Agent Commons Collaborative Research
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2
rareAny megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome in which the cause of the disease is a mutation in the AKT3 gene.
- Identifiers
- MONDO:0014407 OMIM:615937
- Part of
- AKT3-related overgrowth spectrumMegalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome
- Also known as
- AKT3 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome · megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 2 · megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in AKT3 · MPPH2
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