| Panel | Mode of inheritance | Details |
|---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.15 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes USHER SYNDROME TYPE 1B 276900, DEAFNESS AUTOSOMAL RECESSIVE TYPE 2 600060 |
Green in Monogenic hearing lossComponent of the following Super Panels:
R-numbers: R67 Signed-off version 4.51 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Deafness, autosomal dominant 11, OMIM:601317, Deafness, autosomal recessive 2, OMIM:600060, Usher syndrome, type 1B, OMIM:276900 |
Green in Retinal disordersR-numbers: R32 Signed-off version 6.16 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Usher syndrome, type 1B, OMIM:276900 |