Genomics England
GMS Panels
Panels
Genes and Entities

NPHS1

NPHS1, nephrin
OMIM: 602716
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
NEPHROTIC SYNDROME TYPE 1 256300
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
NEPHROTIC SYNDROME TYPE 1
Green
in Proteinuric renal disease
R-numbers: R195
Signed-off version 4.13
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nephrotic syndrome, type 1 #602716
Green
in Unexplained young onset end-stage renal disease
R-numbers: R257
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nephrotic syndrome, type 1 256300