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Gene Information
Gene symbol: HPFH2
Gene name: hereditary persistence of fetal hemoglobin, heterocellular, Indian type
HGNC ID: 5153
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | HBB | 1 hits |
| 2 | HBG1 | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 1984681 | Although some cases of the syndrome of hereditary persistence of fetal hemoglobin (HPFH) have been correlated with mutations causing a change in the binding of trans-acting factors to DNA sequences flanking the gamma-globin gene, this mechanism has not been described in beta-thalassemias upstream of the canonical promoter of the beta-globin gene. |
| 2 | 2448411 | False elevation of hemoglobin A1 by hereditary persistence of fetal hemoglobin. |
| 3 | 2448411 | Hemoglobin electrophoresis revealed that the patient had hereditary persistence of fetal hemoglobin. |
| 4 | 2448411 | False elevation of hemoglobin A1 by hereditary persistence of fetal hemoglobin. |
| 5 | 2448411 | Hemoglobin electrophoresis revealed that the patient had hereditary persistence of fetal hemoglobin. |
| 6 | 10653068 | Spurious elevation of hemoglobin A1c by hereditary persistence of fetal hemoglobin. |
| 7 | 10653068 | We present the case of a 61- year-old black woman with a diagnosis of type 2 diabetes and a falsely elevated hemoglobin A1c (HbA1c) due to hereditary persistence of fetal hemoglobin. |
| 8 | 10653068 | Spurious elevation of hemoglobin A1c by hereditary persistence of fetal hemoglobin. |
| 9 | 10653068 | We present the case of a 61- year-old black woman with a diagnosis of type 2 diabetes and a falsely elevated hemoglobin A1c (HbA1c) due to hereditary persistence of fetal hemoglobin. |
| 10 | 20144281 | The most common Hb variants worldwide are HbS, HbE, HbC, and HbD. |
| 11 | 20144281 | However, elevated HbF levels can occur in certain pathologic conditions or with hereditary persistence of fetal hemoglobin. |
| 12 | 22211024 | We report a case of a diabetic, heterozygote with near normal hematology, marginally low level of hemoglobin A(2)(HbA(2)) having an increased level of hemoglobin F(HbF) that was pancellularly distributed among the red cells. |
| 13 | 22211024 | Flow cytometry and polymerization chain reaction (PCR) based studies were carried out which revealed the case to be that of the common hereditary persistence of fetal hemoglobin (HPFH)-3, an Asian Indian mutation. |