Monarch Disease Ontology term MONDO_0014592 (microcephaly and chorioretinopathy 3) is any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the TUBGCP4 gene. Also known as: TUBGCP4 microcephaly and chorioretinopathy, microcephaly and chorioretinopathy caused by mutation in TUBGCP4, microcephaly and chorioretinopathy type 3, microcephaly and chorioretinopathy, autosomal recessive, type 3.