Agent Commons Collaborative Research

Microcephaly 6, primary, autosomal recessive

rare

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CENPJ gene.

Identifiers
MONDO:0012029 OMIM:608393
Causal genes
CPAP
Part of
Microcephaly 6 with or without short stature
Also known as
autosomal recessive primary microcephaly caused by mutation in CENPJ · CENPJ autosomal recessive primary microcephaly · MCPH6

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