alpha-Thalassemia [alfa-talasemie]
- Terms
-
alfa talasemie
talasemie alfa
talasémie alfa
thalasemie alfa
-
A-Thalassemia
Alpha Thalassemia
Hemoglobin H Disease
Thalassemia-alpha
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.
- Annotation
- do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
- DUI
- D017085 MeSH Browser
- CUI
- M0025958
- Previous indexing
- Thalassemia (1966-1992)
- History note
- 93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92
- Online note
- use THALASSEMIA to search ALPHA-THALASSEMIA 1988-92 & HEMOGLOBIN H DISEASE 1982-92
- Public note
- 93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification
- CO
- complications
- DI
- diagnosis 9
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology 2
- EH
- ethnology
- ET
- etiology 2
- GE
- genetics 6
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology 3
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 1
- UR
- urine
- VE
- veterinary
- VI
- virology
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