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Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.41
Latest signed off version: v4.39
(1 May 2024)
Component of the following Super Panels:
Paediatric disorders
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review
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MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
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Sources
- Expert Review Red
- Radboud University Medical Center, Nijmegen
- Expert
- Emory Genetics Laboratory
- UKGTN
- Illumina TruGenome Clinical Sequencing Services
Phenotypes
- hearing loss
- Nonsyndromic Hearing Loss, Dominant
- Deafness, autosomal dominant 48, 607841
- Deafness,autosomaldominant48,607841
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