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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 63

Autosomal recessive nonsyndromic hearing loss 63

Synonyms
DFNB63 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 63

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LRTOMT gene. [from MONDO]

Available tests

21 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (21 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CFAP111, DFNB63, LRRC51, LRRC51-TOMT, TOMT, LRTOMT
    Summary: leucine rich transmembrane and O-methyltransferase domain containing

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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