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

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

4 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (4 available)

Molecular Genetics 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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Imported from Human Phenotype Ontology (HPO)

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