Pituitary hormone deficiency, combined, 1
MONDO:0024464Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the POU1F1 gene.
Also known as: CPHD1, POU1F1 combined pituitary hormone deficiencies, genetic form, combined pituitary hormone deficiencies, genetic form caused by mutation in POU1F1, pituitary hormone deficiency, combined or isolated, 1, pituitary hormone deficiency, combined, 1, pituitary hormone deficiency, combined 1
2 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsBroader categories
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Newborn screening study aims to catch rare diseases at birth
Diagnosis OngoingThis study offers voluntary screening for newborns in North Carolina to detect a wide range of rare health conditions early. Using a small blood sample already collected at birth, the program tests for dozens of disorders, including spinal muscular atrophy, cystic fibrosis, and m…
Sponsor: RTI International • Aim: Diagnosis
Last updated Jul 03, 2026 00:00 UTC
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Pituitary patients followed for years to uncover key outcomes
Knowledge-focused OngoingThis study follows 1500 patients with pituitary gland disorders to see how they fare over time, whether treated with medication, surgery, or just monitoring. Researchers will track tumor regrowth after surgery to find clues that predict recurrence. The goal is to learn, not to te…
Sponsor: University of Alberta • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:01 UTC