abnormality of the posterior pituitary Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the neurohypophysis, which is also known as the posterior lobe of the hypophysis. (Human Phenotype Ontology, HP_0011751)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011751
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5 genes associated with the abnormality of the posterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AVP arginine vasopressin
GLI2 GLI family zinc finger 2
OTX2 orthodenticle homeobox 2
TBX3 T-box 3
TP63 tumor protein p63