Search results for Atorvastatin

1013 hits were found for Atorvastatin

#	Family	MCID	Name	MIFTS	Score
1	c	HYP836	Hypercholesterolemia, Familial, 1	73	41.479

2		LPD008	Lipid Metabolism Disorder	62	33.141

3	P	CRN300	Coronary Heart Disease 1	73	26.652

4		LPP008	Lipoprotein Quantitative Trait Locus	65	22.274

5		ATH013	Atherosclerosis Susceptibility	63	21.230

6		ART140	Arteries, Anomalies of	53	20.513

7		ISC004	Ischemia	61	19.600

8	P	HRT032	Heart Disease	81	19.371

9	c	TYP009	Type 2 Diabetes Mellitus	92	18.618

10	P	MYP004	Myopathy	67	16.446

11	P	MYC007	Myocardial Infarction	70	15.651

12	P	DBT009	Diabetes Mellitus	67	15.500

13		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	15.022

14	c	FML021	Familial Hypercholesterolemia	72	14.663

15		INT007	Intermediate Coronary Syndrome	54	13.660

16	P	HYP750	Hypertriglyceridemia, Familial	62	13.092

17	P	VSC007	Vascular Disease	63	12.977

18		FML035	Familial Hyperlipidemia	55	12.280

19	c	ACT075	Acute Myocardial Infarction	56	11.779

20		ANG054	Angina Pectoris	66	11.231

21	P	ATR011	Atrial Fibrillation	66	10.736

22		STR067	Stroke, Ischemic	80	10.732

23	c	CHR684	Chronic Kidney Disease	69	10.567

24	c	HYP272	Hypercholesterolemia, Familial, 3	45	10.220

25	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	10.214

26	P	KDN018	Kidney Disease	72	10.092

27		NNL005	Non-Alcoholic Fatty Liver Disease	63	10.086

28		FTT001	Fatty Liver Disease	62	10.062

29		PRT251	Proteinuria, Chronic Benign	57	9.907

30		CRB039	Cerebrovascular Disease	66	9.603

31	P	CRD246	Cardiovascular System Disease	56	9.440

32		PRP027	Peripheral Vascular Disease	71	9.177

33		48X005	48,xyyy	39	9.018

34		CNG034	Congestive Heart Failure	69	8.957

35		TRN015	Transient Cerebral Ischemia	63	8.484

36		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	8.476

37	c	HYP595	Hypertension, Essential	85	8.239

38		NNL006	Non-Alcoholic Steatohepatitis	54	8.236

39	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	8.209

40	c	ATR087	Atrial Standstill 1	74	7.809

41	c	HYP724	Hyperlipoproteinemia, Type Iii	67	7.612

42	P	MLT020	Multiple Sclerosis	79	7.604

43		CRB004	Cerebral Artery Occlusion	45	7.590

44	P	PRD008	Periodontitis	64	7.590

45		HMZ003	Homozygous Familial Hypercholesterolemia	60	7.426

46	P	LPS004	Lupus Erythematosus	61	7.406

47	P	PRS040	Prostate Cancer	95	7.247

48	c	ACT071	Acute Kidney Failure	60	7.196

49	P	HYP838	Hyperlipidemia, Familial Combined, 3	61	7.194

50	P	RHM011	Rheumatoid Arthritis	82	7.121

51		CRT013	Carotid Stenosis	51	7.112

52	P	PLM037	Pulmonary Hypertension	72	7.110

53		HYP066	Hyperglycemia	61	7.094

54		BRN071	Brain Injury	50	6.863

55		IMP005	Impotence	52	6.844

56	P	PLY011	Polycystic Ovary Syndrome	57	6.772

57	P	ART021	Arteriosclerosis	54	6.748

58	c	SYS001	Systemic Lupus Erythematosus	87	6.691

59	P	LVR013	Liver Disease	69	6.514

60	c	MCR130	Microvascular Complications of Diabetes 6	41	6.457

61	c	MCR120	Microvascular Complications of Diabetes 7	47	6.457

62	c	MCR113	Microvascular Complications of Diabetes 3	52	6.457

63	c	MCR133	Microvascular Complications of Diabetes 4	41	6.457

64		ANR040	Aneurysm	61	6.433

65		RPD005	Rapidly Involuting Congenital Hemangioma	46	6.291

66	P	ART022	Arthritis	71	6.261

67		RLP002	Relapsing-Remitting Multiple Sclerosis	56	6.239

68	P	ALZ034	Alzheimer Disease	87	6.212

69		AGN016	Aging	54	6.162

70	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	6.156

71		CYT002	Cytokine Deficiency	43	6.139

72		TRM010	Traumatic Brain Injury	51	6.090

73	P	MYS005	Myositis	56	5.996

74		END086	End Stage Renal Disease	52	5.995

75	P	CRD119	Cardiac Arrest	67	5.976

76		HYP266	Hypoxia	57	5.891

77	c	TYP008	Type 1 Diabetes Mellitus	70	5.855

78	c	PRD040	Periodontitis, Chronic	52	5.718

79	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	5.572

80		ANT039	Antisynthetase Syndrome	55	5.457

81		GLB002	Glioblastoma	67	5.351

82	P	BRS047	Breast Cancer	98	5.347

83		LVR012	Liver Cirrhosis	63	5.330

84		HMC014	Homocysteinemia	52	5.228

85		PRP080	Peripheral Artery Disease	54	5.134

86	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	5.133

87	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	5.133

88	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	5.133

89	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	5.133

90	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	5.133

91	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	5.133

92	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	5.133

93	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	5.133

94	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	5.133

95	c	DLT002	Dilated Cardiomyopathy	78	5.121

96		HYP081	Hypolipoproteinemia	49	5.106

97		THR024	Thrombosis	56	5.014

98	c	BLD140	Blood Group, I System	46	5.011

99		BNR002	Bone Resorption Disease	47	4.971

100		ART016	Aortic Aneurysm	68	4.923

101	P	OST002	Osteoporosis	76	4.854

102	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	4.854

103	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	4.854

104	P	END044	Endometriosis	62	4.816

105	c	THR092	Thrombophilia Due to Thrombin Defect	74	4.808

106	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	4.766

107		OST012	Osteoarthritis	77	4.722

108	P	NPH012	Nephrotic Syndrome	60	4.720

109		GSG001	Gas Gangrene	52	4.706

110	c	HPT001	Hepatitis C	62	4.681

111		ALL014	Allergic Encephalomyelitis	34	4.667

112	P	PSR002	Psoriasis	63	4.639

113		PST011	Pustulosis of Palm and Sole	52	4.639

114		KWS002	Kawasaki Disease	65	4.635

115	P	GRF003	Graft-Versus-Host Disease	71	4.616

116	P	THR014	Thrombocytopenia	66	4.597

117		HMN044	Human Immunodeficiency Virus Type 1	78	4.536

118		PLM129	Pulmonary Disease, Chronic Obstructive	74	4.535

119	c	HPT003	Hepatitis a	63	4.528

120	P	AST005	Asthma	76	4.522

121		CRN030	Coronary Stenosis	50	4.499

122	c	PLM164	Pulmonary Hypertension, Primary, 1	76	4.487

123	c	HPT073	Hepatitis C Virus	71	4.471

124		ATM095	Autoimmune Disease	61	4.464

125		CHL068	Cholestasis	61	4.464

126	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	4.445

127	c	MCR115	Microvascular Complications of Diabetes 5	65	4.365

128		GLC003	Glucose Intolerance	54	4.357

129	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	4.345

130	c	ACT135	Acute Graft Versus Host Disease	51	4.342

131	P	MYC008	Myocarditis	59	4.311

132		CRT016	Carotid Artery Disease	52	4.310

133	P	SLP006	Sleep Apnea	69	4.309

134		OCL069	Ocular Motor Apraxia	57	4.254

135	P	HPT023	Hepatocellular Carcinoma	96	4.162

136	P	SZR006	Seizure Disorder	70	4.130

137		CRD132	Cardiac Conduction Defect	60	4.109

138		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	4.084

139		ADN018	Adenoma	59	4.079

140		SPN186	Spinal Cord Injury	61	4.033

141		SVR004	Severe Combined Immunodeficiency	72	4.025

142		END072	Endotheliitis	36	4.017

143	P	PLM036	Pulmonary Fibrosis	66	3.955

144		IMM167	Immune Deficiency Disease	78	3.943

145	c	HYP740	Hyperlipoproteinemia, Type V	53	3.917

146	P	ANR048	Aniridia 1	64	3.912

147		GLL048	Glial Tumor	52	3.905

148		GLM045	Glioma	63	3.905

149	P	CRN074	Coronary Artery Aneurysm	42	3.903

150		47X002	47,xyy	48	3.891

151	P	EXN002	Exanthem	58	3.874

152		APN008	Apnea, Obstructive Sleep	67	3.847

153	P	PNM007	Pneumonia	67	3.794

154	c	SCL052	Scleroderma, Familial Progressive	61	3.789

155	P	PNC044	Pancreatitis	61	3.774

156		PRM236	Primary Biliary Cholangitis	60	3.747

157	c	ART101	Aortic Valve Disease 2	66	3.744

158	c	ACT027	Acute Pancreatitis	60	3.741

159		CRH001	Crohn's Disease	80	3.707

160	c	ART115	Aortic Valve Disease 1	74	3.672

161	P	BRN022	Bronchiectasis	60	3.670

162	P	HYP086	Hypothyroidism	69	3.668

163	c	PCH010	Pachyonychia Congenita 3	43	3.651

164		BRN004	Brain Edema	54	3.651

165	P	EPL164	Epilepsy	68	3.624

166		URT010	Ureteral Obstruction	45	3.618

167		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	3.606

168		RHB024	Rhabdomyosarcoma 2	67	3.592

169	P	HYP061	Hypertrophic Cardiomyopathy	69	3.553

170	P	HPT021	Hepatitis	69	3.543

171		DPR016	Depression	65	3.536

172	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	3.442

173		CLT003	Colitis	63	3.421

174	P	TBR001	Tuberous Sclerosis	69	3.381

175		CLR108	Colorectal Adenoma	64	3.361

176	P	ADN016	Adenocarcinoma	63	3.357

177		PRT013	Portal Hypertension	59	3.308

178		CNS004	Constipation	56	3.273

179	P	THY032	Thyroiditis	57	3.273

180	P	BCL017	B-Cell Lymphoma	59	3.271

181		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	3.254

182	P	DBT005	Diabetes Insipidus	54	3.244

183		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	3.244

184		HRT012	Heart Valve Disease	53	3.242

185	P	LNG032	Lung Cancer	98	3.230

186		PRP030	Purpura	54	3.219

187	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	3.214

188	P	GLM007	Glomerulonephritis	60	3.161

189		URL001	Urolithiasis	46	3.150

190		LTN004	Late-Onset Retinal Degeneration	60	3.116

191		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	3.089

192		RYN005	Raynaud Phenomenon	45	3.083

193		HMN014	Human Immunodeficiency Virus Infectious Disease	54	3.080

194		ADL002	Adult Syndrome	70	3.065

195		ALC007	Alcohol Dependence	66	3.064

196		RCK004	Rickets	68	3.041

197	P	PNC035	Pancreatic Cancer	86	3.008

198	c	ATM011	Autoimmune Hepatitis	63	2.992

199		DST006	Diastolic Heart Failure	45	2.989

200	c	MJR022	Major Affective Disorder 8	38	2.984

201	c	MJR024	Major Affective Disorder 9	41	2.984

202	P	BPL003	Bipolar Disorder	56	2.984

203		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.969

204		INT030	Intracranial Aneurysm	55	2.969

205		MNT002	Mental Depression	57	2.968

206	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	2.949

207	P	MCR129	Microvascular Complications of Diabetes 1	68	2.941

208	c	MCR112	Microvascular Complications of Diabetes 2	42	2.941

209		GT001	Gout	64	2.925

210		PRT036	Peritonitis	65	2.898

211		HYP056	Hypoglycemia	65	2.885

212	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	2.884

213	c	TBR025	Tuberous Sclerosis 1	84	2.884

214	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	60	2.883

215		CLP006	Clopidogrel Resistance	44	2.881

216	P	LKM062	Leukemia, Acute Lymphoblastic	69	2.879

217	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	2.877

218		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	2.877

219	P	VSC011	Vasculitis	61	2.859

220	P	TRN020	Turner Syndrome	67	2.853

221	P	LYM118	Lymphoma	67	2.846

222		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	2.845

223	c	FML001	Familial Atrial Fibrillation	65	2.836

224		LPT014	Leptin Deficiency or Dysfunction	78	2.833

225	P	INS002	in Situ Carcinoma	53	2.823

226	P	CRC039	Coarctation of Aorta	46	2.823

227	P	PLY041	Polymyositis	59	2.801

228		MLR004	Malaria	80	2.796

229	c	MCL042	Macular Degeneration, Age-Related, 1	85	2.786

230		INT002	Intermittent Claudication	61	2.785

231	P	SYS005	Systemic Scleroderma	74	2.779

232		PLM033	Pulmonary Embolism	58	2.761

233		DFC004	Deficiency Anemia	74	2.757

234		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	2.756

235	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	2.756

236		LKN025	Leukoencephalopathy, Hereditary Diffuse, with Spheroids	66	2.735

237		HYP555	Hypertriglyceridemia, Transient Infantile	38	2.728

238		STT001	Status Epilepticus	59	2.718

239		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	2.716

240		CRT084	Creatinine Clearance Quantitative Trait Locus	25	2.705

241	P	LKM071	Leukemia, Chronic Lymphocytic	75	2.704

242		LYM007	Lymphangioleiomyomatosis	68	2.674

243	P	BRS044	Breast Adenocarcinoma	58	2.674

244		HYP014	Hyperuricemia	51	2.674

245	P	GST044	Gastritis	55	2.658

246	P	BLD134	Bladder Cancer	79	2.657

247	P	DRM010	Dermatomyositis	61	2.633

248	P	NRP001	Neuropathy	60	2.629

249	P	LKM002	Leukemia	67	2.628

250	c	ATM022	Autoimmune Myocarditis	36	2.628

251	c	SML038	Small Cell Cancer of the Lung	69	2.628

252		ENT004	Enthesopathy	51	2.595

253	P	HMN010	Hemangioma	62	2.553

254		NSP002	Nasopharyngitis	45	2.531

255	P	DMN002	Dementia	66	2.531

256	c	HYP839	Hyperlipidemia, Familial Combined, 1	30	2.514

257		LPD009	Lipid Storage Disease	45	2.501

258		CLN015	Colon Adenocarcinoma	65	2.497

259	c	PRS136	Prostate Cancer, Hereditary, 6	33	2.490

260	c	PRS130	Prostate Cancer, Hereditary, 8	32	2.490

261		PRS047	Prostatitis	58	2.490

262	c	HNT004	Huntington Disease-Like 2	52	2.485

263	P	NRB001	Neuroblastoma	66	2.485

264		AMN003	Amnestic Disorder	54	2.485

265		SVR001	Severe Acute Respiratory Syndrome	67	2.451

266	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	2.435

267	P	TMP001	Temporal Lobe Epilepsy	49	2.435

268		MDD011	Mood Disorder	62	2.429

269	P	HYP098	Hypereosinophilic Syndrome	66	2.420

270		ACQ007	Acquired Immunodeficiency Syndrome	59	2.398

271		MYL069	Myeloma, Multiple	77	2.394

272		HYP060	Hyperinsulinism	54	2.388

273	c	CHR711	Chronic Asthma	41	2.384

274	P	FCL005	Focal Segmental Glomerulosclerosis	57	2.384

275	c	VRL010	Viral Hepatitis	53	2.382

276		AGR019	Age-Related Hearing Loss	41	2.382

277	P	FNG006	Feingold Syndrome 1	62	2.374

278	c	HPT016	Hepatitis B	62	2.369

279		HYP025	Hyperphosphatemia	48	2.348

280	c	SPN225	Spondyloarthropathy 1	70	2.341

281		CLB022	Coloboma, Ocular, Autosomal Recessive	28	2.339

282		RNL077	Renal Fibrosis	46	2.339

283	P	SNS001	Sensorineural Hearing Loss	59	2.338

284	c	HNT011	Huntington Disease-Like 3	34	2.329

285		CHL065	Cholangiocarcinoma	58	2.329

286	P	NTR004	Neutropenia	63	2.329

287		INT079	Intrahepatic Cholangiocarcinoma	51	2.329

288	P	ALC033	Alcohol Use Disorder	61	2.311

289		IGG001	Iga Glomerulonephritis	50	2.293

290		SYN036	Syncope	45	2.289

291		SQM006	Squamous Cell Carcinoma	60	2.289

292		PRP016	Paraplegia	52	2.285

293	P	MJR001	Major Depressive Disorder	68	2.273

294		CRB009	Cerebritis	43	2.272

295		MCS002	Mucositis	56	2.259

296		SBC016	Subacute Delirium	43	2.250

297	c	LKM061	Leukemia, Acute Myeloid	83	2.218

298		PRC013	Pericarditis	53	2.183

299	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	2.165

300		TXC005	Toxic Shock Syndrome	62	2.159

301		BCT022	Bacterial Infectious Disease	56	2.154

302		MCL006	Macular Retinal Edema	57	2.154

303		DMY004	Demyelinating Disease	50	2.150

304	P	CLR023	Colorectal Cancer	100	2.146

305		HDN002	Head Injury	44	2.128

306		ART004	Aortic Atherosclerosis	47	2.127

307	P	MTR012	Mitral Valve Disease	57	2.127

308	P	DRR001	Diarrhea	55	2.127

309		GST092	Gastroesophageal Reflux	61	2.104

310		CVD001	Covid-19	57	2.093

311	P	MYS003	Myasthenia Gravis	68	2.091

312		ALL029	Allergic Disease	59	2.091

313		TND004	Tendinopathy	45	2.069

314		TND005	Tendinitis	54	2.069

315	c	BRN108	Branchiootic Syndrome 1	62	2.069

316		INF118	Inflammatory Myopathy with Abundant Macrophages	27	2.069

317		DRM006	Dermatitis	62	2.069

318		KDN013	Kidney Hypertrophy	34	2.069

319		HML018	Homologous Wasting Disease	21	2.043

320		ASP030	Aspirin Resistance	40	2.037

321		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	2.014

322	c	SCN036	Secondary Progressive Multiple Sclerosis	55	2.009

323		HYP043	Hyperandrogenism	48	2.009

324	P	URT039	Urticaria	58	2.002

325		SPN051	Spondylitis	51	1.993

326		INF009	Inflammatory Spondylopathy	30	1.993

327		NTR005	Nutritional Deficiency Disease	61	1.976

328	P	AVS003	Avascular Necrosis	41	1.974

329		PRQ002	Paraquat Poisoning	28	1.954

330		NRT004	Neuritis	53	1.954

331		AND005	Androgen Insensitivity Syndrome, Mild	21	1.950

332	c	MGR028	Migraine with or Without Aura 1	64	1.945

333		HYP540	Hypertension, Diastolic	37	1.945

334		ULC004	Ulcerative Colitis	74	1.945

335	P	MLN008	Melanoma	76	1.945

336		NCR015	Necrotizing Autoimmune Myopathy	27	1.937

337		DWN001	Down Syndrome	70	1.925

338	P	MYL006	Myeloid Leukemia	61	1.918

339	P	CRB048	Cerebral Cavernous Malformations	63	1.910

340		CVR010	Cavernous Malformation	30	1.910

341	P	TRM003	Tremor	48	1.879

342	P	CND004	Candidiasis	58	1.879

343		GYN001	Gynecomastia	47	1.879

344		INF021	Infant Gynecomastia	30	1.879

345	P	PLY019	Polyneuropathy	52	1.879

346	P	RTN024	Retinoblastoma	73	1.879

347		HYP080	Hypogonadism	50	1.879

348	P	INF038	Influenza	68	1.864

349		MYC005	Myocardial Stunning	46	1.856

350	P	PRP019	Peripheral Nervous System Disease	58	1.834

351	c	PRC016	Pre-Eclampsia	65	1.833

352	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	1.819

353		ORL015	Oral Squamous Cell Carcinoma	43	1.819

354	P	LTR001	Lateral Sclerosis	58	1.819

355		FNG017	Fungal Infectious Disease	54	1.819

356		PNC041	Pancreatic Ductal Adenocarcinoma	51	1.819

357	P	RNV001	Renovascular Hypertension	49	1.811

358		OBS082	Obstructive Nephropathy	41	1.808

359		DBT006	Diabetic Macular Edema	48	1.808

360		VSC002	Vascular Dementia	60	1.808

361	P	ENC004	Encephalitis	61	1.808

362		LYM019	Lymphosarcoma	46	1.808

363		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	52	1.757

364		PRS129	Prostatic Hyperplasia, Benign	49	1.755

365		SPP011	Suppression of Tumorigenicity 12	61	1.755

366		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	37	1.755

367		OST159	Osteogenic Sarcoma	66	1.755

368	P	OPN001	Open-Angle Glaucoma	55	1.755

369		BLR008	Bilirubin Metabolic Disorder	57	1.755

370		PRS021	Prostatic Adenoma	43	1.755

371		PRS045	Prostatic Hypertrophy	53	1.755

372		CHR466	Chronic Thromboembolic Pulmonary Hypertension	48	1.755

373	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	1.745

374	P	MYC084	Mycobacterium Tuberculosis 1	68	1.740

375		CHR710	Chronic Spontaneous Urticaria	45	1.733

376		HYP020	Hyperprolactinemia	63	1.733

377		ALL006	Allergic Asthma	56	1.733

378	P	CHL066	Cholangitis	52	1.733

379	P	ENC018	Encephalopathy	62	1.733

380		DRG026	Drug Reaction with Eosinophilia and Systemic Symptoms	45	1.733

381	P	PRS038	Personality Disorder	65	1.726

382		SCK003	Sickle Cell Anemia	74	1.711

383	P	SCK005	Sickle Cell Disease	56	1.711

384	P	ALP008	Alopecia	54	1.711

385		ANX010	Anxiety	70	1.689

386	P	FML011	Familial Adenomatous Polyposis	71	1.689

387	P	AMY004	Amyloidosis	70	1.689

388		HYP005	Hypokalemia	55	1.689

389	P	MNC007	Monocytic Leukemia	47	1.689

390		HLX001	Helix Syndrome	48	1.689

391		OPP002	Opportunistic Mycosis	39	1.689

392		VLV011	Vulvovaginal Candidiasis	49	1.689

393		ORL005	Oral Candidiasis	56	1.689

394	c	SYS043	Systemic Lupus Erythematosus 1	38	1.683

395		OBS002	Obsessive-Compulsive Disorder	68	1.653

396		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	46	1.653

397		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	1.644

398		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	1.633

399		WTH001	Withdrawal Disorder	48	1.618

400		MLD018	Mild Cognitive Impairment	48	1.618

401	c	GLC092	Glaucoma, Primary Open Angle	62	1.618

402		LMY002	Leiomyoma	51	1.618

403	P	STS003	Sitosterolemia	53	1.618

404		MYF001	Myofibroma	42	1.618

405	P	LNG064	Lung Cancer Susceptibility 3	70	1.618

406		AMR003	Amaurosis Fugax	33	1.618

407		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	1.613

408		LYM040	Lymphoblastic Lymphoma	53	1.601

409		CTS005	Catastrophic Antiphospholipid Syndrome	43	1.601

410		CRY008	Cryopyrin-Associated Periodic Syndrome	48	1.601

411	P	OVR042	Ovarian Cancer	88	1.565

412		ANL018	Analbuminemia	53	1.565

413	P	LCH002	Lichen Planus	54	1.565

414		DBT010	Diabetic Neuropathy	54	1.565

415		CHG001	Chagas Disease	66	1.565

416		PLC002	Plica Syndrome	35	1.565

417		SYN007	Synovitis	55	1.565

418	P	INF037	Inflammatory Bowel Disease	53	1.544

419		ATR057	Atrioventricular Block	54	1.544

420		PTN004	Patent Ductus Venosus	31	1.544

421	P	SBR004	Seborrheic Dermatitis	44	1.544

422	P	ART023	Arthropathy	61	1.544

423		LNG039	Lung Squamous Cell Carcinoma	57	1.544

424	P	UVT001	Uveitis	57	1.544

425	P	PST095	Post-Thrombotic Syndrome	51	1.544

426		RTN020	Retinal Vascular Disease	46	1.544

427		JPN002	Japanese Encephalitis	61	1.544

428		GST023	Gastric Ulcer	52	1.544

429		CRS001	Crescentic Glomerulonephritis	42	1.544

430		BCK003	Background Diabetic Retinopathy	47	1.544

431		DCB001	Decubitus Ulcer	62	1.544

432		SYS003	Systolic Heart Failure	49	1.544

433		CNG092	Congenital Extrahepatic Portosystemic Shunt	24	1.544

434		ATX019	Ataxia with Vitamin E Deficiency	44	1.522

435		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	40	1.508

436		THR100	Thrombocytopenic Purpura, Autoimmune	61	1.508

437		KRT002	Keratomalacia	55	1.508

438	P	VSC018	Visceral Steatosis	32	1.508

439	c	CHR064	Chronic Monocytic Leukemia	36	1.508

440	P	NSP012	Nasopharyngeal Carcinoma	61	1.500

441	P	SLP005	Sleep Disorder	61	1.500

442	P	KDN017	Kidney Cancer	61	1.500

443	P	RTN022	Retinal Vein Occlusion	54	1.500

444		DRG024	Drug Allergy	40	1.469

445		CRB086	Cerebral Aneurysms	40	1.469

446		CRD223	Cardiac Arrhythmia	63	1.463

447	c	ATM099	Autoimmune Uveitis	45	1.463

448	c	MYC058	Myocardial Infarction 2	24	1.463

449	P	PSD087	Pseudoxanthoma Elasticum	67	1.463

450		ESP021	Esophageal Cancer	83	1.463

451		SKN016	Skin Disease	63	1.463

452	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	1.463

453		ALC010	Alcoholic Cardiomyopathy	42	1.463

454		CRN017	Coronary Thrombosis	46	1.463

455	P	MYG005	Myoglobinuria	40	1.463

456		TTN003	Tetanus	65	1.463

457		CYS009	Cystadenoma	43	1.463

458	P	ADL010	Adult Respiratory Distress Syndrome	71	1.463

459		ATN005	Autonomic Dysfunction	46	1.463

460		PRQ001	Paraquat Lung	16	1.463

461	c	PRM038	Primary Agammaglobulinemia	47	1.460

462		HYP732	Hyperalphalipoproteinemia 1	52	1.421

463		CYS001	Cystic Fibrosis	78	1.397

464		MYL009	Myelodysplastic Syndrome	67	1.397

465	c	HYP739	Hyperlipoproteinemia, Type Iv	53	1.397

466		PRD004	Prediabetes Syndrome	52	1.397

467		MTC005	Mitochondrial Metabolism Disease	45	1.386

468		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	46	1.386

469		ANX004	Anoxia	40	1.376

470		MTH086	Methotrexate Toxicity	32	1.376

471	P	SCH015	Schizophrenia	74	1.376

472		THR099	Third-Degree Atrioventricular Block	42	1.376

473	c	GRV008	Graves Disease 1	54	1.376

474		HMM004	Hamamy Syndrome	39	1.376

475	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	1.376

476		OST017	Osteomyelitis	63	1.376

477		HPT004	Hepatic Coma	43	1.376

478		ART012	Aortitis	42	1.376

479		BLP005	Blepharitis	50	1.376

480	P	HMR005	Hemorrhoid	49	1.376

481	P	ACN011	Acne	57	1.376

482		RTR001	Retrograde Amnesia	41	1.376

483	P	INT070	Intestinal Obstruction	57	1.376

484		CHR096	Chronic Pulmonary Heart Disease	41	1.376

485	P	GLL022	Guillain-Barre Syndrome	60	1.376

486		HPT019	Hepatic Encephalopathy	59	1.376

487		CRY003	Cryptosporidiosis	56	1.376

488		DRG002	Drug-Induced Hepatitis	42	1.376

489		HYD002	Hydronephrosis	58	1.376

490		CRT015	Carotid Artery Occlusion	45	1.376

491		SPT004	Septic Arthritis	58	1.376

492		EXT006	Extrahepatic Cholestasis	40	1.376

493		PLM010	Pulmonary Edema	55	1.376

494	P	CMP008	Compartment Syndrome	50	1.376

495	P	CRB088	Cerebral Atrophy	33	1.376

496	c	CHR708	Chronic Urticaria	42	1.359

497		OST062	Osteoarthritis with Mild Chondrodysplasia	47	1.344

498		EPT021	Epithelial Recurrent Erosion Dystrophy	46	1.344

499		CMP010	Complex Regional Pain Syndrome	60	1.344

500		ARC025	Arachnoid Cysts, Intracranial	37	1.279

501		MDR006	Moderate and Severe Traumatic Brain Injury	27	1.279

502	c	ACT134	Acute Liver Failure	59	1.279

503		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	1.279

504		VLV047	Volvulus of Midgut	52	1.279

505		CHL152	Childhood Acute Lymphocytic Leukemia	50	1.279

506		KRT019	Keratitis, Hereditary	66	1.279

507		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	1.279

508		HRN029	Hearing Loss, Noise-Induced	37	1.279

509	P	PLM034	Pulmonary Emphysema	58	1.279

510		CMB007	Combined Immunodeficiency	57	1.279

511		ASP007	Aspiration Pneumonia	49	1.279

512		PLR008	Pleurisy	50	1.279

513		ACR007	Acromegaly	70	1.279

514		RTR008	Root Resorption	44	1.279

515		TRN018	Transitional Cell Carcinoma	56	1.279

516		GST033	Gestational Diabetes	61	1.279

517		BRN024	Bronchitis	67	1.279

518	P	TRT010	Teratoma	51	1.279

519		NNC012	Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency	17	1.279

520		DXR001	Doxorubicin Induced Cardiomyopathy	32	1.279

521	P	HYP069	Hyperparathyroidism	62	1.276

522	c	PNS012	Paine Syndrome	60	1.253

523	P	BLD124	Bleeding Disorder, Platelet-Type, 11	67	1.253

524	P	CRB194	Cerebroretinal Microangiopathy with Calcifications and Cysts 1	54	1.253

525	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	1.253

526		PLY105	Polycystic Ovary Syndrome 1	39	1.253

527	P	PRC031	Preeclampsia/eclampsia 1	43	1.253

528		SPR126	Superior Semicircular Canal Dehiscence	41	1.253

529	P	ECL001	Eclampsia	52	1.253

530	P	INT143	Interstitial Cystitis	60	1.253

531		MSC190	Muscular Disease	37	1.253

532	c	HMG029	Hemoglobin Se Disease	40	1.253

533		LYM133	Lymphoma, Hodgkin, Classic	74	1.234

534		GLM044	Glomerular Disease	35	1.234

535		ART002	Arts Syndrome	66	1.234

536		KHL003	Kohlschutter-Tonz Syndrome	59	1.234

537		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	59	1.234

538		LYM143	Lymphoma, Non-Hodgkin, Familial	75	1.234

539		ART001	Arterial Tortuosity Syndrome	65	1.234

540		LYN004	Lynch Syndrome I	58	1.234

541		APR006	Apert Syndrome	70	1.234

542		BLD051	Blood Coagulation Disease	53	1.234

543		PLM001	Pulmonary Tuberculosis	69	1.234

544	P	LYN001	Lynch Syndrome	76	1.234

545		PPL001	Papillary Adenoma	44	1.234

546		PLS009	Plasma Cell Neoplasm	64	1.234

547		CLC006	Calcinosis	47	1.234

548		ADS004	Aids Dementia Complex	40	1.234

549		CYT018	Cytochrome P450 2d6 Variant	26	1.234

550		ESN015	Eosinophilic Fasciitis	47	1.228

551		FSC004	Fasciitis	49	1.228

552		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	1.169

553	c	GLL024	Gallbladder Disease 1	52	1.169

554	c	STS010	Sitosterolemia 1	46	1.169

555		HLC007	Helicobacter Pylori Infection	67	1.169

556	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	1.169

557		MMM006	Mammographic Density	39	1.169

558	P	CRT085	Carotid Intimal Medial Thickness 2	22	1.169

559		SKN019	Skin Melanoma	71	1.169

560	P	FBR017	Fibrosarcoma	56	1.169

561		END040	Endogenous Depression	55	1.169

562		LNG099	Lung Disease	62	1.169

563	c	STS011	Sitosterolemia 2	34	1.169

564	P	HYD006	Hydrocephalus	61	1.169

565		QDR001	Quadriplegia	50	1.169

566	P	MYC033	Myoclonus	47	1.169

567		PRS115	Prosthetic Joint Infection	42	1.169

568		SPS057	Spasticity	42	1.168

569	P	CTN015	Cutaneous T Cell Lymphoma	48	1.160

570	c	PSR028	Psoriasis 7	43	1.160

571	c	PSR017	Psoriasis 2	53	1.160

572	c	PSR018	Psoriasis 13	52	1.160

573	c	PSR023	Psoriasis 1	52	1.160

574	c	PSR032	Psoriasis 11	47	1.160

575	P	MJR007	Major Affective Disorder 1	42	1.106

576		MYL031	Myeloproliferative Neoplasm	66	1.106

577		PST028	Post-Traumatic Stress Disorder	59	1.106

578		FBR089	Fibrosclerosis, Multifocal	35	1.090

579	P	BLR024	Biliary Cirrhosis, Primary, 1	28	1.090

580		SMT004	Smith-Lemli-Opitz Syndrome	70	1.090

581	c	MCL062	Mucolipidosis Ii Alpha/beta	68	1.090

582		DBT092	Diabetes Insipidus, Nephrogenic, X-Linked	38	1.090

583		END057	Endometrial Cancer	72	1.090

584	P	PRP056	Porphyria, Acute Hepatic	49	1.090

585		CRH005	Crohn's Colitis	53	1.090

586		RNL065	Renal Cell Carcinoma, Papillary, 1	79	1.090

587		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	46	1.090

588		ACR041	Acromelic Frontonasal Dysostosis	53	1.090

589	c	SRC023	Sarcoidosis 2	44	1.090

590	P	SRC025	Sarcoidosis 1	71	1.090

591	c	INF071	Inflammatory Bowel Disease 1	65	1.090

592	P	GLM040	Glioma Susceptibility 1	71	1.090

593		NRR001	Neuroretinitis	42	1.090

594		RTN023	Retinitis	46	1.090

595	c	BRS049	Breast Carcinoma in Situ	50	1.090

596		CVR006	Cavernous Hemangioma	51	1.090

597		HMT002	Hematologic Cancer	61	1.090

598		VSL013	Visual Impairment and Progressive Phthisis Bulbi	36	1.090

599		PLM012	Pulmonary Sarcoidosis	53	1.090

600		BLD053	Blood Platelet Disease	51	1.090

601	c	INF023	Inflammatory Breast Carcinoma	49	1.090

602	P	EYD002	Eye Disease	57	1.090

603		BRS099	Breast Ductal Carcinoma	61	1.090

604	P	CPL006	Capillary Hemangioma	53	1.090

605		CRN006	Coronary Aneurysm	41	1.090

606		DFF003	Diffuse Scleroderma	41	1.090

607		IRN002	Iron Metabolism Disease	57	1.090

608		ACT113	Acute Myeloblastic Leukemia with Maturation	46	1.090

609		MST020	Mast Cell Activation Syndrome	28	1.090

610		RTR011	Retroperitoneal Fibrosis	47	1.090

611	c	CHR417	Chronic Graft Versus Host Disease	55	1.090

612		NPH091	Nephrolithiasis, Calcium Oxalate	61	1.085

613	P	RHB003	Rhabdomyosarcoma	66	1.085

614		TRC022	Tricuspid Valve Insufficiency	47	1.085

615		NPH009	Nephrolithiasis	54	1.085

616	c	HRD010	Hereditary Spastic Paraplegia	66	1.059

617	P	VNW001	Von Willebrand's Disease	65	1.058

618		CHR603	Chronic Enteropathy Associated with Slco2a1 Gene	25	1.043

619	c	EHL080	Ehlers-Danlos Syndrome, Musculocontractural Type, 1	52	1.043

620		CMR002	Coumarin Resistance	59	1.043

621		CRV035	Cervical Cancer	73	1.038

622	c	FNC027	Fanconi Anemia, Complementation Group a	81	1.038

623		MTB004	Metabolic Acidosis	48	1.038

624		TND006	Tendinosis	41	1.038

625	c	FNC042	Fanconi Anemia, Complementation Group D2	54	1.038

626		HPT022	Hepatoblastoma	54	1.038

627		CHL067	Cholecystitis	60	1.038

628		PHG002	Phagocyte Bactericidal Dysfunction	34	1.038

629		ESP023	Esophageal Disease	52	1.038

630		INT066	Interstitial Lung Disease	60	1.038

631		PLG002	Plague	58	1.038

632		DBT004	Diabetic Polyneuropathy	50	1.038

633		ANC002	Anca-Associated Vasculitis	44	1.038

634		LNR006	Linear Iga Disease	40	1.038

635	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	1.005

636	P	PRK057	Parkinson Disease, Late-Onset	80	1.005

637		CRB008	Cerebral Atherosclerosis	46	0.950

638		INT074	Intracranial Arteriosclerosis	22	0.950

639		PSR001	Psoriatic Arthritis	62	0.928

640		END062	Endometrial Hyperplasia	48	0.917

641		URM002	Uremia	47	0.917

642	P	ORF001	Orofaciodigital Syndrome	50	0.906

643		PMP009	Pemphigus Erythematosus	29	0.868

644		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.868

645		BRK010	Burkitt Lymphoma	66	0.868

646		TLM001	Telomere Length, Mean Leukocyte	16	0.868

647		HMR023	Hemorrhagic Cystitis	43	0.868

648		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.868

649		KRN002	Kearns-Sayre Syndrome	63	0.868

650	c	PRG020	Paragangliomas 3	39	0.868

651	P	HRD008	Hereditary Hemorrhagic Telangiectasia	65	0.868

652		ART010	Arteriolosclerosis	37	0.868

653	P	PMP001	Pemphigus	55	0.868

654		INT075	Intracranial Hypertension	53	0.868

655	P	CYS018	Cystitis	59	0.868

656		TLN003	Telangiectasis	51	0.868

657		CRY005	Cryptococcosis	60	0.868

658		CHL014	Cholera	62	0.868

659		SCH014	Schistosomiasis	56	0.868

660	P	MYS079	Miyoshi Muscular Dystrophy	54	0.868

661		MNN009	Meningoencephalitis	48	0.868

662	P	INF032	Infertility	57	0.868

663		PLS007	Plasmodium Falciparum Malaria	52	0.868

664		MNN002	Mononeuritis Multiplex	38	0.868

665		LCH013	Lichen Planus Pemphigoides	33	0.868

666		MSC007	Muscle Hypertrophy	64	0.840

667		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.840

668	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	50	0.840

669		ACT017	Acute Chest Syndrome	50	0.840

670	P	PHC003	Pheochromocytoma	69	0.820

671		LMB062	Limb Ischemia	55	0.820

672		APH002	Aphasia	56	0.820

673	c	CRB191	Cerebral Cavernous Malformations 2	45	0.820

674	c	CRB094	Cerebral Cavernous Malformations 3	41	0.820

675		TBC004	Tobacco Addiction	63	0.820

676		HRW001	Hair Whorl	35	0.820

677		ADR040	Adrenal Gland Pheochromocytoma	46	0.820

678		ACT003	Acute Kidney Tubular Necrosis	46	0.820

679	P	EMB005	Embryonal Rhabdomyosarcoma	53	0.820

680		NRM001	Neuromyelitis Optica	61	0.820

681		MCR141	Mucormycosis	59	0.820

682		CHL147	Chlamydia Pneumonia	47	0.820

683	P	ANG015	Angioedema	56	0.820

684		FCL012	Facial Paralysis	49	0.820

685	P	GLY013	Glycogen Storage Disease	60	0.820

686		CHL123	Chlamydia	58	0.820

687	P	RTN018	Retinal Disease	53	0.820

688	P	BNG032	Benign Mesothelioma	53	0.820

689		CND006	Candida Glabrata	30	0.820

690	P	OVR082	Overgrowth Syndrome	49	0.758

691	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	58	0.758

692	P	ANT001	Anterolateral Myocardial Infarction	34	0.758

693	P	ESP024	Esophagitis	60	0.758

694	P	TRC086	Trichohepatoenteric Syndrome 1	59	0.742

695		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	0.742

696		LPT006	Leptin Receptor Deficiency	50	0.742

697	P	NJM001	Nijmegen Breakage Syndrome	76	0.742

698		ATY005	Atypical Teratoid Rhabdoid Tumor	69	0.742

699		DDN006	Duodenitis	50	0.742

700		ACR039	Acromegaloid Hypertrichosis Syndrome	23	0.742

701		GLY081	Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency	47	0.710

702	P	LPR021	Leprosy 3	71	0.710

703		MYC006	Mycosis Fungoides	65	0.710

704		CRT045	Creatine Phosphokinase, Elevated Serum	39	0.710

705		GRN037	Granulomatosis with Polyangiitis	64	0.710

706		ATS010	Autosomal Recessive Disease	42	0.710

707		BRR014	Barrett Esophagus	66	0.710

708		AST006	Astigmatism	47	0.710

709		ACT119	Acute Promyelocytic Leukemia	62	0.710

710		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	42	0.710

711	c	GLY060	Glycogen Storage Disease Ia	63	0.710

712		VRC005	Varicose Veins	60	0.710

713	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	65	0.710

714		INT067	Interstitial Nephritis	46	0.710

715	P	MYP006	Myopia	56	0.710

716	P	MSC003	Muscular Atrophy	52	0.710

717	P	MLG056	Malignant Hyperthermia	66	0.710

718	P	VND001	Vein Disease	42	0.710

719		ADG002	Audiogenic Seizures	25	0.710

720	P	VNT002	Ventricular Septal Defect	58	0.710

721		PNC129	Pancreatic Adenocarcinoma	65	0.710

722		INS001	Insulinoma	59	0.710

723		PPT005	Peptic Ulcer Disease	58	0.710

724		SBC019	Subcutaneous Mycosis	35	0.710

725		SPR010	Sporotrichosis	46	0.710

726		HGH043	High Grade Glioma	45	0.710

727	P	BND020	Bone Disease	59	0.710

728		HMP005	Hemiplegia	54	0.710

729		PRS025	Presbyopia	38	0.710

730		DSS009	Disseminated Intravascular Coagulation	57	0.710

731	P	PRN023	Prion Disease	60	0.710

732		HNS001	Hansen's Disease	32	0.710

733		CRB090	Cerebral Hypoxia	42	0.710

734		FRS019	Farsightedness	36	0.710

735		DYS073	Dysphagia	53	0.710

736		ALN001	Aland Island Eye Disease	55	0.696

737	P	CNR004	Cone-Rod Dystrophy 2	74	0.696

738		HYP781	Hypoascorbemia	52	0.696

739	c	LKM063	Leukemia, Chronic Myeloid	71	0.696

740		MNT001	Mantle Cell Lymphoma	67	0.696

741		LYM012	Lymphoplasmacytic Lymphoma	50	0.696

742		WLD007	Waldenstroem's Macroglobulinemia	63	0.696

743		RHM028	Rheumatic Heart Disease	56	0.696

744		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	64	0.696

745	c	MSM022	Mismatch Repair Cancer Syndrome 1	70	0.696

746	c	FCL025	Focal Segmental Glomerulosclerosis 1	49	0.696

747	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	49	0.696

748	c	MJR006	Major Affective Disorder 5	32	0.696

749	c	MJR023	Major Affective Disorder 7	33	0.696

750	c	MJR004	Major Affective Disorder 4	28	0.696

751	c	MJR003	Major Affective Disorder 6	32	0.696

752	c	MJR008	Major Affective Disorder 2	34	0.696

753		SLT014	Salt and Pepper Developmental Regression Syndrome	43	0.696

754		BHR001	Behr Syndrome	51	0.696

755		CRD220	Cardiac Valvular Defect, Developmental	28	0.696

756	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	69	0.696

757		MCR004	Macroglobulinemia	49	0.696

758		INT003	Intracranial Hypotension	36	0.696

759		BNM001	Bone Marrow Cancer	46	0.696

760		MYL075	Myelodysplastic/myeloproliferative Neoplasm	51	0.696

761		VRL011	Viral Infectious Disease	61	0.696

762		LMN005	Lmna-Related Cardiocutaneous Progeria Syndrome	28	0.696

763		LNG031	Lung Benign Neoplasm	51	0.696

764		ACT084	Acute Stress Disorder	54	0.696

765		EBL001	Ebola Hemorrhagic Fever	56	0.696

766		CHR546	Chronic Mountain Sickness	43	0.696

767		OST003	Osteonecrosis	61	0.696

768		PRL017	Prolymphocytic Leukemia	47	0.696

769		SCN001	Secondary Hyperparathyroidism of Renal Origin	24	0.696

770	c	SCN007	Secondary Hyperparathyroidism	51	0.696

771		LCH001	Leech Infestation	38	0.696

772	P	ACT105	Acute Mountain Sickness	52	0.696

773	P	CLL015	Collagen Disease	48	0.696

774		ATM021	Autoimmune Inner Ear Disease	36	0.696

775		ANG011	Angiodysplasia	42	0.648

776		BCK006	Back Pain	47	0.648

777		CLC053	Colchicine Poisoning	23	0.580

778		PRN061	Prenatal-Onset Spinal Muscular Atrophy with Congenital Bone Fractures	13	0.580

779	P	VTR007	Vitreoretinopathy	46	0.580

780	P	THL005	Thalassemia	56	0.580

781		TNG002	Tangier Disease	64	0.580

782		RTN017	Retinal Detachment	60	0.580

783		FCT001	Factor Viii Deficiency	60	0.580

784	c	MST023	Mesothelioma, Malignant	56	0.580

785	c	BTT014	Beta-Thalassemia	72	0.580

786		INF034	Infective Endocarditis	54	0.580

787		SXL003	Sexual Disorder	49	0.580

788		BTT017	Beta-Thalassemia Major	51	0.580

789		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.580

790	c	HMP029	Hemophilia a	68	0.580

791		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	65	0.580

792		PLY001	Polycythemia Vera	69	0.580

793		SPR004	Supravalvular Aortic Stenosis	57	0.580

794		VTR016	Vater/vacterl Association	49	0.580

795		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.580

796		URT049	Urate Oxidase, Pseudogene	24	0.580

797	P	HNT016	Huntington Disease	73	0.580

798		DSS032	Disease by Infectious Agent	55	0.580

799		CHR431	Chronic Venous Insufficiency	48	0.580

800		SCR011	Scrapie	39	0.580

801	P	CHR012	Chronic Granulomatous Disease	69	0.580

802		CLL003	Cellulitis	53	0.580

803	P	LCT001	Lactic Acidosis	51	0.580

804		LYM027	Lymphopenia	56	0.580

805		FBR047	Fibromyalgia	58	0.580

806	P	CTR002	Cataract	60	0.580

807	P	PLY018	Polycythemia	56	0.580

808	P	MMB011	Membranous Nephropathy	50	0.580

809	P	VNS003	Venous Insufficiency	55	0.580

810		HPT085	Hepatitis, Fulminant Viral	33	0.580

811	P	DNG005	Dengue Virus	56	0.580

812		CRN019	Coronary Artery Vasospasm	47	0.580

813		PNC001	Pancytopenia	53	0.580

814		EPC002	Epicondylitis	44	0.580

815		RYS001	Reye Syndrome	49	0.580

816		PRT014	Protein S Deficiency	41	0.580

817		DBT008	Diabetic Angiopathy	45	0.580

818	P	MCR010	Microcephaly	60	0.580

819		HMP001	Hemopericardium	47	0.580

820	P	PRC012	Pericardial Effusion	50	0.580

821	P	END033	Endocarditis	58	0.580

822	P	RHN004	Rhinitis	57	0.580

823	P	HYP076	Hyperthyroidism	53	0.580

824		ACT058	Active Peptic Ulcer Disease	56	0.580

825	P	THR015	Thrombophilia	51	0.580

826		PTN001	Patent Foramen Ovale	62	0.580

827		VCT001	Vacterl Association	47	0.580

828	P	HMP007	Hemophilia	52	0.580

829		BRK012	Broken Heart Syndrome	42	0.580

830	P	PRD037	Periodontal Ehlers-Danlos Syndrome	49	0.580

831		RNL001	Renal Artery Obstruction	31	0.492

832		SLR005	Solar Urticaria	29	0.458

833		MCR037	Macroglossia	44	0.458

834		HMN047	Human Cytomegalovirus Infection	57	0.458

835		HPT025	Hepatic Lipase Deficiency	47	0.458

836		FXD003	Fixed Drug Eruption	34	0.458

837	P	MLN007	Male Infertility	56	0.458

838		BRN012	Bronchiolitis Obliterans	56	0.458

839		BRN002	Bronchiolitis	57	0.458

840		HDR003	Hidradenitis	50	0.458

841		LYS003	Lysinuric Protein Intolerance	57	0.410

842	c	SBC035	Subacute Cutaneous Lupus Erythematosus	34	0.410

843		ADR022	Adrenomyeloneuropathy	39	0.410

844		SRT004	Serotonin Syndrome	54	0.410

845		DFF031	Diffuse Alveolar Hemorrhage	31	0.410

846		ATR055	Atrial Septal Aneurysm	23	0.410

847		LYS029	Lysosomal Disease	30	0.410

848		THR123	Thrombotic Microangiopathy	40	0.410

849	c	DWL002	Dowling-Degos Disease 1	58	0.410

850	P	FML018	Familial Mediterranean Fever	73	0.410

851		ALL003	Allergic Rhinitis	67	0.410

852	P	SPR120	Supranuclear Palsy, Progressive, 1	69	0.410

853		BDD001	Budd-Chiari Syndrome	62	0.410

854	c	RTN047	Retinitis Pigmentosa 18	46	0.410

855		XNT003	Xanthomatosis	49	0.410

856	P	DRM053	Dermatitis, Atopic	65	0.410

857		BRT054	Brittle Bone Disorder	74	0.410

858	c	LKM070	Leukemia, Acute Monocytic	56	0.410

859		LPM012	Lipomatosis, Multiple	60	0.410

860		ANS021	Anisocoria	25	0.410

861	P	TMP003	Temporal Arteritis	69	0.410

862		HYP457	Hypertrophic Scars	42	0.410

863		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	0.410

864		IGG007	Igg4-Related Disease	48	0.410

865	P	MCL001	Mucolipidosis	49	0.410

866	c	BNG093	Benign Teratoma	39	0.410

867	P	ERY036	Erythema Nodosum	49	0.410

868	c	ATS007	Autism Spectrum Disorder	72	0.410

869	P	LYM033	Lymphoproliferative Syndrome	59	0.410

870		HPT046	Hepatic Veno-Occlusive Disease	62	0.410

871	P	SML001	Small Cell Carcinoma	52	0.410

872		MLT180	Multisystem Inflammatory Syndrome in Children	32	0.410

873	P	TRN034	Transverse Myelitis	47	0.410

874		CRB011	Cerebrotendinous Xanthomatosis	65	0.410

875		WRN001	Werner Syndrome	69	0.410

876		LYS012	Lysosomal Acid Lipase Deficiency	65	0.410

877		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.410

878		NRL016	Neural Tube Defects	81	0.410

879		CNT105	Central Core Disease of Muscle	59	0.410

880		LNG108	Langerhans Cell Histiocytosis	58	0.410

881	P	GST053	Gastric Cancer	83	0.410

882		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.410

883		MYP071	Myopathy Due to Myoadenylate Deaminase Deficiency	43	0.410

884		LPP002	Lipoprotein Glomerulopathy	43	0.410

885		AFB002	Afibrinogenemia, Congenital	64	0.410

886		CYS013	Cystinuria	66	0.410

887	P	SPP010	Suppressor of Tumorigenicity 3	51	0.410

888		LCH016	Lichen Sclerosus Et Atrophicus	42	0.410

889		HMF008	Hemifacial Atrophy, Progressive	38	0.410

890		PRD013	Periodic Fever, Familial, Autosomal Dominant	68	0.410

891	c	HRM017	Hermansky-Pudlak Syndrome 2	55	0.410

892		EST002	Estrogen-Receptor Negative Breast Cancer	45	0.410

893	c	NMN016	Niemann-Pick Disease, Type B	56	0.410

894	P	FLL037	Follicular Lymphoma	74	0.410

895		CRD137	Cardiogenic Shock	56	0.410

896		FGF013	Fgfr3-Related Chondrodysplasia	4	0.410

897		RRC033	Rare Coagulation Disorder	11	0.410

898	c	PST005	Posterior Uveitis	54	0.410

899		PMP014	Pemphigoid	51	0.410

900	P	HRD214	Hereditary Periodic Fever Syndrome	30	0.410

901	P	HYP083	Hypopituitarism	52	0.410

902		AVN001	Avian Influenza	61	0.410

903		SCH012	Schizoaffective Disorder	50	0.410

904	P	HMC002	Homocystinuria	53	0.410

905		CRT008	Carotid Artery Dissection	29	0.410

906	c	BCT013	Bacterial Pneumonia	48	0.410

907	P	MTC133	Mitochondrial Myopathy	50	0.410

908		SPN185	Spinal Cord Infarction	28	0.410

909		PST092	Posttransplant Acute Limbic Encephalitis	28	0.410

910	P	ALP009	Alopecia Areata	59	0.410

911		SPC030	Specific Language Disorder	25	0.410

912		ANR004	Anuria	44	0.410

913	P	ANT006	Antiphospholipid Syndrome	55	0.410

914		NRN001	Neuroendocrine Carcinoma	47	0.410

915	P	OPT006	Optic Nerve Disease	58	0.410

916		HST010	Histiocytosis	49	0.410

917	P	SKN015	Skin Carcinoma	71	0.410

918		CHL050	Cholesterol Ester Storage Disease	31	0.410

919		CHL070	Cholesterol Embolism	39	0.410

920		OVR063	Overnutrition	42	0.410

921		INF013	Inferior Myocardial Infarction	33	0.410

922		MYL001	Myelitis	50	0.410

923		FCL003	Facial Hemiatrophy	29	0.410

924		BLL006	Bullous Pemphigoid	61	0.410

925		PHN011	Phenytoin Toxicity	32	0.410

926		ASY002	Asymptomatic Neurosyphilis	41	0.410

927		PLM005	Pleomorphic Lipoma	40	0.410

928	P	HMP002	Hemophagocytic Lymphohistiocytosis	61	0.410

929	P	CTN003	Cutaneous Lupus Erythematosus	52	0.410

930		ERY003	Erythema Multiforme	56	0.410

931	P	MGR001	Migraine Without Aura	49	0.410

932	P	GRV001	Graves' Disease	55	0.410

933	P	OPT009	Optic Neuritis	57	0.410

934		PCD001	Pica Disease	38	0.410

935		SBC014	Subclavian Steal Syndrome	31	0.410

936		PPL022	Papilloma	53	0.410

937		SQM002	Squamous Cell Papilloma	46	0.410

938	P	NMN002	Niemann-Pick Disease	60	0.410

939		EXS001	Exostosis	49	0.410

940	P	GCH001	Gaucher's Disease	70	0.410

941		CNT016	Central Retinal Vein Occlusion	54	0.410

942	P	CYS017	Cystic Teratoma	41	0.410

943	P	LNG028	Long Qt Syndrome	64	0.410

944		DPH001	Diphtheria	59	0.410

945	P	RNL015	Renal Hypertension	45	0.410

946		BRC012	Brucellosis