Autosomal recessive nonsyndromic hearing loss 97

Synonyms: Deafness, autosomal recessive 97

Summary

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

Available tests

19 tests are in the database for this condition.

Clinical tests (19 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

MET
225 tests
Also known as: AUTS9, DA11, DFNB97, HGFR, RCCP2, c-Met, MET
Summary: MET proto-oncogene, receptor tyrosine kinase

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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