abnormal hypothalamus morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomaly of the hypothalamus. (Human Phenotype Ontology, HP_0012286)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012286
Similar Terms
Downloads & Tools


4 genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GLI3 GLI family zinc finger 3
LEPR leptin receptor
OFD1 oral-facial-digital syndrome 1
SOX2 SRY (sex determining region Y)-box 2