hemoglobinuria hemolytic anemia acquired metabolic disease acquired aplastic anemia inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation disorder of GPI anchor biosynthesis paroxysmal nocturnal hemoglobinuria https://github.com/monarch-initiative/mondo/issues/4232 https://github.com/monarch-initiative/mondo/issues/9097 https://rarediseases.info.nih.gov/diseases/7337/paroxysmal-nocturnal-hemoglobinuria https://www.malacards.org/card/paroxysmal_nocturnal_hemoglobinuria Orphanet:447 HP:0004818 hereditary paroxysmal nocturnal hemoglobinuria icd11.foundation:859588467 Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal hematopoietic stem cell disorder characterized by corpuscular hemolytic anemia, bone marrow failure and frequent thrombotic events. MEDGEN:7471 SCTID:1963002 inherited paroxysmal nocturnal hemoglobinuria MedDRA:10034042 UMLS:C0024790 PNH paroxysmal hemoglobinuria MONDO:0100244 Marchiafava-Micheli disease NCIT:C61233 acquired paroxysmal nocturnal hemoglobinuria NORD:1557 OMIMPS:300818 ICD10CM:D59.5 HGNC:8957 DOID:0060284 GARD:0007337