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| Term | pellagra | ID (Ontology) | DOID:8457 (Human Disease) |
| Definition | A nutritional deficiency disease that is characterized by deficiency of niacin (vitamin B3), has_symptom gastrointestinal disturbance, anorexia, diarrhea, dementia, hallucinations, depression, psychosis, and/or non-specific skin changes, and has_material_basis_in deficiency of niacin, often from inadequate diet, malabsorption, or medication side effects. | ||
| Also Known As | "Niacin deficiency" ; "Niacin-tryptophan deficiency" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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nutrition disease |__nutritional deficiency disease |__pellagra |
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| Is a | nutritional deficiency disease | ||
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GARD:10014 ICD9CM:265.2 MESH:D010383 SNOMEDCT_US_2023_03_01:267491008 UMLS_CUI:C0030783 |
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