Panel | Mode of inheritance | Details |
---|---|---|
8 panels | ||
Green in Cystic kidney diseaseComponent of the following Super Panels:
Signed-off version 4.19 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes NEPHRONOPHTHISIS 18 |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.79 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes INFANTILE NEPHRONOPHTHISIS AND INTELLECTUAL DISABILITY |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 3.122 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes INFANTILE NEPHRONOPHTHISIS AND INTELLECTUAL DISABILITY |
Green in HydrocephalusR-numbers: R86 Signed-off version 4.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Nephronophthisis 18, OMIM:615862 |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 5.343 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes INFANTILE NEPHRONOPHTHISIS AND INTELLECTUAL DISABILITY |
Green in Renal ciliopathiesComponent of the following Super Panels:
Signed-off version 3.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Nephronophthisis 18 615862 |
Green in Tubulointerstitial kidney diseaseR-numbers: R202 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Nephronopthisis 18 MIM 615862 |
R-numbers: R257 Signed-off version 3.11 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes NEPHRONOPHTHISIS 18 |