Autosomal recessive nonsyndromic hearing loss 98

Synonyms: Deafness, autosomal recessive 98

Summary

This form of autosomal recessive nonsyndromic deafness is sensorineural and shows prelingual onset (Delmaghani et al., 2012). [from OMIM]

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.

TSPEAR
31 tests
Also known as: C21orf29, DFNB98, ECTD14, STHAG10, TSP-EAR, TSPEAR
Summary: thrombospondin type laminin G domain and EAR repeats

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

Reviews

Clinical resources

Molecular resources

Consumer resources

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