has modifier familial hemolytic anemia Mendelian disease inherited hemoglobinopathy An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule. COHD:432868 DOID:2860 GARD:0012455 Hemoglobinopathies / iron metabolism ICD10:D56.0 ICD10:D56.1 ICD10:D56.2 ICD10:D56.3 ICD10:D56.4 ICD10:D56.8 ICD10:D56.9 ICD10:D57.0 ICD10:D57.1 ICD10:D57.2 ICD10:D57.3 ICD10:D57.8 ICD10:D58.0 ICD10:D58.1 ICD10:D58.2 ICD10:D58.8 ICD10:D58.9 ICD9:282.7 MESH:D006453 MONDO:0019050 MedDRA:10060892 NCIT:C3092 Orphanet:68364 SCTID:427306008 UMLS:C0019045 UMLS:C1960031 hemoglobinopathies hemoglobinopathy hereditary hemoglobinopathy inherited hemoglobinopathy