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Pellagra

Disease ID: disease_node_5950

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DbxrefGARD:10014, ICD9CM:265.2, MESH:D010383, SNOMEDCT_US_2023_03_01:267491008, UMLS_CUI:C0030783
SubclassofDOID_5113
Data SourceDOID, MESH
SynonymsNiacin deficiency, Niacin-tryptophan deficiency
Mesh IdD010383
Mesh LabelPellagra
Disease Has FeatureDOID_1307
Mesh SubclassofD014804
Doid Labelpellagra
Doid DescriptionA 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.
Has SymptomSYMP_0000570, SYMP_0000607, SYMP_0000022, SYMP_0000523
Disease Node Iddisease_node_5950
Doid IdDOID_8457
LabelPellagra

  • Incoming r'ship ASSOCIATED_WITH_DISEASE to/from Coffea arabica (Plant) Rel Props:Icd11:5B5C.0; Doid:DOID_8457; Mesh:D010383; Reference:ISBN:9788172360481