Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 (MPPH2)

Alias:

Mpph2

Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome, Type 2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2, is also known as mpph2. An important gene associated with Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 2 is AKT3 (AKT Serine/Threonine Kinase 3). Affiliated tissues include liver and skin, and related phenotypes are seizure and hemimegalencephaly

Related ID：

MALACARDS：MGL028

OMIM：615937

MESH：D006849