Panel | Mode of inheritance | Details |
---|---|---|
5 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.79 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME 616577 |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 4.134 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Epilepsy, hearing loss, and mental retardation syndrome 616577 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 3.122 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes EPILEPSY, HEARING LOSS, AND MENTAL RETARDATION SYNDROME |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 5.343 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Epilepsy, hearing loss, and mental retardation syndrome, 616577 |
Green in Monogenic hearing lossComponent of the following Super Panels:
R-numbers: R67 Signed-off version 4.23 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Epilepsy, hearing loss, and mental retardation syndrome 616577 |