FAT1

FAT atypical cadherin 1
OMIM: 600976
PanelMode of inheritanceDetails
3 panels
R-numbers: R21, R412
Signed-off version 4.195
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hand and foot anomalies, nephropathy, ocular anomalies, multiple congenital anomalies
Component of the following Super Panels:
  • - Unexplained young onset end-stage renal disease
R-numbers: R195
Signed-off version 4.15
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Glomerulotubular nephropathy
R-numbers: R36
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes