Search results for Methionine

2451 hits were found for Methionine

#	Family	MCID	Name	MIFTS	Score
1		HYP003	Hypermethioninemia	51	37.736

2		MTH074	Methionine Adenosyltransferase I/iii Deficiency	42	35.587

3		HMC033	Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type	34	24.761

4		HMC014	Homocysteinemia	52	22.617

5		MTH011	Methionine Adenosyltransferase Deficiency	18	20.085

6	P	HMC002	Homocystinuria	53	16.621

7		NNL005	Non-Alcoholic Fatty Liver Disease	63	16.107

8		HMC042	Homocystinuria-Megaloblastic Anemia, Cble Complementation Type	33	14.436

9		FTT001	Fatty Liver Disease	62	14.407

10		NNL006	Non-Alcoholic Steatohepatitis	54	14.099

11		MTH075	Methionine Malabsorption Syndrome	14	14.058

12		GLY015	Glycine N-Methyltransferase Deficiency	40	13.964

13		GLL048	Glial Tumor	52	11.920

14		GLM045	Glioma	63	11.844

15		MTH046	Methylmalonic Acidemia Without Homocystinuria	39	11.507

16		MTH055	Methylmalonic Aciduria and Homocystinuria, Cbld Type	38	11.310

17		ALP077	Alpha-Methylacetoacetic Aciduria	52	11.181

18	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	10.591

19		MTH021	Methylmalonic Acidemia with Homocystinuria	44	10.212

20	P	VSC007	Vascular Disease	63	9.635

21	P	LVR013	Liver Disease	69	9.602

22		NRL016	Neural Tube Defects	81	9.572

23		DSR079	Disorder of Methionine Cycle and Sulfur Amino Acid Metabolism	4	9.357

24		GLB002	Glioblastoma	67	9.084

25		RPD005	Rapidly Involuting Congenital Hemangioma	46	9.032

26		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	50	8.315

27	P	GLM040	Glioma Susceptibility 1	71	7.866

28		VTM002	Vitamin B12 Deficiency	48	7.778

29		CHL068	Cholestasis	61	7.729

30		ADN018	Adenoma	59	7.430

31		CRT072	Creutzfeldt-Jakob Disease	68	7.227

32		HLX001	Helix Syndrome	48	7.131

33	P	NRB001	Neuroblastoma	66	6.934

34		LVR012	Liver Cirrhosis	63	6.931

35	P	HYP069	Hyperparathyroidism	62	6.927

36		HGH043	High Grade Glioma	45	6.763

37		MNT002	Mental Depression	57	6.730

38		DPR016	Depression	65	6.650

39	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	6.549

40		CHL045	Choline Deficiency Disease	39	6.484

41	P	ENC018	Encephalopathy	62	6.425

42	P	PRN023	Prion Disease	60	6.389

43	P	MJR001	Major Depressive Disorder	68	6.339

44		DWN001	Down Syndrome	70	6.335

45	c	INH020	Inherited Metabolic Disorder	48	6.287

46		MLG169	Malignant Astrocytoma	57	6.186

47	P	HPT023	Hepatocellular Carcinoma	96	6.070

48		MGL001	Megaloblastic Anemia	58	5.793

49		ATH013	Atherosclerosis Susceptibility	63	5.769

50	P	HPT021	Hepatitis	69	5.741

51		AGN016	Aging	54	5.731

52		48X005	48,xyyy	39	5.643

53		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	5.560

54		HPT004	Hepatic Coma	43	5.527

55		INS024	Insulin-Like Growth Factor I	78	5.499

56		MYL069	Myeloma, Multiple	77	5.490

57	c	PRM005	Primary Hyperparathyroidism	59	5.377

58		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	5.313

59		HPT019	Hepatic Encephalopathy	59	5.226

60	c	HPT001	Hepatitis C	62	5.218

61	P	MDL005	Medulloblastoma	75	5.130

62	P	MTH008	Methylmalonic Acidemia	52	5.013

63	P	PRS040	Prostate Cancer	95	4.966

64	P	ALZ034	Alzheimer Disease	87	4.907

65		DSR002	Disorders of Intracellular Cobalamin Metabolism	29	4.887

66	P	LYM118	Lymphoma	67	4.751

67		HMN044	Human Immunodeficiency Virus Type 1	78	4.622

68	c	HPT016	Hepatitis B	62	4.620

69		PPL052	Papillomatosis, Confluent and Reticulated	34	4.577

70		LPP008	Lipoprotein Quantitative Trait Locus	65	4.547

71		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	4.544

72	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	4.526

73	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	4.526

74	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	4.526

75	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	4.526

76	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	4.526

77	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	4.526

78	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	4.526

79	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	4.526

80	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	4.526

81	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	4.526

82		MNN043	Meningioma, Familial	79	4.502

83		SCR001	Secretory Meningioma	40	4.502

84		LYM002	Lymphoplasmacyte-Rich Meningioma	35	4.502

85		SPN021	Spinal Meningioma	50	4.502

86		ACQ007	Acquired Immunodeficiency Syndrome	59	4.459

87		HMC041	Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity	48	4.459

88		OST159	Osteogenic Sarcoma	66	4.427

89	P	LKM062	Leukemia, Acute Lymphoblastic	69	4.400

90	P	URN019	Urinary Tract Infection	49	4.379

91	P	PNC035	Pancreatic Cancer	86	4.346

92	P	ALC033	Alcohol Use Disorder	61	4.346

93	P	AMY004	Amyloidosis	70	4.327

94	c	PCH010	Pachyonychia Congenita 3	43	4.294

95		PRM236	Primary Biliary Cholangitis	60	4.293

96	P	OLG002	Oligodendroglioma	66	4.264

97	P	CRD246	Cardiovascular System Disease	56	4.264

98	P	MYP004	Myopathy	67	4.250

99	c	HYP836	Hypercholesterolemia, Familial, 1	73	4.234

100	P	PHC003	Pheochromocytoma	69	4.230

101		LWG006	Low Grade Glioma	41	4.212

102		ADR040	Adrenal Gland Pheochromocytoma	46	4.195

103	P	HRP006	Herpes Simplex	65	4.168

104		SRC014	Sarcoma	65	4.165

105		ALC007	Alcohol Dependence	66	4.155

106		SPN035	Spindle Cell Sarcoma	54	4.136

107	c	PRC016	Pre-Eclampsia	65	4.124

108		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	4.121

109		ART140	Arteries, Anomalies of	53	4.115

110	P	RHB003	Rhabdomyosarcoma	66	4.100

111	P	PLY019	Polyneuropathy	52	4.085

112	c	CHR684	Chronic Kidney Disease	69	4.079

113		47X002	47,xyy	48	4.055

114		PRT029	Parathyroid Adenoma	51	4.022

115	P	ATS364	Autism	69	4.011

116	P	BCL017	B-Cell Lymphoma	59	3.980

117	P	PNC044	Pancreatitis	61	3.936

118	P	FTL002	Fatal Familial Insomnia	50	3.930

119	P	SZR006	Seizure Disorder	70	3.917

120	P	HML002	Hemolytic Anemia	62	3.898

121		HMC030	Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency	34	3.897

122		VSC002	Vascular Dementia	60	3.891

123		DFC004	Deficiency Anemia	74	3.880

124	P	HYP265	Hypotonia	42	3.864

125	c	BRN108	Branchiootic Syndrome 1	62	3.829

126	P	HRT032	Heart Disease	81	3.828

127	P	DMN002	Dementia	66	3.826

128		STM007	Stomatitis	54	3.826

129	P	PTT006	Pituitary Adenoma	55	3.825

130		CYS001	Cystic Fibrosis	78	3.798

131	P	SCH015	Schizophrenia	74	3.786

132		THY029	Thyroid Carcinoma	51	3.784

133	P	ART021	Arteriosclerosis	54	3.784

134	P	BRS047	Breast Cancer	98	3.775

135	c	ACT068	Acute Cystitis	61	3.770

136		HYP814	Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency	34	3.764

137		VCC001	Vaccinia	47	3.730

138		CRB039	Cerebrovascular Disease	66	3.714

139		HRN029	Hearing Loss, Noise-Induced	37	3.700

140	P	BPL003	Bipolar Disorder	56	3.689

141		PYR009	Pyridoxine Deficiency Anemia	35	3.683

142		THR024	Thrombosis	56	3.678

143	P	LTR001	Lateral Sclerosis	58	3.670

144		END086	End Stage Renal Disease	52	3.645

145	c	MJR022	Major Affective Disorder 8	38	3.642

146	c	MJR024	Major Affective Disorder 9	41	3.642

147		ANP005	Anaplastic Astrocytoma	57	3.640

148	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	3.628

149		END040	Endogenous Depression	55	3.598

150		HYP060	Hyperinsulinism	54	3.598

151		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	56	3.594

152		HYP066	Hyperglycemia	61	3.570

153		ATS010	Autosomal Recessive Disease	42	3.568

154	c	HPT003	Hepatitis a	63	3.537

155		ARG004	Argyria	26	3.535

156		LPD008	Lipid Metabolism Disorder	62	3.532

157		CLL010	Cellular Ependymoma	57	3.491

158	P	BNG030	Benign Ependymoma	51	3.491

159	P	MYC084	Mycobacterium Tuberculosis 1	68	3.477

160		EWN003	Ewing Sarcoma	70	3.470

161	P	INF032	Infertility	57	3.461

162	P	KDN018	Kidney Disease	72	3.460

163		ALC006	Alcoholic Hepatitis	61	3.452

164	P	EPL164	Epilepsy	68	3.443

165		MTB004	Metabolic Acidosis	48	3.434

166	c	TYP009	Type 2 Diabetes Mellitus	92	3.402

167		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	3.390

168		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	3.377

169		CHL014	Cholera	62	3.362

170		PTT037	Pituitary Tumors	44	3.360

171	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	3.340

172		PRC051	Paracetamol Poisoning	29	3.316

173	P	SRC025	Sarcoidosis 1	71	3.305

174		BRN028	Brain Cancer	74	3.299

175	P	LNG032	Lung Cancer	98	3.298

176		NWC001	Newcastle Disease	47	3.289

177		CYT002	Cytokine Deficiency	43	3.283

178	P	CRN300	Coronary Heart Disease 1	73	3.280

179		HYP266	Hypoxia	57	3.272

180		CYS019	Cystathioninuria	46	3.257

181	P	RTN024	Retinoblastoma	73	3.252

182	P	RCT021	Rectum Cancer	54	3.246

183		PRT037	Pertussis	65	3.239

184		SFT003	Soft Tissue Sarcoma	57	3.231

185		NRT001	Neurotic Disorder	56	3.226

186	P	GST053	Gastric Cancer	83	3.224

187	c	HYP595	Hypertension, Essential	85	3.219

188		IMM167	Immune Deficiency Disease	78	3.216

189	P	CLR023	Colorectal Cancer	100	3.215

190		CRC021	Carcinosarcoma	64	3.202

191		PRP027	Peripheral Vascular Disease	71	3.198

192		IRN002	Iron Metabolism Disease	57	3.186

193		ADL002	Adult Syndrome	70	3.164

194		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	3.153

195		CRH001	Crohn's Disease	80	3.151

196		CRN036	Craniopharyngioma	64	3.145

197		CLR108	Colorectal Adenoma	64	3.128

198	P	NRP001	Neuropathy	60	3.123

199	c	THR092	Thrombophilia Due to Thrombin Defect	74	3.105

200		BCT022	Bacterial Infectious Disease	56	3.097

201	P	ADN016	Adenocarcinoma	63	3.091

202		LYM019	Lymphosarcoma	46	3.079

203	P	HYP086	Hypothyroidism	69	3.077

204		CLF027	Cleft Palate, Isolated	64	3.069

205		BRN004	Brain Edema	54	3.060

206		PHN003	Phenylketonuria	76	3.056

207		HYP056	Hypoglycemia	65	3.048

208	P	PRK057	Parkinson Disease, Late-Onset	80	3.048

209		MLD018	Mild Cognitive Impairment	48	3.033

210		ATM095	Autoimmune Disease	61	3.016

211	c	TYP008	Type 1 Diabetes Mellitus	70	3.015

212	P	MLT020	Multiple Sclerosis	79	3.013

213		NRL018	Neural Tube Defects, Folate-Sensitive	45	3.010

214		DPH001	Diphtheria	59	2.994

215	P	CTR002	Cataract	60	2.990

216	P	CNT005	Central Nervous System Lymphoma	52	2.984

217		PRM226	Primary Central Nervous System Lymphoma	47	2.984

218		PNG002	Pain Agnosia	51	2.966

219	c	ACT134	Acute Liver Failure	59	2.961

220		OCL069	Ocular Motor Apraxia	57	2.909

221	P	OVR042	Ovarian Cancer	88	2.887

222	P	LKM002	Leukemia	67	2.887

223		HRW001	Hair Whorl	35	2.885

224		ISL099	Isolated Methylmalonic Acidemia	36	2.885

225		SCR011	Scrapie	39	2.870

226		ISC004	Ischemia	61	2.870

227	P	TYR004	Tyrosinemia	50	2.865

228		PLC008	Placenta Disease	49	2.864

229	P	MLN008	Melanoma	76	2.862

230		ANX010	Anxiety	70	2.855

231		HMP009	Haemophilus Influenzae	41	2.846

232	P	OBS001	Obstructive Jaundice	48	2.839

233		LYM143	Lymphoma, Non-Hodgkin, Familial	75	2.836

234	P	MSC005	Muscular Dystrophy	67	2.836

235	P	BNG032	Benign Mesothelioma	53	2.834

236		ANX004	Anoxia	40	2.822

237	c	HPT073	Hepatitis C Virus	71	2.822

238	P	KLZ004	Kala-Azar 1	41	2.808

239		LSH001	Leishmaniasis	64	2.808

240	P	MYC033	Myoclonus	47	2.806

241		THY111	Thyroid Carcinoma, Familial Medullary	67	2.777

242	c	ACT027	Acute Pancreatitis	60	2.759

243		THY125	Thyroid Gland Medullary Carcinoma	48	2.756

244	P	HYP750	Hypertriglyceridemia, Familial	62	2.756

245		HMS001	Hemosiderosis	48	2.749

246		LNG099	Lung Disease	62	2.746

247	P	MLN007	Male Infertility	56	2.734

248	P	MCR010	Microcephaly	60	2.733

249		KR002	Kuru	45	2.710

250		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	2.709

251		CLT003	Colitis	63	2.678

252	P	HNT016	Huntington Disease	73	2.678

253	P	TRM003	Tremor	48	2.673

254		STR067	Stroke, Ischemic	80	2.647

255		SQM013	Squamous Cell Carcinoma, Head and Neck	73	2.645

256		DFF039	Diffuse Midline Glioma, H3 K27m-Mutant	47	2.641

257		LYM133	Lymphoma, Hodgkin, Classic	74	2.621

258	c	MGR028	Migraine with or Without Aura 1	64	2.619

259		ALL014	Allergic Encephalomyelitis	34	2.597

260		ULC004	Ulcerative Colitis	74	2.594

261	P	BLD134	Bladder Cancer	79	2.577

262	P	FBR017	Fibrosarcoma	56	2.569

263		URL001	Urolithiasis	46	2.568

264		CCC002	Coccidiosis	50	2.568

265	P	CHR012	Chronic Granulomatous Disease	69	2.558

266		MTH056	Methylmalonic Aciduria and Homocystinuria, Cblf Type	35	2.554

267		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.546

268	c	ATS007	Autism Spectrum Disorder	72	2.535

269	P	INF037	Inflammatory Bowel Disease	53	2.519

270		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	2.510

271	c	LKM005	Leukemia, T-Cell, Chronic	34	2.510

272		DFF005	Diffuse Large B-Cell Lymphoma	54	2.509

273		NTR005	Nutritional Deficiency Disease	61	2.506

274	P	DBT009	Diabetes Mellitus	67	2.500

275	P	RHM011	Rheumatoid Arthritis	82	2.498

276		CHL065	Cholangiocarcinoma	58	2.495

277		INT079	Intrahepatic Cholangiocarcinoma	51	2.495

278		SVR004	Severe Combined Immunodeficiency	72	2.494

279		LWG005	Low-Grade Astrocytoma	38	2.478

280	P	ISL078	Isolated Ectopia Lentis	58	2.474

281		AMN006	Aminoaciduria	37	2.468

282		PYR016	Pyridoxine Deficiency	29	2.455

283		MCS002	Mucositis	56	2.452

284		WLS001	Wilson Disease	70	2.442

285	P	PRK039	Parkinsonism	55	2.442

286		FBR047	Fibromyalgia	58	2.424

287	P	ENC004	Encephalitis	61	2.415

288		SLP001	Sleeping Sickness	56	2.415

289		GLC003	Glucose Intolerance	54	2.388

290		PLS011	Plasmacytoma	56	2.385

291	P	PLM036	Pulmonary Fibrosis	66	2.383

292		ACT098	Acute Erythroid Leukemia	55	2.366

293		AMY087	Amyloidosis, Hereditary, Transthyretin-Related	65	2.364

294		TRY001	Trypanosomiasis	50	2.364

295	P	ECL001	Eclampsia	52	2.364

296		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	2.361

297		PRT251	Proteinuria, Chronic Benign	57	2.361

298		BNR002	Bone Resorption Disease	47	2.361

299		PTH003	Pathologic Nystagmus	52	2.356

300	P	PRP019	Peripheral Nervous System Disease	58	2.343

301		CRV035	Cervical Cancer	73	2.329

302	P	INT099	Intrahepatic Cholestasis of Pregnancy	62	2.315

303	P	TMP001	Temporal Lobe Epilepsy	49	2.315

304		MLG079	Malignant Pleural Mesothelioma	42	2.315

305		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	2.312

306	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	2.312

307		URM002	Uremia	47	2.312

308	P	DNG005	Dengue Virus	56	2.312

309	P	MYC007	Myocardial Infarction	70	2.305

310		FLT009	Folate Malabsorption, Hereditary	49	2.298

311	P	CRB088	Cerebral Atrophy	33	2.286

312		CHR074	Choriocarcinoma	46	2.271

313	P	PLM006	Pulmonary Alveolar Proteinosis	53	2.269

314		CHL123	Chlamydia	58	2.259

315	P	MYS005	Myositis	56	2.248

316		KWS001	Kwashiorkor	45	2.247

317		ACR007	Acromegaly	70	2.244

318		TBC004	Tobacco Addiction	63	2.234

319	P	INF038	Influenza	68	2.233

320		MST005	Mastitis	53	2.232

321		CLF001	Cleft Lip	53	2.232

322		OST012	Osteoarthritis	77	2.230

323	P	MLT074	Multiple Endocrine Neoplasia	59	2.221

324	c	MCL042	Macular Degeneration, Age-Related, 1	85	2.217

325		CYS013	Cystinuria	66	2.209

326	P	ART022	Arthritis	71	2.204

327	c	DLT002	Dilated Cardiomyopathy	78	2.204

328		PLY150	Polykaryocytosis Inducer	29	2.186

329	c	ACT071	Acute Kidney Failure	60	2.186

330		END057	Endometrial Cancer	72	2.175

331	P	HDC001	Headache	57	2.167

332	c	SCN007	Secondary Hyperparathyroidism	51	2.166

333		BRN024	Bronchitis	67	2.166

334		PRN011	Pernicious Anemia	53	2.157

335		BRK010	Burkitt Lymphoma	66	2.155

336		PRS131	Prostate Cancer/brain Cancer Susceptibility	23	2.155

337	P	HYP076	Hyperthyroidism	53	2.155

338	P	BRS044	Breast Adenocarcinoma	58	2.147

339	P	MPL001	Maple Syrup Urine Disease	70	2.144

340		OLG006	Oligoastrocytoma	34	2.129

341	P	OVR082	Overgrowth Syndrome	49	2.123

342		SQM006	Squamous Cell Carcinoma	60	2.122

343	P	THR015	Thrombophilia	51	2.117

344		TTN003	Tetanus	65	2.091

345		GTR002	Goiter	53	2.087

346		MXD026	Mixed Glioma	45	2.067

347		DFF016	Diffuse Astrocytoma	45	2.061

348		DYS006	Dysembryoplastic Neuroepithelial Tumor	32	2.061

349		GLM004	Gliomatosis Cerebri	52	2.061

350	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	2.057

351	P	LNG064	Lung Cancer Susceptibility 3	70	2.057

352	P	KDN017	Kidney Cancer	61	2.057

353		PPL022	Papilloma	53	2.042

354		MSL001	Measles	61	2.035

355		ANP009	Anaplastic Oligodendroglioma	41	2.026

356		STT001	Status Epilepticus	59	2.024

357		ESP021	Esophageal Cancer	83	2.023

358	c	ACT075	Acute Myocardial Infarction	56	2.023

359	P	MYC008	Myocarditis	59	2.023

360		ANP008	Anaplastic Oligoastrocytoma	29	2.001

361	c	SCL052	Scleroderma, Familial Progressive	61	1.994

362	c	TYR012	Tyrosinemia, Type I	61	1.994

363		TRM010	Traumatic Brain Injury	51	1.994

364		BRN071	Brain Injury	50	1.994

365	P	MTR014	Motor Neuron Disease	65	1.991

366		MLR004	Malaria	80	1.988

367		GRM004	Germinoma	44	1.984

368	P	MJR007	Major Affective Disorder 1	42	1.976

369		BRN032	Brain Glioma	45	1.968

370		SVR001	Severe Acute Respiratory Syndrome	67	1.961

371	P	THL005	Thalassemia	56	1.952

372		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	1.952

373		PRP001	Propionic Acidemia	65	1.952

374		GNG004	Ganglioglioma	53	1.952

375		SCH014	Schistosomiasis	56	1.952

376		ALL029	Allergic Disease	59	1.951

377	c	VRL010	Viral Hepatitis	53	1.949

378		MDD011	Mood Disorder	62	1.949

379		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	1.946

380	P	PSR002	Psoriasis	63	1.946

381		PST011	Pustulosis of Palm and Sole	52	1.946

382		SQM002	Squamous Cell Papilloma	46	1.946

383		PLG002	Plague	58	1.946

384	P	GLM007	Glomerulonephritis	60	1.946

385	P	FLL037	Follicular Lymphoma	74	1.945

386	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	41	1.932

387	P	RTN016	Retinal Degeneration	52	1.928

388	P	PRD008	Periodontitis	64	1.928

389	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	55	1.919

390		INS001	Insulinoma	59	1.919

391		ADR022	Adrenomyeloneuropathy	39	1.915

392		PLM134	Pulmonary Fibrosis, Idiopathic	76	1.915

393		ADR007	Adrenoleukodystrophy	73	1.915

394	P	PLM037	Pulmonary Hypertension	72	1.915

395		NRR001	Neuroretinitis	42	1.915

396		RTN023	Retinitis	46	1.915

397		PNC129	Pancreatic Adenocarcinoma	65	1.915

398		ART016	Aortic Aneurysm	68	1.915

399		DSS032	Disease by Infectious Agent	55	1.904

400		ANR040	Aneurysm	61	1.904

401		AMN012	Aminoacidopathies	20	1.904

402		PLM129	Pulmonary Disease, Chronic Obstructive	74	1.896

403		HYP141	Hyperphenylalaninemia	42	1.888

404	P	RTN008	Retinitis Pigmentosa	80	1.876

405		FCL014	Focal Epilepsy	53	1.876

406	P	CYS018	Cystitis	59	1.862

407	P	PRP029	Porphyria	60	1.862

408	P	OST002	Osteoporosis	76	1.858

409		CLF056	Cleft Lip with or Without Cleft Palate	42	1.858

410		PLM031	Poliomyelitis	63	1.858

411		PLC007	Placental Abruption	47	1.858

412		CHR178	Chromosomal Triplication	34	1.857

413		EXN003	Exencephaly	30	1.857

414		SKN016	Skin Disease	63	1.836

415	P	PLY011	Polycystic Ovary Syndrome	57	1.836

416		CYS009	Cystadenoma	43	1.828

417	c	MCR130	Microvascular Complications of Diabetes 6	41	1.825

418	c	MCR120	Microvascular Complications of Diabetes 7	47	1.825

419	P	SPP010	Suppressor of Tumorigenicity 3	51	1.825

420	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	1.825

421	P	LPS004	Lupus Erythematosus	61	1.825

422	c	MCR113	Microvascular Complications of Diabetes 3	52	1.825

423	c	MCR133	Microvascular Complications of Diabetes 4	41	1.825

424	P	MSC003	Muscular Atrophy	52	1.823

425		PRT010	Parathyroid Carcinoma	68	1.822

426	P	VNW001	Von Willebrand's Disease	65	1.822

427	P	RRH023	Rare Hereditary Hemochromatosis	54	1.822

428		BRN034	Brain Meningioma	33	1.817

429		INT395	Intracranial Meningioma	39	1.817

430		MTH051	Methylmalonic Aciduria and Homocystinuria, Cblj Type	28	1.813

431		MCR025	Microhydranencephaly	33	1.795

432	c	MCR115	Microvascular Complications of Diabetes 5	65	1.792

433	c	HRD039	Hereditary Amyloidosis	45	1.792

434		PRS047	Prostatitis	58	1.785

435		ANN002	Anencephaly	57	1.785

436	P	SML001	Small Cell Carcinoma	52	1.785

437	c	HNT010	Huntington Disease-Like 1	55	1.785

438	P	ADL010	Adult Respiratory Distress Syndrome	71	1.785

439		KRT002	Keratomalacia	55	1.776

440		TRN015	Transient Cerebral Ischemia	63	1.770

441		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	1.766

442	c	SML038	Small Cell Cancer of the Lung	69	1.759

443	P	HML001	Hemolytic-Uremic Syndrome	52	1.759

444		CHC001	Chickenpox	57	1.759

445		HPT022	Hepatoblastoma	54	1.759

446	P	GST044	Gastritis	55	1.759

447		OST017	Osteomyelitis	63	1.753

448		CRV002	Cervix Uteri Carcinoma in Situ	47	1.753

449	P	SYP003	Syphilis	59	1.753

450		CRV045	Cervical Intraepithelial Neoplasia	39	1.753

451		PRT013	Portal Hypertension	59	1.747

452		GST045	Gastroenteritis	58	1.747

453		DMY004	Demyelinating Disease	50	1.747

454	c	SYS001	Systemic Lupus Erythematosus	87	1.737

455	P	CNR004	Cone-Rod Dystrophy 2	74	1.716

456	P	PLV020	Pelvic Organ Prolapse	58	1.716

457		HTC003	Hutchinson-Gilford Progeria Syndrome	65	1.708

458		GST033	Gestational Diabetes	61	1.708

459	P	DBT005	Diabetes Insipidus	54	1.707

460	c	THY107	Thymoma, Familial	42	1.707

461	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	1.707

462	P	THY023	Thymoma	64	1.707

463	c	FML021	Familial Hypercholesterolemia	72	1.707

464	P	RTN022	Retinal Vein Occlusion	54	1.707

465	P	MTC069	Mitochondrial Disorders	57	1.695

466	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	1.690

467		CRD132	Cardiac Conduction Defect	60	1.690

468	c	ATR087	Atrial Standstill 1	74	1.690

469	P	GRV001	Graves' Disease	55	1.690

470	P	HMN010	Hemangioma	62	1.690

471		CHR028	Chronic Wasting Disease	33	1.690

472	P	NRF002	Neurofibromatosis	57	1.690

473		ATN005	Autonomic Dysfunction	46	1.690

474		MCR020	Microsporidiosis	49	1.670

475		HGH041	High-Grade Astrocytoma	36	1.670

476		ANR007	Anorexia Nervosa	60	1.666

477	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	1.666

478	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	1.666

479	P	ALP008	Alopecia	54	1.666

480		TRN018	Transitional Cell Carcinoma	56	1.661

481		MCR017	Macrocytic Anemia	44	1.661

482		SPS057	Spasticity	42	1.654

483	c	LKM061	Leukemia, Acute Myeloid	83	1.654

484	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	67	1.654

485	P	DYS154	Dystonia	64	1.654

486	P	LCT001	Lactic Acidosis	51	1.654

487	P	DRR001	Diarrhea	55	1.654

488		HYP264	Hypertonia	36	1.654

489	P	ANR048	Aniridia 1	64	1.630

490		AMD002	Amed Syndrome, Digenic	37	1.630

491		GRW007	Growth Hormone Deficiency	46	1.623

492		MDD018	Middle East Respiratory Syndrome	44	1.623

493	P	SYS005	Systemic Scleroderma	74	1.623

494		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	58	1.616

495	c	GLL024	Gallbladder Disease 1	52	1.616

496	P	CHL066	Cholangitis	52	1.614

497		CYS010	Cystinosis	62	1.614

498		DRM006	Dermatitis	62	1.612

499	P	BLR024	Biliary Cirrhosis, Primary, 1	28	1.612

500		SHR109	Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities	35	1.612

501		MLD017	Mal De Debarquement Syndrome	29	1.612

502	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	1.587

503		CRB004	Cerebral Artery Occlusion	45	1.579

504		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	1.578

505	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	1.578

506		MTH071	Methane Production	25	1.578

507		LGH007	Leigh Syndrome	70	1.578

508		WST005	West Nile Virus	57	1.578

509		CNS004	Constipation	56	1.578

510		TXC005	Toxic Shock Syndrome	62	1.578

511	c	RNG015	Ring Chromosome 2	22	1.578

512		AKN002	Akinetic Mutism	36	1.571

513		MTS001	Mutism	44	1.571

514		PPT005	Peptic Ulcer Disease	58	1.560

515		IMP005	Impotence	52	1.541

516		CNN005	Connective Tissue Disease	67	1.538

517		RCK004	Rickets	68	1.538

518		CYS005	Cysticercosis	60	1.538

519		CNG034	Congestive Heart Failure	69	1.538

520	P	TCD001	Tic Disorder	49	1.538

521		NRM004	Neuroma	49	1.538

522		PLM012	Pulmonary Sarcoidosis	53	1.533

523		CRH005	Crohn's Colitis	53	1.532

524	P	SNS001	Sensorineural Hearing Loss	59	1.532

525		HMG005	Hemoglobinopathy	56	1.532

526	P	HYP024	Hypoparathyroidism	55	1.532

527		SPL018	Splenomegaly	49	1.532

528	P	CHR345	Chronic Pain	50	1.532

529	P	RSP003	Respiratory Failure	74	1.511

530	P	ADL017	Adult T-Cell Leukemia	56	1.497

531	c	ATM022	Autoimmune Myocarditis	36	1.497

532	P	CND004	Candidiasis	58	1.497

533		PSY004	Psychotic Disorder	66	1.497

534		GST023	Gastric Ulcer	52	1.491

535	c	HNT004	Huntington Disease-Like 2	52	1.483

536	P	END046	Endometritis	46	1.483

537	P	MTH007	Methemoglobinemia	46	1.483

538		CNT019	Central Neurocytoma	46	1.483

539		AMN003	Amnestic Disorder	54	1.483

540		THR123	Thrombotic Microangiopathy	40	1.454

541		MYL020	Myelomeningocele	51	1.454

542	P	GLC113	Galactosemia I	66	1.454

543		MYL013	Myeloperoxidase Deficiency	44	1.454

544	P	PLM034	Pulmonary Emphysema	58	1.454

545	P	VNT002	Ventricular Septal Defect	58	1.454

546		CRT013	Carotid Stenosis	51	1.454

547		RBS001	Rabies	58	1.454

548	P	SLP005	Sleep Disorder	61	1.454

549		SNL007	Senile Cataract	40	1.454

550		PLM033	Pulmonary Embolism	58	1.454

551		PRL019	Prolidase Deficiency	50	1.450

552	P	MYP006	Myopia	56	1.450

553		GNT189	Genetic Prion Disease	20	1.450

554		VSC003	Visceral Leishmaniasis	55	1.446

555		PRG009	Progressive Multifocal Leukoencephalopathy	58	1.446

556		HMZ003	Homozygous Familial Hypercholesterolemia	60	1.431

557	P	MYS003	Myasthenia Gravis	68	1.431

558	P	DRM053	Dermatitis, Atopic	65	1.431

559		ANG054	Angina Pectoris	66	1.431

560		EPD015	Epidemic Typhus	44	1.431

561		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	1.431

562		CLR109	Colorectal Adenocarcinoma	50	1.431

563	P	VSC011	Vasculitis	61	1.431

564		BRN049	Brain Tumor, Childhood	28	1.431

565		MRF001	Marfan Syndrome	76	1.418

566		CLN015	Colon Adenocarcinoma	65	1.418

567	P	DYS021	Dysautonomia	38	1.418

568	P	ATR011	Atrial Fibrillation	66	1.416

569	P	THY032	Thyroiditis	57	1.415

570		MRG013	Mirage Syndrome	44	1.414

571	P	MLG074	Malignant Mesenchymoma	40	1.414

572		CNT033	Central Nervous System Cancer	47	1.414

573		SPN041	Spinal Cord Disease	55	1.414

574	P	NRV006	Nervous System Cancer	48	1.414

575		MSC157	Muscular Dystrophy, Duchenne Type	79	1.410

576		GRS011	Gerstmann-Straussler Disease	56	1.410

577		CHL152	Childhood Acute Lymphocytic Leukemia	50	1.410

578	P	NTR004	Neutropenia	63	1.410

579		LYM017	Lyme Disease	62	1.410

580		AZS001	Azoospermia	45	1.410

581		OVR094	Ovarian Epithelial Cancer	39	1.410

582	P	TRN020	Turner Syndrome	67	1.407

583		ANT018	Anthracosis	51	1.381

584		PPL058	Papilloma of Choroid Plexus	55	1.376

585	c	DFN116	Deafness, Autosomal Recessive 74	30	1.376

586		FNG017	Fungal Infectious Disease	54	1.376

587		HMN009	Hemangioblastoma	54	1.376

588		PRP030	Purpura	54	1.376

589		BBS001	Babesiosis	49	1.376

590		CRB086	Cerebral Aneurysms	40	1.376

591	c	BCT007	Bacterial Meningitis	55	1.363

592		NNS045	Non-Specific Syndromic Intellectual Disability	42	1.363

593		MTH047	Methanol Poisoning	37	1.363

594		CLS049	Classic Phenylketonuria	41	1.363

595	P	HML033	Hemolytic Uremic Syndrome, Atypical 1	69	1.363

596		HYP017	Hypophosphatemia	49	1.363

597		SCK003	Sickle Cell Anemia	74	1.363

598		CTR172	Citrullinemia, Classic	65	1.363

599	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	52	1.363

600		ACT149	Acetaminophen Metabolism	35	1.363

601	c	LRG001	Large Cell Carcinoma	48	1.363

602		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.363

603	P	TBR001	Tuberous Sclerosis	69	1.363

604		TYP007	Typhoid Fever	64	1.363

605		MYT011	Myotonia	39	1.363

606		DWR001	Dwarfism	44	1.363

607		AMN007	Aminoacylase 1 Deficiency	33	1.341

608		PNC041	Pancreatic Ductal Adenocarcinoma	51	1.332

609	P	PRD006	Prader-Willi Syndrome	61	1.320

610		HRT011	Heart Septal Defect	49	1.318

611		PRS045	Prostatic Hypertrophy	53	1.318

612		PRT038	Protein-Energy Malnutrition	53	1.318

613	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	1.316

614		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	61	1.316

615		CRY035	Cryptorchidism, Unilateral or Bilateral	58	1.316

616		PLM020	Pleomorphic Xanthoastrocytoma	40	1.316

617	P	CWD010	Cowden Syndrome	70	1.316

618	P	TRT010	Teratoma	51	1.316

619	P	SPN237	Spina Bifida Aperta	19	1.314

620		PRN071	Parenteral Nutrition-Associated Cholestasis	23	1.314

621	P	NSP012	Nasopharyngeal Carcinoma	61	1.314

622	P	BCK002	Beckwith-Wiedemann Syndrome	62	1.314

623	c	BTT014	Beta-Thalassemia	72	1.314

624		KRT019	Keratitis, Hereditary	66	1.314

625	c	HNT011	Huntington Disease-Like 3	34	1.314

626	P	TTR001	Tetralogy of Fallot	69	1.314

627	c	TBR025	Tuberous Sclerosis 1	84	1.314

628	P	LKD001	Leukodystrophy	59	1.314

629		PST092	Posttransplant Acute Limbic Encephalitis	28	1.314

630		ANT024	Anthrax Disease	58	1.314

631		LYM027	Lymphopenia	56	1.314

632		TCK001	Tick-Borne Encephalitis	59	1.314

633	P	HYP040	Hypospadias	51	1.314

634		INC002	Inclusion Body Myositis	57	1.310

635		ENT004	Enthesopathy	51	1.310

636	c	ATM011	Autoimmune Hepatitis	63	1.282

637	P	HYD006	Hydrocephalus	61	1.282

638		THY030	Thyroid Gland Disease	50	1.268

639		IRR002	Irritable Bowel Syndrome	65	1.268

640		ENC055	Encephalopathy, Ethylmalonic	51	1.262

641		OTT002	Otitis Media	71	1.262

642		PRN001	Purine Nucleoside Phosphorylase Deficiency	53	1.262

643	P	CRP001	Carpal Tunnel Syndrome	66	1.262

644		KPS004	Kaposi Sarcoma	77	1.262

645		PRL045	Proline-Negative Auxotroph of Hamster, Complementation of	16	1.262

646		VRC005	Varicose Veins	60	1.262

647		DGR001	Digeorge Syndrome	62	1.262

648		AVN001	Avian Influenza	61	1.262

649	P	LYN001	Lynch Syndrome	76	1.262

650		VGN019	Vaginal Discharge	47	1.262

651		HYP082	Hypopharynx Cancer	47	1.262

652		CHL147	Chlamydia Pneumonia	47	1.262

653		RYS001	Reye Syndrome	49	1.262

654	P	CRD119	Cardiac Arrest	67	1.262

655		CRC006	Carcinoid Syndrome	55	1.262

656		ETN001	Eating Disorder	59	1.262

657	c	PRS136	Prostate Cancer, Hereditary, 6	33	1.262

658	c	PRS130	Prostate Cancer, Hereditary, 8	32	1.262

659		TRN022	Transcobalamin Ii Deficiency	45	1.260

660		NDL024	Nodal Marginal Zone Lymphoma	37	1.252

661		HYP020	Hyperprolactinemia	63	1.252

662		MST020	Mast Cell Activation Syndrome	28	1.252

663		CHG001	Chagas Disease	66	1.246

664		ANT039	Antisynthetase Syndrome	55	1.243

665	P	VSC018	Visceral Steatosis	32	1.243

666	P	CLS010	Cluster Headache	42	1.229

667		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	26	1.229

668		HSH003	Hashimoto Thyroiditis	60	1.213

669	c	MLT159	Multiple Endocrine Neoplasia, Type Iib	61	1.209

670		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	1.209

671	P	CHN012	Chondrosarcoma	57	1.209

672	c	ACT073	Acute Leukemia	58	1.209

673		PRT036	Peritonitis	65	1.209

674	P	DRM010	Dermatomyositis	61	1.209

675	P	END044	Endometriosis	62	1.209

676		SPP011	Suppression of Tumorigenicity 12	61	1.207

677	c	PLM164	Pulmonary Hypertension, Primary, 1	76	1.207

678		NND010	Nondisjunction	34	1.207

679		SPN221	Spina Bifida Occulta	40	1.207

680		ACT119	Acute Promyelocytic Leukemia	62	1.207

681	c	WLM013	Wilms Tumor 1	66	1.207

682		MLD001	Melioidosis	67	1.207

683		LPD007	Lipoadenoma	26	1.207

684		AMB001	Amebiasis	57	1.207

685		CMB007	Combined Immunodeficiency	57	1.207

686	P	MMP001	Mumps	57	1.207

687		CNT016	Central Retinal Vein Occlusion	54	1.207

688	P	SHR001	Short Bowel Syndrome	53	1.207

689		ENC005	Encephalomalacia	44	1.207

690		CHY002	Chylomicron Retention Disease	64	1.205

691	P	ACT010	Acth-Secreting Pituitary Adenoma	61	1.195

692	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	1.195

693		CNN003	Conn's Syndrome	79	1.195

694	P	PLT029	Platelet Groups--Ko System	15	1.181

695	P	ART023	Arthropathy	61	1.181

696	P	BRB001	Beriberi	44	1.181

697	P	PLY014	Polycystic Kidney Disease	69	1.175

698		ITR003	Iatrogenic Creutzfeldt-Jakob Disease	15	1.171

699	P	MYL006	Myeloid Leukemia	61	1.171

700		MTH009	Mouth Disease	57	1.171

701	P	EYD002	Eye Disease	57	1.171

702		EMB004	Embryonal Carcinoma	56	1.171

703		CND006	Candida Glabrata	30	1.171

704	P	SJG008	Sjogren Syndrome	61	1.153

705		AND005	Androgen Insensitivity Syndrome, Mild	21	1.150

706	c	MTC063	Mitochondrial Dna Depletion Syndrome 3	51	1.148

707		KSH001	Keshan Disease	34	1.148

708	P	FTL001	Fetal Alcohol Syndrome	55	1.148

709	P	CRB048	Cerebral Cavernous Malformations	63	1.148

710	c	PRG020	Paragangliomas 3	39	1.148

711	c	MCR312	Microphthalmia, Syndromic 10	40	1.148

712		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	72	1.148

713		PRM329	Premature Aging	36	1.148

714		CTN007	Cutaneous Leishmaniasis	62	1.148

715		PLM014	Pleomorphic Adenoma	51	1.148

716		CRB001	Cerebral Lymphoma	36	1.148

717		DFF036	Differentiated Thyroid Carcinoma	51	1.148

718		GST040	Gastric Adenocarcinoma	67	1.148

719		OLF005	Olfactory Neuroblastoma	46	1.148

720		MRS001	Marasmus	42	1.148

721		LWC001	Low Compliance Bladder	45	1.148

722	P	INT143	Interstitial Cystitis	60	1.148

723		HMN014	Human Immunodeficiency Virus Infectious Disease	54	1.148

724	c	ATS204	Autosomal Recessive Non-Syndromic Intellectual Disability	48	1.148

725	P	BRN022	Bronchiectasis	60	1.148

726		AGR019	Age-Related Hearing Loss	41	1.148

727		CVR010	Cavernous Malformation	30	1.148

728		SPR166	Sporadic Fatal Insomnia	14	1.131

729	P	EXN002	Exanthem	58	1.131

730		YLL002	Yellow Fever	61	1.131

731	P	OPT006	Optic Nerve Disease	58	1.131

732	c	SRC023	Sarcoidosis 2	44	1.105

733		PLS009	Plasma Cell Neoplasm	64	1.105

734		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	1.105

735		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	1.100

736	c	HYP793	Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1	46	1.100

737		GLY010	Glycine Encephalopathy	57	1.100

738	P	FML068	Familial Hypocalciuric Hypercalcemia	55	1.100

739		ADG002	Audiogenic Seizures	25	1.100

740		WLD005	Wild Type Attr Amyloidosis	29	1.100

741		SLC006	Silicosis	56	1.100

742		CHN004	Chondroblastoma	41	1.100

743		PLZ002	Pelizaeus-Merzbacher-Like Disease	37	1.100

744		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	1.090

745	P	RTT002	Rett Syndrome	79	1.090

746		PRS129	Prostatic Hyperplasia, Benign	49	1.090

747		HLC007	Helicobacter Pylori Infection	67	1.090

748		NPH009	Nephrolithiasis	54	1.090

749		PRS021	Prostatic Adenoma	43	1.090

750	c	ALP101	Alpha-Thalassemia	62	1.083

751		FML037	Female Breast Cancer	51	1.083

752		BRR014	Barrett Esophagus	66	1.083

753		SXL003	Sexual Disorder	49	1.083

754		ANT009	Antithrombin Iii Deficiency	59	1.083

755	P	TRT019	Torticollis	47	1.083

756	c	PNC106	Pancreatic Agenesis 1	51	1.083

757		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	1.083

758		RTC009	Reticulum Cell Sarcoma	44	1.083

759	P	ANG001	Angelman Syndrome	65	1.083

760		STS002	Situs Inversus	45	1.083

761		OVR059	Ovary Adenocarcinoma	49	1.083

762	P	CHR071	Charcot-Marie-Tooth Disease	64	1.083

763		PLC002	Plica Syndrome	35	1.083

764		DYS015	Dysentery	50	1.083

765		PYR004	Pyuria	36	1.083

766		TTH006	Tooth Disease	51	1.083

767		SYN007	Synovitis	55	1.083

768		PNC034	Pancreas Disease	50	1.083

769		MTH081	Mthfr Gene Variant	10	1.083

770		ARG007	Argininemia	58	1.064

771	c	MST023	Mesothelioma, Malignant	56	1.063

772		RTN017	Retinal Detachment	60	1.047

773		VLV047	Volvulus of Midgut	52	1.047

774	c	LKM063	Leukemia, Chronic Myeloid	71	1.047

775	P	PLY041	Polymyositis	59	1.047

776	P	NPH012	Nephrotic Syndrome	60	1.047

777		INT066	Interstitial Lung Disease	60	1.047

778		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	50	1.039

779		MTH040	Methylmalonyl-Coa Epimerase Deficiency	26	1.039

780		INT002	Intermittent Claudication	61	1.017

781	P	ESP024	Esophagitis	60	1.017

782		PNM013	Pneumococcal Meningitis	43	1.012

783		CYN003	Cyanide Poisoning	22	1.012

784		DRV001	Dravet Syndrome	69	1.012

785	c	ANM038	Anemia, Autoimmune Hemolytic	64	1.012

786	c	OPT053	Optic Atrophy 1	62	1.012

787		ALC001	Alcohol-Related Birth Defect	36	1.012

788		MYL009	Myelodysplastic Syndrome	67	1.012

789		HYP241	Hypermethioninemia Due to Adenosine Kinase Deficiency	37	1.012

790	P	CNG436	Congenital Disorder of Deglycosylation	51	1.012

791	c	ERY064	Erythrocytosis, Familial, 6	30	1.012

792		RNL077	Renal Fibrosis	46	1.012

793		CWP001	Cowpox	45	1.012

794		MNG007	Manganese Poisoning	28	1.012

795		CLL003	Cellulitis	53	1.012

796	P	RST002	Restrictive Cardiomyopathy	54	1.012

797	P	ACN011	Acne	57	1.012

798		HYP005	Hypokalemia	55	1.012

799	P	INT070	Intestinal Obstruction	57	1.012

800		PLR008	Pleurisy	50	1.012

801	P	MGR001	Migraine Without Aura	49	1.012

802		LYD001	Leydig Cell Tumor	45	1.012

803		TRC008	Trachoma	53	1.012

804		ART004	Aortic Atherosclerosis	47	1.012

805	P	LRY044	Larynx Cancer	54	1.012

806	P	MNN013	Meningitis	65	1.012

807		GMS001	Gemistocytic Astrocytoma	32	1.012

808		LTH004	Lathyrism	15	1.012

809		CRY036	Cryptogenic Cirrhosis	36	1.012

810	P	FML187	Familial Hypertension	34	1.012

811		ACT228	Acute Radiation Syndrome	30	1.003

812	P	PRP003	Porphyria Cutanea Tarda	66	1.003

813	c	BPL002	Bipolar I Disorder	47	1.003

814		BCT004	Bacteriuria	47	1.003

815		ANT019	Anterograde Amnesia	38	1.003

816		PST028	Post-Traumatic Stress Disorder	59	1.003

817		FRN006	Frontotemporal Dementia	68	1.002

818	c	MCL062	Mucolipidosis Ii Alpha/beta	68	1.002

819	c	THR082	Thrombophilia Due to Activated Protein C Resistance	59	1.002

820		XRD010	Xeroderma Pigmentosum, Variant Type	73	1.002

821		GST050	Gastrointestinal System Disease	55	1.002

822	P	HRD217	Hereditary Optic Neuropathy	36	0.956

823		AND002	Androgen Insensitivity Syndrome	63	0.956

824		PRP080	Peripheral Artery Disease	54	0.956

825		SLF014	Sulfite Oxidase Deficiency, Isolated	53	0.956

826		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.956

827		ALP103	Alpha-1-Antitrypsin Deficiency	68	0.956

828	P	ASP006	Aspergillosis	72	0.956

829		EXT007	Extracutaneous Mastocytoma	38	0.956

830		MST004	Mast Cell Neoplasm	42	0.956

831		TRT001	Teratocarcinoma	42	0.956

832		INT271	Interstitial Lung and Liver Disease	40	0.956

833		TLN003	Telangiectasis	51	0.956

834		BLR001	Biliary Atresia	55	0.956

835		BRC012	Brucellosis	66	0.956

836	P	RHN004	Rhinitis	57	0.956

837		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.956

838	P	EPD016	Epidermolysis Bullosa	53	0.956

839		LYS002	Lysosomal Storage Disease	51	0.956

840	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	59	0.956

841		MTC005	Mitochondrial Metabolism Disease	45	0.936

842	c	PNC108	Pancreatitis, Hereditary	69	0.936

843		GLS018	Glass Syndrome	61	0.934

844	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	0.934

845		ATS252	Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb	41	0.931

846		SDD008	Sudden Sensorineural Hearing Loss	41	0.931

847		CRB151	Cerebral Creatine Deficiency Syndrome 1	50	0.931

848		LSC001	Lesch-Nyhan Syndrome	62	0.931

849		ALP100	Alpha-Thalassemia/mental Retardation Syndrome, X-Linked	64	0.931

850		AND020	Androgen Insensitivity, Partial	55	0.931

851		SHR097	Short Tarsus with Absence of Lower Eyelashes	25	0.931

852		PLS025	Plasmablastic Lymphoma	56	0.931

853	c	ATS006	Autosomal Recessive Nonsyndromic Deafness	27	0.931

854	c	2HY001	2-Hydroxyglutaric Aciduria	38	0.931

855		DBT090	Diabetes and Deafness, Maternally Inherited	45	0.931

856		TRD006	Tardive Dyskinesia	53	0.931

857	c	CHL119	Cholangitis, Primary Sclerosing	58	0.931

858		CHR072	Chordoma	57	0.931

859		GLB001	Gilbert Syndrome	53	0.931

860		HNZ004	Heinz Body Anemias	40	0.931

861		ADN011	Adenoid Cystic Carcinoma	68	0.931

862	P	HYP077	Hypertrichosis	46	0.931

863		URT010	Ureteral Obstruction	45	0.931

864		PDT001	Pediatric Lymphoma	27	0.931

865	P	RNV001	Renovascular Hypertension	49	0.931

866	P	PLY018	Polycythemia	56	0.931

867	P	PLL002	Pellagra	46	0.931

868		THY006	Thymus Lymphoma	27	0.931

869	P	SCL009	Sclerosing Cholangitis	48	0.931

870	P	DDN001	Duodenal Ulcer	53	0.931

871		GLS001	Gliosarcoma	64	0.931

872	P	CNG003	Congenital Dyserythropoietic Anemia	48	0.931

873		SPT005	Spotted Fever	49	0.931

874		HYP043	Hyperandrogenism	48	0.931

875		GST029	Gastric Cardia Adenocarcinoma	29	0.931

876	P	INT068	Intestinal Disease	53	0.931

877		TLR001	Tularemia	56	0.931

878	c	NNS007	Nonsyndromic Deafness	33	0.931

879		AML004	Ameloblastic Carcinoma	39	0.931

880		DSS012	Disseminated Infection with Mycobacterium Avium Complex	19	0.931

881		TTT001	Tatton-Brown-Rahman Syndrome	46	0.908

882		CLF004	Cleft Lip/palate	57	0.907

883	P	AST005	Asthma	76	0.907

884	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.907

885		BTN004	Biotin Deficiency	45	0.907

886		WST001	West Syndrome	59	0.907

887	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	0.907

888		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	0.907

889	P	RBL001	Rubella	58	0.907

890	P	THR014	Thrombocytopenia	66	0.907

891	P	GRF003	Graft-Versus-Host Disease	71	0.907

892		PNC001	Pancytopenia	53	0.907

893	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	0.907

894	P	NRV007	Nervous System Disease	67	0.907

895		CHR682	Chronic Bilirubin Encephalopathy	37	0.892

896	c	FML001	Familial Atrial Fibrillation	65	0.892

897		PTT057	Pituitary Adenoma 4, Acth-Secreting	48	0.892

898	c	MJR006	Major Affective Disorder 5	32	0.892

899	c	MJR023	Major Affective Disorder 7	33	0.892

900	c	MJR004	Major Affective Disorder 4	28	0.892

901	c	MJR003	Major Affective Disorder 6	32	0.892

902	c	MJR008	Major Affective Disorder 2	34	0.892

903		FNC007	Functioning Pituitary Adenoma	42	0.892

904		AMN002	Amino Acid Metabolic Disorder	39	0.892

905		PTT003	Pituitary-Dependent Cushing's Disease	39	0.892

906		MYF002	Myofascial Pain Syndrome	46	0.892

907		PPL001	Papillary Adenoma	44	0.892

908	P	INB001	Inborn Amino Acid Metabolism Disorder	11	0.892

909		HLT002	Halothane Hepatitis	31	0.878

910		FCS002	Fucosidosis	62	0.855

911	P	ATX030	Ataxia-Telangiectasia	80	0.855

912	P	CLC063	Celiac Disease 1	66	0.855

913	P	HYP111	Hyperprolinemia	45	0.855

914	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.855

915		CMP034	Complete Androgen Insensitivity Syndrome	55	0.855

916		SCH038	Schopf-Schulz-Passarge Syndrome	51	0.855

917		GYR004	Gyrate Atrophy of Choroid and Retina	58	0.855

918		MYT030	Myotonia, Potassium-Aggravated	46	0.855

919		LRN003	Learning Disability	49	0.855

920	P	PRD021	Periodic Paralysis	41	0.855

921		TRC003	Trichomoniasis	53	0.855

922	P	HYP061	Hypertrophic Cardiomyopathy	69	0.855

923		ALC009	Alcoholic Liver Cirrhosis	54	0.855

924		ATN004	Autonomic Neuropathy	42	0.855

925	P	BND020	Bone Disease	59	0.855

926	P	SBS003	Substance Abuse	54	0.855

927		LNS001	Lens Subluxation	39	0.855

928	P	OST001	Osteopetrosis	71	0.855

929	P	HRD011	Hereditary Spherocytosis	64	0.855

930		HYP014	Hyperuricemia	51	0.855

931	P	TXP001	Toxoplasmosis	60	0.855

932		PLY100	Polyploidy	36	0.835

933	P	ALB003	Albinism-Deafness Syndrome	34	0.835

934	P	FCS012	Facioscapulohumeral Muscular Dystrophy 1	68	0.835

935	c	ATR062	Atrial Septal Defect 1	39	0.835

936	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.835

937	P	FML011	Familial Adenomatous Polyposis	71	0.835

938	c	VNW010	Von Willebrand Disease, Type 2	48	0.835

939	c	RTN066	Retinitis Pigmentosa 4	42	0.835

940		PYR012	Pyruvate Dehydrogenase E1-Beta Deficiency	41	0.835

941	c	ATM045	Autoimmune Glomerulonephritis	35	0.835

942		BTT017	Beta-Thalassemia Major	51	0.835

943		LPT014	Leptin Deficiency or Dysfunction	78	0.835

944		ARM004	Aromatase Excess Syndrome	51	0.835

945		HND015	Hand Skill, Relative	30	0.835

946	P	FBR003	Fibrous Histiocytoma	43	0.835

947		BRN018	Borna Disease	36	0.835

948		CMP010	Complex Regional Pain Syndrome	60	0.835

949		MLT006	Multidrug-Resistant Tuberculosis	47	0.835

950		HRT012	Heart Valve Disease	53	0.835

9