(Q32146270)
Englisch
hemochromatosis type 1
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22
- symptomatic form of classic hemochromatosis
- symptomatic form of HFE-related hereditary hemochromatosis
- symptomatic form of hemochromatosis type 1
- HFE1
- HFE-associated hereditary hemochromatosis
Statements
1 reference
1 reference
C84764
0 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference