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familial periodic paralysis
MONDO:0000995
hereditary hemochromatosis
MONDO:0006507
acrodermatitis enteropathica
MONDO:0008713
atransferrinemia
MONDO:0008846
sulfite oxidase deficiency due to molybdenum cofactor deficiency type A
MONDO:0009643
sulfite oxidase deficiency due to molybdenum cofactor deficiency type B
MONDO:0009644