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Autosomal recessive severe congenital neutropenia due to CXCR2 deficiency

MONDO:0018487

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Hereditary disease (176) Hematologic disorder (170) Immune system disorder (148) Neutropenia (32) Human disease (14) Leukocyte disorder (6) Leukopenia (6) Severe congenital neutropenia (5) Autosomal recessive disease (4)

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