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DO Term : severe congenital neutropenia 2 [DOID:0112131] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant severe congenital neutropenia that has_material_basis_in heterozygous mutation in the GFI1 gene on chromosome 1p22.1.

synonyms:
613107,
SCN2,
OMIM:613107

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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