Autosomal dominant nonsyndromic hearing loss 69

Synonyms: Deafness, autosomal dominant 69; Deafness, autosomal dominant 69, unilateral or asymmetric

Summary

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

Available tests

11 tests are in the database for this condition.

Clinical tests (11 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

KITLG
41 tests
Also known as: DCUA, DFNA69, FPH2, FPHH, KL-1, Kitl, MGF, SCF, SF, SHEP7, SLF, WS2F, KITLG
Summary: KIT ligand

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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Molecular resources

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