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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal recessive 44

Summary

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the METTL23 gene. [from MONDO]

Available tests

6 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: C17orf95, MRT44, METTL23
    Summary: methyltransferase 23, arginine

Clinical features

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