Descriptor English: | beta-Thalassemia | ||||||
Descriptor Spanish: |
Talasemia beta
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Descriptor Portuguese: | Talassemia beta | ||||||
Descriptor French: | bêta-Thalassémie | ||||||
Entry term(s): |
Anemia, Cooley Anemia, Cooley's Anemia, Cooleys Anemia, Erythroblastic Anemia, Mediterranean Anemias, Erythroblastic Anemias, Mediterranean Cooley's Anemia Disease, Hemoglobin F Erythroblastic Anemia Hemoglobin F Disease Intermedia, Thalassemia Intermedias, Thalassemia Major, Thalassemia (beta-Thalassemia Major) Majors, Thalassemia (beta-Thalassemia Major) Mediterranean Anemia Mediterranean Anemias Microcytemia, beta Type Microcytemias, beta Type Minor, Thalassemia (beta-Thalassemia Minor) Minors, Thalassemia (beta-Thalassemia Minor) Thalassemia Intermedia Thalassemia Intermedias Thalassemia Major Thalassemia Major (beta Thalassemia Major) Thalassemia Major (beta-Thalassemia Major) Thalassemia Majors (beta-Thalassemia Major) Thalassemia Minor Thalassemia Minor (beta Thalassemia Minor) Thalassemia Minor (beta-Thalassemia Minor) Thalassemia Minors (beta-Thalassemia Minor) Thalassemia, beta Thalassemia, beta Type Thalassemias, beta Thalassemias, beta Type Type Microcytemia, beta Type Microcytemias, beta Type Thalassemia, beta Type Thalassemias, beta beta Thalassemia beta Thalassemias beta Type Microcytemia beta Type Microcytemias beta Type Thalassemia beta Type Thalassemias |
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Tree number(s): |
C15.378.050.141.150.875.150 C15.378.420.826.150 C16.320.070.875.150 C16.320.365.826.150 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017086 | ||||||
Scope note: | A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. |
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Annotation: | delta-beta thalassemia = DELTA-THALASSEMIA + BETA-THALASSEMIA |
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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; ANEMIA, ERYTHROBLASTIC was see THALASSEMIA 1965-92, was heading 1963-64; ANEMIA, COOLEY'S was see THALASSEMIA 1963-92; ANEMIA, MEDITERRANEAN was see THALASSEMIA 1965-92; HEMOGLOBIN F DISEASE & THALASSEMIA MAJOR were see THALASSEMIA 1988-92 |
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Online Note: | use THALASSEMIA to search ANEMIA, ERYTHROBLASTIC & ANEMIA, COOLEY'S & ANEMIA, MEDITERRANEAN 1966-92 and HEMOGLOBIN F DISEASE & THALASSEMIA MAJOR 1988-92 |
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History Note: | 93; was see THALASSEMIA 1988-92; ANEMIA, ERYTHROBLASTIC was see THALASSEMIA 1965-92, was heading 1963-64; ANEMIA, COOLEY'S was see THALASSEMIA 1963-92; ANEMIA, MEDITERRANEAN was see THALASSEMIA 1965-92; HEMOGLOBIN F DISEASE & THALASSEMIA MAJOR were see THALASSEMIA 1988-92 |
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DeCS ID: | 30812 | ||||||
Unique ID: | D017086 | ||||||
NLM Classification: | WH 170 | ||||||
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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beta-Thalassemia
- Preferred
Thalassemia Intermedia
- Narrower
Thalassemia Minor
- Narrower
Hemoglobin F Disease
- Narrower
Thalassemia Major
- Narrower
Concept UI |
M0025960 |
Scope note | A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent. |
Preferred term | beta-Thalassemia |
Entry term(s) |
Microcytemia, beta Type Microcytemias, beta Type Thalassemia, beta Thalassemia, beta Type Thalassemias, beta Thalassemias, beta Type Type Microcytemia, beta Type Microcytemias, beta Type Thalassemia, beta Type Thalassemias, beta beta Thalassemia beta Thalassemias beta Type Microcytemia beta Type Microcytemias beta Type Thalassemia beta Type Thalassemias |
Concept UI |
M0542614 |
Preferred term | Thalassemia Intermedia |
Entry term(s) |
Intermedia, Thalassemia Intermedias, Thalassemia Thalassemia Intermedias |
Concept UI |
M0025962 |
Preferred term | Thalassemia Minor |
Entry term(s) |
Minor, Thalassemia (beta-Thalassemia Minor) Minors, Thalassemia (beta-Thalassemia Minor) Thalassemia Minor (beta Thalassemia Minor) Thalassemia Minor (beta-Thalassemia Minor) Thalassemia Minors (beta-Thalassemia Minor) |
Concept UI |
M0025961 |
Preferred term | Hemoglobin F Disease |
Entry term(s) |
Disease, Hemoglobin F |
Concept UI |
M0025959 |
Preferred term | Thalassemia Major |
Entry term(s) |
Anemia, Cooley Anemia, Cooley's Anemia, Cooleys Anemia, Erythroblastic Anemia, Mediterranean Anemias, Erythroblastic Anemias, Mediterranean Cooley's Anemia Erythroblastic Anemia Major, Thalassemia (beta-Thalassemia Major) Majors, Thalassemia (beta-Thalassemia Major) Mediterranean Anemia Mediterranean Anemias Thalassemia Major (beta Thalassemia Major) Thalassemia Major (beta-Thalassemia Major) Thalassemia Majors (beta-Thalassemia Major) |
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