hemoglobin H disease
(Q3144945)
alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other
alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other
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Current Data About
hemoglobin H disease
other details
| aliases |
HBH alpha thalassemia, hemoglobin H type alpha-thalassemia intermedia hemoglobin H disease, deletional Hemoglobin H disease |
| description | alpha thalassemia that has material basis in contiguous gene deletion of the hemoglobin alpha-1 (HBA1) and alpha-2 (HBA2) genes on one chromosome 16, and a defect, deletional or nondeletional, in either HBA1 or HBA2 on the other |
External Links
| (P492) |
613978
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| (P699) |
DOID:0110031
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| (P1550) |
93616
|
| (P2671) |
/g/11c52_z7by
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| (P2892) |
C3161174
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| (P4229) |
D56.0
|
| (P5270) |
MONDO_0013512
|
| (P7329) |
3A50.02
|
| (P7807) |
9436211
|
| (P11430) |
DI-03202
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