Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in Monogenic hearing lossR-numbers: R67 Signed-off version 3.3 | BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal | Phenotypes #600101:Deafness, autosomal dominant 2A |