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Summary Literature (0)
DOID:0060284 - paroxysmal nocturnal hemoglobinuria


Disease Ontology Definition: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:

Xenbase Genes : piga, pigt

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018641 - paroxysmal nocturnal hemoglobinuria

OMIM:
OMIM:300818 - PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1; PNH1
OMIM:615399 - PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2; PNH2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hemoglobinuria (is_a)