Search results for Vitamin C

3280 hits were found for Vitamin C

#	Family	MCID	Name	MIFTS	Score
1		HYP781	Hypoascorbemia	51	4.731

2		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	54	3.602

3		RCK004	Rickets	68	0.962

4	c	HPT001	Hepatitis C	62	0.802

5	c	HPT073	Hepatitis C Virus	72	0.742

6	P	HPT021	Hepatitis	67	0.470

7		KRT002	Keratomalacia	47	0.446

8		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.431

9	P	LVR013	Liver Disease	68	0.406

10		VTM002	Vitamin B12 Deficiency	48	0.368

11	P	KDN018	Kidney Disease	72	0.362

12		LVR012	Liver Cirrhosis	62	0.356

13	P	HYP069	Hyperparathyroidism	63	0.349

14	c	CHR684	Chronic Kidney Disease	70	0.328

15	P	BRS047	Breast Cancer	97	0.323

16	P	OST002	Osteoporosis	74	0.320

17	P	CLR023	Colorectal Cancer	99	0.308

18	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.303

19	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.302

20		ATM095	Autoimmune Disease	62	0.301

21		VTM033	Vitamin K Deficiency Bleeding	48	0.281

22		DFC004	Deficiency Anemia	70	0.277

23	P	HPT023	Hepatocellular Carcinoma	100	0.272

24	c	SCN007	Secondary Hyperparathyroidism	51	0.270

25		BNR002	Bone Resorption Disease	48	0.264

26		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.262

27	P	RTN008	Retinitis Pigmentosa	79	0.253

28	c	HPT016	Hepatitis B	59	0.242

29	c	PRC016	Pre-Eclampsia	63	0.240

30	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.240

31		OST011	Osteomalacia	52	0.239

32	P	BND020	Bone Disease	59	0.237

33		48X005	48,xyyy	39	0.235

34	c	VRL010	Viral Hepatitis	52	0.234

35		FTT001	Fatty Liver Disease	61	0.232

36		END086	End Stage Renal Disease	51	0.232

37	P	PRS040	Prostate Cancer	97	0.231

38	P	CRN300	Coronary Heart Disease 1	63	0.231

39		ATH013	Atherosclerosis Susceptibility	65	0.230

40	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.229

41	c	HPT003	Hepatitis a	62	0.227

42	P	VSC007	Vascular Disease	63	0.225

43	P	DBT009	Diabetes Mellitus	64	0.224

44		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.223

45		IRN002	Iron Metabolism Disease	57	0.219

46	P	DRR001	Diarrhea	55	0.219

47		CYS001	Cystic Fibrosis	81	0.217

48	P	NRP001	Neuropathy	56	0.217

49	P	PSR002	Psoriasis	62	0.217

50		HMC014	Homocysteinemia	53	0.217

51	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.213

52		PST011	Pustulosis of Palm and Sole	52	0.213

53		LPP008	Lipoprotein Quantitative Trait Locus	62	0.210

54	P	INF037	Inflammatory Bowel Disease	54	0.209

55	P	LKM002	Leukemia	68	0.206

56	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.204

57	P	HRT032	Heart Disease	75	0.204

58	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.203

59		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.203

60		LPD008	Lipid Metabolism Disorder	62	0.203

61		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.202

62	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.201

63		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.200

64	P	CRD246	Cardiovascular System Disease	57	0.199

65		ART140	Arteries, Anomalies of	52	0.198

66	P	ALZ034	Alzheimer Disease	88	0.197

67		HLX001	Helix Syndrome	47	0.197

68		CYT002	Cytokine Deficiency	42	0.197

69		HMN044	Human Immunodeficiency Virus Type 1	71	0.197

70	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.197

71		ISC004	Ischemia	58	0.194

72	P	ATR011	Atrial Fibrillation	66	0.193

73	P	SKN015	Skin Carcinoma	66	0.193

74	P	MYL006	Myeloid Leukemia	60	0.193

75		NRL016	Neural Tube Defects	82	0.191

76	P	MLT020	Multiple Sclerosis	72	0.190

77	P	LNG032	Lung Cancer	98	0.190

78		PRN011	Pernicious Anemia	53	0.188

79	P	ADN016	Adenocarcinoma	64	0.187

80	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.186

81		CRH001	Crohn's Disease	74	0.186

82		PRT037	Pertussis	65	0.185

83		DRM006	Dermatitis	61	0.185

84	c	SYS001	Systemic Lupus Erythematosus	86	0.185

85		ADN018	Adenoma	59	0.184

86	c	ATR087	Atrial Standstill 1	75	0.183

87	c	LKM061	Leukemia, Acute Myeloid	84	0.182

88		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.182

89		STR067	Stroke, Ischemic	81	0.181

90	P	BLD134	Bladder Cancer	79	0.181

91	P	LYN001	Lynch Syndrome	77	0.181

92	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.180

93	P	MYP004	Myopathy	70	0.179

94	c	NRF023	Neurofibromatosis, Type Ii	80	0.179

95	P	LYM118	Lymphoma	68	0.178

96	P	GST053	Gastric Cancer	83	0.178

97	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.178

98		IMM167	Immune Deficiency Disease	78	0.177

99	P	OVR042	Ovarian Cancer	88	0.176

100	P	PNC035	Pancreatic Cancer	84	0.175

101		NTR005	Nutritional Deficiency Disease	62	0.174

102	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.174

103	P	PRD008	Periodontitis	64	0.174

104		OST159	Osteogenic Sarcoma	66	0.174

105	P	NRB001	Neuroblastoma	72	0.174

106	P	PLY011	Polycystic Ovary Syndrome	56	0.173

107		CNG034	Congestive Heart Failure	69	0.173

108		TXC005	Toxic Shock Syndrome	62	0.173

109	P	LPS004	Lupus Erythematosus	61	0.173

110	P	THL005	Thalassemia	60	0.173

111	P	PRP019	Peripheral Nervous System Disease	58	0.172

112		HYP066	Hyperglycemia	61	0.171

113		SKN016	Skin Disease	63	0.171

114		CRB039	Cerebrovascular Disease	67	0.171

115		MSL001	Measles	62	0.170

116		INS024	Insulin-Like Growth Factor I	79	0.170

117	P	MYC007	Myocardial Infarction	70	0.170

118		GST033	Gestational Diabetes	61	0.169

119	c	MCR120	Microvascular Complications of Diabetes 7	47	0.169

120	P	HYP086	Hypothyroidism	69	0.169

121		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.167

122	P	ALP008	Alopecia	54	0.167

123	P	THR014	Thrombocytopenia	67	0.167

124	c	MCR113	Microvascular Complications of Diabetes 3	52	0.167

125	P	NTR004	Neutropenia	63	0.166

126		PYR009	Pyridoxine Deficiency Anemia	34	0.166

127	c	MCR130	Microvascular Complications of Diabetes 6	41	0.166

128	c	HYP595	Hypertension, Essential	84	0.165

129	c	MCR133	Microvascular Complications of Diabetes 4	41	0.165

130		CHL068	Cholestasis	61	0.165

131	P	ATX030	Ataxia-Telangiectasia	82	0.165

132		LNG099	Lung Disease	60	0.164

133	P	CTR002	Cataract	60	0.164

134		OST012	Osteoarthritis	78	0.163

135	P	GST044	Gastritis	56	0.162

136		DPR016	Depression	63	0.161

137	P	HYP061	Hypertrophic Cardiomyopathy	70	0.161

138	P	RHM011	Rheumatoid Arthritis	80	0.160

139		TTN003	Tetanus	65	0.159

140		AST005	Asthma	76	0.159

141	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.158

142		VSL002	Visual Epilepsy	59	0.158

143	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.158

144	P	MLN008	Melanoma	69	0.158

145	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.158

146	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.158

147	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.158

148	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.158

149	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.158

150	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.158

151	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.158

152	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.158

153		NNL006	Non-Alcoholic Steatohepatitis	54	0.157

154		PLM001	Pulmonary Tuberculosis	69	0.156

155		ALL026	Allergic Hypersensitivity Disease	62	0.156

156	P	DRM053	Dermatitis, Atopic	66	0.156

157	P	ECL001	Eclampsia	50	0.155

158		THR024	Thrombosis	57	0.155

159		ULC004	Ulcerative Colitis	73	0.155

160	c	PRM005	Primary Hyperparathyroidism	58	0.153

161		AGN016	Aging	56	0.152

162		PRP030	Purpura	54	0.152

163		47X002	47,xyy	49	0.151

164		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.151

165		LGH007	Leigh Syndrome	70	0.151

166		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.149

167	P	BCL017	B-Cell Lymphoma	58	0.149

168		THY029	Thyroid Carcinoma	59	0.149

169		ATX019	Ataxia with Vitamin E Deficiency	42	0.148

170		ALC007	Alcohol Dependence	66	0.148

171		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.147

172	P	GLM007	Glomerulonephritis	57	0.147

173	P	PNM007	Pneumonia	68	0.146

174	P	HML002	Hemolytic Anemia	63	0.146

175		MNT002	Mental Depression	58	0.145

176	P	NGH001	Night Blindness	48	0.143

177	P	GLM045	Glioma	63	0.143

178		SQM006	Squamous Cell Carcinoma	60	0.143

179	P	VSC011	Vasculitis	62	0.143

180		PRT011	Protein C Deficiency	44	0.142

181		MGL001	Megaloblastic Anemia	51	0.141

182		CHL079	Children's Interstitial Lung Disease	26	0.141

183		GLL048	Glial Tumor	45	0.141

184		HMS001	Hemosiderosis	54	0.140

185		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.140

186		GLC003	Glucose Intolerance	54	0.139

187		CLT003	Colitis	62	0.139

188		VRL011	Viral Infectious Disease	61	0.139

189	P	MSC005	Muscular Dystrophy	66	0.139

190		CMM005	Common Cold	57	0.139

191		ACQ007	Acquired Immunodeficiency Syndrome	60	0.139

192	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.138

193		ESP021	Esophageal Cancer	90	0.138

194	P	CNR004	Cone-Rod Dystrophy 2	73	0.138

195	P	SZR006	Seizure Disorder	56	0.136

196		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.136

197	c	ACT075	Acute Myocardial Infarction	57	0.136

198		BCT022	Bacterial Infectious Disease	56	0.136

199		HYP017	Hypophosphatemia	50	0.136

200		CRY004	Cryoglobulinemia	48	0.135

201	P	ART022	Arthritis	69	0.135

202	P	THY032	Thyroiditis	52	0.135

203	P	ENC018	Encephalopathy	61	0.135

204	P	INF032	Infertility	57	0.135

205	c	RHB024	Rhabdomyosarcoma 2	67	0.134

206	P	RRH023	Rare Hereditary Hemochromatosis	41	0.134

207	P	ATS364	Autism	70	0.133

208	P	MCR115	Microvascular Complications of Diabetes 5	66	0.133

209	P	TRN020	Turner Syndrome	67	0.132

210	P	HYP076	Hyperthyroidism	55	0.132

211		KRT001	Keratoconjunctivitis Sicca	49	0.132

212		PRP027	Peripheral Vascular Disease	71	0.132

213		XRP001	Xerophthalmia	41	0.132

214	c	ATS007	Autism Spectrum Disorder	67	0.132

215		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.131

216	P	SRC025	Sarcoidosis 1	70	0.131

217	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.130

218	P	RTN024	Retinoblastoma	73	0.130

219		DWN001	Down Syndrome	70	0.130

220		MYL009	Myelodysplastic Syndrome	70	0.130

221	P	ART021	Arteriosclerosis	54	0.130

222	P	ALC033	Alcohol Use Disorder	58	0.130

223	c	SML038	Small Cell Cancer of the Lung	65	0.129

224	c	DLT002	Dilated Cardiomyopathy	79	0.129

225	P	EXN002	Exanthem	57	0.128

226	c	PRM038	Primary Agammaglobulinemia	44	0.128

227		NPH009	Nephrolithiasis	55	0.128

228	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.128

229	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.127

230	c	NRF024	Neurofibromatosis, Type I	77	0.127

231	P	MYC084	Mycobacterium Tuberculosis 1	68	0.127

232	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.127

233	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.127

234		ATS010	Autosomal Recessive Disease	48	0.127

235	c	FML346	Familial Adenomatous Polyposis 1	66	0.127

236		GST019	Gastrointestinal Stromal Tumor	78	0.126

237	P	PHC003	Pheochromocytoma	71	0.126

238		HYP266	Hypoxia	57	0.126

239		GLB015	Glioblastoma Multiforme	75	0.126

240	c	DBT099	Diabetes Mellitus, Type I	65	0.126

241	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.126

242		STM007	Stomatitis	50	0.125

243	c	BTT014	Beta-Thalassemia	74	0.125

244	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	60	0.125

245	P	NPH012	Nephrotic Syndrome	60	0.124

246	P	LCH002	Lichen Planus	53	0.123

247		URM002	Uremia	49	0.123

248	P	SCK005	Sickle Cell Disease	50	0.122

249	P	HYP750	Hypertriglyceridemia, Familial	62	0.122

250	P	CHR071	Charcot-Marie-Tooth Disease	65	0.122

251	P	INF038	Influenza	68	0.122

252		ANG054	Angina Pectoris	66	0.122

253	P	RHN004	Rhinitis	57	0.122

254		PLM033	Pulmonary Embolism	59	0.121

255	P	CHR345	Chronic Pain	44	0.121

256		LPT014	Leptin Deficiency or Dysfunction	74	0.120

257		IRN001	Iron Deficiency Anemia	59	0.120

258		LYM133	Lymphoma, Hodgkin, Classic	69	0.120

259		MYL069	Myeloma, Multiple	85	0.120

260	P	HYP024	Hypoparathyroidism	56	0.120

261		DPH001	Diphtheria	60	0.120

262	P	DMN002	Dementia	66	0.119

263	P	PLY019	Polyneuropathy	56	0.119

264	P	PRM011	Primary Ciliary Dyskinesia	69	0.119

265		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.119

266	P	PRM006	Primary Biliary Cirrhosis	62	0.119

267		DSR002	Disorders of Intracellular Cobalamin Metabolism	31	0.118

268		CLR108	Colorectal Adenoma	64	0.118

269		TQP001	Taqi Polymorphism	32	0.118

270	c	ACT071	Acute Kidney Failure	60	0.117

271	c	THR082	Thrombophilia Due to Activated Protein C Resistance	61	0.117

272	P	LTR001	Lateral Sclerosis	54	0.116

273	P	HYP726	Hypercalcemia, Infantile, 1	58	0.116

274	P	PRK057	Parkinson Disease, Late-Onset	78	0.116

275	P	HMC002	Homocystinuria	53	0.116

276		HLC007	Helicobacter Pylori Infection	59	0.115

277		SVR004	Severe Combined Immunodeficiency	73	0.115

278	P	MNN013	Meningitis	66	0.115

279	c	TBR025	Tuberous Sclerosis 1	77	0.115

280		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.115

281		PRT013	Portal Hypertension	59	0.114

282	P	CLC063	Celiac Disease 1	66	0.114

283		MNN028	Mononeuropathy of the Median Nerve, Mild	46	0.114

284		HYP025	Hyperphosphatemia	48	0.114

285	P	THR015	Thrombophilia	51	0.113

286	c	FML001	Familial Atrial Fibrillation	65	0.113

287		FND002	Fundus Dystrophy	55	0.113

288		INT007	Intermediate Coronary Syndrome	55	0.113

289		SPN186	Spinal Cord Injury	60	0.113

290	c	FML008	Familial Retinoblastoma	53	0.113

291		HYP056	Hypoglycemia	66	0.113

292	P	MJR001	Major Depressive Disorder	68	0.113

293		LSH001	Leishmaniasis	63	0.113

294	P	KLZ004	Kala-Azar 1	41	0.113

295	c	MGR028	Migraine with or Without Aura 1	67	0.112

296	P	RSP003	Respiratory Failure	74	0.112

297	c	EXD008	Exudative Vitreoretinopathy 1	71	0.112

298	P	MTH008	Methylmalonic Acidemia	50	0.111

299		HYP060	Hyperinsulinism	54	0.111

300	P	END044	Endometriosis	63	0.111

301	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.111

302		VTM028	Vitamin E, Familial Isolated Deficiency of	52	0.111

303		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.111

304	c	PCH010	Pachyonychia Congenita 3	44	0.111

305		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.110

306	P	CRY007	Cryoglobulinemia, Familial Mixed	50	0.109

307	P	GRV001	Graves' Disease	55	0.109

308	c	ATM011	Autoimmune Hepatitis	63	0.109

309	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	46	0.109

310		ALL014	Allergic Encephalomyelitis	38	0.109

311	P	HMP007	Hemophilia	51	0.109

312	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.108

313	c	GLC092	Glaucoma, Primary Open Angle	62	0.108

314		CHL014	Cholera	59	0.108

315	P	HRP006	Herpes Simplex	65	0.108

316	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.108

317		KRT009	Keratosis	51	0.108

318	P	EPL164	Epilepsy	71	0.108

319	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.107

320	c	PRD040	Periodontitis, Chronic	53	0.107

321	P	RCT021	Rectum Cancer	52	0.107

322		CRV035	Cervical Cancer	76	0.107

323	c	INH030	Inherited Retinal Disorder	51	0.107

324		ALL003	Allergic Rhinitis	67	0.107

325		ADL002	Adult Syndrome	70	0.107

326		EYD002	Eye Disease	58	0.106

327		MLR004	Malaria	81	0.106

328	c	NMN015	Niemann-Pick Disease, Type C1	68	0.106

329	P	GRF003	Graft-Versus-Host Disease	72	0.106

330	c	ACT073	Acute Leukemia	58	0.106

331	P	LNG064	Lung Cancer Susceptibility 3	78	0.105

332		CVD001	Covid-19	44	0.105

333	c	DWL002	Dowling-Degos Disease 1	58	0.105

334		RTN023	Retinitis	46	0.105

335		NRR001	Neuroretinitis	42	0.105

336	P	ATR005	Atrophic Gastritis	50	0.105

337	c	ACT027	Acute Pancreatitis	60	0.104

338		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.104

339	P	HYP058	Hypervitaminosis a	48	0.104

340	P	NRP063	Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive	57	0.104

341		SPL018	Splenomegaly	48	0.104

342		RNL011	Renal Osteodystrophy	50	0.104

343		ABT001	Abetalipoproteinemia	69	0.104

344		ANX010	Anxiety	73	0.104

345		DBT010	Diabetic Neuropathy	54	0.103

346		PLM031	Poliomyelitis	64	0.103

347		NSS002	Neisseria Meningitidis Infection	47	0.103

348	c	BRN108	Branchiootic Syndrome 1	62	0.103

349	P	OPN001	Open-Angle Glaucoma	49	0.103

350	c	SPN225	Spondyloarthropathy 1	73	0.102

351		LYM019	Lymphosarcoma	46	0.102

352	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.101

353		CNS004	Constipation	58	0.101

354		KRT019	Keratitis, Hereditary	65	0.101

355		MTC097	Mitochondrial Complex Iv Deficiency	59	0.101

356		MRF001	Marfan Syndrome	77	0.101

357		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.101

358	P	SLP006	Sleep Apnea	69	0.101

359	c	INF071	Inflammatory Bowel Disease 1	67	0.101

360	P	NMN002	Niemann-Pick Disease	59	0.100

361		PLC008	Placenta Disease	50	0.100

362		SCK003	Sickle Cell Anemia	74	0.100

363	P	SYP003	Syphilis	58	0.100

364	P	PRP029	Porphyria	62	0.100

365	P	SCH015	Schizophrenia	74	0.100

366	P	BRB001	Beriberi	46	0.100

367	P	MLN007	Male Infertility	55	0.100

368		PPT005	Peptic Ulcer Disease	59	0.099

369		PNC001	Pancytopenia	54	0.099

370	P	PLM036	Pulmonary Fibrosis	65	0.099

371	P	HDC001	Headache	57	0.099

372		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.099

373		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.098

374		PNC129	Pancreatic Adenocarcinoma	68	0.098

375		MCS002	Mucositis	56	0.098

376		DSS009	Disseminated Intravascular Coagulation	57	0.098

377	P	OVR082	Overgrowth Syndrome	50	0.098

378		BRN056	Bronchopulmonary Dysplasia	57	0.098

379		VTM009	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1	31	0.098

380		PHN003	Phenylketonuria	75	0.097

381		DFF005	Diffuse Large B-Cell Lymphoma	55	0.097

382	P	HMR003	Hemorrhagic Disease	53	0.097

383	c	FML021	Familial Hypercholesterolemia	66	0.097

384	c	SVR001	Severe Acute Respiratory Syndrome	62	0.097

385		HRW001	Hair Whorl	36	0.097

386	c	CNG411	Congenital Disorder of Glycosylation, Type in	68	0.097

387	P	PNC044	Pancreatitis	61	0.097

388	P	CRD119	Cardiac Arrest	67	0.096

389		BRK010	Burkitt Lymphoma	67	0.096

390		TRN015	Transient Cerebral Ischemia	63	0.096

391		HYP081	Hypolipoproteinemia	51	0.096

392		SKN019	Skin Melanoma	68	0.096

393		MDD011	Mood Disorder	62	0.096

394		FDL002	Food Allergy	51	0.096

395	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.096

396	P	IMR002	Imerslund-Grasbeck Syndrome 1	43	0.096

397		PRT036	Peritonitis	64	0.096

398		DNT012	Dental Caries	53	0.096

399	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.096

400	P	TRM003	Tremor	54	0.096

401		BSL036	Basal Cell Nevus Syndrome	73	0.095

402	P	TBR001	Tuberous Sclerosis	70	0.095

403		ENT011	Enterocolitis	51	0.095

404		BRN071	Brain Injury	49	0.095

405		GST050	Gastrointestinal System Disease	56	0.094

406		ORL011	Oral Cancer	60	0.094

407	P	HYP098	Hypereosinophilic Syndrome	67	0.094

408	P	URT039	Urticaria	58	0.094

409		CHL123	Chlamydia	59	0.094

410		URL001	Urolithiasis	45	0.094

411		FBR047	Fibromyalgia	58	0.094

412	c	LKM063	Leukemia, Chronic Myeloid	72	0.094

413	c	HMC039	Hemochromatosis, Type 1	74	0.094

414	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	64	0.094

415		PPL052	Papillomatosis, Confluent and Reticulated	33	0.094

416		GTR002	Goiter	53	0.094

417	P	INS002	in Situ Carcinoma	53	0.094

418		ACT119	Acute Promyelocytic Leukemia	63	0.093

419		OCL069	Ocular Motor Apraxia	51	0.093

420		MSC157	Muscular Dystrophy, Duchenne Type	72	0.093

421		IGR001	Ige Responsiveness, Atopic	59	0.093

422		GST045	Gastroenteritis	59	0.093

423		IRR002	Irritable Bowel Syndrome	65	0.093

424		NPH003	Nephrocalcinosis	51	0.092

425		PRP080	Peripheral Artery Disease	53	0.092

426		SPN051	Spondylitis	51	0.092

427		BRN024	Bronchitis	68	0.092

428		BLR008	Bilirubin Metabolic Disorder	57	0.092

429		INF009	Inflammatory Spondylopathy	31	0.092

430	P	HYP265	Hypotonia	43	0.092

431	P	RTN016	Retinal Degeneration	53	0.091

432	P	SBS003	Substance Abuse	55	0.091

433	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.091

434	c	PNS012	Paine Syndrome	61	0.091

435		END057	Endometrial Cancer	74	0.091

436	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.091

437	P	PLR004	Pleuropulmonary Blastoma	65	0.091

438		ALL006	Allergic Asthma	56	0.091

439		HSH003	Hashimoto Thyroiditis	62	0.090

440	c	SCL052	Scleroderma, Familial Progressive	61	0.090

441		PRS045	Prostatic Hypertrophy	53	0.090

442	P	FBR017	Fibrosarcoma	56	0.090

443		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.090

444		VRC005	Varicose Veins	60	0.090

445		HNS001	Hansen's Disease	34	0.090

446		ERY051	Erythroleukemia, Familial	56	0.090

447		CRH005	Crohn's Colitis	53	0.089

448	P	LPR021	Leprosy 3	69	0.089

449	P	BPL003	Bipolar Disorder	56	0.089

450	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.089

451	P	MSC003	Muscular Atrophy	52	0.089

452	P	ANT006	Antiphospholipid Syndrome	55	0.089

453		PPL022	Papilloma	54	0.089

454		VCC001	Vaccinia	49	0.089

455	c	ACT068	Acute Cystitis	63	0.089

456	c	MJR024	Major Affective Disorder 9	41	0.088

457	c	MJR022	Major Affective Disorder 8	38	0.088

458	c	DRR009	Diarrhea 6	46	0.088

459		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.088

460		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.088

461		TRN018	Transitional Cell Carcinoma	56	0.088

462		THY030	Thyroid Gland Disease	52	0.088

463		BRT054	Brittle Bone Disorder	72	0.088

464	c	NRP053	Neuropathy, Hereditary Sensory and Autonomic, Type Iia	65	0.088

465		PND002	Pendred Syndrome	65	0.088

466	c	HYP057	Hypervitaminosis D	42	0.088

467	P	ANR048	Aniridia 1	63	0.088

468		ORL015	Oral Squamous Cell Carcinoma	43	0.088

469		MST005	Mastitis	53	0.088

470		GST040	Gastric Adenocarcinoma	70	0.087

471		HMP009	Haemophilus Influenzae	43	0.087

472	P	NSP012	Nasopharyngeal Carcinoma	66	0.087

473		DRR016	Diarrhea 2, with Microvillus Atrophy	60	0.087

474	P	AMY004	Amyloidosis	70	0.087

475	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.086

476		CNT047	Contact Dermatitis	58	0.086

477		BRN002	Bronchiolitis	59	0.086

478		PRS129	Prostatic Hyperplasia, Benign	49	0.086

479	P	SYS005	Systemic Scleroderma	68	0.086

480		PSY004	Psychotic Disorder	67	0.085

481	P	MYC008	Myocarditis	59	0.085

482	P	PLM037	Pulmonary Hypertension	67	0.085

483		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.085

484		SRC014	Sarcoma	65	0.085

485		SCH014	Schistosomiasis	57	0.085

486		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.085

487		MSC007	Muscle Hypertrophy	64	0.085

488		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	65	0.085

489		KHL003	Kohlschutter-Tonz Syndrome	65	0.085

490		PRS021	Prostatic Adenoma	51	0.085

491	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.085

492	P	HYD006	Hydrocephalus	66	0.085

493	P	MYP006	Myopia	55	0.084

494		ANR007	Anorexia Nervosa	63	0.084

495		EPL131	Epilepsy, Pyridoxine-Dependent	49	0.084

496		MTH078	Methylmalonic Aciduria, Cblb Type	51	0.084

497		MCR017	Macrocytic Anemia	44	0.084

498		TRM010	Traumatic Brain Injury	51	0.084

499	P	OST001	Osteopetrosis	70	0.084

500	P	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	38	0.084

501		BCK006	Back Pain	42	0.084

502	P	KDN017	Kidney Cancer	60	0.084

503	c	BSL007	Basal Cell Carcinoma	68	0.084

504		CNN005	Connective Tissue Disease	68	0.084

505	P	SLP005	Sleep Disorder	59	0.084

506	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	52	0.084

507	c	MCR129	Microvascular Complications of Diabetes 1	66	0.083

508		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.083

509	P	DYS154	Dystonia	65	0.083

510	P	LCT001	Lactic Acidosis	51	0.083

511	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.083

512		DSS008	Disease of Mental Health	58	0.083

513	c	TBR026	Tuberous Sclerosis 2	72	0.083

514		SQM002	Squamous Cell Papilloma	46	0.083

515		LMY002	Leiomyoma	52	0.083

516	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.083

517		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.083

518	P	PRP003	Porphyria Cutanea Tarda	67	0.083

519	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.082

520	P	OPT006	Optic Nerve Disease	60	0.082

521		MTH077	Methylmalonic Aciduria, Cbla Type	42	0.082

522		ENT004	Enthesopathy	49	0.082

523		PRT038	Protein-Energy Malnutrition	54	0.082

524		CLN015	Colon Adenocarcinoma	65	0.082

525	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.082

526		SPN035	Spindle Cell Sarcoma	53	0.081

527	P	SCL018	Scoliosis	60	0.081

528	P	SPP010	Suppressor of Tumorigenicity 3	51	0.081

529		HPT004	Hepatic Coma	45	0.081

530		PST092	Posttransplant Acute Limbic Encephalitis	29	0.081

531		ORL013	Oral Lichen Planus	45	0.080

532	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.080

533	P	ADL010	Adult Respiratory Distress Syndrome	65	0.080

534		HRD160	Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors	22	0.080

535		SBC016	Subacute Delirium	44	0.080

536		PNG002	Pain Agnosia	51	0.080

537		OTT002	Otitis Media	72	0.080

538		CLC006	Calcinosis	48	0.080

539	c	CWD006	Cowden Syndrome 1	78	0.080

540		DMY004	Demyelinating Disease	52	0.080

541		GNG013	Gingivitis	59	0.080

542	c	HMP029	Hemophilia a	67	0.080

543		CMR002	Coumarin Resistance	56	0.080

544		HPT019	Hepatic Encephalopathy	60	0.080

545		OVR094	Ovarian Epithelial Cancer	38	0.079

546	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.079

547		WRN001	Werner Syndrome	69	0.079

548	P	ART023	Arthropathy	62	0.079

549		CLF027	Cleft Palate, Isolated	64	0.079

550		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.079

551	P	ALP009	Alopecia Areata	60	0.079

552		CHL065	Cholangiocarcinoma	68	0.078

553	P	OCL013	Oculodentodigital Dysplasia	69	0.078

554	c	ACT134	Acute Liver Failure	56	0.078

555		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.078

556		BRC012	Brucellosis	64	0.078

557	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.078

558		MTB004	Metabolic Acidosis	50	0.078

559		CRB037	Cerebral Palsy	69	0.078

560	P	FML018	Familial Mediterranean Fever	73	0.078

561		INT079	Intrahepatic Cholangiocarcinoma	51	0.078

562		HYP080	Hypogonadism	50	0.078

563	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.078

564		PRN019	Perinatal Necrotizing Enterocolitis	59	0.077

565		CRD132	Cardiac Conduction Defect	58	0.077

566		LYM027	Lymphopenia	58	0.077

567		NWC001	Newcastle Disease	45	0.077

568	P	APL001	Aplastic Anemia	74	0.077

569	P	UVT001	Uveitis	57	0.077

570		DYS073	Dysphagia	50	0.077

571		CRB004	Cerebral Artery Occlusion	45	0.077

572		LKP003	Leukoplakia	39	0.077

573	P	MPL001	Maple Syrup Urine Disease	69	0.077

574	P	MVM001	Movement Disease	63	0.077

575	P	ALP004	Alport Syndrome	68	0.077

576		CRP001	Carpal Tunnel Syndrome	67	0.076

577	P	CRN037	Craniosynostosis	68	0.076

578		HYP014	Hyperuricemia	52	0.076

579		PRM020	Premenstrual Tension	40	0.076

580	c	FML035	Familial Hyperlipidemia	55	0.076

581	P	ENC004	Encephalitis	61	0.076

582	c	PSR023	Psoriasis 1	52	0.076

583	P	GLM040	Glioma Susceptibility 1	81	0.076

584	P	AST007	Astrocytoma	51	0.076

585		BRN028	Brain Cancer	74	0.075

586		IMP005	Impotence	52	0.075

587		ERY029	Erythermalgia, Primary	58	0.075

588		ATM052	Autoimmune Disease 1	37	0.075

589	c	SVR005	Severe Pre-Eclampsia	50	0.075

590		CHR066	Chronic Fatigue Syndrome	61	0.075

591		MMM001	Mammary Paget's Disease	53	0.075

592		BLD131	Bladder Urothelial Carcinoma	62	0.074

593		ADR040	Adrenal Gland Pheochromocytoma	46	0.074

594		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.074

595	P	PLL002	Pellagra	46	0.074

596		ANR040	Aneurysm	59	0.074

597		PPL049	Papillon-Lefevre Syndrome	65	0.074

598	c	GRV008	Graves Disease 1	56	0.074

599		HMG005	Hemoglobinopathy	56	0.074

600	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.074

601		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.074

602	c	MCR112	Microvascular Complications of Diabetes 2	41	0.074

603	c	PSR017	Psoriasis 2	53	0.073

604		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.073

605	P	CHL066	Cholangitis	51	0.073

606	P	HYP818	Hypobetalipoproteinemia, Familial, 1	56	0.073

607		TLN003	Telangiectasis	52	0.073

608		HYP005	Hypokalemia	55	0.072

609	P	END033	Endocarditis	57	0.072

610	P	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	64	0.072

611		CRN030	Coronary Stenosis	50	0.072

612		GT001	Gout	64	0.072

613	c	ALP101	Alpha-Thalassemia	62	0.072

614		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.072

615		THY111	Thyroid Carcinoma, Familial Medullary	67	0.072

616		MYL005	Myelofibrosis	70	0.072

617		CMP010	Complex Regional Pain Syndrome	58	0.072

618	P	BNG032	Benign Mesothelioma	46	0.072

619		VSC003	Visceral Leishmaniasis	55	0.072

620	P	DNG005	Dengue Virus	59	0.072

621		NRT004	Neuritis	52	0.072

622		GST023	Gastric Ulcer	53	0.072

623		49X006	49, Xxxxy Syndrome	41	0.072

624		TRD006	Tardive Dyskinesia	54	0.072

625	P	INT068	Intestinal Disease	53	0.072

626		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.071

627		FCT007	Factor Vii Deficiency	67	0.071

628		END040	Endogenous Depression	55	0.071

629		APH001	Aphthous Stomatitis	57	0.071

630		ANX004	Anoxia	40	0.071

631		ART016	Aortic Aneurysm	69	0.071

632	P	SHR001	Short Bowel Syndrome	53	0.071

633		CHR178	Chromosomal Triplication	35	0.071

634		HYP043	Hyperandrogenism	48	0.071

635		DGN001	Degenerative Disc Disease	48	0.071

636		ACR007	Acromegaly	71	0.071

637	P	FRN006	Frontotemporal Dementia	68	0.071

638		PRM329	Premature Aging	35	0.070

639		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.070

640	c	GLL024	Gallbladder Disease 1	53	0.070

641		LNG031	Lung Benign Neoplasm	51	0.070

642	P	LFR001	Li-Fraumeni Syndrome	72	0.070

643	P	PRC031	Preeclampsia/eclampsia 1	38	0.070

644		PSR001	Psoriatic Arthritis	61	0.070

645	P	BRS044	Breast Adenocarcinoma	59	0.070

646		MMB001	Membranoproliferative Glomerulonephritis	55	0.070

647		WLS001	Wilson Disease	71	0.070

648		BLR001	Biliary Atresia	50	0.070

649	P	MLT074	Multiple Endocrine Neoplasia	56	0.070

650		NRT001	Neurotic Disorder	53	0.070

651	c	PNC108	Pancreatitis, Hereditary	70	0.070

652	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.070

653		NWB001	Newborn Respiratory Distress Syndrome	58	0.069

654	c	EPL184	Epileptic Encephalopathy, Early Infantile, 6	70	0.069

655	P	RTN018	Retinal Disease	53	0.069

656		VSC002	Vascular Dementia	57	0.069

657	P	CND004	Candidiasis	58	0.069

658	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.069

659		OST003	Osteonecrosis	61	0.069

660		DYS015	Dysentery	52	0.069

661		SNS003	Sensory Peripheral Neuropathy	54	0.069

662	c	WLM013	Wilms Tumor 1	65	0.069

663	P	SJG008	Sjogren Syndrome	61	0.069

664		CHG001	Chagas Disease	66	0.069

665	c	ACT135	Acute Graft Versus Host Disease	52	0.069

666		BRR014	Barrett Esophagus	65	0.069

667	P	MDL005	Medulloblastoma	77	0.069

668	c	CNG006	Congenital Hypothyroidism	64	0.069

669		MNN020	Meningococcal Infection	46	0.069

670		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	65	0.069

671	P	PSD087	Pseudoxanthoma Elasticum	65	0.069

672		CHC001	Chickenpox	60	0.068

673		MTH009	Mouth Disease	56	0.068

674	P	MTC069	Mitochondrial Disorders	56	0.068

675	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	65	0.068

676		THY125	Thyroid Gland Medullary Carcinoma	50	0.068

677	P	DYS007	Dyskeratosis Congenita	67	0.068

678		RBF001	Riboflavin Deficiency	49	0.068

679	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.068

680		PLY150	Polykaryocytosis Inducer	31	0.068

681		ALP103	Alpha-1-Antitrypsin Deficiency	64	0.068

682	P	PLY014	Polycystic Kidney Disease	62	0.068

683		ADR007	Adrenoleukodystrophy	75	0.068

684		INT066	Interstitial Lung Disease	60	0.068

685	c	LKM005	Leukemia, T-Cell, Chronic	34	0.068

686	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	52	0.068

687	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.068

688		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.067

689	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	41	0.067

690		PLM010	Pulmonary Edema	54	0.067

691		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	52	0.067

692	P	BRL012	Bare Lymphocyte Syndrome, Type Ii	66	0.067

693		OST017	Osteomyelitis	64	0.067

694	P	NRV007	Nervous System Disease	66	0.067

695		KPS004	Kaposi Sarcoma	75	0.067

696	P	MST009	Mastocytosis	64	0.067

697		PYR016	Pyridoxine Deficiency	30	0.067

698		CHR074	Choriocarcinoma	47	0.067

699	c	NMN014	Niemann-Pick Disease, Type C2	51	0.067

700	c	LTN004	Late-Onset Retinal Degeneration	59	0.067

701		ALC006	Alcoholic Hepatitis	61	0.067

702		HRP004	Herpes Zoster	60	0.067

703		FML307	Familial Calcium Pyrophosphate Deposition	40	0.067

704		TNG002	Tangier Disease	65	0.067

705	P	ANG001	Angelman Syndrome	69	0.067

706	c	SPN207	Spinocerebellar Ataxia, Autosomal Recessive 8	49	0.067

707	P	DDN001	Duodenal Ulcer	52	0.066

708		CTN007	Cutaneous Leishmaniasis	62	0.066

709		ISL099	Isolated Methylmalonic Acidemia	29	0.066

710	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.066

711		CRV045	Cervical Intraepithelial Neoplasia	39	0.066

712		STT001	Status Epilepticus	60	0.066

713		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	50	0.066

714		APN008	Apnea, Obstructive Sleep	64	0.066

715		CHN016	Cohen Syndrome	63	0.066

716	P	PRS038	Personality Disorder	65	0.066

717	c	MYT021	Myotonic Dystrophy 1	69	0.066

718	P	VTR007	Vitreoretinopathy	46	0.066

719		BDD001	Budd-Chiari Syndrome	63	0.066

720	P	LBR014	Leber Congenital Amaurosis 4	56	0.066

721		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.066

722	P	CYS018	Cystitis	59	0.066

723	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	0.066

724	P	VSC018	Visceral Steatosis	33	0.066

725		CLR109	Colorectal Adenocarcinoma	51	0.066

726		HYL004	Hyaline Fibromatosis Syndrome	67	0.066

727	P	PLY018	Polycythemia	56	0.066

728		BRS051	Breast Disease	58	0.066

729		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.066

730	P	HML001	Hemolytic-Uremic Syndrome	53	0.066

731	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.066

732	P	HNT016	Huntington Disease	72	0.065

733		INT002	Intermittent Claudication	61	0.065

734		ESP002	Esophageal Varix	51	0.065

735		CYS036	Cystinosis, Nephropathic	51	0.065

736	c	XNT010	Xanthinuria, Type I	53	0.065

737		THR004	Thrombocytosis	51	0.065

738	P	PRP034	Purpura Fulminans	43	0.065

739		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.065

740	c	INH020	Inherited Metabolic Disorder	47	0.065

741	P	ICH004	Ichthyosis	54	0.065

742	P	FLL037	Follicular Lymphoma	67	0.065

743	c	HYP243	Hyperparathyroidism 1	51	0.065

744		SCN001	Secondary Hyperparathyroidism of Renal Origin	27	0.065

745	P	ESP024	Esophagitis	62	0.065

746		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.065

747	P	LYM033	Lymphoproliferative Syndrome	59	0.064

748	P	MYS005	Myositis	56	0.064

749	P	PTY003	Pityriasis Rubra Pilaris	58	0.064

750	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.064

751		CRT013	Carotid Stenosis	50	0.064

752	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.064

753	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.064

754	c	PLY105	Polycystic Ovary Syndrome 1	38	0.064

755	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.064

756	c	PSR032	Psoriasis 11	47	0.064

757	c	PSR028	Psoriasis 7	42	0.064

758	c	PSR018	Psoriasis 13	41	0.064

759	P	PTT014	Pitt-Hopkins Syndrome	63	0.064

760	c	HYP864	Hypoparathyroidism, Familial Isolated, 1	48	0.064

761		LMY014	Leiomyoma, Uterine	56	0.063

762	c	PRD013	Periodic Fever, Familial, Autosomal Dominant	67	0.063

763		PRT029	Parathyroid Adenoma	50	0.063

764	c	BLC008	Bile Acid Synthesis Defect, Congenital, 2	50	0.063

765		GLS007	Glossitis	47	0.063

766		HYP636	Hypocalcemic Vitamin D-Dependent Rickets	39	0.063

767		ORT008	Orotic Aciduria	55	0.063

768	P	MCR010	Microcephaly	59	0.063

769	P	NRF002	Neurofibromatosis	56	0.063

770	c	ART101	Aortic Valve Disease 2	65	0.063

771	c	INF145	Infantile Liver Failure Syndrome 1	50	0.063

772		WGN007	Wagner Vitreoretinopathy	38	0.063

773		WGN003	Wagner Syndrome	36	0.063

774	c	PSD066	Pseudohypoparathyroidism, Type Ib	55	0.063

775	P	PYL005	Pyelonephritis	56	0.063

776		MYF001	Myofibroma	45	0.063

777		GYR004	Gyrate Atrophy of Choroid and Retina	57	0.063

778		ATN005	Autonomic Dysfunction	46	0.063

779	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.063

780		RNL078	Renal Dysplasia	50	0.063

781		RTN020	Retinal Vascular Disease	46	0.063

782	c	CHL119	Cholangitis, Primary Sclerosing	57	0.063

783	P	BRD002	Bardet-Biedl Syndrome	66	0.063

784	P	HYP035	Hypophosphatasia	61	0.063

785	P	CRB101	Cerebrooculofacioskeletal Syndrome 1	60	0.062

786		PTZ001	Peutz-Jeghers Syndrome	70	0.062

787	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.062

788		PRS063	Paresthesia	41	0.062

789		PRT014	Protein S Deficiency	44	0.062

790		OMN001	Omenn Syndrome	67	0.062

791	c	HMG029	Hemoglobin Se Disease	39	0.062

792	P	SPN429	Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2	52	0.062

793		INS001	Insulinoma	60	0.062

794	c	GLY060	Glycogen Storage Disease Ia	63	0.062

795		FDB001	Foodborne Botulism	55	0.062

796		HLC001	Holocarboxylase Synthetase Deficiency	48	0.062

797		PGM030	Pigmentation Anomaly of the Skin	26	0.062

798	c	CHR064	Chronic Monocytic Leukemia	33	0.062

799		ACN002	Acanthosis Nigricans	60	0.062

800		FLT009	Folate Malabsorption, Hereditary	50	0.062

801	P	MTC003	Metachromatic Leukodystrophy	70	0.062

802		BRN004	Brain Edema	56	0.062

803		BTN003	Biotinidase Deficiency	60	0.062

804		BNN003	Bone Inflammation Disease	48	0.062

805		AMN001	Amenorrhea	54	0.061

806		ALL010	Allergic Contact Dermatitis	56	0.061

807	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.061

808	P	CNJ013	Conjunctivitis	65	0.061

809	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.061

810	P	RST001	Restless Legs Syndrome	54	0.061

811	c	BCT007	Bacterial Meningitis	55	0.061

812	c	MLG068	Malignant Glioma	46	0.061

813		PFF001	Pfeiffer Syndrome	79	0.061

814	P	RBL001	Rubella	59	0.061

815	P	SNS001	Sensorineural Hearing Loss	60	0.061

816		BCT002	Bacterial Vaginosis	53	0.061

817		EMB004	Embryonal Carcinoma	56	0.061

818	P	MTC133	Mitochondrial Myopathy	49	0.061

819		CHL067	Cholecystitis	57	0.061

820		KRN002	Kearns-Sayre Syndrome	63	0.061

821	P	MTR014	Motor Neuron Disease	65	0.061

822		CHD001	Chediak-Higashi Syndrome	66	0.061

823		GLY010	Glycine Encephalopathy	62	0.061

824	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	70	0.061

825		GLC106	Glucocorticoid Resistance, Generalized	48	0.061

826	c	HPT007	Hepatitis E	53	0.061

827		ART001	Arterial Tortuosity Syndrome	66	0.060

828	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.060

829		IGG001	Iga Glomerulonephritis	48	0.060

830		PST021	Postpartum Depression	50	0.060

831		CRD223	Cardiac Arrhythmia	60	0.060

832	c	HYP768	Hyperlipoproteinemia, Type I	67	0.060

833		PRD004	Prediabetes Syndrome	47	0.060

834		RHM001	Rheumatic Fever	60	0.060

835	P	GCH001	Gaucher's Disease	63	0.060

836		PRT010	Parathyroid Carcinoma	67	0.060

837	c	MCP052	Mucopolysaccharidosis, Type Vi	67	0.060

838	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.060

839		IDP070	Idiopathic Scoliosis	42	0.060

840		CHY002	Chylomicron Retention Disease	65	0.060

841	c	HMP004	Hemophilia B	68	0.060

842		RFR010	Refractory Anemia	48	0.060

843		GRW007	Growth Hormone Deficiency	46	0.060

844		NRM005	Neuromuscular Disease	64	0.059

845	P	RNL007	Renal Tubular Acidosis	51	0.059

846		CYT018	Cytochrome P450 2d6 Variant	27	0.059

847	c	BLD140	Blood Group, I System	32	0.059

848		ALP077	Alpha-Methylacetoacetic Aciduria	55	0.059

849		SPS150	Spastic Ataxia, Charlevoix-Saguenay Type	58	0.059

850		GLS018	Glass Syndrome	57	0.059

851	c	JVN061	Juvenile Arthritis	60	0.059

852		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	63	0.059

853	P	RTN022	Retinal Vein Occlusion	53	0.059

854		MTH021	Methylmalonic Acidemia with Homocystinuria	46	0.059

855		MNN032	Meningococcal Meningitis	54	0.059

856	c	HYP369	Hypophosphatemic Rickets, Autosomal Recessive, 2	29	0.059

857	P	MMP001	Mumps	58	0.059

858	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.059

859		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.059

860		LMB062	Limb Ischemia	55	0.059

861	P	MNC007	Monocytic Leukemia	53	0.059

862	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.059

863		MCC012	Mccune-Albright Syndrome	70	0.059

864	P	FML011	Familial Adenomatous Polyposis	72	0.059

865	P	PNT019	Pontocerebellar Hypoplasia	46	0.059

866	P	LCT002	Lactose Intolerance	53	0.059

867		BLL006	Bullous Pemphigoid	62	0.059

868	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	62	0.059

869		RNL077	Renal Fibrosis	47	0.059

870		DNN002	Donnai-Barrow Syndrome	56	0.058

871	c	HPT015	Hepatitis D	49	0.058

872	c	CRD184	Ceroid Lipofuscinosis, Neuronal, 5	55	0.058

873	c	DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.058

874	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.058

875		LNG039	Lung Squamous Cell Carcinoma	66	0.058

876		CLF001	Cleft Lip	53	0.058

877		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.058

878	P	PSD015	Pseudohypoparathyroidism	56	0.058

879		DWR001	Dwarfism	44	0.058

880	P	ALP106	Alport Syndrome 1, X-Linked	55	0.058

881		TRP009	Triple X Syndrome	42	0.058

882		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	59	0.058

883		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	60	0.058

884		AZS001	Azoospermia	50	0.058

885		PYR021	Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency	47	0.058

886		BRS099	Breast Ductal Carcinoma	62	0.058

887		MCL006	Macular Retinal Edema	55	0.058

888		ATN011	Autoinflammation with Infantile Enterocolitis	44	0.058

889		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.058

890		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.058

891		PLY001	Polycythemia Vera	69	0.058

892		HYP741	Hyperparathyroidism 2 with Jaw Tumors	53	0.058

893		THR123	Thrombotic Microangiopathy	36	0.058

894		THR013	Thoracic Outlet Syndrome	54	0.057

895	P	PMP001	Pemphigus	54	0.057

896		PRS047	Prostatitis	56	0.057

897	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.057

898	c	ALZ056	Alzheimer Disease 3	57	0.057

899		STT009	Sutton Disease 2	30	0.057

900		PRP001	Propionic Acidemia	65	0.057

901		TRN022	Transcobalamin Ii Deficiency	45	0.057

902		HRP008	Herpes Simiae	25	0.057

903		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.057

904		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.057

905		SPP011	Suppression of Tumorigenicity 12	59	0.057

906	c	PLM127	Pulmonary Hypertension, Primary, 3	34	0.057

907		ACR006	Aceruloplasminemia	65	0.057

908		FND001	Fundus Albipunctatus	60	0.057

909		MCR013	Microphthalmia	57	0.057

910	P	NPH005	Nephronophthisis	59	0.057

911	P	MMB011	Membranous Nephropathy	50	0.057

912	c	PRX059	Peroxisome Biogenesis Disorder 1a	56	0.057

913	P	AGG001	Aggressive Periodontitis	50	0.056

914		APP008	Appendicitis	61	0.056

915		MTC005	Mitochondrial Metabolism Disease	49	0.056

916	c	GCH015	Gaucher Disease, Type I	70	0.056

917	c	GLY008	Glycogen Storage Disease Ii	70	0.056

918		PRT082	Preterm Premature Rupture of the Membranes	54	0.056

919		EHL052	Ehlers-Danlos Syndrome, Vascular Type	56	0.056

920		PHR003	Pharyngitis	57	0.056

921		KRT006	Keratoconjunctivitis	53	0.056

922		PRL032	Perlman Syndrome	57	0.056

923	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.056

924		SYN007	Synovitis	54	0.056

925		PLC002	Plica Syndrome	36	0.056

926		PRT018	Portal Vein Thrombosis	50	0.056

927		ORL012	Oral Leukoplakia	39	0.056

928		WST001	West Syndrome	61	0.056

929		MTH056	Methylmalonic Aciduria and Homocystinuria, Cblf Type	38	0.056

930		ANV001	Anovulation	47	0.056

931		CHR005	Chorioamnionitis	51	0.056

932	P	SCL057	Scoliosis, Isolated 1	41	0.055

933		LBR036	Leber Plus Disease	66	0.055

934		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.055

935		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.055

936	c	USH036	Usher Syndrome, Type I	60	0.055

937	P	OBS001	Obstructive Jaundice	50	0.055

938	P	ASP006	Aspergillosis	69	0.055

939		GRG001	Greig Cephalopolysyndactyly Syndrome	66	0.055

940		CRT017	Cartilage Disease	54	0.055

941		RDN001	Reading Disorder	40	0.055

942	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.055

943	P	KRB001	Krabbe Disease	69	0.055

944		HRT012	Heart Valve Disease	53	0.055

945	P	TXP001	Toxoplasmosis	60	0.055

946		GST092	Gastroesophageal Reflux	67	0.055

947	P	SCL009	Sclerosing Cholangitis	48	0.055

948		CMM004	Common Variable Immunodeficiency	68	0.055

949		LPT006	Leptin Receptor Deficiency	48	0.055

950		LYS012	Lysosomal Acid Lipase Deficiency	65	0.055

951		CHL004	Cholelithiasis	49	0.055

952		MLT092	Multicentric Carpotarsal Osteolysis Syndrome	65	0.055

953		KRT013	Keratolytic Winter Erythema	46	0.055

954		HDN002	Head Injury	46	0.055

955		SXL003	Sexual Disorder	47	0.055

956		GST020	Gastric Antral Vascular Ectasia	41	0.055

957		DRY001	Dry Eye Syndrome	47	0.054

958		TYP007	Typhoid Fever	63	0.054

959	P	MTR004	Maturity-Onset Diabetes of the Young	65	0.054

960		ETN001	Eating Disorder	60	0.054

961		DRR014	Darier-White Disease	60	0.054

962	c	DSB006	Desbuquois Dysplasia 1	48	0.054

963		KWS002	Kawasaki Disease	65	0.054

964		GLL008	Gilles De La Tourette Syndrome	66	0.054

965		FCT034	Factor V and Factor Viii, Combined Deficiency of, 2	41	0.054

966		CYS013	Cystinuria	63	0.054

967		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	68	0.054

968		CLR030	Clear Cell Renal Cell Carcinoma	53	0.054

969		PLG002	Plague	63	0.054

970		GRN017	Granulocytopenia	44	0.054

971		ATX010	Ataxia Neuropathy Spectrum	34	0.054

972		SCH012	Schizoaffective Disorder	50	0.054

973	c	PSD114	Pseudohypoaldosteronism, Type I, Autosomal Recessive	59	0.054

974		MYC006	Mycosis Fungoides	66	0.054

975		CHL109	Childhood Apraxia of Speech	44	0.054

976		INT075	Intracranial Hypertension	53	0.053

977		THR016	Thrombophlebitis	51	0.053

978	c	SZR007	Seizures, Benign Familial Infantile, 3	42	0.053

979		SMT004	Smith-Lemli-Opitz Syndrome	70	0.053

980		ATN004	Autonomic Neuropathy	45	0.053

981		PST028	Post-Traumatic Stress Disorder	58	0.053

982	P	RTT002	Rett Syndrome	80	0.053

983		OBS002	Obsessive-Compulsive Disorder	68	0.053

984		INT303	Intracranial Hypertension, Idiopathic	57	0.053

985	P	PGT001	Paget's Disease of Bone	58	0.053

986		LYM040	Lymphoblastic Lymphoma	54	0.053

987		INT088	Intrinsic Factor Deficiency	34	0.053

988	c	ATS307	Autosomal Recessive Cerebellar Ataxia	42	0.053

989	P	ALG028	Alagille Syndrome 1	73	0.053

990		SFT003	Soft Tissue Sarcoma	56	0.053

991		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	59	0.053

992		HPT022	Hepatoblastoma	56	0.053

993	c	MYS033	Miyoshi Muscular Dystrophy 1	56	0.053

994		LWC001	Low Compliance Bladder	43	0.053

995		RSC001	Rosacea	54	0.053

996	c	MNN043	Meningioma, Familial	74	0.053

997	c	ACT004	Acute Diarrhea	39	0.052

998	c	HNT011	Huntington Disease-Like 3	38	0.052

999		BTT001	Bietti Crystalline Corneoretinal Dystrophy	52	0.052

1000	c	CHL132	Cholestasis, Progressive Familial Intrahepatic, 1	57	0.052

1001	P	PLY041	Polymyositis	57	0.052

1002	P	LRY044	Larynx Cancer	55	0.052

1003	c	MST023	Mesothelioma, Malignant	57	0.052

1004	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.052

1005		CHR103	Charge Syndrome	67	0.052

1006		SPR004	Supravalvular Aortic Stenosis	58	0.052

1007		GLM044	Glomerular Disease	37	0.052

1008	c	OPT053	Optic Atrophy 1	63	0.052

1009	P	BRN022	Bronchiectasis	59	0.052

1010	c	SYS043	Systemic Lupus Erythematosus 1	38	0.052

1011		AYM001	Ayme-Gripp Syndrome	57	0.052

1012	P	KRT007	Keratoconus	50	0.052

1013	P	TRC031	Trichorhinophalangeal Syndrome	40	0.052

1014		GLC042	Glucocorticoid Deficiency 1	53	0.052

1015		ADN011	Adenoid Cystic Carcinoma	70	0.052

1016		MYL031	Myeloproliferative Neoplasm	66	0.052

1017		HMT002	Hematologic Cancer	62	0.052

1018		ACT064	Acute Necrotizing Encephalitis	33	0.052

1019		BLD137	Blood Group--Ahonen	16	0.052

1020	P	MYS003	Myasthenia Gravis	68	0.052

1021	P	SML001	Small Cell Carcinoma	52	0.052

1022	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.052

1023	c	HYP794	Hyperoxaluria, Primary, Type I	63	0.052

1024		EXC002	Exocrine Pancreatic Insufficiency	42	0.052

1025		FML026	Familial Lipoprotein Lipase Deficiency	51	0.052

1026	c	WLM018	Wilms Tumor 5	61	0.052

1027		CHN055	Chanarin-Dorfman Syndrome	61	0.052

1028	c	HNT004	Huntington Disease-Like 2	50	0.052

1029		INF034	Infective Endocarditis	53	0.052

1030	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.052

1031		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.052

1032		ACT084	Acute Stress Disorder	47	0.052

1033		HMR039	Hemorrhage, Intracerebral	57	0.051

1034		MLT157	Multiple System Atrophy 1	70	0.051

1035		AST006	Astigmatism	47	0.051

1036	P	DRM010	Dermatomyositis	61	0.051

1037		PTH003	Pathologic Nystagmus	52	0.051

1038	P	TCD001	Tic Disorder	53	0.051

1039		YLL002	Yellow Fever	61	0.051

1040		FBR012	Fabry Disease	72	0.051

1041		OVR029	Ovarian Hyperstimulation Syndrome	64	0.051

1042		URT010	Ureteral Obstruction	45	0.051

1043	P	PRN023	Prion Disease	57	0.051

1044		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.051

1045		MTC027	Mitochondrial Trifunctional Protein Deficiency	58	0.051

1046		TNS005	Tonsillitis	57	0.051

1047	P	THY023	Thymoma	65	0.051

1048	c	THY107	Thymoma, Familial	52	0.051

1049		MCR018	Microcytic Anemia	47	0.051

1050		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.051

1051		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.051

1052	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.051

1053		SPT004	Septic Arthritis	58	0.051

1054		HYP348	Hyperglycinuria	41	0.051

1055		CYT008	Cytomegalovirus Infection	57	0.051

1056	c	MCL013	Mucolipidosis Iv	66	0.051

1057	P	MYC033	Myoclonus	46	0.051

1058		RFR003	Refractive Error	43	0.051

1059	P	DNT020	Dent Disease 1	62	0.051

1060		ARG004	Argyria	27	0.051

1061		NRN004	Neuroendocrine Tumor	55	0.051

1062	P	STR020	Strabismus	55	0.051

1063		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	45	0.051

1064		PLL001	Pallister-Hall Syndrome	64	0.050

1065	P	GLC113	Galactosemia I	64	0.050

1066		ALP097	Alopecia Universalis Congenita	59	0.050

1067		TRT001	Teratocarcinoma	45	0.050

1068		SPS019	Spastic Paraparesis	38	0.050