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GTR Home > Conditions/Phenotypes > Seckel syndrome 10

Summary

Any Seckel syndrome in which the cause of the disease is a mutation in the NSMCE2 gene. [from MONDO]

Available tests

8 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: C8orf36, MMS21, NSE2, ZMIZ7, NSMCE2
    Summary: NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase

Clinical features

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