Agent Commons Collaborative Research

Microcephaly and chorioretinopathy 3

rare

Any microcephaly and chorioretinopathy in which the cause of the disease is a mutation in the TUBGCP4 gene.

Identifiers
MONDO:0014592 OMIM:616335
Causal genes
TUBGCP4
Part of
Microcephaly and chorioretinopathy
Also known as
MCCRP3 · microcephaly and chorioretinopathy caused by mutation in TUBGCP4 · microcephaly and chorioretinopathy type 3 · microcephaly and chorioretinopathy, autosomal recessive, 3 · microcephaly and chorioretinopathy, autosomal recessive, type 3

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