Panel | Mode of inheritance | Details |
---|---|---|
11 panels | ||
Green in Alstrom syndromeR-numbers: R106 Signed-off version 1.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes ALSTROM SYNDROME 203800 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes ALSTROM SYNDROME |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes ALSTROM SYNDROME, 203800 |
Green in Monogenic hearing lossComponent of the following Super Panels:
R-numbers: R67 Signed-off version 4.42 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes #203800: Alstrom syndrome |
Green in Ophthalmological ciliopathiesComponent of the following Super Panels:
Signed-off version 4.1 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Alstrom Syndrome, Bardet-Biedl Syndrome, 203800, Alstrom syndrome |
Component of the following Super Panels:
R-numbers: R135 Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes OMIM 203800 |
Green in Renal ciliopathiesComponent of the following Super Panels:
Signed-off version 3.7 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Bardet-Biedl Syndrome, Alstrom syndrome, OMIM:203800 |
Green in Retinal disordersR-numbers: R32 Signed-off version 5.4 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Eye Disorders, Alstrom syndrome, 203800 |
Green in Severe early-onset obesityR-numbers: R149 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Alstrom syndrome, OMIM:203800 |
R-numbers: R158 Signed-off version 4.56 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Alstrom syndrome, OMIM:203800 |