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Intellectual developmental disorder, autosomal recessive 74

MONDO:0014951

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the APC2 gene.

Also known as: APC2 Sotos syndrome, Sotos syndrome caused by mutation in APC2, Sotos syndrome type 3, intellectual developmental disorder, autosomal recessive 74

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

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Hereditary disease (172) Neurodevelopmental disorder (125) Intellectual disability (115) Inborn errors of metabolism (42) Human disease (14) Hereditary neurological disease (5) Autosomal recessive disease (4)

Trials to join now! 25 Not yet recruiting 8 Not yet finished but already full! 6 Completed 13