Autosomal dominant nonsyndromic hearing loss 7

Synonyms: Deafness, autosomal dominant 7

Summary

Autosomal dominant deafness-7 (DFNA7) is a form of progressive sensorineural hearing loss with highly variable age at onset and severity, even within families. The age at onset ranges from congenital to mid-adulthood. Some patients may have associated vertigo (summary by Wesdorp et al., 2018). [from OMIM]

Available tests

2 tests are in the database for this condition.

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Clinical tests (2 available)

Molecular Genetics Tests

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Associated genes Help
Genes reported to contribute to the condition.

LMX1A
8 tests
Also known as: DFNA7, LMX1, LMX1.1, LMX1A
Summary: LIM homeobox transcription factor 1 alpha

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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