posterior pituitary dysgenesis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal development of the neurohypophysis during embryonic growth and development. (Human Phenotype Ontology, HP_0011753)
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3 genes associated with the posterior pituitary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GLI2 GLI family zinc finger 2
OTX2 orthodenticle homeobox 2
TBX3 T-box 3