Panel | Mode of inheritance | Details |
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1 panel | ||
Green in Monogenic hearing lossComponent of the following Super Panels:
R-numbers: R67 Signed-off version 4.42 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Nonsyndromic Hearing Loss, Dominant, Deafness, autosomal dominant 22, 606346, Nonsyndromic Hearing Loss, Recessive, #606346:Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy, #607821:Deafness, autosomal recessive 37 |