ORPHA:42738

Severe congenital neutropenia

Body system

Immunological diseases

Inheritance pattern

Autosomal dominant, Autosomal recessive, X-linked recessive

Typical age of onset

Childhood

Estimated prevalence

1-9 / 1 000 000 (Europe)

Rarity class

1-9 / 1 000 000

ORPHA:42738 is classified under "Immunological diseases" in the Orphanet nomenclature.