1 / 1
|
DeCS
|
|
|
Descriptor English:
|
|
alpha-Thalassemia
|
Descriptor Spanish:
|
|
Talasemia alfa
|
Descriptor Portuguese:
|
|
Talassemia alfa
|
Synonyms English:
|
|
A-Thalassemia
Alpha Thalassemia
Disease, Hemoglobin H
Thalassemia alpha
Thalassemia, Alpha
alpha-Thalassemias
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:
|
|
|
Record Number:
|
|
30859
|
Unique Identifier:
|
|
D017085
|
Occurrence in VHL:
|
|
|
Similar:
|
|
DeCS CID-10 LILACS
|