| Digenic hemochromatosis (disorder) | | Digenic hemochromatosis | | A rare subtype of hemochromatosis characterized by the combination of pathogenic variants in two genes involved in iron metabolism (usually a combination of HFE and non-HFE mutations), where the classical HFE-related hemochromatosis is not enough to fully explain the clinical picture of the patient. |
| | Id | 1299153008 | | Status | Primitive |
| SNOMED CT to ICD-10 extended map | | Target | E83.1 | | Rule | TRUE | | Advice | ALWAYS E83.1 | | Correlation | SNOMED CT source code to target map code correlation not specified |
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