Search results for Triglycerides Group D

343 hits were found for Triglycerides Group D

#	Family	MCID	Name	MIFTS	Score
1	c	DBT026	Diabetes Mellitus, Noninsulin-Dependent	92	0.394

2	c	DBT009	Diabetes Mellitus	67	0.393

3	c	HPT021	Hepatitis	74	0.349

4	c	HRT032	Heart Disease	76	0.324

5	c	BRS047	Breast Cancer	100	0.311

6	c	LVR013	Liver Disease	77	0.294

7		RCK004	Rickets	66	0.287

8	c	MYC007	Myocardial Infarction	78	0.258

9	c	CRN018	Coronary Artery Anomaly	74	0.256

10		NTR005	Nutritional Deficiency Disease	60	0.255

11		DPR016	Depression	73	0.254

12	c	KDN018	Kidney Disease	71	0.254

13	c	ART022	Arthritis	78	0.254

14		ART140	Arteries, Anomalies of	67	0.249

15		LPD008	Lipid Metabolism Disorder	65	0.242

16	c	CRN300	Coronary Heart Disease 1	62	0.241

17		FTT001	Fatty Liver Disease	66	0.228

18	c	PRS040	Prostate Cancer	93	0.225

19		ISC004	Ischemia	67	0.224

20	c	OST002	Osteoporosis	74	0.219

21	c	CRD246	Cardiovascular System Disease	57	0.217

22	c	SCH015	Schizophrenia	73	0.215

23	c	ALZ034	Alzheimer Disease	88	0.213

24	P	PRS136	Prostate Cancer, Hereditary, 6	40	0.209

25	P	PRS130	Prostate Cancer, Hereditary, 8	37	0.209

26		ANX010	Anxiety	73	0.208

27	c	PNC044	Pancreatitis	62	0.202

28	c	HYP069	Hyperparathyroidism	59	0.202

29	P	BDY007	Body Mass Index Quantitative Trait Locus 1	48	0.201

30	c	NNL004	Nonalcoholic Fatty Liver Disease	56	0.201

31	c	LNG032	Lung Cancer	99	0.201

32		ISC006	Ischemic Heart Disease	72	0.200

33		GLC008	Glucose Metabolism Disease	54	0.194

34	P	HPT001	Hepatitis C	69	0.194

35	P	CHR089	Chronic Kidney Failure	73	0.193

36		VSC007	Vascular Disease	72	0.190

37		THR024	Thrombosis	64	0.189

38		ACQ007	Acquired Immunodeficiency Syndrome	66	0.189

39		HYP060	Hyperinsulinism	57	0.189

40		MNT002	Mental Depression	65	0.188

41	c	MLT020	Multiple Sclerosis	76	0.188

42		GST033	Gestational Diabetes	63	0.187

43	c	RHM011	Rheumatoid Arthritis	82	0.186

44		HMN014	Human Immunodeficiency Virus Infectious Disease	62	0.184

45	P	HPT016	Hepatitis B	70	0.181

46		PSY004	Psychotic Disorder	74	0.179

47		RRR001	Rere-Related Disorders	55	0.178

48		DRM006	Dermatitis	69	0.176

49		DMN002	Dementia	69	0.175

50	c	ENC018	Encephalopathy	65	0.174

51		OCL033	Oculocerebral Syndrome with Hypopigmentation	46	0.173

52		AGN016	Aging	63	0.171

53	c	ADN016	Adenocarcinoma	71	0.169

54		ATM095	Autoimmune Disease	68	0.167

55	c	DRR001	Diarrhea	58	0.162

56		GLC003	Glucose Intolerance	59	0.159

57	c	LPS004	Lupus Erythematosus	69	0.158

58	c	NRP001	Neuropathy	63	0.157

59	c	ART021	Arteriosclerosis	61	0.156

60	P	ACT027	Acute Pancreatitis	59	0.155

61		CYS001	Cystic Fibrosis	83	0.155

62		CNG034	Congestive Heart Failure	71	0.155

63	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	61	0.152

64	c	HPT023	Hepatocellular Carcinoma	97	0.150

65	P	MCR113	Microvascular Complications of Diabetes 3	58	0.149

66	P	MCR120	Microvascular Complications of Diabetes 7	46	0.149

67	P	MCR130	Microvascular Complications of Diabetes 6	43	0.149

68	P	MCR133	Microvascular Complications of Diabetes 4	43	0.149

69	P	SYS001	Systemic Lupus Erythematosus	88	0.149

70	c	PLY011	Polycystic Ovary Syndrome	64	0.148

71	P	SCN007	Secondary Hyperparathyroidism	56	0.148

72	c	INF037	Inflammatory Bowel Disease	56	0.148

73		URN009	Urinary System Disease	59	0.146

74	c	MYP004	Myopathy	65	0.145

75	P	CNT035	Central Nervous System Disease	65	0.144

76		GST050	Gastrointestinal System Disease	67	0.144

77	P	HPT073	Hepatitis C Virus	73	0.142

78	c	INT068	Intestinal Disease	62	0.142

79	c	PRD008	Periodontitis	66	0.141

80		RPD005	Rapidly Involuting Congenital Hemangioma	24	0.140

81	P	ACT075	Acute Myocardial Infarction	57	0.140

82		ALL026	Allergic Hypersensitivity Disease	68	0.139

83	P	PRC016	Pre-Eclampsia	61	0.138

84	P	HYP595	Hypertension, Essential	77	0.138

85		SPS003	Spastic Diplegia	49	0.137

86		HYP066	Hyperglycemia	65	0.136

87	c	PSR002	Psoriasis	67	0.136

88		HMN044	Human Immunodeficiency Virus Type 1	75	0.133

89		OST012	Osteoarthritis	81	0.132

90		CRH001	Crohn's Disease	79	0.132

91		SKN016	Skin Disease	68	0.130

92	c	HYP086	Hypothyroidism	66	0.130

93		PRD007	Periodontal Disease	66	0.130

94		VRL011	Viral Infectious Disease	69	0.129

95	c	DBT085	Diabetes Mellitus, Insulin-Dependent	73	0.128

96	c	EPL164	Epilepsy	73	0.128

97	c	RTN024	Retinoblastoma	73	0.128

98		CRB039	Cerebrovascular Disease	70	0.126

99		ATH013	Atherosclerosis Susceptibility	61	0.126

100		END057	Endometrial Cancer	69	0.125

101	c	HYP607	Hypercholesterolemia, Familial	82	0.125

102	c	MJR001	Major Depressive Disorder	67	0.125

103	c	NRV007	Nervous System Disease	72	0.122

104		HYP266	Hypoxia	63	0.122

105		NNL002	Nonalcoholic Steatohepatitis	55	0.122

106	c	NRB001	Neuroblastoma	73	0.121

107	P	TRC078	Trichohepatoenteric Syndrome 2	35	0.120

108		ADN018	Adenoma	65	0.120

109		CYT017	Cytophagic Histiocytic Panniculitis	26	0.120

110		GST045	Gastroenteritis	65	0.119

111		MDD011	Mood Disorder	65	0.119

112	c	INF032	Infertility	60	0.119

113		CLT003	Colitis	65	0.119

114		FSH001	Fish-Eye Disease	51	0.118

115		DST081	Distal Trisomy 11q	20	0.118

116		IMM136	Immune System Disease	57	0.116

117	c	TRC086	Trichohepatoenteric Syndrome 1	61	0.115

118	P	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	60	0.115

119		LVR012	Liver Cirrhosis	67	0.115

120	c	ABD014	Abdominal Obesity-Metabolic Syndrome 1	58	0.113

121		END030	End Stage Renal Failure	60	0.110

122		ANG054	Angina Pectoris	70	0.110

123	P	SCL052	Scleroderma, Familial Progressive	68	0.109

124		BRN071	Brain Injury	54	0.109

125	c	ECL001	Eclampsia	59	0.109

126	P	BNM022	Bone Mineral Density Quantitative Trait Locus 8	40	0.108

127	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	46	0.108

128		STR067	Stroke, Ischemic	84	0.106

129		SPN186	Spinal Cord Injury	66	0.106

130	c	CTR002	Cataract	58	0.104

131	c	BPL003	Bipolar Disorder	61	0.104

132		CNT047	Contact Dermatitis	64	0.104

133		DNT012	Dental Caries	52	0.103

134	c	CND004	Candidiasis	63	0.103

135	c	THR014	Thrombocytopenia	65	0.103

136		NRM005	Neuromuscular Disease	61	0.102

137	c	PRP019	Peripheral Nervous System Disease	66	0.102

138	c	THL005	Thalassemia	65	0.101

139	P	PRD040	Periodontitis, Chronic	60	0.101

140	c	ATR011	Atrial Fibrillation	69	0.101

141		ANR007	Anorexia Nervosa	68	0.101

142		URM002	Uremia	53	0.101

143		THR100	Thrombocytopenic Purpura, Autoimmune	68	0.099

144		END040	Endogenous Depression	59	0.099

145	c	CLC063	Celiac Disease 1	72	0.098

146	c	MSC033	Muscle Disorders	56	0.098

147		IMP005	Impotence	58	0.096

148		PRM236	Primary Biliary Cholangitis	63	0.096

149		CLR108	Colorectal Adenoma	64	0.096

150	c	PRM006	Primary Biliary Cirrhosis	54	0.096

151	P	BLR024	Biliary Cirrhosis, Primary, 1	39	0.096

152		LPD009	Lipid Storage Disease	53	0.095

153		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	35	0.095

154	P	VRL010	Viral Hepatitis	60	0.095

155		LYM019	Lymphosarcoma	59	0.094

156		DRL001	Dural Sinus Malformation	23	0.094

157	c	AMY004	Amyloidosis	69	0.094

158		OVR063	Overnutrition	53	0.094

159	c	ART153	Arthrochalasia Ehlers-Danlos Syndrome	22	0.094

160	c	NRF023	Neurofibromatosis, Type Ii	76	0.093

161		HYP056	Hypoglycemia	64	0.093

162		THR013	Thoracic Outlet Syndrome	57	0.092

163	P	THR001	Thrombocytopenia Due to Platelet Alloimmunization	61	0.092

164		ILT001	Ileitis	59	0.092

165		BRR014	Barrett Esophagus	71	0.092

166	c	SLP006	Sleep Apnea	70	0.091

167		DFC004	Deficiency Anemia	65	0.091

168		THY030	Thyroid Gland Disease	51	0.090

169	c	LCT001	Lactic Acidosis	53	0.089

170		PSR001	Psoriatic Arthritis	68	0.089

171	c	MCR115	Microvascular Complications of Diabetes 5	71	0.089

172		MSC190	Muscular Disease	55	0.089

173		MSC004	Muscle Tissue Disease	39	0.089

174		CHL123	Chlamydia	66	0.088

175		CGN005	Cognitive Impairment with or Without Cerebellar Ataxia	37	0.088

176		PRD004	Prediabetes Syndrome	51	0.088

177		FRN020	Frontal Fibrosing Alopecia	32	0.087

178	c	BDY004	Body Mass Index Quantitative Trait Locus 11	74	0.086

179	P	BDY020	Body Mass Index Quantitative Trait Locus 19	43	0.086

180	P	BDY019	Body Mass Index Quantitative Trait Locus 18	43	0.086

181	P	BDY017	Body Mass Index Quantitative Trait Locus 14	41	0.086

182	P	BDY011	Body Mass Index Quantitative Trait Locus 10	41	0.086

183		HYP080	Hypogonadism	53	0.086

184		PRP080	Peripheral Artery Disease	56	0.086

185		DMY004	Demyelinating Disease	60	0.086

186		BNG081	Benign Childhood Occipital Epilepsy, Panayiotopoulos Type	25	0.086

187	c	SZR006	Seizure Disorder	61	0.085

188		PRT036	Peritonitis	67	0.085

189		CRH005	Crohn's Colitis	61	0.084

190		GND003	Gonadal Disease	49	0.083

191		ART016	Aortic Aneurysm	71	0.082

192	c	TRM003	Tremor	56	0.082

193		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.082

194	c	ICH004	Ichthyosis	57	0.082

195		IRN002	Iron Metabolism Disease	60	0.082

196		GT001	Gout	62	0.081

197		CHL068	Cholestasis	60	0.081

198		PRT037	Pertussis	71	0.081

199		DBT010	Diabetic Neuropathy	60	0.081

200	c	CRD132	Cardiac Conduction Defect	64	0.081

201		INS024	Insulin-Like Growth Factor I	83	0.080

202		PRP027	Peripheral Vascular Disease	72	0.079

203	c	DDN001	Duodenal Ulcer	52	0.079

204		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.079

205	c	SHR001	Short Bowel Syndrome	52	0.078

206		HDN002	Head Injury	52	0.078

207		MRB003	Morbid Obesity	62	0.078

208		KWS001	Kwashiorkor	46	0.078

209	c	VSC018	Visceral Steatosis	38	0.078

210		INT002	Intermittent Claudication	64	0.077

211		SCH012	Schizoaffective Disorder	54	0.077

212	P	INF071	Inflammatory Bowel Disease 1	57	0.077

213		NTR027	Neutrophil Actin Dysfunction	32	0.076

214	P	PNC106	Pancreatic Agenesis 1	52	0.076

215		TRN018	Transitional Cell Carcinoma	63	0.075

216	c	OPN001	Open-Angle Glaucoma	53	0.075

217		PNC034	Pancreas Disease	60	0.075

218		SCK003	Sickle Cell Anemia	75	0.075

219		SXL003	Sexual Disorder	53	0.074

220		RTN018	Retinal Disease	58	0.073

221	P	BTT014	Beta-Thalassemia	73	0.073

222	c	FML018	Familial Mediterranean Fever	74	0.073

223		GRW007	Growth Hormone Deficiency	53	0.073

224		TRN015	Transient Cerebral Ischemia	59	0.072

225		BLR001	Biliary Atresia	57	0.072

226		BRN056	Bronchopulmonary Dysplasia	61	0.071

227	P	ART138	Aortic Aneurysm, Familial Abdominal, 1	66	0.071

228	c	GLY013	Glycogen Storage Disease	62	0.071

229		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	29	0.070

230		HYP064	Hypogonadotropism	42	0.070

231		BLM002	Bulimia Nervosa	61	0.070

232		GST092	Gastroesophageal Reflux	66	0.070

233	P	INS002	in Situ Carcinoma	60	0.070

234	c	DLT002	Dilated Cardiomyopathy	74	0.069

235		CYT002	Cytokine Deficiency	39	0.069

236	c	MSC007	Muscle Hypertrophy	64	0.069

237	P	MTR002	Mitral Valve Insufficiency	50	0.068

238		OST003	Osteonecrosis	67	0.066

239	c	NMN002	Niemann-Pick Disease	50	0.066

240	P	PLM164	Pulmonary Hypertension, Primary, 1	71	0.066

241	c	HYP076	Hyperthyroidism	56	0.065

242		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	36	0.065

243		ADR007	Adrenoleukodystrophy	72	0.064

244		KWS002	Kawasaki Disease	72	0.064

245	P	NMN015	Niemann-Pick Disease, Type C1	68	0.064

246	P	PSR017	Psoriasis 2	54	0.063

247		PLM017	Pulmonary Alveolar Microlithiasis	52	0.063

248		STT004	Steatorrhea	43	0.063

249	c	SLL003	Salla Disease	53	0.063

250	c	HYP014	Hyperuricemia	56	0.062

251		CHL004	Cholelithiasis	52	0.062

252		LWC002	Lowe Oculocerebrorenal Syndrome	67	0.062

253		HPR003	Heparin-Induced Thrombocytopenia	49	0.062

254	P	BLD140	Blood Group, I System	26	0.061

255		CRC021	Carcinosarcoma	62	0.060

256		ALL010	Allergic Contact Dermatitis	61	0.060

257		BRN080	Brain Ischemia	43	0.060

258		TRP004	Tropical Sprue	36	0.058

259	P	ATR087	Atrial Standstill 1	69	0.058

260		IRN001	Iron Deficiency Anemia	54	0.057

261	c	PTY003	Pityriasis Rubra Pilaris	52	0.057

262		KRT009	Keratosis	55	0.057

263		OBS082	Obstructive Nephropathy	52	0.056

264		PNC041	Pancreatic Ductal Adenocarcinoma	54	0.056

265		BLR008	Bilirubin Metabolic Disorder	53	0.056

266		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.056

267		HYP730	Hypogonadotropic Hypogonadism	58	0.056

268		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	60	0.056

269	P	PSR028	Psoriasis 7	43	0.055

270	P	PSR032	Psoriasis 11	43	0.055

271	P	PSR018	Psoriasis 13	42	0.055

272		WRN001	Werner Syndrome	74	0.055

273		HPT019	Hepatic Encephalopathy	60	0.055

274		WTH001	Withdrawal Disorder	51	0.054

275		ALC009	Alcoholic Liver Cirrhosis	52	0.054

276		CRC034	Carcinoma Showing Thymus-Like Differentiation	29	0.054

277		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	48	0.052

278		RTN017	Retinal Detachment	62	0.052

279	c	ZLL001	Zellweger Syndrome	57	0.052

280		LSH001	Leishmaniasis	72	0.052

281	c	SHR029	Short Syndrome	57	0.052

282	c	MYT002	Myotonic Dystrophy	52	0.052

283		ACT088	Acute Insulin Response	50	0.052

284		BLR006	Biliary Tract Disease	53	0.051

285		MYC088	Mycobacterium Avium Complex Infections	34	0.051

286		MYT026	Myotonia Atrophica	29	0.051

287		CRN167	Caronte	19	0.051

288		PRP016	Paraplegia	55	0.051

289		DBT084	Diabetes Mellitus, Ketosis-Prone	62	0.050

290		HPT004	Hepatic Coma	45	0.050

291		INS001	Insulinoma	66	0.050

292	P	CNG006	Congenital Hypothyroidism	64	0.050

293		AND005	Androgen Insensitivity Syndrome, Mild	19	0.050

294	c	ACT008	Actinic Keratosis	55	0.050

295		KRT002	Keratomalacia	51	0.050

296		CRN030	Coronary Stenosis	52	0.049

297	c	LYM025	Lymphedema	55	0.049

298	c	CMP008	Compartment Syndrome	52	0.049

299		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	44	0.049

300		PHT003	Phototoxic Dermatitis	44	0.049

301		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	56	0.048

302		NNT019	Neonatal Hypothyroidism	42	0.048

303		HMS001	Hemosiderosis	52	0.048

304		MNS002	Mini Stroke	25	0.047

305	P	TYP024	Type Ii Mixed Cryoglobulinemia	40	0.047

306	c	CRB088	Cerebral Atrophy	42	0.047

307		INT007	Intermediate Coronary Syndrome	50	0.047

308	P	GLL024	Gallbladder Disease 1	45	0.046

309		LNG073	Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency	60	0.046

310		MTR003	Mitral Valve Stenosis	51	0.046

311		FXF002	Fox-Fordyce Disease	41	0.046

312	c	HYP061	Hypertrophic Cardiomyopathy	59	0.046

313		DSM006	Desmoplastic Infantile Ganglioglioma	28	0.045

314		ACT236	Acute Motor and Sensory Axonal Neuropathy	23	0.045

315		ATN004	Autonomic Neuropathy	46	0.045

316	c	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	70	0.044

317		CRY035	Cryptorchidism, Unilateral or Bilateral	61	0.044

318		MTB007	Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration	53	0.044

319		DBT008	Diabetic Angiopathy	48	0.044

320		CHR177	Chromophobe Renal Cell Carcinoma	54	0.043

321		OCL069	Ocular Motor Apraxia	51	0.043

322		FTL021	Fetal Macrosomia	47	0.042

323		CHL147	Chlamydia Pneumonia	42	0.041

324		PRT019	Protein-Losing Enteropathy	41	0.041

325	c	MTC069	Mitochondrial Disorders	51	0.041

326		CHL013	Cholecystolithiasis	37	0.041

327		SPN021	Spinal Meningioma	50	0.041

328		SCR001	Secretory Meningioma	40	0.041

329		DRM009	Dermatomycosis	36	0.041

330		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	48	0.040

331	c	ANL018	Analbuminemia	48	0.040

332		CHL067	Cholecystitis	59	0.040

333		LPD004	Lipoid Nephrosis	51	0.039

334		KRT008	Keratopathy	47	0.039

335		MTC005	Mitochondrial Metabolism Disease	46	0.039

336		VSC003	Visceral Leishmaniasis	61	0.039

337	P	MNN043	Meningioma, Familial	63	0.038

338	c	GLL020	Gallbladder Disease	64	0.036

339		PYR016	Pyridoxine Deficiency	39	0.036

340		HYP264	Hypertonia	37	0.035

341		NTR046	Neutrophil Migration	56	0.034

342		BLP005	Blepharitis	45	0.034

343	P	BRN108	Branchiootic Syndrome 1	48	0.032