| Descriptor English: | alpha-Thalassemia | ||||||
| Descriptor Spanish: |
Talasemia alfa
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| Descriptor Portuguese: | Talassemia alfa | ||||||
| Descriptor French: | alpha-Thalassémie | ||||||
| Entry term(s): |
A-Thalassemia Alpha Thalassemia Disease, Hemoglobin H Hemoglobin H Disease Thalassemia alpha Thalassemia, Alpha Thalassemia-alpha alpha-Thalassemias |
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| Tree number(s): |
C15.378.071.141.150.875.100 C15.378.420.826.100 C16.320.070.875.100 C16.320.365.826.100 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017085 | ||||||
| Scope note: | A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. |
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| Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES |
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| 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 |
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| Previous Indexing: |
Thalassemia (1966-1992) |
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| Public MeSH Note: | 93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92 |
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| Online Note: | use THALASSEMIA to search ALPHA-THALASSEMIA 1988-92 & HEMOGLOBIN H DISEASE 1982-92 |
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| History Note: | 93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92 |
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| Related: |
Hemoglobin H
MeSH | ||||||
| DeCS ID: | 30859 | ||||||
| Unique ID: | D017085 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1993/01/01 | ||||||
| Date of Entry: | 1992/05/07 | ||||||
| Revision Date: | 2013/07/08 |
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alpha-Thalassemia
- Preferred
| Concept UI |
M0025958 |
| Scope note | A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted. |
| Preferred term | alpha-Thalassemia |
| Entry term(s) |
A-Thalassemia Alpha Thalassemia Disease, Hemoglobin H Hemoglobin H Disease Thalassemia alpha Thalassemia, Alpha Thalassemia-alpha alpha-Thalassemias |
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