Search results for Cysteine

3391 hits were found for Cysteine

#	Family	MCID	Name	MIFTS	Score
1		RPD005	Rapidly Involuting Congenital Hemangioma	46	27.317

2		MRC009	Mercaptolactate-Cysteine Disulfiduria	20	23.608

3		GLT040	Glutamate-Cysteine Ligase Deficiency	31	15.828

4		GMM011	Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to	25	15.812

5		CYS043	Cysteine Peptiduria	7	15.445

6		HLX001	Helix Syndrome	48	14.949

7		AMP011	Ampola Syndrome	12	10.665

8		HMC014	Homocysteinemia	52	9.046

9		CHG001	Chagas Disease	66	8.030

10		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	7.743

11	P	PRD008	Periodontitis	64	7.653

12	P	KLZ004	Kala-Azar 1	41	7.627

13		LSH001	Leishmaniasis	64	7.627

14		BNR002	Bone Resorption Disease	47	7.490

15		HMN044	Human Immunodeficiency Virus Type 1	78	7.457

16	P	NRB001	Neuroblastoma	66	7.215

17		HYP266	Hypoxia	57	7.052

18	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	6.873

19	P	HMC002	Homocystinuria	53	6.859

20		SVR001	Severe Acute Respiratory Syndrome	67	6.714

21		AGN016	Aging	54	6.708

22		ISC004	Ischemia	61	6.669

23	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	6.453

24	P	LTR001	Lateral Sclerosis	58	6.453

25		47X002	47,xyy	48	6.430

26		CYT002	Cytokine Deficiency	43	6.230

27		48X005	48,xyyy	39	6.214

28	P	MSC005	Muscular Dystrophy	67	6.113

29		THY029	Thyroid Carcinoma	51	6.109

30		BCT022	Bacterial Infectious Disease	56	6.058

31	P	VSC007	Vascular Disease	63	5.942

32	c	NRP064	Neuropathy, Congenital Hypomyelinating, 2	35	5.933

33	P	ALZ034	Alzheimer Disease	87	5.901

34		CYS013	Cystinuria	66	5.884

35		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	5.840

36		PRT037	Pertussis	65	5.816

37		VCC001	Vaccinia	47	5.781

38	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	5.765

39	P	KDN018	Kidney Disease	72	5.738

40		AMB001	Amebiasis	57	5.670

41	P	PLM036	Pulmonary Fibrosis	66	5.665

42	P	OVR042	Ovarian Cancer	88	5.650

43		GLB002	Glioblastoma	67	5.576

44		IMM167	Immune Deficiency Disease	78	5.534

45		MLR004	Malaria	80	5.498

46	P	MLT074	Multiple Endocrine Neoplasia	59	5.475

47		SQM006	Squamous Cell Carcinoma	60	5.414

48	P	PNC035	Pancreatic Cancer	86	5.399

49		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	5.374

50	P	PHC003	Pheochromocytoma	69	5.365

51		GLL048	Glial Tumor	52	5.361

52		CYS010	Cystinosis	62	5.355

53	c	ACT071	Acute Kidney Failure	60	5.353

54	P	MYC084	Mycobacterium Tuberculosis 1	68	5.348

55		GLM045	Glioma	63	5.345

56	P	INF032	Infertility	57	5.323

57		PPL052	Papillomatosis, Confluent and Reticulated	34	5.318

58		CHL123	Chlamydia	58	5.308

59		SLP001	Sleeping Sickness	56	5.291

60	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	5.267

61		THY111	Thyroid Carcinoma, Familial Medullary	67	5.255

62		TXC005	Toxic Shock Syndrome	62	5.247

63	P	PLY011	Polycystic Ovary Syndrome	57	5.222

64	P	HRP006	Herpes Simplex	65	5.217

65		THY125	Thyroid Gland Medullary Carcinoma	48	5.217

66		ADR040	Adrenal Gland Pheochromocytoma	46	5.183

67		CYS001	Cystic Fibrosis	78	5.170

68		BRN071	Brain Injury	50	5.144

69		TRY001	Trypanosomiasis	50	5.128

70	P	PLM037	Pulmonary Hypertension	72	5.122

71		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	5.097

72		BRT054	Brittle Bone Disorder	74	5.091

73		FTT001	Fatty Liver Disease	62	5.019

74	P	SCH015	Schizophrenia	74	5.003

75	P	LKM002	Leukemia	67	4.959

76	P	HPT021	Hepatitis	69	4.952

77		HMS001	Hemosiderosis	48	4.945

78	P	BPL003	Bipolar Disorder	56	4.944

79		ATH013	Atherosclerosis Susceptibility	63	4.935

80	c	MJR022	Major Affective Disorder 8	38	4.924

81	c	MJR024	Major Affective Disorder 9	41	4.924

82		TRC003	Trichomoniasis	53	4.922

83	P	RRH023	Rare Hereditary Hemochromatosis	54	4.920

84		NNL005	Non-Alcoholic Fatty Liver Disease	63	4.863

85	c	MCR120	Microvascular Complications of Diabetes 7	47	4.831

86	P	PRS040	Prostate Cancer	95	4.815

87	P	PRK039	Parkinsonism	55	4.802

88	P	BCL017	B-Cell Lymphoma	59	4.802

89		TRM010	Traumatic Brain Injury	51	4.794

90		HYP066	Hyperglycemia	61	4.765

91		ALC007	Alcohol Dependence	66	4.751

92		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	50	4.741

93		PLM129	Pulmonary Disease, Chronic Obstructive	74	4.734

94	P	PRK057	Parkinson Disease, Late-Onset	80	4.730

95	P	MYC007	Myocardial Infarction	70	4.721

96	P	BRS047	Breast Cancer	98	4.667

97	P	LVR013	Liver Disease	69	4.658

98	c	HPT003	Hepatitis a	63	4.654

99	c	ACT134	Acute Liver Failure	59	4.651

100	P	ATS364	Autism	69	4.608

101	c	ACT027	Acute Pancreatitis	60	4.607

102		SVR004	Severe Combined Immunodeficiency	72	4.605

103	c	MCL042	Macular Degeneration, Age-Related, 1	85	4.579

104	P	ALC033	Alcohol Use Disorder	61	4.566

105		OST159	Osteogenic Sarcoma	66	4.509

106		VSC003	Visceral Leishmaniasis	55	4.488

107		SCH014	Schistosomiasis	56	4.450

108		BRN024	Bronchitis	67	4.434

109		LVR012	Liver Cirrhosis	63	4.430

110	P	HPT023	Hepatocellular Carcinoma	96	4.427

111	P	MLN008	Melanoma	76	4.421

112		MRF001	Marfan Syndrome	76	4.393

113		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	4.385

114		PRS131	Prostate Cancer/brain Cancer Susceptibility	23	4.378

115	P	AMY004	Amyloidosis	70	4.376

116	P	PNC044	Pancreatitis	61	4.374

117	c	MCR113	Microvascular Complications of Diabetes 3	52	4.354

118	c	CHR684	Chronic Kidney Disease	69	4.347

119		DPR016	Depression	65	4.330

120		HYP056	Hypoglycemia	65	4.323

121	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	67	4.293

122	P	CTR002	Cataract	60	4.265

123	P	GST053	Gastric Cancer	83	4.262

124	P	LNG032	Lung Cancer	98	4.261

125	P	DBT009	Diabetes Mellitus	67	4.224

126		MNT002	Mental Depression	57	4.214

127	P	THR014	Thrombocytopenia	66	4.191

128	P	CLR023	Colorectal Cancer	100	4.187

129	c	HPT073	Hepatitis C Virus	71	4.142

130	P	ADL010	Adult Respiratory Distress Syndrome	71	4.129

131	c	HYP836	Hypercholesterolemia, Familial, 1	73	4.125

132	c	TYP009	Type 2 Diabetes Mellitus	92	4.113

133	P	INF038	Influenza	68	4.087

134		PLM134	Pulmonary Fibrosis, Idiopathic	76	4.083

135	c	MCR115	Microvascular Complications of Diabetes 5	65	4.073

136	P	HNT016	Huntington Disease	73	4.020

137	c	PCH010	Pachyonychia Congenita 3	43	4.008

138	c	MCR130	Microvascular Complications of Diabetes 6	41	3.999

139	c	MCR133	Microvascular Complications of Diabetes 4	41	3.999

140		BRN056	Bronchopulmonary Dysplasia	56	3.996

141		CTN007	Cutaneous Leishmaniasis	62	3.981

142	c	TYP008	Type 1 Diabetes Mellitus	70	3.981

143		MSC157	Muscular Dystrophy, Duchenne Type	79	3.975

144	P	GST044	Gastritis	55	3.954

145		PRG008	Paragonimiasis	37	3.913

146	P	MYP004	Myopathy	67	3.902

147		PNC041	Pancreatic Ductal Adenocarcinoma	51	3.865

148		CYS019	Cystathioninuria	46	3.843

149	c	WLM013	Wilms Tumor 1	66	3.825

150	P	CRN300	Coronary Heart Disease 1	73	3.816

151	P	GLM040	Glioma Susceptibility 1	71	3.816

152	P	FBR017	Fibrosarcoma	56	3.790

153	c	SML038	Small Cell Cancer of the Lung	69	3.774

154		ATM095	Autoimmune Disease	61	3.772

155	P	RTN008	Retinitis Pigmentosa	80	3.767

156		NRR001	Neuroretinitis	42	3.767

157		RTN023	Retinitis	46	3.767

158	c	PRC016	Pre-Eclampsia	65	3.760

159		INS024	Insulin-Like Growth Factor I	78	3.756

160		HMP009	Haemophilus Influenzae	41	3.751

161		IRN002	Iron Metabolism Disease	57	3.729

162	c	HPT001	Hepatitis C	62	3.728

163		MLG169	Malignant Astrocytoma	57	3.701

164	c	LKM061	Leukemia, Acute Myeloid	83	3.699

165	P	MLN007	Male Infertility	56	3.696

166	c	PRD040	Periodontitis, Chronic	52	3.688

167		ACQ007	Acquired Immunodeficiency Syndrome	59	3.656

168	P	ADN016	Adenocarcinoma	63	3.643

169	c	MGR028	Migraine with or Without Aura 1	64	3.642

170	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	3.594

171	c	BRN108	Branchiootic Syndrome 1	62	3.592

172		OST012	Osteoarthritis	77	3.590

173		ANX004	Anoxia	40	3.582

174		CHL014	Cholera	62	3.578

175	P	URN019	Urinary Tract Infection	49	3.571

176	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	3.559

177		PRT251	Proteinuria, Chronic Benign	57	3.552

178		SPN035	Spindle Cell Sarcoma	54	3.548

179		SRC014	Sarcoma	65	3.548

180		CLN003	Clonorchiasis	43	3.541

181		LNG099	Lung Disease	62	3.514

182	c	ACT068	Acute Cystitis	61	3.506

183		PLY150	Polykaryocytosis Inducer	29	3.498

184	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	3.497

185	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	3.497

186	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	3.497

187	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	3.497

188	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	3.497

189	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	3.497

190	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	3.497

191	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	3.497

192	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	3.497

193	c	HYP724	Hyperlipoproteinemia, Type Iii	67	3.479

194		ALL029	Allergic Disease	59	3.479

195	P	RTN016	Retinal Degeneration	52	3.478

196		ATS010	Autosomal Recessive Disease	42	3.469

197	P	MLT020	Multiple Sclerosis	79	3.464

198	P	LKM062	Leukemia, Acute Lymphoblastic	69	3.464

199		CVD001	Covid-19	57	3.452

200		FSC002	Fascioliasis	44	3.448

201	P	ENC018	Encephalopathy	62	3.440

202		NNL006	Non-Alcoholic Steatohepatitis	54	3.421

203		PRC051	Paracetamol Poisoning	29	3.419

204		CLT003	Colitis	63	3.405

205		ART140	Arteries, Anomalies of	53	3.400

206		LPP008	Lipoprotein Quantitative Trait Locus	65	3.400

207	c	FML021	Familial Hypercholesterolemia	72	3.384

208		CYS005	Cysticercosis	60	3.366

209	P	MSC003	Muscular Atrophy	52	3.363

210	P	RTN024	Retinoblastoma	73	3.358

211	P	LNG064	Lung Cancer Susceptibility 3	70	3.358

212	c	INH020	Inherited Metabolic Disorder	48	3.351

213	c	PRT132	Protoporphyria, Erythropoietic, 1	61	3.349

214		PLM001	Pulmonary Tuberculosis	69	3.330

215	P	PRP029	Porphyria	60	3.322

216		TBC004	Tobacco Addiction	63	3.316

217	P	SZR006	Seizure Disorder	70	3.311

218		LYS002	Lysosomal Storage Disease	51	3.302

219	P	MJR001	Major Depressive Disorder	68	3.294

220	P	EPL164	Epilepsy	68	3.288

221		LPD008	Lipid Metabolism Disorder	62	3.286

222		STM007	Stomatitis	54	3.279

223	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	3.278

224	P	HML002	Hemolytic Anemia	62	3.268

225		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	3.251

226	c	LKM005	Leukemia, T-Cell, Chronic	34	3.251

227		RNL114	Renal Cell Carcinoma, Nonpapillary	80	3.246

228	P	DMN002	Dementia	66	3.239

229	c	HPT016	Hepatitis B	62	3.237

230	P	BLD134	Bladder Cancer	79	3.215

231		ENT011	Enterocolitis	55	3.214

232		CRB004	Cerebral Artery Occlusion	45	3.199

233	P	VNW001	Von Willebrand's Disease	65	3.197

234	P	RHM011	Rheumatoid Arthritis	82	3.180

235		SPN186	Spinal Cord Injury	61	3.173

236		STR067	Stroke, Ischemic	80	3.163

237		ALL014	Allergic Encephalomyelitis	34	3.163

238		PRN019	Perinatal Necrotizing Enterocolitis	60	3.146

239		NWC001	Newcastle Disease	47	3.140

240	P	BRS044	Breast Adenocarcinoma	58	3.129

241	P	HRT032	Heart Disease	81	3.118

242		INS001	Insulinoma	59	3.117

243	P	TRN020	Turner Syndrome	67	3.114

244		MSL001	Measles	61	3.089

245		HRN029	Hearing Loss, Noise-Induced	37	3.086

246	P	HYP086	Hypothyroidism	69	3.076

247		OBS002	Obsessive-Compulsive Disorder	68	3.068

248	P	THL005	Thalassemia	56	3.067

249		ALC006	Alcoholic Hepatitis	61	3.064

250		FRN006	Frontotemporal Dementia	68	3.062

251	P	MYL006	Myeloid Leukemia	61	3.059

252	P	HDC001	Headache	57	3.044

253		ARG004	Argyria	26	3.043

254		DPH001	Diphtheria	59	3.043

255	P	ENC004	Encephalitis	61	3.036

256		MLD018	Mild Cognitive Impairment	48	3.005

257		SKN016	Skin Disease	63	3.003

258	c	EXD008	Exudative Vitreoretinopathy 1	71	3.002

259	P	ART022	Arthritis	71	2.987

260		MTB004	Metabolic Acidosis	48	2.985

261		GST045	Gastroenteritis	58	2.985

262	c	NMN015	Niemann-Pick Disease, Type C1	68	2.972

263	P	INF037	Inflammatory Bowel Disease	53	2.971

264		VLV047	Volvulus of Midgut	52	2.966

265		TRC010	Trichotillomania	50	2.934

266	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	2.934

267		PRP030	Purpura	54	2.931

268	P	ALP008	Alopecia	54	2.926

269		VSC002	Vascular Dementia	60	2.923

270		PRP027	Peripheral Vascular Disease	71	2.911

271		BRN002	Bronchiolitis	57	2.911

272	P	THR005	Thrombotic Thrombocytopenic Purpura	64	2.875

273	c	ACT073	Acute Leukemia	58	2.874

274		CRV035	Cervical Cancer	73	2.866

275		CHL068	Cholestasis	61	2.860

276		ESP021	Esophageal Cancer	83	2.853

277		CNT047	Contact Dermatitis	57	2.848

278		SQM013	Squamous Cell Carcinoma, Head and Neck	73	2.845

279	c	ATS007	Autism Spectrum Disorder	72	2.839

280		URM002	Uremia	47	2.838

281		DSS032	Disease by Infectious Agent	55	2.833

282	P	DRM053	Dermatitis, Atopic	65	2.832

283		CRB039	Cerebrovascular Disease	66	2.832

284		DFC004	Deficiency Anemia	74	2.830

285	P	NMN002	Niemann-Pick Disease	60	2.816

286	P	CHR345	Chronic Pain	50	2.799

287		NRL016	Neural Tube Defects	81	2.798

288		TLN003	Telangiectasis	51	2.798

289		ORL011	Oral Cancer	60	2.798

290		ACT119	Acute Promyelocytic Leukemia	62	2.786

291	P	RHN004	Rhinitis	57	2.780

292	c	DLT002	Dilated Cardiomyopathy	78	2.779

293	P	PRP019	Peripheral Nervous System Disease	58	2.777

294	c	HPT007	Hepatitis E	51	2.772

295		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	2.770

296	P	AST005	Asthma	76	2.759

297	P	BND020	Bone Disease	59	2.757

298	c	HYP595	Hypertension, Essential	85	2.756

299	P	KDN017	Kidney Cancer	61	2.744

300		VGN023	Vaginitis	56	2.735

301	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	65	2.733

302		GRD001	Giardiasis	46	2.719

303	P	TRM003	Tremor	48	2.712

304		BBS001	Babesiosis	49	2.712

305		MTH009	Mouth Disease	57	2.700

306	P	SKN015	Skin Carcinoma	71	2.699

307		CHL147	Chlamydia Pneumonia	47	2.698

308		PPL022	Papilloma	53	2.698

309		SPR006	Sparganosis	35	2.698

310	c	ATR087	Atrial Standstill 1	74	2.688

311		BRK010	Burkitt Lymphoma	66	2.679

312		SQM002	Squamous Cell Papilloma	46	2.677

313		MCS002	Mucositis	56	2.676

314		NCR007	Necrotizing Fasciitis	49	2.673

315		FSC004	Fasciitis	49	2.673

316		END086	End Stage Renal Disease	52	2.671

317	P	ATX030	Ataxia-Telangiectasia	80	2.669

318	P	GLM007	Glomerulonephritis	60	2.661

319		ULC004	Ulcerative Colitis	74	2.649

320		PRT036	Peritonitis	65	2.644

321		ALL006	Allergic Asthma	56	2.643

322		MNN009	Meningoencephalitis	48	2.643

323		TTN003	Tetanus	65	2.643

324	P	PLY019	Polyneuropathy	52	2.643

325		NTR005	Nutritional Deficiency Disease	61	2.642

326		HRW001	Hair Whorl	35	2.631

327	P	DBT005	Diabetes Insipidus	54	2.625

328	P	ISL078	Isolated Ectopia Lentis	58	2.625

329		MDD018	Middle East Respiratory Syndrome	44	2.625

330		PTH002	Pathological Gambling	48	2.621

331		CRH001	Crohn's Disease	80	2.616

332	P	END044	Endometriosis	62	2.598

333		DWR001	Dwarfism	44	2.598

334	c	OST080	Osteogenesis Imperfecta, Type Ii	56	2.587

335	P	RTN018	Retinal Disease	53	2.575

336		CHL065	Cholangiocarcinoma	58	2.570

337		INT079	Intrahepatic Cholangiocarcinoma	51	2.570

338	P	OST002	Osteoporosis	76	2.568

339	P	ART021	Arteriosclerosis	54	2.568

340		PSY004	Psychotic Disorder	66	2.557

341	P	PNM007	Pneumonia	67	2.552

342		PYC001	Pycnodysostosis	55	2.549

343		THR024	Thrombosis	56	2.547

344		PRT038	Protein-Energy Malnutrition	53	2.541

345	P	ATR005	Atrophic Gastritis	50	2.535

346	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	2.529

347	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	2.529

348		MYL069	Myeloma, Multiple	77	2.528

349		ALL010	Allergic Contact Dermatitis	56	2.510

350		ART016	Aortic Aneurysm	68	2.490

351		CLN015	Colon Adenocarcinoma	65	2.489

352		ALL003	Allergic Rhinitis	67	2.487

353	P	HYP069	Hyperparathyroidism	62	2.486

354		CHK001	Chikungunya	60	2.483

355		ADN018	Adenoma	59	2.478

356		HMZ003	Homozygous Familial Hypercholesterolemia	60	2.467

357	P	NSP012	Nasopharyngeal Carcinoma	61	2.466

358		CHC001	Chickenpox	57	2.445

359		GLT007	Glutathione Synthetase Deficiency	48	2.433

360		GLC009	Glucosephosphate Dehydrogenase Deficiency	53	2.430

361	c	TRC125	Trichothiodystrophy 7, Nonphotosensitive	19	2.429

362		KRT002	Keratomalacia	55	2.425

363	P	NRP001	Neuropathy	60	2.423

364		BRN004	Brain Edema	54	2.423

365	P	MCR129	Microvascular Complications of Diabetes 1	68	2.419

366	P	PRV006	Pervasive Developmental Disorder	52	2.419

367		PLY105	Polycystic Ovary Syndrome 1	39	2.416

368	P	NRF002	Neurofibromatosis	57	2.410

369		ANT039	Antisynthetase Syndrome	55	2.408

370		MDD011	Mood Disorder	62	2.398

371		BCT002	Bacterial Vaginosis	53	2.393

372	c	HMC039	Hemochromatosis, Type 1	73	2.386

373		HVY002	Heavy Metal Poisoning	22	2.370

374	P	DNG005	Dengue Virus	56	2.365

375		LYM017	Lyme Disease	62	2.365

376	P	BNG032	Benign Mesothelioma	53	2.365

377		ORL015	Oral Squamous Cell Carcinoma	43	2.363

378	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	2.355

379		GLC003	Glucose Intolerance	54	2.355

380	P	TMP001	Temporal Lobe Epilepsy	49	2.355

381	c	OST135	Osteogenesis Imperfecta, Type I	53	2.350

382	c	SYS001	Systemic Lupus Erythematosus	87	2.350

383		APH002	Aphasia	56	2.341

384		DWN001	Down Syndrome	70	2.334

385	P	CLC063	Celiac Disease 1	66	2.334

386		LMY003	Leiomyomatosis	44	2.332

387		INT020	Intravenous Leiomyomatosis	36	2.332

388		PRM004	Primary Amebic Meningoencephalitis	27	2.325

389	P	OVR082	Overgrowth Syndrome	49	2.322

390		ANR040	Aneurysm	61	2.322

391	P	EYD002	Eye Disease	57	2.321

392	P	MRC003	Mercury Poisoning	49	2.309

393	c	PLM164	Pulmonary Hypertension, Primary, 1	76	2.309

394		HYP060	Hyperinsulinism	54	2.309

395	P	EXN002	Exanthem	58	2.300

396		GNG013	Gingivitis	59	2.300

397	P	SCK005	Sickle Cell Disease	56	2.300

398	c	DNT047	Dentinogenesis Imperfecta Type 2	35	2.300

399	c	MCR112	Microvascular Complications of Diabetes 2	42	2.299

400		HPT004	Hepatic Coma	43	2.295

401		HYP014	Hyperuricemia	51	2.288

402		IMP005	Impotence	52	2.277

403		STR077	Streptococcal Toxic-Shock Syndrome	35	2.266

404		CLL003	Cellulitis	53	2.255

405		URL001	Urolithiasis	46	2.255

406	P	MDL005	Medulloblastoma	75	2.255

407		BRN028	Brain Cancer	74	2.255

408	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	2.255

409		MLT135	Multiple Sulfatase Deficiency	53	2.254

410		HYP003	Hypermethioninemia	51	2.234

411	P	LYM118	Lymphoma	67	2.232

412		KPS004	Kaposi Sarcoma	77	2.224

413	P	PRN023	Prion Disease	60	2.224

414	P	SPP010	Suppressor of Tumorigenicity 3	51	2.214

415		CMB007	Combined Immunodeficiency	57	2.211

416		PRS045	Prostatic Hypertrophy	53	2.208

417	P	HRS035	Hirschsprung Disease 1	66	2.203

418		GT001	Gout	64	2.203

419		ANX010	Anxiety	70	2.196

420	P	LPS004	Lupus Erythematosus	61	2.196

421		ANG054	Angina Pectoris	66	2.188

422	P	MJR007	Major Affective Disorder 1	42	2.187

423		HPT019	Hepatic Encephalopathy	59	2.186

424	P	SLP006	Sleep Apnea	69	2.186

425		MNN043	Meningioma, Familial	79	2.184

426		PPL049	Papillon-Lefevre Syndrome	66	2.183

427	P	LKM071	Leukemia, Chronic Lymphocytic	75	2.180

428		RSP019	Respiratory Distress Syndrome in Premature Infants	52	2.180

429	c	BTT014	Beta-Thalassemia	72	2.164

430		PRS129	Prostatic Hyperplasia, Benign	49	2.160

431		CWP001	Cowpox	45	2.160

432		PRS021	Prostatic Adenoma	43	2.160

433		KRT009	Keratosis	53	2.160

434		SPN051	Spondylitis	51	2.158

435		INF009	Inflammatory Spondylopathy	30	2.158

436	P	SNS001	Sensorineural Hearing Loss	59	2.156

437		HYP781	Hypoascorbemia	52	2.144

438	c	LKM063	Leukemia, Chronic Myeloid	71	2.136

439	P	RHB003	Rhabdomyosarcoma	66	2.136

440		DYS015	Dysentery	50	2.136

441	P	ECL001	Eclampsia	52	2.136

442		END057	Endometrial Cancer	72	2.134

443		PLG002	Plague	58	2.134

444		SPN209	Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations	66	2.133

445		NWB001	Newborn Respiratory Distress Syndrome	56	2.116

446		ACT098	Acute Erythroid Leukemia	55	2.112

447	P	PSR002	Psoriasis	63	2.112

448		CCC002	Coccidiosis	50	2.112

449		NRN005	Neuronal Ceroid-Lipofuscinoses	61	2.112

450		SCR001	Secretory Meningioma	40	2.111

451		LYM002	Lymphoplasmacyte-Rich Meningioma	35	2.111

452		SPN021	Spinal Meningioma	50	2.111

453		SPL018	Splenomegaly	49	2.111

454	c	THY107	Thymoma, Familial	42	2.107

455		SLF014	Sulfite Oxidase Deficiency, Isolated	53	2.107

456	P	THY023	Thymoma	64	2.107

457	P	SRC025	Sarcoidosis 1	71	2.106

458	P	GRF003	Graft-Versus-Host Disease	71	2.098

459	c	THR092	Thrombophilia Due to Thrombin Defect	74	2.098

460		HLC007	Helicobacter Pylori Infection	67	2.090

461		LMY002	Leiomyoma	51	2.080

462		OTT002	Otitis Media	71	2.071

463		LYM019	Lymphosarcoma	46	2.071

464	P	DRR001	Diarrhea	55	2.069

465	P	RBL001	Rubella	58	2.065

466		PNC129	Pancreatic Adenocarcinoma	65	2.065

467		END040	Endogenous Depression	55	2.060

468	P	FRD001	Friedreich Ataxia	61	2.060

469	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	70	2.060

470		HPT022	Hepatoblastoma	54	2.060

471		PPT005	Peptic Ulcer Disease	58	2.060

472		PHN003	Phenylketonuria	76	2.052

473		DNT012	Dental Caries	53	2.052

474		BRS099	Breast Ductal Carcinoma	61	2.045

475	P	OPN001	Open-Angle Glaucoma	55	2.036

476		DRM006	Dermatitis	62	2.033

477		FCT001	Factor Viii Deficiency	60	2.023

478	c	HMP029	Hemophilia a	68	2.023

479		VNZ002	Venezuelan Equine Encephalitis	46	2.022

480		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	2.021

481		PST011	Pustulosis of Palm and Sole	52	2.016

482		PRP080	Peripheral Artery Disease	54	2.012

483	P	HMP007	Hemophilia	52	2.006

484	P	MTR014	Motor Neuron Disease	65	2.004

485		CRD223	Cardiac Arrhythmia	63	1.995

486	P	LRY044	Larynx Cancer	54	1.994

487	P	ADL017	Adult T-Cell Leukemia	56	1.980

488	P	CRN037	Craniosynostosis	68	1.980

489		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	1.979

490	P	CYS018	Cystitis	59	1.979

491	c	VRL010	Viral Hepatitis	53	1.979

492		PLS007	Plasmodium Falciparum Malaria	52	1.979

493		MTC108	Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency	32	1.973

494		DBT010	Diabetic Neuropathy	54	1.973

495	P	CRD246	Cardiovascular System Disease	56	1.973

496		KRT019	Keratitis, Hereditary	66	1.966

497	c	SCL052	Scleroderma, Familial Progressive	61	1.964

498		CLR109	Colorectal Adenocarcinoma	50	1.964

499		PRM329	Premature Aging	36	1.964

500		RHB024	Rhabdomyosarcoma 2	67	1.958

501	c	SPN225	Spondyloarthropathy 1	70	1.957

502		TRN015	Transient Cerebral Ischemia	63	1.957

503		HGH043	High Grade Glioma	45	1.957

504	P	MYP006	Myopia	56	1.951

505		INT323	Intraocular Pressure Quantitative Trait Locus	64	1.943

506		PST092	Posttransplant Acute Limbic Encephalitis	28	1.940

507		LNG031	Lung Benign Neoplasm	51	1.936

508	P	THN009	Thanatophoric Dysplasia, Type I	63	1.925

509		TRC008	Trachoma	53	1.925

510	P	HRD011	Hereditary Spherocytosis	64	1.918

511	c	SCN036	Secondary Progressive Multiple Sclerosis	55	1.916

512	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	1.914

513		ACT149	Acetaminophen Metabolism	35	1.914

514	P	HYP098	Hypereosinophilic Syndrome	66	1.914

515	P	NTR004	Neutropenia	63	1.909

516	P	CRN025	Corneal Dystrophy	49	1.908

517	P	LMB006	Limb-Girdle Muscular Dystrophy	52	1.898

518	P	VTR007	Vitreoretinopathy	46	1.893

519	P	GCH001	Gaucher's Disease	70	1.893

520	P	TXP001	Toxoplasmosis	60	1.893

521		HRD029	Hereditary Leiomyomatosis and Renal Cell Cancer	56	1.887

522	P	MYC008	Myocarditis	59	1.887

523	P	DYS154	Dystonia	64	1.885

524		DBT087	Diabetes Insipidus, Neurohypophyseal	58	1.882

525	P	MNN013	Meningitis	65	1.869

526		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	1.864

527	P	EHL001	Ehlers-Danlos Syndrome	58	1.863

528		WLS001	Wilson Disease	70	1.861

529	P	HYP076	Hyperthyroidism	53	1.861

530		ADR022	Adrenomyeloneuropathy	39	1.860

531		ADR007	Adrenoleukodystrophy	73	1.860

532		THR035	Thrombasthenia	48	1.860

533		FLR002	Filariasis	55	1.860

534	P	MYC033	Myoclonus	47	1.859

535	P	SBS003	Substance Abuse	54	1.849

536		RTN020	Retinal Vascular Disease	46	1.833

537		CNG034	Congestive Heart Failure	69	1.833

538		MTC005	Mitochondrial Metabolism Disease	45	1.832

539	P	ART023	Arthropathy	61	1.810

540	c	MJR006	Major Affective Disorder 5	32	1.803

541	c	MJR023	Major Affective Disorder 7	33	1.803

542	c	MJR004	Major Affective Disorder 4	28	1.803

543	c	MJR003	Major Affective Disorder 6	32	1.803

544	c	MJR008	Major Affective Disorder 2	34	1.803

545		PFF001	Pfeiffer Syndrome	77	1.803

546		HYP346	Hypotrichosis and Recurrent Skin Vesicles	29	1.803

547		CLS016	Clostridium Difficile Colitis	49	1.803

548		OCL069	Ocular Motor Apraxia	57	1.803

549	P	HMR003	Hemorrhagic Disease	59	1.803

550		SPN008	Spondyloepiphyseal Dysplasia Congenita	54	1.801

551		RCK004	Rickets	68	1.801

552		LNG039	Lung Squamous Cell Carcinoma	57	1.801

553		CNN005	Connective Tissue Disease	67	1.801

554	c	TBR025	Tuberous Sclerosis 1	84	1.792

555	P	RSP003	Respiratory Failure	74	1.789

556	P	ANR048	Aniridia 1	64	1.787

557	P	ASP006	Aspergillosis	72	1.784

558	P	GRV001	Graves' Disease	55	1.784

559		TLR001	Tularemia	56	1.784

560		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	1.784

561		RNL077	Renal Fibrosis	46	1.774

562		GST040	Gastric Adenocarcinoma	67	1.774

563		PRV004	Periventricular Leukomalacia	52	1.774

564		MST020	Mast Cell Activation Syndrome	28	1.774

565		HDN002	Head Injury	44	1.774

566		CLF027	Cleft Palate, Isolated	64	1.769

567	P	HYP061	Hypertrophic Cardiomyopathy	69	1.758

568		GTR002	Goiter	53	1.758

569	P	ESP024	Esophagitis	60	1.745

570		KWS001	Kwashiorkor	45	1.745

571		MCL006	Macular Retinal Edema	57	1.744

572	c	DWL002	Dowling-Degos Disease 1	58	1.744

573		STT001	Status Epilepticus	59	1.744

574		ACT003	Acute Kidney Tubular Necrosis	46	1.739

575	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	1.735

576		PRM236	Primary Biliary Cholangitis	60	1.735

577		DMY004	Demyelinating Disease	50	1.735

578	c	CNG006	Congenital Hypothyroidism	63	1.731

579	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	1.731

580	P	HYP750	Hypertriglyceridemia, Familial	62	1.731

581	P	SYS005	Systemic Scleroderma	74	1.731

582	c	HPT015	Hepatitis D	49	1.731

583	P	MYC026	Myoclonus Epilepsy	35	1.715

584	P	END033	Endocarditis	58	1.713

585	P	SPN052	Spondyloarthropathy	55	1.713

586		PLM012	Pulmonary Sarcoidosis	53	1.709

587		MYL009	Myelodysplastic Syndrome	67	1.704

588		GST023	Gastric Ulcer	52	1.704

589		SNL007	Senile Cataract	40	1.701

590		ACH004	Achondroplasia	66	1.698

591		HMC030	Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency	34	1.690

592	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	1.683

593		TCK004	Tick Infestation	30	1.682

594		OVR094	Ovarian Epithelial Cancer	39	1.682

595		CRZ001	Crouzon Syndrome	65	1.676

596		GST092	Gastroesophageal Reflux	61	1.676

597	P	SCL018	Scoliosis	57	1.676

598		RBS001	Rabies	58	1.676

599	c	PRG011	Progressive Myoclonus Epilepsy	41	1.671

600	P	STR035	Streptococcal Group a Invasive Disease	24	1.665

601		MYC021	Mycobacterium Xenopi	19	1.665

602		PLY028	Polycystic Bone Disease	17	1.651

603		NPH009	Nephrolithiasis	54	1.649

604	P	EPD016	Epidermolysis Bullosa	53	1.649

605		VRL011	Viral Infectious Disease	61	1.647

606	P	PLM034	Pulmonary Emphysema	58	1.647

607	P	LCT001	Lactic Acidosis	51	1.647

608	P	MNC007	Monocytic Leukemia	47	1.647

609	P	PLY014	Polycystic Kidney Disease	69	1.638

610		ADL002	Adult Syndrome	70	1.635

611	c	ADL066	Adult Neuronal Ceroid Lipofuscinosis	46	1.628

612		SLC006	Silicosis	56	1.628

613		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	1.627

614		PRD013	Periodic Fever, Familial, Autosomal Dominant	68	1.618

615	c	ATS307	Autosomal Recessive Cerebellar Ataxia	39	1.618

616		GST050	Gastrointestinal System Disease	55	1.618

617		CHR100	Chronic Ulcer of Skin	57	1.616

618	c	GLC092	Glaucoma, Primary Open Angle	62	1.616

619		SCR011	Scrapie	39	1.616

620		PYR009	Pyridoxine Deficiency Anemia	35	1.616

621	P	LNG028	Long Qt Syndrome	64	1.616

622	P	HYD006	Hydrocephalus	61	1.616

623		DSS009	Disseminated Intravascular Coagulation	57	1.616

624	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	65	1.609

625		LTN004	Late-Onset Retinal Degeneration	60	1.608

626		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	1.608

627		DBT006	Diabetic Macular Edema	48	1.608

628		CCN002	Cocaine Abuse	49	1.608

629	c	SPR086	Spermatogenic Failure 3	46	1.607

630		ANT024	Anthrax Disease	58	1.604

631		ANC001	Ancylostomiasis	39	1.590

632		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	1.588

633	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	1.588

634		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.588

635	P	RTN022	Retinal Vein Occlusion	54	1.588

636		HMN014	Human Immunodeficiency Virus Infectious Disease	54	1.588

637	c	OVR114	Ovarian Cancer 1	59	1.582

638	P	CNR004	Cone-Rod Dystrophy 2	74	1.582

639		PCK003	Pick Disease of Brain	69	1.582

640		PST021	Postpartum Depression	50	1.581

641		PNM013	Pneumococcal Meningitis	43	1.581

642		MSC152	Muscular Dystrophy, Becker Type	69	1.581

643	P	MLG056	Malignant Hyperthermia	66	1.581

644	P	TBR001	Tuberous Sclerosis	69	1.581

645		BRC012	Brucellosis	66	1.581

646		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	1.557

647		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	1.557

648	P	FML011	Familial Adenomatous Polyposis	71	1.557

649	c	ERL056	Early-Onset Parkinson's Disease	40	1.557

650		CHR066	Chronic Fatigue Syndrome	60	1.557

651		CHR074	Choriocarcinoma	46	1.557

652		PRS047	Prostatitis	58	1.550

653	P	CHN012	Chondrosarcoma	57	1.550

654		RTN003	Retinal Ischemia	49	1.550

655	P	BRC006	Brachydactyly	51	1.546

656	c	ACT075	Acute Myocardial Infarction	56	1.546

657		PYR016	Pyridoxine Deficiency	29	1.546

658		CND006	Candida Glabrata	30	1.534

659	c	NRF024	Neurofibromatosis, Type I	72	1.529

660	c	NRD017	Neurodegeneration with Brain Iron Accumulation 1	63	1.526

661		ILT001	Ileitis	48	1.526

662		MTC004	Mitochondrial Encephalomyopathy	42	1.526

663	P	MGR003	Migraine with Aura	52	1.526

664		HRT015	Heritable Pulmonary Arterial Hypertension	46	1.526

665	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	1.526

666		DSS008	Disease of Mental Health	74	1.518

667		NRT001	Neurotic Disorder	56	1.518

668		CRB009	Cerebritis	43	1.518

669	c	CRN110	Cranioectodermal Dysplasia 3	27	1.509

670		LWG006	Low Grade Glioma	41	1.509

671	P	ACN011	Acne	57	1.509

672		CCC001	Coccidioidomycosis	58	1.509

673	P	ALP004	Alport Syndrome	69	1.509

674		CRB037	Cerebral Palsy	67	1.509

675		TRC096	Trichothiodystrophy	55	1.509

676	P	LPS002	Liposarcoma	64	1.508

677	c	ACT135	Acute Graft Versus Host Disease	51	1.497

678		END072	Endotheliitis	36	1.497

679		GLM044	Glomerular Disease	35	1.494

680		MTH071	Methane Production	25	1.494

681	c	MLT159	Multiple Endocrine Neoplasia, Type Iib	61	1.494

682		LGH007	Leigh Syndrome	70	1.494

683	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	1.494

684		GSG001	Gas Gangrene	52	1.494

685	P	MMP001	Mumps	57	1.494

686		CMM005	Common Cold	56	1.494

687	P	INT068	Intestinal Disease	53	1.494

688		INT066	Interstitial Lung Disease	60	1.494

689		LCH001	Leech Infestation	38	1.494

690		VTM002	Vitamin B12 Deficiency	48	1.485

691		YLL002	Yellow Fever	61	1.485

692	c	VRL005	Viral Pneumonia	53	1.479

693	c	ALP101	Alpha-Thalassemia	62	1.473

694		INF034	Infective Endocarditis	54	1.471

695		FLT009	Folate Malabsorption, Hereditary	49	1.471

696		URT010	Ureteral Obstruction	45	1.471

697		CRC021	Carcinosarcoma	64	1.471

698		HMG002	Hemoglobinuria	50	1.471

699		GRN004	Granulomatous Amebic Encephalitis	30	1.471

700		PHR003	Pharyngitis	58	1.471

701	P	GND004	Gonadal Dysgenesis	47	1.471

702		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	58	1.469

703	c	NMN013	Niemann-Pick Disease, Type a	63	1.469

704		ANV001	Anovulation	47	1.469

705		BRN038	Bronchial Disease	51	1.469

706		ACD003	Acid Sphingomyelinase Deficiency	32	1.469

707		CYN003	Cyanide Poisoning	22	1.464

708		IMP004	Impetigo	48	1.464

709		DNG002	Dengue Hemorrhagic Fever	60	1.464

710		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	1.461

711		MNT001	Mantle Cell Lymphoma	67	1.460

712		PLL012	Pollen Allergy	45	1.460

713	P	MTC003	Metachromatic Leukodystrophy	71	1.460

714	P	LKD001	Leukodystrophy	59	1.460

715		FND002	Fundus Dystrophy	55	1.460

716	P	INS002	in Situ Carcinoma	53	1.460

717		XRD010	Xeroderma Pigmentosum, Variant Type	73	1.460

718	P	MVM001	Movement Disease	61	1.455

719		IDP011	Idiopathic Interstitial Pneumonia	59	1.444

720		TRN018	Transitional Cell Carcinoma	56	1.439

721	P	HYP768	Hyperlipoproteinemia, Type I	67	1.431

722		FCS014	Fucosidase Regulator	15	1.431

723	P	PLY018	Polycythemia	56	1.431

724	c	PLM127	Pulmonary Hypertension, Primary, 3	34	1.431

725		LYM011	Lymphogranuloma Venereum	33	1.431

726		FCL014	Focal Epilepsy	53	1.431

727		MST005	Mastitis	53	1.431

728		SPT004	Septic Arthritis	58	1.431

729		RFT001	Rift Valley Fever	48	1.431

730		ANR007	Anorexia Nervosa	60	1.426

731	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	1.426

732		RTN017	Retinal Detachment	60	1.426

733	c	MST023	Mesothelioma, Malignant	56	1.426

734		HTC003	Hutchinson-Gilford Progeria Syndrome	65	1.426

735	P	VSC011	Vasculitis	61	1.426

736	P	SYP003	Syphilis	59	1.426

737		CNT016	Central Retinal Vein Occlusion	54	1.426

738	P	LMY004	Leiomyosarcoma	62	1.426

739		IRR002	Irritable Bowel Syndrome	65	1.426

740		GLN010	Glanzmann Thrombasthenia	66	1.418

741		CRY003	Cryptosporidiosis	56	1.418

742		LYM133	Lymphoma, Hodgkin, Classic	74	1.409

743	P	NPH012	Nephrotic Syndrome	60	1.409

744		FBR047	Fibromyalgia	58	1.405

745		AND002	Androgen Insensitivity Syndrome	63	1.390

746		MRF007	Marfanoid Hypermobility Syndrome	47	1.390

747		CRT072	Creutzfeldt-Jakob Disease	68	1.390

748		MSC007	Muscle Hypertrophy	64	1.390

749		LYM009	Lymphocytic Choriomeningitis	46	1.390

750	P	HYP265	Hypotonia	42	1.390

751	P	RTT002	Rett Syndrome	79	1.389

752		PLS011	Plasmacytoma	56	1.389

753		PLC008	Placenta Disease	49	1.389

754		AMD002	Amed Syndrome, Digenic	37	1.379

755		SCH003	Schizophreniform Disorder	55	1.379

756	P	ATR011	Atrial Fibrillation	66	1.368

757		VGN020	Vaginal Disease	48	1.367

758		ACT228	Acute Radiation Syndrome	30	1.358

759		UNV001	Unverricht-Lundborg Syndrome	53	1.356

760		STN013	Stenotrophomonas Maltophilia Infection	26	1.353

761		FBR012	Fabry Disease	70	1.353

762	P	APL001	Aplastic Anemia	73	1.353

763		DFF005	Diffuse Large B-Cell Lymphoma	54	1.353

764		SCH038	Schopf-Schulz-Passarge Syndrome	51	1.353

765	c	VNW005	Von Willebrand Disease, Type 1	45	1.353

766	P	PMP001	Pemphigus	55	1.353

767		ACT162	Acute Sensory Ataxic Neuropathy	24	1.353

768	P	THY032	Thyroiditis	57	1.353

769	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	1.353

770		CRB027	Cerebellar Disease	47	1.353

771		MYT011	Myotonia	39	1.353

772	P	PLZ001	Pelizaeus-Merzbacher Disease	65	1.345

773		ACN002	Acanthosis Nigricans	56	1.345

774		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	1.345

775	P	PSD003	Pseudohypoaldosteronism	44	1.345

776		AMN003	Amnestic Disorder	54	1.345

777	P	FCL005	Focal Segmental Glomerulosclerosis	57	1.334

778		AMN006	Aminoaciduria	37	1.334

779		AND014	Androgenic Alopecia	47	1.333

780	P	ALP009	Alopecia Areata	59	1.333

781		CNN001	Cannabis Dependence	38	1.332

782		ACT029	Acute Interstitial Pneumonia	59	1.332

783		NRR002	Norrie Disease	61	1.328

784		LGN006	Legionnaire Disease	52	1.328

785		ANR004	Anuria	44	1.315

786	c	OPT053	Optic Atrophy 1	62	1.315

787	P	PRP003	Porphyria Cutanea Tarda	66	1.315

788		CRD137	Cardiogenic Shock	56	1.315

789	P	PTT006	Pituitary Adenoma	55	1.315

790		FLR001	Filarial Elephantiasis	59	1.315

791		CRT013	Carotid Stenosis	51	1.315

792	P	AGG001	Aggressive Periodontitis	55	1.315

793		LPT001	Leptospirosis	66	1.315

794		GRN055	Granular Corneal Dystrophy	37	1.314

795		WTH001	Withdrawal Disorder	48	1.304

796		HRT012	Heart Valve Disease	53	1.304

797		BLR001	Biliary Atresia	55	1.304

798		CCN001	Cocaine Dependence	48	1.304

799	P	CND004	Candidiasis	58	1.300

800	P	SKL032	Skeletal Muscle Disease	25	1.298

801		GST019	Gastrointestinal Stromal Tumor	78	1.298

802		ATS251	Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna	38	1.298

803		AML001	Amelanotic Melanoma	37	1.298

804	P	END046	Endometritis	46	1.298

805	P	GLL018	Gallbladder Cancer	53	1.298

806		AGR019	Age-Related Hearing Loss	41	1.298

807		TNG009	Tongue Squamous Cell Carcinoma	43	1.297

808	c	GLC111	Galactosemia Ii	50	1.294

809		SKL017	Skeletal Dysplasias	41	1.275

810	P	LPR021	Leprosy 3	71	1.275

811	P	MYS005	Myositis	56	1.275

812	P	OST122	Osteogenesis Imperfecta, Type Iii	57	1.275

813		URT049	Urate Oxidase, Pseudogene	24	1.275

814		NPH091	Nephrolithiasis, Calcium Oxalate	61	1.275

815		ARM004	Aromatase Excess Syndrome	51	1.275

816		HYP005	Hypokalemia	55	1.275

817		MLG079	Malignant Pleural Mesothelioma	42	1.275

818		SCB001	Scabies	50	1.275

819		PLC002	Plica Syndrome	35	1.275

820	c	SCN007	Secondary Hyperparathyroidism	51	1.275

821	P	GLL022	Guillain-Barre Syndrome	60	1.275

822		LRY018	Laryngeal Squamous Cell Carcinoma	44	1.275

823	c	BSL007	Basal Cell Carcinoma	68	1.275

824		SYN007	Synovitis	55	1.275

825		HNS001	Hansen's Disease	32	1.275

826		MNN020	Meningococcal Infection	45	1.275

827	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	60	1.272

828		STC018	Stac3 Disorder	26	1.263

829		ANT009	Antithrombin Iii Deficiency	59	1.257

830		ECH003	Echinococcosis	53	1.257

831	c	HYP819	Hyperlipoproteinemia, Type Id	24	1.249

832	c	ACR088	Aicardi-Goutieres Syndrome 3	39	1.249

833		XLN231	X-Linked Alport Syndrome	41	1.249

834		BNG036	Bone Giant Cell Tumor	49	1.249

835		CNS004	Constipation	56	1.249

836		CRV040	Cervix Carcinoma	50	1.249

837	c	ATM011	Autoimmune Hepatitis	63	1.249

838		ONC002	Onchocerciasis	51	1.249

839		ALB002	Albinism	47	1.249

840		LTH004	Lathyrism	15	1.249

841	c	MSC169	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1	61	1.242

842	P	CNJ013	Conjunctivitis	66	1.242

843		SPN119	Spondylarthropathy	38	1.233

844		SPS057	Spasticity	42	1.233

845	P	MCH002	Machado-Joseph Disease	62	1.233

846		SPP011	Suppression of Tumorigenicity 12	61	1.233

847	c	OST121	Osteogenesis Imperfecta, Type Iv	49	1.233

848		CMP034	Complete Androgen Insensitivity Syndrome	55	1.233

849		RHM035	Rheumatic Fever-Related Antigen	37	1.233

850	P	OVR106	Ovarian Clear Cell Carcinoma	44	1.233

851		EXT007	Extracutaneous Mastocytoma	38	1.233

852		WLD005	Wild Type Attr Amyloidosis	29	1.233

853		MST004	Mast Cell Neoplasm	42	1.233

854		LYM027	Lymphopenia	56	1.233

855	P	NGH001	Night Blindness	52	1.233

856	P	ECT006	Ectodermal Dysplasia	63	1.233

857	P	AGM001	Agammaglobulinemia	68	1.233

858	P	CRD119	Cardiac Arrest	67	1.233

859		HMP005	Hemiplegia	54	1.233

860		RHM001	Rheumatic Fever	59	1.233

861		PTT037	Pituitary Tumors	44	1.233

862		ORL004	Oral Submucous Fibrosis	56	1.212

863		EMB004	Embryonal Carcinoma	56	1.212

864		FCH001	Fuchs' Endothelial Dystrophy	50	1.202

865	c	PNS012	Paine Syndrome	60	1.198

866		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	37	1.198

867		KHL003	Kohlschutter-Tonz Syndrome	59	1.198

868	P	OCY003	Oocyte Maturation Defect 1	46	1.198

869	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	1.198

870		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	67	1.198

871	c	NMN016	Niemann-Pick Disease, Type B	56	1.198

872		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	49	1.198

873		DNT014	Dental Pulp Disease	43	1.198

874	P	CRV039	Cervicitis	52	1.198

875		FRN030	Frontotemporal Dementia with Parkinsonism-17	24	1.198

876		CHR466	Chronic Thromboembolic Pulmonary Hypertension	48	1.198

877		RSP007	Respiratory Distress Syndrome, Infant	40	1.198

878	P	ALP106	Alport Syndrome 1, X-Linked	47	1.195

879		BRN032	Brain Glioma	45	1.195

880		LMY014	Leiomyoma, Uterine	56	1.195

881		DYS165	Dysfibrinogenemia, Congenital	51	1.195

882	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	52	1.195

883	c	HMP004	Hemophilia B	68	1.195

884		ENC005	Encephalomalacia	44	1.195

885	c	AMY009	Amyloidosis Aa	47	1.195

886		TST015	Testicular Disease	42	1.193

887		PLY100	Polyploidy	36	1.189

888		AND020	Androgen Insensitivity, Partial	55	1.189

889		BRR014	Barrett Esophagus	66	1.189

890		MLT157	Multiple System Atrophy 1	69	1.189

891		DCT002	Ductal Carcinoma in Situ	58	1.189

892		AVN001	Avian Influenza	61	1.189

893		FDL002	Food Allergy	47	1.189

894	P	INT070	Intestinal Obstruction	57	1.189

895		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	1.189

896		IRN001	Iron Deficiency Anemia	58	1.189

897		ANP005	Anaplastic Astrocytoma	57	1.189

898	P	TRC031	Trichorhinophalangeal Syndrome	38	1.189

899	c	TBL031	Tubulointerstitial Kidney Disease, Autosomal Dominant, 1	47	1.182

900		PLM010	Pulmonary Edema	55	1.182

901	P	NRV007	Nervous System Disease	67	1.174

902		SKN019	Skin Melanoma	71	1.168

903		3HY010	3-Hydroxyisobutyryl-Coa Hydrolase Deficiency	34	1.167

904		HND015	Hand Skill, Relative	30	1.150

905	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	1.150

906	P	DDN001	Duodenal Ulcer	53	1.150

907	P	OST001	Osteopetrosis	71	1.150

908	P	ICH004	Ichthyosis	56	1.150

909	P	PHT010	Photoparoxysmal Response 1	46	1.146

910		KHN001	Kuhnt-Junius Degeneration	48	1.146

911		NRF007	Neurofibroma	64	1.146

912	c	DFN353	Deafness, Autosomal Dominant 12	38	1.143

913	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	1.143

914	P	EXD001	Exudative Vitreoretinopathy	56	1.143

915		RSP021	Respiratory Allergy	41	1.143

916		CLR108	Colorectal Adenoma	64	1.143

917	P	BRN019	Bernard-Soulier Syndrome	61	1.143

918		THY069	Thyroid Hormone Resistance, Selective Pituitary	36	1.143

919	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	64	1.143

920	P	HYP097	Hyperekplexia	62	1.143

921	P	KLL001	Kallmann Syndrome	65	1.143

922		BRN012	Bronchiolitis Obliterans	56	1.143

923		RCT015	Reactive Arthritis	61	1.143

924		KLB003	Klebsiella Pneumonia	50	1.143

925		OPS001	Opisthorchiasis	41	1.143

926		MGC001	Megacolon	48	1.143

927		CLN039	Cln4 Disease	17	1.143

928	c	CNT101	Central Congenital Hypothyroidism	36	1.143

929	P	KRB001	Krabbe Disease	69	1.139

930		HRD218	Hereditary Stomatocytosis	30	1.139

931		CLS049	Classic Phenylketonuria	41	1.138

932	c	VNW010	Von Willebrand Disease, Type 2	48	1.138

933		PRT129	Prothrombin Deficiency, Congenital	49	1.138

934		OST062	Osteoarthritis with Mild Chondrodysplasia	47	1.138

935		BTT016	Batten-Turner Congenital Myopathy	53	1.138

936		GYN001	Gynecomastia	47	1.138

937		CMP010	Complex Regional Pain Syndrome	60	1.138

938		OCL006	Ocular Hypertension	53	1.138

939	P	CRN028	Corneal Ulcer	47	1.138

940		TNS005	Tonsillitis	57	1.138

941		EXT009	Extratemporal Epilepsy	21	1.138

942		PRT012	Prothrombin Deficiency	49	1.138

943		INF021	Infant Gynecomastia	30	1.138

944		ALV005	Alveolar Soft Part Sarcoma	61	1.118

945		SCK003	Sickle Cell Anemia	74	1.118

946	P	CHR012	Chronic Granulomatous Disease	69	1.118

947		DCB001	Decubitus Ulcer	62	1.114

948	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	1.110

949	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	1.110

950		PRR019	Perioral Myoclonia with Absences	27	1.093

951	c	BCT007	Bacterial Meningitis	55	1.093