ORPHA:169142

Recurrent infections due to specific granule deficiency

Also called Neutrophil-specific granule deficiency

Body system

Immunological diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy, Neonatal

Estimated prevalence

Not documented in Orphadata

Rarity class

Not documented in Orphadata

ORPHA:169142 is classified under "Immunological diseases" in the Orphanet nomenclature.