垂体缺陷

Pituitary deficiency

ORPHA:101957疾病组

相关基因 25来自下位疾病

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
AVP	arginine vasopressin	ORPHA:30925
CDON	cell adhesion associated, oncogene regulated	ORPHA:95496
CHD7	chromodomain helicase DNA binding protein 7	ORPHA:138
DCAF17	DDB1 and CUL4 associated factor 17	ORPHA:3464
DMXL2	Dmx like 2	ORPHA:453533
FOXA2	forkhead box A2	ORPHA:95494
GHSR	growth hormone secretagogue receptor	ORPHA:314811
GLI2	GLI family zinc finger 2	ORPHA:95494
GLI3	GLI family zinc finger 3	ORPHA:672
GPR161	G protein-coupled receptor 161	ORPHA:95496
HESX1	HESX homeobox 1	ORPHA:95496
LEP	leptin	ORPHA:66628
LEPR	leptin receptor	ORPHA:179494
LHX4	LIM homeobox 4	ORPHA:95496
NFKB2	nuclear factor kappa B subunit 2	ORPHA:293978
NR0B1	nuclear receptor subfamily 0 group B member 1	ORPHA:95702
OTX2	orthodenticle homeobox 2	ORPHA:95494
PCSK1	proprotein convertase subtilisin/kexin type 1	ORPHA:71528
PNPLA6	patatin like domain 6, lysophospholipase	ORPHA:1173
POU1F1	POU class 1 homeobox 1	ORPHA:95494
PROP1	PROP paired-like homeobox 1	ORPHA:95494
RBM28	RNA binding motif protein 28	ORPHA:157954
RNF216	ring finger protein 216	ORPHA:1173
ROBO1	roundabout guidance receptor 1	ORPHA:95496
TSHB	thyroid stimulating hormone subunit beta	ORPHA:90674

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