Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | 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 4.42 | 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 5.4 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Usher syndrome, type 1B, OMIM:276900 |