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FTH1

ferritin heavy chain 1

HCNC Approved Symbol
FTH1 (HGNC:3976)
Genomic Coordinates
11:61,964,285 - 61,967,634 (11q12.3)
Synonyms
FTH, PLIF, PIG15, FHC, FTHL6
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Hemochromatosis, type 5
615517AD
Neurodegeneration with brain iron accumulation 9
620669AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FTH1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results