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Human Disease

autosomal dominant severe congenital neutropenia

Term ID

DOID:0112130

Synonyms

Definition

A severe congenital neutropenia that has_material_basis_in heterozygous mutation of an autosomal gene. (2)

References

GARD:9558
ORDO:486

Ontology

Human Disease ( DOID:0112130 )

Relationships

is a type of: autosomal dominant disease severe congenital neutropenia

autosomal dominant disease severe congenital neutropenia Show first 5 Terms
has subtype: severe congenital neutropenia 2 severe congenital neutropenia 8

severe congenital neutropenia 2 severe congenital neutropenia 8 Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models