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Sweeney-Cox syndrome
Disease Summary
Associated Targets (1)
Tbio
1
Uniprot Description An autosomal dominant syndrome characterized by facial dysostosis, including hypertelorism, deficiencies of the eyelids and facial bones, cleft palate/velopharyngeal insufficiency, and low-set cupped ears.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0080538
OMIM:617746
UMLS:C4540299
MONDO:0060592
High level summary of knowledge for a disease, including descriptions and datasource references.