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Up to: Syndromic disease · Inherited retinal dystrophy · Microcephaly and chorioretinopathy
Microcephaly and chorioretinopathy 1
An autosomal recessive disorder caused by mutation(s) in the TUBGCP6 gene, encoding gamma-tubulin complex component 6. It is characterized by microcephaly and chorioretinopathy.
This condition has no sub-types.