Autosomal recessive nonsyndromic hearing loss 86
- Synonyms
- Deafness, autosomal recessive 86
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- GeneReview Scope
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- References
- Chapter Notes
- Authors:
- Bettina E Mucha
- Raoul CM Hennekam
- Sanjay Sisodiya
- view full author information
Available tests
Clinical tests (32 available)
Clinical features
Help- Ear malformation
- Hearing impairment
Hearing impairment
- MedGen UID: 235586
- Concept ID: C1384666
- Finding: Disease or Syndrome
Ear malformation
- Hearing impairment
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