familial hemolytic anemia hereditary spherocytosis https://rarediseases.info.nih.gov/diseases/6639/hereditary-spherocytosis https://www.malacards.org/card/hereditary_spherocytosis UMLS:C0037889 NORD:777 DOID:12971 MEDGEN:52450 congenital spherocytosis MONDO:0019350 NCIT:C97074 icd11.foundation:1305248013 Orphanet:822 NANDO:2200622 ICD10CM:D58.0 SCTID:55995005 congenital spherocytic hemolytic anaemia MedDRA:10019904 MESH:D013103 Minkowski-Chauffard disease hereditary spherocytosis spherocytic anaemia ICD9:282.0 Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis. GARD:0006639