Microcephaly and chorioretinopathy 2

Any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the PLK4 gene.

Also known as: PLK4 microcephaly and chorioretinopathy, microcephaly and chorioretinopathy caused by mutation in PLK4, microcephaly and chorioretinopathy type 2, microcephaly and chorioretinopathy, autosomal recessive, type 2, MCCRP2, microcephaly and chorioretinopathy, autosomal recessive, 2

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