Disease-gene associations mined from literature

Human genes for paroxysmal nocturnal hemoglobinuria

Paroxysmal nocturnal hemoglobinuria [DOID:0060284]

An aquired hemolytic anemia that is characterized by abdominal pain, hematuria, esophageal dysmotility and thrombosis, has_material_basis_in defect in the cell membrane glycosyl phosphatidylinositols that protect red blood cells from the innate complement immune system.

Synonyms:  paroxysmal nocturnal hemoglobinuria,  DOID:0060284,  paroxysmal nocturnal hemoglobinurias