paroxysmal nocturnal hemoglobinuria Disease Ontology Browser

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Disease Ontology Browser

paroxysmal nocturnal hemoglobinuria (DOID:0060284)
Alliance: disease page
Alt IDs: OMIM:300818, OMIM:615399, ICD10CM:D59.5, ICD10CM:D59.6, MESH:D006457, NCI:C61233, ORDO:447, UMLS_CUI:C0019050, UMLS_CUI:C0024790, UMLS_CUI:C0086774
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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