功能性中性粒细胞缺陷

Congenital functional phagocyte defect

ORPHA:183681疾病组

别名

Constitutional functional phagocyte defect、Congenital functional defect of phagocyte

Orphanet 未在本条目上直接标注致病基因。下表由本组所属的下位疾病汇总而来，「来源条目」列给出基因实际标注在哪一个 ORPHA 条目上。

基因	名称	来源条目
CEBPE	CCAAT enhancer binding protein epsilon	ORPHA:169142
CTSC	cathepsin C	ORPHA:678
FERMT3	FERM domain containing kindlin 3	ORPHA:99844
ITGB2	integrin subunit beta 2	ORPHA:99842
MPO	myeloperoxidase	ORPHA:2587
RAC2	Rac family small GTPase 2	ORPHA:183707
SLC35C1	solute carrier family 35 member C1	ORPHA:99843
SMARCD2	SWI/SNF related BAF chromatin remodeling complex subunit D2	ORPHA:169142

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