Holoprosencephaly 9 (HPE9)

Holoprosencephaly 9, also known as pituitary anomalies with holoprosencephaly-like features, is related to culler-jones syndrome and holoprosencephaly, recurrent infections, and monocytosis, and has symptoms including seizures An important gene associated with Holoprosencephaly 9 is GLI2 (GLI Family Zinc Finger 2), and among its related pathways/superpathways are Ciliopathies and Osteoblast differentiation and related diseases. Affiliated tissues include pituitary and brain, and related phenotypes are short stature and hypotelorism