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GTR Home > Conditions/Phenotypes > Hearing loss, autosomal recessive 121

Hearing loss, autosomal recessive 121

Synonyms
Deafness, autosomal recessive 121

Summary

Autosomal recessive deafness-121 (DFNB121) is characterized by congenital or prelingual moderate sensorineural hearing loss (Ramzan et al., 2023). [from OMIM]

Available tests

1 test is in the database for this condition.

Clinical tests (1 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: DFNB121, GABABL, PGR28, GPR156
    Summary: G protein-coupled receptor 156

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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