hemolytic anemia hereditary elliptocytosis https://www.malacards.org/card/hereditary_elliptocytosis ovalocytosis ICD10CM:D58.1 UMLS:C0013902 congenital elliptocytosis hereditary ovalocytosis GARD:0006621 DOID:2373 NORD:1935 MEDGEN:41747 Hereditary elliptocytosis (HE) is a rare clinically and genetically heterogeneous disorder of the red cell membrane characterized by manifestations ranging from mild to severe transfusion-dependent hemolytic anemia but with the majority of patients being asymptomatic. NCIT:C35882 MedDRA:10014490 MESH:D004612 NANDO:2200630 Orphanet:288 HE MONDO:0017319 SCTID:178935009 Hashimoto Encephalopathy icd11.foundation:679955609