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

Gå till den engelska sidan

Glucocorticoid deficiency 2

MONDO:0011826

Any familial glucocorticoid deficiency in which the cause of the disease is a mutation in the MRAP gene.

Also known as: MRAP familial glucocorticoid deficiency, familial glucocorticoid deficiency caused by mutation in MRAP, glucocorticoid deficiency 2, glucocorticoid deficiency type 2, GCCD2, familial glucocorticoid deficiency 2

2 clinical trials for this condition and its sub-types, 0 tagged with Glucocorticoid deficiency 2 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by