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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease hemochromatosis
Comorbidity C0024523|malabsorption
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PubMedID- 24910826 ), malabsorption), infiltration of thyroid, (amyloidosis, sarcoidosis, hemochromatosis, riedel's thyroiditis, cystinosis, acquired immunodeficiency syndrome (aids), primary thyroid lymphoma), central hypothyroidism, toxic substances, industrial and environmental agents, and mutations of tsh receptor gene like g α gene mutations.

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