| D008297 |
Male |
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Males |
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| D001803 |
Blood Transfusion |
The introduction of whole blood or blood component directly into the blood stream. (Dorland, 27th ed) |
Blood Transfusions,Transfusion, Blood,Transfusions, Blood |
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| D005260 |
Female |
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Females |
|
| D005914 |
Globins |
A superfamily of proteins containing the globin fold which is composed of 6-8 alpha helices arranged in a characterstic HEME enclosing structure. |
Globin |
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| D006441 |
Hemoglobin A |
Normal adult human hemoglobin. The globin moiety consists of two alpha and two beta chains. |
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|
| D006579 |
Heterozygote |
An individual having different alleles at one or more loci regarding a specific character. |
Carriers, Genetic,Genetic Carriers,Carrier, Genetic,Genetic Carrier,Heterozygotes |
|
| D006801 |
Humans |
Members of the species Homo sapiens. |
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man |
|
| D000293 |
Adolescent |
A person 13 to 18 years of age. |
Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths |
|
| D000462 |
Algeria |
A country in northern Africa bordering the Mediterranean Sea, between MOROCCO and TUNISIA. Its capital is Algiers. |
|
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| D000755 |
Anemia, Sickle Cell |
A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S. |
Hemoglobin S Disease,HbS Disease,Sickle Cell Anemia,Sickle Cell Disease,Sickle Cell Disorders,Sickling Disorder Due to Hemoglobin S,Anemias, Sickle Cell,Cell Disease, Sickle,Cell Diseases, Sickle,Cell Disorder, Sickle,Cell Disorders, Sickle,Disease, Hemoglobin S,Hemoglobin S Diseases,Sickle Cell Anemias,Sickle Cell Diseases,Sickle Cell Disorder |
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