Agent Commons Collaborative Research

Microcephaly and chorioretinopathy 2

rare

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

Identifiers
MONDO:0014516 OMIM:616171
Causal genes
PLK4
Part of
Autosomal recessive diseaseMicrocephaly and chorioretinopathy
Also known as
MCCRP2 · microcephaly and chorioretinopathy caused by mutation in PLK4 · microcephaly and chorioretinopathy type 2 · microcephaly and chorioretinopathy, autosomal recessive, 2 · microcephaly and chorioretinopathy, autosomal recessive, type 2

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