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 )

Relationships
is a type of: autosomal dominant severe congenital neutropenia