Genomics England
GMS Panels
Panels
Genes and Entities

FAH

fumarylacetoacetate hydrolase
OMIM: 613871
PanelMode of inheritanceDetails
6 panels
Green
in Cholestasis
R-numbers: R171
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neonatal and Adult Cholestasis, Tyrosinaemia, Type 1, 276700, Cholestasis
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
TYROSINEMIA TYPE 1 276700
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
TYROSINEMIA TYPE 1
Green
in Likely inborn error of metabolism
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 5.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Tyrosinemia, type I
Green
in Renal tubulopathies
R-numbers: R198
Signed-off version 4.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Tyrosinemia, type I 276700
Green
in Unexplained young onset end-stage renal disease
R-numbers: R257
Signed-off version 4.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Tyrosinemia, type I, OMIM:276700