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

Gå till den engelska sidan

Intellectual disability, X-linked 21

MONDO:0010256

Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the IL1RAPL1 gene.

Also known as: IL1RAPL1 non-syndromic X-linked intellectual disability, intellectual developmental disorder, X-linked 21, X-linked recessive, intellectual disability, X-linked 21, intellectual disability, X-linked type 21, mental retardation, X-linked type 21, non-syndromic X-linked intellectual disability caused by mutation in IL1RAPL1, MRX21, intellectual disability, X-linked 34

0 clinical trials for this condition and its sub-types, 0 tagged with Intellectual disability, X-linked 21 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.