Pituitary hormone deficiency, combined, 2

MONDO:0009878

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

Also known as: PROP1 combined pituitary hormone deficiencies, genetic form, combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1, pituitary hormone deficiency, combined, 2, pituitary hormone deficiency, combined, type 2, CPHD2, Hanhart dwarfism, ateliotic dwarfism with hypogonadism, panhypopituitarism

1 clinical trial for this condition and its sub-types, 0 tagged with Pituitary hormone deficiency, combined, 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Panhypopituitarism (2)

Including sub-types (1) Tagged with Pituitary hormone deficiency, combined, 2 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.