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

Gå till den engelska sidan

Hypotrichosis 1

MONDO:0011549

Any hypotrichosis in which the cause of the disease is a mutation in the APCDD1 gene.

Also known as: HHS, APCDD1 hypotrichosis, HTS, HYPT1, hereditary generalised hypotrichosis simplex, hypotrichosis 1, hypotrichosis caused by mutation in APCDD1, hypotrichosis type 1

0 clinical trials for this condition and its sub-types, 0 tagged with Hypotrichosis 1 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

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