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Summary Literature (0)
DOID:8457 - pellagra

Disease Ontology 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.

Synonyms: Niacin deficiency, Niacin-tryptophan deficiency, Pellagra,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019975 - pellagra


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): nutritional deficiency disease (is_a)