Cure My Disease

Don't miss your cure!

 Log in / Sign up

Intellectual disability, X-linked 101

MONDO:0010489

Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the MID2 gene.

Also known as: MID2 non-syndromic X-linked intellectual disability, intellectual developmental disorder, X-linked 101, X-linked recessive, intellectual disability, X-linked 101, intellectual disability, X-linked type 101, mental retardation, X-linked type 101, non-syndromic X-linked intellectual disability caused by mutation in MID2, MRX101, mental retardation, X-linked 101

28 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) X-linked disease (16) Human disease (14) Hereditary neurological disease (5) Disease of genetic or genomic mechanism (2) Disease by body system or component (0)
Trials to join now! 12 Not yet recruiting 5 Not yet finished but already full! 3 Completed 8
Sort by