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- Hemoglobinopathy abstract "Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits. Common hemoglobinopathies include sickle-cell disease. It is estimated that 7% of world's population (420 million) are carriers, with 60% of total and 70% pathological being in Africa. Hemoglobinopathies are most common in ethnic populations from Africa, the Mediterranean basin and Southeast Asia.Hemoglobinopathies imply structural abnormalities in the globin proteins themselves. Thalassemias, in contrast, usually result in underproduction of normal globin proteins, often through mutations in regulatory genes. The two conditions may overlap, however, since some conditions which cause abnormalities in globin proteins (hemoglobinopathy) also affect their production (thalassemia). Thus, some hemoglobinopathies are also thalassemias, but most are not.Either hemoglobinopathy or thalassemia, or both, may cause anemia. Some well-known hemoglobin variants such as sickle-cell anemia and congenital dyserythropoietic anemia are responsible for diseases, and are considered hemoglobinopathies. However, many hemoglobin variants do not cause pathology or anemia, and thus are often not classed as hemoglobinopathies, because they are not considered pathologies. Hemoglobin variants are a part of the normal embryonic and fetal development, but may also be pathologic mutant forms of hemoglobin in a population, caused by variations in genetics. Other variants cause no detectable pathology, and are thus considered non-pathological variants.".
- Hemoglobinopathy diseasesdb "19674".
- Hemoglobinopathy icd10 "D58.2".
- Hemoglobinopathy icd9 "282.7".
- Hemoglobinopathy medlineplus "001291".
- Hemoglobinopathy meshId "D006453".
- Hemoglobinopathy wikiPageID "78944".
- Hemoglobinopathy wikiPageRevisionID "597954180".
- Hemoglobinopathy diseasesdb "19674".
- Hemoglobinopathy hasPhotoCollection Hemoglobinopathy.
- Hemoglobinopathy icd "282.7".
- Hemoglobinopathy icd "D58.2".
- Hemoglobinopathy medlineplus "1291".
- Hemoglobinopathy meshid "D006453".
- Hemoglobinopathy name "Hemoglobinopathy".
- Hemoglobinopathy wordnet_type synset-disease-noun-1.
- Hemoglobinopathy subject Category:Disorders_of_globin_and_globulin_proteins.
- Hemoglobinopathy subject Category:Hereditary_hemolytic_anemias.
- Hemoglobinopathy type Disease.
- Hemoglobinopathy type AilmentCondition.
- Hemoglobinopathy type Situation.
- Hemoglobinopathy comment "Hemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits. Common hemoglobinopathies include sickle-cell disease. It is estimated that 7% of world's population (420 million) are carriers, with 60% of total and 70% pathological being in Africa.".
- Hemoglobinopathy label "Emoglobinopatia".
- Hemoglobinopathy label "Hemoglobinopathie".
- Hemoglobinopathy label "Hemoglobinopathy".
- Hemoglobinopathy label "Hemoglobinopatia".
- Hemoglobinopathy label "Hemoglobinopatia".
- Hemoglobinopathy label "Hemoglobinopatía".
- Hemoglobinopathy label "Hämoglobinopathie".
- Hemoglobinopathy label "Hémoglobinopathie".
- Hemoglobinopathy sameAs Hämoglobinopathie.
- Hemoglobinopathy sameAs Hemoglobinopatía.
- Hemoglobinopathy sameAs Hémoglobinopathie.
- Hemoglobinopathy sameAs Emoglobinopatia.
- Hemoglobinopathy sameAs Hemoglobinopathie.
- Hemoglobinopathy sameAs Hemoglobinopatia.
- Hemoglobinopathy sameAs Hemoglobinopatia.
- Hemoglobinopathy sameAs m.0kk5x.
- Hemoglobinopathy sameAs Q1642147.
- Hemoglobinopathy sameAs Q1642147.
- Hemoglobinopathy sameAs C0019045.
- Hemoglobinopathy wasDerivedFrom Hemoglobinopathy?oldid=597954180.
- Hemoglobinopathy isPrimaryTopicOf Hemoglobinopathy.
- Hemoglobinopathy name "Hemoglobinopathy".