Search results for Vitamin C

2030 hits were found for Vitamin C

#	Family	MCID	Name	MIFTS	Score
1		HYP781	Hypoascorbemia	42	4.360

2		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	51	3.564

3	P	HPT021	Hepatitis	76	0.606

4	c	HPT001	Hepatitis C	71	0.562

5	c	HPT073	Hepatitis C Virus	72	0.448

6	P	BRS047	Breast Cancer	100	0.376

7	P	LVR013	Liver Disease	75	0.318

8		RCK004	Rickets	62	0.300

9		VTM002	Vitamin B12 Deficiency	47	0.274

10	c	HPT003	Hepatitis a	61	0.265

11		END072	Endotheliitis	45	0.263

12	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.262

13	P	PRS040	Prostate Cancer	90	0.256

14		VRL011	Viral Infectious Disease	63	0.256

15		PRS047	Prostatitis	60	0.253

16		AGN016	Aging	64	0.240

17	P	DBT009	Diabetes Mellitus	64	0.238

18	P	KDN018	Kidney Disease	68	0.237

19	P	CLR023	Colorectal Cancer	97	0.236

20	P	LYN001	Lynch Syndrome	71	0.231

21	P	LKM002	Leukemia	72	0.229

22	P	HPT023	Hepatocellular Carcinoma	94	0.229

23	P	HYP607	Hypercholesterolemia, Familial	79	0.206

24		TYP041	Type I	56	0.205

25	P	HRT032	Heart Disease	74	0.205

26	P	OST002	Osteoporosis	76	0.205

27	P	HYP061	Hypertrophic Cardiomyopathy	64	0.203

28	P	LNG032	Lung Cancer	98	0.201

29		ISC004	Ischemia	65	0.197

30	P	LYM118	Lymphoma	70	0.195

31	P	FNC027	Fanconi Anemia, Complementation Group a	78	0.195

32		THR024	Thrombosis	61	0.190

33	c	FML346	Familial Adenomatous Polyposis 1	62	0.189

34		ACQ007	Acquired Immunodeficiency Syndrome	63	0.188

35		INS024	Insulin-Like Growth Factor I	82	0.187

36	c	CHR089	Chronic Kidney Failure	72	0.187

37	P	ART022	Arthritis	76	0.186

38		ART140	Arteries, Anomalies of	65	0.185

39	P	HYP069	Hyperparathyroidism	58	0.185

40	P	MYC007	Myocardial Infarction	79	0.184

41	c	MCL042	Macular Degeneration, Age-Related, 1	84	0.184

42	P	LNG028	Long Qt Syndrome	65	0.184

43	P	ATX030	Ataxia-Telangiectasia	79	0.183

44	P	CRN018	Coronary Artery Anomaly	68	0.183

45	c	HPT016	Hepatitis B	67	0.179

46	P	ADN016	Adenocarcinoma	70	0.178

47		BND020	Bone Disease	62	0.176

48		URN009	Urinary System Disease	55	0.176

49	P	THY032	Thyroiditis	55	0.174

50	P	ZLL001	Zellweger Syndrome	56	0.174

51	P	PNC044	Pancreatitis	64	0.173

52	c	NRF024	Neurofibromatosis, Type I	66	0.171

53	P	LBR001	Leber Congenital Amaurosis	64	0.170

54		MTH078	Methylmalonic Aciduria, Cblb Type	61	0.169

55		MLN008	Melanoma	62	0.161

56		GST050	Gastrointestinal System Disease	64	0.160

57		AST005	Asthma	82	0.160

58	c	CRN300	Coronary Heart Disease 1	64	0.159

59	P	THR014	Thrombocytopenia	64	0.158

60		OCL033	Oculocerebral Syndrome with Hypopigmentation	45	0.157

61		CYS001	Cystic Fibrosis	84	0.157

62		GST053	Gastric Cancer	77	0.156

63	P	ALZ034	Alzheimer Disease	87	0.155

64		GLC008	Glucose Metabolism Disease	52	0.155

65	P	PLM037	Pulmonary Hypertension	75	0.154

66		LNG099	Lung Disease	67	0.154

67	P	MLT020	Multiple Sclerosis	78	0.154

68	P	RHM011	Rheumatoid Arthritis	80	0.154

69		LVR012	Liver Cirrhosis	68	0.153

70		NRL016	Neural Tube Defects	78	0.153

71		GST019	Gastrointestinal Stromal Tumor	73	0.153

72		VSC007	Vascular Disease	68	0.153

73		NRN002	Neuronitis	41	0.153

74	P	XRD010	Xeroderma Pigmentosum, Variant Type	68	0.152

75		DPR016	Depression	72	0.151

76	P	NRB001	Neuroblastoma	72	0.151

77	P	PNC035	Pancreatic Cancer	79	0.151

78	P	INF038	Influenza	76	0.151

79	P	NRP001	Neuropathy	63	0.151

80		ATM095	Autoimmune Disease	64	0.150

81	c	PLM164	Pulmonary Hypertension, Primary, 1	66	0.149

82	P	INT068	Intestinal Disease	64	0.148

83	P	MTR004	Maturity-Onset Diabetes of the Young	60	0.148

84		PRT011	Protein C Deficiency	49	0.148

85	P	INF037	Inflammatory Bowel Disease	53	0.147

86		BNF002	Bone Fracture	55	0.146

87		SQM006	Squamous Cell Carcinoma	59	0.145

88	P	LPS004	Lupus Erythematosus	68	0.144

89		MTC097	Mitochondrial Complex Iv Deficiency	54	0.141

90		LGH007	Leigh Syndrome	67	0.139

91		CRH001	Crohn's Disease	78	0.139

92	c	SYS001	Systemic Lupus Erythematosus	86	0.137

93	P	MYL006	Myeloid Leukemia	68	0.137

94	P	PNM007	Pneumonia	69	0.137

95		IMM136	Immune System Disease	56	0.137

96		RTN023	Retinitis	50	0.137

97	c	SML038	Small Cell Cancer of the Lung	68	0.136

98		SKN016	Skin Disease	66	0.136

99	c	THR092	Thrombophilia Due to Thrombin Defect	67	0.136

100	P	MGL001	Megaloblastic Anemia	51	0.136

101		ISC006	Ischemic Heart Disease	72	0.135

102	c	LKM061	Leukemia, Acute Myeloid	80	0.133

103	P	OVR042	Ovarian Cancer	81	0.132

104		SKN027	Skin Conditions	48	0.132

105		ADN018	Adenoma	63	0.131

106	P	PRD008	Periodontitis	66	0.131

107	P	PSR002	Psoriasis	65	0.129

108	P	NNL004	Nonalcoholic Fatty Liver Disease	51	0.129

109	P	ART021	Arteriosclerosis	60	0.129

110	P	ATR011	Atrial Fibrillation	68	0.128

111		ALP046	Alport Syndrome, X-Linked	75	0.127

112		HYP060	Hyperinsulinism	56	0.127

113	c	TBR025	Tuberous Sclerosis 1	62	0.127

114	P	DRR001	Diarrhea	56	0.127

115	c	CNG006	Congenital Hypothyroidism	60	0.127

116		DSR002	Disorders of Intracellular Cobalamin Metabolism	19	0.126

117		FTT001	Fatty Liver Disease	60	0.125

118		NRL018	Neural Tube Defects, Folate-Sensitive	44	0.125

119		RSP006	Respiratory System Disease	63	0.124

120	c	VRL010	Viral Hepatitis	59	0.123

121		DRM006	Dermatitis	66	0.123

122		HMN044	Human Immunodeficiency Virus Type 1	70	0.122

123	c	PRM012	Primary Polycythemia	52	0.121

124	P	OST001	Osteopetrosis	61	0.120

125		CNG034	Congestive Heart Failure	72	0.120

126	c	GLC092	Glaucoma, Primary Open Angle	57	0.120

127	P	CTR002	Cataract	60	0.120

128	P	MYP004	Myopathy	68	0.120

129	P	INF032	Infertility	59	0.119

130		DMN002	Dementia	68	0.119

131		CRB009	Cerebritis	41	0.119

132		VNH007	Von Hippel-Lindau Syndrome	69	0.118

133	P	HRD008	Hereditary Hemorrhagic Telangiectasia	61	0.118

134		WRN001	Werner Syndrome	69	0.118

135		BSL036	Basal Cell Nevus Syndrome	65	0.118

136		ATX019	Ataxia with Vitamin E Deficiency	31	0.117

137		CLN019	Colonic Disease	54	0.117

138	c	PRC016	Pre-Eclampsia	59	0.116

139	c	ACT075	Acute Myocardial Infarction	58	0.116

140		HYP266	Hypoxia	61	0.116

141		FND002	Fundus Dystrophy	49	0.116

142		SPS003	Spastic Diplegia	54	0.115

143	P	THL005	Thalassemia	64	0.115

144		ACR006	Aceruloplasminemia	73	0.114

145	P	DYS154	Dystonia	64	0.114

146	P	ENC018	Encephalopathy	62	0.114

147	P	NRV007	Nervous System Disease	73	0.114

148		PRP019	Peripheral Nervous System Disease	60	0.113

149	P	ANR048	Aniridia 1	65	0.113

150		CNG008	Congenital Ichthyosiform Erythroderma	60	0.113

151	P	SCH015	Schizophrenia	69	0.113

152		OST012	Osteoarthritis	82	0.113

153	P	GLM045	Glioma	54	0.112

154	P	HYP818	Hypobetalipoproteinemia, Familial, 1	54	0.112

155		VTM028	Vitamin E, Familial Isolated Deficiency of	52	0.112

156		MNT002	Mental Depression	57	0.111

157		GLB002	Glioblastoma	72	0.111

158	P	FCL005	Focal Segmental Glomerulosclerosis	59	0.110

159	P	TBR001	Tuberous Sclerosis	68	0.110

160	P	FRN006	Frontotemporal Dementia	67	0.110

161		MYL069	Myeloma, Multiple	83	0.109

162		CRB039	Cerebrovascular Disease	67	0.109

163	P	PLY011	Polycystic Ovary Syndrome	63	0.109

164	P	THR015	Thrombophilia	57	0.109

165	P	CRV039	Cervicitis	49	0.108

166	P	EXN002	Exanthem	61	0.108

167	P	ESP024	Esophagitis	63	0.108

168	c	3MT016	3-Methylglutaconic Aciduria, Type Iii	59	0.108

169		PLC008	Placenta Disease	61	0.107

170	P	RTN024	Retinoblastoma	70	0.106

171	c	BTT014	Beta-Thalassemia	69	0.106

172		SCN001	Secondary Hyperparathyroidism of Renal Origin	50	0.106

173	P	SZR006	Seizure Disorder	56	0.106

174	P	LNG064	Lung Cancer Susceptibility 3	76	0.105

175		END030	End Stage Renal Failure	56	0.105

176	c	FTT008	Fatty Liver Disease, Nonalcoholic 1	39	0.105

177		ESP021	Esophageal Cancer	77	0.105

178		CHL061	Childhood Leukemia	55	0.104

179	c	PRM005	Primary Hyperparathyroidism	59	0.104

180	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	62	0.104

181		CMM005	Common Cold	61	0.104

182	c	CNT035	Central Nervous System Disease	63	0.103

183		VTM001	Vitamin K Deficiency Hemorrhagic Disease	40	0.103

184		ABT001	Abetalipoproteinemia	63	0.103

185	P	BLD134	Bladder Cancer	69	0.103

186		GST045	Gastroenteritis	64	0.103

187	P	NPH012	Nephrotic Syndrome	59	0.103

188		PSY004	Psychotic Disorder	71	0.103

189	P	ECL001	Eclampsia	57	0.103

190	P	RTN016	Retinal Degeneration	54	0.102

191		BRN106	Burns	56	0.102

192		SKN019	Skin Melanoma	69	0.102

193		CLT003	Colitis	62	0.102

194		PRT118	Protoporphyria, Erythropoietic	58	0.102

195	P	ALP008	Alopecia	58	0.102

196		RNL065	Renal Cell Carcinoma, Papillary, 1	70	0.102

197	P	NGH001	Night Blindness	51	0.102

198		HYP066	Hyperglycemia	63	0.101

199	P	DRM053	Dermatitis, Atopic	67	0.101

200		ANR040	Aneurysm	60	0.101

201		LPD008	Lipid Metabolism Disorder	58	0.101

202	P	MLT074	Multiple Endocrine Neoplasia	55	0.100

203		NNL002	Nonalcoholic Steatohepatitis	50	0.100

204		MLR004	Malaria	83	0.100

205	P	BLD051	Blood Coagulation Disease	50	0.100

206	P	MNN013	Meningitis	70	0.100

207		PLM129	Pulmonary Disease, Chronic Obstructive	72	0.099

208		LYM019	Lymphosarcoma	55	0.099

209	P	LYM033	Lymphoproliferative Syndrome	55	0.099

210		BRS051	Breast Disease	66	0.099

211		CRY004	Cryoglobulinemia	49	0.099

212		CLR108	Colorectal Adenoma	60	0.099

213	P	HMR003	Hemorrhagic Disease	60	0.099

214		RCT017	Rectal Disease	39	0.099

215		PRP030	Purpura	61	0.099

216		RNL114	Renal Cell Carcinoma, Nonpapillary	59	0.098

217		ANX010	Anxiety	72	0.098

218		GLC003	Glucose Intolerance	56	0.098

219		PNC034	Pancreas Disease	57	0.098

220	c	ERL006	Early-Onset Familial Alzheimer Disease	38	0.098

221		BRN028	Brain Cancer	72	0.098

222		NRM005	Neuromuscular Disease	60	0.097

223		WVR001	Weaver Syndrome	61	0.097

224		TTN003	Tetanus	64	0.097

225		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	53	0.097

226		RHM027	Rheumatic Disease	62	0.097

227	P	HYP086	Hypothyroidism	64	0.097

228	P	TRC086	Trichohepatoenteric Syndrome 1	54	0.097

229	c	ATM006	Autoimmune Lymphoproliferative Syndrome	70	0.096

230		ERY029	Erythermalgia, Primary	54	0.096

231	P	CRN037	Craniosynostosis	67	0.096

232	P	CRV035	Cervical Cancer	69	0.096

233	P	DLT002	Dilated Cardiomyopathy	76	0.096

234		CNN005	Connective Tissue Disease	64	0.096

235		ENT004	Enthesopathy	46	0.096

236		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.096

237	c	MYT021	Myotonic Dystrophy 1	68	0.096

238		PRN011	Pernicious Anemia	50	0.096

239	P	MTC003	Metachromatic Leukodystrophy	71	0.096

240		PLM001	Pulmonary Tuberculosis	71	0.095

241		PNC033	Pancreas Adenocarcinoma	64	0.095

242		NRT004	Neuritis	57	0.095

243	P	BCL006	B-Cell Lymphomas	65	0.095

244	P	ART023	Arthropathy	67	0.095

245		GST040	Gastric Adenocarcinoma	63	0.094

246		PDT001	Pediatric Lymphoma	45	0.094

247	c	ADL001	Adult Lymphoma	39	0.094

248		CYS036	Cystinosis, Nephropathic	48	0.094

249		OST015	Osteochondrodysplasia	53	0.094

250	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	59	0.094

251	P	RTN008	Retinitis Pigmentosa	81	0.093

252	P	HML002	Hemolytic Anemia	62	0.093

253	c	TRC078	Trichohepatoenteric Syndrome 2	34	0.093

254	c	PRC031	Preeclampsia/eclampsia 1	39	0.093

255	P	HMC002	Homocystinuria	50	0.093

256		BRN038	Bronchial Disease	56	0.093

257		MYL009	Myelodysplastic Syndrome	70	0.093

258	P	HMP002	Hemophagocytic Lymphohistiocytosis	67	0.093

259		SRC014	Sarcoma	68	0.092

260	P	VSC018	Visceral Steatosis	37	0.092

261		LYM024	Lymphatic System Disease	54	0.092

262		SZR026	Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance	55	0.092

263		CYS010	Cystinosis	54	0.092

264	P	NJM001	Nijmegen Breakage Syndrome	70	0.092

265	c	LKM071	Leukemia, Chronic Lymphocytic	75	0.091

266		JNT002	Joint Disorders	59	0.091

267		CLC006	Calcinosis	51	0.090

268		LPD012	Lipoid Congenital Adrenal Hyperplasia	69	0.090

269		EPL131	Epilepsy, Pyridoxine-Dependent	37	0.090

270	P	MDL005	Medulloblastoma	75	0.090

271		IRN002	Iron Metabolism Disease	55	0.089

272		ANG054	Angina Pectoris	66	0.089

273		SQM013	Squamous Cell Carcinoma, Head and Neck	76	0.089

274	c	ATS307	Autosomal Recessive Cerebellar Ataxia	27	0.089

275	P	DBT085	Diabetes Mellitus, Insulin-Dependent	65	0.089

276		CNS004	Constipation	56	0.088

277	P	GST044	Gastritis	60	0.088

278		HLC001	Holocarboxylase Synthetase Deficiency	58	0.088

279	c	WLM018	Wilms Tumor 5	60	0.088

280		ULC004	Ulcerative Colitis	72	0.088

281	P	CLL015	Collagen Disease	52	0.088

282	c	ATS007	Autism Spectrum Disorder	61	0.087

283	P	LYM026	Lymphoblastic Leukemia	64	0.087

284		PHN003	Phenylketonuria	73	0.087

285		BLD131	Bladder Urothelial Carcinoma	60	0.086

286	P	MYP006	Myopia	56	0.086

287		FCT034	Factor V and Factor Viii, Combined Deficiency of, 2	36	0.086

288		PLM033	Pulmonary Embolism	62	0.086

289		MSC157	Muscular Dystrophy, Duchenne Type	68	0.086

290		MTH009	Mouth Disease	63	0.086

291		SLP005	Sleep Disorder	59	0.086

292		STM007	Stomatitis	52	0.086

293		MSL001	Measles	64	0.086

294	P	ATS364	Autism	70	0.085

295	P	GLM007	Glomerulonephritis	61	0.085

296	c	OVR114	Ovarian Cancer 1	62	0.085

297		SPP011	Suppression of Tumorigenicity 12	61	0.085

298	P	EHL052	Ehlers-Danlos Syndrome, Vascular Type	55	0.085

299		PRT036	Peritonitis	66	0.085

300		PGT001	Paget's Disease of Bone	59	0.085

301		PRX028	Peroxisomal Acyl-Coa Oxidase Deficiency	52	0.085

302	c	BRT028	Brittle Cornea Syndrome 1	28	0.085

303		PRS042	Prostate Disease	44	0.084

304	P	EPL164	Epilepsy	69	0.084

305		RTN018	Retinal Disease	56	0.084

306		TNG002	Tangier Disease	64	0.084

307		STR067	Stroke, Ischemic	82	0.084

308		PRP080	Peripheral Artery Disease	53	0.083

309	P	PRX010	Paroxysmal Ventricular Fibrillation	28	0.083

310		MSC004	Muscle Tissue Disease	39	0.083

311		HDC001	Headache	59	0.083

312		MDD011	Mood Disorder	63	0.083

313		CHD001	Chediak-Higashi Syndrome	65	0.083

314		DMY004	Demyelinating Disease	57	0.083

315	c	INF071	Inflammatory Bowel Disease 1	53	0.083

316	P	PRM002	Primary Hyperoxaluria	53	0.082

317	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.082

318		PRT030	Parathyroid Gland Disease	49	0.082

319	P	MSC033	Muscle Disorders	52	0.082

320	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	50	0.082

321	P	GRV001	Graves' Disease	61	0.082

322		FND001	Fundus Albipunctatus	53	0.082

323		VSC008	Vascular Hemostatic Disease	36	0.082

324	P	DMN001	Diamond-Blackfan Anemia	69	0.081

325		PLM134	Pulmonary Fibrosis, Idiopathic	73	0.081

326		VSC011	Vasculitis	65	0.081

327		BRC012	Brucellosis	70	0.081

328	P	PSD087	Pseudoxanthoma Elasticum	67	0.081

329	P	NTR004	Neutropenia	60	0.081

330	c	MCP004	Mucopolysaccharidosis Iv	59	0.081

331	c	RHB011	Rhabdoid Tumor Predisposition Syndrome 2	26	0.081

332		GST033	Gestational Diabetes	60	0.080

333	c	PNS012	Paine Syndrome	62	0.080

334	c	VSC019	Vesicoureteral Reflux 1	57	0.080

335		SCK005	Sickle Cell Disease	54	0.080

336		SCK003	Sickle Cell Anemia	72	0.080

337	P	CRY007	Cryoglobulinemia, Familial Mixed	54	0.080

338	c	LKM062	Leukemia, Acute Lymphoblastic	69	0.080

339		HMS001	Hemosiderosis	51	0.080

340		IRN001	Iron Deficiency Anemia	55	0.080

341	P	MRQ003	Morquio Syndrome	31	0.080

342		ALP103	Alpha-1-Antitrypsin Deficiency	61	0.079

343	c	HMC039	Hemochromatosis, Type 1	70	0.079

344		MCS002	Mucositis	60	0.079

345	P	KRB001	Krabbe Disease	69	0.078

346		KRT019	Keratitis, Hereditary	52	0.078

347		NPH009	Nephrolithiasis	55	0.078

348	P	NSP012	Nasopharyngeal Carcinoma	67	0.078

349	P	FML018	Familial Mediterranean Fever	73	0.078

350		KND001	Kindler Syndrome	50	0.077

351		HMG005	Hemoglobinopathy	53	0.077

352		PRD007	Periodontal Disease	64	0.077

353	c	PRM196	Premature Ovarian Failure 1	71	0.077

354	c	MCP024	Mucopolysaccharidosis Type Vi	62	0.077

355	P	RHN004	Rhinitis	61	0.077

356	P	ORT004	Orthostatic Intolerance	68	0.077

357		FLT009	Folate Malabsorption, Hereditary	35	0.077

358	c	ART101	Aortic Valve Disease 2	73	0.077

359		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.077

360		CD4003	Cd40 Ligand Deficiency	44	0.076

361		MTC008	Mitochondrial Complex Iii Deficiency	32	0.076

362		LYM133	Lymphoma, Hodgkin, Classic	71	0.076

363		SPR004	Supravalvular Aortic Stenosis	53	0.076

364		HYP810	Hypereosinophilic Syndrome, Idiopathic	58	0.076

365		MTY001	Mutyh-Associated Polyposis	48	0.076

366	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	59	0.076

367		VTM027	Vitamin D-Dependent Rickets, Type 2a	51	0.076

368	c	CRD187	Cardiomyopathy, Dilated, 3b	46	0.076

369	P	MCR115	Microvascular Complications of Diabetes 5	71	0.076

370	P	MSC005	Muscular Dystrophy	66	0.076

371	P	GNT009	Giant Axonal Neuropathy	51	0.076

372	c	GNT049	Giant Axonal Neuropathy 1, Autosomal Recessive	37	0.076

373		WLL001	Williams-Beuren Syndrome	63	0.075

374		PHR003	Pharyngitis	59	0.075

375		DFC004	Deficiency Anemia	61	0.075

376		HMT018	Hematopoietic Stem Cell Transplantation	57	0.075

377	P	END044	Endometriosis	64	0.075

378	P	MJR001	Major Depressive Disorder	65	0.075

379		OVR063	Overnutrition	53	0.075

380	P	HYP802	Hypocalcemia, Autosomal Dominant 1	62	0.075

381		APL001	Aplastic Anemia	73	0.074

382	c	LKM004	Leukemia, B-Cell, Chronic	36	0.074

383		GRN017	Granulocytopenia	43	0.074

384		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	40	0.074

385	P	PRK057	Parkinson Disease, Late-Onset	76	0.074

386	P	AMY004	Amyloidosis	68	0.074

387		ACT118	Acute Non Lymphoblastic Leukemia	32	0.074

388		PRM236	Primary Biliary Cholangitis	55	0.074

389		DFF005	Diffuse Large B-Cell Lymphoma	56	0.074

390		LNG039	Lung Squamous Cell Carcinoma	59	0.074

391	c	PRG126	Progressive Familial Heart Block	47	0.074

392	P	PRP029	Porphyria	62	0.074

393	c	ACT071	Acute Kidney Failure	54	0.074

394		EWN002	Ewing's Family of Tumors	56	0.074

395		GNG013	Gingivitis	63	0.073

396		THY030	Thyroid Gland Disease	51	0.073

397		GND003	Gonadal Disease	46	0.073

398		CHL068	Cholestasis	60	0.073

399		SPN186	Spinal Cord Injury	68	0.073

400		ANX004	Anoxia	49	0.073

401		HYP458	Hyper Ige Syndrome	49	0.072

402		THY028	Thyroid Cancer	66	0.072

403		ILT001	Ileitis	56	0.072

404	P	ESS003	Essential Thrombocythemia	70	0.072

405		OPT006	Optic Nerve Disease	57	0.072

406	P	CMR001	Camurati-Engelmann Disease	61	0.072

407	c	HYP595	Hypertension, Essential	76	0.072

408		GYR004	Gyrate Atrophy of Choroid and Retina	50	0.072

409	P	PRM006	Primary Biliary Cirrhosis	53	0.072

410	P	PRP003	Porphyria Cutanea Tarda	66	0.071

411	c	HYP794	Hyperoxaluria, Primary, Type I	41	0.071

412		HYP348	Hyperglycinuria	33	0.071

413		BTT001	Bietti Crystalline Corneoretinal Dystrophy	36	0.071

414		ADR007	Adrenoleukodystrophy	71	0.071

415		NRN004	Neuroendocrine Tumor	58	0.071

416	P	OVR049	Ovarian Disease	59	0.071

417	c	THR082	Thrombophilia Due to Activated Protein C Resistance	46	0.071

418	c	SVR003	Severe Congenital Neutropenia	58	0.071

419	c	MTR002	Mitral Valve Insufficiency	46	0.070

420	c	BLR024	Biliary Cirrhosis, Primary, 1	36	0.070

421	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	55	0.070

422		TRN018	Transitional Cell Carcinoma	61	0.070

423	P	AST007	Astrocytoma	51	0.070

424		HPD002	Hepadnavirus Infection	25	0.070

425		FBR012	Fabry Disease	71	0.070

426		HLC007	Helicobacter Pylori Infection	63	0.070

427		BTN003	Biotinidase Deficiency	56	0.070

428		THR100	Thrombocytopenic Purpura, Autoimmune	62	0.070

429		ATX010	Ataxia Neuropathy Spectrum	35	0.070

430	P	ALP009	Alopecia Areata	63	0.070

431	c	GLY008	Glycogen Storage Disease Ii	64	0.070

432	c	ACT210	Acute Respiratory Distress Syndrome	61	0.070

433		BRN080	Brain Ischemia	44	0.069

434	c	HMP029	Hemophilia a	68	0.069

435	c	PNC108	Pancreatitis, Hereditary	59	0.069

436	P	FML052	Familial Cold Autoinflammatory Syndrome	53	0.069

437		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	48	0.069

438		PRD004	Prediabetes Syndrome	45	0.069

439		MLN007	Male Infertility	53	0.069

440	P	GRF003	Graft-Versus-Host Disease	71	0.069

441	P	LTR001	Lateral Sclerosis	58	0.069

442		TRN022	Transcobalamin Ii Deficiency	46	0.068

443	P	HYP035	Hypophosphatasia	58	0.068

444		WLS001	Wilson Disease	71	0.068

445		FDL002	Food Allergy	55	0.068

446	P	BRN120	Bronchus Cancer	49	0.068

447	P	HYP111	Hyperprolinemia	34	0.068

448	c	CRP023	Carpenter Syndrome 1	54	0.068

449		NSP002	Nasopharyngitis	46	0.068

450	P	SLP006	Sleep Apnea	66	0.068

451		URT039	Urticaria	60	0.068

452	P	LCH002	Lichen Planus	57	0.067

453		BRN071	Brain Injury	53	0.067

454		FCT007	Factor Vii Deficiency	61	0.067

455		ATN005	Autonomic Dysfunction	50	0.067

456		ART016	Aortic Aneurysm	69	0.067

457		PRP027	Peripheral Vascular Disease	70	0.067

458	P	TYR004	Tyrosinemia	48	0.067

459		IRR002	Irritable Bowel Syndrome	62	0.067

460	P	SCK002	Sick Sinus Syndrome	53	0.067

461	P	CHR345	Chronic Pain	51	0.067

462	P	ATR005	Atrophic Gastritis	48	0.067

463		CHN016	Cohen Syndrome	47	0.066

464		GLC006	Galactosemia	65	0.066

465		TRN015	Transient Cerebral Ischemia	56	0.066

466		PRT014	Protein S Deficiency	47	0.066

467		BLD044	Bladder Disease	55	0.066

468		CHL065	Cholangiocarcinoma	63	0.066

469		LYM067	Lymphoid Leukemia	44	0.066

470		HYP056	Hypoglycemia	62	0.066

471		RLP002	Relapsing-Remitting Multiple Sclerosis	57	0.066

472	c	HMP004	Hemophilia B	67	0.066

473	c	LKM063	Leukemia, Chronic Myeloid	70	0.066

474	P	KDN017	Kidney Cancer	58	0.066

475	P	SCL057	Scoliosis, Isolated 1	40	0.066

476		OVR012	Ovarian Serous Cystadenocarcinoma	48	0.066

477		FCT006	Factor V Deficiency	53	0.066

478		URM002	Uremia	52	0.066

479	P	MYL005	Myelofibrosis	70	0.065

480	c	BSL007	Basal Cell Carcinoma	64	0.065

481	P	CRB048	Cerebral Cavernous Malformations	57	0.065

482		DBT010	Diabetic Neuropathy	59	0.065

483	P	ALG028	Alagille Syndrome 1	73	0.065

484	P	DST101	Distal Hereditary Motor Neuropathies	28	0.065

485		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	61	0.065

486		GT001	Gout	57	0.065

487	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	60	0.065

488	P	ACT074	Acute Lymphocytic Leukemia	59	0.065

489		BCK006	Back Pain	44	0.065

490	P	ADL010	Adult Respiratory Distress Syndrome	66	0.065

491		OST097	Osteoporotic Fracture	41	0.065

492	c	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	35	0.065

493	P	PLY019	Polyneuropathy	57	0.065

494		PRT037	Pertussis	68	0.064

495		CRD119	Cardiac Arrest	62	0.064

496	P	CNG003	Congenital Dyserythropoietic Anemia	41	0.064

497		PNG002	Pain Agnosia	42	0.064

498	P	LRY019	Laryngitis	56	0.064

499		ALL003	Allergic Rhinitis	67	0.064

500		NWB001	Newborn Respiratory Distress Syndrome	52	0.064

501		RSP007	Respiratory Distress Syndrome, Infant	34	0.064

502	P	CHR084	Chromosomal Disease	40	0.064

503	P	HYP599	Hypoparathyroidism, Familial Isolated	37	0.064

504	P	HMP007	Hemophilia	60	0.064

505		CYS013	Cystinuria	63	0.063

506	c	HYP793	Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1	40	0.063

507		APH001	Aphthous Stomatitis	63	0.063

508		HYP017	Hypophosphatemia	46	0.063

509	P	VTL001	Vitelliform Macular Dystrophy	42	0.063

510		APN008	Apnea, Obstructive Sleep	67	0.063

511		HRP008	Herpes Simiae	16	0.063

512		DNN002	Donnai-Barrow Syndrome	43	0.063

513		BRN056	Bronchopulmonary Dysplasia	60	0.063

514		PRT038	Protein-Energy Malnutrition	51	0.063

515	P	OPN001	Open-Angle Glaucoma	51	0.063

516	P	CHR012	Chronic Granulomatous Disease	69	0.063

517		MTC027	Mitochondrial Trifunctional Protein Deficiency	54	0.063

518		GLN010	Glanzmann Thrombasthenia	65	0.063

519	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	21	0.063

520		FCT002	Factor Xi Deficiency	64	0.062

521		ISL003	Isolated Growth Hormone Deficiency	55	0.062

522	P	BPL003	Bipolar Disorder	59	0.062

523		CRD223	Cardiac Arrhythmia	54	0.062

524	P	PSD015	Pseudohypoparathyroidism	50	0.062

525	c	WLM013	Wilms Tumor 1	64	0.062

526	c	MSC121	Muscular Dystrophy, Limb-Girdle, Type 2a	58	0.062

527		OCL006	Ocular Hypertension	53	0.062

528	P	CLC063	Celiac Disease 1	71	0.062

529		ACQ031	Acquired Idiopathic Sideroblastic Anemia	36	0.062

530	P	NRN021	Neuronal Ceroid Lipofuscinosis	61	0.062

531	c	PYR007	Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia	30	0.062

532		BRR014	Barrett Esophagus	63	0.062

533	c	MGL018	Megaloblastic Anemia 1	42	0.062

534		DRR014	Darier-White Disease	61	0.062

535		UTR024	Uterine Carcinosarcoma	59	0.062

536	P	RTN022	Retinal Vein Occlusion	52	0.062

537		GLC022	Glucose/galactose Malabsorption	41	0.062

538		PYR015	Pyridoxal 5'-Phosphate-Dependent Epilepsy	17	0.062

539		ERY003	Erythema Multiforme	60	0.061

540		RFS006	Refsum Disease, Classic	62	0.061

541	P	MCL013	Mucolipidosis Iv	67	0.061

542		CLN015	Colon Adenocarcinoma	53	0.061

543	P	MSC003	Muscular Atrophy	54	0.061

544		INT007	Intermediate Coronary Syndrome	52	0.061

545	P	HYP058	Hypervitaminosis a	47	0.061

546		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	56	0.061

547	c	MCR130	Microvascular Complications of Diabetes 6	40	0.061

548		ART001	Arterial Tortuosity Syndrome	53	0.061

549		PRP001	Propionic Acidemia	62	0.061

550	c	CHR579	Chiari Malformation Type Ii	45	0.061

551		BLD137	Blood Group--Ahonen	17	0.061

552	P	FLL037	Follicular Lymphoma	69	0.061

553		END057	Endometrial Cancer	65	0.061

554	P	OVR046	Ovarian Cyst	50	0.061

555	P	RTT002	Rett Syndrome	82	0.060

556	c	AFB002	Afibrinogenemia, Congenital	60	0.060

557		SPN041	Spinal Cord Disease	51	0.060

558		BRN002	Bronchiolitis	59	0.060

559	c	MCR113	Microvascular Complications of Diabetes 3	52	0.060

560	c	MCR120	Microvascular Complications of Diabetes 7	37	0.060

561	c	MCR133	Microvascular Complications of Diabetes 4	35	0.060

562		SPS150	Spastic Ataxia, Charlevoix-Saguenay Type	50	0.060

563	P	ANG001	Angelman Syndrome	61	0.060

564		FBR047	Fibromyalgia	57	0.060

565		CRT016	Carotid Artery Disease	57	0.060

566	P	AST055	Asthma-Related Traits 1	30	0.060

567		SPN051	Spondylitis	55	0.060

568		ATM052	Autoimmune Disease 1	34	0.060

569	P	HYP076	Hyperthyroidism	56	0.060

570	P	PTY003	Pityriasis Rubra Pilaris	50	0.060

571	c	LYN004	Lynch Syndrome I	58	0.060

572	c	EHL078	Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1	44	0.060

573		GLB015	Glioblastoma Multiforme	60	0.059

574		MYL031	Myeloproliferative Neoplasm	63	0.059

575	P	TYS001	Tay-Sachs Disease	71	0.059

576	c	HYP543	Hypoplastic Left Heart Syndrome 1	42	0.059

577	c	EXD008	Exudative Vitreoretinopathy 1	69	0.059

578		INC002	Inclusion Body Myositis	63	0.059

579		FXF002	Fox-Fordyce Disease	40	0.059

580		CHR619	Chromosome 2q35 Duplication Syndrome	55	0.059

581	P	RSP003	Respiratory Failure	70	0.059

582	P	DYS021	Dysautonomia	43	0.059

583	c	AMG001	Amegakaryocytic Thrombocytopenia, Congenital	52	0.059

584		PYR021	Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency	27	0.059

585		GNG011	Gingival Disease	49	0.058

586		RST001	Restless Legs Syndrome	52	0.058

587		ALP012	Alpha-Methylacyl-Coa Racemase Deficiency	46	0.058

588	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	64	0.058

589	P	CNJ013	Conjunctivitis	63	0.058

590		PHT003	Phototoxic Dermatitis	40	0.058

591		RSS026	Roussy-Levy Hereditary Areflexic Dystasia	46	0.058

592		SMT004	Smith-Lemli-Opitz Syndrome	68	0.058

593	P	PRP034	Purpura Fulminans	45	0.058

594		PRP056	Porphyria, Acute Hepatic	42	0.058

595	P	ORF002	Orofacial Cleft	41	0.058

596	c	ACT027	Acute Pancreatitis	60	0.058

597	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	0.058

598		CRN024	Corneal Disease	47	0.058

599		PRS063	Paresthesia	37	0.057

600		PRS129	Prostatic Hyperplasia, Benign	48	0.057

601		HYP080	Hypogonadism	51	0.057

602		ORL011	Oral Cancer	59	0.057

603		KRT009	Keratosis	53	0.057

604		MVM001	Movement Disease	60	0.057

605		CRB011	Cerebrotendinous Xanthomatosis	63	0.057

606	P	LCT002	Lactose Intolerance	47	0.057

607		CMP010	Complex Regional Pain Syndrome	57	0.057

608		OVR094	Ovarian Epithelial Cancer	38	0.057

609		DWN001	Down Syndrome	69	0.057

610		ENT011	Enterocolitis	54	0.057

611		DPH001	Diphtheria	62	0.057

612		CRB045	Cerebellar Hypoplasia	48	0.057

613		ALC006	Alcoholic Hepatitis	62	0.056

614		BDY007	Body Mass Index Quantitative Trait Locus 1	26	0.056

615		PLS009	Plasma Cell Neoplasm	51	0.056

616		PNC001	Pancytopenia	51	0.056

617	c	ATM011	Autoimmune Hepatitis	62	0.056

618	P	SHR001	Short Bowel Syndrome	51	0.056

619	P	SNS014	Sinusitis	62	0.056

620		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	44	0.056

621	c	PLY105	Polycystic Ovary Syndrome 1	30	0.056

622		HMP009	Haemophilus Influenzae	49	0.056

623	P	ENC004	Encephalitis	65	0.056

624		MCK007	Muckle-Wells Syndrome	64	0.056

625		ALC007	Alcohol Dependence	65	0.056

626	c	INS002	in Situ Carcinoma	56	0.056

627		DNT012	Dental Caries	51	0.056

628		PLC007	Placental Abruption	50	0.056

629		HML018	Homologous Wasting Disease	18	0.056

630		PNC041	Pancreatic Ductal Adenocarcinoma	52	0.056

631	c	LKM056	Leukemia, Chronic Lymphocytic 2	41	0.055

632		CHY002	Chylomicron Retention Disease	52	0.055

633		ARM001	Aromatase Deficiency	52	0.055

634		ATN002	Autonomic Nervous System Disease	51	0.055

635		DGN001	Degenerative Disc Disease	53	0.055

636		HMC014	Homocysteinemia	48	0.055

637	P	ALC004	Alcohol Abuse	63	0.055

638	P	UVT001	Uveitis	60	0.055

639		MCR017	Macrocytic Anemia	45	0.055

640		CHR074	Choriocarcinoma	47	0.055

641	P	GCH001	Gaucher's Disease	62	0.055

642		ATR013	Atrichia with Papular Lesions	35	0.055

643	c	MLG068	Malignant Glioma	38	0.055

644		FNC005	Functional Colonic Disease	31	0.054

645	P	MYS005	Myositis	63	0.054

646		DYS073	Dysphagia	46	0.054

647		VTM009	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1	21	0.054

648		NSD001	Nose Disease	50	0.054

649		STT009	Sutton Disease 2	29	0.054

650		MNS002	Mini Stroke	23	0.054

651		HRP004	Herpes Zoster	60	0.054

652	P	MTC069	Mitochondrial Disorders	49	0.054

653		BRN024	Bronchitis	66	0.054

654	P	ACT008	Actinic Keratosis	54	0.054

655		GTR002	Goiter	52	0.054

656	c	SCL052	Scleroderma, Familial Progressive	64	0.054

657	c	STR084	Stargardt Disease 1	48	0.054

658		TRD006	Tardive Dyskinesia	59	0.054

659		HRT012	Heart Valve Disease	44	0.054

660		SPS057	Spasticity	41	0.054

661		SWL001	Swallowing Disorders	36	0.054

662		ASP002	Aspartylglucosaminuria	56	0.054

663	c	SPN225	Spondyloarthropathy 1	71	0.054

664		ACT119	Acute Promyelocytic Leukemia	59	0.054

665		ADR054	Adrenocortical Carcinoma, Hereditary	70	0.053

666		OTT002	Otitis Media	66	0.053

667		THY111	Thyroid Carcinoma, Familial Medullary	69	0.053

668		URN022	Urinary Tract Infections, Recurrent	29	0.053

669		GNR004	Generalized Anxiety Disorder	53	0.053

670		BSL008	Basal Ganglia Disease	46	0.053

671		VGN023	Vaginitis	58	0.053

672		CRV040	Cervix Carcinoma	53	0.053

673		GST092	Gastroesophageal Reflux	64	0.053

674		LMY002	Leiomyoma	57	0.053

675	c	ACT073	Acute Leukemia	60	0.053

676	P	ANT006	Antiphospholipid Syndrome	59	0.053

677		STM006	Stomach Disease	52	0.053

678	c	BCT007	Bacterial Meningitis	58	0.053

679		OPT009	Optic Neuritis	53	0.053

680		HYD046	Hydatidiform Mole, Recurrent, 1	52	0.053

681		MTC061	Mitochondrial Dna Depletion Syndrome 1	44	0.053

682		ORL013	Oral Lichen Planus	51	0.053

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

684		CHR008	Choroiditis	46	0.053

685		SFT003	Soft Tissue Sarcoma	58	0.053

686	P	ANP001	Anaplastic Large Cell Lymphoma	59	0.053

687	P	ERY053	Erythrokeratodermia Variabilis Et Progressiva 1	51	0.052

688		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	44	0.052

689		ADN011	Adenoid Cystic Carcinoma	65	0.052

690		MTR014	Motor Neuron Disease	61	0.052

691		INT088	Intrinsic Factor Deficiency	35	0.052

692		AMN002	Amino Acid Metabolic Disorder	47	0.052

693	P	PLY014	Polycystic Kidney Disease	60	0.052

694	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.052

695	P	TCL004	T-Cell Leukemia	50	0.052

696		CHR005	Chorioamnionitis	51	0.052

697		BRN004	Brain Edema	55	0.052

698		ESP023	Esophageal Disease	56	0.052

699		SPN369	Spinal Disease	42	0.052

700		SCH014	Schistosomiasis	62	0.052

701		OVR029	Ovarian Hyperstimulation Syndrome	64	0.052

702		LSH001	Leishmaniasis	70	0.052

703		TTH006	Tooth Disease	53	0.051

704		PPL022	Papilloma	58	0.051

705		PLS011	Plasmacytoma	60	0.051

706		HYP636	Hypocalcemic Vitamin D-Dependent Rickets	31	0.051

707	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.051

708		DHY002	Dihydropyrimidine Dehydrogenase Deficiency	55	0.051

709		CYS019	Cystathioninuria	30	0.051

710		ORL015	Oral Squamous Cell Carcinoma	45	0.051

711		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	47	0.051

712		BRK010	Burkitt Lymphoma	68	0.051

713	c	CNT016	Central Retinal Vein Occlusion	49	0.051

714		HDN002	Head Injury	47	0.051

715		MRB003	Morbid Obesity	60	0.051

716		HPT070	Hepatosplenic T-Cell Lymphoma	43	0.051

717		PRT018	Portal Vein Thrombosis	50	0.051

718		NRV006	Nervous System Cancer	60	0.051

719		RFR010	Refractory Anemia	49	0.051

720		RFL001	Reflex Sympathetic Dystrophy	51	0.051

721	c	LBR014	Leber Congenital Amaurosis 4	49	0.051

722		RFR003	Refractive Error	44	0.050

723		SPN404	Spinal and Bulbar Muscular Atrophy, X-Linked 1	63	0.050

724	P	CHR071	Charcot-Marie-Tooth Disease	65	0.050

725	P	FBR017	Fibrosarcoma	61	0.050

726		PST021	Postpartum Depression	53	0.050

727		HYP025	Hyperphosphatemia	48	0.050

728		PYR016	Pyridoxine Deficiency	36	0.050

729	P	DYS007	Dyskeratosis Congenita	67	0.050

730		LKC009	Leukocyte Adhesion Deficiency, Type I	57	0.050

731		SNS003	Sensory Peripheral Neuropathy	53	0.050

732	P	PRT013	Portal Hypertension	59	0.050

733		HMC016	Homocystinuria Due to Cbs Deficiency	20	0.050

734		CNC002	Cinca Syndrome	62	0.050

735	P	FML068	Familial Hypocalciuric Hypercalcemia	48	0.050

736	P	TRM003	Tremor	54	0.050

737		SCH012	Schizoaffective Disorder	54	0.050

738	P	DBT005	Diabetes Insipidus	54	0.050

739		AZS001	Azoospermia	45	0.050

740	P	SCL018	Scoliosis	55	0.050

741		SPC010	Speech and Communication Disorders	52	0.050

742		ALG001	Algoneurodystrophy	39	0.050

743		BCT002	Bacterial Vaginosis	54	0.050

744		AMN012	Aminoacidopathies	24	0.050

745		FLL027	Fallopian Tube Carcinoma	62	0.050

746		HYP005	Hypokalemia	53	0.050

747		HMT002	Hematologic Cancer	63	0.050

748	P	SML001	Small Cell Carcinoma	58	0.049

749		BLD053	Blood Platelet Disease	55	0.049

750		MTC005	Mitochondrial Metabolism Disease	44	0.049

751		LKP003	Leukoplakia	42	0.049

752		BRT054	Brittle Bone Disorder	69	0.049

753		SPH010	Sphingolipidosis	47	0.049

754		NPH003	Nephrocalcinosis	48	0.049

755		PRV006	Pervasive Developmental Disorder	55	0.049

756		LRG015	Large Intestine Adenoma	17	0.049

757		PSR001	Psoriatic Arthritis	65	0.049

758	P	AGG001	Aggressive Periodontitis	54	0.049

759	c	MCL066	Macular Dystrophy, Vitelliform, 2	42	0.049

760		GLT007	Glutathione Synthetase Deficiency	46	0.049

761		CMP028	Complement Component 2 Deficiency	45	0.049

762	P	CNN004	Connective Tissue Cancer	45	0.049

763		CLR030	Clear Cell Renal Cell Carcinoma	49	0.049

764		PRN019	Perinatal Necrotizing Enterocolitis	56	0.049

765		CNR004	Cone-Rod Dystrophy 2	67	0.049

766		INB001	Inborn Amino Acid Metabolism Disorder	16	0.049

767	P	HRP006	Herpes Simplex	69	0.049

768		VNW001	Von Willebrand's Disease	60	0.049

769		LMY014	Leiomyoma, Uterine	53	0.048

770		HYP043	Hyperandrogenism	50	0.048

771		SYN036	Syncope	47	0.048

772	c	CRD089	Cardiomyopathy, Familial Hypertrophic, 14	22	0.048

773		SPP010	Suppressor of Tumorigenicity 3	54	0.048

774		LPD009	Lipid Storage Disease	51	0.048

775		MTB004	Metabolic Acidosis	48	0.048

776	P	PLM036	Pulmonary Fibrosis	69	0.048

777		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	45	0.048

778		PRT029	Parathyroid Adenoma	49	0.048

779	P	ATS366	Autism X-Linked 2	43	0.048

780		PRP036	Peripheral T-Cell Lymphoma	56	0.048

781	c	ART115	Aortic Valve Disease 1	61	0.048

782		PLM031	Poliomyelitis	58	0.048

783		TXC002	Toxic Encephalopathy	55	0.048

784		THM002	Thiamine-Responsive Megaloblastic Anemia Syndrome	41	0.048

785	c	CHR417	Chronic Graft Versus Host Disease	64	0.047

786	P	HRD018	Hair Disease	51	0.047

787	P	THR005	Thrombotic Thrombocytopenic Purpura	63	0.047

788		KLD001	Keloids	49	0.047

789	c	MNN047	Mannosidosis, Alpha B, Lysosomal	56	0.047

790		LYS002	Lysosomal Storage Disease	56	0.047

791	P	MSC007	Muscle Hypertrophy	58	0.047

792	c	AMY087	Amyloidosis, Hereditary, Transthyretin-Related	57	0.047

793		HYP776	Hyperparathyroidism, Neonatal Severe	40	0.047

794	c	JVN004	Juvenile Myelomonocytic Leukemia	67	0.047

795	P	ASP006	Aspergillosis	65	0.047

796		BLR006	Biliary Tract Disease	54	0.047

797	P	PMP001	Pemphigus	54	0.047

798		PRT035	Peritoneum Cancer	42	0.047

799	P	LRY044	Larynx Cancer	60	0.047

800		MTH077	Methylmalonic Aciduria, Cbla Type	26	0.047

801		NRR001	Neuroretinitis	46	0.046

802		CRN031	Cranial Nerve Disease	45	0.046

803	P	SPN046	Spinal Muscular Atrophy	63	0.046

804	P	MTC133	Mitochondrial Myopathy	54	0.046

805	P	FRG001	Fragile X Syndrome	69	0.046

806		CRB085	Cerebral Hemorrhage	47	0.046

807		SYS003	Systolic Heart Failure	46	0.046

808		DYS014	Dyspepsia	54	0.046

809	c	SVR005	Severe Pre-Eclampsia	53	0.046

810		SBC017	Sebaceous Gland Disease	38	0.046

811		MNK001	Menkes Disease	63	0.046

812		MYF002	Myofascial Pain Syndrome	43	0.046

813		BRS099	Breast Ductal Carcinoma	56	0.046

814	P	CYS018	Cystitis	56	0.046

815		DCT002	Ductal Carcinoma in Situ	55	0.046

816		HMR039	Hemorrhage, Intracerebral	57	0.046

817	P	CTN003	Cutaneous Lupus Erythematosus	52	0.046

818		CHC001	Chickenpox	49	0.046

819	c	PSR017	Psoriasis 2	39	0.046

820		DBF001	D-Bifunctional Protein Deficiency	57	0.046

821	c	BNG091	Benign Chronic Pemphigus	52	0.046

822	P	AGM019	Agammaglobulinemia, X-Linked	68	0.046

823		OST003	Osteonecrosis	63	0.046

824	P	ORL007	Oral Cavity Cancer	61	0.045

825		CRV002	Cervix Uteri Carcinoma in Situ	47	0.045

826		HYP457	Hypertrophic Scars	47	0.045

827	c	MLG079	Malignant Pleural Mesothelioma	46	0.045

828		DSS009	Disseminated Intravascular Coagulation	55	0.045

829	P	BRN035	Brain Stem Glioma	50	0.045

830	P	PLY018	Polycythemia	58	0.045

831	P	CHR285	Chronic Myelomonocytic Leukemia	62	0.045

832		MST005	Mastitis	55	0.045

833		FNT004	Fainting	36	0.045

834	P	MCR010	Microcephaly	57	0.045

835	P	CTN015	Cutaneous T Cell Lymphoma	55	0.045

836		CLC001	Calciphylaxis	52	0.045

837		DBT008	Diabetic Angiopathy	47	0.045

838		BRB001	Beriberi	41	0.045

839		PCK003	Pick Disease of Brain	65	0.045

840		VCC001	Vaccinia	50	0.045

841	P	UTR058	Uterine Anomalies	59	0.045

842		ORL012	Oral Leukoplakia	47	0.045

843	P	VTM029	Vitamin D Hydroxylation-Deficient Rickets, Type 1b	24	0.045

844	c	ALP101	Alpha-Thalassemia	59	0.045

845		ALR002	Al-Raqad Syndrome	31	0.045

846	c	ACT135	Acute Graft Versus Host Disease	56	0.045

847		BLR001	Biliary Atresia	57	0.045

848		LNS003	Lens Disease	39	0.045

849		RCT018	Rectal Neoplasm	54	0.045

850	c	MSC120	Muscular Dystrophy, Limb-Girdle, Type 2c	51	0.045

851	c	SPN327	Spinocerebellar Ataxia, Autosomal Recessive 1	60	0.045

852		IRN004	Iron-Refractory Iron Deficiency Anemia	42	0.045

853	P	TMP003	Temporal Arteritis	66	0.045

854	c	RTN162	Retinitis Pigmentosa 2	50	0.045

855		CRV045	Cervical Intraepithelial Neoplasia	43	0.045

856		PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	62	0.045

857	P	MLN069	Melanoma, Uveal	58	0.045

858		GRW007	Growth Hormone Deficiency	51	0.044

859	c	ANM036	Anemia, Sideroblastic, 1	55	0.044

860	P	FML011	Familial Adenomatous Polyposis	71	0.044

861	P	LCT001	Lactic Acidosis	50	0.044

862		HYP189	Hypoadrenalism	43	0.044

863		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	69	0.044

864	P	GLL020	Gallbladder Disease	64	0.044

865	P	GST049	Gastrointestinal System Cancer	59	0.044

866	c	CHL119	Cholangitis, Primary Sclerosing	59	0.044

867		MRG003	Marginal Zone B-Cell Lymphoma	56	0.044

868		EXC002	Exocrine Pancreatic Insufficiency	43	0.044

869		ICH054	Ichthyosis, X-Linked	58	0.044

870		VSC002	Vascular Dementia	58	0.044

871		SPS019	Spastic Paraparesis	35	0.044

872		CYT008	Cytomegalovirus Infection	56	0.044

873		SKL017	Skeletal Dysplasias	48	0.044

874	c	ALZ056	Alzheimer Disease 3	47	0.044

875	P	HYP087	Hypotrichosis	48	0.044

876		IDP070	Idiopathic Scoliosis	41	0.044

877		NTH001	Netherton Syndrome	60	0.044

878		THR004	Thrombocytosis	54	0.044

879		MNT001	Mantle Cell Lymphoma	73	0.043

880	P	GRM010	Germ Cells Tumors	36	0.043

881		RTC005	Reticulosarcoma	49	0.043

882		BDY004	Body Mass Index Quantitative Trait Locus 11	68	0.043

883		CHR177	Chromophobe Renal Cell Carcinoma	55	0.043

884		PPT005	Peptic Ulcer Disease	61	0.043

885		NRF026	Neurofibromatosis, Type Iv, of Riccardi	73	0.043

886		PLM010	Pulmonary Edema	56	0.043

887		CRV069	Cervix Disease	35	0.043

888		MNN020	Meningococcal Infection	47	0.043

889	c	GCH015	Gaucher Disease, Type I	57	0.043

890		CLS016	Clostridium Difficile Colitis	47	0.043

891		HTC003	Hutchinson-Gilford Progeria Syndrome	62	0.043

892	P	EPD009	Epidermolysis Bullosa Dystrophica	58	0.043

893		HST017	Histiocytosis-Lymphadenopathy Plus Syndrome	40	0.043

894	P	MYS003	Myasthenia Gravis	72	0.043

895		BLL006	Bullous Pemphigoid	63	0.043

896	P	MNC007	Monocytic Leukemia	57	0.043

897		CHL067	Cholecystitis	57	0.043

898		MCR004	Macroglobulinemia	53	0.043

899	c	PYR010	Peyronie's Disease	53	0.043

900		INT303	Intracranial Hypertension, Idiopathic	50	0.043

901		DYS015	Dysentery	43	0.043

902	P	BRN009	Burning Mouth Syndrome	53	0.043

903		FCL044	Fecal Incontinence	38	0.043

904		MSC152	Muscular Dystrophy, Becker Type	60	0.043

905		INT002	Intermittent Claudication	61	0.042

906	P	PYL005	Pyelonephritis	56	0.042

907		KRT006	Keratoconjunctivitis	55	0.042

908		MCL006	Macular Retinal Edema	51	0.042

909		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.042

910		CNJ012	Conjunctival Disease	48	0.042

911		TTH004	Tethered Spinal Cord Syndrome	38	0.042

912	c	MLG074	Malignant Mesenchymoma	54	0.042

913		NRF007	Neurofibroma	65	0.042

914	P	HYP614	Hyperlipidemia, Familial Combined	56	0.042

915	c	ADL017	Adult T-Cell Leukemia	62	0.042

916	P	ATS308	Autosomal Dominant Cerebellar Ataxia	54	0.042

917	c	DNR003	Duane Retraction Syndrome 1	34	0.042

918		NST002	Nestor-Guillermo Progeria Syndrome	25	0.042

919	P	INT001	Intrahepatic Cholestasis	60	0.042

920	c	FCL025	Focal Segmental Glomerulosclerosis 1	59	0.042

921		PRT082	Preterm Premature Rupture of the Membranes	52	0.042

922	c	INH004	Inherited Blood Coagulation Disease	41	0.042

923		SND001	Sandhoff Disease	64	0.042

924		RHB001	Rhabdoid Cancer	62	0.042

925	P	MMB011	Membranous Nephropathy	57	0.042

926	c	CRD147	Cardiomyopathy, Familial Hypertrophic, 20	36	0.042

927	P	INT070	Intestinal Obstruction	56	0.042

928		BRN022	Bronchiectasis	55	0.042

929	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	52	0.042

930		CRT013	Carotid Stenosis	52	0.042

931		CHL123	Chlamydia	64	0.042

932		PRP032	Porphyria Variegata	55	0.042

933	P	SYP003	Syphilis	51	0.042

934		HPT019	Hepatic Encephalopathy	58	0.042

935	P	BRS044	Breast Adenocarcinoma	58	0.042

936		DDN006	Duodenitis	48	0.042

937	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.042

938	P	KRT007	Keratoconus	48	0.042

939		MLT157	Multiple System Atrophy 1	73	0.042

940	P	SBS003	Substance Abuse	57	0.042

941		GLC009	Glucosephosphate Dehydrogenase Deficiency	48	0.042

942	P	CRD132	Cardiac Conduction Defect	59	0.041

943	P	HYP014	Hyperuricemia	55	0.041

944	P	HMG032	Hemoglobin H Disease	52	0.041

945		KRT008	Keratopathy	43	0.041

946		GRY002	Gray Platelet Syndrome	55	0.041

947	P	DYS193	Dystonia 11, Myoclonic	51	0.041

948		MGK001	Megakaryocytic Leukemia	63	0.041

949		CRP001	Carpal Tunnel Syndrome	66	0.041

950		MYM001	Myoma	55	0.041

951		PGM003	Pigmentation Disease	45	0.041

952		HYP064	Hypogonadotropism	40	0.041

953		FLL029	Fallopian Tube Disease	35	0.041

954		INT074	Intracranial Arteriosclerosis	15	0.041

955		NSS002	Neisseria Meningitidis Infection	49	0.041

956	P	TRN020	Turner Syndrome	68	0.041

957		RTC009	Reticulum Cell Sarcoma	52	0.041

958		INT038	Interdigitating Dendritic Cell Sarcoma	44	0.041

959	P	ENC011	Encephalomyopathy	40	0.041

960		APP008	Appendicitis	64	0.041

961		GLL018	Gallbladder Cancer	51	0.041

962	P	FRD012	Friedreich Ataxia 1	64	0.041

963		CLF027	Cleft Palate, Isolated	63	0.041

964	P	PLM034	Pulmonary Emphysema	58	0.041

965		INT075	Intracranial Hypertension	52	0.041

966		PRX077	Peroxisomal Biogenesis Disorders	40	0.041

967		TST014	Testicular Cancer	53	0.041

968		SPL018	Splenomegaly	46	0.041

969		VRC005	Varicose Veins	64	0.041

970		PST028	Post-Traumatic Stress Disorder	58	0.041

971		PLS007	Plasmodium Falciparum Malaria	57	0.041

972		INT066	Interstitial Lung Disease	62	0.041

973		INT079	Intrahepatic Cholangiocarcinoma	52	0.041

974		HMC041	Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity	41	0.041

975	P	ANG015	Angioedema	57	0.040

976		HLL004	Hellp Syndrome	52	0.040

977	P	EST001	Estrogen-Receptor Positive Breast Cancer	51	0.040

978	P	RFR008	Refractory Anemia with Excess Blasts	33	0.040

979	P	EPN002	Ependymoma	55	0.040

980		CLR109	Colorectal Adenocarcinoma	53	0.040

981	P	PTT006	Pituitary Adenoma	52	0.040

982	c	ACT134	Acute Liver Failure	52	0.040

983		FCT003	Factor X Deficiency	57	0.040

984		MN1001	Mn1	35	0.040

985		HRW001	Hair Whorl	32	0.040

986		APH002	Aphasia	58	0.040

987	c	CRD093	Cardiomyopathy, Dilated, 1a	57	0.040

988		ATN007	Autoinflammation, Lipodystrophy, and Dermatosis Syndrome	69	0.040

989	P	CHL066	Cholangitis	52	0.040

990	c	PSR028	Psoriasis 7	38	0.040

991	c	PSR032	Psoriasis 11	38	0.040

992	c	PSR018	Psoriasis 13	37	0.040

993	c	CHR020	Chronic Interstitial Cystitis	43	0.040

994		MCR018	Microcytic Anemia	43	0.040

995	c	PRM126	Primary Peritoneal Carcinoma	60	0.040

996	P	FCS002	Fucosidosis	60	0.040

997	P	MYC008	Myocarditis	58	0.040

998		CMB081	Combined Immunodeficiency, X-Linked	64	0.040

999		PRP083	Porphyria, Acute Intermittent	61	0.040

1000	P	BRN019	Bernard-Soulier Syndrome	59	0.040

1001		CMM004	Common Variable Immunodeficiency	70	0.040

1002	P	LKD001	Leukodystrophy	57	0.040

1003		ACL001	Acalculous Cholecystitis	38	0.040

1004		CNT047	Contact Dermatitis	63	0.040

1005	P	HMR012	Hemorrhagic Fever	57	0.040

1006		IGG001	Iga Glomerulonephritis	55	0.040

1007		CRN030	Coronary Stenosis	51	0.040

1008		DFF036	Differentiated Thyroid Carcinoma	49	0.040

1009	c	PRD040	Periodontitis, Chronic	49	0.040

1010		ANG046	Angioimmunoblastic T-Cell Lymphoma	47	0.040

1011		PSD088	Pseudobulbar Affect	37	0.040

1012		NSP003	Nasopharyngeal Disease	32	0.040

1013		PRN021	Paranasal Sinus Disease	50	0.040

1014		MYF001	Myofibroma	39	0.040

1015		KPS004	Kaposi Sarcoma	73	0.040

1016		NKJ001	Nakajo Syndrome	26	0.040

1017		PLG002	Plague	56	0.040

1018		FRN030	Frontotemporal Dementia with Parkinsonism-17	31	0.040

1019		GLB001	Gilbert Syndrome	56	0.039

1020		RHM001	Rheumatic Fever	58	0.039

1021		GLS001	Gliosarcoma	58	0.039

1022		IMP005	Impotence	55	0.039

1023		PRT129	Prothrombin Deficiency, Congenital	49	0.039

1024		MRG013	Mirage Syndrome	43	0.039

1025		CLN044	Colon Adenoma	42	0.039

1026		RHM035	Rheumatic Fever-Related Antigen	39	0.039

1027		PRM155	Primary Cutaneous Anaplastic Large Cell Lymphoma	39	0.039

1028		MMM006	Mammographic Density	43	0.039

1029	c	MCP049	Mucopolysaccharidosis, Type Vii	63	0.039

1030	c	CHL132	Cholestasis, Progressive Familial Intrahepatic, 1	52	0.039

1031		LYM040	Lymphoblastic Lymphoma	57	0.039

1032		PLS025	Plasmablastic Lymphoma	53	0.039

1033		THR016	Thrombophlebitis	52	0.039

1034		HPT082	Hepatic Adenomas, Familial	53	0.039

1035		PLY001	Polycythemia Vera	74	0.039

1036	P	RHB003	Rhabdomyosarcoma	56	0.039

1037	c	LKM060	Leukemia, Acute Lymphoblastic 3	53	0.039

1038		LRY017	Laryngeal Disease	38	0.039

1039		ACT094	Acute Articular Rheumatism	26	0.039

1040	P	RBL001	Rubella	62	0.039

1041	P	ATX024	Ataxia-Oculomotor Apraxia 3	40	0.039

1042		LBR002	Leber Hereditary Optic Neuropathy	57	0.039

1043		OCC006	Occipital Horn Syndrome	49	0.039

1044		CRB037	Cerebral Palsy	71	0.038

1045		EXP004	Exophthalmos	51	0.038

1046		CHL004	Cholelithiasis	50	0.038

1047		PNN001	Panniculitis	49	0.038

1048	c	WSK002	Wiskott-Aldrich Syndrome 2	27	0.038

1049		PTT009	Pituitary Gland Disease	56	0.038

1050		EPL166	Epilepsy, Early-Onset, Vitamin B6-Dependent	18	0.038

1051		BNC003	Bone Cancer	59	0.038

1052		DBT062	Diabetic Foot Ulcers	59	0.038

1053	P	FNC004	Fanconi Syndrome	52	0.038

1054		DBT006	Diabetic Macular Edema	48	0.038

1055		ASP004	Asphyxia Neonatorum	43	0.038

1056		NDL024	Nodal Marginal Zone Lymphoma	41	0.038

1057		RFR001	Refractory Plasma Cell Neoplasm	19	0.038

1058	P	PRS038	Personality Disorder	64	0.038

1059		OST017	Osteomyelitis	63	0.038

1060	c	HMN021	Human T-Cell Leukemia Virus Type 1	52	0.038

1061		SPL004	Splenic Marginal Zone Lymphoma	51	0.038

1062	c	ANT034	Anterior Uveitis	50	0.038

1063	c	MCP050	Mucopolysaccharidosis, Type Ii	63	0.038

1064		ALL006	Allergic Asthma	59	0.038

1065		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	52	0.038

1066		TNG003	Tongue Cancer	58	0.038

1067		SNS001	Sensorineural Hearing Loss	56	0.038

1068	c	ADL096	Adult Hepatocellular Carcinoma	48	0.038

1069	P	MTC004	Mitochondrial Encephalomyopathy	43	0.038

1070		MYC006	Mycosis Fungoides	72	0.038

1071	P	CMP008	Compartment Syndrome	47	0.038

1072		HDG004	Hodgkin's Granuloma	28	0.038

1073		HDG006	Hodgkin's Paragranuloma	21	0.038

1074		ADR012	Adrenal Gland Disease	51	0.038

1075		EPD070	Epidermoid Cysts	47	0.038

1076		ULC007	Ulcerative Stomatitis	46	0.038

1077		END041	Endometrial Adenocarcinoma	60	0.038

1078		INS001	Insulinoma	65	0.038

1079		FCT001	Factor Viii Deficiency	51	0.038

1080		PRR002	Pure Red-Cell Aplasia	51	0.038

1081	P	TXP001	Toxoplasmosis	64	0.037

1082	P	LMY004	Leiomyosarcoma	58	0.037

1083		TRM010	Traumatic Brain Injury	55	0.037

1084		ALC009	Alcoholic Liver Cirrhosis	52	0.037

1085		DRG003	Drug Dependence	51	0.037

1086		PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	38	0.037

1087		PHS023	Phosphoserine Aminotransferase Deficiency	30	0.037

1088		GLT005	Glutamate Formiminotransferase Deficiency	28	0.037

1089	P	WSK001	Wiskott-Aldrich Syndrome	77	0.037

1090	P	ICH004	Ichthyosis	54	0.037

1091		SWN001	Swine Influenza	42	0.037

1092	P	HYP265	Hypotonia	40	0.037

1093	c	BSL024	Basal Cell Carcinoma 1	35	0.037

1094		TNS005	Tonsillitis	60	0.037

1095	P	ART084	Arteriovenous Fistula	45	0.037

1096		AND014	Androgenic Alopecia	39	0.037

1097	c	HYP602	Hyperoxaluria, Primary, Type Ii	37	0.037

1098		RFR007	Refractory Anemia with Excess Blasts in Transformation	24	0.037

1099	c	JVN010	Juvenile Rheumatoid Arthritis	69	0.037

1100		ACT103	Acute Lymphoblastic Leukemia, Childhood	48	0.037

1101	P	CRN028	Corneal Ulcer	47	0.037

1102	c	ACT042	Acute Pyelonephritis	46	0.037

1103		PRT012	Prothrombin Deficiency	45	0.037

1104		CHL013	Cholecystolithiasis	40	0.037

1105		ARG006	Aregenerative Anemia	25	0.037

1106		OBS002	Obsessive-Compulsive Disorder	66	0.037

1107		MYL004	Myelodysplastic Myeloproliferative Cancer	53	0.037

1108		LKC003	Leukocyte Disease	46	0.037

1109		RNL021	Renal Tubular Transport Disease	38	0.037

1110		TRT001	Teratocarcinoma	40	0.037

1111	c	OST163	Osteopetrosis, Autosomal Recessive 3	33	0.037

1112	P