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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)
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| 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)
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| ICD9 | 282.7 |
| English | Globin abnormality, Haemoglobin disease, Haemoglobin disorder, Haemoglobinopathy, Hemoglobin disease, Hemoglobin disorder, hemoglobin disorders, Hemoglobinopathies, Hemoglobinopathies / Iron Metabolism, Hemoglobinopathy |
| Spanish | alteración de la hemoglobina, alteracion de la hemoglobina, hemoglobinopatÃa, hemoglobinopatia, trastorno de la hemoglobina |
| Credits | Derived from the NIH UMLS (Unified Medical Language System)
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