Genomics England
GMS Panels
Panels
Genes and Entities

PAH

phenylalanine hydroxylase
OMIM: 612349
PanelMode of inheritanceDetails
5 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
NON-PHENYLKETONURIA HYPERPHENYLALANINEMIA 261600, PHENYLKETONURIA 261600
Green
in Genetic epilepsy syndromes
R-numbers: R59
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Phenylketonuria 261600
Green
in Inborn errors of metabolism
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R98
Signed-off version 3.2
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Phenylketonuria
Green
in Intellectual disability
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Phenylketonuria, 261600[Hyperphenylalaninemia, non-PKU mild], 261600, NON-PHENYLKETONURIA HYPERPHENYLALANINEMIA (NON-PKU HPA)
Green
in White matter disorders - adult onset
R-numbers: R62
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Phenylketonuria, [Hyperphenylalaninemia, non-PKU mild], 261600