http://www.fpnotebook.com/
HemoglobinopathyAka: Hemoglobin disorders
- Sickle Cell Syndromes
- Sickle Cell Trait
- Sickle Cell Anemia
- Combination disorders
- Sickle B Thalassemia
- Sickle C Disease (SC)
- Sickle D Disease (SD)
- Unstable Hemoglobins
- Congenital Heinz body Hemolytic Anemia
- Methemoglobinemia
- Thalassemia
- Alpha Thalassemia
- Beta Thalassemia minor
- Beta Thalassemia major
Hemoglobinopathies (C0019045) | |
|---|---|
| Definition (MSH) | A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. |
| Definition (CSP) | group of inherited disorders characterized by structural alterations within the hemoglobin molecule. |
| Concepts | Disease or Syndrome (T047) |
| ICD9 | 282.7 |
| MSH | D006453 |
| English | Globin abnormality, Haemoglobin disease, Haemoglobin disorder, Haemoglobinopathy, Hemoglobin disease, Hemoglobin disorder, hemoglobin disorders, Hemoglobinopathies, Hemoglobinopathies / Iron Metabolism, Hemoglobinopathy |
| Spanish | alteracion de la hemoglobina, hemoglobinopatia, trastorno de la hemoglobina |
| Parent Concepts | Disorder of protein metabolism (C0597300), Blood Protein Disorders (C0005830), Hereditary Diseases (C0019247), Hematological Disease (C0018939), Abnormality of red blood cells (C0391870), Genetic Diseases, Inborn (C0950123), Non-Neoplastic Hematologic and Lymphocytic Disorder (C1518374), Red blood cell disorder (C0221016) |
| Sources | AOD, COSTAR, CSP, CST, LCH, LNC, MSH, MTH, MTHICD9, NCI, NDFRT, SCTSPA, SNOMEDCT Derived from the NIH UMLS (Unified Medical Language System) |
