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DO Term : autosomal dominant severe congenital neutropenia [DOID:0112130] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene.

synonyms:
GARD:9558,
ORDO:486

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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