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1 hemoglobin C disease
Медицина: гемоглобиноз С (наследственная мутациия в 6 позиции гемоглобина, проявляется как лёгкая форма серповидно-клеточной анемии) -
2 hemoglobin H disease
Медицина: Н-гемоглобинопатия (наследственная мутациия в альфа-цепи гемоглобина, проявляется в виде альфа-талассемии) -
3 hemoglobin C disease
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4 hemoglobin E disease
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5 hemoglobin M disease
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6 sickle cell-hemoglobin C disease
داء الهيموغلوبين المنجليC* * *داءُ الهِيموغلوبينِ المِنْجَلِيّCEnglish-Arabic Medical Dictionary > sickle cell-hemoglobin C disease
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7 sickle cell-hemoglobin D disease
داء الهيموغلوبين المنجليD* * *داءُ الهِيموغلوبينِ المِنْجَلِيّDEnglish-Arabic Medical Dictionary > sickle cell-hemoglobin D disease
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8 hemoglobin C-thalassemia disease
داء التلاسيمية مع الهيموغلوبين C* * *داءُ التَّلاَسيمية مع الهِيمُوغلُوبينِ CEnglish-Arabic Medical Dictionary > hemoglobin C-thalassemia disease
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9 hemoglobin E-thalassemia disease
داء التلاسيمية مع الهيموغلوبينE* * *داءُ الَّتلاسيمية مع الهِيمُوغلُوبينِEEnglish-Arabic Medical Dictionary > hemoglobin E-thalassemia disease
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10 hemoglobin S-C disease
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11 داء الهيموغلوبين C
hemoglobin C disease -
12 Н-гемоглобинопатия
Medicine: hemoglobin H disease (наследственная мутациия в альфа-цепи гемоглобина, проявляется в виде альфа-талассемии)Универсальный русско-английский словарь > Н-гемоглобинопатия
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13 гемоглобиноз С
Medicine: hemoglobin C disease (наследственная мутациия в 6 позиции гемоглобина, проявляется как лёгкая форма серповидно-клеточной анемии) -
14 داء الهيموغلوبين المنجليC
sickle cell-hemoglobin C diseaseArabic-English Medical Dictionary > داء الهيموغلوبين المنجليC
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15 داء الهيموغلوبين المنجليD
sickle cell-hemoglobin D diseaseArabic-English Medical Dictionary > داء الهيموغلوبين المنجليD
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16 داء التلاسيمية مع الهيموغلوبين C
hemoglobin C-thalassemia diseaseArabic-English Medical Dictionary > داء التلاسيمية مع الهيموغلوبين C
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17 داء التلاسيمية مع الهيموغلوبينE
hemoglobin E-thalassemia diseaseArabic-English Medical Dictionary > داء التلاسيمية مع الهيموغلوبينE
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18 داء هيموغلوبيني
hemoglobin disease
См. также в других словарях:
hemoglobin C disease — n an inherited hemolytic anemia that occurs esp. in individuals of African descent and is characterized esp. by splenomegaly and the presence of target cells and hemoglobin C in the blood * * * the state of being homozygous for hemoglobin C,… … Medical dictionary
hemoglobin D disease — the state of being homozygous for hemoglobin D, characterized by mild hemolytic anemia with numerous target cells in the peripheral blood … Medical dictionary
hemoglobin E disease — the state of being homozygous for hemoglobin E; many patients are asymptomatic, but others have mild hemolytic anemia, usually without splenomegaly, and increased numbers of normochromic target cells in the peripheral blood … Medical dictionary
hemoglobin H disease — α thalassemia in individuals heterozygous for hemoglobin H, characterized by chronic hemolytic anemia associated with splenomegaly; red blood cell hypochromia, anisocytosis, and poikilocytosis are accompanied by inclusion bodies detectable… … Medical dictionary
hemoglobin SC disease — sickle cell–hemoglobin C d … Medical dictionary
hemoglobin SD disease — sickle cell–hemoglobin D d … Medical dictionary
Hemoglobin — Hemoglobin, human, adult (heterotetramer, (αβ)2) Structure of human hemoglobin. The protein s α and β subunits are in red and blue, and the iron containing heme groups in green. Fro … Wikipedia
hemoglobin C — n an abnormal hemoglobin that differs from hemoglobin A in having a lysine residue substituted for the glutamic acid residue at position 6 in two of the four polypeptide chains making up the hemoglobin molecule * * * a common abnormal hemoglobin… … Medical dictionary
sickle cell–hemoglobin C disease — a genetically determined anemia in which the erythrocytes contain both hemoglobin S and hemoglobin C; symptoms are similar to but less severe than those of sickle cell anemia and may include abdominal and skeletal pain, splenomegaly, splenic… … Medical dictionary
sickle cell–hemoglobin D disease — a genetically determined anemia in which the erythrocytes contain both hemoglobin S and hemoglobin D, with symptoms like those of mild sickle cell anemia. Called also hemoglobin SD d … Medical dictionary
hemoglobin H — a rapidly migrating abnormal hemoglobin composed of four β chains, having a high oxygen affinity, found mainly in Southeast Asians, natives of the Mediterranean region, and a few other ethnic groups. Infants may be born with a mixture of… … Medical dictionary