has material basis in germline mutation in TUBGCP4 microcephaly and chorioretinopathy microcephaly and chorioretinopathy 3 https://www.malacards.org/card/microcephaly_and_chorioretinopathy_3 https://www.malacards.org/card/microcephaly_and_chorioretinopathy_autosomal_recessive_3 microcephaly and chorioretinopathy, autosomal recessive, 3 MONDO:0014592 GARD:0018482 DOID:0080107 TUBGCP4 microcephaly and chorioretinopathy OMIM:616335 MCCRP3 microcephaly and chorioretinopathy type 3 MEDGEN:902924 microcephaly and chorioretinopathy, autosomal recessive, type 3 UMLS:C4225362 Any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the TUBGCP4 gene. microcephaly and chorioretinopathy caused by mutation in TUBGCP4