Rare hereditary hemochromatosis

Orpha code: 220489OMIM code:

Definition

Rare hereditary hemochromatosis comprises the rare forms of hereditary hemochromatosis (HH), a group of diseases characterized by excessive tissue iron deposition. These rare forms are hemochromatosis type 2 (juvenile), type 3 (TFR2-related), and type 4 (ferroportin disease) (see these terms). Hemochromatosis type 1 (also called classic hemochromatosis; see this term) is not a rare disease.

Disease data
Classification

Category

Synonyms
Iron overload disease
Choroba przeładowania żelazem
ORPHA code
220489
OMIM code
-
ICD10 code
E83.1
ICD11 code
-

No additional description.

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