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Intellectual disability, X-linked 103

MONDO:0010508

Any non-syndromic X-linked intellectual disability in which the cause of the disease is a mutation in the KLHL15 gene.

Also known as: KLHL15 non-syndromic X-linked intellectual disability, MRX103, intellectual developmental disorder, X-linked 103, X-linked recessive, intellectual disability, X-linked 103, intellectual disability, X-linked type 103, mental retardation, X-linked 103, mental retardation, X-linked type 103, non-syndromic X-linked intellectual disability caused by mutation in KLHL15

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

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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
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