrafish Models