Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3

Any megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome in which the cause of the disease is a mutation in the CCND2 gene.

Also known as: CCND2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome, megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3, megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 3, megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in CCND2, MPPH3

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