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GTR Home > Conditions/Phenotypes > Microcephaly 8, primary, autosomal recessive

Summary

Any autosomal recessive primary microcephaly in which the cause of the disease is a mutation in the CEP135 gene. [from MONDO]

Available tests

20 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: CEP4, KIAA0635, MCPH8, CEP135
    Summary: centrosomal protein 135

Clinical features

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