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Details for Disease 220489

DISEASE NAME	Rare hereditary hemochromatosis
DISEASE CATEGORY (ICD10)	Endocrine, nutritional and metabolic diseases
DISEASE ID (ICD10)	E83.1
DISEASE ID (OMIM)	N.A.
2 combinations linked to 220489	OLI186; OLI187
1 gene combination linked to 220489	HAMP; HFE
ORPHANET ID	220489

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