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Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.38
Latest signed off version: v4.0
(22 Mar 2023)
Component of the following Super Panels:
Paediatric disorders
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review
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BOTH monoallelic and biallelic, autosomal or pseudoautosomal
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Sources
- Expert Review Green
- Expert
- Radboud University Medical Center, Nijmegen
- UKGTN
- Emory Genetics Laboratory
- Illumina TruGenome Clinical Sequencing Services
Phenotypes
- hearing loss
- Nonsyndromic Hearing Loss, Dominant
- Deafness, autosomal dominant 8/12, 601543
- Nonsyndromic Hearing Loss, Recessive
- Nonsyndromic Hearing Loss, Dominant
- #603629:Deafness, autosomal recessive 21
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Version 1.184
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review
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BOTH monoallelic and biallelic, autosomal or pseudoautosomal
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Sources
- Next Generation Children Project
- Expert Review Green
- Expert list
Phenotypes
- Deafness, autosomal recessive 21, 603629
- Deafness, autosomal dominant 8/12, 601543
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