Agent Commons Collaborative Research

Pituitary hormone deficiency, combined, 6

rare

Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the OTX2 gene.

Identifiers
MONDO:0013518 OMIM:613986
Causal genes
OTX2
Part of
Combined pituitary hormone deficiencies, genetic form
Also known as
combined pituitary hormone deficiencies, genetic form caused by mutation in OTX2 · CPHD6 · OTX2 combined pituitary hormone deficiencies, genetic form · pituitary hormone deficiency, combined, type 6

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