Search results for Nateglinide

97 hits were found for Nateglinide

#	Family	MCID	Name	MIFTS	Score
1	c	TYP009	Type 2 Diabetes Mellitus	92	19.520

2		HYP066	Hyperglycemia	61	13.990

3		HYP056	Hypoglycemia	65	13.769

4	P	DBT009	Diabetes Mellitus	67	11.525

5		HYP060	Hyperinsulinism	54	6.537

6		LPD008	Lipid Metabolism Disorder	62	6.315

7	c	BLD140	Blood Group, I System	46	5.533

8	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	5.331

9	P	HYP750	Hypertriglyceridemia, Familial	62	4.728

10		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	4.263

11		GLC003	Glucose Intolerance	54	4.205

12		PRD004	Prediabetes Syndrome	52	4.205

13	P	TRN020	Turner Syndrome	67	3.531

14	P	KDN018	Kidney Disease	72	3.399

15	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	3.223

16		INT007	Intermediate Coronary Syndrome	54	3.129

17		FTT001	Fatty Liver Disease	62	2.927

18	P	ART021	Arteriosclerosis	54	2.830

19	c	DVL042	Developmental and Epileptic Encephalopathy 14	50	2.732

20		MLG120	Malignant Migrating Partial Seizures of Infancy	43	2.732

21	P	ANR048	Aniridia 1	64	2.707

22	P	MTR004	Maturity-Onset Diabetes of the Young	68	2.629

23		OCL069	Ocular Motor Apraxia	57	2.629

24		CLN015	Colon Adenocarcinoma	65	2.629

25	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	2.520

26	c	CHR684	Chronic Kidney Disease	69	2.520

27	P	TRM003	Tremor	48	2.520

28	P	HYP050	Hyperinsulinemic Hypoglycemia	57	2.520

29		HYP026	Hypoglycemic Coma	37	2.520

30		NNL006	Non-Alcoholic Steatohepatitis	54	2.404

31		CNG034	Congestive Heart Failure	69	2.323

32		GLC036	Glucagonoma	46	2.279

33	P	EXN002	Exanthem	58	2.143

34		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	2.029

35	c	THR092	Thrombophilia Due to Thrombin Defect	74	1.993

36		HRW001	Hair Whorl	35	1.993

37	P	ATR011	Atrial Fibrillation	66	1.822

38		CLR109	Colorectal Adenocarcinoma	50	1.799

39		ATH013	Atherosclerosis Susceptibility	63	1.620

40	P	CRN300	Coronary Heart Disease 1	73	1.620

41	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	51	1.620

42	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	53	1.620

43		CRB039	Cerebrovascular Disease	66	1.620

44		CRB004	Cerebral Artery Occlusion	45	1.357

45		ISC004	Ischemia	61	1.357

46		END072	Endotheliitis	36	1.318

47	P	RHM011	Rheumatoid Arthritis	82	1.272

48		INS001	Insulinoma	59	1.272

49		CNN005	Connective Tissue Disease	67	1.272

50	P	ART022	Arthritis	71	1.272

51	P	DRR001	Diarrhea	55	1.272

52	c	MCR130	Microvascular Complications of Diabetes 6	41	1.102

53	c	MCR120	Microvascular Complications of Diabetes 7	47	1.102

54		HPT004	Hepatic Coma	43	1.102

55	c	MCR113	Microvascular Complications of Diabetes 3	52	1.102

56	c	MCR133	Microvascular Complications of Diabetes 4	41	1.102

57		ACR007	Acromegaly	70	1.102

58		HPT019	Hepatic Encephalopathy	59	1.102

59		LVR012	Liver Cirrhosis	63	1.102

60		ART140	Arteries, Anomalies of	53	0.900

61		LPP008	Lipoprotein Quantitative Trait Locus	65	0.900

62		DBT010	Diabetic Neuropathy	54	0.900

63	P	LCT001	Lactic Acidosis	51	0.900

64	P	SKN015	Skin Carcinoma	71	0.721

65	c	EHL080	Ehlers-Danlos Syndrome, Musculocontractural Type, 1	52	0.640

66	P	PNC035	Pancreatic Cancer	86	0.640

67		RHB024	Rhabdomyosarcoma 2	67	0.640

68	c	ACT027	Acute Pancreatitis	60	0.640

69	P	HRT032	Heart Disease	81	0.640

70	P	PNC044	Pancreatitis	61	0.640

71	P	CRD246	Cardiovascular System Disease	56	0.640

72		ALL001	Allan-Herndon-Dudley Syndrome	54	0.636

73	P	CLR023	Colorectal Cancer	100	0.636

74		PRP027	Peripheral Vascular Disease	71	0.636

75	c	MCR115	Microvascular Complications of Diabetes 5	65	0.636

76	P	INF037	Inflammatory Bowel Disease	53	0.636

77		ATR057	Atrioventricular Block	54	0.636

78		NNL005	Non-Alcoholic Fatty Liver Disease	63	0.636

79		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.636

80		MNC019	Monocarboxylate Transporter 1 Deficiency	47	0.636

81		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.636

82	P	MYC007	Myocardial Infarction	70	0.636

83		HRD218	Hereditary Stomatocytosis	30	0.636

84	P	LPS004	Lupus Erythematosus	61	0.636

85		CRN020	Coronary Restenosis	39	0.636

86	P	HYP098	Hypereosinophilic Syndrome	66	0.636

87		SYN036	Syncope	45	0.636

88	P	LVR013	Liver Disease	69	0.636

89		END086	End Stage Renal Disease	52	0.636

90		ALL029	Allergic Disease	59	0.636

91	P	VSC007	Vascular Disease	63	0.636

92		ATN004	Autonomic Neuropathy	42	0.636

93		GST033	Gestational Diabetes	61	0.636

94	P	CNJ013	Conjunctivitis	66	0.636

95	P	EYD002	Eye Disease	57	0.636

96		PRP030	Purpura	54	0.636

97	c	BCT006	Bacterial Conjunctivitis	42	0.636