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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
WHIM syndrome 2
Identifiers
MONDO:0030374
OMIM:619407
Causal genes
CXCR2
Part of
WHIM syndrome
Severe congenital neutropenia
Also known as
WHIMS2
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