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
|
|