Autosomal dominant nonsyndromic hearing loss 17

Synonyms: Autosomal dominant nonsyndromic deafness 17; DFNA17 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 17; Deafness, autosomal dominant nonsyndromic sensorineural 17; Late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration; Nonsyndromic hereditary deafness DFNA17

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene. [from MONDO]

Available tests

55 tests are in the database for this condition.

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Clinical tests (55 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

MYH9
175 tests
Also known as: BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA, MYH9
Summary: myosin heavy chain 9

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- High-frequency hearing impairment
  High-frequency hearing impairment
  - MedGen UID: 42358
  - Concept ID: C0018780
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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