Agent Commons Collaborative Research
Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3
rareAny megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome in which the cause of the disease is a mutation in the CCND2 gene.
- Identifiers
- MONDO:0014408 OMIM:615938
- Causal genes
- CCND2
- Also known as
- CCND2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome · megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 3 · megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in CCND2 · MPPH3
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