CEP164

centrosomal protein 164
OMIM: 614848
PanelMode of inheritanceDetails
7 panels
Component of the following Super Panels:
  • - Cystic renal disease
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliopathy genes associated with cystic kidney disease
R-numbers: R21, R412
Signed-off version 2.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nephronophthisis 15 614845
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ciliopathies, Nephronophthisis 15, Senior-Loken syndrome, Nephronophthisis 15, 614845
Component of the following Super Panels:
  • - Cystic renal disease
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
ciliopathies, Nephronophthisis 15, Senior-Loken syndrome, Nephronophthisis 15, 614845
R-numbers: R32
Signed-off version 3.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Genetic Retinal Degeneration Conditions
R-numbers: R202
Signed-off version 2.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nephronopthisis 15 MIM 614845
R-numbers: R257
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Ciliopathy genes associated with cystic kidney disease, Nephronophthisis 15 614845