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GTR Home > Conditions/Phenotypes > Meier-Gorlin syndrome 6

Meier-Gorlin syndrome 6

Summary

Any Meier-Gorlin syndrome in which the cause of the disease is a mutation in the GMNN gene. [from MONDO]

Available tests

19 tests are in the database for this condition.

Clinical tests (18 available)

Molecular Genetics Tests

Research tests

Genes See tests for all associated and related genes

  • Also known as: Gem, MGORS6, GMNN
    Summary: geminin DNA replication inhibitor

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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