| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 16p13.3 | Erythrocytosis, familial, 7 | 617981 | AD | 3 |
| Heinz body anemias, alpha- | 140700 | AD | 3 | |
| Hemoglobin H disease, nondeletional | 613978 | 3 | ||
| Methemoglobinemia, alpha type | 617973 | AD | 3 | |
| Thalassemias, alpha- | 604131 | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
|---|---|---|---|---|
| 16p13.3 | Erythrocytosis, familial, 7 | 617981 | AD | 3 |
| Heinz body anemia | 140700 | AD | 3 | |
| Hemoglobin H disease, deletional and nondeletional | 613978 | 3 | ||
| Thalassemia, alpha- | 604131 | 3 |
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| Location | Phenotype |
Phenotype MIM number |
Inheritance |
Phenotype mapping key |
Gene/Locus |
Gene/Locus MIM number |
|---|---|---|---|---|---|---|
| 16p13.3 | Thalassemia, alpha- | 604131 | 3 | HBA2 | 141850 | |
| 16p13.3 | Thalassemias, alpha- | 604131 | 3 | HBA1 | 141800 |
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