Search results for Vitamin C

3237 hits were found for Vitamin C

#	Family	MCID	Name	MIFTS	Score
1		HYP781	Hypoascorbemia	50	4.723

2		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	53	3.589

3		RCK004	Rickets	69	0.982

4	c	HPT001	Hepatitis C	63	0.852

5	c	HPT073	Hepatitis C Virus	70	0.788

6	P	HPT021	Hepatitis	67	0.501

7		KRT002	Keratomalacia	48	0.456

8		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	53	0.441

9	P	LVR013	Liver Disease	68	0.426

10		LVR012	Liver Cirrhosis	63	0.374

11		VTM002	Vitamin B12 Deficiency	48	0.374

12	P	KDN018	Kidney Disease	70	0.373

13	P	HYP069	Hyperparathyroidism	62	0.356

14	c	CHR684	Chronic Kidney Disease	66	0.339

15	P	OST002	Osteoporosis	73	0.330

16	P	BRS047	Breast Cancer	96	0.329

17	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.313

18	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	41	0.312

19		ATM095	Autoimmune Disease	61	0.308

20	P	CLR023	Colorectal Cancer	98	0.298

21		DFC004	Deficiency Anemia	75	0.288

22	P	HPT023	Hepatocellular Carcinoma	100	0.287

23		VTM033	Vitamin K Deficiency Bleeding	48	0.286

24	c	SCN007	Secondary Hyperparathyroidism	50	0.277

25		BNR002	Bone Resorption Disease	48	0.272

26	c	HPT016	Hepatitis B	59	0.256

27	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.250

28		END030	End Stage Renal Failure	58	0.250

29		48X005	48,xyyy	39	0.248

30	c	PRC016	Pre-Eclampsia	63	0.246

31		OST011	Osteomalacia	52	0.245

32	c	VRL010	Viral Hepatitis	51	0.245

33	c	HYP836	Hypercholesterolemia, Familial, 1	72	0.243

34	P	CRN300	Coronary Heart Disease 1	63	0.242

35		ATH013	Atherosclerosis Susceptibility	66	0.242

36	P	BND020	Bone Disease	59	0.241

37	P	PRS040	Prostate Cancer	97	0.241

38		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.240

39		FTT001	Fatty Liver Disease	61	0.238

40	c	HPT003	Hepatitis a	63	0.238

41	P	VSC007	Vascular Disease	63	0.234

42	P	DBT009	Diabetes Mellitus	64	0.233

43	P	PSR002	Psoriasis	62	0.227

44	P	DRR001	Diarrhea	57	0.226

45		CYS001	Cystic Fibrosis	80	0.225

46	P	NRP001	Neuropathy	56	0.224

47		IRN002	Iron Metabolism Disease	57	0.224

48		PST011	Pustulosis of Palm and Sole	52	0.224

49		HMC014	Homocysteinemia	53	0.222

50	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.221

51	P	INF037	Inflammatory Bowel Disease	56	0.220

52	P	CRN018	Coronary Artery Anomaly	63	0.218

53	P	HRT032	Heart Disease	75	0.217

54	P	LKM002	Leukemia	66	0.215

55	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	89	0.214

56	P	HYP724	Hyperlipoproteinemia, Type Iii	72	0.211

57		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.211

58		HLX001	Helix Syndrome	47	0.209

59		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.208

60	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.208

61		LPD008	Lipid Metabolism Disorder	62	0.207

62		HMN044	Human Immunodeficiency Virus Type 1	71	0.207

63		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.206

64		ART140	Arteries, Anomalies of	53	0.205

65	P	CRD246	Cardiovascular System Disease	56	0.205

66		ISC004	Ischemia	60	0.204

67		CYT002	Cytokine Deficiency	44	0.204

68	P	ATR011	Atrial Fibrillation	66	0.203

69	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.202

70	P	ALZ034	Alzheimer Disease	88	0.201

71	P	LNG032	Lung Cancer	97	0.201

72	P	SKN015	Skin Carcinoma	67	0.198

73	P	ADN016	Adenocarcinoma	64	0.198

74		PRT037	Pertussis	65	0.195

75	P	MLT020	Multiple Sclerosis	72	0.193

76		CRH001	Crohn's Disease	74	0.193

77		DRM006	Dermatitis	61	0.193

78		ADN018	Adenoma	58	0.193

79		CRB039	Cerebrovascular Disease	69	0.193

80	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.192

81	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.192

82		PRN011	Pernicious Anemia	52	0.192

83	c	SYS001	Systemic Lupus Erythematosus	86	0.192

84		NRL016	Neural Tube Defects	82	0.191

85	P	BLD134	Bladder Cancer	78	0.191

86	P	GST053	Gastric Cancer	83	0.190

87		ATX038	Ataxia and Polyneuropathy, Adult-Onset	44	0.190

88	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.189

89		IMM167	Immune Deficiency Disease	78	0.189

90	c	LKM061	Leukemia, Acute Myeloid	83	0.189

91	P	MYL006	Myeloid Leukemia	60	0.188

92	P	PNC035	Pancreatic Cancer	84	0.188

93	P	LYM118	Lymphoma	68	0.188

94		STR067	Stroke, Ischemic	80	0.187

95	P	OVR042	Ovarian Cancer	89	0.184

96	P	MYP004	Myopathy	64	0.184

97	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.183

98		ALL026	Allergic Hypersensitivity Disease	64	0.182

99	c	ATR087	Atrial Standstill 1	74	0.182

100		CNG034	Congestive Heart Failure	70	0.182

101	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	57	0.181

102	P	NRB001	Neuroblastoma	71	0.181

103		OST159	Osteogenic Sarcoma	66	0.180

104		HYP066	Hyperglycemia	61	0.180

105	P	THL005	Thalassemia	60	0.180

106	P	LPS004	Lupus Erythematosus	61	0.180

107		NTR005	Nutritional Deficiency Disease	61	0.178

108	P	LYN001	Lynch Syndrome	77	0.177

109	P	PRD008	Periodontitis	62	0.177

110	P	PRP019	Peripheral Nervous System Disease	57	0.177

111	P	THR014	Thrombocytopenia	68	0.177

112		TXC005	Toxic Shock Syndrome	61	0.176

113	P	MYC007	Myocardial Infarction	70	0.176

114		SKN016	Skin Disease	63	0.176

115	P	NRF023	Neurofibromatosis, Type Ii	76	0.176

116	P	PLY011	Polycystic Ovary Syndrome	56	0.176

117	c	MCR120	Microvascular Complications of Diabetes 7	47	0.175

118		MSL001	Measles	61	0.174

119	P	HYP086	Hypothyroidism	68	0.174

120	P	ALP008	Alopecia	56	0.173

121	c	HYP595	Hypertension, Essential	84	0.173

122	P	NTR004	Neutropenia	63	0.173

123	c	MCR113	Microvascular Complications of Diabetes 3	52	0.173

124	c	MCR130	Microvascular Complications of Diabetes 6	41	0.171

125		CHL068	Cholestasis	60	0.171

126	c	MCR133	Microvascular Complications of Diabetes 4	41	0.171

127		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.170

128	P	CTR002	Cataract	60	0.170

129		PYR009	Pyridoxine Deficiency Anemia	34	0.170

130	P	LYM031	Lymphocytic Leukemia	55	0.170

131		GST033	Gestational Diabetes	57	0.170

132		OST012	Osteoarthritis	78	0.168

133	P	GST044	Gastritis	55	0.167

134	P	HYP061	Hypertrophic Cardiomyopathy	66	0.167

135	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.167

136	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.167

137		DPR016	Depression	63	0.166

138	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.166

139	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.166

140	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.166

141	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.166

142	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.166

143	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.166

144	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.166

145	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.166

146		THR024	Thrombosis	56	0.166

147		LNG099	Lung Disease	61	0.166

148		TTN003	Tetanus	64	0.166

149		MLN008	Melanoma	69	0.166

150		INS024	Insulin-Like Growth Factor I	79	0.166

151	P	RHM011	Rheumatoid Arthritis	80	0.164

152		VSL002	Visual Epilepsy	58	0.164

153		AST005	Asthma	77	0.163

154		PLM001	Pulmonary Tuberculosis	70	0.162

155	P	MGL001	Megaloblastic Anemia	55	0.162

156		ATX019	Ataxia with Vitamin E Deficiency	48	0.160

157	P	DRM053	Dermatitis, Atopic	66	0.160

158		47X002	47,xyy	49	0.159

159	P	ECL001	Eclampsia	51	0.158

160		ULC004	Ulcerative Colitis	73	0.158

161		PRP030	Purpura	55	0.157

162	c	PRM005	Primary Hyperparathyroidism	58	0.157

163		AGN016	Aging	56	0.157

164		NNL006	Non-Alcoholic Steatohepatitis	51	0.156

165	P	GLM007	Glomerulonephritis	57	0.156

166	P	BCL017	B-Cell Lymphoma	58	0.155

167		THY029	Thyroid Carcinoma	59	0.154

168		PRT011	Protein C Deficiency	45	0.154

169		ALC007	Alcohol Dependence	66	0.154

170	P	ATX030	Ataxia-Telangiectasia	83	0.154

171		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.154

172		LGH007	Leigh Syndrome	70	0.151

173	P	GLM045	Glioma	63	0.151

174	P	VSC011	Vasculitis	62	0.150

175		SQM006	Squamous Cell Carcinoma	60	0.150

176		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.149

177		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.149

178		MNT002	Mental Depression	57	0.149

179		GLL048	Glial Tumor	45	0.148

180		HMS001	Hemosiderosis	54	0.147

181	P	HML002	Hemolytic Anemia	62	0.147

182	P	PNM007	Pneumonia	68	0.147

183	P	NRP063	Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive	61	0.146

184	c	RHB024	Rhabdomyosarcoma 2	65	0.145

185		ACQ007	Acquired Immunodeficiency Syndrome	60	0.144

186	P	MSC005	Muscular Dystrophy	66	0.144

187		CRY004	Cryoglobulinemia	49	0.144

188		GLC003	Glucose Intolerance	54	0.144

189		VRL011	Viral Infectious Disease	61	0.144

190		CHL079	Children's Interstitial Lung Disease	27	0.143

191	P	MTH008	Methylmalonic Acidemia	51	0.143

192	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.142

193		CMM005	Common Cold	56	0.142

194		BCT022	Bacterial Infectious Disease	56	0.142

195	c	ACT075	Acute Myocardial Infarction	56	0.142

196		ESP021	Esophageal Cancer	90	0.142

197		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.142

198	P	ENC018	Encephalopathy	61	0.141

199	c	FML001	Familial Atrial Fibrillation	66	0.141

200		CLT003	Colitis	62	0.141

201	P	NGH001	Night Blindness	47	0.141

202	P	RRH023	Rare Hereditary Hemochromatosis	41	0.140

203	P	SZR006	Seizure Disorder	58	0.140

204	P	THY032	Thyroiditis	53	0.140

205		HYP017	Hypophosphatemia	49	0.140

206	P	ART022	Arthritis	70	0.139

207	P	INF032	Infertility	57	0.139

208	P	TRN020	Turner Syndrome	65	0.139

209	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.139

210	P	HYP076	Hyperthyroidism	55	0.138

211		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.138

212		DWN001	Down Syndrome	70	0.137

213		PRP027	Peripheral Vascular Disease	71	0.137

214	P	NPH012	Nephrotic Syndrome	63	0.137

215		MYL009	Myelodysplastic Syndrome	70	0.136

216		KRT001	Keratoconjunctivitis Sicca	50	0.136

217	P	ALC033	Alcohol Use Disorder	58	0.136

218	c	SML038	Small Cell Cancer of the Lung	65	0.136

219	P	SRC025	Sarcoidosis 1	70	0.136

220		XRP001	Xerophthalmia	42	0.136

221	P	ART021	Arteriosclerosis	54	0.135

222		GLB015	Glioblastoma Multiforme	75	0.135

223	P	ATS364	Autism	65	0.135

224	P	MCR115	Microvascular Complications of Diabetes 5	66	0.135

225	P	EXN002	Exanthem	57	0.134

226	c	PRM038	Primary Agammaglobulinemia	43	0.133

227	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	66	0.133

228	c	ATS007	Autism Spectrum Disorder	67	0.132

229		ATS010	Autosomal Recessive Disease	48	0.132

230	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.132

231	P	RTN024	Retinoblastoma	72	0.131

232	P	PHC003	Pheochromocytoma	71	0.131

233	P	MYC084	Mycobacterium Tuberculosis 1	68	0.131

234		HYP266	Hypoxia	56	0.129

235	c	DLT002	Dilated Cardiomyopathy	79	0.129

236	c	CNG411	Congenital Disorder of Glycosylation, Type in	68	0.129

237	P	LCH002	Lichen Planus	54	0.129

238		STM007	Stomatitis	49	0.129

239	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.128

240	P	DBT085	Diabetes Mellitus, Insulin-Dependent	67	0.128

241	c	BTT014	Beta-Thalassemia	72	0.128

242		MYL069	Myeloma, Multiple	85	0.127

243		URM002	Uremia	49	0.127

244	c	FML346	Familial Adenomatous Polyposis 1	70	0.126

245	P	RHN004	Rhinitis	57	0.126

246	P	HYP750	Hypertriglyceridemia, Familial	61	0.126

247		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.126

248		PLM033	Pulmonary Embolism	59	0.125

249	P	INF038	Influenza	68	0.125

250		LYM133	Lymphoma, Hodgkin, Classic	69	0.125

251		DPH001	Diphtheria	60	0.125

252	P	SCK005	Sickle Cell Disease	50	0.125

253		ANG054	Angina Pectoris	66	0.125

254	P	CHR345	Chronic Pain	50	0.125

255		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.124

256		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.124

257	P	DMN002	Dementia	67	0.124

258		IRN001	Iron Deficiency Anemia	58	0.123

259	P	HMC002	Homocystinuria	54	0.123

260	P	PRM006	Primary Biliary Cirrhosis	61	0.123

261	P	PLY019	Polyneuropathy	56	0.123

262		CLR108	Colorectal Adenoma	64	0.122

263	P	HYP024	Hypoparathyroidism	55	0.122

264	P	PRM011	Primary Ciliary Dyskinesia	69	0.122

265	c	THR082	Thrombophilia Due to Activated Protein C Resistance	60	0.122

266		TQP001	Taqi Polymorphism	32	0.121

267		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.120

268	P	RTN008	Retinitis Pigmentosa	77	0.120

269		SVR004	Severe Combined Immunodeficiency	73	0.120

270	P	LTR001	Lateral Sclerosis	53	0.120

271		HLC007	Helicobacter Pylori Infection	59	0.120

272		PRT013	Portal Hypertension	60	0.120

273	c	ACT071	Acute Kidney Failure	59	0.120

274	c	FML008	Familial Retinoblastoma	53	0.119

275		GST019	Gastrointestinal Stromal Tumor	76	0.119

276	P	MNN013	Meningitis	65	0.119

277	P	THR015	Thrombophilia	50	0.118

278		INT007	Intermediate Coronary Syndrome	55	0.118

279		LPT014	Leptin Deficiency or Dysfunction	73	0.117

280		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.116

281		SPN186	Spinal Cord Injury	60	0.116

282		HYP025	Hyperphosphatemia	47	0.116

283	P	CRY007	Cryoglobulinemia, Familial Mixed	50	0.116

284		HYP056	Hypoglycemia	66	0.116

285		VTM027	Vitamin D-Dependent Rickets, Type 2a	55	0.115

286		LSH001	Leishmaniasis	63	0.115

287	P	KLZ004	Kala-Azar 1	41	0.115

288	P	CLC063	Celiac Disease 1	68	0.115

289	c	MGR028	Migraine with or Without Aura 1	69	0.115

290	c	NRF024	Neurofibromatosis, Type I	71	0.115

291	P	MJR001	Major Depressive Disorder	68	0.115

292	c	ATM011	Autoimmune Hepatitis	62	0.114

293		CHL014	Cholera	55	0.114

294	c	PCH010	Pachyonychia Congenita 3	43	0.114

295	P	EPL164	Epilepsy	71	0.114

296	P	LBR001	Leber Congenital Amaurosis	67	0.114

297	P	HRP006	Herpes Simplex	65	0.114

298		HYP060	Hyperinsulinism	54	0.114

299	P	HMP007	Hemophilia	51	0.114

300	P	GRV001	Graves' Disease	55	0.114

301	P	END044	Endometriosis	62	0.114

302	P	PRK057	Parkinson Disease, Late-Onset	76	0.114

303	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.113

304		CRV035	Cervical Cancer	76	0.113

305		ALL014	Allergic Encephalomyelitis	39	0.113

306		KRT009	Keratosis	53	0.113

307	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	60	0.113

308	c	GLC092	Glaucoma, Primary Open Angle	62	0.112

309		DSR002	Disorders of Intracellular Cobalamin Metabolism	30	0.112

310	c	PRD040	Periodontitis, Chronic	54	0.112

311		ALL003	Allergic Rhinitis	67	0.111

312	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.111

313	c	ACT073	Acute Leukemia	58	0.110

314		MLR004	Malaria	80	0.110

315	P	RCT021	Rectum Cancer	53	0.110

316	c	LKM063	Leukemia, Chronic Myeloid	71	0.110

317	c	TBR025	Tuberous Sclerosis 1	76	0.110

318		SPL018	Splenomegaly	48	0.109

319		ANX010	Anxiety	72	0.109

320	P	TBR001	Tuberous Sclerosis	70	0.109

321		VTM028	Vitamin E, Familial Isolated Deficiency of	52	0.109

322	c	DWL002	Dowling-Degos Disease 1	58	0.109

323	P	ZLL001	Zellweger Syndrome	64	0.109

324		RTN023	Retinitis	46	0.109

325		NRR001	Neuroretinitis	43	0.109

326	c	NMN015	Niemann-Pick Disease, Type C1	68	0.109

327	P	RSP003	Respiratory Failure	74	0.109

328		EYD002	Eye Disease	58	0.109

329		ADL002	Adult Syndrome	69	0.109

330		RHM027	Rheumatic Disease	56	0.108

331	P	LNG064	Lung Cancer Susceptibility 3	77	0.108

332	P	ATR005	Atrophic Gastritis	50	0.108

333	P	GRF003	Graft-Versus-Host Disease	71	0.108

334		RNL011	Renal Osteodystrophy	49	0.107

335		PLM031	Poliomyelitis	57	0.107

336	P	HYP058	Hypervitaminosis a	49	0.107

337	P	NMN002	Niemann-Pick Disease	60	0.107

338	P	OPN001	Open-Angle Glaucoma	49	0.106

339	P	CNR004	Cone-Rod Dystrophy 2	71	0.106

340		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.106

341	c	SPN225	Spondyloarthropathy 1	73	0.106

342	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	0.105

343	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.105

344	P	SCH015	Schizophrenia	75	0.105

345		LYM019	Lymphosarcoma	47	0.105

346		DBT010	Diabetic Neuropathy	55	0.105

347	P	PRP029	Porphyria	62	0.105

348	P	SYP003	Syphilis	59	0.105

349		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.105

350		MTC097	Mitochondrial Complex Iv Deficiency	56	0.105

351	P	SLP006	Sleep Apnea	69	0.104

352	c	PRX059	Peroxisome Biogenesis Disorder 1a	57	0.104

353		CNS004	Constipation	57	0.104

354		BRK010	Burkitt Lymphoma	67	0.104

355		PPT005	Peptic Ulcer Disease	58	0.104

356		PLC008	Placenta Disease	49	0.103

357		PNC001	Pancytopenia	54	0.103

358	P	MLN007	Male Infertility	56	0.103

359	P	HDC001	Headache	57	0.102

360	P	CRD119	Cardiac Arrest	67	0.102

361	P	BRB001	Beriberi	44	0.102

362	P	PNC044	Pancreatitis	61	0.102

363		MRF001	Marfan Syndrome	75	0.101

364		PRT036	Peritonitis	65	0.101

365		MDD011	Mood Disorder	62	0.101

366	P	DYS154	Dystonia	65	0.101

367		SCK003	Sickle Cell Anemia	72	0.101

368		KRT019	Keratitis, Hereditary	67	0.101

369		DSS009	Disseminated Intravascular Coagulation	57	0.101

370		ACR006	Aceruloplasminemia	73	0.101

371	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.101

372	P	HMR003	Hemorrhagic Disease	52	0.101

373		PNC129	Pancreatic Adenocarcinoma	67	0.100

374		HRW001	Hair Whorl	36	0.100

375		RLP002	Relapsing-Remitting Multiple Sclerosis	55	0.100

376		BRN056	Bronchopulmonary Dysplasia	57	0.100

377		DFF005	Diffuse Large B-Cell Lymphoma	56	0.100

378		MCS002	Mucositis	55	0.100

379	c	FML021	Familial Hypercholesterolemia	68	0.100

380	P	OST001	Osteopetrosis	71	0.099

381		CHL123	Chlamydia	59	0.099

382	P	HYP726	Hypercalcemia, Infantile, 1	57	0.099

383		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.099

384	P	TRM003	Tremor	53	0.099

385	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	59	0.099

386		BRN071	Brain Injury	49	0.099

387		DNT012	Dental Caries	51	0.099

388	P	OVR082	Overgrowth Syndrome	50	0.099

389		HYP081	Hypolipoproteinemia	50	0.099

390	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.099

391		SKN019	Skin Melanoma	67	0.099

392		IDP011	Idiopathic Interstitial Pneumonia	63	0.099

393	P	HYP098	Hypereosinophilic Syndrome	66	0.099

394		FDL002	Food Allergy	49	0.098

395		TRN015	Transient Cerebral Ischemia	62	0.098

396	P	PLM036	Pulmonary Fibrosis	61	0.098

397		GTR002	Goiter	52	0.098

398		ORL011	Oral Cancer	60	0.098

399		OCL069	Ocular Motor Apraxia	51	0.098

400	P	INS002	in Situ Carcinoma	52	0.098

401	c	HMC039	Hemochromatosis, Type 1	74	0.098

402		GST045	Gastroenteritis	59	0.097

403		GST050	Gastrointestinal System Disease	56	0.097

404		FBR047	Fibromyalgia	59	0.097

405		ACT119	Acute Promyelocytic Leukemia	63	0.097

406	P	RTN016	Retinal Degeneration	53	0.097

407	P	SBS003	Substance Abuse	54	0.097

408		PPL052	Papillomatosis, Confluent and Reticulated	34	0.097

409	c	LKM071	Leukemia, Chronic Lymphocytic	79	0.096

410		IRR002	Irritable Bowel Syndrome	63	0.096

411	c	PNS012	Paine Syndrome	61	0.096

412		ENT011	Enterocolitis	50	0.096

413	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	64	0.096

414		IGR001	Ige Responsiveness, Atopic	59	0.096

415		BLR008	Bilirubin Metabolic Disorder	57	0.095

416		NPH003	Nephrocalcinosis	51	0.095

417	c	INF071	Inflammatory Bowel Disease 1	68	0.095

418		NSS002	Neisseria Meningitidis Infection	46	0.095

419	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	65	0.095

420	P	FBR017	Fibrosarcoma	56	0.095

421		BRN024	Bronchitis	68	0.095

422		PRP080	Peripheral Artery Disease	53	0.095

423		SPN051	Spondylitis	52	0.095

424		ERY051	Erythroleukemia, Familial	56	0.095

425	P	URT039	Urticaria	58	0.095

426		PHN003	Phenylketonuria	75	0.095

427	c	ACT027	Acute Pancreatitis	59	0.095

428	c	SCL052	Scleroderma, Familial Progressive	62	0.094

429		END057	Endometrial Cancer	74	0.094

430		VCC001	Vaccinia	49	0.094

431		HSH003	Hashimoto Thyroiditis	62	0.094

432		PPL022	Papilloma	54	0.094

433		INF009	Inflammatory Spondylopathy	32	0.094

434		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.094

435		HNS001	Hansen's Disease	34	0.094

436	c	BRN108	Branchiootic Syndrome 1	61	0.094

437		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	57	0.093

438	P	LPR021	Leprosy 3	67	0.093

439	P	MSC003	Muscular Atrophy	52	0.093

440		VRC005	Varicose Veins	60	0.093

441		TRN018	Transitional Cell Carcinoma	56	0.093

442		PRS045	Prostatic Hypertrophy	52	0.093

443	P	BPL003	Bipolar Disorder	56	0.093

444	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	59	0.093

445	P	HYP265	Hypotonia	42	0.092

446	P	CHR071	Charcot-Marie-Tooth Disease	64	0.092

447	P	ANT006	Antiphospholipid Syndrome	54	0.092

448		HMP009	Haemophilus Influenzae	42	0.092

449	c	MJR024	Major Affective Disorder 9	41	0.092

450	c	MJR022	Major Affective Disorder 8	38	0.092

451	P	AMY004	Amyloidosis	70	0.092

452	P	NSP012	Nasopharyngeal Carcinoma	67	0.092

453		THY030	Thyroid Gland Disease	51	0.091

454		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.091

455		ABT001	Abetalipoproteinemia	67	0.091

456		GST040	Gastric Adenocarcinoma	70	0.091

457	P	BRD002	Bardet-Biedl Syndrome	66	0.091

458	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.091

459		MST005	Mastitis	53	0.091

460	c	ACT068	Acute Cystitis	63	0.091

461		CRH005	Crohn's Colitis	52	0.090

462		ALL006	Allergic Asthma	56	0.090

463	c	CNG006	Congenital Hypothyroidism	65	0.089

464		BRN002	Bronchiolitis	59	0.089

465	P	ANR048	Aniridia 1	63	0.089

466	P	MTR004	Maturity-Onset Diabetes of the Young	66	0.089

467	c	HYP057	Hypervitaminosis D	41	0.089

468	P	SYS005	Systemic Scleroderma	70	0.089

469		TRM010	Traumatic Brain Injury	53	0.088

470		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.088

471	P	PLM037	Pulmonary Hypertension	68	0.088

472		ORL015	Oral Squamous Cell Carcinoma	43	0.088

473	P	LYM033	Lymphoproliferative Syndrome	60	0.088

474	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.088

475	P	HYD006	Hydrocephalus	65	0.088

476		PSY004	Psychotic Disorder	67	0.088

477	P	MYP006	Myopia	55	0.088

478		SRC014	Sarcoma	65	0.088

479		SQM002	Squamous Cell Papilloma	42	0.088

480		CLN015	Colon Adenocarcinoma	63	0.088

481		PRS129	Prostatic Hyperplasia, Benign	49	0.088

482	c	NRP053	Neuropathy, Hereditary Sensory and Autonomic, Type Iia	66	0.087

483	P	KDN017	Kidney Cancer	61	0.087

484		MSC157	Muscular Dystrophy, Duchenne Type	71	0.087

485		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.087

486		CNT047	Contact Dermatitis	57	0.087

487		BCK006	Back Pain	42	0.087

488		BSL036	Basal Cell Nevus Syndrome	72	0.087

489	P	MYC008	Myocarditis	59	0.087

490		ANR007	Anorexia Nervosa	63	0.087

491	c	EXD008	Exudative Vitreoretinopathy 1	69	0.086

492	c	BSL007	Basal Cell Carcinoma	68	0.086

493		SCH014	Schistosomiasis	56	0.086

494		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.086

495		SPP010	Suppressor of Tumorigenicity 3	51	0.086

496		PRS021	Prostatic Adenoma	51	0.086

497	P	PRP003	Porphyria Cutanea Tarda	67	0.086

498	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.086

499		CNN005	Connective Tissue Disease	66	0.086

500	P	LCT001	Lactic Acidosis	51	0.086

501	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.086

502	P	FCL005	Focal Segmental Glomerulosclerosis	58	0.086

503	P	SLP005	Sleep Disorder	59	0.085

504		MCR017	Macrocytic Anemia	41	0.085

505		HPT004	Hepatic Coma	43	0.085

506		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	57	0.085

507		LMY002	Leiomyoma	50	0.085

508		PST092	Posttransplant Acute Limbic Encephalitis	29	0.085

509	c	LRG017	Large Intestine Cancer	47	0.085

510		ENT004	Enthesopathy	48	0.084

511		MSC007	Muscle Hypertrophy	63	0.084

512	c	MCR129	Microvascular Complications of Diabetes 1	66	0.084

513		CMR002	Coumarin Resistance	56	0.084

514		SPN035	Spindle Cell Sarcoma	51	0.084

515		OTT002	Otitis Media	71	0.084

516		PRT038	Protein-Energy Malnutrition	54	0.084

517		KHL003	Kohlschutter-Tonz Syndrome	64	0.084

518		ORL013	Oral Lichen Planus	45	0.084

519		HPT019	Hepatic Encephalopathy	60	0.083

520	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.083

521	P	OPT006	Optic Nerve Disease	57	0.083

522		PNG002	Pain Agnosia	51	0.083

523	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.083

524	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.083

525		DSS008	Disease of Mental Health	57	0.082

526	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.082

527	P	ENC004	Encephalitis	61	0.082

528		CLF027	Cleft Palate, Isolated	64	0.082

529		GNG013	Gingivitis	59	0.082

530		CLC006	Calcinosis	48	0.082

531		OVR094	Ovarian Epithelial Cancer	38	0.082

532	P	ALP009	Alopecia Areata	60	0.082

533	P	GLM040	Glioma Susceptibility 1	81	0.082

534		MTB004	Metabolic Acidosis	50	0.081

535		CHL065	Cholangiocarcinoma	67	0.081

536		DMY004	Demyelinating Disease	52	0.081

537		CRB037	Cerebral Palsy	68	0.081

538		HYP080	Hypogonadism	50	0.081

539	P	AST007	Astrocytoma	50	0.081

540		INT079	Intrahepatic Cholangiocarcinoma	50	0.081

541		HYP064	Hypogonadotropism	40	0.080

542		BRN028	Brain Cancer	73	0.080

543	c	ACT134	Acute Liver Failure	51	0.080

544	P	ART023	Arthropathy	62	0.080

545		NWC001	Newcastle Disease	44	0.080

546	P	BLD124	Bleeding Disorder, Platelet-Type, 11	61	0.080

547	P	UVT001	Uveitis	57	0.080

548		CRD132	Cardiac Conduction Defect	59	0.080

549		PRN019	Perinatal Necrotizing Enterocolitis	54	0.080

550		SBC016	Subacute Delirium	44	0.080

551		PRM020	Premenstrual Tension	39	0.080

552	c	CWD006	Cowden Syndrome 1	77	0.080

553	P	APL001	Aplastic Anemia	74	0.079

554		PLM134	Pulmonary Fibrosis, Idiopathic	75	0.079

555		EPL131	Epilepsy, Pyridoxine-Dependent	49	0.079

556	c	HMP029	Hemophilia a	65	0.079

557		LKP003	Leukoplakia	39	0.079

558		DYS073	Dysphagia	50	0.079

559	P	SCL018	Scoliosis	60	0.079

560	c	SVR005	Severe Pre-Eclampsia	49	0.079

561	c	PSR023	Psoriasis 1	49	0.079

562		CRB004	Cerebral Artery Occlusion	44	0.079

563		FND002	Fundus Dystrophy	51	0.078

564	P	MVM001	Movement Disease	61	0.078

565		MMM001	Mammary Paget's Disease	53	0.078

566	c	FML035	Familial Hyperlipidemia	55	0.078

567		CRP001	Carpal Tunnel Syndrome	67	0.078

568		HYP014	Hyperuricemia	51	0.078

569		IMP005	Impotence	52	0.078

570		CHR066	Chronic Fatigue Syndrome	61	0.078

571		TLN003	Telangiectasis	51	0.077

572		NRL018	Neural Tube Defects, Folate-Sensitive	49	0.077

573		BLD131	Bladder Urothelial Carcinoma	61	0.077

574	P	PLR004	Pleuropulmonary Blastoma	65	0.077

575		HMG005	Hemoglobinopathy	55	0.077

576	P	EPS003	Episodic Ataxia	60	0.077

577		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	64	0.077

578	P	MLT074	Multiple Endocrine Neoplasia	55	0.077

579	c	GRV008	Graves Disease 1	55	0.077

580		LYM027	Lymphopenia	57	0.077

581		ADR040	Adrenal Gland Pheochromocytoma	46	0.077

582		PPL049	Papillon-Lefevre Syndrome	63	0.077

583		ANR040	Aneurysm	58	0.077

584	P	FRN006	Frontotemporal Dementia	70	0.077

585		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.077

586	P	PLL002	Pellagra	45	0.076

587		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.076

588		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.076

589	P	BNG032	Benign Mesothelioma	45	0.076

590	P	CRN037	Craniosynostosis	68	0.076

591		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	52	0.076

592	P	OCL013	Oculodentodigital Dysplasia	69	0.076

593	P	END033	Endocarditis	57	0.076

594		MYL005	Myelofibrosis	67	0.076

595		WRN001	Werner Syndrome	69	0.075

596	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.075

597		CRN030	Coronary Stenosis	50	0.075

598	c	MCR112	Microvascular Complications of Diabetes 2	41	0.075

599		HYP005	Hypokalemia	55	0.075

600	P	FML018	Familial Mediterranean Fever	72	0.075

601		NRT004	Neuritis	53	0.075

602		CMP010	Complex Regional Pain Syndrome	58	0.075

603		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.075

604		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.074

605		ANX004	Anoxia	42	0.074

606		CHR178	Chromosomal Triplication	35	0.074

607	P	CHL066	Cholangitis	50	0.074

608		MMB001	Membranoproliferative Glomerulonephritis	53	0.074

609		GT001	Gout	63	0.074

610		PRT014	Protein S Deficiency	50	0.074

611		TRD006	Tardive Dyskinesia	55	0.074

612	P	TRC086	Trichohepatoenteric Syndrome 1	59	0.074

613	P	HML033	Hemolytic Uremic Syndrome, Atypical 1	69	0.074

614		GST023	Gastric Ulcer	53	0.074

615		LNG031	Lung Benign Neoplasm	50	0.074

616	P	SHR001	Short Bowel Syndrome	52	0.074

617		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.074

618	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.074

619		APH001	Aphthous Stomatitis	57	0.074

620		END040	Endogenous Depression	54	0.074

621	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	51	0.074

622	c	GLL024	Gallbladder Disease 1	52	0.073

623		FCT001	Factor Viii Deficiency	55	0.073

624		VSC003	Visceral Leishmaniasis	55	0.073

625	P	BRS044	Breast Adenocarcinoma	59	0.073

626	c	ALP101	Alpha-Thalassemia	62	0.073

627		THY111	Thyroid Carcinoma, Familial Medullary	67	0.073

628		DYS015	Dysentery	50	0.073

629		HYP043	Hyperandrogenism	48	0.073

630	P	INT068	Intestinal Disease	52	0.072

631		BLR001	Biliary Atresia	50	0.072

632	P	PLY014	Polycystic Kidney Disease	59	0.072

633	P	NPH005	Nephronophthisis	58	0.072

634		SNS003	Sensory Peripheral Neuropathy	53	0.072

635	c	ATS013	Autosomal Recessive Congenital Ichthyosis	66	0.072

636		PSR001	Psoriatic Arthritis	62	0.072

637	c	INH030	Inherited Retinal Disorder	47	0.072

638	P	CND004	Candidiasis	57	0.072

639	P	PSD087	Pseudoxanthoma Elasticum	67	0.072

640		VSC002	Vascular Dementia	57	0.072

641	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	50	0.072

642		DGN001	Degenerative Disc Disease	48	0.072

643		NRT001	Neurotic Disorder	52	0.072

644	c	EPL184	Epileptic Encephalopathy, Early Infantile, 6	69	0.072

645		FCT007	Factor Vii Deficiency	66	0.072

646		ERY029	Erythermalgia, Primary	58	0.072

647		CHG001	Chagas Disease	66	0.072

648		ATM052	Autoimmune Disease 1	37	0.072

649		PLY150	Polykaryocytosis Inducer	31	0.072

650		CYS010	Cystinosis	60	0.072

651	P	RTN018	Retinal Disease	52	0.072

652		ACR007	Acromegaly	71	0.071

653	P	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	38	0.071

654	P	PRC031	Preeclampsia/eclampsia 1	37	0.071

655		CHC001	Chickenpox	60	0.071

656	P	NJM001	Nijmegen Breakage Syndrome	72	0.071

657	c	PSR017	Psoriasis 2	52	0.071

658		RRS014	Rare Surgical Neurologic Disease	32	0.071

659		BRR014	Barrett Esophagus	64	0.071

660	P	DNG005	Dengue Virus	57	0.071

661		LPD012	Lipoid Congenital Adrenal Hyperplasia	71	0.071

662	c	PNC108	Pancreatitis, Hereditary	69	0.071

663		CHR074	Choriocarcinoma	46	0.071

664	P	HML001	Hemolytic-Uremic Syndrome	52	0.071

665		PRM329	Premature Aging	39	0.071

666		OST003	Osteonecrosis	61	0.071

667		KPS004	Kaposi Sarcoma	75	0.071

668		OST017	Osteomyelitis	64	0.071

669		MTH009	Mouth Disease	56	0.071

670		INT066	Interstitial Lung Disease	59	0.070

671	c	MGL018	Megaloblastic Anemia 1	48	0.070

672		PLM010	Pulmonary Edema	55	0.070

673		49X006	49, Xxxxy Syndrome	41	0.070

674		ART016	Aortic Aneurysm	68	0.070

675	c	TBR026	Tuberous Sclerosis 2	71	0.070

676	P	ADL010	Adult Respiratory Distress Syndrome	63	0.070

677	P	MPL001	Maple Syrup Urine Disease	69	0.070

678	P	CHN059	Chondrocalcinosis	51	0.070

679		ALC006	Alcoholic Hepatitis	61	0.070

680	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.070

681		BRT054	Brittle Bone Disorder	70	0.070

682	P	PRS038	Personality Disorder	65	0.070

683	c	CRV002	Cervix Uteri Carcinoma in Situ	44	0.070

684		CRV045	Cervical Intraepithelial Neoplasia	39	0.070

685		CLR109	Colorectal Adenocarcinoma	50	0.070

686	P	DDN001	Duodenal Ulcer	50	0.070

687		HRP004	Herpes Zoster	60	0.069

688	P	PRP034	Purpura Fulminans	42	0.069

689	c	ACT135	Acute Graft Versus Host Disease	51	0.069

690	P	LFR001	Li-Fraumeni Syndrome	72	0.069

691	P	MDL005	Medulloblastoma	77	0.069

692		THR004	Thrombocytosis	51	0.069

693		PYR016	Pyridoxine Deficiency	30	0.069

694	P	HYP818	Hypobetalipoproteinemia, Familial, 1	58	0.069

695	P	PGT001	Paget's Disease of Bone	60	0.069

696	P	ANG001	Angelman Syndrome	67	0.069

697		THY125	Thyroid Gland Medullary Carcinoma	51	0.069

698	P	SJG008	Sjogren Syndrome	56	0.069

699		INT002	Intermittent Claudication	61	0.069

700	P	FLL037	Follicular Lymphoma	66	0.069

701	P	PLY018	Polycythemia	55	0.068

702	P	NRV007	Nervous System Disease	66	0.068

703	P	PNT019	Pontocerebellar Hypoplasia	46	0.068

704		RBF001	Riboflavin Deficiency	45	0.068

705		BRS051	Breast Disease	58	0.068

706	P	HNT016	Huntington Disease	71	0.068

707	P	CYS018	Cystitis	59	0.068

708	P	MYS005	Myositis	56	0.068

709		STT001	Status Epilepticus	59	0.068

710	P	HYP733	Hypercalciuria, Absorptive, 2	46	0.068

711		APN008	Apnea, Obstructive Sleep	65	0.068

712	c	INH020	Inherited Metabolic Disorder	46	0.068

713	P	ICH004	Ichthyosis	54	0.067

714	P	VSC018	Visceral Steatosis	33	0.067

715		ESP002	Esophageal Varix	51	0.067

716		ISL099	Isolated Methylmalonic Acidemia	30	0.067

717		PLS011	Plasmacytoma	56	0.067

718	c	HYP272	Hypercholesterolemia, Familial, 3	43	0.067

719		WLS001	Wilson Disease	70	0.067

720	P	TCL004	T-Cell Leukemia	47	0.067

721		ALP103	Alpha-1-Antitrypsin Deficiency	63	0.067

722		CYS036	Cystinosis, Nephropathic	51	0.066

723	P	MTC069	Mitochondrial Disorders	56	0.066

724		NRF026	Neurofibromatosis, Type Iv, of Riccardi	63	0.066

725	c	CHR682	Chronic Bilirubin Encephalopathy	38	0.066

726	P	MST009	Mastocytosis	63	0.066

727	c	PSR028	Psoriasis 7	39	0.066

728	c	PSR032	Psoriasis 11	38	0.066

729	c	PSR018	Psoriasis 13	38	0.066

730	c	DNT047	Dentinogenesis Imperfecta Type 2	33	0.066

731		SCN001	Secondary Hyperparathyroidism of Renal Origin	28	0.066

732		BDD001	Budd-Chiari Syndrome	62	0.066

733	c	CHR064	Chronic Monocytic Leukemia	34	0.066

734		INS001	Insulinoma	60	0.066

735	c	INF145	Infantile Liver Failure Syndrome 1	50	0.066

736		PFF001	Pfeiffer Syndrome	79	0.066

737		CRT013	Carotid Stenosis	50	0.066

738	P	ESP024	Esophagitis	62	0.066

739		LMY014	Leiomyoma, Uterine	56	0.066

740	c	ATS307	Autosomal Recessive Cerebellar Ataxia	41	0.066

741		GLS007	Glossitis	47	0.065

742		FDB001	Foodborne Botulism	56	0.065

743	c	CHL119	Cholangitis, Primary Sclerosing	57	0.065

744	P	ALP004	Alport Syndrome	68	0.065

745		IGG001	Iga Glomerulonephritis	48	0.065

746		PRT029	Parathyroid Adenoma	50	0.065

747		WLL001	Williams-Beuren Syndrome	62	0.065

748	P	PYL005	Pyelonephritis	56	0.065

749		ATX010	Ataxia Neuropathy Spectrum	38	0.064

750		PRS063	Paresthesia	43	0.064

751		BNN003	Bone Inflammation Disease	48	0.064

752		ACN002	Acanthosis Nigricans	60	0.064

753	P	MCR010	Microcephaly	58	0.064

754	c	PLY105	Polycystic Ovary Syndrome 1	38	0.064

755	c	WLM018	Wilms Tumor 5	62	0.064

756		RTN020	Retinal Vascular Disease	48	0.064

757	P	CNJ013	Conjunctivitis	65	0.064

758		AZS001	Azoospermia	50	0.064

759		EMB004	Embryonal Carcinoma	57	0.064

760		PGM030	Pigmentation Anomaly of the Skin	25	0.064

761		MYF001	Myofibroma	42	0.064

762		NWB001	Newborn Respiratory Distress Syndrome	58	0.064

763	c	JVN010	Juvenile Rheumatoid Arthritis	67	0.064

764		BRN004	Brain Edema	55	0.064

765	P	MTR014	Motor Neuron Disease	64	0.064

766		KRN002	Kearns-Sayre Syndrome	63	0.064

767		ADR007	Adrenoleukodystrophy	74	0.064

768	P	MTC133	Mitochondrial Myopathy	49	0.064

769		RFR010	Refractory Anemia	48	0.063

770	c	MYT021	Myotonic Dystrophy 1	66	0.063

771	P	GCH001	Gaucher's Disease	64	0.063

772		CHL067	Cholecystitis	58	0.063

773		ALL010	Allergic Contact Dermatitis	55	0.063

774	P	MTC003	Metachromatic Leukodystrophy	70	0.063

775	c	HPT007	Hepatitis E	52	0.063

776	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	0.063

777		ARB001	Ariboflavinosis	36	0.063

778		ATN005	Autonomic Dysfunction	47	0.063

779		RHM001	Rheumatic Fever	61	0.063

780		BCT002	Bacterial Vaginosis	52	0.063

781		FML307	Familial Calcium Pyrophosphate Deposition	38	0.063

782		WGN007	Wagner Vitreoretinopathy	38	0.063

783		WGN003	Wagner Syndrome	35	0.063

784		BTN003	Biotinidase Deficiency	60	0.063

785	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.063

786	c	BCT007	Bacterial Meningitis	55	0.063

787	P	RTN022	Retinal Vein Occlusion	52	0.063

788	c	PRD013	Periodic Fever, Familial, Autosomal Dominant	65	0.063

789	c	MLG068	Malignant Glioma	45	0.063

790		PST021	Postpartum Depression	50	0.063

791	P	SNS001	Sensorineural Hearing Loss	61	0.062

792		AMN001	Amenorrhea	54	0.062

793	P	LCT002	Lactose Intolerance	53	0.062

794		PND002	Pendred Syndrome	60	0.062

795		CTN007	Cutaneous Leishmaniasis	61	0.062

796		GYR004	Gyrate Atrophy of Choroid and Retina	56	0.062

797		CRD223	Cardiac Arrhythmia	60	0.062

798	c	HPT015	Hepatitis D	49	0.062

799	c	MCL062	Mucolipidosis Ii Alpha/beta	66	0.062

800	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	0.062

801		MCC012	Mccune-Albright Syndrome	70	0.062

802	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.062

803		CHY002	Chylomicron Retention Disease	64	0.062

804		NRM005	Neuromuscular Disease	63	0.062

805		MTH021	Methylmalonic Acidemia with Homocystinuria	46	0.061

806		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.061

807		FRY006	Fryns Microphthalmia Syndrome	54	0.061

808	P	FML011	Familial Adenomatous Polyposis	72	0.061

809	c	THY112	Thyroid Hormone Resistance, Generalized, Autosomal Dominant	51	0.061

810	P	VTR007	Vitreoretinopathy	46	0.061

811	P	RST001	Restless Legs Syndrome	54	0.061

812		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.061

813	c	ART101	Aortic Valve Disease 2	63	0.061

814	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	59	0.061

815	P	MMB011	Membranous Nephropathy	50	0.061

816	P	ALP106	Alport Syndrome 1, X-Linked	55	0.061

817		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.061

818		TNG002	Tangier Disease	65	0.061

819		HRT012	Heart Valve Disease	53	0.061

820	P	RNL007	Renal Tubular Acidosis	50	0.061

821		THR013	Thoracic Outlet Syndrome	53	0.061

822		RRD056	Rare Disease in Surgical Orthopedic	28	0.061

823	c	HMP022	Hemophagocytic Lymphohistiocytosis, Familial, 1	65	0.061

824		BRS099	Breast Ductal Carcinoma	62	0.061

825		BRC012	Brucellosis	61	0.061

826		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	65	0.061

827		DWR001	Dwarfism	44	0.061

828	P	PSD015	Pseudohypoparathyroidism	56	0.061

829		LNG039	Lung Squamous Cell Carcinoma	65	0.061

830		LMB062	Limb Ischemia	55	0.060

831		CLF001	Cleft Lip	53	0.060

832	P	RBL001	Rubella	58	0.060

833		BLL006	Bullous Pemphigoid	62	0.060

834		MCL006	Macular Retinal Edema	55	0.060

835		RNL077	Renal Fibrosis	47	0.060

836		PRD004	Prediabetes Syndrome	47	0.060

837		HRP008	Herpes Simiae	25	0.060

838	c	HMP004	Hemophilia B	67	0.060

839		PLY001	Polycythemia Vera	69	0.060

840		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	51	0.060

841	c	PLM127	Pulmonary Hypertension, Primary, 3	33	0.060

842		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.060

843	P	MMP001	Mumps	57	0.060

844	P	PTY003	Pityriasis Rubra Pilaris	58	0.060

845		APP008	Appendicitis	60	0.060

846		FML063	Familial Glucocorticoid Deficiency	51	0.060

847		SPP011	Suppression of Tumorigenicity 12	59	0.060

848	c	GCH015	Gaucher Disease, Type I	70	0.059

849	P	HYP035	Hypophosphatasia	60	0.059

850		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	59	0.059

851		SYN007	Synovitis	55	0.059

852	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.059

853	P	BRL012	Bare Lymphocyte Syndrome, Type Ii	65	0.059

854		GLS018	Glass Syndrome	53	0.059

855		STT009	Sutton Disease 2	30	0.059

856		THY124	Thyroid Gland Papillary Carcinoma	52	0.059

857	P	AGG001	Aggressive Periodontitis	50	0.059

858		ORT008	Orotic Aciduria	54	0.059

859		PRS047	Prostatitis	56	0.059

860	P	MNC007	Monocytic Leukemia	54	0.059

861	P	PMP001	Pemphigus	55	0.059

862	c	MLT156	Multiple Endocrine Neoplasia, Type I	71	0.059

863		DBT084	Diabetes Mellitus, Ketosis-Prone	59	0.059

864		TRP009	Triple X Syndrome	42	0.059

865		PHR003	Pharyngitis	56	0.058

866		INT075	Intracranial Hypertension	53	0.058

867		GLY010	Glycine Encephalopathy	60	0.058

868	c	SVR001	Severe Acute Respiratory Syndrome	55	0.058

869	P	ASP006	Aspergillosis	66	0.058

870		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	58	0.058

871		THR123	Thrombotic Microangiopathy	38	0.058

872		CHD001	Chediak-Higashi Syndrome	66	0.058

873		PRT018	Portal Vein Thrombosis	50	0.058

874	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	67	0.058

875		ORL012	Oral Leukoplakia	39	0.058

876		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.058

877		PLG002	Plague	57	0.058

878	c	HMG029	Hemoglobin Se Disease	38	0.058

879	P	TXP001	Toxoplasmosis	60	0.058

880	P	CHR453	Charcot-Marie-Tooth Hereditary Neuropathy	45	0.058

881	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	69	0.058

882	c	PRG047	Progressive Familial Intrahepatic Cholestasis	62	0.058

883		MCR013	Microphthalmia	60	0.057

884	c	GLY060	Glycogen Storage Disease Ia	61	0.057

885		PRT082	Preterm Premature Rupture of the Membranes	54	0.057

886	P	OBS001	Obstructive Jaundice	48	0.057

887		CMB003	Combined T Cell and B Cell Immunodeficiency	52	0.057

888		HLC001	Holocarboxylase Synthetase Deficiency	48	0.057

889	P	SCL009	Sclerosing Cholangitis	47	0.057

890		TYP007	Typhoid Fever	63	0.057

891		CHR005	Chorioamnionitis	51	0.057

892		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	62	0.057

893	c	PRM196	Premature Ovarian Failure 1	68	0.057

894		MYC006	Mycosis Fungoides	66	0.057

895	P	FRD001	Friedreich Ataxia	63	0.057

896		MTC005	Mitochondrial Metabolism Disease	48	0.057

897		CHL004	Cholelithiasis	49	0.057

898		GST092	Gastroesophageal Reflux	65	0.057

899		MYL031	Myeloproliferative Neoplasm	65	0.057

900	P	PRM002	Primary Hyperoxaluria	62	0.057

901	P	KRB001	Krabbe Disease	69	0.057

902	P	PTT014	Pitt-Hopkins Syndrome	60	0.057

903		RDN001	Reading Disorder	40	0.057

904		KRT006	Keratoconjunctivitis	53	0.056

905		MTH078	Methylmalonic Aciduria, Cblb Type	50	0.056

906	c	MCP052	Mucopolysaccharidosis, Type Vi	67	0.056

907		CRT017	Cartilage Disease	54	0.056

908		GRN017	Granulocytopenia	44	0.056

909	P	TCD001	Tic Disorder	54	0.056

910		PRT010	Parathyroid Carcinoma	66	0.056

911	P	EXD001	Exudative Vitreoretinopathy	56	0.056

912		ETN001	Eating Disorder	59	0.056

913		GRW007	Growth Hormone Deficiency	43	0.056

914		ART001	Arterial Tortuosity Syndrome	66	0.056

915		SCH012	Schizoaffective Disorder	50	0.056

916		SXL003	Sexual Disorder	48	0.056

917		CLR030	Clear Cell Renal Cell Carcinoma	53	0.056

918	c	MYS033	Miyoshi Muscular Dystrophy 1	56	0.056

919		PTZ001	Peutz-Jeghers Syndrome	69	0.056

920	P	CHR012	Chronic Granulomatous Disease	67	0.056

921		GLM044	Glomerular Disease	39	0.056

922		VTM009	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1	26	0.056

923		GST020	Gastric Antral Vascular Ectasia	41	0.056

924	P	ACR001	Aicardi-Goutieres Syndrome	65	0.056

925	c	HYP768	Hyperlipoproteinemia, Type I	52	0.056

926	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.056

927		KWS002	Kawasaki Disease	64	0.056

928		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.056

929		THR016	Thrombophlebitis	51	0.056

930		HYP741	Hyperparathyroidism 2 with Jaw Tumors	53	0.056

931		ANV001	Anovulation	47	0.056

932		CYT018	Cytochrome P450 2d6 Variant	27	0.056

933		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	49	0.056

934		EHL052	Ehlers-Danlos Syndrome, Vascular Type	56	0.056

935	P	MLG056	Malignant Hyperthermia	67	0.055

936		INT303	Intracranial Hypertension, Idiopathic	56	0.055

937		CMM004	Common Variable Immunodeficiency	67	0.055

938	P	TRC031	Trichorhinophalangeal Syndrome	40	0.055

939		KRT013	Keratolytic Winter Erythema	46	0.055

940		LYM040	Lymphoblastic Lymphoma	54	0.055

941		IDP070	Idiopathic Scoliosis	37	0.055

942		OBS002	Obsessive-Compulsive Disorder	68	0.055

943	c	WLM013	Wilms Tumor 1	65	0.055

944		RSC001	Rosacea	55	0.055

945	c	HNT011	Huntington Disease-Like 3	38	0.055

946		FND001	Fundus Albipunctatus	61	0.055

947		DRY001	Dry Eye Syndrome	47	0.055

948		LWC001	Low Compliance Bladder	42	0.055

949		ADN011	Adenoid Cystic Carcinoma	70	0.055

950	c	MST023	Mesothelioma, Malignant	57	0.055

951	P	PLY041	Polymyositis	57	0.055

952	P	LRY044	Larynx Cancer	54	0.055

953		PST028	Post-Traumatic Stress Disorder	58	0.055

954		HDN002	Head Injury	45	0.055

955		DNN002	Donnai-Barrow Syndrome	56	0.055

956		MNN020	Meningococcal Infection	45	0.055

957	P	MYS003	Myasthenia Gravis	68	0.054

958	P	SML001	Small Cell Carcinoma	52	0.054

959		PYR021	Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency	39	0.054

960		MNN032	Meningococcal Meningitis	46	0.054

961		RNL078	Renal Dysplasia	49	0.054

962		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.054

963		TRN022	Transcobalamin Ii Deficiency	45	0.054

964	P	ALG028	Alagille Syndrome 1	73	0.054

965	P	KRT007	Keratoconus	49	0.054

966	P	RTT002	Rett Syndrome	80	0.054

967	c	ACT004	Acute Diarrhea	39	0.054

968	c	HNT004	Huntington Disease-Like 2	49	0.054

969		SPS150	Spastic Ataxia, Charlevoix-Saguenay Type	59	0.054

970	c	SYS043	Systemic Lupus Erythematosus 1	38	0.054

971	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	0.054

972	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.054

973		ACT064	Acute Necrotizing Encephalitis	32	0.054

974		BLD137	Blood Group--Ahonen	19	0.054

975		ATN004	Autonomic Neuropathy	44	0.054

976		OMN001	Omenn Syndrome	66	0.054

977		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.054

978	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.054

979		YLL002	Yellow Fever	60	0.054

980	P	TYR004	Tyrosinemia	58	0.054

981		GLL008	Gilles De La Tourette Syndrome	66	0.054

982	P	THY023	Thymoma	65	0.054

983	c	THY107	Thymoma, Familial	54	0.054

984		TNS005	Tonsillitis	57	0.054

985		CYT008	Cytomegalovirus Infection	56	0.054

986		URT010	Ureteral Obstruction	46	0.053

987		HPT022	Hepatoblastoma	56	0.053

988	c	DPH024	Diaphragmatic Hernia, Congenital	64	0.053

989	P	BRN022	Bronchiectasis	59	0.053

990		EXC002	Exocrine Pancreatic Insufficiency	41	0.053

991		CHL152	Childhood Acute Lymphocytic Leukemia	43	0.053

992		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	62	0.053

993	c	VSC019	Vesicoureteral Reflux 1	59	0.053

994	c	GLY008	Glycogen Storage Disease Ii	70	0.053

995		FCT029	Factor V and Factor Viii, Combined Deficiency of, 1	30	0.053

996		TRT001	Teratocarcinoma	46	0.053

997		FLT009	Folate Malabsorption, Hereditary	39	0.053

998		PTH003	Pathologic Nystagmus	51	0.053

999		PRP001	Propionic Acidemia	66	0.053

1000		RFR003	Refractive Error	44	0.053

1001	P	OPT009	Optic Neuritis	56	0.053

1002		FBR012	Fabry Disease	71	0.053

1003		SFT003	Soft Tissue Sarcoma	56	0.053

1004		ACT084	Acute Stress Disorder	48	0.053

1005		LPT006	Leptin Receptor Deficiency	47	0.053

1006		HMR039	Hemorrhage, Intracerebral	57	0.053

1007		CLL003	Cellulitis	54	0.053

1008	P	MYC033	Myoclonus	46	0.053

1009		NRN004	Neuroendocrine Tumor	55	0.053

1010	P	DRM010	Dermatomyositis	61	0.053

1011		LYS012	Lysosomal Acid Lipase Deficiency	64	0.053

1012	P	DMN001	Diamond-Blackfan Anemia	69	0.053

1013	P	PRN023	Prion Disease	57	0.053

1014		SPS019	Spastic Paraparesis	40	0.053

1015	P	ACT008	Actinic Keratosis	52	0.053

1016		PLC007	Placental Abruption	48	0.053

1017		WST001	West Syndrome	60	0.052

1018		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	45	0.052

1019		GRG001	Greig Cephalopolysyndactyly Syndrome	67	0.052

1020		HMT002	Hematologic Cancer	62	0.052

1021		CHL109	Childhood Apraxia of Speech	44	0.052

1022		INT088	Intrinsic Factor Deficiency	34	0.052

1023		GLL018	Gallbladder Cancer	56	0.052

1024		MLT092	Multicentric Carpotarsal Osteolysis Syndrome	60	0.052

1025		RFL001	Reflex Sympathetic Dystrophy	53	0.052

1026	c	MNN043	Meningioma, Familial	74	0.052

1027		PLL001	Pallister-Hall Syndrome	64	0.052

1028		SMT004	Smith-Lemli-Opitz Syndrome	69	0.052

1029		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.052

1030		KLD004	Keloid Disorder	40	0.052

1031		PRP036	Peripheral T-Cell Lymphoma	53	0.052

1032		SPR004	Supravalvular Aortic Stenosis	58	0.052

1033	c	PSD114	Pseudohypoaldosteronism, Type I, Autosomal Recessive	58	0.052

1034		THY122	Thyroid Gland Cancer	58	0.052

1035	P	VNW001	Von Willebrand's Disease	64	0.052

1036		ARG004	Argyria	28	0.052

1037		NNT012	Neonatal Jaundice	53	0.052

1038		ATN011	Autoinflammation with Infantile Enterocolitis	43	0.052

1039	P	LYM025	Lymphedema	53	0.051

1040		OVR029	Ovarian Hyperstimulation Syndrome	63	0.051

1041	P	ANG015	Angioedema	54	0.051

1042		MLT157	Multiple System Atrophy 1	70	0.051

1043		CYS013	Cystinuria	62	0.051

1044		PRT058	Pure Autonomic Failure	59	0.051

1045		CRT016	Carotid Artery Disease	52	0.051

1046	c	DSB006	Desbuquois Dysplasia 1	48	0.051

1047		SPT004	Septic Arthritis	57	0.051

1048		GRD001	Giardiasis	45	0.051

1049		SPS057	Spasticity	41	0.051

1050		INC002	Inclusion Body Myositis	64	0.051

1051		DRR014	Darier-White Disease	61	0.051

1052		ILS001	Ileus	51	0.051

1053		GLC006	Galactosemia	65	0.051

1054	c	CNT016	Central Retinal Vein Occlusion	49	0.051

1055	P	NRN021	Neuronal Ceroid Lipofuscinosis	63	0.051

1056		GSG001	Gas Gangrene	50	0.051

1057	c	HYP794	Hyperoxaluria, Primary, Type I	48	0.051

1058	P	END047	Endophthalmitis	52	0.051

1059		CHR103	Charge Syndrome	66	0.051

1060	P	TRT010	Teratoma	51	0.051

1061		GLC106	Glucocorticoid Resistance, Generalized	48	0.051

1062		DCT002	Ductal Carcinoma in Situ	59	0.051

1063		CLN045	Colonic Benign Neoplasm	49	0.051

1064	P	SCL057	Scoliosis, Isolated 1	41	0.051

1065		SYS071	Systemic Autoimmune Disease	37	0.051

1066	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	35	0.051

1067		PRS034	Parasitic Helminthiasis Infectious Disease	49	0.050

1068	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	60	0.050

1069	P	STR020	Strabismus	56	0.050

1070	c	LTN004	Late-Onset Retinal Degeneration	52	0.050

1071	c	MCL013	Mucolipidosis Iv	64