Search results for Coagulation factor VII human

972 hits were found for Coagulation factor VII human

#	Family	MCID	Name	MIFTS	Score
1		DSS009	Disseminated Intravascular Coagulation	58	0.654

2	P	HMP007	Hemophilia	58	0.593

3		IMM167	Immune Deficiency Disease	79	0.533

4	P	CLR023	Colorectal Cancer	100	0.481

5	P	BRS047	Breast Cancer	99	0.476

6		HMN044	Human Immunodeficiency Virus Type 1	73	0.457

7	c	HMP029	Hemophilia a	69	0.448

8		FCT007	Factor Vii Deficiency	65	0.448

9		FCT001	Factor Viii Deficiency	54	0.446

10	P	HPT023	Hepatocellular Carcinoma	99	0.426

11	P	LKM002	Leukemia	69	0.425

12	P	ADN016	Adenocarcinoma	65	0.421

13	P	LNG032	Lung Cancer	99	0.415

14	P	LVR013	Liver Disease	71	0.403

15	P	CRN300	Coronary Heart Disease 1	59	0.395

16	P	OVR042	Ovarian Cancer	89	0.394

17	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.391

18	P	THR014	Thrombocytopenia	67	0.389

19		LVR012	Liver Cirrhosis	67	0.389

20	P	VSC007	Vascular Disease	65	0.387

21		ATH013	Atherosclerosis Susceptibility	68	0.381

22		THR024	Thrombosis	58	0.374

23		GLB002	Glioblastoma	74	0.369

24		ATM095	Autoimmune Disease	62	0.366

25		GLB015	Glioblastoma Multiforme	60	0.365

26		SQM006	Squamous Cell Carcinoma	60	0.363

27	P	KDN018	Kidney Disease	73	0.361

28		CYT002	Cytokine Deficiency	46	0.361

29	P	GLM045	Glioma	64	0.359

30	c	PRC016	Pre-Eclampsia	63	0.354

31	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	82	0.350

32		CRV035	Cervical Cancer	77	0.349

33		GLL048	Glial Tumor	48	0.345

34		HYP266	Hypoxia	58	0.342

35	P	PNC035	Pancreatic Cancer	86	0.341

36	P	NRB010	Neuroblastoma 1	66	0.340

37	P	LYM031	Lymphocytic Leukemia	56	0.337

38	P	PRS040	Prostate Cancer	97	0.335

39	P	BLD134	Bladder Cancer	79	0.331

40		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.331

41		HLX001	Helix Syndrome	46	0.331

42	P	HRT032	Heart Disease	78	0.326

43		SVR004	Severe Combined Immunodeficiency	74	0.325

44	P	NTR004	Neutropenia	64	0.322

45		ADN018	Adenoma	60	0.321

46		MLN008	Melanoma	68	0.321

47		TXC005	Toxic Shock Syndrome	63	0.315

48	c	HMP004	Hemophilia B	66	0.313

49	P	DRR001	Diarrhea	55	0.307

50		CRB039	Cerebrovascular Disease	71	0.306

51	P	CRN018	Coronary Artery Anomaly	67	0.303

52		48X005	48,xyyy	37	0.299

53	c	SYS001	Systemic Lupus Erythematosus	88	0.296

54	P	MYL006	Myeloid Leukemia	61	0.295

55	P	INF032	Infertility	60	0.295

56	P	BLD051	Blood Coagulation Disease	48	0.294

57		RNL114	Renal Cell Carcinoma, Nonpapillary	79	0.290

58	P	VNW001	Von Willebrand's Disease	64	0.290

59		ISC004	Ischemia	62	0.290

60		ACQ007	Acquired Immunodeficiency Syndrome	61	0.290

61	c	SML038	Small Cell Cancer of the Lung	67	0.289

62	P	MCR115	Microvascular Complications of Diabetes 5	67	0.287

63	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.287

64	c	LKM061	Leukemia, Acute Myeloid	84	0.286

65	P	LYM118	Lymphoma	70	0.285

66		LPD008	Lipid Metabolism Disorder	64	0.283

67		LNG099	Lung Disease	62	0.281

68	P	INF037	Inflammatory Bowel Disease	57	0.280

69	P	HRP006	Herpes Simplex	66	0.279

70		ART140	Arteries, Anomalies of	60	0.278

71		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	67	0.276

72	P	GLM007	Glomerulonephritis	58	0.275

73		PRT037	Pertussis	66	0.275

74		STR067	Stroke, Ischemic	82	0.274

75	P	LPS004	Lupus Erythematosus	62	0.273

76	c	HYP836	Hypercholesterolemia, Familial, 1	74	0.273

77		PPL022	Papilloma	56	0.273

78	P	MYC007	Myocardial Infarction	74	0.271

79	P	DBT009	Diabetes Mellitus	66	0.268

80	c	BDY007	Body Mass Index Quantitative Trait Locus 1	43	0.268

81	P	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.268

82		MYL069	Myeloma, Multiple	85	0.265

83	c	ACT210	Acute Respiratory Distress Syndrome	59	0.264

84		ALL026	Allergic Hypersensitivity Disease	65	0.264

85		THY029	Thyroid Carcinoma	62	0.261

86		PRP030	Purpura	56	0.260

87		SKN016	Skin Disease	64	0.260

88		PLM033	Pulmonary Embolism	60	0.260

89		SQM002	Squamous Cell Papilloma	49	0.259

90		CNG034	Congestive Heart Failure	69	0.257

91		DFC004	Deficiency Anemia	77	0.255

92	c	CHR684	Chronic Kidney Disease	68	0.254

93		END057	Endometrial Cancer	74	0.254

94	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.253

95		HYP066	Hyperglycemia	63	0.253

96	P	THR015	Thrombophilia	51	0.253

97	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.253

98	P	PRD008	Periodontitis	66	0.253

99	c	MCL042	Macular Degeneration, Age-Related, 1	88	0.250

100	P	LNG064	Lung Cancer Susceptibility 3	79	0.246

101		END030	End Stage Renal Failure	60	0.246

102		ANR040	Aneurysm	60	0.246

103	P	ALZ034	Alzheimer Disease	90	0.246

104	c	HYP595	Hypertension, Essential	87	0.245

105		CRH001	Crohn's Disease	75	0.243

106		MLR004	Malaria	82	0.243

107		TRM010	Traumatic Brain Injury	54	0.243

108	P	RHM011	Rheumatoid Arthritis	82	0.241

109		HYP056	Hypoglycemia	68	0.241

110		PRS045	Prostatic Hypertrophy	55	0.239

111	P	ECL001	Eclampsia	53	0.239

112	P	END044	Endometriosis	63	0.239

113		BRN071	Brain Injury	51	0.238

114		OST012	Osteoarthritis	80	0.237

115		47X002	47,xyy	49	0.237

116	c	ACT075	Acute Myocardial Infarction	59	0.237

117		ESP021	Esophageal Cancer	90	0.237

118	P	RTN024	Retinoblastoma	74	0.236

119	c	FML008	Familial Retinoblastoma	46	0.236

120		BNR002	Bone Resorption Disease	51	0.235

121	P	CTR002	Cataract	62	0.235

122		ULC004	Ulcerative Colitis	75	0.235

123	P	BCL017	B-Cell Lymphoma	61	0.235

124	P	EPD016	Epidermolysis Bullosa	54	0.234

125	P	ART021	Arteriosclerosis	56	0.232

126	P	ATR011	Atrial Fibrillation	67	0.232

127		FTT001	Fatty Liver Disease	63	0.231

128		PRS021	Prostatic Adenoma	52	0.231

129	c	BDY021	Body Mass Index Quantitative Trait Locus 20	50	0.230

130	c	BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.230

131		CRV045	Cervical Intraepithelial Neoplasia	41	0.230

132	c	CRV002	Cervix Uteri Carcinoma in Situ	47	0.230

133	c	BDY006	Body Mass Index Quantitative Trait Locus 8	45	0.230

134	c	BDY010	Body Mass Index Quantitative Trait Locus 4	48	0.230

135	c	BDY015	Body Mass Index Quantitative Trait Locus 12	48	0.230

136	c	BDY011	Body Mass Index Quantitative Trait Locus 10	47	0.230

137	c	BDY012	Body Mass Index Quantitative Trait Locus 7	45	0.230

138	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.230

139	c	BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.230

140	c	BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.230

141	P	GRF003	Graft-Versus-Host Disease	71	0.230

142		OCL069	Ocular Motor Apraxia	53	0.229

143	c	ACT071	Acute Kidney Failure	60	0.228

144		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.228

145		CHL014	Cholera	58	0.228

146		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.228

147		AGN016	Aging	58	0.228

148		SPP010	Suppressor of Tumorigenicity 3	54	0.227

149	P	PSR002	Psoriasis	63	0.227

150	c	ACT073	Acute Leukemia	59	0.226

151	c	HPT001	Hepatitis C	62	0.226

152		PRS129	Prostatic Hyperplasia, Benign	49	0.226

153		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.224

154	P	HYP086	Hypothyroidism	70	0.224

155	P	VSC011	Vasculitis	64	0.223

156		ART016	Aortic Aneurysm	71	0.222

157		PST011	Pustulosis of Palm and Sole	51	0.222

158		PRP027	Peripheral Vascular Disease	72	0.221

159	P	PNM007	Pneumonia	71	0.220

160		DRM006	Dermatitis	63	0.219

161	P	ENC018	Encephalopathy	64	0.217

162	P	CRD119	Cardiac Arrest	71	0.217

163	c	HPT016	Hepatitis B	63	0.216

164		ALC007	Alcohol Dependence	68	0.216

165	P	AST007	Astrocytoma	52	0.215

166		HMT018	Hematopoietic Stem Cell Transplantation	54	0.215

167		PRT036	Peritonitis	66	0.214

168	P	EXN002	Exanthem	58	0.214

169		SRC014	Sarcoma	67	0.214

170	P	INF038	Influenza	69	0.213

171		DPR016	Depression	64	0.212

172	P	RSP003	Respiratory Failure	75	0.211

173		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.210

174	P	NRP001	Neuropathy	57	0.210

175		KPS004	Kaposi Sarcoma	75	0.210

176	P	RHN004	Rhinitis	59	0.209

177	P	ENC004	Encephalitis	64	0.208

178		BCT022	Bacterial Infectious Disease	57	0.208

179		LSH001	Leishmaniasis	64	0.207

180	P	KLZ004	Kala-Azar 1	43	0.207

181	P	SYP003	Syphilis	59	0.206

182		TTN003	Tetanus	62	0.206

183	P	HYP750	Hypertriglyceridemia, Familial	62	0.204

184		SPN035	Spindle Cell Sarcoma	57	0.204

185		PLM001	Pulmonary Tuberculosis	72	0.204

186		GST045	Gastroenteritis	60	0.202

187		HDN002	Head Injury	47	0.202

188		ANX010	Anxiety	75	0.201

189		CLT003	Colitis	63	0.201

190		SCH014	Schistosomiasis	57	0.201

191		SCH060	Schistosoma Mansoni Infection, Susceptibility/	40	0.199

192	c	ACT027	Acute Pancreatitis	60	0.199

193	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.199

194		ANG054	Angina Pectoris	66	0.199

195	P	PLM037	Pulmonary Hypertension	69	0.199

196		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.199

197	P	PNC044	Pancreatitis	61	0.198

198	P	OST002	Osteoporosis	79	0.197

199	P	END033	Endocarditis	58	0.197

200		IDP011	Idiopathic Interstitial Pneumonia	65	0.196

201	P	PLM036	Pulmonary Fibrosis	66	0.196

202		VCC001	Vaccinia	50	0.195

203		PPT005	Peptic Ulcer Disease	60	0.195

204		RRS014	Rare Surgical Neurologic Disease	33	0.194

205		MYL009	Myelodysplastic Syndrome	72	0.194

206		CYS001	Cystic Fibrosis	84	0.194

207	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.194

208	P	NPH012	Nephrotic Syndrome	65	0.193

209		ORL015	Oral Squamous Cell Carcinoma	44	0.193

210		AST005	Asthma	80	0.193

211		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.190

212		DWN001	Down Syndrome	70	0.189

213	P	DRM053	Dermatitis, Atopic	68	0.189

214		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.189

215	P	AMY004	Amyloidosis	71	0.188

216		INT007	Intermediate Coronary Syndrome	58	0.187

217	P	BLD124	Bleeding Disorder, Platelet-Type, 11	66	0.187

218	P	ART022	Arthritis	71	0.187

219	P	FBR017	Fibrosarcoma	57	0.186

220	c	VRL010	Viral Hepatitis	56	0.186

221	c	ACT134	Acute Liver Failure	53	0.186

222	P	HYP098	Hypereosinophilic Syndrome	67	0.185

223		RTN017	Retinal Detachment	62	0.185

224		CYT008	Cytomegalovirus Infection	58	0.184

225	c	ACT068	Acute Cystitis	63	0.184

226	P	ART023	Arthropathy	61	0.184

227		IRN002	Iron Metabolism Disease	58	0.183

228		HMN014	Human Immunodeficiency Virus Infectious Disease	56	0.182

229	P	GST044	Gastritis	58	0.182

230	P	HPT021	Hepatitis	69	0.181

231	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	62	0.181

232	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	51	0.181

233	c	CNG216	Congenital Hydrocephalus	55	0.180

234	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	43	0.180

235	P	NSP012	Nasopharyngeal Carcinoma	67	0.180

236	P	ALC033	Alcohol Use Disorder	58	0.180

237	P	HYD006	Hydrocephalus	68	0.180

238	P	MLT020	Multiple Sclerosis	73	0.180

239	c	SCL052	Scleroderma, Familial Progressive	62	0.179

240	P	INS002	in Situ Carcinoma	55	0.179

241		BCK006	Back Pain	44	0.179

242		MSL001	Measles	61	0.178

243		HRW001	Hair Whorl	36	0.177

244	P	CHR345	Chronic Pain	52	0.177

245		MNT002	Mental Depression	60	0.176

246	c	ACQ014	Acquired Hemophilia	47	0.176

247	P	SCK005	Sickle Cell Disease	53	0.176

248		LYM133	Lymphoma, Hodgkin, Classic	70	0.175

249		DNT012	Dental Caries	52	0.174

250	P	RCT021	Rectum Cancer	54	0.174

251		VRC005	Varicose Veins	61	0.174

252	c	ATR087	Atrial Standstill 1	76	0.173

253	P	HML002	Hemolytic Anemia	64	0.173

254	P	MSC005	Muscular Dystrophy	68	0.173

255	P	MNN013	Meningitis	67	0.172

256	c	LKM071	Leukemia, Chronic Lymphocytic	81	0.172

257		TLN003	Telangiectasis	53	0.171

258		ALL003	Allergic Rhinitis	69	0.171

259	P	SLP006	Sleep Apnea	71	0.171

260		ENT011	Enterocolitis	51	0.170

261		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.170

262		GTR002	Goiter	54	0.169

263		BND020	Bone Disease	60	0.169

264		RHM027	Rheumatic Disease	56	0.169

265		CHC001	Chickenpox	53	0.169

266	P	SZR006	Seizure Disorder	59	0.169

267	c	PRM038	Primary Agammaglobulinemia	45	0.168

268	P	KDN017	Kidney Cancer	60	0.168

269		DPH001	Diphtheria	61	0.168

270		IMP005	Impotence	53	0.168

271		NRR001	Neuroretinitis	46	0.168

272	P	THL005	Thalassemia	62	0.168

273		RTN023	Retinitis	46	0.168

274		MNN042	Meningioma, Radiation-Induced	64	0.167

275	P	ANT006	Antiphospholipid Syndrome	56	0.167

276	c	MLG068	Malignant Glioma	46	0.167

277		HNS001	Hansen's Disease	35	0.167

278		PRT013	Portal Hypertension	61	0.167

279		STM007	Stomatitis	51	0.167

280	P	LPR021	Leprosy 3	67	0.166

281		ERY051	Erythroleukemia, Familial	58	0.166

282	P	HYP076	Hyperthyroidism	55	0.166

283	P	DMN002	Dementia	68	0.166

284		BRC012	Brucellosis	62	0.166

285		FCT002	Factor Xi Deficiency	59	0.166

286	P	DBT085	Diabetes Mellitus, Insulin-Dependent	68	0.165

287		FCT003	Factor X Deficiency	57	0.165

288		CHL068	Cholestasis	61	0.165

289		BRK010	Burkitt Lymphoma	68	0.164

290	P	HMR003	Hemorrhagic Disease	54	0.163

291	c	HPT003	Hepatitis a	60	0.163

292		PLM010	Pulmonary Edema	56	0.163

293		CHR178	Chromosomal Triplication	36	0.162

294		SPN021	Spinal Meningioma	40	0.162

295	c	MNN043	Meningioma, Familial	74	0.162

296	P	MYP004	Myopathy	63	0.162

297	P	TXP001	Toxoplasmosis	61	0.162

298		BRN024	Bronchitis	70	0.162

299		FCT005	Factor Xiii Deficiency	50	0.161

300		SCR001	Secretory Meningioma	38	0.161

301		LYM002	Lymphoplasmacyte-Rich Meningioma	40	0.161

302	P	EPL164	Epilepsy	73	0.161

303	P	SCH015	Schizophrenia	76	0.161

304		AVN001	Avian Influenza	56	0.160

305	c	MGR028	Migraine with or Without Aura 1	70	0.160

306		BLL006	Bullous Pemphigoid	63	0.159

307	P	RHB003	Rhabdomyosarcoma	62	0.158

308		GST040	Gastric Adenocarcinoma	67	0.158

309	c	DLT002	Dilated Cardiomyopathy	81	0.157

310		VTM033	Vitamin K Deficiency Bleeding	47	0.157

311	c	SPN225	Spondyloarthropathy 1	74	0.157

312		OVR082	Overgrowth Syndrome	51	0.156

313		ATS010	Autosomal Recessive Disease	49	0.156

314		LPT001	Leptospirosis	60	0.156

315		VSL002	Visual Epilepsy	58	0.156

316		PNC129	Pancreatic Adenocarcinoma	69	0.156

317		HLC007	Helicobacter Pylori Infection	61	0.156

318	P	APL001	Aplastic Anemia	76	0.156

319	P	MLN007	Male Infertility	57	0.156

320	c	BRN108	Branchiootic Syndrome 1	62	0.155

321	P	CND004	Candidiasis	61	0.155

322		DYS073	Dysphagia	52	0.155

323		CMB003	Combined T Cell and B Cell Immunodeficiency	53	0.155

324	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.155

325		THR035	Thrombasthenia	42	0.154

326		URM002	Uremia	50	0.153

327	P	SCL018	Scoliosis	61	0.153

328	P	PYL005	Pyelonephritis	58	0.153

329		OTT002	Otitis Media	71	0.153

330	P	SYS005	Systemic Scleroderma	68	0.152

331	P	MJR001	Major Depressive Disorder	69	0.152

332		EYD002	Eye Disease	59	0.152

333	c	MCR129	Microvascular Complications of Diabetes 1	67	0.151

334	c	ACT135	Acute Graft Versus Host Disease	52	0.150

335	P	ATS364	Autism	68	0.150

336		PLM031	Poliomyelitis	58	0.150

337	c	THR082	Thrombophilia Due to Activated Protein C Resistance	61	0.149

338		VRL011	Viral Infectious Disease	62	0.149

339		FCT006	Factor V Deficiency	53	0.149

340		ADL002	Adult Syndrome	62	0.149

341	P	GRV001	Graves' Disease	57	0.149

342		PLC007	Placental Abruption	47	0.148

343		TRY001	Trypanosomiasis	50	0.148

344		PRN019	Perinatal Necrotizing Enterocolitis	55	0.148

345	P	MYP006	Myopia	58	0.148

346	P	TRN020	Turner Syndrome	66	0.148

347	P	THY032	Thyroiditis	52	0.148

348		THR004	Thrombocytosis	52	0.147

349		ANT024	Anthrax Disease	56	0.147

350		CRT013	Carotid Stenosis	50	0.146

351	P	UVT001	Uveitis	58	0.146

352		GLC003	Glucose Intolerance	55	0.146

353		LMY002	Leiomyoma	52	0.146

354	P	MYC084	Mycobacterium Tuberculosis 1	69	0.145

355	P	DDN001	Duodenal Ulcer	50	0.145

356		SPL018	Splenomegaly	48	0.145

357	P	CYS018	Cystitis	59	0.145

358	c	MCR112	Microvascular Complications of Diabetes 2	42	0.145

359	P	HYP069	Hyperparathyroidism	64	0.144

360		SKN019	Skin Melanoma	68	0.144

361		PLY150	Polykaryocytosis Inducer	31	0.144

362		ALL014	Allergic Encephalomyelitis	40	0.143

363		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	0.143

364		PNG002	Pain Agnosia	52	0.143

365		BRR014	Barrett Esophagus	67	0.143

366		MST005	Mastitis	55	0.142

367		CHG001	Chagas Disease	66	0.142

368		HMP009	Haemophilus Influenzae	46	0.141

369	P	PRS038	Personality Disorder	66	0.141

370		ANR007	Anorexia Nervosa	64	0.141

371		APP008	Appendicitis	61	0.140

372		VSC003	Visceral Leishmaniasis	55	0.140

373	P	HMN010	Hemangioma	62	0.140

374		RRD056	Rare Disease in Surgical Orthopedic	29	0.139

375	P	PRK057	Parkinson Disease, Late-Onset	77	0.139

376		ECH003	Echinococcosis	54	0.139

377		CRB037	Cerebral Palsy	69	0.139

378		SPN051	Spondylitis	53	0.138

379		TYP007	Typhoid Fever	61	0.138

380		INF009	Inflammatory Spondylopathy	29	0.138

381		MDD011	Mood Disorder	62	0.137

382	P	PLY018	Polycythemia	56	0.136

383		SQM013	Squamous Cell Carcinoma, Head and Neck	81	0.136

384		FCT004	Factor Xii Deficiency	54	0.136

385	c	PLM164	Pulmonary Hypertension, Primary, 1	79	0.136

386	P	ATX030	Ataxia-Telangiectasia	83	0.136

387	P	PTT006	Pituitary Adenoma	53	0.136

388		HYP014	Hyperuricemia	52	0.135

389	P	CHL066	Cholangitis	53	0.135

390		IGG001	Iga Glomerulonephritis	50	0.135

391		NRL016	Neural Tube Defects	83	0.134

392		GST023	Gastric Ulcer	53	0.134

393		PLG002	Plague	54	0.134

394		CHL067	Cholecystitis	60	0.134

395		THR016	Thrombophlebitis	50	0.133

396	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	0.133

397		PLM017	Pulmonary Alveolar Microlithiasis	54	0.133

398	P	HDC001	Headache	59	0.133

399		ACR007	Acromegaly	70	0.132

400		ENT004	Enthesopathy	46	0.132

401	P	SRC025	Sarcoidosis 1	72	0.131

402	P	MSC003	Muscular Atrophy	52	0.131

403		LMB062	Limb Ischemia	50	0.131

404	P	RTN018	Retinal Disease	53	0.131

405	P	ADL010	Adult Respiratory Distress Syndrome	61	0.131

406		CNS004	Constipation	59	0.131

407		KRT019	Keratitis, Hereditary	69	0.130

408		HPT022	Hepatoblastoma	58	0.130

409	c	THY109	Thyroid Cancer, Nonmedullary, 1	58	0.129

410		MCS002	Mucositis	56	0.129

411		TRN015	Transient Cerebral Ischemia	62	0.129

412		ANG005	Anogenital Venereal Wart	51	0.129

413	P	CNJ013	Conjunctivitis	67	0.129

414	c	WLM018	Wilms Tumor 5	63	0.129

415		ETN001	Eating Disorder	61	0.129

416		GRW007	Growth Hormone Deficiency	48	0.129

417		ANX004	Anoxia	44	0.128

418	c	SVR001	Severe Acute Respiratory Syndrome	56	0.128

419	c	EXD008	Exudative Vitreoretinopathy 1	69	0.128

420		PNM008	Pneumothorax	56	0.127

421		SYN007	Synovitis	55	0.127

422	P	PLY019	Polyneuropathy	55	0.127

423	c	JVN010	Juvenile Rheumatoid Arthritis	67	0.127

424		THR123	Thrombotic Microangiopathy	41	0.127

425	P	SLM003	Salmonellosis	54	0.126

426		CLF027	Cleft Palate, Isolated	67	0.126

427		CRN017	Coronary Thrombosis	45	0.126

428		ATX019	Ataxia with Vitamin E Deficiency	46	0.126

429		SLP001	Sleeping Sickness	47	0.126

430	P	HYP061	Hypertrophic Cardiomyopathy	68	0.126

431	P	CRD132	Cardiac Conduction Defect	61	0.126

432		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	36	0.125

433		BLR008	Bilirubin Metabolic Disorder	58	0.125

434		BRN028	Brain Cancer	75	0.125

435		CHR100	Chronic Ulcer of Skin	53	0.125

436	c	GLL024	Gallbladder Disease 1	53	0.125

437	c	PRD040	Periodontitis, Chronic	56	0.124

438		INF034	Infective Endocarditis	53	0.124

439	P	GLY013	Glycogen Storage Disease	59	0.124

440		GRN017	Granulocytopenia	46	0.124

441	c	LKM060	Leukemia, Acute Lymphoblastic 3	57	0.124

442	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.123

443		NTR005	Nutritional Deficiency Disease	61	0.123

444		PRT011	Protein C Deficiency	45	0.123

445		DNG002	Dengue Hemorrhagic Fever	59	0.122

446	P	TRM003	Tremor	55	0.122

447		PRM236	Primary Biliary Cholangitis	57	0.122

448		CNN005	Connective Tissue Disease	68	0.122

449		OST017	Osteomyelitis	65	0.122

450		KRT009	Keratosis	52	0.121

451		HRT011	Heart Septal Defect	52	0.121

452		HYP064	Hypogonadotropism	40	0.121

453		SCK003	Sickle Cell Anemia	74	0.121

454		HYP080	Hypogonadism	51	0.121

455		GNG013	Gingivitis	60	0.120

456	P	PRM006	Primary Biliary Cirrhosis	54	0.120

457		INT066	Interstitial Lung Disease	61	0.120

458	P	MTR003	Mitral Valve Stenosis	54	0.119

459		GT001	Gout	63	0.119

460		ARG004	Argyria	28	0.119

461	c	RHB024	Rhabdomyosarcoma 2	64	0.119

462		HPR003	Heparin-Induced Thrombocytopenia	49	0.119

463		CLR108	Colorectal Adenoma	64	0.119

464	P	ANG015	Angioedema	54	0.119

465		HPT004	Hepatic Coma	42	0.118

466	P	ART005	Arteriovenous Malformation	63	0.118

467	P	SLP005	Sleep Disorder	58	0.118

468		ALL006	Allergic Asthma	56	0.117

469	P	RTN016	Retinal Degeneration	56	0.117

470	P	RTN022	Retinal Vein Occlusion	50	0.117

471	P	PMP001	Pemphigus	56	0.117

472	P	PLY014	Polycystic Kidney Disease	61	0.117

473		CHR005	Chorioamnionitis	51	0.117

474	P	CLC063	Celiac Disease 1	66	0.117

475		DYS015	Dysentery	45	0.117

476		PPL052	Papillomatosis, Confluent and Reticulated	34	0.117

477		LYM019	Lymphosarcoma	48	0.116

478		PRT014	Protein S Deficiency	50	0.116

479		PST092	Posttransplant Acute Limbic Encephalitis	29	0.116

480	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	62	0.115

481	c	DNG003	Dengue Disease	61	0.115

482		HRP004	Herpes Zoster	58	0.115

483	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	65	0.114

484		DYS014	Dyspepsia	51	0.114

485		NRF026	Neurofibromatosis, Type Iv, of Riccardi	65	0.114

486		RCK004	Rickets	70	0.113

487	P	SNS001	Sensorineural Hearing Loss	62	0.113

488		NRL005	Neurilemmoma	62	0.113

489		BRS051	Breast Disease	59	0.113

490		MSC157	Muscular Dystrophy, Duchenne Type	70	0.112

491		AMN001	Amenorrhea	54	0.112

492	P	LMY004	Leiomyosarcoma	63	0.112

493		RTN020	Retinal Vascular Disease	49	0.112

494		PRT018	Portal Vein Thrombosis	50	0.111

495	c	MTR002	Mitral Valve Insufficiency	49	0.111

496		PLY001	Polycythemia Vera	70	0.110

497		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.110

498	c	BTT014	Beta-Thalassemia	73	0.109

499		CHL004	Cholelithiasis	50	0.109

500		CRN030	Coronary Stenosis	49	0.109

501	P	OPT006	Optic Nerve Disease	59	0.109

502		SHW001	Shwartzman Phenomenon	35	0.109

503		ESP002	Esophageal Varix	49	0.109

504	P	ESP024	Esophagitis	62	0.108

505		DBT010	Diabetic Neuropathy	56	0.108

506		HYD012	Hydrops Fetalis	49	0.108

507		PLS007	Plasmodium Falciparum Malaria	53	0.108

508		LPT014	Leptin Deficiency or Dysfunction	72	0.107

509		MYL005	Myelofibrosis	69	0.107

510		INT052	Intestinal Volvulus	44	0.106

511		THY030	Thyroid Gland Disease	53	0.106

512	P	FML011	Familial Adenomatous Polyposis	73	0.105

513		HPT019	Hepatic Encephalopathy	60	0.105

514		HRT012	Heart Valve Disease	56	0.105

515		MNN009	Meningoencephalitis	50	0.105

516		FTL016	Fetal Edema	24	0.104

517	P	MCR010	Microcephaly	56	0.104

518		RHM001	Rheumatic Fever	56	0.104

519		PRP016	Paraplegia	54	0.104

520		GLN010	Glanzmann Thrombasthenia	66	0.104

521		STT001	Status Epilepticus	61	0.103

522	P	CNR004	Cone-Rod Dystrophy 2	72	0.103

523	c	HRD002	Hereditary Angioedema	59	0.103

524		GST050	Gastrointestinal System Disease	57	0.103

525		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	49	0.102

526		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	54	0.102

527	P	HMC002	Homocystinuria	52	0.102

528	P	LCH002	Lichen Planus	55	0.102

529	P	PK3005	Pik3ca-Related Overgrowth Syndrome	35	0.102

530	P	EHL001	Ehlers-Danlos Syndrome	60	0.102

531	P	OBS001	Obstructive Jaundice	49	0.101

532	P	MST009	Mastocytosis	62	0.101

533		ILS001	Ileus	51	0.101

534		ACT058	Active Peptic Ulcer Disease	55	0.101

535		PLS011	Plasmacytoma	57	0.100

536		TNS005	Tonsillitis	58	0.100

537		CRY035	Cryptorchidism, Unilateral or Bilateral	61	0.099

538		SPT005	Spotted Fever	48	0.099

539	c	FML021	Familial Hypercholesterolemia	67	0.099

540		HYD002	Hydronephrosis	58	0.099

541		KWS002	Kawasaki Disease	65	0.098

542		LKP003	Leukoplakia	40	0.098

543		ANG020	Angiosarcoma	59	0.098

544	c	DNT047	Dentinogenesis Imperfecta Type 2	34	0.098

545		MCR011	Microinvasive Gastric Cancer	43	0.098

546	P	SCL009	Sclerosing Cholangitis	47	0.098

547	P	DYS154	Dystonia	65	0.098

548		PLC009	Placenta Praevia	35	0.097

549	P	GCH001	Gaucher's Disease	63	0.097

550	P	VNT002	Ventricular Septal Defect	61	0.097

551		GST019	Gastrointestinal Stromal Tumor	76	0.097

552	P	LYM025	Lymphedema	54	0.097

553		PPL002	Papillary Carcinoma	47	0.097

554		HMR002	Hemarthrosis	46	0.097

555	P	MMB011	Membranous Nephropathy	54	0.097

556		INT075	Intracranial Hypertension	54	0.096

557		NRM005	Neuromuscular Disease	62	0.096

558		ING001	Inguinal Hernia	61	0.096

559		PRS047	Prostatitis	57	0.096

560	P	PRP029	Porphyria	58	0.096

561		PFF001	Pfeiffer Syndrome	79	0.096

562	P	DRM010	Dermatomyositis	62	0.096

563		HMR039	Hemorrhage, Intracerebral	59	0.095

564	P	LCT001	Lactic Acidosis	52	0.095

565		LMY014	Leiomyoma, Uterine	57	0.095

566		EPD015	Epidemic Typhus	47	0.095

567	P	CRN037	Craniosynostosis	69	0.095

568		HLL004	Hellp Syndrome	53	0.095

569		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	33	0.094

570		NRT004	Neuritis	52	0.094

571		PRT082	Preterm Premature Rupture of the Membranes	53	0.094

572	P	PLY041	Polymyositis	57	0.094

573		PTH003	Pathologic Nystagmus	53	0.094

574	P	NRV007	Nervous System Disease	68	0.094

575	P	CMP008	Compartment Syndrome	45	0.093

576		PMP006	Pemphigus Vulgaris, Familial	56	0.093

577		ACN002	Acanthosis Nigricans	62	0.093

578	c	DWL002	Dowling-Degos Disease 1	59	0.093

579		MYL031	Myeloproliferative Neoplasm	66	0.092

580	P	AGM001	Agammaglobulinemia	66	0.092

581	c	PNS012	Paine Syndrome	61	0.092

582		QFV001	Q Fever	58	0.092

583		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.092

584		HPT046	Hepatic Veno-Occlusive Disease	56	0.091

585		BDD001	Budd-Chiari Syndrome	62	0.091

586		CRD137	Cardiogenic Shock	50	0.091

587		CRB086	Cerebral Aneurysms	41	0.091

588	P	AFB001	Afibrinogenemia	49	0.091

589	c	FML035	Familial Hyperlipidemia	56	0.091

590		ACS001	Acoustic Neuroma	57	0.091

591		CMM005	Common Cold	57	0.091

592		SLC006	Silicosis	55	0.091

593	P	MYS005	Myositis	54	0.091

594	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	48	0.091

595		FDL002	Food Allergy	52	0.090

596		PRN011	Pernicious Anemia	51	0.090

597	c	ATM011	Autoimmune Hepatitis	63	0.090

598		HYP005	Hypokalemia	55	0.090

599	c	GRV008	Graves Disease 1	55	0.089

600		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	49	0.089

601	c	CNT016	Central Retinal Vein Occlusion	48	0.089

602	P	INT143	Interstitial Cystitis	62	0.089

603	c	ACQ042	Acquired Hemophilia a	38	0.089

604		TNG003	Tongue Cancer	57	0.089

605	P	FCL005	Focal Segmental Glomerulosclerosis	63	0.089

606		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	0.088

607	P	ANR048	Aniridia 1	64	0.088

608		ADN011	Adenoid Cystic Carcinoma	71	0.088

609		UND005	Undifferentiated Pleomorphic Sarcoma	66	0.088

610	P	PLV020	Pelvic Organ Prolapse	61	0.088

611		PRS034	Parasitic Helminthiasis Infectious Disease	48	0.088

612		HMP001	Hemopericardium	44	0.087

613	P	HYP024	Hypoparathyroidism	56	0.087

614		YLL002	Yellow Fever	58	0.087

615		RYN005	Raynaud Phenomenon	50	0.087

616	P	ATR010	Atrial Heart Septal Defect	61	0.086

617	c	ACQ017	Acquired Von Willebrand Syndrome	42	0.086

618		RLP002	Relapsing-Remitting Multiple Sclerosis	57	0.086

619		HYP020	Hyperprolactinemia	62	0.086

620	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.085

621		MRF001	Marfan Syndrome	75	0.085

622		BRT054	Brittle Bone Disorder	71	0.084

623	P	FRG001	Fragile X Syndrome	69	0.084

624	P	INT070	Intestinal Obstruction	60	0.084

625		PRC013	Pericarditis	54	0.084

626	P	CLL015	Collagen Disease	46	0.084

627	P	HMP002	Hemophagocytic Lymphohistiocytosis	68	0.084

628	P	PRP034	Purpura Fulminans	42	0.084

629	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	29	0.083

630		INT030	Intracranial Aneurysm	57	0.083

631	P	PLM034	Pulmonary Emphysema	55	0.083

632		NRN004	Neuroendocrine Tumor	59	0.083

633	P	BRN019	Bernard-Soulier Syndrome	60	0.083

634		THR013	Thoracic Outlet Syndrome	49	0.083

635	c	PRM005	Primary Hyperparathyroidism	60	0.083

636		HYP457	Hypertrophic Scars	44	0.083

637		TRG002	Trigeminal Neuralgia	58	0.083

638	P	ART018	Aortic Valve Insufficiency	47	0.082

639		KRT008	Keratopathy	46	0.082

640		HRY003	Hairy Cell Leukemia	57	0.082

641	c	CNT035	Central Nervous System Disease	56	0.082

642	P	GNT008	Giant Cell Tumor	45	0.082

643	P	FBR031	Febrile Seizures	54	0.082

644	c	WLM013	Wilms Tumor 1	69	0.082

645		MST004	Mast Cell Neoplasm	40	0.082

646		CRD001	Cardiac Tamponade	45	0.082

647		EXT007	Extracutaneous Mastocytoma	39	0.081

648	P	DBT005	Diabetes Insipidus	54	0.081

649		KRT006	Keratoconjunctivitis	53	0.081

650		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	56	0.080

651	c	FNC043	Fanconi Anemia, Complementation Group E	64	0.080

652	P	PRC012	Pericardial Effusion	51	0.080

653		MLD001	Melioidosis	66	0.080

654		CRP001	Carpal Tunnel Syndrome	68	0.080

655		TRC008	Trachoma	49	0.080

656		SPT004	Septic Arthritis	55	0.080

657		PHR003	Pharyngitis	56	0.079

658	c	ACT004	Acute Diarrhea	38	0.079

659	P	HYP265	Hypotonia	43	0.079

660		CRC021	Carcinosarcoma	62	0.079

661	P	TRC086	Trichohepatoenteric Syndrome 1	57	0.079

662	c	AFB002	Afibrinogenemia, Congenital	62	0.079

663	P	HST010	Histiocytosis	54	0.079

664		THY122	Thyroid Gland Cancer	59	0.078

665		END040	Endogenous Depression	55	0.078

666		BLD053	Blood Platelet Disease	51	0.078

667		AND002	Androgen Insensitivity Syndrome	66	0.078

668		URT001	Urethritis	44	0.078

669		ANT009	Antithrombin Iii Deficiency	57	0.078

670		APH002	Aphasia	56	0.078

671	P	DYS026	Dysfibrinogenemia	42	0.078

672	c	GCH015	Gaucher Disease, Type I	65	0.077

673		MMM001	Mammary Paget's Disease	53	0.077

674	P	ANG001	Angelman Syndrome	65	0.077

675		DNG001	Dengue Shock Syndrome	43	0.076

676		HMP005	Hemiplegia	55	0.076

677		RRC033	Rare Coagulation Disorder	16	0.076

678		NRT001	Neurotic Disorder	53	0.076

679	c	DPH024	Diaphragmatic Hernia, Congenital	66	0.076

680		END062	Endometrial Hyperplasia	49	0.075

681	c	ALM001	Al Amyloidosis	50	0.075

682		FCT034	Factor V and Factor Viii, Combined Deficiency of, 2	37	0.075

683		VRS002	Virus-Associated Trichodysplasia Spinulosa	33	0.075

684		MNN020	Meningococcal Infection	46	0.075

685		ATN004	Autonomic Neuropathy	43	0.075

686	P	ORT004	Orthostatic Intolerance	68	0.075

687	c	FML001	Familial Atrial Fibrillation	67	0.075

688		GNG003	Gingival Recession	43	0.075

689	P	ACT232	Acute Necrotizing Encephalopathy	28	0.075

690		NRM004	Neuroma	50	0.075

691		ATR057	Atrioventricular Block	56	0.074

692	c	INF145	Infantile Liver Failure Syndrome 1	50	0.073

693		PNM001	Pneumocystosis	53	0.073

694	c	ANM038	Anemia, Autoimmune Hemolytic	61	0.073

695		SCT005	Scott Syndrome	48	0.073

696		HMR023	Hemorrhagic Cystitis	40	0.073

697	P	OVR049	Ovarian Disease	55	0.073

698		PLL012	Pollen Allergy	46	0.073

699		LYM021	Lymphadenitis	58	0.073

700		VTM009	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1	25	0.072

701		ANG011	Angiodysplasia	45	0.072

702	P	SPN046	Spinal Muscular Atrophy	65	0.072

703		ATX010	Ataxia Neuropathy Spectrum	39	0.072

704		ORN001	Ornithosis	40	0.072

705		VGN023	Vaginitis	54	0.072

706		BLD137	Blood Group--Ahonen	17	0.072

707		INT078	Intracranial Thrombosis	48	0.072

708		PRT012	Prothrombin Deficiency	37	0.071

709		LPD004	Lipoid Nephrosis	48	0.071

710		ORL013	Oral Lichen Planus	47	0.071

711	P	ACT008	Actinic Keratosis	50	0.071

712		SNL007	Senile Cataract	41	0.070

713	c	PRS130	Prostate Cancer, Hereditary, 8	33	0.070

714		CRY004	Cryoglobulinemia	47	0.070

715	P	PTS002	Ptosis	53	0.070

716	c	PRS136	Prostate Cancer, Hereditary, 6	34	0.070

717	c	TRC022	Tricuspid Valve Insufficiency	41	0.070

718		ERY004	Erysipelas	46	0.070

719		LRN003	Learning Disability	51	0.070

720		MYL020	Myelomeningocele	51	0.069

721		INT051	Intussusception	48	0.069

722	P	END046	Endometritis	49	0.069

723	P	CRN024	Corneal Disease	42	0.069

724		MCP006	Mucoepidermoid Carcinoma	53	0.069

725	c	RRH015	Rare Hemorrhagic Disorder	21	0.069

726		MSN004	Mesenchymal Cell Neoplasm	45	0.069

727		HRD083	Hereditary Antithrombin Deficiency	30	0.069

728		DVR002	Diverticulitis	44	0.069

729	P	MTR012	Mitral Valve Disease	59	0.069

730		CCN002	Cocaine Abuse	48	0.068

731		TBR011	Tuberculous Meningitis	50	0.068

732		TLR001	Tularemia	44	0.068

733		RCK002	Rocky Mountain Spotted Fever	40	0.068

734		CLC006	Calcinosis	48	0.067

735		URN010	Urinary Tract Obstruction	59	0.067

736		HRN026	Hernia, Hiatus	46	0.067

737		PLC001	Placenta Accreta	44	0.067

738	P	RNL015	Renal Hypertension	47	0.066

739		HPT082	Hepatic Adenomas, Familial	40	0.066

740		AMB001	Amebiasis	44	0.066

741	P	RNV001	Renovascular Hypertension	49	0.066

742		PLP001	Pulpitis	48	0.066

743		BLL003	Bell's Palsy	50	0.066

744	P	AXN002	Axenfeld-Rieger Syndrome	58	0.066

745		EXP004	Exophthalmos	53	0.066

746	P	MLG056	Malignant Hyperthermia	60	0.066

747		CMR002	Coumarin Resistance	56	0.066

748		SPN027	Spinal Stenosis	58	0.066

749		PRT129	Prothrombin Deficiency, Congenital	52	0.065

750		CRT004	Carotid Artery Thrombosis	37	0.065

751		ORL012	Oral Leukoplakia	42	0.064

752		EBL001	Ebola Hemorrhagic Fever	48	0.064

753		CHL061	Childhood Leukemia	49	0.064

754		RDC006	Red Cell Aplasia	45	0.064

755		INT067	Interstitial Nephritis	46	0.064

756	P	OPT009	Optic Neuritis	55	0.064

757	P	FML018	Familial Mediterranean Fever	70	0.064

758		THY128	Thyroid Tumor	49	0.064

759	P	PST095	Post-Thrombotic Syndrome	50	0.064

760		CRT017	Cartilage Disease	54	0.063

761		CRT016	Carotid Artery Disease	53	0.063

762		ART031	Aortic Coarctation	45	0.063

763		PNM013	Pneumococcal Meningitis	45	0.062

764	P	BCK002	Beckwith-Wiedemann Syndrome	62	0.062

765	c	VNW005	Von Willebrand Disease, Type 1	49	0.062

766		MGK001	Megakaryocytic Leukemia	65	0.062

767		PYD002	Pyoderma	51	0.062

768		DFF031	Diffuse Alveolar Hemorrhage	28	0.062

769	c	CHR682	Chronic Bilirubin Encephalopathy	36	0.062

770	c	VNW010	Von Willebrand Disease, Type 2	58	0.061

771		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	63	0.061

772		WLS001	Wilson Disease	69	0.061

773	P	PLY017	Polyarteritis Nodosa	52	0.061

774		END011	Endometriosis of Ovary	35	0.061

775	P	HYP055	Hypoplastic Left Heart Syndrome	63	0.061

776	P	PRR002	Pure Red-Cell Aplasia	47	0.061

777		HYP781	Hypoascorbemia	48	0.061

778		NRG002	Neurogenic Bladder	55	0.061

779		MST024	Mastocytosis, Cutaneous	65	0.061

780	P	GLM040	Glioma Susceptibility 1	68	0.060

781		ANC002	Anca-Associated Vasculitis	43	0.060

782		ERY069	Erythrokeratoderma ''en Cocardes''	30	0.060

783	c	OVR114	Ovarian Cancer 1	39	0.060

784	P	OTS001	Otosclerosis	51	0.060

785		MCR141	Mucormycosis	48	0.060

786	P	HRD011	Hereditary Spherocytosis	59	0.060

787		ART017	Aortic Disease	49	0.059

788		C1N001	C1 Inhibitor Deficiency	39	0.059

789		MDS022	Mediastinitis	42	0.059

790		DBN001	Dubin-Johnson Syndrome	58	0.059

791		BRN032	Brain Glioma	44	0.059

792		CHR073	Choreatic Disease	52	0.059

793		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	45	0.059

794		LNG108	Langerhans Cell Histiocytosis	60	0.059

795		CMP040	Complement Component 4, Partial Deficiency of	34	0.058

796		CVR006	Cavernous Hemangioma	49	0.058

797		GLS018	Glass Syndrome	51	0.058

798		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	48	0.058

799		CYS009	Cystadenoma	43	0.058

800	P	MGL001	Megaloblastic Anemia	54	0.058

801		ALR002	Al-Raqad Syndrome	32	0.058

802	P	HMF004	Hemifacial Spasm	40	0.058

803	c	HMF011	Hemifacial Spasm, Familial	34	0.058

804	P	CRN028	Corneal Ulcer	49	0.058

805		LCH001	Leech Infestation	40	0.057

806		KRT001	Keratoconjunctivitis Sicca	53	0.057

807		APH001	Aphthous Stomatitis	56	0.057

808	P	RTN014	Retinal Artery Occlusion	46	0.057

809		GLL008	Gilles De La Tourette Syndrome	66	0.057

810		BLL004	Bullous Keratopathy	47	0.057

811		HMP018	Hemophilic Arthropathy	35	0.057

812		MYC088	Mycobacterium Avium Complex Infections	30	0.057

813		MCR088	Microscopic Polyangiitis	51	0.057

814		ANC001	Ancylostomiasis	39	0.056

815		GLC006	Galactosemia	63	0.055

816		PPL049	Papillon-Lefevre Syndrome	63	0.055

817		LWC002	Lowe Oculocerebrorenal Syndrome	63	0.055

818		ART001	Arterial Tortuosity Syndrome	60	0.055

819		GST037	Gastroparesis	52	0.055

820	c	PST005	Posterior Uveitis	52	0.055

821	P	ALP106	Alport Syndrome 1, X-Linked	55	0.054

822		TKY002	Takayasu Arteritis	61	0.054

823		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	53	0.054

824		PYD001	Pyoderma Gangrenosum	53	0.054

825		VLV044	Vulvar Intraepithelial Neoplasia	44	0.054

826		HYP458	Hyper Ige Syndrome	60	0.054

827	P	MYG005	Myoglobinuria	43	0.054

828		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	56	0.054

829		HNT002	Hantavirus Pulmonary Syndrome	48	0.054

830		ANG046	Angioimmunoblastic T-Cell Lymphoma	49	0.054

831		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	63	0.053

832		FRN014	Fournier Gangrene	38	0.053

833	P	NMN002	Niemann-Pick Disease	60	0.053

834		HMN035	Hemangioma-Thrombocytopenia Syndrome	40	0.053

835		AML001	Amelanotic Melanoma	38	0.053

836	c	INH004	Inherited Blood Coagulation Disease	31	0.053

837	c	BLD140	Blood Group, I System	29	0.052

838		DDN006	Duodenitis	44	0.052

839		ELP001	Elephantiasis	37	0.052

840	c	GLY008	Glycogen Storage Disease Ii	68	0.051

841		ADP007	Adie Pupil	40	0.051

842		HNM002	Hinman Syndrome	26	0.051

843		ORC001	Orchitis	41	0.051

844		CHL013	Cholecystolithiasis	37	0.051

845	c	LSS005	Lissencephaly 1	54	0.051

846		UMB002	Umbilical Hernia	45	0.051

847	P	PRM011	Primary Ciliary Dyskinesia	67	0.051

848		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	65	0.050

849		AND005	Androgen Insensitivity Syndrome, Mild	20	0.050

850	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.050

851	P	ACR001	Aicardi-Goutieres Syndrome	63	0.050

852		APR006	Apert Syndrome	70	0.050

853		HYD038	Hydrops Fetalis, Nonimmune	55	0.050

854		49X002	49,xxxxy Syndrome	39	0.050

855		CHD001	Chediak-Higashi Syndrome	68	0.050

856	P	SYR001	Syringomyelia	51	0.050

857		SYR010	Syringomyelia, Noncommunicating Isolated	37	0.050

858		ACR008	Acrocallosal Syndrome	66	0.049

859		OBS524	Obsolete: Benign Exophthalmos Syndrome	13	0.049

860		MSC165	Muscular Dystrophy, Congenital, Lmna-Related	66	0.048

861	P	ALP004	Alport Syndrome	66	0.048

862		HMN016	Hemangioendothelioma	41	0.048

863	P	HRM001	Hermansky-Pudlak Syndrome	64	0.048

864	c	ACR116	Aicardi-Goutieres Syndrome 1	53	0.048

865		ICH001	Ichthyosis Vulgaris	54	0.048

866		ANL022	Anal Fistula	47	0.048

867		END081	Endosteal Hyperostosis, Autosomal Dominant	59	0.047

868		VRL017	Viral Hemorrhagic Fever	36	0.047

869		CHR008	Choroiditis	41	0.047

870		PRC051	Paracetamol Poisoning	31	0.047

871		SCR015	Scarlet Fever	41	0.047

872	P	HMN036	Hemangiopericytoma, Malignant	57	0.047

873		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	46	0.047

874		ACT049	Acute Disseminated Encephalomyelitis	50	0.046

875		DFF015	Diffuse Glomerulonephritis	33	0.046

876		ENT001	Enterocele	44	0.046

877		SPL006	Splenic Infarction	35	0.046

878	P	ECT005	Ectropion	44	0.046

879		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	48	0.046

880		PPL058	Papilloma of Choroid Plexus	57	0.046

881		HYD005	Hydrocele	47	0.045

882		CRD016	Cardiac Rupture	33	0.045

883		CLD007	Cold Agglutinin Disease	47	0.045

884	P	OMP004	Omphalocele	51	0.045

885		ACT055	Actinomycosis	43	0.044

886	P	CNT110	Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a	61	0.044

887		LYM022	Lymphangioma	52	0.044

888		CRB079	Cerebrospinal Fluid Leak	36	0.044

889		WTR001	Waterhouse-Friderichsen Syndrome	39	0.044

890		IMM001	Immune-Complex Glomerulonephritis	40	0.044

891	c	LTN004	Late-Onset Retinal Degeneration	49	0.044

892		CRB009	Cerebritis	31	0.044

893		HRD160	Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors	15	0.044

894		HMT008	Hematuria, Benign Familial	53	0.043

895		SWL001	Swallowing Disorders	39	0.043

896		BLD163	Blood Group, Dombrock System	24	0.043

897		CRB132	Cerebral Sinovenous Thrombosis	33	0.043

898	P	SHR029	Short Syndrome	56	0.043

899		IRT001	Iritis	37	0.043

900		LYM014	Lymphangitis	32	0.043

901		KLP010	Klippel-Trenaunay-Weber Syndrome	55	0.042

902		VTM010	Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2	18	0.042

903		DFF003	Diffuse Scleroderma	43	0.042

904		HYP706	Hypermobile Ehlers-Danlos Syndrome	44	0.042

905		CMP064	Complement Component 3 Deficiency	30	0.042

906	c	RRL003	Rare Lymphatic Malformation	32	0.042

907		LYM116	Lymph Node Disease	43	0.042

908	P	HRN001	Horner's Syndrome	46	0.042

909	P	JNC001	Junctional Epidermolysis Bullosa	54	0.042

910		SPC030	Specific Language Disorder	27	0.042

911		CNS002	Constrictive Pericarditis	37	0.041

912	P	ANT088	Anterior Segment Dysgenesis	41	0.041

913	P	BLP003	Blepharospasm	43	0.040

914		MLL004	Mallory-Weiss Syndrome	28	0.040

915		GST007	Gastric Dilatation	30	0.040

916		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	43	0.040

917		MRS001	Marasmus	39	0.040

918		PCT003	Pectus Excavatum	48	0.040

919		NRN002	Neuronitis	37	0.040

920		RNL012	Renal Tuberculosis	36	0.040

921	c	PSD048	Pseudo-Von Willebrand Disease	44	0.039

922		RTR011	Retroperitoneal Fibrosis	41	0.039

923		CHR177	Chromophobe Renal Cell Carcinoma	58	0.039

924		END072	Endotheliitis	36	0.039

925		CHR103	Charge Syndrome	62	0.039

926		PYR041	Pyruvate Kinase Deficiency of Red Cells	58	0.038

927		RYN001	Raynaud Disease	48	0.038

928	c	CNG124	Congenital Rubella	44	0.038

929		ANK010	Ankylostomiasis	30	0.037

930		HPT081	Hepatic Infarction	32	0.037

931		HMN004	Hemangioma of Liver	35	0.037

932		TRG019	Trigonocephaly with Short Stature and Developmental Delay	31	0.037

933		BLD165	Blood Group, Colton System	21	0.036

934		BRR002	Barrett's Adenocarcinoma	36	0.036

935	P	MLT007	Multiple Epiphyseal Dysplasia	56	0.036

936	P	LRS001	Larsen Syndrome	55	0.036

937		HYP814	Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency	27	0.036

938		WHM001	Whim Syndrome	55	0.036

939		ALT002	Aleutian Mink Disease	35	0.035

940	c	RNG019	Ring Chromosome 3	22	0.035

941	P	CRB045	Cerebellar Hypoplasia	53	0.035

942	P	RST002	Restrictive Cardiomyopathy	55	0.035

943	c	CLR131	Ciliary Dyskinesia, Primary, 1	59	0.035

944		FMR003	Femoral Neuropathy	36	0.034

945		RGH009	Right Atrial Isomerism	52	0.034

946		ARC007	Arachnoid Cysts	40	0.034

947		SLV025	Salivary Gland Adenoma, Pleomorphic	37	0.034

948		MLK003	Melkersson-Rosenthal Syndrome	50	0.033

949		CHL109	Childhood Apraxia of Speech	43	0.033

950		FBR089	Fibrosclerosis, Multifocal	37	0.033

951		PLM180	Pulmonary Artery Disease	33	0.033

952		BCL010	B-Cell Expansion with Nfkb and T-Cell Anergy	58	0.033

953		EPT010	Epithelial-Myoepithelial Carcinoma	53	0.032

954	c	PLM127	Pulmonary Hypertension, Primary, 3	33	0.032

955	P	BRN120	Bronchus Cancer	45	0.032

956	P	PLM149	Palmoplantar Keratoderma and Congenital Alopecia 2	35	0.032

957		HYP774	Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome	52	0.032

958	c	PTT056	Pituitary Adenoma 1, Multiple Types	59	0.032

959		SPN331	Spondyloocular Syndrome	35	0.031

960	P	CWD010	Cowden Syndrome	66	0.031

961		WRF003	Warfarin Syndrome	29	0.031

962	c	WLM011	Wilms Tumor 6	38	0.031

963	c	CWD006	Cowden Syndrome 1	76	0.030

964		KLT001	Klatskin's Tumor	50	0.030

965	P	EPT020	Epithelioid Hemangioendothelioma	45	0.030

966		KND001	Kindler Syndrome	58	0.029

967		FLT006	Floating-Harbor Syndrome	46	0.028

968	P	APL006	Aplasia Cutis Congenita	49	0.027

969		RTN179	Retinal Arteries, Tortuosity of	42	0.027

970		FNT005	Fontaine Progeroid Syndrome	43	0.027

971		DHY016	Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema	41	0.026

972	c	LYM150	Lymphatic Malformation 7	40	0.025