has modifier hemolytic anemia familial hemolytic anemia A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies. COHD:28396 DOID:589 GARD:0006167 ICD10:D58.9 ICD9:282 ICD9:282.9 MESH:D000745 MONDO:0003689 NCIT:C34379 SCTID:42601008 anemia hemolytic congenital congenital hemolytic anemia hereditary hemolytic anemia https://rarediseases.info.nih.gov/diseases/6167/congenital-hemolytic-anemia Mendelian disease inherited