Combined Pituitary Hormone Deficiencies, Genetic Forms, also known as multiple pituitary hormone deficiencies, genetic forms, is related to hypopituitarism and pituitary hormone deficiency, combined, 2. An important gene associated with Combined Pituitary Hormone Deficiencies, Genetic Forms is PROP1 (PROP Paired-Like Homeobox 1), and among its related pathways/superpathways are Embryonic and Induced Pluripotent Stem Cells and Lineage-specific Markers and Endoderm differentiation. Affiliated tissues include pituitary and eye, and related phenotypes are hypopituitarism and hypotension