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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Severe congenital neutropenia
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Autosomal recessive severe congenital neutropenia
Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
rare
Identifiers
MONDO:0018487
Orphanet:420699
Causal genes
CXCR2
Part of
Autosomal recessive severe congenital neutropenia
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