Panel | Mode of inheritance | Details |
---|---|---|
7 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.79 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Nephrotic syndrome with primary microcephaly |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 3.122 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Galloway-Mowat syndrome 3, OMIM:617729, Galloway-Mowat syndrome 3, MONDO:0033007 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 5.343 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Galloway-Mowat syndrome 3, 617729, Intellectual disability |
Component of the following Super Panels:
Signed-off version 4.12 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Galloway-Mowat syndrome 3 617729 |
Green in Proteinuric renal diseaseR-numbers: R195 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Galloway-Mowat syndrome 3 617729 |
Green in Severe microcephalyR-numbers: R88 Signed-off version 4.41 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Galloway-Mowat syndrome 3, OMIM:617729 |
R-numbers: R257 Signed-off version 3.11 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Galloway-Mowat syndrome 3 617729 |