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:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   30859 
Unique Identifier:   D017085 

Occurrence in VHL:
 

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