Search results for Vitamin C

4751 hits were found for Vitamin C

#	Family	MCID	Name	MIFTS	Score
1		RCK004	Rickets	68	166.036

2	c	HPT001	Hepatitis C	62	126.171

3	c	HPT073	Hepatitis C Virus	71	109.627

4		KRT002	Keratomalacia	55	103.419

5	P	HPT021	Hepatitis	69	78.294

6		HYP781	Hypoascorbemia	52	72.879

7		VTM002	Vitamin B12 Deficiency	48	63.739

8		VTM033	Vitamin K Deficiency Bleeding	48	60.854

9	P	HYP069	Hyperparathyroidism	62	50.955

10	c	CHR684	Chronic Kidney Disease	69	50.265

11	c	TYP009	Type 2 Diabetes Mellitus	92	49.466

12	P	VTM027	Vitamin D-Dependent Rickets, Type 2a	53	49.041

13	P	OST002	Osteoporosis	76	49.001

14		PRT011	Protein C Deficiency	47	48.969

15		LVR012	Liver Cirrhosis	63	48.438

16	P	LVR013	Liver Disease	69	48.194

17	c	HYP836	Hypercholesterolemia, Familial, 1	73	48.079

18		VTM028	Vitamin E, Familial Isolated Deficiency of	53	48.048

19	P	DBT009	Diabetes Mellitus	67	47.441

20	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	47.410

21	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	47.358

22	c	THR082	Thrombophilia Due to Activated Protein C Resistance	59	45.940

23	P	KDN018	Kidney Disease	72	45.369

24		LPD008	Lipid Metabolism Disorder	62	44.547

25		NNL005	Non-Alcoholic Fatty Liver Disease	63	44.481

26		ATX019	Ataxia with Vitamin E Deficiency	44	43.894

27		DFC004	Deficiency Anemia	74	43.254

28		FTT001	Fatty Liver Disease	62	42.402

29	c	HPT016	Hepatitis B	62	42.179

30	P	BRS047	Breast Cancer	98	42.062

31		ATH013	Atherosclerosis Susceptibility	63	41.229

32		BNR002	Bone Resorption Disease	47	40.534

33	P	CRN300	Coronary Heart Disease 1	73	40.322

34	c	NMN015	Niemann-Pick Disease, Type C1	68	40.306

35		48X005	48,xyyy	39	40.230

36	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	40.126

37	c	SCN007	Secondary Hyperparathyroidism	51	39.784

38		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	39.727

39	P	HPT023	Hepatocellular Carcinoma	96	39.250

40	P	ATR011	Atrial Fibrillation	66	39.087

41	c	PRC016	Pre-Eclampsia	65	38.791

42		THR068	Thrombophilia Due to Protein C Deficiency, Autosomal Recessive	38	38.255

43	P	CLR023	Colorectal Cancer	100	38.146

44		IRN002	Iron Metabolism Disease	57	38.016

45		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	35	37.919

46	P	BND020	Bone Disease	59	37.875

47		LPP008	Lipoprotein Quantitative Trait Locus	65	37.635

48		HMC014	Homocysteinemia	52	37.407

49		END086	End Stage Renal Disease	52	37.384

50		IMM167	Immune Deficiency Disease	78	37.333

51		CRH001	Crohn's Disease	80	37.297

52		ART140	Arteries, Anomalies of	53	37.283

53		PYR009	Pyridoxine Deficiency Anemia	35	36.789

54		INS024	Insulin-Like Growth Factor I	78	36.766

55		CYS001	Cystic Fibrosis	78	36.498

56	P	HRT032	Heart Disease	81	36.394

57	c	HPT003	Hepatitis a	63	36.329

58	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	65	36.326

59		AGN016	Aging	54	36.131

60		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	56	36.119

61	P	VSC007	Vascular Disease	63	35.860

62		RPD005	Rapidly Involuting Congenital Hemangioma	46	35.558

63	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	35.394

64	c	ATR087	Atrial Standstill 1	74	35.167

65	P	AST005	Asthma	76	35.143

66	P	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	45	34.942

67	P	MLT020	Multiple Sclerosis	79	34.802

68	P	NRP001	Neuropathy	60	34.789

69	c	THR092	Thrombophilia Due to Thrombin Defect	74	34.587

70		HLX001	Helix Syndrome	48	34.579

71	c	VRL010	Viral Hepatitis	53	34.283

72		CSY001	C Syndrome	61	34.221

73	P	DRR001	Diarrhea	55	33.574

74		HMN044	Human Immunodeficiency Virus Type 1	78	33.531

75	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	33.495

76	P	RHM011	Rheumatoid Arthritis	82	33.457

77	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	33.413

78	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	33.408

79	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	33.371

80	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	33.370

81	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	33.368

82	c	LKM061	Leukemia, Acute Myeloid	83	33.359

83		OST011	Osteomalacia	52	33.331

84	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	33.271

85	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	33.269

86	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	33.268

87	P	PRS040	Prostate Cancer	95	32.899

88		CHL123	Chlamydia	58	32.824

89	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	32.718

90	P	INF037	Inflammatory Bowel Disease	53	32.646

91		CYT002	Cytokine Deficiency	43	32.515

92		SCK003	Sickle Cell Anemia	74	32.257

93	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	32.190

94		ISC004	Ischemia	61	32.040

95	P	ALZ034	Alzheimer Disease	87	32.033

96		PRT251	Proteinuria, Chronic Benign	57	31.990

97	c	TYP008	Type 1 Diabetes Mellitus	70	31.834

98		MGL001	Megaloblastic Anemia	58	31.827

99	P	LKM002	Leukemia	67	31.769

100	P	NRB001	Neuroblastoma	66	31.591

101		VTM009	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1	31	31.537

102		MTH077	Methylmalonic Aciduria, Cbla Type	43	31.507

103	P	PSR002	Psoriasis	63	31.488

104		MTH078	Methylmalonic Aciduria, Cblb Type	42	31.419

105	P	ART022	Arthritis	71	31.183

106		HYP066	Hyperglycemia	61	31.151

107	P	PRD008	Periodontitis	64	30.872

108	P	THL005	Thalassemia	56	30.705

109		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	30.588

110		PST011	Pustulosis of Palm and Sole	52	30.507

111		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	30.472

112	P	PRP019	Peripheral Nervous System Disease	58	30.459

113		ATM095	Autoimmune Disease	61	30.253

114	P	LNG032	Lung Cancer	98	30.214

115	P	MYP004	Myopathy	67	30.094

116	c	HMG001	Hemoglobin C Disease	41	30.023

117	P	PLY011	Polycystic Ovary Syndrome	57	29.989

118		TXC005	Toxic Shock Syndrome	62	29.981

119		THR067	Thrombophilia Due to Protein C Deficiency, Autosomal Dominant	29	29.874

120	P	SKN015	Skin Carcinoma	71	29.850

121	P	PNC035	Pancreatic Cancer	86	29.780

122	P	BLD134	Bladder Cancer	79	29.757

123		STR067	Stroke, Ischemic	80	29.580

124	c	MCL042	Macular Degeneration, Age-Related, 1	85	29.389

125	P	OVR042	Ovarian Cancer	88	29.299

126	P	MYC007	Myocardial Infarction	70	29.247

127		CNG034	Congestive Heart Failure	69	29.158

128		PRT037	Pertussis	65	29.115

129		ULC004	Ulcerative Colitis	74	29.059

130	P	MYC084	Mycobacterium Tuberculosis 1	68	28.980

131		PLM129	Pulmonary Disease, Chronic Obstructive	74	28.862

132	P	MYL006	Myeloid Leukemia	61	28.718

133	P	GST053	Gastric Cancer	83	28.614

134		47X002	47,xyy	48	28.541

135	P	LYM118	Lymphoma	67	28.496

136	P	LPS004	Lupus Erythematosus	61	28.481

137		CLT003	Colitis	63	28.474

138	P	HYP086	Hypothyroidism	69	28.439

139	c	SYS001	Systemic Lupus Erythematosus	87	28.430

140	P	PNM007	Pneumonia	67	28.325

141	P	GST044	Gastritis	55	28.291

142	P	RTN008	Retinitis Pigmentosa	80	28.256

143	P	HRD086	Hereditary Hypophosphatemic Rickets	40	27.921

144		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	27.907

145	P	INF032	Infertility	57	27.892

146	P	MLN008	Melanoma	76	27.841

147		GST033	Gestational Diabetes	61	27.779

148	P	BCL017	B-Cell Lymphoma	59	27.745

149	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	27.727

150	c	MCR120	Microvascular Complications of Diabetes 7	47	27.671

151		OST159	Osteogenic Sarcoma	66	27.447

152		OST012	Osteoarthritis	77	27.384

153	c	MCR113	Microvascular Complications of Diabetes 3	52	27.338

154		VTM029	Vitamin D Hydroxylation-Deficient Rickets, Type 1b	27	27.299

155		THR024	Thrombosis	56	27.068

156		DRM006	Dermatitis	62	26.890

157	P	ENC018	Encephalopathy	62	26.888

158		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	50	26.825

159	P	SZR006	Seizure Disorder	70	26.817

160		ALL029	Allergic Disease	59	26.816

161		ALC007	Alcohol Dependence	66	26.791

162		CHL068	Cholestasis	61	26.771

163	c	MCR130	Microvascular Complications of Diabetes 6	41	26.761

164	c	MCR133	Microvascular Complications of Diabetes 4	41	26.631

165	P	THR014	Thrombocytopenia	66	26.498

166		VTM010	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2	23	26.406

167		LNG099	Lung Disease	62	26.363

168		NNL006	Non-Alcoholic Steatohepatitis	54	26.358

169	c	FML021	Familial Hypercholesterolemia	72	26.259

170	P	ADN016	Adenocarcinoma	63	26.235

171	c	HYP595	Hypertension, Essential	85	26.156

172	P	DRM053	Dermatitis, Atopic	65	26.049

173		NRL016	Neural Tube Defects	81	26.040

174	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	25.949

175	P	ALC033	Alcohol Use Disorder	61	25.890

176	P	ECL001	Eclampsia	52	25.856

177	P	CTR002	Cataract	60	25.796

178		HYP266	Hypoxia	57	25.697

179	c	SML038	Small Cell Cancer of the Lung	69	25.563

180		MSL001	Measles	61	25.544

181		SKN016	Skin Disease	63	25.492

182		RNL114	Renal Cell Carcinoma, Nonpapillary	80	25.487

183		ADN018	Adenoma	59	25.222

184		INT323	Intraocular Pressure Quantitative Trait Locus	64	25.216

185	P	HYP750	Hypertriglyceridemia, Familial	62	25.098

186	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	25.067

187		TTN003	Tetanus	65	25.010

188		GLL048	Glial Tumor	52	24.944

189	P	PNC044	Pancreatitis	61	24.903

190		DPR016	Depression	65	24.876

191		BCT022	Bacterial Infectious Disease	56	24.829

192		CRB039	Cerebrovascular Disease	66	24.817

193	P	LKM062	Leukemia, Acute Lymphoblastic	69	24.746

194		ESP021	Esophageal Cancer	83	24.687

195		CVD001	Covid-19	57	24.678

196	P	NTR004	Neutropenia	63	24.555

197		MYL069	Myeloma, Multiple	77	24.516

198		DSS032	Disease by Infectious Agent	55	24.456

199		PRP027	Peripheral Vascular Disease	71	24.440

200	P	ALP008	Alopecia	54	24.302

201	P	CND004	Candidiasis	58	24.275

202	P	ATS364	Autism	69	24.258

203		SVR001	Severe Acute Respiratory Syndrome	67	24.218

204		SQM006	Squamous Cell Carcinoma	60	24.200

205		MNT002	Mental Depression	57	23.974

206		GLM045	Glioma	63	23.958

207		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	23.899

208		THY029	Thyroid Carcinoma	51	23.898

209	P	EPL164	Epilepsy	68	23.748

210		GLB002	Glioblastoma	67	23.736

211	P	THY032	Thyroiditis	57	23.597

212	c	ATS007	Autism Spectrum Disorder	72	23.442

213		PRP030	Purpura	54	23.252

214	P	IMR002	Imerslund-Grasbeck Syndrome 1	42	23.222

215		ATS010	Autosomal Recessive Disease	42	23.222

216	c	PRM005	Primary Hyperparathyroidism	59	23.169

217	c	DLT002	Dilated Cardiomyopathy	78	23.160

218	P	INF038	Influenza	68	23.134

219		MYL009	Myelodysplastic Syndrome	67	23.057

220	c	ACT075	Acute Myocardial Infarction	56	23.013

221		STM007	Stomatitis	54	22.832

222	c	BTT014	Beta-Thalassemia	72	22.760

223		PRN011	Pernicious Anemia	53	22.757

224		SPN186	Spinal Cord Injury	61	22.739

225		PLM001	Pulmonary Tuberculosis	69	22.738

226	c	MCR115	Microvascular Complications of Diabetes 5	65	22.721

227		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	22.704

228	P	VSC011	Vasculitis	61	22.663

229	P	RTN024	Retinoblastoma	73	22.655

230	c	FNC027	Fanconi Anemia, Complementation Group a	81	22.601

231	P	SCK005	Sickle Cell Disease	56	22.505

232		MTH056	Methylmalonic Aciduria and Homocystinuria, Cblf Type	35	22.405

233		HLC007	Helicobacter Pylori Infection	67	22.382

234	P	CRD246	Cardiovascular System Disease	56	22.352

235	P	MSC005	Muscular Dystrophy	67	22.228

236	P	RHN004	Rhinitis	57	22.188

237		MLR004	Malaria	80	22.167

238	P	BRB001	Beriberi	44	22.157

239		SVR004	Severe Combined Immunodeficiency	72	22.126

240	P	SCH015	Schizophrenia	74	22.068

241		GLC003	Glucose Intolerance	54	22.037

242		CRV035	Cervical Cancer	73	22.029

243		CNS004	Constipation	56	22.019

244	c	ACT027	Acute Pancreatitis	60	22.016

245	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	65	21.952

246	P	HML002	Hemolytic Anemia	62	21.947

247		EPL131	Epilepsy, Pyridoxine-Dependent	45	21.941

248		ACQ007	Acquired Immunodeficiency Syndrome	59	21.812

249		PRT036	Peritonitis	65	21.793

250	P	GLM007	Glomerulonephritis	60	21.748

251		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	21.698

252	P	DMN002	Dementia	66	21.664

253		PYR016	Pyridoxine Deficiency	29	21.629

254		HMN014	Human Immunodeficiency Virus Infectious Disease	54	21.621

255	P	CLC063	Celiac Disease 1	66	21.521

256		IRR002	Irritable Bowel Syndrome	65	21.472

257		GST045	Gastroenteritis	58	21.375

258	P	HYP061	Hypertrophic Cardiomyopathy	69	21.372

259	P	ADL010	Adult Respiratory Distress Syndrome	71	21.360

260	P	CRD119	Cardiac Arrest	67	21.346

261		MLD018	Mild Cognitive Impairment	48	21.341

262	P	ATX030	Ataxia-Telangiectasia	80	21.339

263	P	ACN011	Acne	57	21.308

264		HYP636	Hypocalcemic Vitamin D-Dependent Rickets	38	21.162

265		FCT002	Factor Xi Deficiency	62	21.141

266		PLM033	Pulmonary Embolism	58	21.136

267		IRN001	Iron Deficiency Anemia	58	21.132

268	P	NGH001	Night Blindness	52	21.129

269	P	CHR345	Chronic Pain	50	21.012

270	P	EXN002	Exanthem	58	21.001

271	c	MGR028	Migraine with or Without Aura 1	64	20.920

272	P	MJR001	Major Depressive Disorder	68	20.915

273		HYP056	Hypoglycemia	65	20.898

274		HYP060	Hyperinsulinism	54	20.855

275	c	ACT071	Acute Kidney Failure	60	20.682

276		EPL166	Epilepsy, Early-Onset, Vitamin B6-Dependent	23	20.672

277		NPH009	Nephrolithiasis	54	20.664

278	P	LTR001	Lateral Sclerosis	58	20.497

279	P	RRH023	Rare Hereditary Hemochromatosis	54	20.483

280		HRW001	Hair Whorl	35	20.450

281	P	PLY019	Polyneuropathy	52	20.389

282		HYP017	Hypophosphatemia	49	20.367

283		HMS001	Hemosiderosis	48	20.349

284	P	SRC025	Sarcoidosis 1	71	20.292

285		NRR001	Neuroretinitis	42	20.283

286		RTN023	Retinitis	46	20.254

287	P	LNG064	Lung Cancer Susceptibility 3	70	19.987

288		WRF003	Warfarin Syndrome	29	19.975

289	P	RSP003	Respiratory Failure	74	19.927

290		DWN001	Down Syndrome	70	19.882

291	P	HYP024	Hypoparathyroidism	55	19.852

292	P	HMC002	Homocystinuria	53	19.831

293		URM002	Uremia	47	19.802

294		DPH001	Diphtheria	59	19.789

295	P	HRP006	Herpes Simplex	65	19.785

296	P	THR015	Thrombophilia	51	19.744

297		LYM133	Lymphoma, Hodgkin, Classic	74	19.698

298	P	EYD002	Eye Disease	57	19.635

299		LPT014	Leptin Deficiency or Dysfunction	78	19.635

300		GST019	Gastrointestinal Stromal Tumor	78	19.613

301		CMM005	Common Cold	56	19.611

302	P	PRK057	Parkinson Disease, Late-Onset	80	19.575

303		DSS008	Disease of Mental Health	74	19.573

304		MTH021	Methylmalonic Acidemia with Homocystinuria	44	19.561

305	P	HYP076	Hyperthyroidism	53	19.515

306	P	LYN001	Lynch Syndrome	76	19.504

307		ADN090	Adenosylcobalamin Deficiency	32	19.499

308	P	ART021	Arteriosclerosis	54	19.486

309	P	OPN001	Open-Angle Glaucoma	55	19.481

310		ALL003	Allergic Rhinitis	67	19.427

311		LSH001	Leishmaniasis	64	19.379

312		LYM143	Lymphoma, Non-Hodgkin, Familial	75	19.343

313	c	BRN108	Branchiootic Syndrome 1	62	19.289

314	P	KLZ004	Kala-Azar 1	41	19.256

315		ANG054	Angina Pectoris	66	19.241

316	P	CNR004	Cone-Rod Dystrophy 2	74	19.195

317	P	NPH012	Nephrotic Syndrome	60	19.154

318	P	RCT021	Rectum Cancer	54	19.090

319		CHL014	Cholera	62	19.067

320	P	URN019	Urinary Tract Infection	49	18.885

321	P	SLP006	Sleep Apnea	69	18.757

322	P	END044	Endometriosis	62	18.738

323		SKN019	Skin Melanoma	71	18.599

324		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	18.548

325		PRM236	Primary Biliary Cholangitis	60	18.534

326		DBT010	Diabetic Neuropathy	54	18.501

327	c	ACT073	Acute Leukemia	58	18.458

328	P	PRK039	Parkinsonism	55	18.438

329	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	18.341

330		BRN071	Brain Injury	50	18.303

331		INT007	Intermediate Coronary Syndrome	54	18.236

332	c	LKM063	Leukemia, Chronic Myeloid	71	18.212

333		PPL052	Papillomatosis, Confluent and Reticulated	34	18.153

334	P	MNN013	Meningitis	65	18.122

335	P	MLN007	Male Infertility	56	18.052

336		BRK010	Burkitt Lymphoma	66	18.031

337		RBF001	Riboflavin Deficiency	49	17.855

338		HYP025	Hyperphosphatemia	48	17.825

339		CLR108	Colorectal Adenoma	64	17.821

340		PRT013	Portal Hypertension	59	17.795

341		PRT002	Paratyphoid Fever	54	17.742

342	P	PLM036	Pulmonary Fibrosis	66	17.739

343		FCT013	Factor V Leiden Thrombophilia	20	17.718

344	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	17.671

345	P	GRF003	Graft-Versus-Host Disease	71	17.647

346		ANX010	Anxiety	70	17.629

347		ENT011	Enterocolitis	55	17.569

348	P	OVR082	Overgrowth Syndrome	49	17.527

349		VRL011	Viral Infectious Disease	61	17.522

350		OCL069	Ocular Motor Apraxia	57	17.510

351		END057	Endometrial Cancer	72	17.500

352		MTC206	Mitochondrial Complex Iv Deficiency, Nuclear Type 5	52	17.457

353	P	PLM037	Pulmonary Hypertension	72	17.452

354	P	GRV001	Graves' Disease	55	17.402

355		PST092	Posttransplant Acute Limbic Encephalitis	28	17.334

356		NTR005	Nutritional Deficiency Disease	61	17.313

357	P	VTM031	Vitamin B12 Plasma Level Quantitative Trait Locus 1	14	17.293

358	c	PCH010	Pachyonychia Congenita 3	43	17.228

359		RLP002	Relapsing-Remitting Multiple Sclerosis	56	17.211

360	P	MTH008	Methylmalonic Acidemia	52	17.211

361		CND006	Candida Glabrata	30	17.205

362	P	LKM071	Leukemia, Chronic Lymphocytic	75	17.192

363		CHL147	Chlamydia Pneumonia	47	17.162

364	P	ANR048	Aniridia 1	64	17.116

365		CRY004	Cryoglobulinemia	48	17.032

366	P	PHC003	Pheochromocytoma	69	17.030

367		DSS009	Disseminated Intravascular Coagulation	57	16.985

368		PLC008	Placenta Disease	49	16.972

369		MCS002	Mucositis	56	16.950

370		SRC014	Sarcoma	65	16.950

371	P	HYP265	Hypotonia	42	16.875

372	P	BRL012	Bare Lymphocyte Syndrome, Type Ii	65	16.834

373	P	SCL018	Scoliosis	57	16.761

374		PNC129	Pancreatic Adenocarcinoma	65	16.753

375	P	NMN002	Niemann-Pick Disease	60	16.744

376		HRD160	Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors	25	16.718

377	c	PRD040	Periodontitis, Chronic	52	16.718

378	P	TRM003	Tremor	48	16.701

379		SPL018	Splenomegaly	49	16.689

380	P	ATR005	Atrophic Gastritis	50	16.669

381	P	NSP012	Nasopharyngeal Carcinoma	61	16.547

382		KRT001	Keratoconjunctivitis Sicca	50	16.538

383		SPN035	Spindle Cell Sarcoma	54	16.537

384	P	LCH002	Lichen Planus	54	16.505

385		XRP001	Xerophthalmia	41	16.463

386	P	BRN019	Bernard-Soulier Syndrome	61	16.447

387		DFF005	Diffuse Large B-Cell Lymphoma	54	16.438

388		HYP080	Hypogonadism	50	16.436

389	c	DWL002	Dowling-Degos Disease 1	58	16.399

390	P	HMP007	Hemophilia	52	16.398

391	P	HYP098	Hypereosinophilic Syndrome	66	16.324

392	c	GLC092	Glaucoma, Primary Open Angle	62	16.292

393	c	SCL052	Scleroderma, Familial Progressive	61	16.264

394		KRT009	Keratosis	53	16.221

395		MDD011	Mood Disorder	62	16.186

396	P	AMY004	Amyloidosis	70	16.170

397		TRN015	Transient Cerebral Ischemia	63	16.158

398		BRN024	Bronchitis	67	16.114

399		XRD010	Xeroderma Pigmentosum, Variant Type	73	16.106

400		PNG002	Pain Agnosia	51	16.082

401	P	HDC001	Headache	57	16.053

402		HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	16.025

403		NPH091	Nephrolithiasis, Calcium Oxalate	61	15.951

404		NSS002	Neisseria Meningitidis Infection	47	15.950

405		TRM010	Traumatic Brain Injury	51	15.946

406	P	BPL003	Bipolar Disorder	56	15.938

407	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	53	15.912

408	P	FBR017	Fibrosarcoma	56	15.818

409		DYS073	Dysphagia	53	15.800

410		ORL011	Oral Cancer	60	15.791

411		BCK006	Back Pain	47	15.762

412	c	TBR025	Tuberous Sclerosis 1	84	15.756

413		PHN003	Phenylketonuria	76	15.729

414		SPN051	Spondylitis	51	15.726

415		BRN056	Bronchopulmonary Dysplasia	56	15.710

416		IGR001	Ige Responsiveness, Atopic	59	15.706

417	c	SPN225	Spondyloarthropathy 1	70	15.667

418	P	HMR003	Hemorrhagic Disease	59	15.665

419	P	MSC003	Muscular Atrophy	52	15.636

420		HMP009	Haemophilus Influenzae	41	15.624

421	P	TRN020	Turner Syndrome	67	15.523

422	P	MYP006	Myopia	56	15.518

423		PLM134	Pulmonary Fibrosis, Idiopathic	76	15.499

424		RNL011	Renal Osteodystrophy	49	15.444

425		CHL065	Cholangiocarcinoma	58	15.428

426	P	CNJ013	Conjunctivitis	66	15.394

427	P	URT039	Urticaria	58	15.393

428	P	CHR071	Charcot-Marie-Tooth Disease	64	15.354

429		BLR008	Bilirubin Metabolic Disorder	57	15.352

430		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	61	15.339

431	P	PRS038	Personality Disorder	65	15.330

432		ACT119	Acute Promyelocytic Leukemia	62	15.310

433		INF009	Inflammatory Spondylopathy	30	15.304

434	P	KDN017	Kidney Cancer	61	15.279

435	c	ATM011	Autoimmune Hepatitis	63	15.266

436	c	OVR114	Ovarian Cancer 1	59	15.254

437		ALL014	Allergic Encephalomyelitis	34	15.247

438		PRS045	Prostatic Hypertrophy	53	15.240

439	c	ACT068	Acute Cystitis	61	15.215

440		PNC001	Pancytopenia	53	15.167

441		VRC005	Varicose Veins	60	15.134

442		ABT001	Abetalipoproteinemia	68	15.111

443		FBR047	Fibromyalgia	58	15.086

444	c	MJR022	Major Affective Disorder 8	38	15.083

445	c	MJR024	Major Affective Disorder 9	41	15.083

446		PRP080	Peripheral Artery Disease	54	15.080

447		GST040	Gastric Adenocarcinoma	67	15.072

448	c	BSL007	Basal Cell Carcinoma	68	15.032

449		ANR040	Aneurysm	61	15.022

450		MST005	Mastitis	53	14.987

451		SQM013	Squamous Cell Carcinoma, Head and Neck	73	14.966

452		BRT054	Brittle Bone Disorder	74	14.938

453	P	SYP003	Syphilis	59	14.929

454	P	INS002	in Situ Carcinoma	53	14.904

455		INT079	Intrahepatic Cholangiocarcinoma	51	14.880

456		ORL015	Oral Squamous Cell Carcinoma	43	14.801

457		ALL006	Allergic Asthma	56	14.792

458		DNT012	Dental Caries	53	14.784

459		CRH005	Crohn's Colitis	53	14.716

460	P	ANT006	Antiphospholipid Syndrome	55	14.700

461		PRS021	Prostatic Adenoma	43	14.694

462		GNG013	Gingivitis	59	14.691

463	P	HYP058	Hypervitaminosis a	47	14.686

464	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	14.637

465		THY030	Thyroid Gland Disease	50	14.602

466	P	LCT001	Lactic Acidosis	51	14.584

467		GTR002	Goiter	53	14.568

468	P	GCH001	Gaucher's Disease	70	14.559

469	P	DYS154	Dystonia	64	14.514

470		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	14.500

471		PRS129	Prostatic Hyperplasia, Benign	49	14.484

472	P	GLM040	Glioma Susceptibility 1	71	14.470

473		VCC001	Vaccinia	47	14.465

474	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	14.463

475		HSH003	Hashimoto Thyroiditis	60	14.459

476		CRD223	Cardiac Arrhythmia	63	14.435

477		KRT019	Keratitis, Hereditary	66	14.416

478		HYP014	Hyperuricemia	51	14.357

479		LMY002	Leiomyoma	51	14.334

480	P	ENC004	Encephalitis	61	14.329

481		MSC157	Muscular Dystrophy, Duchenne Type	79	14.327

482		PLM031	Poliomyelitis	63	14.322

483		PRS047	Prostatitis	58	14.314

484		FDL002	Food Allergy	47	14.309

485		CNN005	Connective Tissue Disease	67	14.301

486		MTB004	Metabolic Acidosis	48	14.296

487		PPL022	Papilloma	53	14.291

488	P	RTN016	Retinal Degeneration	52	14.290

489		PPT005	Peptic Ulcer Disease	58	14.253

490	c	HMC039	Hemochromatosis, Type 1	73	14.224

491		URL001	Urolithiasis	46	14.069

492		CRD132	Cardiac Conduction Defect	60	14.045

493	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	14.021

494	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	14.005

495		BRC012	Brucellosis	66	14.000

496	P	SYS005	Systemic Scleroderma	74	13.966

497	P	ART023	Arthropathy	61	13.962

498	P	CHL066	Cholangitis	52	13.941

499	c	EXD008	Exudative Vitreoretinopathy 1	71	13.929

500		FND002	Fundus Dystrophy	55	13.928

501	P	MCR010	Microcephaly	60	13.925

502	P	CRY007	Cryoglobulinemia, Familial Mixed	49	13.924

503		PST028	Post-Traumatic Stress Disorder	59	13.914

504		THY111	Thyroid Carcinoma, Familial Medullary	67	13.914

505		BRN002	Bronchiolitis	57	13.895

506	P	MYC008	Myocarditis	59	13.883

507	P	SLP005	Sleep Disorder	61	13.828

508	P	SNS001	Sensorineural Hearing Loss	59	13.822

509	P	SPP010	Suppressor of Tumorigenicity 3	51	13.809

510	P	BNG032	Benign Mesothelioma	53	13.785

511	P	OPT006	Optic Nerve Disease	58	13.781

512	c	HMP029	Hemophilia a	68	13.779

513		PSY004	Psychotic Disorder	66	13.749

514		SCH014	Schistosomiasis	56	13.742

515		TLN003	Telangiectasis	51	13.739

516		HMZ003	Homozygous Familial Hypercholesterolemia	60	13.736

517		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	13.733

518		MTH055	Methylmalonic Aciduria and Homocystinuria, Cbld Type	38	13.696

519	c	GLL024	Gallbladder Disease 1	52	13.668

520		OTT002	Otitis Media	71	13.659

521		CLF027	Cleft Palate, Isolated	64	13.652

522		MTC116	Mitochondrial Myopathy, Infantile, Transient	42	13.643

523		CLN015	Colon Adenocarcinoma	65	13.640

524	c	BLD140	Blood Group, I System	46	13.579

525		CRB037	Cerebral Palsy	67	13.560

526		SQM002	Squamous Cell Papilloma	46	13.552

527		GST050	Gastrointestinal System Disease	55	13.536

528		IMP005	Impotence	52	13.513

529		FCT001	Factor Viii Deficiency	60	13.476

530	P	HYD006	Hydrocephalus	61	13.474

531	P	END033	Endocarditis	58	13.460

532	P	SBS003	Substance Abuse	54	13.442

533		HPT004	Hepatic Coma	43	13.406

534		ART016	Aortic Aneurysm	68	13.402

535		IDP085	Idiopathic Infantile Hypercalcemia	32	13.395

536		LGH007	Leigh Syndrome	70	13.386

537	P	PRN023	Prion Disease	60	13.382

538	P	ESP024	Esophagitis	60	13.370

539		OST003	Osteonecrosis	61	13.350

540		TRN018	Transitional Cell Carcinoma	56	13.350

541		ENT004	Enthesopathy	51	13.328

542		LYM019	Lymphosarcoma	46	13.311

543		ACT098	Acute Erythroid Leukemia	55	13.290

544	c	ACT134	Acute Liver Failure	59	13.280

545		PRN019	Perinatal Necrotizing Enterocolitis	60	13.274

546	P	MCR129	Microvascular Complications of Diabetes 1	68	13.272

547		CMP010	Complex Regional Pain Syndrome	60	13.244

548		HMC042	Homocystinuria-Megaloblastic Anemia, Cble Complementation Type	33	13.210

549	c	NRF024	Neurofibromatosis, Type I	72	13.206

550		NPH003	Nephrocalcinosis	49	13.192

551		KPS004	Kaposi Sarcoma	77	13.187

552		OST017	Osteomyelitis	63	13.168

553		ANX004	Anoxia	40	13.143

554	P	PRP029	Porphyria	60	13.118

555		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	13.105

556	P	UVT001	Uveitis	57	13.061

557		WST001	West Syndrome	59	13.054

558	P	LNG028	Long Qt Syndrome	64	13.026

559		INT066	Interstitial Lung Disease	60	12.997

560		VTM035	Vitamin D-Dependent Rickets, Type 3	16	12.966

561		HMG005	Hemoglobinopathy	56	12.939

562		CRY003	Cryptosporidiosis	56	12.923

563		OVR094	Ovarian Epithelial Cancer	39	12.888

564	P	DNG005	Dengue Virus	56	12.884

565		QFV001	Q Fever	62	12.882

566		GT001	Gout	64	12.881

567	c	PLM164	Pulmonary Hypertension, Primary, 1	76	12.878

568	P	TBR001	Tuberous Sclerosis	69	12.873

569		FRN006	Frontotemporal Dementia	68	12.855

570		NWC001	Newcastle Disease	47	12.850

571		HPT019	Hepatic Encephalopathy	59	12.817

572	P	PRM011	Primary Ciliary Dyskinesia	69	12.783

573		CRN030	Coronary Stenosis	50	12.767

574		CHC001	Chickenpox	57	12.761

575		CRB004	Cerebral Artery Occlusion	45	12.758

576		MCR013	Microphthalmia	60	12.747

577		ADR040	Adrenal Gland Pheochromocytoma	46	12.742

578	P	INT068	Intestinal Disease	53	12.739

579		PRT038	Protein-Energy Malnutrition	53	12.739

580	c	CHL119	Cholangitis, Primary Sclerosing	58	12.701

581	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	12.694

582		SBC016	Subacute Delirium	43	12.669

583	c	HNT004	Huntington Disease-Like 2	52	12.665

584	P	PLY014	Polycystic Kidney Disease	69	12.654

585	P	APL001	Aplastic Anemia	73	12.646

586		PRT014	Protein S Deficiency	41	12.610

587		LYM027	Lymphopenia	56	12.605

588		PSR001	Psoriatic Arthritis	62	12.599

589	P	SHR001	Short Bowel Syndrome	53	12.598

590	P	FML011	Familial Adenomatous Polyposis	71	12.584

591	P	LPR021	Leprosy 3	71	12.577

592		PLY150	Polykaryocytosis Inducer	29	12.528

593	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	12.525

594		RHB024	Rhabdomyosarcoma 2	67	12.442

595		DMY004	Demyelinating Disease	50	12.432

596		HNS001	Hansen's Disease	32	12.336

597		APH001	Aphthous Stomatitis	58	12.315

598	P	MVM001	Movement Disease	61	12.299

599	c	BRS111	Breast-Ovarian Cancer, Familial 2	53	12.284

600		ISL116	Isolated Complex Iii Deficiency	23	12.278

601		VSC003	Visceral Leishmaniasis	55	12.262

602		GST092	Gastroesophageal Reflux	61	12.247

603		BTT017	Beta-Thalassemia Major	51	12.241

604		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	12.229

605		PNC041	Pancreatic Ductal Adenocarcinoma	51	12.221

606	c	HNT011	Huntington Disease-Like 3	34	12.202

607	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	12.181

608	P	CRP001	Carpal Tunnel Syndrome	66	12.164

609		VSC002	Vascular Dementia	60	12.147

610	c	LKM005	Leukemia, T-Cell, Chronic	34	12.142

611	P	BRS044	Breast Adenocarcinoma	58	12.094

612		BRN028	Brain Cancer	74	12.079

613	P	RBL001	Rubella	58	12.017

614		BLR001	Biliary Atresia	55	12.010

615	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	11.999

616		CRY005	Cryptococcosis	60	11.983

617	c	DNT047	Dentinogenesis Imperfecta Type 2	35	11.968

618		TQP001	Taqi Polymorphism	29	11.933

619		ANR007	Anorexia Nervosa	60	11.932

620	c	INH020	Inherited Metabolic Disorder	48	11.931

621	P	USH001	Usher Syndrome	64	11.900

622		CHG001	Chagas Disease	66	11.898

623	P	FML018	Familial Mediterranean Fever	73	11.892

624		MTC008	Mitochondrial Complex Iii Deficiency	35	11.863

625	P	RTN018	Retinal Disease	53	11.846

626		MTH009	Mouth Disease	57	11.819

627		BLD131	Bladder Urothelial Carcinoma	60	11.815

628	P	ALP009	Alopecia Areata	59	11.807

629		HYP005	Hypokalemia	55	11.804

630		ALC006	Alcoholic Hepatitis	61	11.790

631	P	HNT016	Huntington Disease	73	11.784

632		MSC007	Muscle Hypertrophy	64	11.757

633		ADL002	Adult Syndrome	70	11.753

634	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	11.736

635		HYP057	Hypervitaminosis D	37	11.713

636		CMM004	Common Variable Immunodeficiency	72	11.703

637	P	HYP818	Hypobetalipoproteinemia, Familial, 1	60	11.697

638		MLG169	Malignant Astrocytoma	57	11.692

639		MCR017	Macrocytic Anemia	44	11.683

640	P	HYP726	Hypercalcemia, Infantile, 1	58	11.681

641	P	HMN038	Human Coronavirus Sensitivity	30	11.667

642		ISL099	Isolated Methylmalonic Acidemia	36	11.667

643		ANT039	Antisynthetase Syndrome	55	11.660

644	P	NRF002	Neurofibromatosis	57	11.648

645		PRP016	Paraplegia	52	11.634

646	c	JVN010	Juvenile Rheumatoid Arthritis	66	11.627

647		ORL013	Oral Lichen Planus	46	11.576

648	c	ATS239	Autosomal Recessive Hypophosphatemic Rickets	50	11.572

649		CHL067	Cholecystitis	60	11.564

650		THR004	Thrombocytosis	53	11.508

651		CRT013	Carotid Stenosis	51	11.504

652	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	11.484

653		PTH003	Pathologic Nystagmus	52	11.466

654	P	PRP003	Porphyria Cutanea Tarda	66	11.459

655	P	ICH004	Ichthyosis	56	11.458

656		CNT047	Contact Dermatitis	57	11.445

657		INS001	Insulinoma	59	11.400

658		LBR036	Leber Plus Disease	66	11.383

659	c	MCR112	Microvascular Complications of Diabetes 2	42	11.358

660	c	NMN014	Niemann-Pick Disease, Type C2	49	11.354

661		CLC006	Calcinosis	47	11.344

662		NRT004	Neuritis	53	11.328

663		MRF001	Marfan Syndrome	76	11.321

664		CLF001	Cleft Lip	53	11.313

665	P	MDL005	Medulloblastoma	75	11.306

666	P	ASP006	Aspergillosis	72	11.288

667	P	PYL005	Pyelonephritis	57	11.285

668		GST023	Gastric Ulcer	52	11.249

669		HGH043	High Grade Glioma	45	11.238

670	P	MTR014	Motor Neuron Disease	65	11.233

671		ETN001	Eating Disorder	59	11.216

672		ACR007	Acromegaly	70	11.212

673		PYR037	Pyruvate Carboxylase Deficiency	45	11.203

674	P	MYS005	Myositis	56	11.183

675	P	DDN001	Duodenal Ulcer	53	11.172

676		THY125	Thyroid Gland Medullary Carcinoma	48	11.171

677	P	CRV039	Cervicitis	52	11.159

678		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	64	11.157

679	P	NJM001	Nijmegen Breakage Syndrome	76	11.152

680	P	MST009	Mastocytosis	64	11.152

681	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	69	11.146

682		CTN007	Cutaneous Leishmaniasis	62	11.125

683		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	11.082

684		PRM329	Premature Aging	36	11.057

685		NNH002	Non-a-E Hepatitis	21	11.046

686		FDB001	Foodborne Botulism	55	11.024

687		ESP002	Esophageal Varix	51	11.013

688		SNS003	Sensory Peripheral Neuropathy	52	11.004

689	P	ANP001	Anaplastic Large Cell Lymphoma	61	11.000

690	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	65	10.972

691	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	10.955

692		BCT002	Bacterial Vaginosis	53	10.945

693		CLS016	Clostridium Difficile Colitis	49	10.901

694	P	PLY018	Polycythemia	56	10.891

695	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	10.876

696	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	10.857

697	P	OST001	Osteopetrosis	71	10.812

698		MTH071	Methane Production	25	10.785

699		MLT157	Multiple System Atrophy 1	69	10.777

700	c	ACT135	Acute Graft Versus Host Disease	51	10.773

701	P	SCL009	Sclerosing Cholangitis	48	10.769

702		DGN001	Degenerative Disc Disease	49	10.766

703		WRN001	Werner Syndrome	69	10.761

704		PLS011	Plasmacytoma	56	10.751

705		ORL005	Oral Candidiasis	56	10.748

706		HYP043	Hyperandrogenism	48	10.743

707		GLC009	Glucosephosphate Dehydrogenase Deficiency	53	10.737

708		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	10.732

709	P	HYP035	Hypophosphatasia	62	10.728

710	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	10.713

711		APN008	Apnea, Obstructive Sleep	67	10.698

712		KWS002	Kawasaki Disease	65	10.691

713	P	MTC069	Mitochondrial Disorders	57	10.690

714	P	RST001	Restless Legs Syndrome	52	10.685

715		STT001	Status Epilepticus	59	10.679

716	P	PSD015	Pseudohypoparathyroidism	55	10.659

717	c	INF071	Inflammatory Bowel Disease 1	65	10.655

718		LKP003	Leukoplakia	39	10.642

719		BRR014	Barrett Esophagus	66	10.626

720		CHR074	Choriocarcinoma	46	10.605

721	c	GRV008	Graves Disease 1	54	10.601

722		HRP004	Herpes Zoster	61	10.597

723	P	MTR004	Maturity-Onset Diabetes of the Young	68	10.578

724		CHY002	Chylomicron Retention Disease	64	10.558

725		SYN007	Synovitis	55	10.556

726	c	SVR005	Severe Pre-Eclampsia	50	10.554

727		CMB007	Combined Immunodeficiency	57	10.551

728	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	10.534

729	P	BRG001	Brugada Syndrome	69	10.525

730		CHR066	Chronic Fatigue Syndrome	60	10.519

731		PRS063	Paresthesia	39	10.502

732		HDN002	Head Injury	44	10.493

733		NRM005	Neuromuscular Disease	63	10.490

734		PLC002	Plica Syndrome	35	10.470

735		CHL004	Cholelithiasis	49	10.470

736	c	ALP101	Alpha-Thalassemia	62	10.467

737		DYS015	Dysentery	50	10.443

738	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	10.439

739	P	GLL022	Guillain-Barre Syndrome	60	10.438

740		MYL005	Myelofibrosis	71	10.416

741		PLM010	Pulmonary Edema	55	10.408

742		IGG001	Iga Glomerulonephritis	50	10.402

743		CHR178	Chromosomal Triplication	34	10.399

744	P	CYS018	Cystitis	59	10.362

745		CRV002	Cervix Uteri Carcinoma in Situ	47	10.359

746		CRV045	Cervical Intraepithelial Neoplasia	39	10.359

747		SCR011	Scrapie	39	10.323

748		MMM001	Mammary Paget's Disease	53	10.302

749	c	PLM127	Pulmonary Hypertension, Primary, 3	34	10.280

750	c	PSR023	Psoriasis 1	52	10.256

751		BSL036	Basal Cell Nevus Syndrome	73	10.243

752	P	BRN022	Bronchiectasis	60	10.221

753		CMR002	Coumarin Resistance	59	10.215

754	P	THR005	Thrombotic Thrombocytopenic Purpura	64	10.212

755		CLR109	Colorectal Adenocarcinoma	50	10.194

756	c	HPT007	Hepatitis E	51	10.164

757	c	HYP788	Hypophosphatemic Rickets, Autosomal Recessive, 1	28	10.161

758		SPS057	Spasticity	42	10.160

759		MYF001	Myofibroma	42	10.156

760	c	PNC108	Pancreatitis, Hereditary	69	10.150

761		BNN003	Bone Inflammation Disease	48	10.117

762		MNN043	Meningioma, Familial	79	10.114

763		CMP002	Campylobacteriosis	50	10.107

764		BTN003	Biotinidase Deficiency	62	10.080

765	c	HPT015	Hepatitis D	49	10.054

766	c	HMP004	Hemophilia B	68	10.026

767		HMN047	Human Cytomegalovirus Infection	57	10.019

768	P	CHR012	Chronic Granulomatous Disease	69	10.019

769	P	ERL057	Early Infantile Epileptic Encephalopathy	60	10.017

770	P	MYS003	Myasthenia Gravis	68	10.015

771	P	MLT074	Multiple Endocrine Neoplasia	59	10.012

772		AMN001	Amenorrhea	54	10.008

773		BRS051	Breast Disease	58	9.990

774		ART002	Arts Syndrome	66	9.989

775		INT002	Intermittent Claudication	61	9.989

776		PRM020	Premenstrual Tension	39	9.972

777	P	KRT007	Keratoconus	50	9.972

778	c	USH036	Usher Syndrome, Type I	61	9.963

779		PPL049	Papillon-Lefevre Syndrome	66	9.962

780	P	FLL037	Follicular Lymphoma	74	9.955

781	P	TXP001	Toxoplasmosis	60	9.953

782		LMY014	Leiomyoma, Uterine	56	9.946

783		AVN001	Avian Influenza	61	9.936

784	P	STR022	Stargardt Disease	61	9.930

785		FML035	Familial Hyperlipidemia	55	9.883

786		KRN002	Kearns-Sayre Syndrome	63	9.878

787		OBS002	Obsessive-Compulsive Disorder	68	9.845

788		DSR002	Disorders of Intracellular Cobalamin Metabolism	29	9.838

789		BRN004	Brain Edema	54	9.836

790		LMB062	Limb Ischemia	55	9.834

791		ADR007	Adrenoleukodystrophy	73	9.799

792	P	NRV007	Nervous System Disease	67	9.797

793		ATN005	Autonomic Dysfunction	46	9.794

794	P	PSD087	Pseudoxanthoma Elasticum	67	9.791

795	P	PRP034	Purpura Fulminans	41	9.790

796	P	CNG001	Congenital Myasthenic Syndrome	68	9.781

797	P	HML001	Hemolytic-Uremic Syndrome	52	9.780

798		END040	Endogenous Depression	55	9.757

799		APP008	Appendicitis	62	9.750

800		PRM155	Primary Cutaneous Anaplastic Large Cell Lymphoma	34	9.746

801		RNL065	Renal Cell Carcinoma, Papillary, 1	79	9.742

802	P	VTR007	Vitreoretinopathy	46	9.721

803		CRT084	Creatinine Clearance Quantitative Trait Locus	25	9.720

804		RTN020	Retinal Vascular Disease	46	9.710

805		STT009	Sutton Disease 2	29	9.710

806	c	PRM038	Primary Agammaglobulinemia	47	9.700

807	P	NNN008	Noonan Syndrome 1	77	9.699

808	c	FML346	Familial Adenomatous Polyposis 1	65	9.689

809	P	SJG008	Sjogren Syndrome	61	9.676

810	c	GLY008	Glycogen Storage Disease Ii	72	9.664

811		MCL006	Macular Retinal Edema	57	9.661

812		ATN004	Autonomic Neuropathy	42	9.653

813	P	PLL002	Pellagra	46	9.645

814		GRW007	Growth Hormone Deficiency	46	9.643

815	P	MYC033	Myoclonus	47	9.642

816		CHP002	Chops Syndrome	47	9.637

817		TTH006	Tooth Disease	51	9.628

818		GSG001	Gas Gangrene	52	9.623

819	P	VNW001	Von Willebrand's Disease	65	9.587

820	P	HYP838	Hyperlipidemia, Familial Combined, 3	61	9.573

821	c	WLM013	Wilms Tumor 1	66	9.564

822	P	FCL005	Focal Segmental Glomerulosclerosis	57	9.555

823		TRD006	Tardive Dyskinesia	53	9.545

824	P	THY023	Thymoma	64	9.542

825		INT075	Intracranial Hypertension	53	9.540

826		PRT018	Portal Vein Thrombosis	50	9.539

827	P	JBR020	Joubert Syndrome 1	74	9.537

828	P	BRD002	Bardet-Biedl Syndrome	66	9.525

829		GLC086	Glucocorticoid-Induced Osteoporosis	43	9.505

830		IDP070	Idiopathic Scoliosis	42	9.497

831	P	SCL057	Scoliosis, Isolated 1	40	9.489

832	P	MTC133	Mitochondrial Myopathy	50	9.482

833	P	ANG015	Angioedema	56	9.471

834		SYN036	Syncope	45	9.459

835	P	GLC113	Galactosemia I	66	9.444

836	P	RHB003	Rhabdomyosarcoma	66	9.438

837	c	BCT007	Bacterial Meningitis	55	9.428

838	P	AGM001	Agammaglobulinemia	68	9.423

839	P	MMP001	Mumps	57	9.419

840		EMB004	Embryonal Carcinoma	56	9.418

841		PRT029	Parathyroid Adenoma	51	9.405

842	c	HYP724	Hyperlipoproteinemia, Type Iii	67	9.392

843		CHL152	Childhood Acute Lymphocytic Leukemia	50	9.391

844		PRM013	Premature Menopause	58	9.387

845		TRC008	Trachoma	53	9.385

846		RNL077	Renal Fibrosis	46	9.361

847	P	RTT002	Rett Syndrome	79	9.343

848		VGN023	Vaginitis	56	9.343

849		HRD143	Hereditary Hypercarotenemia and Vitamin a Deficiency	6	9.340

850	P	PRM002	Primary Hyperoxaluria	65	9.335

851		ARG004	Argyria	26	9.310

852		SXL003	Sexual Disorder	49	9.310

853	P	ZLL001	Zellweger Syndrome	65	9.298

854		PLG002	Plague	58	9.288

855		PLY001	Polycythemia Vera	69	9.276

856		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	9.264

857		LNG031	Lung Benign Neoplasm	51	9.263

858	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	70	9.261

859		INF034	Infective Endocarditis	54	9.247

860		WRN003	Wernicke Encephalopathy	46	9.243

861	P	CRN037	Craniosynostosis	68	9.226

862		DBT084	Diabetes Mellitus, Ketosis-Prone	60	9.219

863		SPP011	Suppression of Tumorigenicity 12	61	9.214

864	P	LCT002	Lactose Intolerance	52	9.190

865		RFR003	Refractive Error	41	9.190

866		MDD018	Middle East Respiratory Syndrome	44	9.189

867	P	RTN022	Retinal Vein Occlusion	54	9.179

868	P	MLG056	Malignant Hyperthermia	66	9.171

869	c	ART101	Aortic Valve Disease 2	66	9.169

870		HRT012	Heart Valve Disease	53	9.145

871		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	50	9.141

872		PHR003	Pharyngitis	58	9.133

873		ACT084	Acute Stress Disorder	54	9.125

874		FBR012	Fabry Disease	70	9.113

875	c	PNS012	Paine Syndrome	60	9.111

876	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	60	9.097

877		BRS099	Breast Ductal Carcinoma	61	9.077

878		MNN020	Meningococcal Infection	45	9.077

879	c	THY107	Thymoma, Familial	42	9.049

880		HPT022	Hepatoblastoma	54	9.018

881		PRT058	Pure Autonomic Failure	58	9.016

882		DWR001	Dwarfism	44	9.013

883	P	AGG001	Aggressive Periodontitis	55	9.005

884		RTN017	Retinal Detachment	60	9.001

885		AZS001	Azoospermia	45	8.985

886	c	MST023	Mesothelioma, Malignant	56	8.969

887	c	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	63	8.953

888	P	ESS003	Essential Thrombocythemia	69	8.953

889		EXC002	Exocrine Pancreatic Insufficiency	42	8.950

890		ALP103	Alpha-1-Antitrypsin Deficiency	68	8.944

891	P	ALP004	Alport Syndrome	69	8.937

892		AVD001	Avoidant Personality Disorder	49	8.936

893	c	TBR026	Tuberous Sclerosis 2	71	8.935

894		BDD001	Budd-Chiari Syndrome	62	8.893

895	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	8.893

896		DNG003	Dengue Disease	65	8.881

897		PSD059	Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency	29	8.878

898		PST021	Postpartum Depression	50	8.875

899		RYN005	Raynaud Phenomenon	45	8.869

900		MMB001	Membranoproliferative Glomerulonephritis	56	8.847

901	P	LYM033	Lymphoproliferative Syndrome	59	8.844

902		WLS001	Wilson Disease	70	8.834

903		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	8.831

904		MNN009	Meningoencephalitis	48	8.831

905		CLR030	Clear Cell Renal Cell Carcinoma	54	8.811

906		ILS001	Ileus	50	8.804

907	c	FML191	Familial Long Qt Syndrome	55	8.795

908		LYS002	Lysosomal Storage Disease	51	8.768

909		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	8.751

910	P	LRY044	Larynx Cancer	54	8.734

911	c	OPT053	Optic Atrophy 1	62	8.701

912	P	STR020	Strabismus	56	8.693

913	P	RNL007	Renal Tubular Acidosis	50	8.666

914	c	PSR017	Psoriasis 2	53	8.647

915	P	NPH005	Nephronophthisis	56	8.563

916		WST005	West Nile Virus	57	8.553

917		HTC003	Hutchinson-Gilford Progeria Syndrome	65	8.551

918		THR123	Thrombotic Microangiopathy	40	8.549

919	P	MNC007	Monocytic Leukemia	47	8.540

920	P	OBS001	Obstructive Jaundice	48	8.537

921		NRN004	Neuroendocrine Tumor	59	8.530

922		GLM044	Glomerular Disease	35	8.528

923		RFR010	Refractory Anemia	49	8.525

924		CLL003	Cellulitis	53	8.512

925	P	DVL113	Developmental and Epileptic Encephalopathy	43	8.511

926	P	GLL018	Gallbladder Cancer	53	8.506

927		THR100	Thrombocytopenic Purpura, Autoimmune	61	8.494

928	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	67	8.481

929		NRT001	Neurotic Disorder	56	8.473

930	P	PMP001	Pemphigus	55	8.463

931	c	USH035	Usher Syndrome Type 2	52	8.447

932		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	8.420

933	c	CHR708	Chronic Urticaria	42	8.381

934		ALL010	Allergic Contact Dermatitis	56	8.375

935		NRN005	Neuronal Ceroid-Lipofuscinoses	61	8.370

936		SFT003	Soft Tissue Sarcoma	57	8.362

937		PLY100	Polyploidy	36	8.359

938		MYL031	Myeloproliferative Neoplasm	66	8.340

939		GLS007	Glossitis	47	8.338

940	c	MCP001	Mucopolysaccharidosis Iii	69	8.336

941		PRT082	Preterm Premature Rupture of the Membranes	57	8.323

942	P	MMB011	Membranous Nephropathy	50	8.316

943	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	8.315

944		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	8.313

945	P	MTR003