Autosomal dominant nonsyndromic hearing loss 28

Synonyms: DFNA28 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 28

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GRHL2 gene. [from MONDO]

Available tests

21 tests are in the database for this condition.

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Clinical tests (21 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

GRHL2
59 tests
Also known as: BOM, DFNA28, ECTDS, PPCD4, TFCP2L3, GRHL2
Summary: grainyhead like transcription factor 2

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Sensorineural hearing loss disorder
  Sensorineural hearing loss disorder
  - MedGen UID: 9164
  - Concept ID: C0018784
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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