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DOID:0060284 - paroxysmal nocturnal hemoglobinuria
Disease Ontology Definition:An acquired 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:
Echinobase Genes
:
pigt
| MIM:300818 - paroxysmal nocturnal hemoglobinuria 1; pnh1 |
| MIM:615399 - paroxysmal nocturnal hemoglobinuria 2; pnh2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hemoglobinuria (is_a)