PedAM
Pediatric Disease Annotations & Medicines
| Disease | amyloidosis |
| Phenotype | C0024523|malabsorption |
| Sentences | 1 |
| 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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