Search results for cholesterol

3744 hits were found for cholesterol

#	Family	MCID	Name	MIFTS	Score
1	c	HYP836	Hypercholesterolemia, Familial, 1	73	89.925

2		LPD008	Lipid Metabolism Disorder	62	57.962

3	P	CRN300	Coronary Heart Disease 1	73	50.817

4		ATH013	Atherosclerosis Susceptibility	63	49.865

5	c	GLL024	Gallbladder Disease 1	52	37.364

6	P	HYP750	Hypertriglyceridemia, Familial	62	36.810

7	c	FML021	Familial Hypercholesterolemia	72	35.831

8		LPP008	Lipoprotein Quantitative Trait Locus	65	35.089

9		ART140	Arteries, Anomalies of	53	31.857

10		CHL070	Cholesterol Embolism	39	31.820

11		FTT001	Fatty Liver Disease	62	30.164

12	c	HNT004	Huntington Disease-Like 2	52	30.111

13	c	TYP009	Type 2 Diabetes Mellitus	92	29.894

14		NNL005	Non-Alcoholic Fatty Liver Disease	63	29.874

15	P	NMN002	Niemann-Pick Disease	60	29.517

16	c	HNT011	Huntington Disease-Like 3	34	29.347

17	c	NMN015	Niemann-Pick Disease, Type C1	68	29.168

18	P	HRT032	Heart Disease	81	28.798

19		LCT022	Lecithin:cholesterol Acyltransferase Deficiency	58	28.463

20		LYS012	Lysosomal Acid Lipase Deficiency	65	27.578

21		TNG002	Tangier Disease	64	27.529

22		HYP732	Hyperalphalipoproteinemia 1	52	26.505

23		CHL050	Cholesterol Ester Storage Disease	31	25.925

24	P	VSC007	Vascular Disease	63	25.729

25	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	25.461

26	P	DBT009	Diabetes Mellitus	67	23.642

27		RPD005	Rapidly Involuting Congenital Hemangioma	46	23.620

28	P	STS003	Sitosterolemia	53	23.397

29	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	49	21.260

30	P	ART021	Arteriosclerosis	54	20.023

31	P	CHL139	Cholesterol Level Quantitative Trait Locus 1	11	19.670

32		CHL084	Cholesterol Pneumonia	19	19.575

33		SMT004	Smith-Lemli-Opitz Syndrome	70	19.569

34	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	19.155

35	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	19.133

36	c	HYP272	Hypercholesterolemia, Familial, 3	45	18.554

37		PRP027	Peripheral Vascular Disease	71	18.470

38	P	MYC007	Myocardial Infarction	70	18.332

39	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	18.236

40	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	18.236

41	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	18.234

42	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	18.234

43	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	18.234

44	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	18.234

45	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	18.234

46	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	18.234

47	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	18.231

48		HYP066	Hyperglycemia	61	18.220

49		CHL004	Cholelithiasis	49	18.001

50	P	LVR013	Liver Disease	69	17.735

51	P	HGH038	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6	12	17.641

52	c	OPT051	Opitz Gbbb Syndrome, Type I	46	17.618

53	P	CRD246	Cardiovascular System Disease	56	17.300

54		HYP060	Hyperinsulinism	54	17.254

55	c	HYP595	Hypertension, Essential	85	17.000

56		ANG054	Angina Pectoris	66	16.919

57	c	CHR684	Chronic Kidney Disease	69	16.890

58		NNL006	Non-Alcoholic Steatohepatitis	54	16.682

59		ISC004	Ischemia	61	16.651

60	P	HYP086	Hypothyroidism	69	16.396

61		CRB039	Cerebrovascular Disease	66	16.304

62	c	LWD007	Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 7	13	16.297

63		PRT251	Proteinuria, Chronic Benign	57	16.023

64		FSH001	Fish-Eye Disease	44	15.962

65		GLC003	Glucose Intolerance	54	15.845

66	c	LWD008	Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 8	9	15.820

67	c	NMN014	Niemann-Pick Disease, Type C2	49	15.757

68	c	HGH039	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 12	12	15.193

69		CHL068	Cholestasis	61	15.021

70		CHL141	Cholesterol Level Quantitative Trait Locus 2	6	14.949

71		MDD006	Middle Ear Cholesterol Granuloma	13	14.734

72		HMZ003	Homozygous Familial Hypercholesterolemia	60	14.724

73	c	HGH035	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 3	8	14.637

74	P	LWD006	Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6	13	14.432

75	P	ALZ034	Alzheimer Disease	87	14.373

76		FML330	Familial Lcat Deficiency	33	14.326

77	c	HGH032	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 14	8	14.255

78	P	PLY011	Polycystic Ovary Syndrome	57	14.250

79		SQL002	Squalene Synthase Deficiency	28	14.181

80	P	KDN018	Kidney Disease	72	14.126

81	c	ACT075	Acute Myocardial Infarction	56	14.092

82		STR067	Stroke, Ischemic	80	13.965

83		48X005	48,xyyy	39	13.946

84		INT007	Intermediate Coronary Syndrome	54	13.802

85	P	NPH012	Nephrotic Syndrome	60	13.469

86		ART004	Aortic Atherosclerosis	47	13.401

87	c	TYP008	Type 1 Diabetes Mellitus	70	13.223

88	c	MCR113	Microvascular Complications of Diabetes 3	52	13.124

89		FML035	Familial Hyperlipidemia	55	13.123

90	P	HYP838	Hyperlipidemia, Familial Combined, 3	61	12.830

91	c	MCR130	Microvascular Complications of Diabetes 6	41	12.705

92	c	MCR120	Microvascular Complications of Diabetes 7	47	12.705

93	c	MCR133	Microvascular Complications of Diabetes 4	41	12.705

94		END086	End Stage Renal Disease	52	12.507

95	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	12.381

96		PRC052	Pericardial Effusion, Chronic	19	12.368

97	c	HGH042	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 7	8	12.018

98	P	HYP768	Hyperlipoproteinemia, Type I	67	11.953

99	P	RHM011	Rheumatoid Arthritis	82	11.900

100		XNT003	Xanthomatosis	49	11.815

101	P	MYP004	Myopathy	67	11.330

102	c	46X062	46,xy Disorder of Sex Development Due to a Cholesterol Synthesis Defect	4	11.218

103	P	HYP121	Hypoalphalipoproteinemia	43	11.186

104		GST033	Gestational Diabetes	61	10.854

105		LVR012	Liver Cirrhosis	63	10.622

106		47X002	47,xyy	48	10.479

107	P	ART022	Arthritis	71	10.458

108	c	MCL042	Macular Degeneration, Age-Related, 1	85	10.413

109		CRB011	Cerebrotendinous Xanthomatosis	65	10.352

110		AGN016	Aging	54	10.299

111	c	MCR115	Microvascular Complications of Diabetes 5	65	10.257

112		HMC014	Homocysteinemia	52	10.142

113	P	NRB001	Neuroblastoma	66	10.140

114		PRP080	Peripheral Artery Disease	54	10.118

115	c	HPT001	Hepatitis C	62	10.088

116		HYP014	Hyperuricemia	51	10.082

117		HLX001	Helix Syndrome	48	9.998

118	c	HYP724	Hyperlipoproteinemia, Type Iii	67	9.980

119		HYP081	Hypolipoproteinemia	49	9.916

120		RCK004	Rickets	68	9.856

121		CRN030	Coronary Stenosis	50	9.847

122		TRN015	Transient Cerebral Ischemia	63	9.763

123	c	HGH033	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 1	9	9.677

124	P	LPS004	Lupus Erythematosus	61	9.500

125		HYP485	Hypercholesterolemia Due to Cholesterol 7alpha-Hydroxylase Deficiency	11	9.295

126	P	HYP076	Hyperthyroidism	53	9.241

127	P	HNT016	Huntington Disease	73	9.166

128	c	HGH037	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 5	5	9.096

129	P	HYP818	Hypobetalipoproteinemia, Familial, 1	60	9.092

130	c	PRC016	Pre-Eclampsia	65	9.077

131	c	HGH036	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 4	6	9.023

132		ABT001	Abetalipoproteinemia	68	8.969

133	c	ACT027	Acute Pancreatitis	60	8.938

134		LWD005	Low Density Lipoprotein Cholesterol, Mild Elevation of	4	8.880

135	c	HPT073	Hepatitis C Virus	71	8.874

136		CRT013	Carotid Stenosis	51	8.767

137		CNG034	Congestive Heart Failure	69	8.743

138		CHL014	Cholera	62	8.720

139		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	8.572

140		LPT014	Leptin Deficiency or Dysfunction	78	8.545

141		PST011	Pustulosis of Palm and Sole	52	8.532

142	P	PRD008	Periodontitis	64	8.506

143	c	SYS001	Systemic Lupus Erythematosus	87	8.506

144	P	PSR002	Psoriasis	63	8.500

145	c	HGH034	High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 2	6	8.425

146		ATS010	Autosomal Recessive Disease	42	8.304

147	P	SLP006	Sleep Apnea	69	8.283

148	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	8.278

149		HYP056	Hypoglycemia	65	8.272

150	P	PRS040	Prostate Cancer	95	8.246

151	c	ACT071	Acute Kidney Failure	60	8.227

152	P	SCH015	Schizophrenia	74	8.135

153		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	8.115

154		IMP005	Impotence	52	8.108

155		INS024	Insulin-Like Growth Factor I	78	8.108

156		IMM167	Immune Deficiency Disease	78	8.082

157	c	HNT010	Huntington Disease-Like 1	55	8.077

158	P	NRP001	Neuropathy	60	8.077

159		PRM236	Primary Biliary Cholangitis	60	8.056

160		CHL067	Cholecystitis	60	7.976

161		ADN018	Adenoma	59	7.838

162	P	DMN002	Dementia	66	7.826

163	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	7.801

164		MNT002	Mental Depression	57	7.772

165		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	7.664

166		MLD018	Mild Cognitive Impairment	48	7.628

167		DPR016	Depression	65	7.620

168		ART016	Aortic Aneurysm	68	7.601

169	P	PNC044	Pancreatitis	61	7.576

170		VSC002	Vascular Dementia	60	7.468

171	P	HPT021	Hepatitis	69	7.433

172	P	BPL003	Bipolar Disorder	56	7.433

173		DSM002	Desmosterolosis	39	7.420

174	P	EYD002	Eye Disease	57	7.398

175	c	MJR022	Major Affective Disorder 8	38	7.373

176	c	MJR024	Major Affective Disorder 9	41	7.373

177		PLY150	Polykaryocytosis Inducer	29	7.369

178		HYP080	Hypogonadism	50	7.341

179		CNS004	Constipation	56	7.330

180		URM002	Uremia	47	7.328

181		LYS002	Lysosomal Storage Disease	51	7.302

182		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	7.171

183	P	MJR001	Major Depressive Disorder	68	7.137

184		DFC004	Deficiency Anemia	74	7.106

185		HMN044	Human Immunodeficiency Virus Type 1	78	7.105

186		CYT002	Cytokine Deficiency	43	7.079

187		GRW007	Growth Hormone Deficiency	46	7.073

188	P	ICH004	Ichthyosis	56	7.069

189		BNR002	Bone Resorption Disease	47	7.068

190		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	7.033

191	P	ALC033	Alcohol Use Disorder	61	6.996

192		CHL123	Chlamydia	58	6.974

193		INT002	Intermittent Claudication	61	6.947

194	P	ATR011	Atrial Fibrillation	66	6.937

195	P	GLM007	Glomerulonephritis	60	6.886

196	P	HYP098	Hypereosinophilic Syndrome	66	6.831

197		CHL122	Cholesteatoma of Middle Ear	51	6.830

198		CRT016	Carotid Artery Disease	52	6.828

199	P	BRS047	Breast Cancer	98	6.778

200		MVL001	Mevalonic Aciduria	66	6.766

201		CRD132	Cardiac Conduction Defect	60	6.751

202		RST023	Resting Heart Rate, Variation in	40	6.688

203	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	6.680

204		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	6.615

205	P	OST002	Osteoporosis	76	6.590

206		ALC007	Alcohol Dependence	66	6.537

207		STM007	Stomatitis	54	6.498

208	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	6.497

209	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	6.497

210		PRT036	Peritonitis	65	6.474

211		GT001	Gout	64	6.445

212	P	PRP019	Peripheral Nervous System Disease	58	6.409

213		GLB002	Glioblastoma	67	6.382

214	P	ACN011	Acne	57	6.379

215		HYP043	Hyperandrogenism	48	6.371

216		THR024	Thrombosis	56	6.334

217		CYS001	Cystic Fibrosis	78	6.316

218	P	CTR002	Cataract	60	6.292

219	P	VSC011	Vasculitis	61	6.290

220		OST012	Osteoarthritis	77	6.289

221		HYP266	Hypoxia	57	6.211

222	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	6.170

223		ANR040	Aneurysm	61	6.159

224	c	ART101	Aortic Valve Disease 2	66	6.147

225		LPD009	Lipid Storage Disease	45	6.130

226	P	LTR001	Lateral Sclerosis	58	6.106

227		CHL147	Chlamydia Pneumonia	47	6.096

228	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	6.090

229		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	6.081

230		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	6.081

231	P	GLL020	Gallbladder Disease	56	6.072

232		OTT002	Otitis Media	71	6.050

233	c	INH020	Inherited Metabolic Disorder	48	6.017

234		CNG184	Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects	56	6.009

235	P	OBS001	Obstructive Jaundice	48	6.004

236	P	MYC084	Mycobacterium Tuberculosis 1	68	5.971

237	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	50	5.971

238	P	CLR023	Colorectal Cancer	100	5.957

239		LTH002	Lathosterolosis	38	5.933

240	P	AMY004	Amyloidosis	70	5.927

241		MDD011	Mood Disorder	62	5.911

242	P	CHL066	Cholangitis	52	5.901

243	c	VRL010	Viral Hepatitis	53	5.884

244	P	ECL001	Eclampsia	52	5.873

245	P	HML002	Hemolytic Anemia	62	5.859

246		CLB022	Coloboma, Ocular, Autosomal Recessive	28	5.851

247		ATM095	Autoimmune Disease	61	5.843

248	P	TRN020	Turner Syndrome	67	5.837

249		SPN186	Spinal Cord Injury	61	5.829

250	P	MYS005	Myositis	56	5.826

251	P	INF032	Infertility	57	5.813

252		PRS045	Prostatic Hypertrophy	53	5.728

253		PRD004	Prediabetes Syndrome	52	5.694

254		RNL114	Renal Cell Carcinoma, Nonpapillary	80	5.644

255	P	INF038	Influenza	68	5.637

256		SPL018	Splenomegaly	49	5.579

257	P	MLT020	Multiple Sclerosis	79	5.572

258		PRS021	Prostatic Adenoma	43	5.570

259	P	HPT023	Hepatocellular Carcinoma	96	5.566

260	c	HPT016	Hepatitis B	62	5.561

261	P	EXN002	Exanthem	58	5.554

262		HYP290	Hypobetalipoproteinemia, Familial, 2	36	5.548

263		HPT025	Hepatic Lipase Deficiency	47	5.510

264		LKN025	Leukoencephalopathy, Hereditary Diffuse, with Spheroids	66	5.479

265	c	THR092	Thrombophilia Due to Thrombin Defect	74	5.478

266		END057	Endometrial Cancer	72	5.471

267		HPT022	Hepatoblastoma	54	5.458

268		IRN002	Iron Metabolism Disease	57	5.452

269	P	SNS001	Sensorineural Hearing Loss	59	5.441

270		HLC007	Helicobacter Pylori Infection	67	5.426

271	P	ENC018	Encephalopathy	62	5.425

272	c	STS010	Sitosterolemia 1	46	5.415

273		CLF027	Cleft Palate, Isolated	64	5.390

274	P	PRS038	Personality Disorder	65	5.373

275		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	5.368

276		PLM129	Pulmonary Disease, Chronic Obstructive	74	5.334

277	P	INF037	Inflammatory Bowel Disease	53	5.273

278		PRS129	Prostatic Hyperplasia, Benign	49	5.248

279		DSS032	Disease by Infectious Agent	55	5.237

280		ICH054	Ichthyosis, X-Linked	52	5.229

281		GLM045	Glioma	63	5.198

282	P	GCH001	Gaucher's Disease	70	5.196

283	P	DRR001	Diarrhea	55	5.158

284	P	BCL017	B-Cell Lymphoma	59	5.153

285		GLL048	Glial Tumor	52	5.151

286	P	PLY019	Polyneuropathy	52	5.145

287		ANR007	Anorexia Nervosa	60	5.113

288	c	ATR087	Atrial Standstill 1	74	5.110

289	P	GST053	Gastric Cancer	83	5.097

290		PRC013	Pericarditis	53	5.062

291	P	KLZ004	Kala-Azar 1	41	5.055

292		LSH001	Leishmaniasis	64	5.055

293	c	PCH010	Pachyonychia Congenita 3	43	5.036

294		SKN016	Skin Disease	63	5.019

295	P	PNC035	Pancreatic Cancer	86	5.002

296	P	SCK005	Sickle Cell Disease	56	4.964

297		HRW001	Hair Whorl	35	4.954

298		DWN001	Down Syndrome	70	4.921

299		BCT022	Bacterial Infectious Disease	56	4.920

300		CRB008	Cerebral Atherosclerosis	46	4.872

301		HMS001	Hemosiderosis	48	4.866

302		PPL052	Papillomatosis, Confluent and Reticulated	34	4.851

303		ANX010	Anxiety	70	4.846

304		PRT037	Pertussis	65	4.841

305	P	OVR042	Ovarian Cancer	88	4.811

306	P	RRH023	Rare Hereditary Hemochromatosis	54	4.806

307		ACR007	Acromegaly	70	4.770

308	P	CRD119	Cardiac Arrest	67	4.762

309	P	HYP069	Hyperparathyroidism	62	4.744

310		CHL013	Cholecystolithiasis	37	4.739

311	P	HYP083	Hypopituitarism	52	4.732

312	P	MCR010	Microcephaly	60	4.731

313	P	PLM037	Pulmonary Hypertension	72	4.704

314		ALL029	Allergic Disease	59	4.698

315	P	PRN023	Prion Disease	60	4.666

316	P	LKM062	Leukemia, Acute Lymphoblastic	69	4.662

317		CRH001	Crohn's Disease	80	4.651

318		ALL014	Allergic Encephalomyelitis	34	4.627

319	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	4.604

320	P	THL005	Thalassemia	56	4.591

321	P	CHN044	Chondrodysplasia Punctata Syndrome	43	4.587

322	P	CLC063	Celiac Disease 1	66	4.586

323		SPN051	Spondylitis	51	4.581

324		INF009	Inflammatory Spondylopathy	30	4.581

325	c	LKM061	Leukemia, Acute Myeloid	83	4.573

326	c	SPN225	Spondyloarthropathy 1	70	4.570

327		ANL018	Analbuminemia	53	4.540

328		SCH076	Schnyder Corneal Dystrophy	47	4.539

329		NTR005	Nutritional Deficiency Disease	61	4.527

330	P	DNG005	Dengue Virus	56	4.518

331	P	HLP001	Holoprosencephaly	69	4.507

332		THY029	Thyroid Carcinoma	51	4.506

333		ULC004	Ulcerative Colitis	74	4.496

334		CLT003	Colitis	63	4.494

335	c	PRD040	Periodontitis, Chronic	52	4.491

336	P	GST044	Gastritis	55	4.473

337	P	PNM007	Pneumonia	67	4.451

338		PRP016	Paraplegia	52	4.441

339	c	HYP840	Hypercholesterolemia, Familial, 4	46	4.433

340	c	NMN016	Niemann-Pick Disease, Type B	56	4.431

341		ADR016	Adrenal Cortical Carcinoma	62	4.426

342	P	END044	Endometriosis	62	4.425

343		SVR004	Severe Combined Immunodeficiency	72	4.420

344	c	MGR028	Migraine with or Without Aura 1	64	4.406

345	P	GLL018	Gallbladder Cancer	53	4.400

346	P	LKM002	Leukemia	67	4.398

347	P	EPL164	Epilepsy	68	4.391

348	c	DNT047	Dentinogenesis Imperfecta Type 2	35	4.390

349	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	4.380

350		BLR008	Bilirubin Metabolic Disorder	57	4.379

351	P	PNC025	Panic Disorder	52	4.371

352	c	ATS007	Autism Spectrum Disorder	72	4.360

353		AMN001	Amenorrhea	54	4.344

354	P	THR014	Thrombocytopenia	66	4.331

355		TXC005	Toxic Shock Syndrome	62	4.316

356		DFC001	Defective Apolipoprotein B-100	24	4.316

357	P	ATS364	Autism	69	4.282

358	P	ALG028	Alagille Syndrome 1	73	4.281

359		VSC003	Visceral Leishmaniasis	55	4.280

360	c	DLT002	Dilated Cardiomyopathy	78	4.273

361	P	PRK057	Parkinson Disease, Late-Onset	80	4.256

362	P	FCL005	Focal Segmental Glomerulosclerosis	57	4.246

363		CLR108	Colorectal Adenoma	64	4.239

364		PRT013	Portal Hypertension	59	4.236

365		ADR022	Adrenomyeloneuropathy	39	4.232

366		ADR007	Adrenoleukodystrophy	73	4.222

367		ADR054	Adrenocortical Carcinoma, Hereditary	47	4.205

368		ADR004	Adrenal Cortical Adenocarcinoma	38	4.205

369	P	CRT085	Carotid Intimal Medial Thickness 2	22	4.197

370		PHN003	Phenylketonuria	76	4.195

371		LNG099	Lung Disease	62	4.185

372		APN008	Apnea, Obstructive Sleep	67	4.168

373		ARC023	Arcus Corneae	36	4.165

374		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	4.148

375		PSR001	Psoriatic Arthritis	62	4.140

376	P	MLN008	Melanoma	76	4.137

377		PPT005	Peptic Ulcer Disease	58	4.127

378	P	ALP008	Alopecia	54	4.121

379		BLT003	Blue Toe Syndrome	24	4.117

380		INT323	Intraocular Pressure Quantitative Trait Locus	64	4.115

381		PLR008	Pleurisy	50	4.095

382		HNS001	Hansen's Disease	32	4.094

383	P	LPR021	Leprosy 3	71	4.082

384	P	MNC007	Monocytic Leukemia	47	4.069

385		OVR063	Overnutrition	42	4.069

386		SCH012	Schizoaffective Disorder	50	4.059

387		ESP021	Esophageal Cancer	83	4.039

388		GLM044	Glomerular Disease	35	4.038

389		NWC001	Newcastle Disease	47	4.014

390		CHY002	Chylomicron Retention Disease	64	4.011

391		DBT010	Diabetic Neuropathy	54	4.007

392	P	RNL015	Renal Hypertension	45	3.999

393	P	MSC005	Muscular Dystrophy	67	3.993

394		GRN013	Greenberg Dysplasia	55	3.974

395		MYL069	Myeloma, Multiple	77	3.972

396		GTR002	Goiter	53	3.966

397		KRT002	Keratomalacia	55	3.961

398		ACQ007	Acquired Immunodeficiency Syndrome	59	3.955

399	c	ART115	Aortic Valve Disease 1	74	3.939

400		KWS002	Kawasaki Disease	65	3.928

401		ATN004	Autonomic Neuropathy	42	3.926

402	P	HRP006	Herpes Simplex	65	3.922

403		ADR056	Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete	55	3.914

404		PLM033	Pulmonary Embolism	58	3.913

405		ACL001	Acalculous Cholecystitis	38	3.911

406		CRN017	Coronary Thrombosis	46	3.899

407	P	ADN016	Adenocarcinoma	63	3.875

408	P	ZLL001	Zellweger Syndrome	65	3.860

409	c	STS011	Sitosterolemia 2	34	3.854

410		CHR619	Chromosome 2q35 Duplication Syndrome	64	3.847

411		HMP001	Hemopericardium	47	3.839

412	P	PRC012	Pericardial Effusion	50	3.839

413	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	3.827

414	P	CRN025	Corneal Dystrophy	49	3.823

415		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	3.810

416		BRN024	Bronchitis	67	3.809

417		HMN014	Human Immunodeficiency Virus Infectious Disease	54	3.800

418	P	DRM053	Dermatitis, Atopic	65	3.783

419		BRS051	Breast Disease	58	3.776

420		PRM013	Premature Menopause	58	3.770

421	P	SRC025	Sarcoidosis 1	71	3.766

422		ETN001	Eating Disorder	59	3.761

423	c	HYP837	Hypercholesterolemia, Familial, 2	46	3.760

424		PST028	Post-Traumatic Stress Disorder	59	3.751

425		MLR004	Malaria	80	3.750

426		ACN002	Acanthosis Nigricans	56	3.743

427		PSY004	Psychotic Disorder	66	3.740

428		PLM010	Pulmonary Edema	55	3.735

429		HYP005	Hypokalemia	55	3.735

430	P	AST005	Asthma	76	3.716

431		ANT039	Antisynthetase Syndrome	55	3.714

432		NPH009	Nephrolithiasis	54	3.712

433	c	BTT014	Beta-Thalassemia	72	3.693

434		ANV001	Anovulation	47	3.690

435	c	GRV008	Graves Disease 1	54	3.690

436	P	MYL006	Myeloid Leukemia	61	3.678

437	P	PHC003	Pheochromocytoma	69	3.673

438	P	LKM071	Leukemia, Chronic Lymphocytic	75	3.662

439		HYP540	Hypertension, Diastolic	37	3.657

440		ADR040	Adrenal Gland Pheochromocytoma	46	3.647

441	P	BND020	Bone Disease	59	3.646

442		DRM006	Dermatitis	62	3.640

443	c	HYP739	Hyperlipoproteinemia, Type Iv	53	3.638

444		DMY004	Demyelinating Disease	50	3.627

445	P	RTN016	Retinal Degeneration	52	3.627

446	P	MLN007	Male Infertility	56	3.627

447	P	GLY013	Glycogen Storage Disease	60	3.623

448	P	THY032	Thyroiditis	57	3.623

449	P	URN019	Urinary Tract Infection	49	3.618

450		IRN001	Iron Deficiency Anemia	58	3.610

451	P	MCR129	Microvascular Complications of Diabetes 1	68	3.610

452		PRT038	Protein-Energy Malnutrition	53	3.597

453	P	LNG064	Lung Cancer Susceptibility 3	70	3.578

454	P	MMB011	Membranous Nephropathy	50	3.577

455		MCL006	Macular Retinal Edema	57	3.569

456		ACT088	Acute Insulin Response	39	3.567

457		ART008	Arteriosclerosis Obliterans	40	3.565

458		SVR001	Severe Acute Respiratory Syndrome	67	3.565

459		PRP030	Purpura	54	3.558

460		HRT012	Heart Valve Disease	53	3.554

461	P	SCL009	Sclerosing Cholangitis	48	3.553

462		OST003	Osteonecrosis	61	3.552

463	P	GLM040	Glioma Susceptibility 1	71	3.534

464		MLG169	Malignant Astrocytoma	57	3.534

465		HST010	Histiocytosis	49	3.522

466		SCK003	Sickle Cell Anemia	74	3.521

467		CYN002	Cyanosis, Transient Neonatal	43	3.514

468		HPT004	Hepatic Coma	43	3.512

469	P	SYP003	Syphilis	59	3.512

470	P	OPN001	Open-Angle Glaucoma	55	3.512

471		SCR011	Scrapie	39	3.511

472	P	ADL010	Adult Respiratory Distress Syndrome	71	3.507

473		RTN020	Retinal Vascular Disease	46	3.503

474	P	SBS003	Substance Abuse	54	3.499

475		KWS001	Kwashiorkor	45	3.490

476	c	ACT134	Acute Liver Failure	59	3.482

477		INS001	Insulinoma	59	3.480

478	P	PLM006	Pulmonary Alveolar Proteinosis	53	3.469

479		CRB004	Cerebral Artery Occlusion	45	3.467

480		SPH010	Sphingolipidosis	47	3.466

481	P	LNG032	Lung Cancer	98	3.454

482	P	MYC008	Myocarditis	59	3.444

483	P	HYP730	Hypogonadotropic Hypogonadism	53	3.442

484	P	END033	Endocarditis	58	3.431

485		GST023	Gastric Ulcer	52	3.423

486		IGG001	Iga Glomerulonephritis	50	3.421

487	P	SZR006	Seizure Disorder	70	3.421

488	P	CHN074	Chondrodysplasia Punctata 2, X-Linked Dominant	48	3.415

489	P	GND004	Gonadal Dysgenesis	47	3.411

490		BRN071	Brain Injury	50	3.395

491	c	BRN108	Branchiootic Syndrome 1	62	3.395

492	P	HMC002	Homocystinuria	53	3.391

493		TRM010	Traumatic Brain Injury	51	3.389

494		THR004	Thrombocytosis	53	3.388

495		CHL039	Choledocholithiasis	37	3.376

496		SXL003	Sexual Disorder	49	3.374

497		SQM006	Squamous Cell Carcinoma	60	3.362

498		LMB062	Limb Ischemia	55	3.361

499	c	PLM164	Pulmonary Hypertension, Primary, 1	76	3.350

500	P	SKN015	Skin Carcinoma	71	3.340

501		CLN015	Colon Adenocarcinoma	65	3.339

502	P	BLD134	Bladder Cancer	79	3.333

503		OCL069	Ocular Motor Apraxia	57	3.321

504		IRR002	Irritable Bowel Syndrome	65	3.316

505	c	HPT003	Hepatitis a	63	3.314

506		HYP025	Hyperphosphatemia	48	3.313

507	P	GRV001	Graves' Disease	55	3.307

508	P	RCT021	Rectum Cancer	54	3.307

509	c	NMN013	Niemann-Pick Disease, Type a	63	3.301

510	P	KDN017	Kidney Cancer	61	3.294

511		KRT009	Keratosis	53	3.265

512		END062	Endometrial Hyperplasia	48	3.260

513		MSL001	Measles	61	3.256

514	P	LYM118	Lymphoma	67	3.249

515		PLM001	Pulmonary Tuberculosis	69	3.249

516	P	ANT006	Antiphospholipid Syndrome	55	3.246

517	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	65	3.233

518		END040	Endogenous Depression	55	3.229

519		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	3.224

520		SCH014	Schistosomiasis	56	3.224

521		CRN036	Craniopharyngioma	64	3.216

522		MDD010	Middle Ear Disease	46	3.213

523		CHR074	Choriocarcinoma	46	3.212

524	P	FML018	Familial Mediterranean Fever	73	3.212

525		HMN047	Human Cytomegalovirus Infection	57	3.207

526	P	BLR006	Biliary Tract Disease	46	3.195

527	c	HYP740	Hyperlipoproteinemia, Type V	53	3.193

528		ENT004	Enthesopathy	51	3.186

529	c	LKM070	Leukemia, Acute Monocytic	56	3.175

530		ACT200	Acute Monoblastic Leukemia	41	3.175

531	P	HYP040	Hypospadias	51	3.162

532	P	RNV001	Renovascular Hypertension	49	3.157

533	P	SLP005	Sleep Disorder	61	3.150

534	P	PLM036	Pulmonary Fibrosis	66	3.148

535		CKS001	Ck Syndrome	40	3.138

536	c	SCN036	Secondary Progressive Multiple Sclerosis	55	3.125

537		PLC008	Placenta Disease	49	3.111

538	c	HMC039	Hemochromatosis, Type 1	73	3.109

539		SDD008	Sudden Sensorineural Hearing Loss	41	3.109

540		QDR001	Quadriplegia	50	3.109

541	P	PRK039	Parkinsonism	55	3.109

542		FML026	Familial Lipoprotein Lipase Deficiency	52	3.104

543		INT078	Intracranial Thrombosis	50	3.101

544		MTB004	Metabolic Acidosis	48	3.086

545	P	PTS002	Ptosis	52	3.078

546		VRC005	Varicose Veins	60	3.072

547		ART074	Aortic Dissection	53	3.072

548		GST045	Gastroenteritis	58	3.062

549		EXP004	Exophthalmos	51	3.054

550		AVD001	Avoidant Personality Disorder	49	3.052

551	c	MCR112	Microvascular Complications of Diabetes 2	42	3.046

552	P	RHN004	Rhinitis	57	3.044

553	c	LKM063	Leukemia, Chronic Myeloid	71	3.041

554	P	FML187	Familial Hypertension	34	3.041

555		TST014	Testicular Cancer	52	3.037

556		ASP026	Asplenia, Isolated Congenital	43	3.025

557		CNN003	Conn's Syndrome	79	3.025

558		GNR003	Generalized Atherosclerosis	43	3.017

559	P	MTR004	Maturity-Onset Diabetes of the Young	68	3.014

560		NRR001	Neuroretinitis	42	3.009

561		CRV035	Cervical Cancer	73	3.003

562	P	PLY014	Polycystic Kidney Disease	69	3.002

563		URL001	Urolithiasis	46	3.002

564		VTM002	Vitamin B12 Deficiency	48	2.997

565		DYS015	Dysentery	50	2.994

566		LYM133	Lymphoma, Hodgkin, Classic	74	2.993

567		WLL004	Wallerian Degeneration	38	2.993

568	c	HRM017	Hermansky-Pudlak Syndrome 2	55	2.993

569		HYP748	Hypertelorism	46	2.984

570		HPT019	Hepatic Encephalopathy	59	2.983

571		TBC004	Tobacco Addiction	63	2.978

572		NPH010	Nephrosclerosis	50	2.964

573		THY030	Thyroid Gland Disease	50	2.963

574		CRN019	Coronary Artery Vasospasm	47	2.959

575	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	41	2.956

576		FBR012	Fabry Disease	70	2.952

577	P	ART023	Arthropathy	61	2.945

578		INF034	Infective Endocarditis	54	2.941

579		EPD070	Epidermoid Cysts	35	2.929

580	c	SCN007	Secondary Hyperparathyroidism	51	2.928

581		3MT013	3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome	45	2.916

582		ALC006	Alcoholic Hepatitis	61	2.915

583	P	RTN018	Retinal Disease	53	2.912

584		OST159	Osteogenic Sarcoma	66	2.912

585	P	DYS154	Dystonia	64	2.901

586	P	HDC001	Headache	57	2.901

587	P	THR015	Thrombophilia	51	2.887

588	P	PLY017	Polyarteritis Nodosa	60	2.881

589		LYD001	Leydig Cell Tumor	45	2.878

590	c	CHL119	Cholangitis, Primary Sclerosing	58	2.863

591		RLP002	Relapsing-Remitting Multiple Sclerosis	56	2.861

592		RNL077	Renal Fibrosis	46	2.849

593		TTN003	Tetanus	65	2.847

594	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	2.839

595	P	FTL001	Fetal Alcohol Syndrome	55	2.838

596		PTT037	Pituitary Tumors	44	2.838

597		ANX004	Anoxia	40	2.838

598	P	FBR017	Fibrosarcoma	56	2.838

599		LMY002	Leiomyoma	51	2.834

600	P	TRM003	Tremor	48	2.834

601		ANT024	Anthrax Disease	58	2.833

602	P	OVR082	Overgrowth Syndrome	49	2.822

603		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	2.820

604		CHL045	Choline Deficiency Disease	39	2.810

605	P	LKD001	Leukodystrophy	59	2.806

606		GST050	Gastrointestinal System Disease	55	2.806

607		GNT167	Genetic Obesity	30	2.805

608		INT067	Interstitial Nephritis	46	2.803

609		ADL002	Adult Syndrome	70	2.797

610		MCR315	Microcephaly, Congenital Cataract, and Psoriasiform Dermatitis	27	2.792

611	c	GLC092	Glaucoma, Primary Open Angle	62	2.792

612		PNC041	Pancreatic Ductal Adenocarcinoma	51	2.792

613	P	GNG009	Gangliosidosis	44	2.792

614		PST092	Posttransplant Acute Limbic Encephalitis	28	2.790

615		CVD001	Covid-19	57	2.788

616		ACT098	Acute Erythroid Leukemia	55	2.788

617		ACT239	Acetyl-Coa Acetyltransferase-2 Deficiency	20	2.788

618		ORL015	Oral Squamous Cell Carcinoma	43	2.772

619	P	NTR004	Neutropenia	63	2.761

620		ATN005	Autonomic Dysfunction	46	2.761

621	c	PRM005	Primary Hyperparathyroidism	59	2.760

622		ALC001	Alcohol-Related Birth Defect	36	2.753

623		BLR004	Biliary Dyskinesia	37	2.753

624	P	MSC003	Muscular Atrophy	52	2.745

625	P	RTT002	Rett Syndrome	79	2.738

626		CHG001	Chagas Disease	66	2.736

627		LWC002	Lowe Oculocerebrorenal Syndrome	68	2.724

628	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	2.723

629	P	OVR049	Ovarian Disease	52	2.720

630		IGR001	Ige Responsiveness, Atopic	59	2.718

631		ALC009	Alcoholic Liver Cirrhosis	54	2.718

632		AND014	Androgenic Alopecia	47	2.714

633	P	INT099	Intrahepatic Cholestasis of Pregnancy	62	2.713

634	P	RSP003	Respiratory Failure	74	2.713

635		BNS003	Binswanger's Disease	41	2.713

636		MNN043	Meningioma, Familial	79	2.713

637		SCR001	Secretory Meningioma	40	2.713

638		LYM002	Lymphoplasmacyte-Rich Meningioma	35	2.713

639		SPN021	Spinal Meningioma	50	2.713

640		ADT003	Auditory System Disease	49	2.711

641		KRT019	Keratitis, Hereditary	66	2.706

642	P	DDN001	Duodenal Ulcer	53	2.706

643		ALL003	Allergic Rhinitis	67	2.700

644		FRN006	Frontotemporal Dementia	68	2.697

645		PLT031	Platelet Membrane Fluidity	28	2.697

646	c	PRG047	Progressive Familial Intrahepatic Cholestasis	64	2.694

647		HYP781	Hypoascorbemia	52	2.694

648	P	RTN022	Retinal Vein Occlusion	54	2.692

649		BCK006	Back Pain	47	2.691

650		GNR004	Generalized Anxiety Disorder	55	2.689

651		TND005	Tendinitis	54	2.680

652	c	ACT073	Acute Leukemia	58	2.671

653		HYP088	Hyper-Igd Syndrome	51	2.669

654	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	2.667

655	P	ASP006	Aspergillosis	72	2.664

656	P	BRS044	Breast Adenocarcinoma	58	2.664

657		CLR030	Clear Cell Renal Cell Carcinoma	54	2.664

658		DBT006	Diabetic Macular Edema	48	2.661

659		CHD004	Chudley-Mccullough Syndrome	48	2.654

660		CHL065	Cholangiocarcinoma	58	2.647

661		INT079	Intrahepatic Cholangiocarcinoma	51	2.647

662		NSP002	Nasopharyngitis	45	2.646

663		CRN020	Coronary Restenosis	39	2.631

664	P	PLY018	Polycythemia	56	2.619

665	c	BPL002	Bipolar I Disorder	47	2.619

666	P	MYG005	Myoglobinuria	40	2.619

667		EXT006	Extrahepatic Cholestasis	40	2.606

668	P	PRK001	Porokeratosis	55	2.605

669	c	SCL052	Scleroderma, Familial Progressive	61	2.603

670		DPH001	Diphtheria	59	2.601

671		HYP063	Hypersplenism	52	2.599

672	c	SML038	Small Cell Cancer of the Lung	69	2.594

673	P	OPT006	Optic Nerve Disease	58	2.590

674		IDP091	Idiopathic Nephrotic Syndrome	47	2.586

675		ORL011	Oral Cancer	60	2.586

676	c	MLG069	Malignant Hypertension	46	2.584

677		GNG013	Gingivitis	59	2.583

678		ATP014	Atp8b1 Deficiency	28	2.583

679		APH002	Aphasia	56	2.580

680		BLM002	Bulimia Nervosa	57	2.579

681	P	SHR001	Short Bowel Syndrome	53	2.579

682		LYM143	Lymphoma, Non-Hodgkin, Familial	75	2.574

683	P	SPP010	Suppressor of Tumorigenicity 3	51	2.574

684	P	FML355	Familial Intrahepatic Cholestasis	42	2.571

685	P	NSP012	Nasopharyngeal Carcinoma	61	2.566

686		APD001	Apo a-I Deficiency	16	2.564

687		DBT002	Diabetic Autonomic Neuropathy	41	2.561

688		RTN023	Retinitis	46	2.554

689		INC002	Inclusion Body Myositis	57	2.553

690		CRY035	Cryptorchidism, Unilateral or Bilateral	58	2.547

691		CND006	Candida Glabrata	30	2.546

692		DYS073	Dysphagia	53	2.539

693		CRD223	Cardiac Arrhythmia	63	2.537

694	P	RTN008	Retinitis Pigmentosa	80	2.537

695	c	JVN010	Juvenile Rheumatoid Arthritis	66	2.537

696	c	GM1007	Gm1 Gangliosidosis	65	2.533

697		WRN001	Werner Syndrome	69	2.532

698		ART010	Arteriolosclerosis	37	2.526

699		ESP002	Esophageal Varix	51	2.515

700		HYP020	Hyperprolactinemia	63	2.514

701	P	ENC004	Encephalitis	61	2.513

702	c	XLN229	X-Linked Chondrodysplasia Punctata 2	46	2.506

703		ANT003	Antley-Bixler Syndrome	49	2.506

704	c	GLY060	Glycogen Storage Disease Ia	63	2.505

705		GST092	Gastroesophageal Reflux	61	2.503

706		MYX004	Myxedema	43	2.498

707		TND004	Tendinopathy	45	2.490

708		BRN028	Brain Cancer	74	2.490

709		PLC002	Plica Syndrome	35	2.489

710		SYN007	Synovitis	55	2.489

711	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	2.486

712		MST005	Mastitis	53	2.486

713		MDD018	Middle East Respiratory Syndrome	44	2.485

714		ISC015	Ischemic Colitis	43	2.484

715		BRC012	Brucellosis	66	2.483

716		TYP007	Typhoid Fever	64	2.474

717	P	PLY006	Polydactyly	59	2.473

718	P	MVM001	Movement Disease	61	2.472

719	c	HYP839	Hyperlipidemia, Familial Combined, 1	30	2.472

720	c	ACT068	Acute Cystitis	61	2.469

721		ACT003	Acute Kidney Tubular Necrosis	46	2.467

722		MRS001	Marasmus	42	2.464

723	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	2.462

724		DSS009	Disseminated Intravascular Coagulation	57	2.460

725		LYS003	Lysinuric Protein Intolerance	57	2.459

726		NSD002	Nsdhl-Related Disorders	12	2.453

727		BLR001	Biliary Atresia	55	2.451

728		AMN003	Amnestic Disorder	54	2.435

729		PRX001	Peroxisomal Disease	46	2.431

730		AZS001	Azoospermia	45	2.431

731		HYP006	Hypertensive Heart Disease	49	2.427

732		ADR005	Adrenal Carcinoma	62	2.421

733	c	BLD140	Blood Group, I System	46	2.421

734		HMN002	Human Granulocytic Anaplasmosis	31	2.416

735		ART017	Aortic Disease	49	2.416

736		FCL012	Facial Paralysis	49	2.416

737	P	HYP061	Hypertrophic Cardiomyopathy	69	2.411

738		BTT017	Beta-Thalassemia Major	51	2.410

739		NPH091	Nephrolithiasis, Calcium Oxalate	61	2.400

740		HDN002	Head Injury	44	2.397

741		SYS003	Systolic Heart Failure	49	2.391

742		SBL008	Sea-Blue Histiocyte Disease	42	2.378

743		LYM027	Lymphopenia	56	2.374

744	c	THY107	Thymoma, Familial	42	2.371

745	P	HYD006	Hydrocephalus	61	2.371

746	P	THY023	Thymoma	64	2.371

747	P	FML011	Familial Adenomatous Polyposis	71	2.358

748		PRS042	Prostate Disease	42	2.358

749		PRT018	Portal Vein Thrombosis	50	2.357

750	c	ATS013	Autosomal Recessive Congenital Ichthyosis	66	2.355

751	P	ART018	Aortic Valve Insufficiency	52	2.353

752	P	RTN024	Retinoblastoma	73	2.350

753		CRD137	Cardiogenic Shock	56	2.350

754		DSS008	Disease of Mental Health	74	2.343

755		TQP001	Taqi Polymorphism	29	2.341

756		ACT084	Acute Stress Disorder	54	2.338

757		PLG002	Plague	58	2.338

758		ACD003	Acid Sphingomyelinase Deficiency	32	2.338

759		PST021	Postpartum Depression	50	2.328

760		OVR094	Ovarian Epithelial Cancer	39	2.326

761		HYP114	Hypertensive Nephropathy	36	2.325

762		BLP005	Blepharitis	50	2.319

763		BRN002	Bronchiolitis	57	2.312

764		VCC001	Vaccinia	47	2.307

765	P	RTN014	Retinal Artery Occlusion	47	2.307

766		BRN026	Branch Retinal Artery Occlusion	41	2.307

767	c	BSL007	Basal Cell Carcinoma	68	2.306

768		BRD004	Borderline Personality Disorder	53	2.303

769		APL024	Apolipoprotein C-Iii Deficiency	32	2.301

770		PRM329	Premature Aging	36	2.298

771		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	42	2.290

772	P	CHR345	Chronic Pain	50	2.287

773	c	SVR005	Severe Pre-Eclampsia	50	2.285

774		RTN017	Retinal Detachment	60	2.278

775		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	2.278

776		YLL002	Yellow Fever	61	2.267

777		DFF036	Differentiated Thyroid Carcinoma	51	2.267

778		DFF005	Diffuse Large B-Cell Lymphoma	54	2.265

779		ADR041	Adrenal Cortical Adenoma	49	2.265

780		CNS002	Constrictive Pericarditis	40	2.260

781	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	55	2.259

782	c	PRG020	Paragangliomas 3	39	2.253

783		FRZ001	Frozen Shoulder	55	2.253

784		CRT084	Creatinine Clearance Quantitative Trait Locus	25	2.248

785		PLC005	Placental Insufficiency	56	2.248

786	P	DBT005	Diabetes Insipidus	54	2.238

787		PLY001	Polycythemia Vera	69	2.228

788		DBT084	Diabetes Mellitus, Ketosis-Prone	60	2.224

789		PLT004	Platelet Glycoprotein Iv Deficiency	56	2.221

790		HYP008	Hypertensive Retinopathy	39	2.214

791		SLN001	Silent Myocardial Infarction	33	2.214

792		ASP030	Aspirin Resistance	40	2.209

793	P	LCT002	Lactose Intolerance	52	2.209

794	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	2.200

795		FBR047	Fibromyalgia	58	2.200

796	P	HRD011	Hereditary Spherocytosis	64	2.200

797		LNG108	Langerhans Cell Histiocytosis	58	2.198

798		PRT058	Pure Autonomic Failure	58	2.195

799		THR016	Thrombophlebitis	50	2.189

800		GLB001	Gilbert Syndrome	53	2.188

801	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	2.188

802	P	RHZ001	Rhizomelic Chondrodysplasia Punctata	57	2.185

803		KRT008	Keratopathy	46	2.181

804	P	ESP024	Esophagitis	60	2.177

805		CRD001	Cardiac Tamponade	43	2.173

806		CHK001	Chikungunya	60	2.172

807		KRN002	Kearns-Sayre Syndrome	63	2.172

808		CHR178	Chromosomal Triplication	34	2.172

809		ANN002	Anencephaly	57	2.168

810		ACT058	Active Peptic Ulcer Disease	56	2.167

811		DNT012	Dental Caries	53	2.162

812		LYM017	Lyme Disease	62	2.162

813		PRS047	Prostatitis	58	2.152

814		SPS057	Spasticity	42	2.147

815		ADR008	Adrenal Adenoma	55	2.147

816	P	SYS005	Systemic Scleroderma	74	2.139

817	P	RHB003	Rhabdomyosarcoma	66	2.128

818		CMM005	Common Cold	56	2.128

819		OBS002	Obsessive-Compulsive Disorder	68	2.127

820		HSH003	Hashimoto Thyroiditis	60	2.124

821	P	HYP265	Hypotonia	42	2.124

822		LFT001	Left Bundle Branch Hemiblock	47	2.113

823		MSC157	Muscular Dystrophy, Duchenne Type	79	2.105

824		KPS004	Kaposi Sarcoma	77	2.105

825	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	70	2.105

826	P	PSD087	Pseudoxanthoma Elasticum	67	2.105

827		HRT037	Heart and Brain Malformation Syndrome	31	2.105

828		MLT157	Multiple System Atrophy 1	69	2.105

829		URT010	Ureteral Obstruction	45	2.105

830	P	BRB001	Beriberi	44	2.105

831	c	HRD088	Hereditary Neuropathies	33	2.105

832		KFM001	Kaufman Oculocerebrofacial Syndrome	55	2.105

833		CLC001	Calciphylaxis	51	2.104

834		SPN185	Spinal Cord Infarction	28	2.099

835		CRB087	Cerebral Arteriosclerosis	17	2.088

836		OCL006	Ocular Hypertension	53	2.085

837		LTN004	Late-Onset Retinal Degeneration	60	2.085

838	c	CHL132	Cholestasis, Progressive Familial Intrahepatic, 1	57	2.085

839	P	MNN013	Meningitis	65	2.084

840		PNG002	Pain Agnosia	51	2.082

841	P	OVR046	Ovarian Cyst	46	2.082

842	P	RBL001	Rubella	58	2.079

843		LPR001	Lepromatous Leprosy	49	2.079

844	P	PTT006	Pituitary Adenoma	55	2.062

845		PNC129	Pancreatic Adenocarcinoma	65	2.062

846		HRN029	Hearing Loss, Noise-Induced	37	2.059

847		CLC006	Calcinosis	47	2.059

848	P	MTR003	Mitral Valve Stenosis	53	2.059

849		MST019	Mastoiditis	41	2.059

850		ICH001	Ichthyosis Vulgaris	53	2.056

851		CMP034	Complete Androgen Insensitivity Syndrome	55	2.054

852	P	BNG032	Benign Mesothelioma	53	2.054

853		MTR002	Mitral Valve Insufficiency	52	2.050

854		SPN035	Spindle Cell Sarcoma	54	2.049

855		SRC014	Sarcoma	65	2.049

856		GSG001	Gas Gangrene	52	2.045

857	P	INT070	Intestinal Obstruction	57	2.040

858		HYP141	Hyperphenylalaninemia	42	2.040

859	c	BCT007	Bacterial Meningitis	55	2.035

860		LPD001	Lipid Pneumonia	29	2.033

861	P	MMP001	Mumps	57	2.029

862	P	RPD001	Rapidly Progressive Glomerulonephritis	44	2.026

863	c	ATM011	Autoimmune Hepatitis	63	2.025

864	P	TBR001	Tuberous Sclerosis	69	2.018

865		CNT047	Contact Dermatitis	57	2.018

866		GLL029	Gallbladder Adenoma	30	2.011

867		DNG001	Dengue Shock Syndrome	40	2.011

868		BCT002	Bacterial Vaginosis	53	2.011

869		DWR001	Dwarfism	44	2.011

870	P	VNB005	Van Buchem Disease	58	2.010

871	P	OPT048	Opitz-Gbbb Syndrome	49	2.010

872		HYP555	Hypertriglyceridemia, Transient Infantile	38	2.010

873	c	PRG042	Progressive Familial Heart Block, Type Ia	66	2.004

874		PYR016	Pyridoxine Deficiency	29	1.997

875	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	1.995

876	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	1.995

877		CMB007	Combined Immunodeficiency	57	1.995

878		NCR009	Necrobiotic Xanthogranuloma	26	1.995

879		NRT001	Neurotic Disorder	56	1.995

880		RHM028	Rheumatic Heart Disease	56	1.987

881		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	1.983

882	P	END046	Endometritis	46	1.983

883	P	PRL003	Proliferative Glomerulonephritis	43	1.983

884	P	ANG015	Angioedema	56	1.974

885		SNS003	Sensory Peripheral Neuropathy	52	1.972

886		INT066	Interstitial Lung Disease	60	1.972

887	P	MTR014	Motor Neuron Disease	65	1.972

888		RKT003	Rokitansky-Aschoff Sinuses of the Gallbladder	13	1.972

889	c	CNG617	Congenital Disorder of Glycosylation, Type Iit	25	1.969

890	P	MXL015	Maxillary Sinusitis	38	1.963

891	c	CNG006	Congenital Hypothyroidism	63	1.962

892		NRL016	Neural Tube Defects	81	1.962

893		TST015	Testicular Disease	42	1.962

894	P	MTC003	Metachromatic Leukodystrophy	71	1.962

895	P	UVT001	Uveitis	57	1.962

896		HRY003	Hairy Cell Leukemia	61	1.962

897	P	INS002	in Situ Carcinoma	53	1.962

898	P	TRC031	Trichorhinophalangeal Syndrome	38	1.962

899		BRT005	Barth Syndrome	56	1.959

900		CRT072	Creutzfeldt-Jakob Disease	68	1.949

901	c	TBR025	Tuberous Sclerosis 1	84	1.949

902	P	MYT002	Myotonic Dystrophy	51	1.949

903	P	TXP001	Toxoplasmosis	60	1.949

904	P	VNW001	Von Willebrand's Disease	65	1.944

905	P	GRF003	Graft-Versus-Host Disease	71	1.944

906		ALX002	Alexithymia	37	1.941

907		SYN036	Syncope	45	1.941

908		EXT007	Extracutaneous Mastocytoma	38	1.936

909		MST004	Mast Cell Neoplasm	42	1.936

910		NRL005	Neurilemmoma	60	1.936

911	c	46X082	46,xy Sex Reversal	52	1.936

912		SQM013	Squamous Cell Carcinoma, Head and Neck	73	1.935

913		BRS064	Bursitis	51	1.931

914	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	1.925

915		PTT046	Pituitary Hormone Deficiency, Combined, 2	62	1.925

916	P	ATR005	Atrophic Gastritis	50	1.925

917		TRY001	Trypanosomiasis	50	1.925

918	c	HRD010	Hereditary Spastic Paraplegia	66	1.925

919		MCR004	Macroglobulinemia	49	1.922

920		RBS001	Rabies	58	1.922

921	P	CND004	Candidiasis	58	1.919

922		ALC005	Alcoholic Pancreatitis	38	1.919

923		PHR003	Pharyngitis	58	1.919

924		MMM006	Mammographic Density	39	1.910

925		BCK003	Background Diabetic Retinopathy	47	1.908

926		MSC007	Muscle Hypertrophy	64	1.903

927	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	1.902

928		SND001	Sandhoff Disease	66	1.901

929	P	CTN015	Cutaneous T Cell Lymphoma	48	1.901

930		DNG003	Dengue Disease	65	1.901

931	c	HPT007	Hepatitis E	51	1.901

932		PLR005	Pleuropneumonia	33	1.901

933	P	PRP029	Porphyria	60	1.901

934	P	AVS003	Avascular Necrosis	41	1.897

935		DBT004	Diabetic Polyneuropathy	50	1.897

936	c	FML015	Familial Nephrotic Syndrome	48	1.891

937	P	ALP061	Alopecia, Androgenetic, 1	49	1.890

938	c	LPD015	Lipodystrophy, Familial Partial, Type 2	61	1.889

939		MYT011	Myotonia	39	1.886

940		NRM001	Neuromyelitis Optica	61	1.884

941		CTS003	Coats Disease	53	1.884

942		INT010	Intracranial Embolism	48	1.883

943		VTM033	Vitamin K Deficiency Bleeding	48	1.883

944		PLM134	Pulmonary Fibrosis, Idiopathic	76	1.877

945		WST005	West Nile Virus	57	1.877

946		MYM001	Myoma	54	1.877