Search results for B2

2217 hits were found for B2

#	Family	MCID	Name	MIFTS	Score
1	c	BRC052	Brachydactyly, Type B2	40	40.800

2	c	MSC044	Muscular Dystrophy-Dystroglycanopathy , Type B, 2	31	16.799

3		RBF001	Riboflavin Deficiency	49	13.276

4	c	CHR651	Charcot-Marie-Tooth Disease, Axonal, Type 2b2	40	13.005

5		CRT005	Cortical Thymoma	22	9.458

6		ISC004	Ischemia	61	3.925

7	P	THY023	Thymoma	64	3.731

8	c	THY107	Thymoma, Familial	42	3.725

9	c	MGR028	Migraine with or Without Aura 1	64	3.483

10	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	79	3.380

11	c	ACT068	Acute Cystitis	61	3.348

12	c	PRC016	Pre-Eclampsia	64	3.347

13	c	HYP595	Hypertension, Essential	84	3.312

14	P	ANG015	Angioedema	56	3.237

15	P	BRS047	Breast Cancer	97	3.212

16		CRB039	Cerebrovascular Disease	65	3.164

17		CRH001	Crohn's Disease	80	3.120

18	c	MCR133	Microvascular Complications of Diabetes 4	41	3.008

19	c	MCR113	Microvascular Complications of Diabetes 3	52	3.008

20	c	MCR130	Microvascular Complications of Diabetes 6	41	3.008

21	c	MCR120	Microvascular Complications of Diabetes 7	47	3.008

22	P	URN019	Urinary Tract Infection	49	2.978

23	P	ADN016	Adenocarcinoma	63	2.760

24		BRN004	Brain Edema	54	2.738

25	c	HPT016	Hepatitis B	62	2.729

26		PRT037	Pertussis	49	2.703

27	P	KDN018	Kidney Disease	72	2.633

28		LPP008	Lipoprotein Quantitative Trait Locus	65	2.594

29	c	CHR684	Chronic Kidney Disease	74	2.581

30	P	PRS040	Prostate Cancer	95	2.532

31		KRT002	Keratomalacia	54	2.510

32	P	AST005	Asthma	76	2.505

33		ART140	Arteries, Anomalies of	52	2.502

34	P	MYC008	Myocarditis	59	2.494

35		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	2.465

36		48X005	48,xyyy	39	2.443

37		HLX001	Helix Syndrome	47	2.387

38	P	INF032	Infertility	60	2.358

39	P	CLR023	Colorectal Cancer	100	2.313

40		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	2.313

41	c	HYP836	Hypercholesterolemia, Familial, 1	73	2.291

42	P	LVR013	Liver Disease	68	2.267

43		CRV035	Cervical Cancer	72	2.262

44	P	BLD134	Bladder Cancer	79	2.234

45		ANG054	Angina Pectoris	65	2.182

46	P	ECL001	Eclampsia	52	2.178

47	P	INF037	Inflammatory Bowel Disease	53	2.176

48		PST011	Pustulosis of Palm and Sole	52	2.168

49	P	PSR002	Psoriasis	63	2.168

50		47X002	47,xyy	48	2.164

51		OST012	Osteoarthritis	77	2.159

52		AZS001	Azoospermia	45	2.145

53		TRM010	Traumatic Brain Injury	50	2.138

54	c	HRD002	Hereditary Angioedema	61	2.123

55	P	HPT023	Hepatocellular Carcinoma	95	2.108

56	P	HRT032	Heart Disease	84	2.102

57	P	PLM037	Pulmonary Hypertension	69	2.100

58		GLM045	Glioma	62	2.098

59	P	RHN004	Rhinitis	57	2.089

60		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	2.068

61		ATH013	Atherosclerosis Susceptibility	63	2.067

62		PLM129	Pulmonary Disease, Chronic Obstructive	74	2.054

63	P	CRN300	Coronary Heart Disease 1	73	2.048

64		END086	End Stage Renal Disease	54	2.041

65	P	ANR048	Aniridia 1	66	2.037

66		GLL048	Glial Tumor	52	2.019

67		FTT001	Fatty Liver Disease	61	1.994

68		STR067	Stroke, Ischemic	79	1.974

69	P	RCT021	Rectum Cancer	54	1.972

70		INT007	Intermediate Coronary Syndrome	53	1.952

71	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	1.945

72		CRB004	Cerebral Artery Occlusion	46	1.926

73		TXC005	Toxic Shock Syndrome	62	1.903

74	c	ATR087	Atrial Standstill 1	74	1.903

75		HYP066	Hyperglycemia	60	1.900

76		PRT251	Proteinuria, Chronic Benign	58	1.886

77		DWN001	Down Syndrome	70	1.880

78	P	MLN007	Male Infertility	56	1.865

79	P	NRB001	Neuroblastoma	66	1.863

80	P	HPT021	Hepatitis	68	1.861

81	P	NRP001	Neuropathy	59	1.858

82		SPN186	Spinal Cord Injury	61	1.837

83		BCT022	Bacterial Infectious Disease	56	1.831

84		ATM095	Autoimmune Disease	61	1.831

85		BRN071	Brain Injury	50	1.829

86		ALL029	Allergic Disease	61	1.816

87	P	DBT009	Diabetes Mellitus	67	1.809

88	P	MYC007	Myocardial Infarction	69	1.797

89	P	THL005	Thalassemia	56	1.767

90	P	LNG032	Lung Cancer	98	1.763

91		END057	Endometrial Cancer	71	1.763

92	P	VSC007	Vascular Disease	62	1.762

93		BNR002	Bone Resorption Disease	47	1.758

94		MTH009	Mouth Disease	57	1.758

95	P	FBR017	Fibrosarcoma	55	1.739

96	P	LPS004	Lupus Erythematosus	61	1.726

97	P	THR014	Thrombocytopenia	66	1.722

98	P	MYS003	Myasthenia Gravis	68	1.721

99		ALL003	Allergic Rhinitis	66	1.704

100		CLR109	Colorectal Adenocarcinoma	50	1.693

101		LNG099	Lung Disease	62	1.693

102		EMB004	Embryonal Carcinoma	55	1.688

103		PRS047	Prostatitis	58	1.682

104	P	PRK057	Parkinson Disease, Late-Onset	79	1.681

105		NNL005	Non-Alcoholic Fatty Liver Disease	63	1.676

106		RPD005	Rapidly Involuting Congenital Hemangioma	48	1.673

107		CLT003	Colitis	63	1.673

108		HYP266	Hypoxia	56	1.672

109		CNG034	Congestive Heart Failure	69	1.660

110	c	BLD156	Bleeding Disorder, Platelet-Type, 14	33	1.648

111		NTR005	Nutritional Deficiency Disease	60	1.640

112	P	GST053	Gastric Cancer	82	1.629

113	c	ACT075	Acute Myocardial Infarction	55	1.624

114		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.615

115	P	CRD246	Cardiovascular System Disease	55	1.606

116	P	MNN013	Meningitis	65	1.600

117		C1N001	C1 Inhibitor Deficiency	43	1.596

118		NRL016	Neural Tube Defects	81	1.591

119		ADN018	Adenoma	58	1.590

120		ULC004	Ulcerative Colitis	74	1.590

121		URT010	Ureteral Obstruction	45	1.585

122		NNT021	Neonatal Meningitis	22	1.585

123		INT323	Intraocular Pressure Quantitative Trait Locus	63	1.585

124		CLN015	Colon Adenocarcinoma	64	1.584

125		HMC014	Homocysteinemia	52	1.578

126	c	TYP009	Type 2 Diabetes Mellitus	92	1.578

127	P	SLP006	Sleep Apnea	69	1.577

128	c	PRM038	Primary Agammaglobulinemia	47	1.569

129		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	1.568

130		AGN016	Aging	54	1.564

131	c	CTR132	Cataract 3, Multiple Types	41	1.563

132	P	FNG006	Feingold Syndrome 1	61	1.556

133	c	HPT001	Hepatitis C	61	1.541

134	P	DRR001	Diarrhea	55	1.538

135	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	1.533

136	c	SML038	Small Cell Cancer of the Lung	69	1.532

137		RNL077	Renal Fibrosis	46	1.528

138	c	SPR162	Spermatogenic Failure 50	42	1.527

139	P	HDC001	Headache	56	1.516

140	P	CTR002	Cataract	59	1.516

141		ESP021	Esophageal Cancer	84	1.513

142		KRT019	Keratitis, Hereditary	66	1.507

143		CYT002	Cytokine Deficiency	43	1.503

144		STT002	Status Asthmaticus	49	1.502

145		DBT010	Diabetic Neuropathy	54	1.499

146	P	MTR012	Mitral Valve Disease	57	1.495

147		IRN002	Iron Metabolism Disease	56	1.495

148	P	ENC004	Encephalitis	61	1.492

149	P	CYS018	Cystitis	59	1.487

150	P	TMP001	Temporal Lobe Epilepsy	49	1.486

151		FDB001	Foodborne Botulism	55	1.474

152	P	GLM007	Glomerulonephritis	59	1.461

153	P	PYL005	Pyelonephritis	56	1.452

154		ADR040	Adrenal Gland Pheochromocytoma	45	1.447

155	P	PHC003	Pheochromocytoma	70	1.447

156	P	LCT001	Lactic Acidosis	50	1.441

157		PRT036	Peritonitis	65	1.441

158	P	PRD008	Periodontitis	64	1.429

159		SQM006	Squamous Cell Carcinoma	59	1.425

160		SKN016	Skin Disease	62	1.422

161	P	ADL010	Adult Respiratory Distress Syndrome	71	1.414

162		DFC004	Deficiency Anemia	74	1.408

163	P	CLC063	Celiac Disease 1	66	1.396

164		HND002	Hand, Foot and Mouth Disease	50	1.396

165	P	NPH012	Nephrotic Syndrome	62	1.394

166		SVR004	Severe Combined Immunodeficiency	71	1.379

167	P	NTR004	Neutropenia	62	1.377

168		GLB002	Glioblastoma	67	1.372

169	P	AMY004	Amyloidosis	69	1.371

170		ALL006	Allergic Asthma	56	1.371

171	c	SYS001	Systemic Lupus Erythematosus	86	1.370

172	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	1.370

173	P	HYP750	Hypertriglyceridemia, Familial	62	1.370

174		PLM010	Pulmonary Edema	54	1.366

175	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	1.361

176	c	BDY012	Body Mass Index Quantitative Trait Locus 7	43	1.361

177	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	1.361

178	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	1.361

179	c	BDY006	Body Mass Index Quantitative Trait Locus 8	43	1.361

180	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	1.361

181	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	1.361

182	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	1.361

183	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	1.361

184	P	INS002	in Situ Carcinoma	53	1.357

185		MTB004	Metabolic Acidosis	48	1.353

186	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	1.352

187	P	ANT006	Antiphospholipid Syndrome	55	1.346

188		MNN009	Meningoencephalitis	48	1.346

189		PLR008	Pleurisy	49	1.333

190		CHL014	Cholera	62	1.327

191		ART016	Aortic Aneurysm	69	1.327

192	P	PNC044	Pancreatitis	61	1.314

193	P	ART021	Arteriosclerosis	53	1.313

194		HGH043	High Grade Glioma	46	1.306

195		ASP030	Aspirin Resistance	40	1.305

196	P	GST044	Gastritis	55	1.303

197	P	RNV001	Renovascular Hypertension	49	1.299

198		ASP003	Aseptic Meningitis	51	1.294

199	P	PLY019	Polyneuropathy	53	1.293

200		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	1.284

201	c	LKM005	Leukemia, T-Cell, Chronic	33	1.284

202	P	MYC084	Mycobacterium Tuberculosis 1	68	1.283

203		HDN002	Head Injury	44	1.282

204		ALC007	Alcohol Dependence	65	1.270

205		CLR108	Colorectal Adenoma	63	1.269

206		OST017	Osteomyelitis	63	1.268

207	P	MTC069	Mitochondrial Disorders	57	1.258

208		OST159	Osteogenic Sarcoma	66	1.256

209		RCK004	Rickets	65	1.254

210	P	RTN024	Retinoblastoma	72	1.250

211	P	KLZ004	Kala-Azar 1	41	1.250

212	c	DLT002	Dilated Cardiomyopathy	79	1.250

213		LSH001	Leishmaniasis	63	1.250

214		PHR003	Pharyngitis	57	1.244

215		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	1.239

216		LVR012	Liver Cirrhosis	62	1.237

217		DSS032	Disease by Infectious Agent	55	1.231

218	P	END044	Endometriosis	62	1.231

219	c	ACT071	Acute Kidney Failure	60	1.231

220	c	BTT014	Beta-Thalassemia	72	1.219

221		OCL069	Ocular Motor Apraxia	57	1.217

222		DCT002	Ductal Carcinoma in Situ	58	1.217

223	P	HRP006	Herpes Simplex	65	1.217

224		HLC007	Helicobacter Pylori Infection	67	1.216

225	c	MCR115	Microvascular Complications of Diabetes 5	65	1.203

226	P	ALZ034	Alzheimer Disease	87	1.197

227		LMB062	Limb Ischemia	55	1.190

228		SRC014	Sarcoma	64	1.190

229		TRN018	Transitional Cell Carcinoma	56	1.190

230		SPN035	Spindle Cell Sarcoma	51	1.190

231		MSL001	Measles	61	1.190

232		RNL114	Renal Cell Carcinoma, Nonpapillary	79	1.186

233	c	PCH010	Pachyonychia Congenita 3	43	1.183

234		MCR004	Macroglobulinemia	48	1.183

235	c	FML021	Familial Hypercholesterolemia	71	1.182

236	P	LYM118	Lymphoma	69	1.176

237	P	LKM002	Leukemia	66	1.176

238		BRN009	Burning Mouth Syndrome	51	1.174

239		APN008	Apnea, Obstructive Sleep	66	1.172

240		CHR619	Chromosome 2q35 Duplication Syndrome	64	1.167

241	c	ACT027	Acute Pancreatitis	60	1.165

242	P	LKM062	Leukemia, Acute Lymphoblastic	69	1.160

243		THR024	Thrombosis	56	1.154

244	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	1.145

245		THY089	Thymic Epithelial Neoplasm	27	1.144

246	P	MSC005	Muscular Dystrophy	66	1.142

247		THY042	Thymic Epithelial Tumor	26	1.138

248		MCS002	Mucositis	55	1.137

249	P	EXN002	Exanthem	58	1.137

250	c	HPT073	Hepatitis C Virus	71	1.137

251	P	INF038	Influenza	68	1.136

252	P	PRK039	Parkinsonism	55	1.135

253	P	RHB003	Rhabdomyosarcoma	66	1.128

254		BRS099	Breast Ductal Carcinoma	61	1.121

255		GST040	Gastric Adenocarcinoma	66	1.121

256		HMN044	Human Immunodeficiency Virus Type 1	76	1.118

257		LPD008	Lipid Metabolism Disorder	61	1.118

258		CHL068	Cholestasis	61	1.113

259		PLM001	Pulmonary Tuberculosis	69	1.113

260		CRN027	Corneal Neovascularization	47	1.113

261		ORL015	Oral Squamous Cell Carcinoma	43	1.112

262	P	MYP006	Myopia	55	1.112

263	P	PNC035	Pancreatic Cancer	86	1.103

264		BLD131	Bladder Urothelial Carcinoma	59	1.094

265	P	ALC033	Alcohol Use Disorder	67	1.090

266		HPT014	Hepatorenal Syndrome	49	1.090

267	P	LKM071	Leukemia, Chronic Lymphocytic	74	1.086

268		HTC003	Hutchinson-Gilford Progeria Syndrome	65	1.085

269		IMP005	Impotence	52	1.085

270		PRP030	Purpura	54	1.085

271	P	MYP004	Myopathy	67	1.085

272		RTN020	Retinal Vascular Disease	45	1.080

273	P	MYL006	Myeloid Leukemia	60	1.080

274		MYL069	Myeloma, Multiple	77	1.079

275		MLR004	Malaria	78	1.078

276		PLC008	Placenta Disease	49	1.078

277		STM007	Stomatitis	52	1.066

278		SBC016	Subacute Delirium	42	1.065

279		PRP027	Peripheral Vascular Disease	71	1.059

280		CTN007	Cutaneous Leishmaniasis	61	1.054

281		INS024	Insulin-Like Growth Factor I	77	1.052

282	P	RSP003	Respiratory Failure	74	1.052

283		HMG005	Hemoglobinopathy	55	1.046

284		CMP040	Complement Component 4, Partial Deficiency of	34	1.038

285		KPS004	Kaposi Sarcoma	76	1.038

286	P	CRN026	Corneal Edema	42	1.038

287	P	CNJ013	Conjunctivitis	66	1.038

288		ACT003	Acute Kidney Tubular Necrosis	46	1.024

289		GT001	Gout	63	1.024

290		DRM006	Dermatitis	62	1.024

291		CRN017	Coronary Thrombosis	46	1.023

292	P	SRC025	Sarcoidosis 1	70	1.022

293	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	1.015

294	P	BND020	Bone Disease	60	1.015

295		PPT005	Peptic Ulcer Disease	58	1.015

296		PRT049	Partial Deletion of Y	33	1.015

297		BRN024	Bronchitis	67	1.013

298		ALC006	Alcoholic Hepatitis	61	1.012

299		THY022	Thymic Carcinoma	56	1.011

300		SYN007	Synovitis	54	1.007

301		PLC002	Plica Syndrome	35	1.007

302		TRT001	Teratocarcinoma	41	1.007

303		ALL014	Allergic Encephalomyelitis	34	1.007

304		INT078	Intracranial Thrombosis	50	1.000

305	P	PLM036	Pulmonary Fibrosis	65	0.999

306		PST092	Posttransplant Acute Limbic Encephalitis	29	0.999

307		ANT039	Antisynthetase Syndrome	55	0.998

308	P	CRP001	Carpal Tunnel Syndrome	66	0.987

309		DBT004	Diabetic Polyneuropathy	50	0.987

310	P	SZR006	Seizure Disorder	69	0.983

311		CRD137	Cardiogenic Shock	56	0.983

312		ACT098	Acute Erythroid Leukemia	55	0.974

313		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.974

314	P	BRC006	Brachydactyly	52	0.958

315	P	PRP019	Peripheral Nervous System Disease	57	0.957

316		ACT119	Acute Promyelocytic Leukemia	62	0.957

317	P	NSP012	Nasopharyngeal Carcinoma	60	0.957

318		PYR009	Pyridoxine Deficiency Anemia	35	0.957

319		ARG004	Argyria	26	0.957

320		ADL002	Adult Syndrome	69	0.954

321	c	PNS012	Paine Syndrome	60	0.954

322		RHB024	Rhabdomyosarcoma 2	65	0.954

323		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.954

324	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.954

325	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.954

326	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.954

327	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.954

328		RFR003	Refractive Error	41	0.954

329	c	BLD123	Bleeding Disorder, Platelet-Type, 13	22	0.951

330		PRC013	Pericarditis	53	0.948

331	P	ALP008	Alopecia	53	0.948

332	P	CHR345	Chronic Pain	50	0.944

333	P	BCL017	B-Cell Lymphoma	57	0.939

334		SFT003	Soft Tissue Sarcoma	57	0.938

335	P	PLY018	Polycythemia	56	0.938

336	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.933

337	c	TYP008	Type 1 Diabetes Mellitus	77	0.933

338	P	SPP010	Suppressor of Tumorigenicity 3	51	0.928

339	P	ESS003	Essential Thrombocythemia	68	0.928

340	P	DDN001	Duodenal Ulcer	53	0.928

341		THR004	Thrombocytosis	52	0.928

342	P	BNG032	Benign Mesothelioma	53	0.928

343		SPP011	Suppression of Tumorigenicity 12	61	0.928

344	P	HYP086	Hypothyroidism	69	0.926

345	P	ADL017	Adult T-Cell Leukemia	54	0.918

346		ENT011	Enterocolitis	55	0.918

347	P	ATR011	Atrial Fibrillation	66	0.908

348	P	LSS002	Lissencephaly	53	0.908

349		FBR047	Fibromyalgia	58	0.908

350	c	LKM063	Leukemia, Chronic Myeloid	71	0.907

351		MST005	Mastitis	52	0.907

352	c	MLT156	Multiple Endocrine Neoplasia, Type I	71	0.897

353		DSS009	Disseminated Intravascular Coagulation	56	0.897

354	P	MLT074	Multiple Endocrine Neoplasia	58	0.897

355	P	PRX021	Proximal Symphalangism	50	0.892

356		ANK001	Ankylosis	51	0.892

357	c	ALP101	Alpha-Thalassemia	62	0.887

358		STT001	Status Epilepticus	58	0.886

359		BRN028	Brain Cancer	73	0.886

360		GNG013	Gingivitis	59	0.886

361	P	VNW001	Von Willebrand's Disease	64	0.886

362		GST045	Gastroenteritis	58	0.886

363	P	EST010	Esterase B	13	0.880

364		BRN002	Bronchiolitis	57	0.880

365	P	DRM053	Dermatitis, Atopic	65	0.874

366	P	NRF002	Neurofibromatosis	60	0.874

367	P	FML187	Familial Hypertension	34	0.874

368		TRS002	Tarsal-Carpal Coalition Syndrome	42	0.871

369		SYN005	Synostosis	43	0.871

370		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.866

371	P	MTC133	Mitochondrial Myopathy	51	0.862

372	c	ACT076	Acute Myocarditis	47	0.862

373	P	RNL007	Renal Tubular Acidosis	52	0.858

374	c	BRN108	Branchiootic Syndrome 1	63	0.849

375		RNL025	Renal Hypoplasia	46	0.849

376	P	HML001	Hemolytic-Uremic Syndrome	52	0.849

377		PLN006	Poland Syndrome	45	0.846

378	P	MLT072	Multiple Synostoses Syndrome	44	0.846

379		STP011	Stapes Ankylosis with Broad Thumbs and Toes	28	0.846

380		BRK010	Burkitt Lymphoma	66	0.843

381	c	MST023	Mesothelioma, Malignant	56	0.836

382	P	SKN015	Skin Carcinoma	71	0.836

383	P	MLN008	Melanoma	75	0.828

384		MTR002	Mitral Valve Insufficiency	51	0.828

385		IMM165	Immunoglobulin Switch Sequences	14	0.821

386		PRP080	Peripheral Artery Disease	54	0.820

387	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	0.820

388	P	MMB011	Membranous Nephropathy	50	0.820

389	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.820

390	P	INT068	Intestinal Disease	53	0.820

391		GTR002	Goiter	52	0.820

392		GLM044	Glomerular Disease	34	0.820

393	c	BRC051	Brachydactyly, Type B1	50	0.813

394		RCT020	Rectum Adenocarcinoma	48	0.812

395	P	DST107	Distal Renal Tubular Acidosis	48	0.812

396		NRR001	Neuroretinitis	42	0.811

397		RTN023	Retinitis	45	0.811

398		IRN001	Iron Deficiency Anemia	58	0.806

399		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.804

400	P	MYS005	Myositis	56	0.804

401	P	OST002	Osteoporosis	77	0.804

402	c	SVR005	Severe Pre-Eclampsia	50	0.804

403		CLN045	Colonic Benign Neoplasm	48	0.789

404	P	OST001	Osteopetrosis	70	0.789

405		ECH003	Echinococcosis	52	0.789

406	P	ZLL001	Zellweger Syndrome	65	0.789

407		VRC005	Varicose Veins	59	0.786

408		ART074	Aortic Dissection	53	0.786

409		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.786

410		PLM031	Poliomyelitis	62	0.786

411	P	PTT006	Pituitary Adenoma	55	0.786

412	P	GLL018	Gallbladder Cancer	53	0.786

413		HYP056	Hypoglycemia	65	0.786

414	P	MLT020	Multiple Sclerosis	79	0.782

415		CYS008	Cystic Echinococcosis	57	0.770

416	P	HMP007	Hemophilia	52	0.770

417	P	RTN016	Retinal Degeneration	52	0.770

418	c	LKM061	Leukemia, Acute Myeloid	83	0.768

419	c	JVN010	Juvenile Rheumatoid Arthritis	66	0.768

420	c	BSL007	Basal Cell Carcinoma	68	0.759

421	P	PLY011	Polycystic Ovary Syndrome	57	0.759

422		ANR040	Aneurysm	60	0.759

423		IRR002	Irritable Bowel Syndrome	65	0.759

424	P	SCH015	Schizophrenia	74	0.757

425		NNL006	Non-Alcoholic Steatohepatitis	54	0.752

426		MCN001	Mucinous Adenocarcinoma	49	0.752

427		APP009	Appendix Adenocarcinoma	47	0.752

428		CHR603	Chronic Enteropathy Associated with Slco2a1 Gene	25	0.752

429	c	TBR025	Tuberous Sclerosis 1	84	0.749

430	P	TBR001	Tuberous Sclerosis	69	0.749

431	c	ACT249	Acute Asthma	40	0.749

432		URM002	Uremia	47	0.749

433		TYP007	Typhoid Fever	63	0.749

434	P	HYD006	Hydrocephalus	63	0.749

435		INS001	Insulinoma	59	0.749

436	P	SLP005	Sleep Disorder	62	0.749

437	P	KRT007	Keratoconus	50	0.740

438		PNC129	Pancreatic Adenocarcinoma	65	0.739

439	c	ACQ012	Acquired Angioedema	37	0.739

440		MTC100	Metacarpal 4-5 Fusion	31	0.734

441		SGR001	Sugarman Brachydactyly	32	0.734

442	c	BRC078	Brachydactyly, Type A1	53	0.734

443	c	BRC079	Brachydactyly, Type A2	50	0.734

444	c	BRC099	Brachydactyly, Type A4	30	0.734

445		ADP007	Adie Pupil	40	0.734

446		DPN005	Du Pan Syndrome	47	0.734

447		LCR014	Lacrimoauriculodentodigital Syndrome	58	0.734

448		OSS012	Osseous Heteroplasia, Progressive	61	0.734

449	c	BRC075	Brachydactyly, Type A1, C	33	0.734

450	c	MCR109	Microphthalmia, Isolated 4	37	0.734

451		SYN086	Synostoses, Tarsal, Carpal, and Digital	37	0.734

452		SYM024	Symphalangism, Distal	21	0.734

453	P	SYN060	Syndactyly, Type Iii	40	0.734

454		ICH054	Ichthyosis, X-Linked	51	0.734

455	c	BRC080	Brachydactyly, Type A1, B	37	0.734

456		HNM002	Hinman Syndrome	26	0.734

457		PLY001	Polycythemia Vera	69	0.729

458	P	OPN001	Open-Angle Glaucoma	55	0.729

459		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.729

460	c	GLC092	Glaucoma, Primary Open Angle	61	0.729

461	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.729

462		CHG001	Chagas Disease	65	0.729

463		AVN001	Avian Influenza	61	0.729

464	P	HYP098	Hypereosinophilic Syndrome	66	0.729

465		EPT021	Epithelial Recurrent Erosion Dystrophy	46	0.724

466		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	0.724

467		MTC004	Mitochondrial Encephalomyopathy	43	0.724

468		PYR016	Pyridoxine Deficiency	29	0.724

469		DFF005	Diffuse Large B-Cell Lymphoma	55	0.718

470	P	SCL018	Scoliosis	57	0.718

471	P	CRC039	Coarctation of Aorta	46	0.718

472		HMP001	Hemopericardium	47	0.718

473	P	PRC012	Pericardial Effusion	50	0.718

474		SQM013	Squamous Cell Carcinoma, Head and Neck	75	0.718

475	P	MSC003	Muscular Atrophy	52	0.718

476		PDT035	Pediatric Systemic Lupus Erythematosus	46	0.718

477		CRH005	Crohn's Colitis	53	0.711

478		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.707

479		CRN019	Coronary Artery Vasospasm	47	0.707

480	P	CND004	Candidiasis	57	0.707

481	P	HML002	Hemolytic Anemia	62	0.707

482		SCH014	Schistosomiasis	56	0.707

483		GST023	Gastric Ulcer	52	0.707

484	P	PTN014	Patent Ductus Arteriosus 1	59	0.707

485		PLM033	Pulmonary Embolism	58	0.707

486		CNS004	Constipation	56	0.701

487	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.695

488		PNG002	Pain Agnosia	51	0.695

489		BNB002	Bainbridge-Ropers Syndrome	45	0.695

490		HYD002	Hydronephrosis	58	0.695

491	c	DPH024	Diaphragmatic Hernia, Congenital	64	0.695

492		NWC001	Newcastle Disease	48	0.695

493	P	BRS044	Breast Adenocarcinoma	58	0.695

494		HRT012	Heart Valve Disease	53	0.695

495		PRN019	Perinatal Necrotizing Enterocolitis	60	0.695

496		CYS014	Cystadenocarcinoma	51	0.695

497	c	CTR130	Cataract 9, Multiple Types	39	0.691

498		LST001	Listeriosis	59	0.691

499		CTR014	Cataract Microcornea Syndrome	35	0.691

500	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	0.691

501		SLP001	Sleeping Sickness	56	0.683

502		IFP003	Ifap Syndrome 2	42	0.683

503	P	ART005	Arteriovenous Malformation	65	0.683

504	P	GLM040	Glioma Susceptibility 1	70	0.683

505	P	OPT006	Optic Nerve Disease	57	0.683

506		ASP038	Aspirin-Induced Respiratory Disease	16	0.683

507		BTT017	Beta-Thalassemia Major	53	0.683

508	P	ESP024	Esophagitis	60	0.683

509		MCL006	Macular Retinal Edema	56	0.683

510		TRN015	Transient Cerebral Ischemia	62	0.683

511		LYM126	Lymphoma Aids Related	44	0.683

512	P	ATR005	Atrophic Gastritis	50	0.683

513		HRD224	Hereditary Nonpolyposis Colon Cancer	51	0.683

514		THY025	Thymus Cancer	56	0.681

515	c	HPT003	Hepatitis a	63	0.680

516	P	TRN020	Turner Syndrome	67	0.680

517		ART141	Arteriovenous Malformations of the Brain	58	0.670

518		MSC007	Muscle Hypertrophy	64	0.670

519		END062	Endometrial Hyperplasia	48	0.670

520	P	MMP001	Mumps	56	0.670

521		GLL029	Gallbladder Adenoma	30	0.670

522		MTB008	Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration	42	0.670

523		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	52	0.670

524		MLG169	Malignant Astrocytoma	57	0.670

525	P	PRN023	Prion Disease	60	0.670

526	P	HYP069	Hyperparathyroidism	62	0.670

527		MSC157	Muscular Dystrophy, Duchenne Type	79	0.670

528	P	TRM003	Tremor	50	0.670

529	c	HMN021	Human T-Cell Leukemia Virus Type 1	46	0.670

530	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	0.670

531	c	ACT134	Acute Liver Failure	57	0.670

532		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.669

533		HMN014	Human Immunodeficiency Virus Infectious Disease	54	0.669

534		PST028	Post-Traumatic Stress Disorder	59	0.657

535	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	0.657

536		INT395	Intracranial Meningioma	48	0.656

537		TRY001	Trypanosomiasis	50	0.656

538		END041	Endometrial Adenocarcinoma	63	0.656

539		DNT012	Dental Caries	53	0.656

540		CRB037	Cerebral Palsy	67	0.656

541		HRT011	Heart Septal Defect	49	0.656

542	P	KRT005	Keratoacanthoma	47	0.656

543	P	EPD016	Epidermolysis Bullosa	53	0.656

544		PHN003	Phenylketonuria	76	0.656

545		MNN043	Meningioma, Familial	79	0.656

546		SCR001	Secretory Meningioma	40	0.656

547		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.656

548		THR035	Thrombasthenia	48	0.656

549		EXN003	Exencephaly	30	0.656

550		PRQ002	Paraquat Poisoning	28	0.656

551		PRS063	Paresthesia	39	0.645

552		ADN027	Adenomyosis	59	0.642

553		LYM143	Lymphoma, Non-Hodgkin, Familial	79	0.642

554		BRR014	Barrett Esophagus	66	0.642

555		TNG007	Tongue Carcinoma	55	0.642

556		CMM005	Common Cold	55	0.642

557		PLC001	Placenta Accreta	44	0.642

558		URN010	Urinary Tract Obstruction	55	0.642

559	P	HYP040	Hypospadias	51	0.642

560		LPT001	Leptospirosis	66	0.642

561		CHL067	Cholecystitis	59	0.642

562		HYP014	Hyperuricemia	51	0.642

563	P	VNT002	Ventricular Septal Defect	58	0.642

564	P	RTN022	Retinal Vein Occlusion	54	0.642

565	P	PLL002	Pellagra	46	0.642

566		MLG079	Malignant Pleural Mesothelioma	42	0.642

567		GRN017	Granulocytopenia	42	0.642

568		ORL011	Oral Cancer	60	0.642

569	P	HMC002	Homocystinuria	52	0.642

570	P	OVR082	Overgrowth Syndrome	42	0.642

571		HYP005	Hypokalemia	55	0.632

572	P	PLY041	Polymyositis	59	0.627

573		BCL014	B-Cell Growth Factor	32	0.627

574		SPS007	Spastic Cerebral Palsy	46	0.627

575		SRC027	Sarcoma, Synovial	58	0.627

576		PRL045	Proline-Negative Auxotroph of Hamster, Complementation of	16	0.627

577		MYL031	Myeloproliferative Neoplasm	66	0.627

578		DBT007	Diabetic Cataract	35	0.627

579		HMS001	Hemosiderosis	48	0.627

580		CRT004	Carotid Artery Thrombosis	39	0.627

581		CLL003	Cellulitis	53	0.627

582		CCC002	Coccidiosis	50	0.627

583		BRS051	Breast Disease	58	0.627

584		LYS002	Lysosomal Storage Disease	51	0.627

585		ANX004	Anoxia	40	0.627

586		ADG002	Audiogenic Seizures	25	0.627

587	P	RRH023	Rare Hereditary Hemochromatosis	53	0.627

588	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.619

589	P	LTR001	Lateral Sclerosis	58	0.619

590		END040	Endogenous Depression	54	0.619

591		DPR016	Depression	65	0.619

592		GST050	Gastrointestinal System Disease	55	0.619

593		CPR004	Coproporphyria, Hereditary	57	0.613

594		EPL199	Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure	36	0.613

595		NNT012	Neonatal Jaundice	53	0.613

596		RNL078	Renal Dysplasia	46	0.613

597		CHR005	Chorioamnionitis	50	0.610

598	P	LYM033	Lymphoproliferative Syndrome	59	0.610

599	P	ACN011	Acne	55	0.610

600	c	VRL007	Viral Encephalitis	50	0.610

601	P	HYP050	Hyperinsulinemic Hypoglycemia	56	0.610

602		PLS007	Plasmodium Falciparum Malaria	52	0.610

603		ASP004	Asphyxia Neonatorum	50	0.610

604	P	MST009	Mastocytosis	64	0.610

605		SKN005	Skin Atrophy	41	0.610

606		THL004	Theileriasis	26	0.610

607		VSC003	Visceral Leishmaniasis	54	0.610

608		PTH003	Pathologic Nystagmus	52	0.610

609	P	RBL001	Rubella	58	0.610

610		FSC002	Fascioliasis	44	0.610

611		CNG092	Congenital Extrahepatic Portosystemic Shunt	24	0.610

612		LMN011	Laminopathy	35	0.610

613		PLY100	Polyploidy	36	0.610

614	c	VRL010	Viral Hepatitis	52	0.604

615		LMY002	Leiomyoma	51	0.604

616		APH001	Aphthous Stomatitis	57	0.604

617		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.602

618		CHR682	Chronic Bilirubin Encephalopathy	37	0.602

619	c	NRF023	Neurofibromatosis, Type Ii	70	0.591

620		RST011	Restrictive Dermopathy, Lethal	51	0.591

621	c	FTL067	Fetal Hemoglobin Quantitative Trait Locus 6	24	0.591

622	c	AST034	Asthma-Related Traits 4	28	0.591

623	P	THR005	Thrombotic Thrombocytopenic Purpura	64	0.591

624		TNG009	Tongue Squamous Cell Carcinoma	43	0.591

625		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.591

626	c	CRD150	Cardiomyopathy, Familial Hypertrophic, 18	25	0.591

627		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	33	0.591

628		RNL051	Renal Cysts and Diabetes Syndrome	57	0.591

629	P	BRB001	Beriberi	44	0.591

630		NPH009	Nephrolithiasis	54	0.591

631	P	RTN018	Retinal Disease	53	0.591

632		KWS001	Kwashiorkor	44	0.591

633		ALC009	Alcoholic Liver Cirrhosis	54	0.591

634	P	HYP061	Hypertrophic Cardiomyopathy	69	0.591

635		DBT008	Diabetic Angiopathy	47	0.591

636	P	INT099	Intrahepatic Cholestasis of Pregnancy	61	0.591

637		INT075	Intracranial Hypertension	52	0.591

638	P	SBR004	Seborrheic Dermatitis	44	0.591

639		ART008	Arteriosclerosis Obliterans	40	0.591

640		TCL027	T-Cell Acute Lymphoblastic Leukemia	52	0.591

641		DSS012	Disseminated Infection with Mycobacterium Avium Complex	18	0.591

642		HPR003	Heparin-Induced Thrombocytopenia	47	0.591

643		LRY026	Laryngeal Cleft	28	0.591

644		CVD001	Covid-19	58	0.589

645	P	MJR001	Major Depressive Disorder	68	0.589

646		MNT002	Mental Depression	56	0.589

647		PRT038	Protein-Energy Malnutrition	53	0.589

648	P	BRN022	Bronchiectasis	59	0.589

649	P	PLY014	Polycystic Kidney Disease	71	0.583

650	P	RHM011	Rheumatoid Arthritis	81	0.583

651		PMP014	Pemphigoid	49	0.572

652	P	MCR129	Microvascular Complications of Diabetes 1	68	0.572

653		INT002	Intermittent Claudication	61	0.572

654	P	MTR014	Motor Neuron Disease	65	0.572

655		MTC005	Mitochondrial Metabolism Disease	45	0.572

656		BLL006	Bullous Pemphigoid	61	0.572

657		THL010	Thalassemia Minor	31	0.570

658		CYS005	Cysticercosis	60	0.570

659	P	BRN019	Bernard-Soulier Syndrome	61	0.570

660		VLV047	Volvulus of Midgut	55	0.570

661		WTH001	Withdrawal Disorder	47	0.570

662		HND015	Hand Skill, Relative	29	0.570

663	P	TMP003	Temporal Arteritis	68	0.570

664		CRC001	Cercarial Dermatitis	28	0.570

665		ATR057	Atrioventricular Block	54	0.570

666	c	PST001	Posterior Myocardial Infarction	20	0.570

667		MGS001	Megaesophagus	44	0.570

668	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.570

669	P	AGG001	Aggressive Periodontitis	55	0.570

670		DPH001	Diphtheria	59	0.570

671	P	CHR012	Chronic Granulomatous Disease	69	0.570

672		SYS004	Systemic Mastocytosis	62	0.570

673		BLR008	Bilirubin Metabolic Disorder	57	0.570

674	c	SCN007	Secondary Hyperparathyroidism	51	0.570

675	P	JNC001	Junctional Epidermolysis Bullosa	53	0.570

676		PRS042	Prostate Disease	42	0.570

677	P	MLG074	Malignant Mesenchymoma	40	0.570

678		CRL001	Cerulean Cataract	26	0.570

679	c	ATM075	Autoimmune Encephalitis	39	0.570

680		ILS001	Ileus	49	0.570

681	c	BCT007	Bacterial Meningitis	55	0.570

682		ERY069	Erythrokeratoderma ''en Cocardes''	26	0.570

683		PCH007	Pouchitis	42	0.570

684		BHR001	Behr Syndrome	50	0.558

685	P	PRC031	Preeclampsia/eclampsia 1	43	0.558

686		CLN002	Colon Mucinous Adenocarcinoma	28	0.558

687		BRN038	Bronchial Disease	51	0.558

688		AST006	Astigmatism	46	0.553

689		MMM006	Mammographic Density	39	0.553

690	P	CRN028	Corneal Ulcer	47	0.553

691		LGH007	Leigh Syndrome	70	0.545

692	c	DFN036	Deafness, X-Linked 2	44	0.545

693	P	TMR010	Tumor Predisposition Syndrome	69	0.545

694		MRG003	Marginal Zone B-Cell Lymphoma	52	0.545

695	c	DWL002	Dowling-Degos Disease 1	58	0.545

696	P	SCL047	Sclerocornea	32	0.545

697	P	PRP034	Purpura Fulminans	41	0.545

698	P	FLL037	Follicular Lymphoma	73	0.545

699		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.545

700		ANG046	Angioimmunoblastic T-Cell Lymphoma	51	0.545

701		DYS015	Dysentery	50	0.545

702		LKS001	Leukostasis	40	0.545

703		CNT047	Contact Dermatitis	57	0.545

704		ANR004	Anuria	44	0.545

705	P	PNC025	Panic Disorder	52	0.545

706		FNG003	Fungal Esophagitis	21	0.545

707		ORL005	Oral Candidiasis	55	0.545

708		DRF001	Dirofilariasis	32	0.545

709		CNS002	Constrictive Pericarditis	39	0.545

710	c	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.545

711	P	END047	Endophthalmitis	53	0.545

712		PRP007	Priapism	46	0.545

713		PRN008	Peroneal Nerve Paralysis	24	0.545

714		MNN004	Meningothelial Meningioma	25	0.545

715		HRN003	Heroin Dependence	44	0.545

716		GNT019	Giant Cell Myocarditis	29	0.545

717		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	44	0.545

718	P	ACT105	Acute Mountain Sickness	52	0.545

719	P	RSS029	Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha	16	0.545

720	P	PRS038	Personality Disorder	65	0.532

721	P	SBS003	Substance Abuse	54	0.532

722		MYF001	Myofibroma	42	0.532

723	P	EYD002	Eye Disease	57	0.532

724	c	HMC039	Hemochromatosis, Type 1	73	0.512

725		GLN010	Glanzmann Thrombasthenia	66	0.512

726		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	40	0.512

727		XRP001	Xerophthalmia	42	0.512

728		PRM013	Premature Menopause	57	0.512

729		PLY150	Polykaryocytosis Inducer	29	0.512

730		WND001	Wound Botulism	35	0.512

731		ORG002	Organic Acidemia	43	0.512

732		INT146	Intervertebral Disc Disease	61	0.512

733		PLP001	Pulpitis	48	0.512

734	P	TLN014	Tl Antigen	18	0.512

735		KRT001	Keratoconjunctivitis Sicca	49	0.512

736	c	INF023	Inflammatory Breast Carcinoma	48	0.512

737	P	ICH004	Ichthyosis	56	0.512

738	P	MTR003	Mitral Valve Stenosis	53	0.512

739		CHR073	Choreatic Disease	53	0.512

740		EPC002	Epicondylitis	43	0.512

741		CHR096	Chronic Pulmonary Heart Disease	41	0.512

742		SLC006	Silicosis	55	0.512

743		SKN022	Skin Squamous Cell Carcinoma	54	0.512

744		GST007	Gastric Dilatation	29	0.512

745		INC021	Incontinentia Pigmenti	63	0.512

746	c	RTN047	Retinitis Pigmentosa 18	45	0.512

747	c	RNG019	Ring Chromosome 3	19	0.512

748		OPD006	Opioid Addiction	48	0.512

749		TBR011	Tuberculous Meningitis	48	0.512

750		BRK012	Broken Heart Syndrome	42	0.512

751		ECC004	Eccrine Porocarcinoma	40	0.512

752	P	HYP121	Hypoalphalipoproteinemia	42	0.512

753		PNM013	Pneumococcal Meningitis	43	0.512

754		HYP855	Hyperpigmentation of the Skin	26	0.512

755		RSP019	Respiratory Distress Syndrome in Premature Infants	52	0.507

756		HYP781	Hypoascorbemia	52	0.507

757		DSS008	Disease of Mental Health	74	0.507

758	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.507

759		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	58	0.507

760		NWB001	Newborn Respiratory Distress Syndrome	56	0.507

761	c	HPT007	Hepatitis E	50	0.507

762		NRT001	Neurotic Disorder	56	0.507

763		FNG016	Fungal Keratitis	39	0.507

764		HRW001	Hair Whorl	35	0.506

765	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.475

766		LMY014	Leiomyoma, Uterine	55	0.475

767		VTM033	Vitamin K Deficiency Bleeding	50	0.475

768		MLT157	Multiple System Atrophy 1	69	0.475

769		CNN001	Cannabis Dependence	38	0.475

770		PLM012	Pulmonary Sarcoidosis	53	0.475

771		DBT002	Diabetic Autonomic Neuropathy	40	0.475

772	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.475

773		CTS005	Catastrophic Antiphospholipid Syndrome	43	0.475

774		CCN002	Cocaine Abuse	49	0.475

775		PLL009	Pellucid Marginal Degeneration	21	0.475

776		CNN002	Cannabis Abuse	44	0.475

777		CRN030	Coronary Stenosis	50	0.474

778		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.453

779		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	64	0.433

780	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	58	0.433

781		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	48	0.433

782		CNR001	Coenurosis	26	0.433

783	c	MCR382	Microcephaly 26, Primary, Autosomal Dominant	18	0.433

784	c	MCR383	Microcephaly 27, Primary, Autosomal Dominant	12	0.433

785	P	AST056	Asthma-Related Traits 2	28	0.433

786		IMM064	Immunodeficiency, Common Variable, 10	43	0.433

787		LRY018	Laryngeal Squamous Cell Carcinoma	47	0.433

788	P	CYS039	Cystic Kidney Disease	52	0.433

789	P	MCR010	Microcephaly	59	0.433

790	c	PRM212	Primary Microcephaly	40	0.433

791		PST053	Postherpetic Neuralgia	40	0.433

792		RSC001	Rosacea	55	0.433

793		PST021	Postpartum Depression	50	0.433

794		PRN035	Perniosis	27	0.433

795		MYC006	Mycosis Fungoides	65	0.433

796		VCC001	Vaccinia	49	0.425

797	P	LNG064	Lung Cancer Susceptibility 3	70	0.418

798		MDD018	Middle East Respiratory Syndrome	44	0.410

799		PPL052	Papillomatosis, Confluent and Reticulated	34	0.410

800	P	OVR042	Ovarian Cancer	88	0.403

801	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.396

802	P	JBR020	Joubert Syndrome 1	74	0.396

803	c	DSB006	Desbuquois Dysplasia 1	48	0.396

804		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	0.396

805		ABL002	Ablepharon-Macrostomia Syndrome	50	0.396

806	c	MCL062	Mucolipidosis Ii Alpha/beta	69	0.396

807	c	INF071	Inflammatory Bowel Disease 1	65	0.396

808		IMM166	Immunodeficiency 27a	58	0.396

809		ATX049	Ataxia with Vitamin 3 Deficiency	52	0.396

810		ATM052	Autoimmune Disease 1	36	0.396

811		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	46	0.396

812	c	SRC023	Sarcoidosis 2	44	0.396

813		FCT002	Factor Xi Deficiency	61	0.396

814	c	PSR032	Psoriasis 11	47	0.396

815	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	62	0.396

816		VSL013	Visual Impairment and Progressive Phthisis Bulbi	36	0.396

817		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.396

818		ATN013	Autoinflammation, Panniculitis, and Dermatosis Syndrome	48	0.396

819	c	HYP724	Hyperlipoproteinemia, Type Iii	66	0.396

820	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	0.396

821		RSP027	Respiratory Papillomatosis, Juvenile Recurrent, Congenital	47	0.396

822	P	PRG092	Pregnancy Loss, Recurrent 1	42	0.396

823	c	DRR009	Diarrhea 6	46	0.396

824	c	NRP036	Neuropathy, Hereditary Sensory, Type if	33	0.396

825		MYC004	Mycotic Corneal Ulcer	14	0.396

826		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	57	0.396

827	c	EHL078	Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1	51	0.396

828	P	NJM001	Nijmegen Breakage Syndrome	75	0.396

829		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.396

830	c	PSR023	Psoriasis 1	52	0.396

831		ARM010	Arima Syndrome	56	0.396

832		ERY003	Erythema Multiforme	56	0.396

833		SVR097	Severe Cutaneous Adverse Reaction	68	0.396

834	c	SYS043	Systemic Lupus Erythematosus 1	38	0.396

835	c	HYP272	Hypercholesterolemia, Familial, 3	46	0.396

836		URN022	Urinary Tract Infections, Recurrent	27	0.396

837	c	PRM092	Primary Lateral Sclerosis, Adult, 1	38	0.396

838		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	49	0.396

839	P	PHT010	Photoparoxysmal Response 1	45	0.396

840		ADR038	Adermatoglyphia	51	0.396

841	c	BLD140	Blood Group, I System	47	0.396

842		OCL020	Ocular Cicatricial Pemphigoid	52	0.396

843		HYP555	Hypertriglyceridemia, Transient Infantile	38	0.396

844	c	CNG413	Congenital Short Bowel Syndrome	42	0.396

845		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.396

846		MCS006	Macs Syndrome	57	0.396

847	c	PSR018	Psoriasis 13	40	0.396

848	c	PSR028	Psoriasis 7	43	0.396

849		NRL018	Neural Tube Defects, Folate-Sensitive	45	0.396

850		BWN001	Bowen-Conradi Syndrome	54	0.396

851		ACD008	Acid-Labile Subunit Deficiency	52	0.396

852		BLL004	Bullous Keratopathy	47	0.396

853		ACT011	Acute Contagious Conjunctivitis	42	0.396

854		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	30	0.396

855		KRT008	Keratopathy	46	0.396

856	P	CRV039	Cervicitis	52	0.396

857		IRR001	Irregular Astigmatism	32	0.396

858	P	EHL001	Ehlers-Danlos Syndrome	57	0.396

859		RDN001	Reading Disorder	40	0.396

860		GRN055	Granular Corneal Dystrophy	36	0.396

861		CCT002	Cicatricial Pemphigoid	53	0.396

862		MYF002	Myofascial Pain Syndrome	46	0.396

863	c	PSR017	Psoriasis 2	53	0.396

864		MYC088	Mycobacterium Avium Complex Infections	27	0.396

865		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	41	0.396

866		FRS019	Farsightedness	35	0.396

867		ATX019	Ataxia with Vitamin E Deficiency	44	0.396

868		PHT003	Phototoxic Dermatitis	27	0.396

869		PRS011	Persian Gulf Syndrome	35	0.396

870		RSP007	Respiratory Distress Syndrome, Infant	40	0.396

871	P	BRT047	Brittle Cornea Syndrome	42	0.396

872		CNT060	Central Serous Chorioretinopathy	39	0.396

873		AND005	Androgen Insensitivity Syndrome, Mild	21	0.396

874		CHL079	Children's Interstitial Lung Disease	26	0.396

875		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.396

876		CCN001	Cocaine Dependence	48	0.396

877		WSR001	Was-Related Disorders	19	0.396

878		CRY008	Cryopyrin-Associated Periodic Syndrome	48	0.396

879		NNN007	Non-Involuting Congenital Hemangioma	40	0.396

880	c	PLD003	Plod1-Related Kyphoscoliotic Ehlers-Danlos Syndrome	20	0.396

881		END072	Endotheliitis	36	0.396

882		ERY066	Erythema Multiforme Major	29	0.396

883		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	31	0.396

884		CHL065	Cholangiocarcinoma	58	0.395

885		INT079	Intrahepatic Cholangiocarcinoma	51	0.395

886	c	WLM018	Wilms Tumor 5	54	0.391

887	P	SPR093	Spermatogenic Failure, Y-Linked, 2	32	0.387

888		HYP060	Hyperinsulinism	53	0.387

889		DND003	Dendritic Cell Thymoma	23	0.387

890	c	THY086	Thymoma Type B	12	0.387

891		LYM027	Lymphopenia	56	0.379

892		BCK006	Back Pain	43	0.379

893	P	PNM007	Pneumonia	64	0.379

894	P	HYP076	Hyperthyroidism	53	0.379

895	P	GRV001	Graves' Disease	54	0.370

896		THY029	Thyroid Carcinoma	54	0.370

897	c	TYP010	Type C Thymoma	25	0.362

898	P	AVS003	Avascular Necrosis	41	0.362

899		RNL065	Renal Cell Carcinoma, Papillary, 1	79	0.356

900		DNG003	Dengue Disease	65	0.356

901		DNG002	Dengue Hemorrhagic Fever	59	0.356

902		CYS001	Cystic Fibrosis	77	0.353

903	c	PLM164	Pulmonary Hypertension, Primary, 1	80	0.353

904		SPL018	Splenomegaly	47	0.353

905	P	UVT001	Uveitis	57	0.344

906		IGG001	Iga Glomerulonephritis	50	0.344

907	P	ART022	Arthritis	70	0.344

908	c	HNT004	Huntington Disease-Like 2	51	0.335

909		PRT013	Portal Hypertension	59	0.335

910		SVR001	Severe Acute Respiratory Syndrome	68	0.335

911		NRM005	Neuromuscular Disease	63	0.335

912		IMM167	Immune Deficiency Disease	77	0.326

913	P	CTN015	Cutaneous T Cell Lymphoma	48	0.326

914	P	SLM003	Salmonellosis	54	0.326

915	c	SCL052	Scleroderma, Familial Progressive	60	0.326

916		IGR001	Ige Responsiveness, Atopic	59	0.326

917	P	EPL164	Epilepsy	70	0.326

918		PRS045	Prostatic Hypertrophy	52	0.326

919		BCT004	Bacteriuria	48	0.326

920		CRT016	Carotid Artery Disease	52	0.326

921		RYN005	Raynaud Phenomenon	45	0.326

922		PRS129	Prostatic Hyperplasia, Benign	48	0.316

923		TQP001	Taqi Polymorphism	29	0.316

924	P	GRF003	Graft-Versus-Host Disease	71	0.316

925	c	CHR098	Chronic Pyelonephritis	34	0.316

926	P	ATS364	Autism	72	0.316

927		PRS021	Prostatic Adenoma	43	0.316

928	P	OBS001	Obstructive Jaundice	49	0.316

929	P	URT039	Urticaria	57	0.316

930	P	ART023	Arthropathy	60	0.316

931		HMP009	Haemophilus Influenzae	41	0.316

932	P	SCK005	Sickle Cell Disease	56	0.316

933	P	FML011	Familial Adenomatous Polyposis	71	0.306

934	P	CRD119	Cardiac Arrest	68	0.306

935	c	PRG020	Paragangliomas 3	39	0.306

936		CRT013	Carotid Stenosis	51	0.306

937		CHR074	Choriocarcinoma	46	0.306

938	P	TRT010	Teratoma	50	0.306

939		MST020	Mast Cell Activation Syndrome	27	0.306

940		ANT024	Anthrax Disease	58	0.306

941	P	PRC019	Precocious Puberty	49	0.306

942		ACN019	Acanthamoeba Keratitis	30	0.306

943		GLC003	Glucose Intolerance	53	0.295

944	P	THR015	Thrombophilia	51	0.295

945		VRL011	Viral Infectious Disease	60	0.295

946	c	PRD040	Periodontitis, Chronic	52	0.285

947		KWS002	Kawasaki Disease	65	0.285

948		MNT001	Mantle Cell Lymphoma	65	0.285

949		OTT002	Otitis Media	71	0.285

950		BRN012	Bronchiolitis Obliterans	56	0.285

951		HRY003	Hairy Cell Leukemia	61	0.285

952		IMM001	Immune-Complex Glomerulonephritis	36	0.285

953	P	GND004	Gonadal Dysgenesis	46	0.285

954		GST033	Gestational Diabetes	61	0.285

955		TTN003	Tetanus	64	0.285

956