Microcephaly 13, primary, autosomal recessive

MONDO:0014473

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

Also known as: CENPE autosomal recessive primary microcephaly, autosomal recessive primary microcephaly caused by mutation in CENPE, microcephaly 13, primary, autosomal recessive, MCPH13

58 clinical trials for this condition and its sub-types.

Follow this condition — get notified about new trials

Broader categories

Sort by