Genomics England
GMS Panels
Panels
Genes and Entities

PRODH

proline dehydrogenase 1
OMIM: 606810
PanelMode of inheritanceDetails
1 panel
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 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Hyperprolinemia, type I, OMIM:239500, hyperprolinemia type 1, MONDO:0009400