Disease #00004 (HPFH (Hereditary persistence of fetal hemoglobin))

Official abbreviation HPFH
Name Hereditary persistence of fetal hemoglobin
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease -
Associated with 5 genes HBB, HBD, HBE1, HBG1, HBG2
Associated tissues -
Disease features -
Remarks -


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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α-thal genotype     

β-thal genotype     

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00000109 Shang X,et al.(2017) Medical Genetics Department of Southern Medical University N/N (SEA)-HPFH/CD41-42 F 23 beta-thal, HPFH - BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2, HBS1L, MYB BCL11A, HBB, HBD, HBE1, HBG1, HBG2 70 1 Qi Ming
00000201 Shang X,et al.(2017) Medical Genetics Department of Southern Medical University N/N (SEA)-HPFH/CD41-42 M 27 beta-thal, HPFH - BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2, HBS1L, MYB BCL11A, HBB, HBD, HBE1, HBG1, HBG2 70 1 Qi Ming
00000458 Shang X,et al.(2017) Medical Genetics Department of Southern Medical University N/N (SEA)-HPFH/CD41-42 - - beta-thal, HPFH - BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2, MYB BCL11A, HBB, HBD, HBE1, HBG1, HBG2 57 1 Qi Ming
00000464 Shang X,et al.(2017) Medical Genetics Department of Southern Medical University N/N (SEA)-HPFH/IVS-II-654 - - beta-thal, HPFH - BCL11A, HBB, HBD, HBE1, HBG1, HBG2 BCL11A, HBB, HBD, HBE1, HBG1, HBG2 62 1 Qi Ming
00000823 Shang X,et al.(2017) Medical Genetics Department of Southern Medical University N/N (SEA)-HPFH/IVS-II-654 - - beta-thal, HPFH - BCL11A, HBB, HBD, HBE1, HBG1, HBG2 BCL11A, HBB, HBD, HBE1, HBG1, HBG2 62 1 Qi Ming
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