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GTR Home > Conditions/Phenotypes > Autosomal recessive nonsyndromic hearing loss 67

Autosomal recessive nonsyndromic hearing loss 67

Synonyms
DFNB67 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 67

Summary

Autosomal recessive deafness-67 (DFNB67) is characterized by congenital bilateral severe to profound sensorineural deafness, with or without vestibular dysfunction (Shabbir et al., 2006; Kalay et al., 2006; Lerat et al., 2019). [from OMIM]

Available tests

24 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (24 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DFNB67, TMHS, dJ510O8.8, LHFPL5
    Summary: LHFPL tetraspan subfamily member 5

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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