Search on: ALPHA-THALASSEMIA 
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Descriptor English:   alpha-Thalassemia 
Descriptor Spanish:   Talasemia alfa 
Descriptor Portuguese:   Talassemia alfa 
Synonyms English:   Hemoglobin H Disease
Thalassemia-alpha  
Tree Number:   C15.378.071.141.150.875.100
C15.378.420.826.100
C16.320.070.875.100
C16.320.365.826.100
Definition English:   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. 
Indexing Annotation English:   do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
See Related English:   Hemoglobin H
 
History Note English:   93; was see THALASSEMIA 1988-92; HEMOGLOBIN H DISEASE was see THALASSEMIA 1982-92 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
urine ultrasonography
veterinary virology
Record Number:   30859 
Unique Identifier:   D017085 

Occurrence in VHL:
 

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