Search on: HEMOGLOBIN H DISEASE 
Descriptors Found: 1
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Descriptor English:   alpha-Thalassemia 
Descriptor Spanish:   Talasemia alfa 
Descriptor Portuguese:   Talassemia alfa 
Synonyms English:   A-Thalassemia
Alpha Thalassemia
Disease, Hemoglobin H
Hemoglobin H Disease
Thalassemia alpha
Thalassemia, Alpha
Thalassemia-alpha
alpha-Thalassemias  
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
DG diagnostic imaging 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 RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   30859 
Unique Identifier:   D017085 

Occurrence in VHL:
 
LILACS    
MEDLINE    
BDENF    
MedCarib    
PAHO    
WHOLIS    
IBECS    

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