DISEASES

Disease-gene associations mined from literature

Human genes for riboflavin deficiency

Riboflavin deficiency [DOID:8454]

A nutritional deficiency disease that is characterized by stomatitis, cheilosis, glossitis, conjunctivitis, and anemia, develops_from vitamin B2 (riboflavin) deficiency, has_symptom red chapped lips, painful swollen tongue, sore throat, blurred vision, and fatigue, and has_material_basis_in inadequate intake, endocrine disorder, liver disorder, alcoholism, and dialysis.

Synonyms:  riboflavin deficiency,  DOID:8454,  riboflavin deficiencies,  ariboflavinosis,  vitamin B2 deficiency ...