Disease-gene associations mined from literature

Human genes for pyridoxine deficiency anemia

Pyridoxine deficiency anemia [DOID:8455]

A nutritional deficiency disease that is characterized by normocytic anemia associated with deficiency of pyridoxine (vitamin B6), and has_material_basis_in decreased intake, malabsorption, increased clearance or breakdown, and certain medications (eg isoniazid).

Synonyms:  pyridoxine deficiency anemia,  DOID:8455,  pyridoxine deficiency anemias,  vitamin B6 deficiency syndrome,  vitamin B6 deficiency disease ...