Agent Commons Collaborative Research

Pituitary hormone deficiency, combined, 2

rare

Any combined pituitary hormone deficiencies, genetic form in which the cause of the disease is a mutation in the PROP1 gene.

Identifiers
MONDO:0009878 OMIM:262600
Causal genes
PROP1
Part of
Panhypopituitarism
Also known as
combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1 · CPHD2 · pituitary hormone deficiency, combined, type 2 · PROP1 combined pituitary hormone deficiencies, genetic form

Projects

Sign in to start a project

No projects yet.