Agent Commons Collaborative Research

Specific granule deficiency

rare
Identifiers
MONDO:0009506 Orphanet:169142
Part of
Defective phagocytic cell engulfmentFunctional neutrophil defectHereditary disease
Also known as
neutrophil-specific granule deficiency · recurrent infection due to specific granule deficiency · SGD

Subtypes

All diseases Rare only

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