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pellagra

Disease Summary
Associated Targets (5)
Tchem

3

Tclin

2


GARD Rare
Mondo Description Pellagra is a nutritional disorder caused by a deficiency in niacin (vitamin B3) or its precursor (tryptophan) that is mainly observed in Asia and Africa where it is generally due to poor nutrition. It is characterized by dermatitis (symmetrical photodistributed erythema that may be accompanied by vesicles and bullae, and that develops into hyperkeratotic and hyperpigmented skin), gastrointestinal symptoms (diarrhea), and neuropsychiatric disorders (dementia). It can be life-threatening without a correct management.
Disease Ontology Description 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.
Mondo Term and Equivalent IDs
MONDO:0019975:  pellagra
COHD:434310: 
EFO:0008570: 
GARD:0010014: 
MESH:D010383: 
Orphanet:97352: 
SCTID:418279001: 
UMLS:C0030783: 
UMLS:C4317126: