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GTR Home > Conditions/Phenotypes > Usher syndrome type 3A

Usher syndrome type 3A

Synonyms
USHER SYNDROME, TYPE IIIA

Summary

Any Usher syndrome in which the cause of the disease is a mutation in the CLRN1 gene. [from MONDO]

Available tests

22 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (22 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: RP61, USH3, USH3A, CLRN1
    Summary: clarin 1

Clinical features

Help
Imported from Human Phenotype Ontology (HPO)

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