| Disease ID | Source | Name | Description |
| 266140 | OMIM | Hereditary pyropoikilocytosis (HPP) | Autosomal recessive hematologic disorder characterized by hemolytic anemia, microspherocytosis, poikilocytosis, and an unusual thermal sensitivity of red cells. The disease is caused by variants affecting the gene represented in this entry. |
| 270970 | OMIM | Spherocytosis 3 (SPH3) | Spherocytosis is a hematologic disorder leading to chronic hemolytic anemia and characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. SPH3 is characterized by severe hemolytic anemia. Inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry. |
| 130600 | OMIM | Elliptocytosis 2 (EL2) | A Rhesus-unlinked form of hereditary elliptocytosis, a genetically heterogeneous, autosomal dominant hematologic disorder. It is characterized by variable hemolytic anemia and elliptical or oval red cell shape. The disease is caused by variants affecting the gene represented in this entry. |