Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Monogenic hearing lossComponent of the following Super Panels:
R-numbers: R67 Signed-off version 4.57 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes hearing loss, Febrile seizures, familial, 4, 604352, Syndromic and Non Syndromic Hearing Loss, Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472, Usher syndrome, type 2C, 605472 |
Green in Retinal disordersR-numbers: R32 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Usher syndrome, type 2C, 605472, Eye Disorders, Usher syndrome, type 2C, GPR98/PDZD7 digenic, 605472 |