| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0019025 | Hemoglobin F Disease | ICD10 | Hereditary persistence of fetal haemoglobin [HPFH] | D56.4 |
| C0019025 | Hemoglobin F Disease | ICD10CM | Hereditary persistence of fetal hemoglobin [HPFH] | D56.4 |
| C0019025 | Hemoglobin F Disease | MONDO | hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome | 0018749 |
| C0019025 | Hemoglobin F Disease | MONDO | hereditary persistence of fetal hemoglobin | 0020989 |
| C0019025 | Hemoglobin F Disease | MSH | Anemia, Cooley's | D017086 |
| C0019025 | Hemoglobin F Disease | MSH | beta-Thalassemia | D017086 |
| C0019025 | Hemoglobin F Disease | MSH | beta Thalassemia | D017086 |
| C0019025 | Hemoglobin F Disease | MSH | Hemoglobin F Disease | D017086 |
| C0019025 | Hemoglobin F Disease | MSH | Thalassemia Minor | D017086 |
| C0019025 | Hemoglobin F Disease | MSH | Thalassemia Intermedia | D017086 |
| C0019025 | Hemoglobin F Disease | NCI | Hereditary Persistence of Fetal Hemoglobin | C129072 |
| C0019025 | Hemoglobin F Disease | ORDO | Hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome | 46532 |