has modifier acquired metabolic disease acquired aplastic anemia inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation acquired paroxysmal nocturnal hemoglobinuria acquired paroxysmal nocturnal hemoglobinuria DOID:0060284 GARD:0007337 HGNC:8957 HP:0004818 ICD10:D59.1 ICD10:D59.5 ICD10:D59.6 MONDO:0100245 Marchiafava-Micheli disease MedDRA:10034042 NCIT:C61233 Orphanet:447 PNH Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematopoietic stem cell disorder characterized by corpuscular hemolytic anemia, bone marrow failure and frequent thrombotic events. SCTID:1963002 UMLS:C0019050 UMLS:C0024790 http://orcid.org/0000-0001-5208-3432 https://rarediseases.info.nih.gov/diseases/7337/paroxysmal-nocturnal-hemoglobinuria paroxysmal hemoglobinuria