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AKT3-related overgrowth spectrum

MONDO:0800485

Any overgrowth syndrome where the cause of the disease is a gain-of-function variant in the AKT3 gene.

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

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Sub-types

Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 (0)

Broader categories

Disease (618) Hereditary disease (172) Human disease (14) Disease of genetic or genomic mechanism (2) Overgrowth syndrome (1) Disease by developmental or physiological process (0) Disease by etiologic mechanism (0) Disorder of development or morphogenesis (0)

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