Disease-gene associations mined from literature

Human genes for pellagra

Pellagra [DOID:8457]

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:  pellagra,  DOID:8457,  pellagras,  Niacin deficiency,  Niacin-tryptophan deficiency ...

Linkouts:  OMIM