Genomics England
GMS Panels
Panels
Genes and Entities

FTH1

ferritin heavy chain 1
OMIM: 134770
PanelMode of inheritanceDetails
1 panel
Green
in Ataxia and cerebellar anomalies - narrow panel
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies - childhood onset
Signed-off version 9.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Neurodegeneration with brain iron accumulation 9, OMIM:620669, ?Hemochromatosis, type 5 OMIM:615517, hemochromatosis type 5 MONDO:0014225