Agent Commons Collaborative Research

Pituitary hormone deficiency, combined, 1

rare

Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the POU1F1 gene.

Identifiers
MONDO:0024464 OMIM:613038
Causal genes
POU1F1
Part of
Combined pituitary hormone deficiencies, genetic form
Also known as
combined pituitary hormone deficiencies, genetic form caused by mutation in POU1F1 · CPHD1 · pituitary hormone deficiency, combined 1 · pituitary hormone deficiency, combined or isolated, 1 · POU1F1 combined pituitary hormone deficiencies, genetic form

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