Hearing loss, autosomal dominant 88

Synonyms: Deafness, autosomal dominant 88

Summary

Autosomal dominant deafness-88 (DFNA88) is characterized by nonsyndromic postlingual progressive severe sensorineural hearing loss with tinnitus (Jiang et al., 2011; Huang et al., 2023). [from OMIM]

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Associated genes Help
Genes reported to contribute to the condition.

EPHA10
1 test
Also known as: DFNA88, EPHA10
Summary: EPH receptor A10

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Hearing impairment
  Hearing impairment
  - MedGen UID: 235586
  - Concept ID: C1384666
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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