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GTR Home > Conditions/Phenotypes > Intellectual disability, autosomal recessive 27

Summary

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the LINS1 gene. [from MONDO]

Available tests

7 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: LINS, MRT27, WINS1, LINS1
    Summary: lines homolog 1

Clinical features

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