Abnormality Of The Sella Turcica Gene Set

Dataset DisGeNET Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormality of the sella turcica, a saddle-shaped depression in the sphenoid bone at the base of the human skull. (Human Phenotype Ontology, HP_0002679)
External Link https://www.disgenet.org/browser/0/1/0/C4021754
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3 genes associated with the phenotype Abnormality Of The Sella Turcica in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Symbol Name
CDH11 cadherin 11, type 2, OB-cadherin (osteoblast)
NKX2-1 NK2 homeobox 1
STUB1 STIP1 homology and U-box containing protein 1, E3 ubiquitin protein ligase