Search results for Vitamin C

2455 hits were found for Vitamin C

#	Family	MCID	Name	MIFTS	Score
1		HYP781	Hypoascorbemia	49	4.417

2		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	51	3.602

3	c	HPT021	Hepatitis	74	0.722

4	P	HPT001	Hepatitis C	69	0.678

5	P	HPT073	Hepatitis C Virus	73	0.525

6	c	BRS047	Breast Cancer	100	0.403

7		RCK004	Rickets	66	0.362

8	c	LVR013	Liver Disease	77	0.344

9		KRT002	Keratomalacia	51	0.340

10		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	56	0.338

11		ACT236	Acute Motor and Sensory Axonal Neuropathy	23	0.312

12		VTM002	Vitamin B12 Deficiency	48	0.306

13		NTR005	Nutritional Deficiency Disease	60	0.271

14	c	DBT026	Diabetes Mellitus, Noninsulin-Dependent	92	0.266

15	c	DBT009	Diabetes Mellitus	67	0.266

16	c	LYN001	Lynch Syndrome	72	0.260

17	c	KDN018	Kidney Disease	71	0.260

18	P	HPT003	Hepatitis a	66	0.253

19	c	HPT023	Hepatocellular Carcinoma	97	0.252

20	c	LKM002	Leukemia	72	0.247

21	c	PRS040	Prostate Cancer	93	0.243

22		VRL011	Viral Infectious Disease	69	0.234

23	c	OST002	Osteoporosis	74	0.222

24	c	HYP069	Hyperparathyroidism	59	0.220

25	c	CLR023	Colorectal Cancer	99	0.219

26	P	HPT016	Hepatitis B	70	0.218

27	c	HYP061	Hypertrophic Cardiomyopathy	59	0.218

28	c	HRT032	Heart Disease	76	0.213

29	P	PRS136	Prostate Cancer, Hereditary, 6	40	0.207

30	P	PRS130	Prostate Cancer, Hereditary, 8	37	0.207

31	c	ATX030	Ataxia-Telangiectasia	83	0.203

32		CYS001	Cystic Fibrosis	83	0.203

33	P	CHR089	Chronic Kidney Failure	73	0.202

34	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.200

35	c	ART022	Arthritis	78	0.200

36	c	LYM118	Lymphoma	69	0.199

37		VTM033	Vitamin K Deficiency Bleeding	47	0.197

38	c	HYP607	Hypercholesterolemia, Familial	82	0.196

39	c	LNG032	Lung Cancer	99	0.195

40		LVR012	Liver Cirrhosis	67	0.191

41		ISC004	Ischemia	67	0.191

42	c	MYC007	Myocardial Infarction	78	0.191

43		THR024	Thrombosis	64	0.189

44	P	FML346	Familial Adenomatous Polyposis 1	67	0.188

45		HMN014	Human Immunodeficiency Virus Infectious Disease	62	0.188

46	P	MCL042	Macular Degeneration, Age-Related, 1	84	0.185

47		NRL016	Neural Tube Defects	79	0.184

48	c	ADN016	Adenocarcinoma	71	0.182

49		BND020	Bone Disease	65	0.182

50		ART140	Arteries, Anomalies of	67	0.180

51	c	CRN018	Coronary Artery Anomaly	74	0.180

52		ACQ007	Acquired Immunodeficiency Syndrome	66	0.179

53	c	LNG028	Long Qt Syndrome	65	0.176

54	c	MLT020	Multiple Sclerosis	76	0.175

55		INS024	Insulin-Like Growth Factor I	83	0.174

56		AST005	Asthma	81	0.173

57	c	NRP001	Neuropathy	63	0.173

58	P	NRF024	Neurofibromatosis, Type I	69	0.170

59		MLN008	Melanoma	64	0.169

60	c	ATR011	Atrial Fibrillation	69	0.167

61	c	INF037	Inflammatory Bowel Disease	56	0.166

62	c	CRN300	Coronary Heart Disease 1	62	0.165

63	c	HRD086	Hereditary Hypophosphatemic Rickets	45	0.163

64	c	RHM011	Rheumatoid Arthritis	82	0.163

65	c	ALZ034	Alzheimer Disease	88	0.163

66		URN009	Urinary System Disease	59	0.163

67	c	CRD246	Cardiovascular System Disease	57	0.161

68		FTT001	Fatty Liver Disease	66	0.161

69	c	ZLL001	Zellweger Syndrome	57	0.160

70	P	TBR025	Tuberous Sclerosis 1	72	0.160

71	c	NNL004	Nonalcoholic Fatty Liver Disease	56	0.160

72	P	PRC016	Pre-Eclampsia	61	0.159

73		NRL018	Neural Tube Defects, Folate-Sensitive	47	0.159

74	c	LBR001	Leber Congenital Amaurosis	64	0.157

75		DPR016	Depression	73	0.157

76		RRR001	Rere-Related Disorders	55	0.157

77	c	LPS004	Lupus Erythematosus	69	0.157

78	c	THR014	Thrombocytopenia	65	0.157

79		DRM006	Dermatitis	69	0.156

80	P	PRX059	Peroxisome Biogenesis Disorder 1a	51	0.156

81		ATM095	Autoimmune Disease	68	0.156

82		AGN016	Aging	63	0.154

83	c	OVR042	Ovarian Cancer	83	0.153

84		GST050	Gastrointestinal System Disease	67	0.151

85		VSC007	Vascular Disease	72	0.151

86		LNG099	Lung Disease	70	0.150

87	P	SYS001	Systemic Lupus Erythematosus	88	0.149

88		XRD010	Xeroderma Pigmentosum, Variant Type	71	0.149

89	c	MTH008	Methylmalonic Acidemia	47	0.148

90	c	PNC035	Pancreatic Cancer	83	0.148

91		GST019	Gastrointestinal Stromal Tumor	74	0.147

92	c	PLY011	Polycystic Ovary Syndrome	64	0.147

93		GST053	Gastric Cancer	78	0.146

94	c	TBR001	Tuberous Sclerosis	69	0.146

95	c	INF038	Influenza	75	0.146

96		OCL033	Oculocerebral Syndrome with Hypopigmentation	46	0.146

97	c	PSR002	Psoriasis	67	0.146

98	P	SCN007	Secondary Hyperparathyroidism	56	0.144

99	c	NRB001	Neuroblastoma	73	0.143

100	c	INT068	Intestinal Disease	62	0.143

101	c	NRF023	Neurofibromatosis, Type Ii	76	0.142

102		PRN011	Pernicious Anemia	52	0.142

103	c	DRR001	Diarrhea	58	0.142

104		HMN044	Human Immunodeficiency Virus Type 1	75	0.141

105		PRT011	Protein C Deficiency	49	0.140

106	P	VRL010	Viral Hepatitis	60	0.139

107		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.139

108		SQM006	Squamous Cell Carcinoma	59	0.138

109		GLC008	Glucose Metabolism Disease	54	0.138

110	c	THL005	Thalassemia	65	0.138

111	c	MTR004	Maturity-Onset Diabetes of the Young	61	0.138

112	c	LYM033	Lymphoproliferative Syndrome	63	0.138

113	P	PLM164	Pulmonary Hypertension, Primary, 1	71	0.138

114		ISC006	Ischemic Heart Disease	72	0.138

115	c	MYL006	Myeloid Leukemia	68	0.137

116	P	BDY007	Body Mass Index Quantitative Trait Locus 1	48	0.137

117	c	CTR002	Cataract	58	0.136

118		CRH001	Crohn's Disease	79	0.136

119	c	PRD008	Periodontitis	66	0.136

120		MTC097	Mitochondrial Complex Iv Deficiency	55	0.135

121		BNF002	Bone Fracture	50	0.135

122	P	LKM061	Leukemia, Acute Myeloid	83	0.134

123	c	PNM007	Pneumonia	72	0.133

124	P	THR092	Thrombophilia Due to Thrombin Defect	70	0.133

125		ALL026	Allergic Hypersensitivity Disease	68	0.133

126		PYR016	Pyridoxine Deficiency	39	0.132

127		LGH007	Leigh Syndrome	66	0.131

128	P	SML038	Small Cell Cancer of the Lung	69	0.131

129	c	ART021	Arteriosclerosis	61	0.130

130		CMM005	Common Cold	62	0.129

131		CNG034	Congestive Heart Failure	71	0.128

132		END030	End Stage Renal Failure	60	0.127

133	c	PRP019	Peripheral Nervous System Disease	66	0.127

134	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	61	0.125

135		SKN016	Skin Disease	68	0.125

136	c	ECL001	Eclampsia	59	0.125

137	P	BTT014	Beta-Thalassemia	73	0.124

138		CNN005	Connective Tissue Disease	67	0.124

139	c	MGL001	Megaloblastic Anemia	52	0.124

140	c	BLD134	Bladder Cancer	71	0.124

141		DMN002	Dementia	69	0.124

142		HYP060	Hyperinsulinism	57	0.123

143	c	MYP004	Myopathy	65	0.123

144	c	HML002	Hemolytic Anemia	65	0.123

145		OST012	Osteoarthritis	81	0.123

146		CLT003	Colitis	65	0.123

147	c	DRM053	Dermatitis, Atopic	73	0.122

148	c	EPL164	Epilepsy	73	0.122

149		IMM136	Immune System Disease	57	0.122

150		BCT022	Bacterial Infectious Disease	63	0.121

151	P	ACT075	Acute Myocardial Infarction	57	0.121

152		GST033	Gestational Diabetes	63	0.121

153		ADN018	Adenoma	65	0.121

154		BNR002	Bone Resorption Disease	54	0.121

155		SKN027	Skin Conditions	51	0.120

156		BSL036	Basal Cell Nevus Syndrome	68	0.120

157		GST071	Gastrointestinal Carcinoma	46	0.119

158	c	INF032	Infertility	60	0.119

159		GST049	Gastrointestinal System Cancer	62	0.119

160	P	CNG006	Congenital Hypothyroidism	64	0.119

161	c	RTN024	Retinoblastoma	73	0.119

162		NNL002	Nonalcoholic Steatohepatitis	55	0.119

163		DFC004	Deficiency Anemia	65	0.119

164		WRN001	Werner Syndrome	74	0.119

165	P	PRM005	Primary Hyperparathyroidism	60	0.118

166		HYP266	Hypoxia	63	0.118

167	c	LYM031	Lymphocytic Leukemia	61	0.118

168	c	OST001	Osteopetrosis	63	0.117

169	P	MCR130	Microvascular Complications of Diabetes 6	43	0.117

170		TTN003	Tetanus	66	0.117

171	c	NRP053	Neuropathy, Hereditary Sensory and Autonomic, Type Iia	52	0.117

172	c	RTN008	Retinitis Pigmentosa	79	0.117

173	c	SCH015	Schizophrenia	73	0.117

174	P	MCR113	Microvascular Complications of Diabetes 3	58	0.116

175	P	MCR120	Microvascular Complications of Diabetes 7	46	0.116

176	P	MCR133	Microvascular Complications of Diabetes 4	43	0.116

177		DSR002	Disorders of Intracellular Cobalamin Metabolism	17	0.116

178		MYL069	Myeloma, Multiple	85	0.116

179	P	GLC092	Glaucoma, Primary Open Angle	58	0.115

180		IRN002	Iron Metabolism Disease	60	0.115

181	c	DYS154	Dystonia	66	0.115

182		ACR006	Aceruloplasminemia	72	0.115

183	c	ENC018	Encephalopathy	65	0.114

184	c	HRD008	Hereditary Hemorrhagic Telangiectasia	61	0.113

185	P	ATS007	Autism Spectrum Disorder	68	0.112

186	c	TRC086	Trichohepatoenteric Syndrome 1	61	0.112

187		RSP006	Respiratory System Disease	64	0.112

188		ESP021	Esophageal Cancer	84	0.112

189	c	DBT085	Diabetes Mellitus, Insulin-Dependent	73	0.112

190		CLN019	Colonic Disease	62	0.111

191		PLM001	Pulmonary Tuberculosis	74	0.111

192		THY028	Thyroid Cancer	72	0.111

193		GLB002	Glioblastoma	75	0.111

194	c	ANR048	Aniridia 1	63	0.110

195	c	ATS364	Autism	68	0.110

196		MNT002	Mental Depression	65	0.110

197	c	ALP008	Alopecia	56	0.110

198		HYP066	Hyperglycemia	65	0.110

199	c	DLT002	Dilated Cardiomyopathy	74	0.109

200	c	SKN015	Skin Carcinoma	65	0.109

201		VSL002	Visual Epilepsy	33	0.109

202		CRB039	Cerebrovascular Disease	70	0.109

203		SLF012	Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency	23	0.109

204		LPD008	Lipid Metabolism Disorder	65	0.109

205		MLR004	Malaria	85	0.108

206	P	LRG017	Large Intestine Cancer	63	0.108

207		ATX019	Ataxia with Vitamin E Deficiency	34	0.108

208	P	NMN015	Niemann-Pick Disease, Type C1	68	0.107

209		PHN003	Phenylketonuria	75	0.107

210		FND002	Fundus Dystrophy	51	0.107

211	c	GLM045	Glioma	56	0.107

212	c	NPH012	Nephrotic Syndrome	59	0.106

213	c	HYP086	Hypothyroidism	66	0.106

214	c	NRV007	Nervous System Disease	72	0.106

215		SPS003	Spastic Diplegia	49	0.105

216		GST045	Gastroenteritis	65	0.105

217		PLM129	Pulmonary Disease, Chronic Obstructive	75	0.105

218		CRY004	Cryoglobulinemia	50	0.105

219	c	EXN002	Exanthem	62	0.104

220		RHM027	Rheumatic Disease	65	0.104

221	c	LNG064	Lung Cancer Susceptibility 3	80	0.104

222	c	HYP818	Hypobetalipoproteinemia, Familial, 1	51	0.103

223		VTM028	Vitamin E, Familial Isolated Deficiency of	52	0.103

224	c	RTN016	Retinal Degeneration	56	0.103

225	c	FRN006	Frontotemporal Dementia	69	0.103

226	c	MNN013	Meningitis	71	0.103

227		GLC003	Glucose Intolerance	59	0.103

228	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	63	0.103

229	P	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	67	0.102

230	c	FCL005	Focal Segmental Glomerulosclerosis	60	0.101

231		PRP030	Purpura	62	0.101

232		NPH009	Nephrolithiasis	58	0.101

233		LYM019	Lymphosarcoma	59	0.100

234		TXC005	Toxic Shock Syndrome	66	0.100

235		MSC157	Muscular Dystrophy, Duchenne Type	66	0.100

236		PLC008	Placenta Disease	59	0.100

237	P	INF071	Inflammatory Bowel Disease 1	57	0.100

238	c	THY032	Thyroiditis	54	0.100

239	c	LCH002	Lichen Planus	59	0.100

240	c	GST044	Gastritis	61	0.099

241		SRC014	Sarcoma	70	0.099

242	c	NMN002	Niemann-Pick Disease	50	0.099

243	c	BCL006	B-Cell Lymphomas	66	0.099

244	c	PNC044	Pancreatitis	62	0.099

245		BRN106	Burns	59	0.098

246		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.098

247		WVR001	Weaver Syndrome	61	0.098

248		ULC004	Ulcerative Colitis	80	0.098

249		ANX010	Anxiety	73	0.098

250	c	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	60	0.098

251	P	ATS013	Autosomal Recessive Congenital Ichthyosis	63	0.098

252		ABT001	Abetalipoproteinemia	67	0.098

253		PRD007	Periodontal Disease	66	0.097

254		BNG081	Benign Childhood Occipital Epilepsy, Panayiotopoulos Type	25	0.097

255		NPH091	Nephrolithiasis, Calcium Oxalate	54	0.097

256		LYM143	Lymphoma, Non-Hodgkin, Familial	74	0.097

257		RNL114	Renal Cell Carcinoma, Nonpapillary	63	0.097

258	c	LFR001	Li-Fraumeni Syndrome	71	0.097

259		CLR108	Colorectal Adenoma	64	0.096

260		RNL065	Renal Cell Carcinoma, Papillary, 1	71	0.096

261		INT253	Intestinal Benign Neoplasm	57	0.096

262		PSY004	Psychotic Disorder	74	0.096

263	c	NGH001	Night Blindness	50	0.096

264	P	BNM022	Bone Mineral Density Quantitative Trait Locus 8	40	0.096

265	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	46	0.096

266	P	AMY091	Amyotrophic Lateral Sclerosis 1	90	0.095

267	c	FML018	Familial Mediterranean Fever	74	0.095

268		DSS008	Disease of Mental Health	70	0.095

269	c	NJM001	Nijmegen Breakage Syndrome	70	0.095

270		BRS051	Breast Disease	68	0.095

271		RCT017	Rectal Disease	42	0.095

272		ANG054	Angina Pectoris	70	0.094

273		PNC033	Pancreas Adenocarcinoma	67	0.094

274		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	35	0.094

275	c	HMR003	Hemorrhagic Disease	59	0.094

276		NRT004	Neuritis	58	0.094

277	c	BLD051	Blood Coagulation Disease	51	0.093

278	P	PRT132	Protoporphyria, Erythropoietic, 1	59	0.093

279		BRN028	Brain Cancer	74	0.093

280		MSL001	Measles	66	0.093

281		NRM005	Neuromuscular Disease	61	0.093

282		HMC014	Homocysteinemia	52	0.093

283	c	HMC002	Homocystinuria	51	0.093

284	P	ACT210	Acute Respiratory Distress Syndrome	66	0.093

285	c	CRN037	Craniosynostosis	66	0.092

286		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.092

287	c	LKM062	Leukemia, Acute Lymphoblastic	70	0.092

288		CRV035	Cervical Cancer	76	0.092

289		ERY029	Erythermalgia, Primary	58	0.091

290	c	MSC033	Muscle Disorders	56	0.091

291	P	CNT035	Central Nervous System Disease	65	0.091

292	P	THR082	Thrombophilia Due to Activated Protein C Resistance	60	0.091

293		MYL009	Myelodysplastic Syndrome	71	0.091

294		IMM106	Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked	73	0.091

295		IRN001	Iron Deficiency Anemia	54	0.090

296		SCK005	Sickle Cell Disease	57	0.090

297		CLC006	Calcinosis	53	0.090

298	P	ATM006	Autoimmune Lymphoproliferative Syndrome	71	0.090

299	c	ACR001	Aicardi-Goutieres Syndrome	63	0.090

300		STM007	Stomatitis	53	0.090

301	P	PNC106	Pancreatic Agenesis 1	52	0.090

302	c	PTY003	Pityriasis Rubra Pilaris	52	0.090

303	c	MTC003	Metachromatic Leukodystrophy	71	0.089

304	c	NTR004	Neutropenia	61	0.089

305	P	TRC078	Trichohepatoenteric Syndrome 2	35	0.089

306		PNC034	Pancreas Disease	60	0.089

307		LPD012	Lipoid Congenital Adrenal Hyperplasia	72	0.089

308	c	CHN059	Chondrocalcinosis	47	0.089

309	P	HYP595	Hypertension, Essential	77	0.089

310	P	PRD040	Periodontitis, Chronic	60	0.089

311	c	ART023	Arthropathy	68	0.089

312	c	FML011	Familial Adenomatous Polyposis	72	0.088

313	P	PRC031	Preeclampsia/eclampsia 1	41	0.088

314		LYM024	Lymphatic System Disease	55	0.088

315		STR067	Stroke, Ischemic	84	0.088

316		CNS004	Constipation	58	0.088

317	c	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	52	0.088

318		LNG031	Lung Benign Neoplasm	56	0.088

319		ATX010	Ataxia Neuropathy Spectrum	39	0.088

320	c	HYP073	Hypersensitivity Reaction Type Iv Disease	51	0.088

321	c	GRV001	Graves' Disease	61	0.088

322		BRN038	Bronchial Disease	58	0.087

323		HDC001	Headache	63	0.087

324	c	GLM007	Glomerulonephritis	62	0.087

325		SQM013	Squamous Cell Carcinoma, Head and Neck	82	0.087

326		MTH009	Mouth Disease	66	0.087

327	c	PSD087	Pseudoxanthoma Elasticum	68	0.086

328		CYS010	Cystinosis	55	0.086

329		CYS036	Cystinosis, Nephropathic	51	0.086

330		RTN023	Retinitis	48	0.086

331		JNT002	Joint Disorders	64	0.086

332		HLC007	Helicobacter Pylori Infection	66	0.086

333	c	ABD014	Abdominal Obesity-Metabolic Syndrome 1	58	0.086

334		PLM134	Pulmonary Fibrosis, Idiopathic	74	0.086

335	P	OVR114	Ovarian Cancer 1	66	0.086

336	c	PRK057	Parkinson Disease, Late-Onset	77	0.086

337	c	MCR115	Microvascular Complications of Diabetes 5	71	0.086

338	P	RHB011	Rhabdoid Tumor Predisposition Syndrome 2	27	0.086

339		CHL068	Cholestasis	60	0.086

340	c	VSC018	Visceral Steatosis	38	0.086

341	P	MYT021	Myotonic Dystrophy 1	72	0.085

342	c	HMP002	Hemophagocytic Lymphohistiocytosis	68	0.085

343	c	VSC011	Vasculitis	67	0.085

344		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	59	0.085

345		GST040	Gastric Adenocarcinoma	66	0.085

346	P	SPN225	Spondyloarthropathy 1	76	0.085

347	P	LKM071	Leukemia, Chronic Lymphocytic	78	0.085

348		PRM236	Primary Biliary Cholangitis	63	0.085

349		LYM133	Lymphoma, Hodgkin, Classic	73	0.085

350		SPN186	Spinal Cord Injury	66	0.084

351		BLD131	Bladder Urothelial Carcinoma	62	0.084

352		SZR026	Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance	59	0.084

353		MDD011	Mood Disorder	65	0.084

354	c	HML033	Hemolytic Uremic Syndrome, Atypical 1	65	0.084

355		PLM033	Pulmonary Embolism	64	0.084

356		SCK003	Sickle Cell Anemia	75	0.084

357	c	MDL005	Medulloblastoma	77	0.083

358		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	63	0.083

359		EPL131	Epilepsy, Pyridoxine-Dependent	38	0.083

360	c	END044	Endometriosis	65	0.083

361		HLC001	Holocarboxylase Synthetase Deficiency	53	0.083

362	P	ATS307	Autosomal Recessive Cerebellar Ataxia	28	0.083

363	P	ALP106	Alport Syndrome 1, X-Linked	49	0.083

364		IRR002	Irritable Bowel Syndrome	64	0.083

365		MSC190	Muscular Disease	55	0.083

366	c	RHN004	Rhinitis	63	0.083

367	c	PRM006	Primary Biliary Cirrhosis	54	0.082

368	c	CLC063	Celiac Disease 1	72	0.082

369		DST089	Distal Trisomy 3p	22	0.082

370		CGN005	Cognitive Impairment with or Without Cerebellar Ataxia	37	0.082

371	P	BLR024	Biliary Cirrhosis, Primary, 1	39	0.082

372		BRK010	Burkitt Lymphoma	69	0.082

373	c	PLY006	Polydactyly	58	0.082

374		CHN016	Cohen Syndrome	54	0.082

375	c	HYP802	Hypocalcemia, Autosomal Dominant 1	66	0.081

376		RTN018	Retinal Disease	58	0.081

377	P	MCP052	Mucopolysaccharidosis, Type Vi	62	0.081

378	c	EHL052	Ehlers-Danlos Syndrome, Vascular Type	56	0.081

379		DMY004	Demyelinating Disease	60	0.081

380	P	EXD008	Exudative Vitreoretinopathy 1	73	0.081

381		BRR014	Barrett Esophagus	71	0.081

382	c	SLP006	Sleep Apnea	70	0.081

383		HMT018	Hematopoietic Stem Cell Transplantation	59	0.081

384		SKN019	Skin Melanoma	67	0.081

385	c	CLL015	Collagen Disease	52	0.080

386	c	PRP029	Porphyria	60	0.080

387	P	ATM011	Autoimmune Hepatitis	66	0.080

388	c	PGT001	Paget's Disease of Bone	62	0.080

389		PRP080	Peripheral Artery Disease	56	0.080

390	P	HMC039	Hemochromatosis, Type 1	74	0.080

391		PRT010	Parathyroid Carcinoma	65	0.080

392	P	WLM018	Wilms Tumor 5	64	0.079

393		HMS001	Hemosiderosis	52	0.079

394	c	GRF003	Graft-Versus-Host Disease	72	0.079

395		VSC008	Vascular Hemostatic Disease	45	0.079

396	c	KRB001	Krabbe Disease	66	0.079

397	c	NSP012	Nasopharyngeal Carcinoma	66	0.079

398	c	THR015	Thrombophilia	56	0.079

399		CHD001	Chediak-Higashi Syndrome	67	0.079

400	c	MSC005	Muscular Dystrophy	66	0.079

401	P	LYN004	Lynch Syndrome I	59	0.079

402		URT039	Urticaria	60	0.079

403		BRN056	Bronchopulmonary Dysplasia	61	0.079

404		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	61	0.079

405		KRT019	Keratitis, Hereditary	63	0.079

406		FML063	Familial Glucocorticoid Deficiency	41	0.078

407	c	MLN007	Male Infertility	52	0.078

408	c	CRY007	Cryoglobulinemia, Familial Mixed	55	0.078

409	c	BRT029	Brittle Cornea Syndrome 2	54	0.078

410		OPT006	Optic Nerve Disease	60	0.078

411		WLS001	Wilson Disease	71	0.078

412	P	BRT028	Brittle Cornea Syndrome 1	29	0.078

413		PRX028	Peroxisomal Acyl-Coa Oxidase Deficiency	52	0.078

414		URM002	Uremia	53	0.078

415		ANR007	Anorexia Nervosa	68	0.078

416	c	MJR001	Major Depressive Disorder	67	0.077

417	c	ANG001	Angelman Syndrome	65	0.077

418		FRY006	Fryns Microphthalmia Syndrome	51	0.077

419		HYP056	Hypoglycemia	64	0.077

420		PFF001	Pfeiffer Syndrome	79	0.077

421	c	ALP009	Alopecia Areata	68	0.077

422		HMG005	Hemoglobinopathy	54	0.077

423	P	THR001	Thrombocytopenia Due to Platelet Alloimmunization	61	0.077

424		BNG080	Benign Childhood Occipital Epilepsy, Gastaut Type	19	0.077

425		ALP103	Alpha-1-Antitrypsin Deficiency	62	0.077

426	c	OPN001	Open-Angle Glaucoma	53	0.077

427		TNG002	Tangier Disease	64	0.077

428	c	ART106	Arterial Calcification, Generalized, of Infancy, 1	37	0.077

429		BRN071	Brain Injury	54	0.077

430		ALL014	Allergic Encephalomyelitis	43	0.077

431		APL001	Aplastic Anemia	75	0.076

432		MSC004	Muscle Tissue Disease	39	0.076

433	P	ACT074	Acute Lymphocytic Leukemia	62	0.076

434		PRS042	Prostate Disease	47	0.076

435		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.076

436		FND001	Fundus Albipunctatus	56	0.076

437		SPR004	Supravalvular Aortic Stenosis	53	0.076

438		SLP005	Sleep Disorder	60	0.076

439		ATM052	Autoimmune Disease 1	41	0.076

440		DBT010	Diabetic Neuropathy	60	0.076

441		FBR047	Fibromyalgia	62	0.075

442		SPP011	Suppression of Tumorigenicity 12	62	0.075

443	c	HMP007	Hemophilia	62	0.075

444	P	LKM063	Leukemia, Chronic Myeloid	74	0.075

445		ALL003	Allergic Rhinitis	69	0.075

446		FSH001	Fish-Eye Disease	51	0.075

447	c	PRM002	Primary Hyperoxaluria	54	0.075

448	c	DMN001	Diamond-Blackfan Anemia	71	0.075

449		HYP017	Hypophosphatemia	48	0.075

450		THR100	Thrombocytopenic Purpura, Autoimmune	68	0.075

451	P	MCP004	Mucopolysaccharidosis Iv	60	0.075

452	c	MRQ003	Morquio Syndrome	32	0.075

453		PRT030	Parathyroid Gland Disease	51	0.075

454	c	LTR001	Lateral Sclerosis	60	0.075

455		SPN051	Spondylitis	55	0.075

456		BRC012	Brucellosis	71	0.075

457	c	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	56	0.074

458		END035	Endocrine Gland Cancer	57	0.074

459		WLL001	Williams-Beuren Syndrome	64	0.074

460		TRN018	Transitional Cell Carcinoma	63	0.074

461	P	VSC019	Vesicoureteral Reflux 1	58	0.074

462		CRH005	Crohn's Colitis	61	0.074

463	c	AMY004	Amyloidosis	69	0.074

464		ENT011	Enterocolitis	55	0.074

465		DFF005	Diffuse Large B-Cell Lymphoma	58	0.073

466	P	ACT071	Acute Kidney Failure	54	0.073

467		HMP009	Haemophilus Influenzae	51	0.073

468	P	PNC128	Pain - Chronic	46	0.073

469		GLB015	Glioblastoma Multiforme	64	0.073

470	c	SCL057	Scoliosis, Isolated 1	46	0.073

471		TRD006	Tardive Dyskinesia	61	0.073

472		MYL005	Myelofibrosis	70	0.073

473		INT002	Intermittent Claudication	64	0.073

474	P	LBR014	Leber Congenital Amaurosis 4	55	0.073

475		ART001	Arterial Tortuosity Syndrome	59	0.073

476		MLR006	Male Reproductive Organ Cancer	50	0.073

477	P	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	60	0.072

478		PRP027	Peripheral Vascular Disease	72	0.072

479		MTC008	Mitochondrial Complex Iii Deficiency	32	0.072

480		ORL013	Oral Lichen Planus	53	0.072

481	c	MYP006	Myopia	62	0.072

482		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	67	0.072

483	P	CRD187	Cardiomyopathy, Dilated, 3b	48	0.072

484		BTN003	Biotinidase Deficiency	55	0.071

485		ADR007	Adrenoleukodystrophy	72	0.071

486	P	PRM196	Premature Ovarian Failure 1	69	0.071

487		ACT118	Acute Non Lymphoblastic Leukemia	33	0.071

488	P	ACT068	Acute Cystitis	56	0.071

489	c	SBS003	Substance Abuse	61	0.071

490		OST097	Osteoporotic Fracture	36	0.071

491		PRT037	Pertussis	71	0.071

492		PLR023	Polr3-Related Leukodystrophy	36	0.071

493		ALC007	Alcohol Dependence	70	0.071

494	P	LKM004	Leukemia, B-Cell, Chronic	38	0.071

495		CD4003	Cd40 Ligand Deficiency	45	0.071

496		RLP002	Relapsing-Remitting Multiple Sclerosis	59	0.071

497		CHL065	Cholangiocarcinoma	65	0.071

498	c	MSC007	Muscle Hypertrophy	64	0.071

499		FDL002	Food Allergy	54	0.071

500		CHL109	Childhood Apraxia of Speech	36	0.071

501	c	CMR001	Camurati-Engelmann Disease	62	0.070

502		ART016	Aortic Aneurysm	71	0.070

503	c	CRD119	Cardiac Arrest	66	0.070

504	P	PSR017	Psoriasis 2	54	0.070

505		END057	Endometrial Cancer	69	0.070

506	P	ATR087	Atrial Standstill 1	69	0.070

507	P	GLY008	Glycogen Storage Disease Ii	67	0.070

508	c	GNT009	Giant Axonal Neuropathy	52	0.070

509	P	GNT049	Giant Axonal Neuropathy 1, Autosomal Recessive	43	0.070

510		FLT009	Folate Malabsorption, Hereditary	34	0.070

511		GRN017	Granulocytopenia	52	0.070

512	P	MTR002	Mitral Valve Insufficiency	50	0.070

513	c	ORT004	Orthostatic Intolerance	69	0.070

514		PHR003	Pharyngitis	58	0.070

515		LSH001	Leishmaniasis	72	0.070

516	c	ESS003	Essential Thrombocythemia	70	0.070

517		PLM017	Pulmonary Alveolar Microlithiasis	52	0.070

518		THY030	Thyroid Gland Disease	51	0.070

519	c	HYP076	Hyperthyroidism	56	0.070

520	c	BDY004	Body Mass Index Quantitative Trait Locus 11	74	0.070

521	c	RSP003	Respiratory Failure	72	0.069

522	P	HYD046	Hydatidiform Mole, Recurrent, 1	56	0.069

523		PLS011	Plasmacytoma	62	0.069

524		OVR063	Overnutrition	53	0.069

525		GND003	Gonadal Disease	49	0.069

526		BRN080	Brain Ischemia	43	0.069

527		HYP458	Hyper Ige Syndrome	52	0.069

528	P	INS002	in Situ Carcinoma	60	0.069

529		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	47	0.069

530	P	SCL052	Scleroderma, Familial Progressive	68	0.068

531		GT001	Gout	62	0.068

532		ATH013	Atherosclerosis Susceptibility	61	0.068

533	P	ACT027	Acute Pancreatitis	59	0.068

534		GYR004	Gyrate Atrophy of Choroid and Retina	51	0.068

535		MDL020	Midline Interhemispheric Variant of Holoprosencephaly	46	0.068

536	c	PRP003	Porphyria Cutanea Tarda	67	0.068

537		ILT001	Ileitis	59	0.068

538		APH001	Aphthous Stomatitis	65	0.068

539	c	OVR049	Ovarian Disease	63	0.068

540	P	PRG126	Progressive Familial Heart Block	51	0.068

541		CRN239	Carnitine Deficiency, Systemic Primary	54	0.068

542	P	HMP029	Hemophilia a	70	0.068

543	c	RCT021	Rectum Cancer	58	0.068

544		LNG039	Lung Squamous Cell Carcinoma	62	0.068

545	c	PLY019	Polyneuropathy	58	0.068

546	c	KBK002	Kabuki Syndrome 1	67	0.067

547		PRD004	Prediabetes Syndrome	51	0.067

548		LYM067	Lymphoid Leukemia	47	0.067

549		BRN039	Bronchial Neoplasm	43	0.067

550	P	HYP794	Hyperoxaluria, Primary, Type I	43	0.067

551	P	SZR007	Seizures, Benign Familial Infantile, 3	46	0.067

552	c	ART153	Arthrochalasia Ehlers-Danlos Syndrome	22	0.067

553		CMP010	Complex Regional Pain Syndrome	64	0.067

554		CRD223	Cardiac Arrhythmia	56	0.067

555	c	RTT002	Rett Syndrome	83	0.067

556		TRN015	Transient Cerebral Ischemia	59	0.066

557		DNN002	Donnai-Barrow Syndrome	55	0.066

558		DPH001	Diphtheria	63	0.066

559		EWN002	Ewing's Family of Tumors	57	0.066

560	P	MGR028	Migraine with or Without Aura 1	69	0.066

561		MCS002	Mucositis	60	0.066

562	c	BPL003	Bipolar Disorder	61	0.066

563		OVR094	Ovarian Epithelial Cancer	41	0.066

564		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	60	0.066

565	P	CNG027	Congenital Hemolytic Anemia	52	0.066

566	c	MSC003	Muscular Atrophy	56	0.066

567		ACN002	Acanthosis Nigricans	65	0.066

568		SPP010	Suppressor of Tumorigenicity 3	60	0.066

569	c	AST007	Astrocytoma	51	0.066

570	c	ATT013	Attention Deficit-Hyperactivity Disorder	67	0.065

571		HYP810	Hypereosinophilic Syndrome, Idiopathic	60	0.065

572	c	ALC004	Alcohol Abuse	69	0.065

573		HYP348	Hyperglycinuria	36	0.065

574	c	SZR006	Seizure Disorder	61	0.065

575		PRM050	Primary Orthostatic Tremor	34	0.065

576		HPD002	Hepadnavirus Infection	25	0.065

577	c	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	65	0.065

578		BTT001	Bietti Crystalline Corneoretinal Dystrophy	46	0.065

579	c	PRG047	Progressive Familial Intrahepatic Cholestasis	56	0.065

580	P	SVR003	Severe Congenital Neutropenia	58	0.065

581		PNG002	Pain Agnosia	54	0.065

582		PRS129	Prostatic Hyperplasia, Benign	53	0.065

583		FBR012	Fabry Disease	72	0.064

584	c	ATR005	Atrophic Gastritis	49	0.064

585		TRN022	Transcobalamin Ii Deficiency	48	0.064

586	P	ART138	Aortic Aneurysm, Familial Abdominal, 1	66	0.064

587		GLC006	Galactosemia	65	0.064

588		DST081	Distal Trisomy 11q	20	0.064

589		PRP001	Propionic Acidemia	61	0.064

590		NWB001	Newborn Respiratory Distress Syndrome	61	0.064

591		NRN004	Neuroendocrine Tumor	56	0.064

592	c	KDN017	Kidney Cancer	59	0.064

593	P	MGL018	Megaloblastic Anemia 1	46	0.064

594		DWN001	Down Syndrome	72	0.064

595	c	MYC084	Mycobacterium Tuberculosis 1	68	0.064

596		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	45	0.064

597		DNT012	Dental Caries	52	0.064

598		NPH003	Nephrocalcinosis	51	0.064

599		ORL015	Oral Squamous Cell Carcinoma	48	0.064

600		PRN019	Perinatal Necrotizing Enterocolitis	58	0.064

601	c	ADL010	Adult Respiratory Distress Syndrome	64	0.063

602	c	NRN021	Neuronal Ceroid Lipofuscinosis	62	0.063

603		RGD002	Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal	40	0.063

604		THR013	Thoracic Outlet Syndrome	57	0.063

605	c	SLL003	Salla Disease	53	0.063

606	c	SCL018	Scoliosis	59	0.063

607	c	SYP003	Syphilis	58	0.063

608		BLD044	Bladder Disease	57	0.063

609		OST159	Osteogenic Sarcoma	67	0.063

610		CRB011	Cerebrotendinous Xanthomatosis	65	0.063

611		HSH003	Hashimoto Thyroiditis	67	0.063

612	P	CRP023	Carpenter Syndrome 1	59	0.063

613	c	PNS012	Paine Syndrome	63	0.063

614	P	HYP752	Hypocalciuric Hypercalcemia, Familial, Type I	42	0.063

615	P	PNC108	Pancreatitis, Hereditary	61	0.062

616	c	HYP035	Hypophosphatasia	58	0.062

617		PRM020	Premenstrual Tension	53	0.062

618	c	GLM040	Glioma Susceptibility 1	64	0.062

619		KRT009	Keratosis	55	0.062

620	c	HYP111	Hyperprolinemia	35	0.062

621	c	RST001	Restless Legs Syndrome	60	0.062

622	c	ENC004	Encephalitis	66	0.062

623	P	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	63	0.062

624	c	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	37	0.062

625		PRT038	Protein-Energy Malnutrition	53	0.062

626		RSP007	Respiratory Distress Syndrome, Infant	38	0.062

627	c	OVR046	Ovarian Cyst	52	0.062

628		ERY003	Erythema Multiforme	63	0.062

629		CYT002	Cytokine Deficiency	39	0.062

630	P	HMP004	Hemophilia B	67	0.062

631		FCT002	Factor Xi Deficiency	63	0.062

632		DRR014	Darier-White Disease	62	0.062

633	c	FBR017	Fibrosarcoma	61	0.062

634		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	46	0.062

635		CRV045	Cervical Intraepithelial Neoplasia	45	0.062

636	c	SCK002	Sick Sinus Syndrome	54	0.062

637	c	DNT020	Dent Disease 1	60	0.062

638		GLL008	Gilles De La Tourette Syndrome	69	0.061

639		SMT004	Smith-Lemli-Opitz Syndrome	69	0.061

640		SPS150	Spastic Ataxia, Charlevoix-Saguenay Type	50	0.061

641	c	TYR004	Tyrosinemia	49	0.061

642		DRL001	Dural Sinus Malformation	23	0.061

643		OCL006	Ocular Hypertension	56	0.061

644	c	HRP006	Herpes Simplex	71	0.061

645	P	ATS347	Autosomal Dominant Polycystic Kidney Disease	61	0.061

646		MVM001	Movement Disease	67	0.061

647	c	ALG028	Alagille Syndrome 1	71	0.061

648		BRN002	Bronchiolitis	62	0.061

649	c	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	49	0.061

650		HRN028	Horns in Sheep	24	0.061

651		PRT036	Peritonitis	67	0.061

652		BRT054	Brittle Bone Disorder	71	0.061

653		IMP005	Impotence	58	0.061

654	c	CRB048	Cerebral Cavernous Malformations	65	0.061

655	c	UVT001	Uveitis	62	0.061

656		END040	Endogenous Depression	59	0.061

657	P	WLM013	Wilms Tumor 1	68	0.061

658	c	CHR012	Chronic Granulomatous Disease	70	0.061

659		PLC007	Placental Abruption	51	0.061

660		RSS026	Roussy-Levy Hereditary Areflexic Dystasia	48	0.061

661		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	45	0.061

662		CRP001	Carpal Tunnel Syndrome	72	0.061

663		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	65	0.061

664		HML018	Homologous Wasting Disease	25	0.060

665		THY111	Thyroid Carcinoma, Familial Medullary	71	0.060

666		OVR012	Ovarian Serous Cystadenocarcinoma	52	0.060

667	P	HYP793	Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1	41	0.060

668		PST011	Pustulosis of Palm and Sole	50	0.060

669	c	CHR084	Chromosomal Disease	40	0.060

670		MST005	Mastitis	57	0.060

671		PNC041	Pancreatic Ductal Adenocarcinoma	54	0.060

672		BRN024	Bronchitis	70	0.060

673		BLD054	Blood Protein Disease	43	0.060

674	c	ANT006	Antiphospholipid Syndrome	60	0.060

675	P	PSR028	Psoriasis 7	43	0.060

676	P	PSR032	Psoriasis 11	43	0.060

677	P	PSR018	Psoriasis 13	42	0.060

678		NTR027	Neutrophil Actin Dysfunction	32	0.060

679		ORL011	Oral Cancer	60	0.060

680		GTR002	Goiter	54	0.060

681	P	HMG001	Hemoglobin C Disease	43	0.060

682		CLN015	Colon Adenocarcinoma	57	0.060

683	c	GCH001	Gaucher's Disease	66	0.060

684	c	TYS001	Tay-Sachs Disease	70	0.060

685		MTC005	Mitochondrial Metabolism Disease	46	0.060

686		INC002	Inclusion Body Myositis	64	0.060

687		MTC027	Mitochondrial Trifunctional Protein Deficiency	55	0.059

688		MRB003	Morbid Obesity	62	0.059

689	P	CHR579	Chiari Malformation Type Ii	49	0.059

690		APN008	Apnea, Obstructive Sleep	68	0.059

691		FCT007	Factor Vii Deficiency	61	0.059

692		CHL123	Chlamydia	66	0.059

693	c	VTL001	Vitelliform Macular Dystrophy	43	0.059

694		RFS006	Refsum Disease, Classic	63	0.059

695		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	38	0.059

696	P	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	41	0.059

697	c	CNG003	Congenital Dyserythropoietic Anemia	42	0.059

698	c	PLY018	Polycythemia	60	0.059

699		CHR066	Chronic Fatigue Syndrome	68	0.059

700	c	SHR001	Short Bowel Syndrome	52	0.058

701	c	PLM036	Pulmonary Fibrosis	70	0.058

702	c	TRM003	Tremor	56	0.058

703		SPN041	Spinal Cord Disease	55	0.058

704		HYP080	Hypogonadism	53	0.058

705	c	HYP599	Hypoparathyroidism, Familial Isolated	37	0.058

706		INT007	Intermediate Coronary Syndrome	50	0.058

707	P	MCL013	Mucolipidosis Iv	59	0.058

708	c	ACT232	Acute Necrotizing Encephalopathy	30	0.058

709		BLD137	Blood Group--Ahonen	21	0.058

710	c	RTN022	Retinal Vein Occlusion	54	0.058

711	c	HYP058	Hypervitaminosis a	48	0.058

712	P	ACT134	Acute Liver Failure	53	0.058

713		LMY014	Leiomyoma, Uterine	57	0.058

714	c	AXN002	Axenfeld-Rieger Syndrome	62	0.058

715	P	ATS406	Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2	37	0.058

716		GNG013	Gingivitis	63	0.058

717		LYM040	Lymphoblastic Lymphoma	58	0.058

718		CYS013	Cystinuria	65	0.057

719	c	PRT013	Portal Hypertension	61	0.057

720		STT009	Sutton Disease 2	32	0.057

721	P	BCT007	Bacterial Meningitis	61	0.057

722		DSS009	Disseminated Intravascular Coagulation	58	0.057

723		PLY001	Polycythemia Vera	76	0.057

724		ACT058	Active Peptic Ulcer Disease	53	0.057

725		OTT002	Otitis Media	68	0.057

726	P	BSL007	Basal Cell Carcinoma	65	0.057

727		HRP008	Herpes Simiae	16	0.057

728		CNT047	Contact Dermatitis	64	0.057

729	P	ART101	Aortic Valve Disease 2	68	0.057

730		OST003	Osteonecrosis	67	0.057

731		NWC001	Newcastle Disease	53	0.057

732	c	CHR071	Charcot-Marie-Tooth Disease	65	0.057

733		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.057

734		ISL003	Isolated Growth Hormone Deficiency	53	0.057

735	c	MTC133	Mitochondrial Myopathy	52	0.057

736		PYR015	Pyridoxal 5'-Phosphate-Dependent Epilepsy	17	0.057

737		BLR001	Biliary Atresia	57	0.057

738		LMY002	Leiomyoma	58	0.056

739		PNC001	Pancytopenia	53	0.056

740	c	PLM037	Pulmonary Hypertension	77	0.056

741		HMC016	Homocystinuria Due to Cbs Deficiency	24	0.056

742		GLC022	Glucose/galactose Malabsorption	44	0.056

743		RPD005	Rapidly Involuting Congenital Hemangioma	24	0.056

744		PRT014	Protein S Deficiency	46	0.056

745	P	LKM056	Leukemia, Chronic Lymphocytic 2	43	0.056

746		DGS002	Degos 'en Cocarde' Erythrokeratoderma	26	0.056

747		BRN139	Brain Small Vessel Disease 1 with or Without Ocular Anomalies	36	0.056

748		DYS073	Dysphagia	53	0.056

749		APP008	Appendicitis	66	0.056

750	P	AMY087	Amyloidosis, Hereditary, Transthyretin-Related	60	0.056

751		CRD220	Cardiac Valvular Defect, Developmental	36	0.056

752		BRB001	Beriberi	43	0.056

753		ALC006	Alcoholic Hepatitis	62	0.056

754		PST021	Postpartum Depression	55	0.056

755	c	OPT009	Optic Neuritis	55	0.056

756		STH001	Saethre-Chotzen Syndrome	64	0.056

757	c	MYS005	Myositis	62	0.056

758	c	AST055	Asthma-Related Traits 1	34	0.055

759		VRC005	Varicose Veins	67	0.055

760		PRT082	Preterm Premature Rupture of the Membranes	57	0.055

761	P	PLY105	Polycystic Ovary Syndrome 1	43	0.055

762	c	PSD015	Pseudohypoparathyroidism	51	0.055

763		PHT003	Phototoxic Dermatitis	44	0.055

764	c	FLL037	Follicular Lymphoma	71	0.055

765		PSR001	Psoriatic Arthritis	68	0.055

766		PLY112	Polyarteritis Nodosa, Childhood-Onset	51	0.055

767		MYL031	Myeloproliferative Neoplasm	64	0.055

768		TRM010	Traumatic Brain Injury	56	0.055

769		ACT119	Acute Promyelocytic Leukemia	61	0.055

770	c	PLY041	Polymyositis	59	0.055

771		PRS063	Paresthesia	45	0.055

772	P	EHL078	Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1	45	0.055

773		CHR074	Choriocarcinoma	50	0.055

774		FNC005	Functional Colonic Disease	29	0.055

775	c	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	30	0.055

776		ASP002	Aspartylglucosaminuria	56	0.055

777	P	AMG001	Amegakaryocytic Thrombocytopenia, Congenital	49	0.055

778		MCR017	Macrocytic Anemia	46	0.055

779		HYP005	Hypokalemia	56	0.055

780		CRT016	Carotid Artery Disease	58	0.055

781	c	CRD132	Cardiac Conduction Defect	64	0.054

782	c	FML068	Familial Hypocalciuric Hypercalcemia	50	0.054

783	P	SVR005	Severe Pre-Eclampsia	55	0.054

784	P	MSC169	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1	48	0.054

785	c	PLY014	Polycystic Kidney Disease	63	0.054

786		SCH014	Schistosomiasis	62	0.054

787		CHR619	Chromosome 2q35 Duplication Syndrome	58	0.054

788		ALP012	Alpha-Methylacyl-Coa Racemase Deficiency	49	0.054

789	c	SNS014	Sinusitis	64	0.054

790	c	KRT007	Keratoconus	50	0.054

791		PRP056	Porphyria, Acute Hepatic	47	0.054

792		PYR021	Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency	29	0.054

793		MNN028	Mononeuropathy of the Median Nerve, Mild	46	0.054

794		DHY002	Dihydropyrimidine Dehydrogenase Deficiency	57	0.054

795	P	HYP543	Hypoplastic Left Heart Syndrome 1	44	0.054

796		INT079	Intrahepatic Cholangiocarcinoma	55	0.054

797		MTR014	Motor Neuron Disease	60	0.054

798	c	DNG005	Dengue Virus	64	0.054

799		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	29	0.053

800	P	STR084	Stargardt Disease 1	54	0.053

801		ATR013	Atrichia with Papular Lesions	42	0.053

802		RHM001	Rheumatic Fever	63	0.053

803		RHM035	Rheumatic Fever-Related Antigen	44	0.053

804	c	DYS021	Dysautonomia	49	0.053

805		CLF027	Cleft Palate, Isolated	66	0.053

806		HRP004	Herpes Zoster	63	0.053

807		HDN002	Head Injury	52	0.053

808		MTH078	Methylmalonic Aciduria, Cblb Type	40	0.053

809	P	ACT073	Acute Leukemia	62	0.053

810	c	JVN024	Juvenile Hereditary Hemochromatosis	44	0.053

811		LNG073	Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency	60	0.053

812	c	LCT001	Lactic Acidosis	53	0.053

813		CYS019	Cystathioninuria	42	0.053

814		TXC002	Toxic Encephalopathy	57	0.053

815	c	SRC025	Sarcoidosis 1	76	0.053

816		ALL010	Allergic Contact Dermatitis	61	0.053

817		SXL003	Sexual Disorder	53	0.053

818		HRT012	Heart Valve Disease	57	0.053

819		CYT017	Cytophagic Histiocytic Panniculitis	26	0.053

820	P	JVN010	Juvenile Rheumatoid Arthritis	72	0.053

821		GST092	Gastroesophageal Reflux	66	0.052

822		CRN024	Corneal Disease	45	0.052

823	c	SPN046	Spinal Muscular Atrophy	65	0.052

824		IDP070	Idiopathic Scoliosis	38	0.052

825		RST011	Restrictive Dermopathy, Lethal	45	0.052

826	c	PRS038	Personality Disorder	68	0.052

827		BSL008	Basal Ganglia Disease	49	0.052

828		CRB045	Cerebellar Hypoplasia	50	0.052

829		MTB004	Metabolic Acidosis	51	0.052

830	c	LCT002	Lactose Intolerance	47	0.052

831		VSC002	Vascular Dementia	58	0.052

832		AND002	Androgen Insensitivity Syndrome	62	0.052

833		ALC009	Alcoholic Liver Cirrhosis	52	0.052

834		BRN004	Brain Edema	59	0.052

835		SWL001	Swallowing Disorders	36	0.052

836		WST001	West Syndrome	60	0.052

837		OBS002	Obsessive-Compulsive Disorder	69	0.052

838		INT146	Intervertebral Disc Disease	65	0.052

839		PRD013	Periodic Fever, Familial, Autosomal Dominant	64	0.052

840		MCK007	Muckle-Wells Syndrome	64	0.051

841	c	ERY053	Erythrokeratodermia Variabilis Et Progressiva 1	52	0.051

842		TTH006	Tooth Disease	54	0.051

843		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	55	0.051

844		CHC001	Chickenpox	50	0.051

845		ATN002	Autonomic Nervous System Disease	54	0.051

846		INT075	Intracranial Hypertension	58	0.051

847		URN022	Urinary Tract Infections, Recurrent	34	0.051

848		SNS003	Sensory Peripheral Neuropathy	56	0.051

849	c	ORF002	Orofacial Cleft	40	0.051

850		LKP003	Leukoplakia	43	0.051

851	c	NRV006	Nervous System Cancer	60	0.051

852		CNN004	Connective Tissue Cancer	46	0.051

853	P	MTC061	Mitochondrial Dna Depletion Syndrome 1	46	0.051

854		ALL006	Allergic Asthma	61	0.051

855		IGG001	Iga Glomerulonephritis	58	0.051

856		DGN001	Degenerative Disc Disease	51	0.051

857		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	51	0.051

858		RBR001	Roberts Syndrome	56	0.051

859	c	SML001	Small Cell Carcinoma	61	0.051

860	P	JVN004	Juvenile Myelomonocytic Leukemia	70	0.051

861		ARM001	Aromatase Deficiency	52	0.051

862		KPS004	Kaposi Sarcoma	77	0.051

863		KWS002	Kawasaki Disease	72	0.051

864		PRV006	Pervasive Developmental Disorder	56	0.050

865		VTM009	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1	21	0.050

866	P	ART115	Aortic Valve Disease 1	70	0.050

867		NSD001	Nose Disease	52	0.050

868	P	DPH024	Diaphragmatic Hernia, Congenital	66	0.050

869		GRW007	Growth Hormone Deficiency	53	0.050

870	c	PRP034	Purpura Fulminans	46	0.050

871		NRR001	Neuroretinitis	48	0.050

872		ADN011	Adenoid Cystic Carcinoma	67	0.050

873		HYP636	Hypocalcemic Vitamin D-Dependent Rickets	32	0.050

874	P	ACT135	Acute Graft Versus Host Disease	58	0.050

875	c	MCR010	Microcephaly	59	0.050

876	c	CNJ013	Conjunctivitis	65	0.050

877	P	CRD089	Cardiomyopathy, Familial Hypertrophic, 14	23	0.050

878	c	AGG001	Aggressive Periodontitis	56	0.050

879	P	HYP304	Hyperinsulinemic Hypoglycemia, Familial, 1	56	0.050

880	c	SJG008	Sjogren Syndrome	60	0.050

881		CRV040	Cervix Carcinoma	53	0.050

882		EMB004	Embryonal Carcinoma	60	0.050

883		CHR005	Chorioamnionitis	53	0.050

884		FXF002	Fox-Fordyce Disease	41	0.050

885	c	THR005	Thrombotic Thrombocytopenic Purpura	65	0.050

886	P	USH036	Usher Syndrome, Type I	60	0.050

887		ACT088	Acute Insulin Response	50	0.050

888	c	PYL005	Pyelonephritis	57	0.050

889		VCC001	Vaccinia	52	0.050

890		OVR029	Ovarian Hyperstimulation Syndrome	65	0.050

891		DBT002	Diabetic Autonomic Neuropathy	46	0.049

892		PPL022	Papilloma	58	0.049

893		SPH010	Sphingolipidosis	50	0.049

894		INT066	Interstitial Lung Disease	65	0.049

895	c	ACT008	Actinic Keratosis	55	0.049

896		GNR004	Generalized Anxiety Disorder	55	0.049

897		MNS002	Mini Stroke	25	0.049

898	P	MLG068	Malignant Glioma	47	0.049

899		SYN036	Syncope	49	0.049

900	c	OCL013	Oculodentodigital Dysplasia	59	0.049

901	P	MYT029	Myotonia Congenita, Autosomal Recessive	38	0.049

902		BCT002	Bacterial Vaginosis	56	0.049

903	P	MCR129	Microvascular Complications of Diabetes 1	66	0.049

904	c	HYP014	Hyperuricemia	56	0.049

905	c	SNS001	Sensorineural Hearing Loss	60	0.049

906	c	DBT005	Diabetes Insipidus	55	0.049

907		BWN003	Bowenoid Papulosis	43	0.049

908		INT088	Intrinsic Factor Deficiency	36	0.049

909	c	TCL004	T-Cell Leukemia	53	0.049

910		HMT002	Hematologic Cancer	64	0.049

911		THR004	Thrombocytosis	55	0.049

912	c	CYT020	Cytomegalic Congenital Adrenal Hypoplasia	25	0.049

913	c	CHR285	Chronic Myelomonocytic Leukemia	65	0.049

914		LWC002	Lowe Oculocerebrorenal Syndrome	67	0.049

915		DYS014	Dyspepsia	56	0.048

916		AMN002	Amino Acid Metabolic Disorder	49	0.048

917		PLR009	Pol Iii-Related Leukodystrophies	31	0.048

918		BLR008	Bilirubin Metabolic Disorder	53	0.048

919		SPN369	Spinal Disease	47	0.048

920		SCR035	Sacral Agenesis with Vertebral Anomalies	40	0.048

921		CYT008	Cytomegalovirus Infection	61	0.048

922		STM006	Stomach Disease	56	0.048

923		PLM031	Poliomyelitis	61	0.048

924	P	BDY020	Body Mass Index Quantitative Trait Locus 19	43	0.048

925	P	BDY019	Body Mass Index Quantitative Trait Locus 18	43	0.048

926	P	BDY017	Body Mass Index Quantitative Trait Locus 14	41	0.048

927	P	BDY011	Body Mass Index Quantitative Trait Locus 10	41	0.048

928	P	THY109	Thyroid Cancer, Nonmedullary, 1	60	0.048

929	c	DYS007	Dyskeratosis Congenita	67	0.048

930	c	PMP001	Pemphigus	56	0.048

931		AMN012	Aminoacidopathies	25	0.048

932	c	TTR001	Tetralogy of Fallot	71	0.048

933	P	BNG091	Benign Chronic Pemphigus	54	0.048

934	c	CYS018	Cystitis	58	0.048

935		CRB085	Cerebral Hemorrhage	46	0.048

936		SFT003	Soft Tissue Sarcoma	60	0.048

937		CMM004	Common Variable Immunodeficiency	71	0.048

938	c	ASP006	Aspergillosis	67	0.048

939	c	ESP024	Esophagitis	62	0.048

940		SPC010	Speech and Communication Disorders	51	0.048

941		MTH021	Methylmalonic Acidemia with Homocystinuria	39	0.048

942		CLR030	Clear Cell Renal Cell Carcinoma	49	0.048

943		RDN004	Radin Blood Group Antigen	29	0.048

944		HYP025	Hyperphosphatemia	49	0.048

945		ARB001	Ariboflavinosis	40	0.048

946		ACT103	Acute Lymphoblastic Leukemia, Childhood	55	0.048

947	P	CNT016	Central Retinal Vein Occlusion	50	0.047

948	P	MCL066	Macular Dystrophy, Vitelliform, 2	44	0.047

949		PYG003	Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne	38	0.047

950	P	MNN047	Mannosidosis, Alpha B, Lysosomal	58	0.047

951	P	MLG079	Malignant Pleural Mesothelioma	45	0.047

952		ACR007	Acromegaly	71	0.047

953		PLM010	Pulmonary Edema	60	0.047

954		INB001	Inborn Amino Acid Metabolism Disorder	16	0.047

955		BLD053	Blood Platelet Disease	56	0.047

956	c	OBS001	Obstructive Jaundice	54	0.047

957		GLM004	Gliomatosis Cerebri	58	0.047

958		RFR003	Refractive Error	46	0.047

959	P	PTT056	Pituitary Adenoma 1, Multiple Types	51	0.047

960		LKC009	Leukocyte Adhesion Deficiency, Type I	61	0.047

961		FCT001	Factor Viii Deficiency	56	0.047

962		ATN011	Autoinflammation with Infantile Enterocolitis	43	0.047

963		LPD009	Lipid Storage Disease	53	0.047

964	c	CHL066	Cholangitis	52	0.047

965		SNS008	Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis	51	0.047

966		MNT001	Mantle Cell Lymphoma	75	0.047

967		SDD001	Sudden Infant Death Syndrome	63	0.047

968		HMR039	Hemorrhage, Intracerebral	62	0.047

969		DBF001	D-Bifunctional Protein Deficiency	56	0.047

970	P	ATS383	Autosomal Dominant Non-Syndromic Intellectual Disability 1	23	0.047

971		INT303	Intracranial Hypertension, Idiopathic	53	0.047

972	P	CHL119	Cholangitis, Primary Sclerosing	63	0.047

973		ESP023	Esophageal Disease	59	0.047

974	P	MCR112	Microvascular Complications of Diabetes 2	42	0.047

975		DBT084	Diabetes Mellitus, Ketosis-Prone	62	0.047

976	P	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	65	0.047

977		SCH012	Schizoaffective Disorder	54	0.046

978		CHY002	Chylomicron Retention Disease	53	0.046

979		EPD015	Epidemic Typhus	52	0.046

980		HYP064	Hypogonadotropism	42	0.046

981		KLD001	Keloids	51	0.046

982	c	DYS193	Dystonia 11, Myoclonic	56	0.046

983	P	GCH015	Gaucher Disease, Type I	65	0.046

984		CNC002	Cinca Syndrome	65	0.046

985		PRS034	Parasitic Helminthiasis Infectious Disease	51	0.046

986		VSC003	Visceral Leishmaniasis	61	0.046

987	c	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	57	0.046

988		MCL006	Macular Retinal Edema	55	0.046

989		CLN045	Colonic Benign Neoplasm	48	0.046

990		RFL001	Reflex Sympathetic Dystrophy	55	0.046

991	P	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	59	0.046

992		MYC006	Mycosis Fungoides	74	0.046

993		PRS047	Prostatitis	57	0.046

994	P	HPT007	Hepatitis E	56	0.046

995	c	ANP001	Anaplastic Large Cell Lymphoma	60	0.046

996		DRY001	Dry Eye Syndrome	53	0.046

997	c	BRS044	Breast Adenocarcinoma	60	0.046

998		CLR109	Colorectal Adenocarcinoma	54	0.046

999	c	AGM019	Agammaglobulinemia, X-Linked	73	0.046

1000	c	CTN003	Cutaneous Lupus Erythematosus	55	0.046

1001		AZS001	Azoospermia	47	0.046

1002		CRB037	Cerebral Palsy	71	0.045

1003		MTH077	Methylmalonic Aciduria, Cbla Type	30	0.045

1004		LYS002	Lysosomal Storage Disease	56	0.045

1005	c	EPD009	Epidermolysis Bullosa Dystrophica	58	0.045

1006		GLY022	Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency	30	0.045

1007		KRT006	Keratoconjunctivitis	55	0.045

1008		DBT008	Diabetic Angiopathy	48	0.045

1009	c	ATS366	Autism X-Linked 2	45	0.045

1010		ALG001	Algoneurodystrophy	40	0.045

1011	c	HYD006	Hydrocephalus	66	0.045

1012		EPD002	Epidermolytic Hyperkeratosis	56	0.045

1013		MYM001	Myoma	57	0.045

1014	P	ALP101	Alpha-Thalassemia	61	0.045

1015	c	MYC008	Myocarditis	59	0.045

1016	c	HML001	Hemolytic-Uremic Syndrome	55	0.045

1017	c	ATS411	Autosomal Dominant Epidermolytic Ichthyosis	35	0.045

1018		SND001	Sandhoff Disease	66	0.045

1019		MMM001	Mammary Paget's Disease	56	0.045

1020		MLT157	Multiple System Atrophy 1	73	0.045

1021		MMM006	Mammographic Density	47	0.045

1022		DYS015	Dysentery	45	0.045

1023		LRG015	Large Intestine Adenoma	17	0.045

1024		PPT005	Peptic Ulcer Disease	64	0.045

1025		SYS003	Systolic Heart Failure	46	0.045

1026		GLT007	Glutathione Synthetase Deficiency	46	0.045

1027		THM002	Thiamine-Responsive Megaloblastic Anemia Syndrome	47	0.045

1028	P	MSC171	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5	39	0.045

1029	c	ICH004	Ichthyosis	57	0.045

1030		NSS002	Neisseria Meningitidis Infection	51	0.045

1031		BRN022	Bronchiectasis	58	0.045

1032	P	PYR010	Peyronie's Disease	55	0.044

1033	c	MYS003	Myasthenia Gravis	74	0.044

1034		DCT002	Ductal Carcinoma in Situ	58	0.044

1035		OST017	Osteomyelitis	65	0.044

1036		PRP036	Peripheral T-Cell Lymphoma	57	0.044

1037		CLF001	Cleft Lip	56	0.044

1038	c	HRD018	Hair Disease	50	0.044

1039		SBC017	Sebaceous Gland Disease	45	0.044

1040		TRD008	Triiodothyronine Receptor Auxiliary Protein	27	0.044

1041		PCK003	Pick Disease of Brain	66	0.044

1042	P	RTN162	Retinitis Pigmentosa 2	52	0.044

1043		PRT035	Peritoneum Cancer	47	0.044

1044		FLL027	Fallopian Tube Carcinoma	64	0.044

1045	P	MJR004	Major Affective Disorder 4	40	0.044

1046	P	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	69	0.044

1047		INT323	Intraocular Pressure Quantitative Trait Locus	38	0.044

1048		SPN404	Spinal and Bulbar Muscular Atrophy, X-Linked 1	62	0.044

1049		PLS007	Plasmodium Falciparum Malaria	58	0.044

1050		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	49	0.044

1051	c	CND004	Candidiasis	63	0.044

1052		HPT082	Hepatic Adenomas, Familial	49	0.044

1053		ADP007	Adie Pupil	43	0.044

1054		HNM002	Hinman Syndrome	29	0.044

1055	c	INT070	Intestinal Obstruction	55	0.044

1056		THR016	Thrombophlebitis	54	0.044

1057		CRT013	Carotid Stenosis	52	0.044

1058		HNS001	Hansen's Disease	36	0.044

1059		CHL014	Cholera	61	0.044

1060	c	TMP003	Temporal Arteritis	68	0.044

1061		CHL067	Cholecystitis	59	0.044

1062		MYF001	Myofibroma	38	0.044

1063	c	MNC007	Monocytic Leukemia	57	0.044

1064		CRN030	Coronary Stenosis	52	0.044

1065		IRN004	Iron-Refractory Iron Deficiency Anemia	42	0.044

1066	c	BRN035	Brain Stem Glioma	52	0.043

1067	c	UTR058	Uterine Anomalies	60	0.043

1068		NRF026	Neurofibromatosis, Type Iv, of Riccardi	76	0.043

1069	c	FRG001	Fragile X Syndrome	70	0.043

1070	c	ANG015	Angioedema	58	0.043

1071		DFF036	Differentiated Thyroid Carcinoma	55	0.043