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PedAM

Pediatric Disease Annotations & Medicines




Disease sarcoidosis
Phenotype 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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