| Descriptor in English: | Hemoglobinopathies |
| Descriptor in Spanish: | Hemoglobinopatías |
| Descriptor in Portuguese: | Hemoglobinopatias |
| Descriptor in French: | Hémoglobinopathies |
| Entry term(s): |
Hemoglobinopathy |
| Tree number(s): |
C15.378.420 C16.320.365 |
| Scope note: | A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. |
| Annotation: | do not confuse with HEMOGLOBINS, ABNORMAL (D12): use term in the text; coord IM with specific abnormal hemoglobin (IM) but HEMOGLOBIN C DISEASE; THALASSEMIA (hemoglobin H disease) & ANEMIA, SICKLE CELL (hemoglobin S disease) are available |
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
| History Note: | 68 |
| See also the descriptors: |
Hemoglobins, Abnormal
MeSH |
| DeCS UI: | 6603 |
| Descriptor UI: | D006453 |
| Date Established: | 1968/01/01 |
| Date of Entry: | 1999/01/01 |
| Revision Date: | 2001/07/25 |
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Hemoglobinopathies
- Preferred
| Concept UI |
M0010129 |
| Scope note | A group of inherited disorders characterized by structural alterations within the hemoglobin molecule. |
| Preferred term | Hemoglobinopathies |
| Entry term(s) |
Hemoglobinopathy |
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