Autosomal dominant nonsyndromic hearing loss 4A

Synonyms: DFNA 4 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal dominant 4; Deafness, autosomal dominant 4A

Summary

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH14 gene. [from MONDO]

Available tests

22 tests are in the database for this condition.

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Clinical tests (22 available)

Molecular Genetics Tests

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Associated genes Help
Genes reported to contribute to the condition.

MYH14
63 tests
Also known as: DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C, NMHC-II-C, PNMHH, myosin, MYH14
Summary: myosin heavy chain 14

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Progressive sensorineural hearing impairment
  Progressive sensorineural hearing impairment
  - MedGen UID: 335894
  - Concept ID: C1843156
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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