Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Pituitary hormone deficiency, combined, 6

MONDO:0013518

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

Also known as: OTX2 combined pituitary hormone deficiencies, genetic form, combined pituitary hormone deficiencies, genetic form caused by mutation in OTX2, pituitary hormone deficiency, combined, 6, pituitary hormone deficiency, combined, type 6, CPHD6

1 clinical trial for this condition and its sub-types, 0 tagged with Pituitary hormone deficiency, combined, 6 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by