hemochromatosis type 1 (Q32146270)
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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
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hemochromatosis type 1 |
hemochromatosis that has material basis in homozygous or compound heterozygous mutation in the HFE gene on chromosome 6p22 |
|
Statements
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C84764
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