#term ID	term description	observed gene count	background gene count	strength	signal	false discovery rate	matching proteins in your network (IDs)	matching proteins in your network (labels)
DOID:626	Complement deficiency	8	23	1.9	2.43	3.36e-09	9606.ENSP00000223642,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000299367,9606.ENSP00000314299,9606.ENSP00000378131,9606.ENSP00000416561,9606.ENSP00000493985	C5,C9,KLKB1,C2,CFHR1,CFI,CFB,KNG1
DOID:9120	Amyloidosis	10	75	1.48	2.06	8.72e-09	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000278222,9606.ENSP00000315130,9606.ENSP00000346839,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000450540	APOE,APCS,LYZ,C9,SAA4,CLU,FN1,APOA4,GSN,SERPINA3
DOID:1247	Blood coagulation disease	10	89	1.41	1.9	2.75e-08	9606.ENSP00000215727,9606.ENSP00000232003,9606.ENSP00000255030,9606.ENSP00000264690,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000377783,9606.ENSP00000415941,9606.ENSP00000493985	SERPIND1,HRG,CRP,KLKB1,FGB,F2,PLG,PROS1,C4B,KNG1
DOID:2452	Thrombophilia	7	21	1.88	2.16	3.14e-08	9606.ENSP00000215727,9606.ENSP00000232003,9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000377783,9606.ENSP00000415941	SERPIND1,HRG,CRP,F2,PLG,PROS1,C4B
DOID:2914	Immune system disease	19	675	0.8	1.15	1.22e-07	9606.ENSP00000223642,9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000257198,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000278222,9606.ENSP00000299367,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000346839,9606.ENSP00000378131,9606.ENSP00000396688,9606.ENSP00000415941,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000493985	C5,APOE,CRP,APCS,DSC1,C9,KLKB1,SAA4,C2,F2,PLG,CFHR1,FN1,CFI,C4A,C4B,CFB,JCHAIN,KNG1
DOID:557	Kidney disease	12	275	0.99	1.17	3.56e-06	9606.ENSP00000223642,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000278222,9606.ENSP00000308541,9606.ENSP00000314299,9606.ENSP00000346839,9606.ENSP00000350425,9606.ENSP00000355627,9606.ENSP00000378131,9606.ENSP00000415941,9606.ENSP00000416561	C5,CRP,APCS,SAA4,F2,CFHR1,FN1,APOA4,AGT,CFI,C4B,CFB
DOID:10871	Age related macular degeneration	6	44	1.49	1.21	4.74e-05	9606.ENSP00000252486,9606.ENSP00000263408,9606.ENSP00000299367,9606.ENSP00000314299,9606.ENSP00000378131,9606.ENSP00000416561	APOE,C9,C2,CFHR1,CFI,CFB
DOID:4	Disease	52	6291	0.27	0.47	4.74e-05	9606.ENSP00000215727,9606.ENSP00000217407,9606.ENSP00000222381,9606.ENSP00000223642,9606.ENSP00000231751,9606.ENSP00000232003,9606.ENSP00000241052,9606.ENSP00000251595,9606.ENSP00000252486,9606.ENSP00000254722,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000257198,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264381,9606.ENSP00000264613,9606.ENSP00000264690,9606.ENSP00000266041,9606.ENSP00000266718,9606.ENSP00000273784,9606.ENSP00000278222,9606.ENSP00000291009,9606.ENSP00000296280,9606.ENSP00000299367,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000329374,9606.ENSP00000342850,9606.ENSP00000346839,9606.ENSP00000350425,9606.ENSP00000355627,9606.ENSP00000360281,9606.ENSP00000360522,9606.ENSP00000360687,9606.ENSP00000362238,9606.ENSP00000362924,9606.ENSP00000363770,9606.ENSP00000370473,9606.ENSP00000377783,9606.ENSP00000378131,9606.ENSP00000385035,9606.ENSP00000389814,9606.ENSP00000396688,9606.ENSP00000415941,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,LBP,PON1,C5,LTF,HRG,CAT,HBA2,APOE,SERPINF1,CRP,APCS,DSC1,LYZ,C9,BCHE,CP,KLKB1,ITIH4,LUM,AHSG,SAA4,PIP,MASP1,C2,FGB,F2,PLG,CFHR1,CLU,SERPINA7,SERPINA6,FN1,APOA4,AGT,C8B,RBP4,PTGDS,POF1B,GSN,C1QC,IGFBP3,PROS1,CFI,C1S,ADIPOQ,C4A,C4B,CFB,JCHAIN,SERPINA3,KNG1
DOID:7	Disease of anatomical entity	44	4798	0.32	0.5	5.32e-05	9606.ENSP00000215727,9606.ENSP00000217407,9606.ENSP00000223642,9606.ENSP00000231751,9606.ENSP00000232003,9606.ENSP00000251595,9606.ENSP00000252486,9606.ENSP00000254722,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000257198,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000266718,9606.ENSP00000273784,9606.ENSP00000278222,9606.ENSP00000291009,9606.ENSP00000299367,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000329374,9606.ENSP00000342850,9606.ENSP00000346839,9606.ENSP00000350425,9606.ENSP00000355627,9606.ENSP00000360281,9606.ENSP00000360522,9606.ENSP00000360687,9606.ENSP00000362238,9606.ENSP00000362924,9606.ENSP00000363770,9606.ENSP00000377783,9606.ENSP00000378131,9606.ENSP00000385035,9606.ENSP00000389814,9606.ENSP00000396688,9606.ENSP00000415941,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,LBP,C5,LTF,HRG,HBA2,APOE,SERPINF1,CRP,APCS,DSC1,C9,KLKB1,LUM,AHSG,SAA4,PIP,C2,FGB,F2,PLG,CFHR1,CLU,SERPINA7,SERPINA6,FN1,APOA4,AGT,C8B,RBP4,PTGDS,POF1B,GSN,C1QC,PROS1,CFI,C1S,ADIPOQ,C4A,C4B,CFB,JCHAIN,SERPINA3,KNG1
DOID:612	Primary immunodeficiency disease	13	470	0.8	0.84	7.04e-05	9606.ENSP00000223642,9606.ENSP00000255030,9606.ENSP00000257198,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000299367,9606.ENSP00000308541,9606.ENSP00000314299,9606.ENSP00000378131,9606.ENSP00000396688,9606.ENSP00000415941,9606.ENSP00000416561,9606.ENSP00000493985	C5,CRP,DSC1,C9,KLKB1,C2,F2,CFHR1,CFI,C4A,C4B,CFB,KNG1
DOID:0050637	Finnish type amyloidosis	4	9	2.0	1.23	8.55e-05	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000263408,9606.ENSP00000362924	APOE,APCS,C9,GSN
DOID:0070029	ITM2B-related cerebral amyloid angiopathy 1	4	12	1.88	1.11	0.00019	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000315130,9606.ENSP00000450540	APOE,APCS,CLU,SERPINA3
DOID:0050117	Disease by infectious agent	11	368	0.83	0.79	0.00023	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000264613,9606.ENSP00000266041,9606.ENSP00000273784,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000355627,9606.ENSP00000363770,9606.ENSP00000396688	APOE,CRP,APCS,CP,ITIH4,AHSG,F2,PLG,AGT,C1QC,C4A
DOID:0070030	ITM2B-related cerebral amyloid angiopathy 2	4	13	1.84	1.09	0.00023	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000315130,9606.ENSP00000450540	APOE,APCS,CLU,SERPINA3
DOID:74	Hematopoietic system disease	12	473	0.76	0.73	0.00033	9606.ENSP00000215727,9606.ENSP00000232003,9606.ENSP00000251595,9606.ENSP00000255030,9606.ENSP00000264690,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000377783,9606.ENSP00000415941,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,HRG,HBA2,CRP,KLKB1,FGB,F2,PLG,PROS1,C4B,SERPINA3,KNG1
DOID:0050639	Primary cutaneous amyloidosis	4	19	1.68	0.94	0.00064	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000263408,9606.ENSP00000362924	APOE,APCS,C9,GSN
DOID:934	Viral infectious disease	7	133	1.08	0.82	0.00064	9606.ENSP00000255030,9606.ENSP00000264613,9606.ENSP00000266041,9606.ENSP00000273784,9606.ENSP00000308541,9606.ENSP00000355627,9606.ENSP00000396688	CRP,CP,ITIH4,AHSG,F2,AGT,C4A
DOID:0014667	Disease of metabolism	17	1076	0.55	0.56	0.00086	9606.ENSP00000241052,9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264613,9606.ENSP00000273784,9606.ENSP00000278222,9606.ENSP00000308541,9606.ENSP00000315130,9606.ENSP00000346839,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000377783,9606.ENSP00000389814,9606.ENSP00000450540	CAT,APOE,CRP,APCS,LYZ,C9,CP,AHSG,SAA4,F2,CLU,FN1,APOA4,GSN,PROS1,ADIPOQ,SERPINA3
DOID:0050636	Familial visceral amyloidosis	4	21	1.63	0.9	0.00086	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000350425	APOE,APCS,LYZ,APOA4
DOID:0060449	Gelatinous drop-like corneal dystrophy	3	5	2.13	0.94	0.00086	9606.ENSP00000231751,9606.ENSP00000252486,9606.ENSP00000315130	LTF,APOE,CLU
DOID:0070028	APP-related cerebral amyloid angiopathy	3	5	2.13	0.94	0.00086	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000450540	APOE,APCS,SERPINA3
DOID:1936	Atherosclerosis	4	21	1.63	0.9	0.00086	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000355627,9606.ENSP00000389814	APOE,CRP,AGT,ADIPOQ
DOID:2451	Protein S deficiency	3	5	2.13	0.94	0.00086	9606.ENSP00000308541,9606.ENSP00000377783,9606.ENSP00000415941	F2,PROS1,C4B
DOID:5614	Eye disease	14	749	0.63	0.6	0.00090	9606.ENSP00000231751,9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000263408,9606.ENSP00000266718,9606.ENSP00000299367,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000360522,9606.ENSP00000362924,9606.ENSP00000378131,9606.ENSP00000416561	LTF,APOE,CRP,APCS,C9,LUM,C2,PLG,CFHR1,CLU,RBP4,GSN,CFI,CFB
DOID:14735	Hereditary angioedema	3	6	2.05	0.91	0.0010	9606.ENSP00000264690,9606.ENSP00000385035,9606.ENSP00000493985	KLKB1,C1S,KNG1
DOID:9352	Type 2 diabetes mellitus	4	25	1.56	0.86	0.0011	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000389814	APOE,CRP,APCS,ADIPOQ
DOID:0050736	Autosomal dominant disease	19	1386	0.49	0.52	0.0012	9606.ENSP00000215727,9606.ENSP00000232003,9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000299367,9606.ENSP00000308541,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000378131,9606.ENSP00000385035,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,HRG,APOE,APCS,LYZ,C9,KLKB1,C2,F2,CFHR1,CLU,APOA4,GSN,CFI,C1S,CFB,JCHAIN,SERPINA3,KNG1
DOID:16	Integumentary system disease	12	575	0.67	0.6	0.0013	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000257198,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000273784,9606.ENSP00000291009,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000385035,9606.ENSP00000493985	APOE,CRP,APCS,DSC1,C9,KLKB1,AHSG,PIP,APOA4,GSN,C1S,KNG1
DOID:5844	Myocardial infarction	4	27	1.53	0.84	0.0013	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000308938,9606.ENSP00000355627	APOE,CRP,PLG,AGT
DOID:7693	Abdominal aortic aneurysm	3	7	1.99	0.88	0.0013	9606.ENSP00000252486,9606.ENSP00000308938,9606.ENSP00000355627	APOE,PLG,AGT
DOID:9477	Pulmonary embolism	3	7	1.99	0.88	0.0013	9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000308938	CRP,F2,PLG
DOID:3973	Thyroid gland medullary carcinoma	3	8	1.93	0.86	0.0015	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000350425	APOE,APCS,APOA4
DOID:0050155	Sensory system disease	15	929	0.56	0.54	0.0016	9606.ENSP00000231751,9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000263408,9606.ENSP00000266718,9606.ENSP00000299367,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000360522,9606.ENSP00000360687,9606.ENSP00000362924,9606.ENSP00000378131,9606.ENSP00000416561	LTF,APOE,CRP,APCS,C9,LUM,C2,PLG,CFHR1,CLU,RBP4,PTGDS,GSN,CFI,CFB
DOID:11949	Creutzfeldt-Jakob disease	3	9	1.88	0.82	0.0019	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000363770	APOE,APCS,C1QC
DOID:5200	Urinary tract obstruction	3	9	1.88	0.82	0.0019	9606.ENSP00000255030,9606.ENSP00000346839,9606.ENSP00000355627	CRP,FN1,AGT
DOID:37	Skin disease	11	518	0.68	0.57	0.0021	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000257198,9606.ENSP00000263408,9606.ENSP00000264690,9606.ENSP00000291009,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000385035,9606.ENSP00000493985	APOE,CRP,APCS,DSC1,C9,KLKB1,PIP,APOA4,GSN,C1S,KNG1
DOID:520	Aortic disease	4	34	1.43	0.76	0.0023	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000308938,9606.ENSP00000355627	APOE,CRP,PLG,AGT
DOID:0050828	Artery disease	6	130	1.02	0.66	0.0028	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000355627,9606.ENSP00000389814	APOE,CRP,F2,PLG,AGT,ADIPOQ
DOID:0080301	Atypical hemolytic-uremic syndrome	3	11	1.79	0.77	0.0028	9606.ENSP00000314299,9606.ENSP00000378131,9606.ENSP00000416561	CFHR1,CFI,CFB
DOID:10652	Alzheimers disease	4	41	1.34	0.68	0.0041	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000315130,9606.ENSP00000450540	APOE,APCS,CLU,SERPINA3
DOID:12554	Hemolytic-uremic syndrome	3	14	1.69	0.7	0.0046	9606.ENSP00000314299,9606.ENSP00000378131,9606.ENSP00000416561	CFHR1,CFI,CFB
DOID:2529	Splenic disease	3	17	1.6	0.64	0.0073	9606.ENSP00000255030,9606.ENSP00000278222,9606.ENSP00000308541	CRP,SAA4,F2
DOID:50	Thyroid gland disease	4	50	1.26	0.6	0.0075	9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000329374,9606.ENSP00000350425	APOE,APCS,SERPINA7,APOA4
DOID:630	Genetic disease	32	3778	0.28	0.35	0.0078	9606.ENSP00000215727,9606.ENSP00000231751,9606.ENSP00000232003,9606.ENSP00000241052,9606.ENSP00000251595,9606.ENSP00000252486,9606.ENSP00000254722,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264613,9606.ENSP00000264690,9606.ENSP00000296280,9606.ENSP00000299367,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000342850,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000370473,9606.ENSP00000377783,9606.ENSP00000378131,9606.ENSP00000385035,9606.ENSP00000389814,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,LTF,HRG,CAT,HBA2,APOE,SERPINF1,CRP,APCS,LYZ,C9,CP,KLKB1,MASP1,C2,FGB,F2,PLG,CFHR1,CLU,SERPINA6,APOA4,GSN,IGFBP3,PROS1,CFI,C1S,ADIPOQ,CFB,JCHAIN,SERPINA3,KNG1
DOID:0050177	Monogenic disease	29	3266	0.3	0.35	0.0083	9606.ENSP00000215727,9606.ENSP00000231751,9606.ENSP00000232003,9606.ENSP00000251595,9606.ENSP00000252486,9606.ENSP00000254722,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264613,9606.ENSP00000264690,9606.ENSP00000296280,9606.ENSP00000299367,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000342850,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000370473,9606.ENSP00000377783,9606.ENSP00000378131,9606.ENSP00000385035,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,LTF,HRG,HBA2,APOE,SERPINF1,APCS,LYZ,C9,CP,KLKB1,MASP1,C2,FGB,F2,PLG,CFHR1,CLU,SERPINA6,APOA4,GSN,IGFBP3,PROS1,CFI,C1S,CFB,JCHAIN,SERPINA3,KNG1
DOID:0111676	High molecular weight kininogen deficiency	2	2	2.35	0.64	0.0087	9606.ENSP00000264690,9606.ENSP00000493985	KLKB1,KNG1
DOID:115	Cardiac tamponade	2	2	2.35	0.64	0.0087	9606.ENSP00000255030,9606.ENSP00000308541	CRP,F2
DOID:2533	Splenic infarction	2	2	2.35	0.64	0.0087	9606.ENSP00000255030,9606.ENSP00000308541	CRP,F2
DOID:866	Vein disease	3	19	1.55	0.61	0.0087	9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000396688	CRP,F2,C4A
DOID:178	Vascular disease	7	249	0.8	0.5	0.0097	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000355627,9606.ENSP00000389814,9606.ENSP00000396688	APOE,CRP,F2,PLG,AGT,ADIPOQ,C4A
DOID:0050739	Autosomal genetic disease	26	2802	0.32	0.35	0.0098	9606.ENSP00000215727,9606.ENSP00000231751,9606.ENSP00000232003,9606.ENSP00000251595,9606.ENSP00000252486,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264613,9606.ENSP00000264690,9606.ENSP00000296280,9606.ENSP00000299367,9606.ENSP00000306099,9606.ENSP00000308541,9606.ENSP00000308938,9606.ENSP00000314299,9606.ENSP00000315130,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000370473,9606.ENSP00000378131,9606.ENSP00000385035,9606.ENSP00000416561,9606.ENSP00000440066,9606.ENSP00000450540,9606.ENSP00000493985	SERPIND1,LTF,HRG,HBA2,APOE,APCS,LYZ,C9,CP,KLKB1,MASP1,C2,FGB,F2,PLG,CFHR1,CLU,APOA4,GSN,IGFBP3,CFI,C1S,CFB,JCHAIN,SERPINA3,KNG1
DOID:0060903	Thrombosis	3	21	1.51	0.58	0.0108	9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000308938	CRP,F2,PLG
DOID:1074	Kidney failure	3	23	1.47	0.55	0.0134	9606.ENSP00000255030,9606.ENSP00000308541,9606.ENSP00000355627	CRP,F2,AGT
DOID:0060002	C1 inhibitor deficiency	2	4	2.05	0.53	0.0189	9606.ENSP00000264690,9606.ENSP00000493985	KLKB1,KNG1
DOID:10128	Venous insufficiency	2	4	2.05	0.53	0.0189	9606.ENSP00000308541,9606.ENSP00000396688	F2,C4A
DOID:12549	Hepatitis A	2	4	2.05	0.53	0.0189	9606.ENSP00000264613,9606.ENSP00000308541	CP,F2
DOID:3572	Intracranial sinus thrombosis	2	4	2.05	0.53	0.0189	9606.ENSP00000255030,9606.ENSP00000308541	CRP,F2
DOID:5199	Ureteral obstruction	2	4	2.05	0.53	0.0189	9606.ENSP00000346839,9606.ENSP00000355627	FN1,AGT
DOID:8943	Lattice corneal dystrophy	2	4	2.05	0.53	0.0189	9606.ENSP00000252486,9606.ENSP00000315130	APOE,CLU
DOID:0050830	Peripheral artery disease	2	5	1.96	0.5	0.0242	9606.ENSP00000255030,9606.ENSP00000308938	CRP,PLG
DOID:11249	Vitamin K deficiency bleeding	2	5	1.96	0.5	0.0242	9606.ENSP00000308541,9606.ENSP00000377783	F2,PROS1
DOID:28	Endocrine system disease	8	398	0.66	0.39	0.0242	9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000329374,9606.ENSP00000342850,9606.ENSP00000350425,9606.ENSP00000362238,9606.ENSP00000389814	APOE,CRP,APCS,SERPINA7,SERPINA6,APOA4,POF1B,ADIPOQ
DOID:864	Phlebitis	2	5	1.96	0.5	0.0242	9606.ENSP00000255030,9606.ENSP00000308541	CRP,F2
DOID:8725	Vascular dementia	2	5	1.96	0.5	0.0242	9606.ENSP00000252486,9606.ENSP00000264381	APOE,BCHE
DOID:9074	Systemic lupus erythematosus	3	31	1.34	0.47	0.0253	9606.ENSP00000255030,9606.ENSP00000396688,9606.ENSP00000415941	CRP,C4A,C4B
DOID:0050855	Renal fibrosis	2	6	1.88	0.47	0.0295	9606.ENSP00000346839,9606.ENSP00000355627	FN1,AGT
DOID:1884	Viral hepatitis	2	6	1.88	0.47	0.0295	9606.ENSP00000273784,9606.ENSP00000308541	AHSG,F2
DOID:3407	Carotid artery disease	2	6	1.88	0.47	0.0295	9606.ENSP00000252486,9606.ENSP00000255030	APOE,CRP
DOID:10124	Corneal disease	4	85	1.03	0.41	0.0338	9606.ENSP00000231751,9606.ENSP00000252486,9606.ENSP00000266718,9606.ENSP00000315130	LTF,APOE,LUM,CLU
DOID:10873	Kuhnt-Junius degeneration	2	7	1.81	0.44	0.0352	9606.ENSP00000299367,9606.ENSP00000416561	C2,CFB
DOID:11247	Disseminated intravascular coagulation	2	7	1.81	0.44	0.0352	9606.ENSP00000255030,9606.ENSP00000308541	CRP,F2
DOID:11716	Prediabetes syndrome	2	7	1.81	0.44	0.0352	9606.ENSP00000255030,9606.ENSP00000389814	CRP,ADIPOQ
DOID:0060158	Acquired metabolic disease	5	162	0.84	0.37	0.0413	9606.ENSP00000264613,9606.ENSP00000273784,9606.ENSP00000308541,9606.ENSP00000377783,9606.ENSP00000389814	CP,AHSG,F2,PROS1,ADIPOQ
DOID:3118	Hepatobiliary disease	5	168	0.83	0.36	0.0474	9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000273784,9606.ENSP00000278222,9606.ENSP00000308541	CRP,APCS,AHSG,SAA4,F2
DOID:655	Inherited metabolic disorder	12	949	0.46	0.3	0.0474	9606.ENSP00000241052,9606.ENSP00000252486,9606.ENSP00000255030,9606.ENSP00000255040,9606.ENSP00000261267,9606.ENSP00000263408,9606.ENSP00000264613,9606.ENSP00000315130,9606.ENSP00000350425,9606.ENSP00000362924,9606.ENSP00000389814,9606.ENSP00000450540	CAT,APOE,CRP,APCS,LYZ,C9,CP,CLU,APOA4,GSN,ADIPOQ,SERPINA3
DOID:409	Liver disease	4	97	0.97	0.37	0.0483	9606.ENSP00000255040,9606.ENSP00000273784,9606.ENSP00000278222,9606.ENSP00000308541	APCS,AHSG,SAA4,F2