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GTR Home > Conditions/Phenotypes > Microcephaly 13, primary, autosomal recessive

Summary

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

Available tests

6 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Genes See tests for all associated and related genes

  • Also known as: CENP-E, KIF10, MCPH13, PPP1R61, CENPE
    Summary: centromere protein E

Clinical features

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