| Term Name: | severe congenital neutropenia 2 |
|---|---|
| Synonyms: | SCN2 |
| Definition: | An autosomal dominant severe congenital neutropenia that has_material_basis_in heterozygous mutation in the GFI1 gene on chromosome 1p22.1. |
| Ontology: | Human Disease [DOID:0112131] ( DOID:0112131 ) |