| Disease ID | Source | Name | Description |
| 617014 | OMIM | Neutropenia, severe congenital 7, autosomal recessive (SCN7) | A form of severe congenital neutropenia, a disorder of hematopoiesis characterized by maturation arrest of granulopoiesis at the level of promyelocytes with peripheral blood absolute neutrophil counts below 0.5 x 10(9)/l and early onset of severe bacterial infections. The disease is caused by variants affecting the gene represented in this entry. |
| 162830 | OMIM | Hereditary neutrophilia (NEUTROPHILIA) | A form of lifelong, persistent neutrophilia, a condition characterized by an increase in the number of neutrophils in the blood. The disease is caused by variants affecting the gene represented in this entry. |