Search results for Clofibrate

244 hits were found for Clofibrate

#	Family	MCID	Name	MIFTS	Score
1	P	DBT005	Diabetes Insipidus	55	0.249

2	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.204

3	P	HYP750	Hypertriglyceridemia, Familial	62	0.201

4	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.184

5	P	HRT032	Heart Disease	75	0.176

6		BLR008	Bilirubin Metabolic Disorder	57	0.162

7	P	MYP004	Myopathy	70	0.152

8	P	DBT009	Diabetes Mellitus	64	0.147

9	P	CRN300	Coronary Heart Disease 1	63	0.147

10	P	VSC007	Vascular Disease	63	0.136

11	P	ART021	Arteriosclerosis	54	0.136

12	P	KDN018	Kidney Disease	72	0.130

13		ATH013	Atherosclerosis Susceptibility	65	0.130

14	c	FML021	Familial Hypercholesterolemia	66	0.118

15	P	MCR115	Microvascular Complications of Diabetes 5	66	0.111

16		MYT011	Myotonia	34	0.111

17	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.104

18	P	MYC007	Myocardial Infarction	70	0.104

19	c	GLL024	Gallbladder Disease 1	53	0.104

20		48X005	48,xyyy	39	0.104

21		PPL052	Papillomatosis, Confluent and Reticulated	33	0.104

22		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.096

23		LPP008	Lipoprotein Quantitative Trait Locus	62	0.096

24		LVR012	Liver Cirrhosis	62	0.096

25		FTT001	Fatty Liver Disease	61	0.096

26		NNT012	Neonatal Jaundice	53	0.096

27	P	HYP086	Hypothyroidism	69	0.088

28		LPD008	Lipid Metabolism Disorder	62	0.088

29	P	NPH012	Nephrotic Syndrome	60	0.088

30	P	CRD246	Cardiovascular System Disease	57	0.088

31		ANG054	Angina Pectoris	66	0.079

32		ISC004	Ischemia	58	0.079

33		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.079

34	P	NRP001	Neuropathy	56	0.079

35		HYP014	Hyperuricemia	52	0.079

36		XNT003	Xanthomatosis	49	0.079

37		CHL004	Cholelithiasis	49	0.079

38	P	KRN004	Kernicterus	47	0.079

39		ADR007	Adrenoleukodystrophy	75	0.068

40		PRP027	Peripheral Vascular Disease	71	0.068

41	P	HYP098	Hypereosinophilic Syndrome	67	0.068

42	P	PRM006	Primary Biliary Cirrhosis	62	0.068

43		CHL068	Cholestasis	61	0.068

44	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.068

45	c	FML035	Familial Hyperlipidemia	55	0.068

46		HYP060	Hyperinsulinism	54	0.068

47		GLC003	Glucose Intolerance	54	0.068

48		DBT010	Diabetic Neuropathy	54	0.068

49		ART140	Arteries, Anomalies of	52	0.068

50	P	CRC039	Coarctation of Aorta	47	0.068

51		ATX019	Ataxia with Vitamin E Deficiency	42	0.068

52		ADR022	Adrenomyeloneuropathy	38	0.068

53	c	HNT011	Huntington Disease-Like 3	38	0.068

54	P	HPT023	Hepatocellular Carcinoma	100	0.056

55	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.056

56	P	OVR042	Ovarian Cancer	88	0.056

57	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.056

58	c	LKM063	Leukemia, Chronic Myeloid	72	0.056

59	P	LVR013	Liver Disease	68	0.056

60	P	HPT021	Hepatitis	67	0.056

61		CRB039	Cerebrovascular Disease	67	0.056

62		HYP056	Hypoglycemia	66	0.056

63	P	ADN016	Adenocarcinoma	64	0.056

64		INT002	Intermittent Claudication	61	0.056

65	P	MYL006	Myeloid Leukemia	60	0.056

66	c	ACT027	Acute Pancreatitis	60	0.056

67	c	ACT071	Acute Kidney Failure	60	0.056

68		ADN018	Adenoma	59	0.056

69		ERY003	Erythema Multiforme	58	0.056

70		EYD002	Eye Disease	58	0.056

71	P	GLL020	Gallbladder Disease	57	0.056

72	P	ZLL001	Zellweger Syndrome	57	0.056

73	P	HYP076	Hyperthyroidism	55	0.056

74		IMP005	Impotence	52	0.056

75		HPT014	Hepatorenal Syndrome	50	0.056

76		47X002	47,xyy	49	0.056

77	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.056

78	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	35	0.056

79	P	CLR023	Colorectal Cancer	99	0.039

80	P	BRS047	Breast Cancer	97	0.039

81		MYL069	Myeloma, Multiple	85	0.039

82	c	HYP595	Hypertension, Essential	84	0.039

83	P	PNC035	Pancreatic Cancer	84	0.039

84		IMM167	Immune Deficiency Disease	78	0.039

85	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.039

86	c	ATR087	Atrial Standstill 1	75	0.039

87		LPT014	Leptin Deficiency or Dysfunction	74	0.039

88	c	SPN225	Spondyloarthropathy 1	73	0.039

89	P	FML018	Familial Mediterranean Fever	73	0.039

90		HMN044	Human Immunodeficiency Virus Type 1	71	0.039

91		DFC004	Deficiency Anemia	70	0.039

92	P	AMY004	Amyloidosis	70	0.039

93		MYL009	Myelodysplastic Syndrome	70	0.039

94		LGH007	Leigh Syndrome	70	0.039

95		CNG034	Congestive Heart Failure	69	0.039

96	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.039

97	P	ART022	Arthritis	69	0.039

98		SVR097	Severe Cutaneous Adverse Reaction	69	0.039

99	P	SLP006	Sleep Apnea	69	0.039

100	P	PNM007	Pneumonia	68	0.039

101	P	TRN020	Turner Syndrome	67	0.039

102	c	MCR129	Microvascular Complications of Diabetes 1	66	0.039

103	P	ATR011	Atrial Fibrillation	66	0.039

104	P	DRM053	Dermatitis, Atopic	66	0.039

105	c	FML001	Familial Atrial Fibrillation	65	0.039

106		TNG002	Tangier Disease	65	0.039

107		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.039

108	P	HRP006	Herpes Simplex	65	0.039

109		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.039

110		CLN015	Colon Adenocarcinoma	65	0.039

111	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.039

112		APN008	Apnea, Obstructive Sleep	64	0.039

113		BRC012	Brucellosis	64	0.039

114	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.039

115	c	ATS013	Autosomal Recessive Congenital Ichthyosis	63	0.039

116		KRN002	Kearns-Sayre Syndrome	63	0.039

117	c	ACT068	Acute Cystitis	63	0.039

118	c	ATM011	Autoimmune Hepatitis	63	0.039

119	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.039

120	P	PSR002	Psoriasis	62	0.039

121	c	HPT003	Hepatitis a	62	0.039

122	c	BRN108	Branchiootic Syndrome 1	62	0.039

123		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.039

124		ALL026	Allergic Hypersensitivity Disease	62	0.039

125		CRC021	Carcinosarcoma	62	0.039

126		NTR005	Nutritional Deficiency Disease	62	0.039

127		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.039

128		HYP066	Hyperglycemia	61	0.039

129		CHN055	Chanarin-Dorfman Syndrome	61	0.039

130		DRM006	Dermatitis	61	0.039

131	P	ENC018	Encephalopathy	61	0.039

132	P	PNC044	Pancreatitis	61	0.039

133	P	LPS004	Lupus Erythematosus	61	0.039

134		HPT019	Hepatic Encephalopathy	60	0.039

135		ACQ007	Acquired Immunodeficiency Syndrome	60	0.039

136	P	BND020	Bone Disease	59	0.039

137		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.039

138		DBT087	Diabetes Insipidus, Neurohypophyseal	58	0.039

139		GLB001	Gilbert Syndrome	58	0.039

140	P	ALC033	Alcohol Use Disorder	58	0.039

141		BRG013	Buerger Disease	58	0.039

142	P	GLM007	Glomerulonephritis	57	0.039

143	c	CHL119	Cholangitis, Primary Sclerosing	57	0.039

144	P	PLY041	Polymyositis	57	0.039

145		DSS009	Disseminated Intravascular Coagulation	57	0.039

146	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.039

147	c	ACT075	Acute Myocardial Infarction	57	0.039

148		THR024	Thrombosis	57	0.039

149	P	PYL005	Pyelonephritis	56	0.039

150	P	MYS005	Myositis	56	0.039

151	P	MTC069	Mitochondrial Disorders	56	0.039

152		NRL004	Neuroleptic Malignant Syndrome	56	0.039

153	P	HYP838	Hyperlipidemia, Familial Combined, 3	56	0.039

154		AGN016	Aging	56	0.039

155	P	GST044	Gastritis	56	0.039

156		HYP005	Hypokalemia	55	0.039

157		MCL006	Macular Retinal Edema	55	0.039

158	P	DRR001	Diarrhea	55	0.039

159		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.039

160	P	PTT006	Pituitary Adenoma	55	0.039

161		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.039

162		ANL018	Analbuminemia	54	0.039

163		PPL022	Papilloma	54	0.039

164		TRC023	Trichinosis	53	0.039

165	P	HYP083	Hypopituitarism	53	0.039

166		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.039

167		PRP080	Peripheral Artery Disease	53	0.039

168	P	RTN018	Retinal Disease	53	0.039

169	c	MCR113	Microvascular Complications of Diabetes 3	52	0.039

170	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.039

171		PST011	Pustulosis of Palm and Sole	52	0.039

172		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.039

173	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.039

174	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	52	0.039

175		LMY002	Leiomyoma	52	0.039

176		SPN051	Spondylitis	51	0.039

177		THR016	Thrombophlebitis	51	0.039

178		LNG031	Lung Benign Neoplasm	51	0.039

179		END086	End Stage Renal Disease	51	0.039

180	P	CHL066	Cholangitis	51	0.039

181		HYP081	Hypolipoproteinemia	51	0.039

182	c	HNT004	Huntington Disease-Like 2	50	0.039

183	P	ESN008	Eosinophilic Pneumonia	50	0.039

184		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.039

185	c	HYP739	Hyperlipoproteinemia, Type Iv	50	0.039

186		RBF001	Riboflavin Deficiency	49	0.039

187	P	MYT002	Myotonic Dystrophy	49	0.039

188	P	MTC133	Mitochondrial Myopathy	49	0.039

189	P	OPN001	Open-Angle Glaucoma	49	0.039

190		MTC005	Mitochondrial Metabolism Disease	49	0.039

191		URM002	Uremia	49	0.039

192		VCC001	Vaccinia	49	0.039

193		ATS010	Autosomal Recessive Disease	48	0.039

194	P	SCL009	Sclerosing Cholangitis	48	0.039

195		INT067	Interstitial Nephritis	48	0.039

196	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.039

197		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.039

198		THY128	Thyroid Tumor	47	0.039

199	c	MCR120	Microvascular Complications of Diabetes 7	47	0.039

200	c	INH020	Inherited Metabolic Disorder	47	0.039

201	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.039

202		LPD009	Lipid Storage Disease	46	0.039

203	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.039

204	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.039

205		SQM002	Squamous Cell Papilloma	46	0.039

206		PRX001	Peroxisomal Disease	46	0.039

207	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.039

208	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.039

209		HPT004	Hepatic Coma	45	0.039

210		FSH001	Fish-Eye Disease	45	0.039

211		ORG002	Organic Acidemia	44	0.039

212	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.039

213	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.039

214	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.039

215	P	MYG005	Myoglobinuria	44	0.039

216	P	HYP121	Hypoalphalipoproteinemia	43	0.039

217	c	ICH049	Ichthyosis, Congenital, Autosomal Recessive 2	43	0.039

218		MNN017	Mononeuropathy	42	0.039

219	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.039

220		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.039

221	c	SZR022	Seizures, Benign Familial Neonatal, 1	42	0.039

222	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	41	0.039

223		NTR007	Neutral Lipid Storage Disease with Myopathy	41	0.039

224	c	MCR130	Microvascular Complications of Diabetes 6	41	0.039

225	c	MCR133	Microvascular Complications of Diabetes 4	41	0.039

226	c	MCR112	Microvascular Complications of Diabetes 2	41	0.039

227		PYL004	Pyelitis	40	0.039

228		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.039

229		MSC190	Muscular Disease	37	0.039

230		GRN009	Granulomatous Hepatitis	33	0.039

231		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.039

232		KDN013	Kidney Hypertrophy	32	0.039

233		INF009	Inflammatory Spondylopathy	31	0.039

234		SPR017	Spermatocele	31	0.039

235		LCH014	Lichen Amyloidosis	31	0.039

236		ERY066	Erythema Multiforme Major	30	0.039

237	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.039

238		ANG037	Angiomatosis	28	0.039

239	c	RNG015	Ring Chromosome 2	26	0.039

240		STN013	Stenotrophomonas Maltophilia Infection	25	0.039

241		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.039

242		URT049	Urate Oxidase, Pseudogene	25	0.039

243		DPS001	Dipsogenic Diabetes Insipidus	23	0.039

244		ORN004	Ornithinemia	17	0.039