Search results for Liver Extracts

2650 hits were found for Liver Extracts

#	Family	MCID	Name	MIFTS	Score
1	P	LVR013	Liver Disease	71	1.303

2		FTT001	Fatty Liver Disease	63	0.891

3		LVR012	Liver Cirrhosis	67	0.884

4	P	HPT023	Hepatocellular Carcinoma	99	0.746

5		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.724

6	P	CTR002	Cataract	62	0.526

7	c	ACT134	Acute Liver Failure	53	0.479

8	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	58	0.454

9	P	CLR023	Colorectal Cancer	100	0.427

10		NNL006	Non-Alcoholic Steatohepatitis	53	0.417

11		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.412

12	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.383

13		CHL068	Cholestasis	61	0.376

14	c	HPT001	Hepatitis C	62	0.363

15		PRT013	Portal Hypertension	61	0.361

16	c	VRL010	Viral Hepatitis	56	0.360

17	c	HPT073	Hepatitis C Virus	74	0.358

18	c	HPT016	Hepatitis B	63	0.339

19		HYP066	Hyperglycemia	63	0.325

20	P	CHL066	Cholangitis	53	0.318

21		LPD008	Lipid Metabolism Disorder	64	0.306

22	P	HPT021	Hepatitis	69	0.297

23	P	ENC018	Encephalopathy	64	0.292

24		ISC004	Ischemia	62	0.289

25		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.286

26		HPT004	Hepatic Coma	42	0.283

27		48X005	48,xyyy	37	0.280

28		HPT019	Hepatic Encephalopathy	60	0.265

29		CHL065	Cholangiocarcinoma	68	0.265

30		PRM236	Primary Biliary Cholangitis	57	0.265

31		INT079	Intrahepatic Cholangiocarcinoma	54	0.264

32	P	PRM006	Primary Biliary Cirrhosis	54	0.257

33		VRC005	Varicose Veins	61	0.257

34	c	ATM011	Autoimmune Hepatitis	63	0.256

35		PRT036	Peritonitis	66	0.252

36	P	DRR001	Diarrhea	55	0.249

37		ADN018	Adenoma	60	0.245

38	c	HYP836	Hypercholesterolemia, Familial, 1	74	0.244

39	P	HMN010	Hemangioma	62	0.243

40		CYT002	Cytokine Deficiency	46	0.243

41	P	KDN018	Kidney Disease	73	0.239

42	P	SCL009	Sclerosing Cholangitis	47	0.234

43		ALC007	Alcohol Dependence	68	0.234

44		ALL026	Allergic Hypersensitivity Disease	65	0.229

45		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.226

46	c	HPT003	Hepatitis a	60	0.225

47		HYP056	Hypoglycemia	68	0.222

48		ALC006	Alcoholic Hepatitis	60	0.220

49	P	ALC033	Alcohol Use Disorder	58	0.219

50		HMS001	Hemosiderosis	54	0.218

51		OCL069	Ocular Motor Apraxia	53	0.217

52		BLR001	Biliary Atresia	51	0.212

53	P	RRH023	Rare Hereditary Hemochromatosis	41	0.211

54	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	82	0.209

55	P	GST053	Gastric Cancer	85	0.207

56		HRW001	Hair Whorl	36	0.207

57	P	DBT009	Diabetes Mellitus	66	0.206

58	c	CHL119	Cholangitis, Primary Sclerosing	59	0.206

59		BCT022	Bacterial Infectious Disease	57	0.205

60	P	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.204

61		ECH003	Echinococcosis	54	0.204

62	P	PNC035	Pancreatic Cancer	86	0.204

63		DRM006	Dermatitis	63	0.203

64	P	BRS047	Breast Cancer	99	0.203

65	P	ADN016	Adenocarcinoma	65	0.201

66		SCH014	Schistosomiasis	57	0.197

67	P	INF037	Inflammatory Bowel Disease	57	0.197

68		ATM095	Autoimmune Disease	62	0.196

69		SCH060	Schistosoma Mansoni Infection, Susceptibility/	40	0.196

70	c	DNT047	Dentinogenesis Imperfecta Type 2	34	0.194

71	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.194

72	c	BDY021	Body Mass Index Quantitative Trait Locus 20	50	0.194

73	c	BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.194

74	c	BDY010	Body Mass Index Quantitative Trait Locus 4	48	0.194

75	c	BDY015	Body Mass Index Quantitative Trait Locus 12	48	0.194

76	c	BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.194

77	c	BDY011	Body Mass Index Quantitative Trait Locus 10	47	0.194

78	c	BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.194

79	c	BDY006	Body Mass Index Quantitative Trait Locus 8	45	0.194

80	c	BDY012	Body Mass Index Quantitative Trait Locus 7	45	0.194

81		BNR002	Bone Resorption Disease	51	0.193

82		HYP060	Hyperinsulinism	55	0.192

83	P	THR014	Thrombocytopenia	67	0.192

84		47X002	47,xyy	49	0.192

85		DFC004	Deficiency Anemia	77	0.192

86		ATH013	Atherosclerosis Susceptibility	68	0.190

87		PRT018	Portal Vein Thrombosis	50	0.190

88		CLT003	Colitis	63	0.188

89		PLM017	Pulmonary Alveolar Microlithiasis	54	0.188

90		GLC003	Glucose Intolerance	55	0.187

91		HYP266	Hypoxia	58	0.187

92	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.185

93	P	HYP750	Hypertriglyceridemia, Familial	62	0.185

94		ESP002	Esophageal Varix	49	0.185

95		GST023	Gastric Ulcer	53	0.184

96		ULC004	Ulcerative Colitis	75	0.184

97		SPL018	Splenomegaly	48	0.184

98	P	HRP006	Herpes Simplex	66	0.183

99	P	BCL017	B-Cell Lymphoma	61	0.183

100		PPL052	Papillomatosis, Confluent and Reticulated	34	0.181

101	c	BDY007	Body Mass Index Quantitative Trait Locus 1	43	0.181

102		ALC009	Alcoholic Liver Cirrhosis	53	0.180

103		SKN016	Skin Disease	64	0.179

104		THR024	Thrombosis	58	0.178

105	P	RHN004	Rhinitis	59	0.177

106	P	OST002	Osteoporosis	79	0.175

107	c	HMC039	Hemochromatosis, Type 1	73	0.175

108		SPN035	Spindle Cell Sarcoma	57	0.175

109		SRC014	Sarcoma	67	0.174

110	P	PRD008	Periodontitis	66	0.172

111	P	VSC007	Vascular Disease	65	0.171

112		RHM027	Rheumatic Disease	56	0.171

113		BLR008	Bilirubin Metabolic Disorder	58	0.171

114	P	RCT021	Rectum Cancer	54	0.169

115	c	ACT071	Acute Kidney Failure	60	0.168

116	P	GST044	Gastritis	58	0.166

117		HPT022	Hepatoblastoma	58	0.165

118	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	51	0.165

119	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	43	0.165

120	P	DRM053	Dermatitis, Atopic	68	0.164

121	P	PSR002	Psoriasis	63	0.164

122		CYS001	Cystic Fibrosis	84	0.164

123		TXC005	Toxic Shock Syndrome	63	0.164

124		ALL003	Allergic Rhinitis	69	0.163

125	P	OBS001	Obstructive Jaundice	49	0.163

126	P	NRB010	Neuroblastoma 1	66	0.163

127		PST011	Pustulosis of Palm and Sole	51	0.162

128	P	NTR004	Neutropenia	64	0.162

129	P	HYP086	Hypothyroidism	70	0.161

130	P	MYP006	Myopia	58	0.161

131	c	HYP595	Hypertension, Essential	87	0.161

132		END030	End Stage Renal Failure	60	0.160

133		AZS001	Azoospermia	51	0.160

134	c	CHR684	Chronic Kidney Disease	68	0.159

135		ENT004	Enthesopathy	46	0.158

136	P	AMY004	Amyloidosis	71	0.158

137		CNG034	Congestive Heart Failure	69	0.158

138		HPT014	Hepatorenal Syndrome	49	0.158

139		PPT005	Peptic Ulcer Disease	60	0.156

140		LSH001	Leishmaniasis	64	0.154

141		CHL067	Cholecystitis	60	0.152

142	c	MCR113	Microvascular Complications of Diabetes 3	55	0.152

143	c	MCR130	Microvascular Complications of Diabetes 6	42	0.152

144	c	MCR133	Microvascular Complications of Diabetes 4	42	0.152

145		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.152

146	c	MCR120	Microvascular Complications of Diabetes 7	48	0.152

147	P	KLZ004	Kala-Azar 1	43	0.152

148		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.151

149	P	END033	Endocarditis	58	0.151

150	P	NRP001	Neuropathy	57	0.151

151		BRN024	Bronchitis	70	0.150

152	P	LYM118	Lymphoma	70	0.150

153	c	PRC016	Pre-Eclampsia	63	0.150

154		SVR004	Severe Combined Immunodeficiency	74	0.150

155	P	HMP007	Hemophilia	58	0.149

156	P	HYP098	Hypereosinophilic Syndrome	67	0.148

157		DYS014	Dyspepsia	51	0.147

158		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.147

159		DYS015	Dysentery	45	0.147

160		PRS045	Prostatic Hypertrophy	55	0.147

161		PLY023	Polycystic Liver Disease	55	0.147

162	P	END047	Endophthalmitis	50	0.147

163		PRS021	Prostatic Adenoma	52	0.147

164		CLN015	Colon Adenocarcinoma	65	0.146

165		MLN008	Melanoma	68	0.146

166		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	67	0.145

167	P	HRT032	Heart Disease	78	0.144

168	c	ACT027	Acute Pancreatitis	60	0.143

169	P	CRD119	Cardiac Arrest	71	0.143

170	c	GLL024	Gallbladder Disease 1	53	0.143

171		INS024	Insulin-Like Growth Factor I	79	0.142

172	P	SKN015	Skin Carcinoma	67	0.141

173	P	PRS040	Prostate Cancer	97	0.141

174		OST012	Osteoarthritis	80	0.141

175		BND020	Bone Disease	60	0.141

176		ANX010	Anxiety	75	0.140

177	P	GRF003	Graft-Versus-Host Disease	71	0.140

178		PRS129	Prostatic Hyperplasia, Benign	49	0.139

179		AGN016	Aging	58	0.139

180	P	CND004	Candidiasis	61	0.138

181		DNT012	Dental Caries	52	0.138

182		BDD001	Budd-Chiari Syndrome	62	0.138

183		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.138

184	P	LNG032	Lung Cancer	99	0.138

185		CRY036	Cryptogenic Cirrhosis	38	0.137

186		CYT008	Cytomegalovirus Infection	58	0.137

187		CNS004	Constipation	59	0.136

188	P	PLY019	Polyneuropathy	55	0.136

189	P	HYP076	Hyperthyroidism	55	0.135

190		PNG002	Pain Agnosia	52	0.135

191	c	ACT210	Acute Respiratory Distress Syndrome	59	0.135

192		LNG099	Lung Disease	62	0.135

193	P	PNC044	Pancreatitis	61	0.134

194		MLR004	Malaria	82	0.134

195		IMM167	Immune Deficiency Disease	79	0.134

196	P	RSP003	Respiratory Failure	75	0.134

197		CHL014	Cholera	58	0.134

198		CHL004	Cholelithiasis	50	0.134

199		HYP014	Hyperuricemia	52	0.133

200		DSS009	Disseminated Intravascular Coagulation	58	0.133

201		ALP103	Alpha-1-Antitrypsin Deficiency	63	0.132

202		OVR082	Overgrowth Syndrome	51	0.132

203		PLM033	Pulmonary Embolism	60	0.131

204		RTN017	Retinal Detachment	62	0.131

205	P	BLD134	Bladder Cancer	79	0.131

206	c	INF145	Infantile Liver Failure Syndrome 1	50	0.130

207		GT001	Gout	63	0.130

208		HLX001	Helix Syndrome	46	0.130

209	P	OVR042	Ovarian Cancer	89	0.129

210	P	EXN002	Exanthem	58	0.129

211		PRT037	Pertussis	66	0.127

212	P	LKM002	Leukemia	69	0.127

213		GLB002	Glioblastoma	74	0.127

214		GLB015	Glioblastoma Multiforme	60	0.126

215	P	PLM037	Pulmonary Hypertension	69	0.126

216	P	FBR017	Fibrosarcoma	57	0.125

217	P	THL005	Thalassemia	62	0.125

218	c	HPT007	Hepatitis E	53	0.125

219	c	LRG017	Large Intestine Cancer	53	0.125

220		IMP005	Impotence	53	0.124

221	P	LYM031	Lymphocytic Leukemia	56	0.124

222		RNL114	Renal Cell Carcinoma, Nonpapillary	79	0.123

223	P	DDN001	Duodenal Ulcer	50	0.123

224		IRN002	Iron Metabolism Disease	58	0.123

225		LPT014	Leptin Deficiency or Dysfunction	72	0.123

226	P	GLY013	Glycogen Storage Disease	59	0.122

227	P	ALZ034	Alzheimer Disease	90	0.122

228	P	ASP006	Aspergillosis	67	0.121

229		CRB039	Cerebrovascular Disease	71	0.121

230	P	PRP029	Porphyria	58	0.121

231		TLN003	Telangiectasis	53	0.121

232		CRH001	Crohn's Disease	75	0.120

233		WLS001	Wilson Disease	69	0.120

234	P	UVT001	Uveitis	58	0.120

235		NDL013	Nodular Regenerative Hyperplasia	48	0.120

236	P	MCR115	Microvascular Complications of Diabetes 5	67	0.118

237		HLL004	Hellp Syndrome	53	0.118

238	P	NRF023	Neurofibromatosis, Type Ii	77	0.118

239		CLR109	Colorectal Adenocarcinoma	51	0.118

240		STM007	Stomatitis	51	0.118

241		OST003	Osteonecrosis	62	0.118

242		NTR005	Nutritional Deficiency Disease	61	0.118

243		SQM006	Squamous Cell Carcinoma	60	0.118

244		PLM001	Pulmonary Tuberculosis	72	0.118

245		GST019	Gastrointestinal Stromal Tumor	76	0.117

246	P	TRM003	Tremor	55	0.117

247		ANG020	Angiosarcoma	59	0.117

248	P	PLY014	Polycystic Kidney Disease	61	0.117

249		ORL011	Oral Cancer	62	0.116

250		OST159	Osteogenic Sarcoma	67	0.116

251		HPT046	Hepatic Veno-Occlusive Disease	56	0.115

252		HMN044	Human Immunodeficiency Virus Type 1	73	0.115

253	c	PCH010	Pachyonychia Congenita 3	43	0.115

254	P	SRC025	Sarcoidosis 1	72	0.115

255	P	ART021	Arteriosclerosis	56	0.115

256	P	SYP003	Syphilis	59	0.114

257	P	BRS044	Breast Adenocarcinoma	59	0.114

258	P	HML002	Hemolytic Anemia	64	0.114

259	c	SYS001	Systemic Lupus Erythematosus	88	0.114

260		HPT009	Hepatopulmonary Syndrome	49	0.114

261	P	CRN300	Coronary Heart Disease 1	59	0.114

262	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.113

263		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	56	0.113

264	c	RHB024	Rhabdomyosarcoma 2	64	0.113

265	P	INF032	Infertility	60	0.113

266	P	ART022	Arthritis	71	0.113

267		ESP021	Esophageal Cancer	90	0.112

268	P	SZR006	Seizure Disorder	59	0.112

269		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.112

270		CVR006	Cavernous Hemangioma	49	0.112

271	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.112

272	P	CRN018	Coronary Artery Anomaly	67	0.112

273		PNM008	Pneumothorax	56	0.111

274		DPR016	Depression	64	0.111

275		PRN011	Pernicious Anemia	51	0.111

276	P	RHM011	Rheumatoid Arthritis	82	0.111

277		NRN004	Neuroendocrine Tumor	59	0.111

278		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.111

279		BRN004	Brain Edema	57	0.111

280	P	LNG064	Lung Cancer Susceptibility 3	79	0.111

281	P	PRP019	Peripheral Nervous System Disease	64	0.110

282	c	CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	59	0.109

283		GST045	Gastroenteritis	60	0.109

284	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	65	0.109

285	P	GLM007	Glomerulonephritis	58	0.109

286		PST092	Posttransplant Acute Limbic Encephalitis	29	0.109

287		FDL002	Food Allergy	52	0.109

288		DWN001	Down Syndrome	70	0.109

289	P	LPR021	Leprosy 3	67	0.108

290		HNS001	Hansen's Disease	35	0.108

291		ART140	Arteries, Anomalies of	60	0.108

292		GST050	Gastrointestinal System Disease	57	0.108

293		VCC001	Vaccinia	50	0.108

294		PST046	Post-Transplant Lymphoproliferative Disease	55	0.108

295		ALV002	Alveolar Echinococcosis	50	0.108

296		HPT067	Hepatocellular Adenoma	45	0.107

297		VSL002	Visual Epilepsy	58	0.107

298		ARG004	Argyria	28	0.107

299		ANX004	Anoxia	44	0.107

300		HYP063	Hypersplenism	51	0.106

301		MYL069	Myeloma, Multiple	85	0.106

302		ACQ007	Acquired Immunodeficiency Syndrome	61	0.106

303	P	ECL001	Eclampsia	53	0.106

304		CNT047	Contact Dermatitis	58	0.106

305	P	TRN020	Turner Syndrome	66	0.106

306	P	LPS004	Lupus Erythematosus	62	0.106

307	P	PLY011	Polycystic Ovary Syndrome	58	0.105

308		PLL012	Pollen Allergy	46	0.105

309	P	LYM033	Lymphoproliferative Syndrome	62	0.105

310	P	PHC003	Pheochromocytoma	71	0.104

311		CHL079	Children's Interstitial Lung Disease	27	0.104

312		PRP030	Purpura	56	0.104

313	c	ATR087	Atrial Standstill 1	76	0.104

314	P	ALP008	Alopecia	58	0.104

315		CHL039	Choledocholithiasis	37	0.103

316		ADR040	Adrenal Gland Pheochromocytoma	51	0.103

317	P	LMY004	Leiomyosarcoma	63	0.103

318	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	62	0.103

319		ALL006	Allergic Asthma	56	0.103

320		CRV035	Cervical Cancer	77	0.103

321	c	ACT068	Acute Cystitis	63	0.103

322		GNG013	Gingivitis	60	0.102

323	P	RTN024	Retinoblastoma	74	0.102

324		MCL006	Macular Retinal Edema	52	0.102

325	P	INF038	Influenza	69	0.101

326	P	APL001	Aplastic Anemia	76	0.101

327		GST040	Gastric Adenocarcinoma	67	0.101

328		MTB004	Metabolic Acidosis	48	0.101

329	c	FML008	Familial Retinoblastoma	46	0.101

330	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.101

331	P	SLP006	Sleep Apnea	71	0.100

332		HYP080	Hypogonadism	51	0.100

333		GLL048	Glial Tumor	48	0.100

334		MNT002	Mental Depression	60	0.100

335	P	NSP012	Nasopharyngeal Carcinoma	67	0.099

336	P	VSC011	Vasculitis	64	0.099

337	P	BLR006	Biliary Tract Disease	49	0.099

338		AMB001	Amebiasis	44	0.099

339	P	GLM045	Glioma	64	0.099

340		TYP007	Typhoid Fever	61	0.099

341		ADL002	Adult Syndrome	62	0.099

342	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	61	0.099

343		THY029	Thyroid Carcinoma	62	0.099

344		HYP005	Hypokalemia	55	0.099

345		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	0.098

346	P	MYL006	Myeloid Leukemia	61	0.098

347		HYP064	Hypogonadotropism	40	0.098

348		ATX019	Ataxia with Vitamin E Deficiency	46	0.098

349	P	MYC007	Myocardial Infarction	74	0.098

350	P	PLM036	Pulmonary Fibrosis	66	0.097

351		IDP011	Idiopathic Interstitial Pneumonia	65	0.097

352	c	SML038	Small Cell Cancer of the Lung	67	0.097

353	P	SDR002	Siderosis	42	0.096

354		KLB003	Klebsiella Pneumonia	36	0.096

355		FCT001	Factor Viii Deficiency	54	0.096

356	P	DNG005	Dengue Virus	57	0.096

357	P	LCT001	Lactic Acidosis	52	0.096

358	P	URT039	Urticaria	61	0.096

359		AMN003	Amnestic Disorder	55	0.096

360		SNL007	Senile Cataract	41	0.096

361		INS001	Insulinoma	60	0.096

362	c	DWL002	Dowling-Degos Disease 1	59	0.096

363		HLC007	Helicobacter Pylori Infection	61	0.096

364		CNN005	Connective Tissue Disease	68	0.095

365	P	RRT020	Rare Tumor	43	0.095

366		URM002	Uremia	50	0.095

367	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	61	0.095

368		MCS002	Mucositis	56	0.094

369		OST017	Osteomyelitis	65	0.094

370		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	56	0.094

371		TTN003	Tetanus	62	0.094

372		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	0.094

373	c	HMP029	Hemophilia a	69	0.094

374		VSC003	Visceral Leishmaniasis	55	0.093

375		MST021	Meester-Loeys Syndrome	32	0.093

376		ILS001	Ileus	51	0.093

377		CRB004	Cerebral Artery Occlusion	38	0.093

378	P	SCK005	Sickle Cell Disease	53	0.093

379	c	HPT015	Hepatitis D	49	0.093

380	c	LKM061	Leukemia, Acute Myeloid	84	0.093

381	P	TYR004	Tyrosinemia	54	0.093

382		INF034	Infective Endocarditis	53	0.092

383	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	0.092

384		FSC002	Fascioliasis	44	0.092

385	P	MYP004	Myopathy	63	0.091

386		CHC001	Chickenpox	53	0.091

387	c	PNS012	Paine Syndrome	61	0.091

388		NTR046	Neutrophil Migration	49	0.091

389	P	PK3005	Pik3ca-Related Overgrowth Syndrome	35	0.091

390		PLY150	Polykaryocytosis Inducer	31	0.091

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

392	P	BLD062	Bile Duct Cancer	66	0.090

393		STR067	Stroke, Ischemic	82	0.090

394	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.090

395		PLM010	Pulmonary Edema	56	0.090

396	P	PRM002	Primary Hyperoxaluria	60	0.090

397		ATS010	Autosomal Recessive Disease	49	0.089

398	P	TXP001	Toxoplasmosis	61	0.089

399	c	INH020	Inherited Metabolic Disorder	51	0.089

400	P	CHR345	Chronic Pain	52	0.089

401		AST005	Asthma	80	0.089

402	c	DNG003	Dengue Disease	61	0.089

403	P	PNM007	Pneumonia	71	0.089

404	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	61	0.089

405	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.089

406		SPP010	Suppressor of Tumorigenicity 3	54	0.089

407	P	ENC004	Encephalitis	64	0.089

408	c	MGR028	Migraine with or Without Aura 1	70	0.089

409		KRT002	Keratomalacia	47	0.088

410		HPT082	Hepatic Adenomas, Familial	40	0.088

411	P	CNJ013	Conjunctivitis	67	0.088

412		KRT019	Keratitis, Hereditary	69	0.088

413		CND006	Candida Glabrata	33	0.088

414	P	CLC063	Celiac Disease 1	66	0.087

415	P	END044	Endometriosis	63	0.087

416		CMB003	Combined T Cell and B Cell Immunodeficiency	53	0.087

417	c	GRV008	Graves Disease 1	55	0.087

418		CYS008	Cystic Echinococcosis	47	0.087

419	P	TRT010	Teratoma	52	0.087

420		YLL002	Yellow Fever	58	0.087

421		HMC014	Homocysteinemia	54	0.087

422		MSL001	Measles	61	0.087

423	P	MSC003	Muscular Atrophy	52	0.086

424		SKN019	Skin Melanoma	68	0.086

425		ENT011	Enterocolitis	51	0.086

426		SXL003	Sexual Disorder	49	0.086

427		IRR002	Irritable Bowel Syndrome	65	0.086

428		SPN186	Spinal Cord Injury	63	0.086

429		INT075	Intracranial Hypertension	54	0.086

430		PPL022	Papilloma	56	0.085

431	c	ACT073	Acute Leukemia	59	0.085

432		VRL011	Viral Infectious Disease	62	0.085

433		LYM133	Lymphoma, Hodgkin, Classic	70	0.085

434		APP008	Appendicitis	61	0.085

435		CMM005	Common Cold	57	0.085

436		SBC016	Subacute Delirium	43	0.085

437	P	ATR011	Atrial Fibrillation	67	0.085

438	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.085

439		CYS014	Cystadenocarcinoma	51	0.085

440		PNC129	Pancreatic Adenocarcinoma	69	0.085

441		PLR007	Pleural Empyema	44	0.085

442		GLL018	Gallbladder Cancer	57	0.085

443		PNC001	Pancytopenia	54	0.085

444		HMT018	Hematopoietic Stem Cell Transplantation	54	0.085

445		FLR002	Filariasis	56	0.084

446		END057	Endometrial Cancer	74	0.084

447	P	MLN069	Melanoma, Uveal	59	0.084

448	c	MCL042	Macular Degeneration, Age-Related, 1	88	0.084

449		CRD001	Cardiac Tamponade	45	0.084

450		CYS009	Cystadenoma	43	0.084

451		RCK004	Rickets	70	0.084

452		PRS047	Prostatitis	57	0.084

453	P	KDN017	Kidney Cancer	60	0.084

454		DPH001	Diphtheria	61	0.084

455		PLM186	Pulmonary Arterial Hypertension Associated with Portal Hypertension	26	0.084

456		PLR008	Pleurisy	50	0.084

457		BRN071	Brain Injury	51	0.083

458		LYM019	Lymphosarcoma	48	0.083

459		ANR040	Aneurysm	60	0.083

460		LMY002	Leiomyoma	52	0.083

461	P	INT068	Intestinal Disease	56	0.083

462		OPS001	Opisthorchiasis	39	0.082

463		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	55	0.082

464		EXT006	Extrahepatic Cholestasis	38	0.082

465		PLY100	Polyploidy	41	0.082

466		BRC012	Brucellosis	62	0.082

467		ENC038	Encephalopathy, Progressive, with or Without Lipodystrophy	38	0.081

468	P	NPH012	Nephrotic Syndrome	65	0.081

469	c	TRC022	Tricuspid Valve Insufficiency	41	0.081

470	P	CRN026	Corneal Edema	44	0.081

471	P	MSC005	Muscular Dystrophy	68	0.081

472	P	GCH001	Gaucher's Disease	63	0.081

473		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.081

474	P	RHB003	Rhabdomyosarcoma	62	0.081

475	P	ALG028	Alagille Syndrome 1	70	0.081

476	P	MLN007	Male Infertility	57	0.081

477		MCR013	Microphthalmia	62	0.081

478	P	SHR001	Short Bowel Syndrome	50	0.080

479		LYM143	Lymphoma, Non-Hodgkin, Familial	74	0.080

480	c	FML035	Familial Hyperlipidemia	56	0.080

481		LVR002	Liver Angiosarcoma	52	0.080

482		BNN003	Bone Inflammation Disease	51	0.080

483	P	LTR001	Lateral Sclerosis	56	0.080

484		CHG001	Chagas Disease	66	0.079

485		SQM002	Squamous Cell Papilloma	49	0.079

486	P	ATX030	Ataxia-Telangiectasia	83	0.079

487		MST005	Mastitis	55	0.079

488		CRC021	Carcinosarcoma	62	0.079

489	c	LKM060	Leukemia, Acute Lymphoblastic 3	57	0.079

490	P	SLP005	Sleep Disorder	58	0.079

491		NWC001	Newcastle Disease	45	0.079

492	P	HDC001	Headache	59	0.079

493	P	MYC008	Myocarditis	60	0.079

494		DRG002	Drug-Induced Hepatitis	41	0.078

495		ANG018	Angiomyolipoma	46	0.078

496		HRP004	Herpes Zoster	58	0.078

497	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.078

498	P	MLT020	Multiple Sclerosis	73	0.078

499	P	MYC084	Mycobacterium Tuberculosis 1	69	0.078

500	c	PRM038	Primary Agammaglobulinemia	45	0.078

501		ANG054	Angina Pectoris	66	0.078

502	P	DMN002	Dementia	68	0.077

503		INT052	Intestinal Volvulus	44	0.077

504		HYP081	Hypolipoproteinemia	51	0.077

505		CCC002	Coccidiosis	46	0.077

506	c	INV001	Invasive Aspergillosis	48	0.076

507		SCK003	Sickle Cell Anemia	74	0.076

508	P	ADL010	Adult Respiratory Distress Syndrome	61	0.076

509	P	BLD124	Bleeding Disorder, Platelet-Type, 11	66	0.076

510		HMP001	Hemopericardium	44	0.076

511		EYD002	Eye Disease	59	0.076

512	c	PRG047	Progressive Familial Intrahepatic Cholestasis	59	0.076

513	c	ACT075	Acute Myocardial Infarction	59	0.076

514		HMN004	Hemangioma of Liver	35	0.076

515	P	HMR005	Hemorrhoid	47	0.075

516	P	VNS003	Venous Insufficiency	55	0.075

517	P	MNN013	Meningitis	67	0.075

518		ORL015	Oral Squamous Cell Carcinoma	44	0.075

519		DFF005	Diffuse Large B-Cell Lymphoma	56	0.075

520		CHL045	Choline Deficiency Disease	39	0.075

521		ALL010	Allergic Contact Dermatitis	56	0.074

522	P	HST010	Histiocytosis	54	0.074

523	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.074

524		CYN002	Cyanosis, Transient Neonatal	45	0.074

525	P	FML355	Familial Intrahepatic Cholestasis	49	0.073

526	P	SBS003	Substance Abuse	56	0.073

527		ACT003	Acute Kidney Tubular Necrosis	42	0.073

528		ACT055	Actinomycosis	43	0.073

529		WTH001	Withdrawal Disorder	47	0.073

530		PRT038	Protein-Energy Malnutrition	56	0.073

531		CTN007	Cutaneous Leishmaniasis	61	0.072

532		MDD011	Mood Disorder	62	0.072

533		ALL014	Allergic Encephalomyelitis	40	0.072

534	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	61	0.072

535	P	SYS005	Systemic Scleroderma	68	0.072

536	P	PRC012	Pericardial Effusion	51	0.072

537		DYS073	Dysphagia	52	0.072

538	P	HYP069	Hyperparathyroidism	64	0.072

539		KRT009	Keratosis	52	0.072

540	c	PRT132	Protoporphyria, Erythropoietic, 1	59	0.072

541	P	CNG048	Congenital Hepatic Fibrosis	39	0.072

542		KPS004	Kaposi Sarcoma	75	0.072

543	c	FML021	Familial Hypercholesterolemia	67	0.072

544		MSC007	Muscle Hypertrophy	65	0.071

545		CHL123	Chlamydia	60	0.071

546		GTR002	Goiter	54	0.071

547		IMM064	Immunodeficiency, Common Variable, 10	51	0.071

548		CLL003	Cellulitis	56	0.071

549		BNT001	Banti's Syndrome	22	0.071

550		IGR001	Ige Responsiveness, Atopic	61	0.070

551	P	ESP024	Esophagitis	62	0.070

552		RYS001	Reye Syndrome	49	0.070

553		NRN001	Neuroendocrine Carcinoma	48	0.070

554	P	CYS018	Cystitis	59	0.070

555		BRK010	Burkitt Lymphoma	68	0.070

556		BCK006	Back Pain	44	0.070

557	c	CHR431	Chronic Venous Insufficiency	48	0.070

558		XRD010	Xeroderma Pigmentosum, Variant Type	72	0.070

559		AMN001	Amenorrhea	54	0.070

560	c	HMP004	Hemophilia B	66	0.070

561		INT017	Intestinal Schistosomiasis	49	0.070

562	P	THY032	Thyroiditis	52	0.070

563	P	DBT085	Diabetes Mellitus, Insulin-Dependent	68	0.069

564	P	SLM003	Salmonellosis	54	0.069

565	P	AST007	Astrocytoma	52	0.069

566	P	THY023	Thymoma	64	0.069

567	c	THY107	Thymoma, Familial	55	0.069

568	P	DBT005	Diabetes Insipidus	54	0.069

569	P	HRD008	Hereditary Hemorrhagic Telangiectasia	64	0.069

570	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	0.069

571		HMP009	Haemophilus Influenzae	46	0.069

572	P	ART023	Arthropathy	61	0.069

573	c	SVR005	Severe Pre-Eclampsia	50	0.069

574	c	SCL052	Scleroderma, Familial Progressive	62	0.069

575	c	LKM071	Leukemia, Chronic Lymphocytic	81	0.069

576		ANR007	Anorexia Nervosa	64	0.068

577		MCR141	Mucormycosis	48	0.068

578		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	41	0.068

579	c	BTT014	Beta-Thalassemia	73	0.068

580	P	MJR001	Major Depressive Disorder	69	0.068

581		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.068

582		PRC051	Paracetamol Poisoning	31	0.068

583		FCT007	Factor Vii Deficiency	65	0.068

584	c	AMY087	Amyloidosis, Hereditary, Transthyretin-Related	59	0.068

585		PFF001	Pfeiffer Syndrome	79	0.068

586	P	GLL020	Gallbladder Disease	60	0.068

587		CHR074	Choriocarcinoma	47	0.067

588		PRP027	Peripheral Vascular Disease	72	0.067

589	c	GCH015	Gaucher Disease, Type I	65	0.067

590		CRR012	Cirrhotic Cardiomyopathy	23	0.067

591		ZLL002	Zollinger-Ellison Syndrome	54	0.067

592		PRN019	Perinatal Necrotizing Enterocolitis	55	0.067

593	P	CRG003	Crigler-Najjar Syndrome, Type I	61	0.067

594		GLB001	Gilbert Syndrome	58	0.067

595		PLS002	Peliosis Hepatis	37	0.067

596	P	OPT006	Optic Nerve Disease	59	0.067

597		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.066

598	P	TCL004	T-Cell Leukemia	48	0.066

599		CRY004	Cryoglobulinemia	47	0.066

600		ASC001	Ascaridiasis	36	0.066

601	c	MCR129	Microvascular Complications of Diabetes 1	67	0.066

602		CYS005	Cysticercosis	55	0.066

603		PLS011	Plasmacytoma	57	0.066

604		GSG001	Gas Gangrene	52	0.066

605		VSC002	Vascular Dementia	57	0.066

606		DBT010	Diabetic Neuropathy	56	0.066

607		ASC010	Ascaris Lumbricoides Infection	51	0.066

608	P	NMN002	Niemann-Pick Disease	60	0.066

609		GST033	Gestational Diabetes	58	0.066

610	P	INT070	Intestinal Obstruction	60	0.066

611		RTR008	Root Resorption	44	0.066

612		PTT037	Pituitary Tumors	47	0.066

613	P	INS002	in Situ Carcinoma	55	0.066

614		OST011	Osteomalacia	51	0.066

615	P	ART005	Arteriovenous Malformation	63	0.065

616	c	PRD040	Periodontitis, Chronic	56	0.065

617	c	ANT034	Anterior Uveitis	48	0.065

618	P	PYL005	Pyelonephritis	58	0.065

619	P	RNL015	Renal Hypertension	47	0.065

620		LPT001	Leptospirosis	60	0.065

621		HDN002	Head Injury	47	0.065

622		TRM010	Traumatic Brain Injury	54	0.065

623	c	DLT002	Dilated Cardiomyopathy	81	0.065

624	P	BNG032	Benign Mesothelioma	47	0.065

625	c	LKM005	Leukemia, T-Cell, Chronic	35	0.065

626		MYL009	Myelodysplastic Syndrome	72	0.065

627	c	LPM012	Lipomatosis, Multiple	60	0.065

628	P	CRD132	Cardiac Conduction Defect	61	0.065

629		ACT119	Acute Promyelocytic Leukemia	63	0.065

630		FSC004	Fasciitis	47	0.065

631		HMN014	Human Immunodeficiency Virus Infectious Disease	56	0.064

632	c	LKM063	Leukemia, Chronic Myeloid	74	0.064

633	P	PRK057	Parkinson Disease, Late-Onset	77	0.064

634		ACT058	Active Peptic Ulcer Disease	55	0.064

635		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.064

636		IRN001	Iron Deficiency Anemia	59	0.064

637	c	LKM004	Leukemia, B-Cell, Chronic	35	0.064

638		URT049	Urate Oxidase, Pseudogene	26	0.064

639		STS002	Situs Inversus	46	0.063

640		MTH009	Mouth Disease	56	0.063

641		PRC013	Pericarditis	54	0.063

642		CRC006	Carcinoid Syndrome	55	0.063

643	c	PRS136	Prostate Cancer, Hereditary, 6	34	0.063

644	c	PRS130	Prostate Cancer, Hereditary, 8	33	0.063

645		CRD223	Cardiac Arrhythmia	61	0.063

646	P	SJG008	Sjogren Syndrome	57	0.063

647	c	PLM164	Pulmonary Hypertension, Primary, 1	79	0.063

648		OVR063	Overnutrition	47	0.063

649	P	ANG015	Angioedema	54	0.063

650	P	ATS364	Autism	68	0.063

651		CRD137	Cardiogenic Shock	50	0.063

652		CLR108	Colorectal Adenoma	64	0.063

653		RNL077	Renal Fibrosis	49	0.063

654		ART016	Aortic Aneurysm	71	0.063

655		PLG002	Plague	54	0.062

656		LYM027	Lymphopenia	58	0.062

657		PRS063	Paresthesia	46	0.062

658		NNT012	Neonatal Jaundice	48	0.062

659	P	INT099	Intrahepatic Cholestasis of Pregnancy	50	0.062

660		ORL005	Oral Candidiasis	56	0.062

661	P	FML011	Familial Adenomatous Polyposis	73	0.062

662	P	RBL001	Rubella	56	0.062

663	P	HNT016	Huntington Disease	72	0.062

664	P	EPL164	Epilepsy	73	0.061

665		TST014	Testicular Cancer	49	0.061

666	c	WLM018	Wilms Tumor 5	63	0.061

667	P	PLY018	Polycythemia	56	0.061

668		PNC034	Pancreas Disease	51	0.061

669		ENH001	Enhanced S-Cone Syndrome	56	0.061

670		GRN017	Granulocytopenia	46	0.061

671		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	54	0.061

672		THR016	Thrombophlebitis	50	0.061

673		LNG108	Langerhans Cell Histiocytosis	60	0.061

674		DNG002	Dengue Hemorrhagic Fever	59	0.061

675		PLM031	Poliomyelitis	58	0.061

676		STT001	Status Epilepticus	61	0.060

677	c	SVR001	Severe Acute Respiratory Syndrome	56	0.060

678		CTR172	Citrullinemia, Classic	62	0.060

679	P	ANR048	Aniridia 1	64	0.060

680		HRT011	Heart Septal Defect	52	0.060

681		GST092	Gastroesophageal Reflux	68	0.060

682		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	63	0.060

683	P	SML001	Small Cell Carcinoma	55	0.060

684	c	ACT135	Acute Graft Versus Host Disease	52	0.059

685	P	PLM034	Pulmonary Emphysema	55	0.059

686		LST001	Listeriosis	55	0.059

687		THR004	Thrombocytosis	52	0.059

688		CRY005	Cryptococcosis	51	0.059

689	c	FNC043	Fanconi Anemia, Complementation Group E	64	0.059

690		NRR001	Neuroretinitis	46	0.059

691		PHR003	Pharyngitis	56	0.059

692		HYP781	Hypoascorbemia	48	0.059

693		RTN020	Retinal Vascular Disease	49	0.059

694	P	LCH002	Lichen Planus	55	0.059

695		ATN005	Autonomic Dysfunction	48	0.059

696		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	36	0.059

697		AVN001	Avian Influenza	56	0.059

698	c	MCR112	Microvascular Complications of Diabetes 2	42	0.059

699	P	VNW001	Von Willebrand's Disease	64	0.059

700	P	BLD036	Bile Duct Disease	46	0.059

701		IGG001	Iga Glomerulonephritis	50	0.059

702	c	SPN225	Spondyloarthropathy 1	74	0.058

703	P	HYP061	Hypertrophic Cardiomyopathy	68	0.058

704		RTN023	Retinitis	46	0.058

705		TXC011	Toxocariasis	43	0.058

706		SFT003	Soft Tissue Sarcoma	57	0.058

707		QFV001	Q Fever	58	0.058

708		NCR007	Necrotizing Fasciitis	47	0.058

709		VTM033	Vitamin K Deficiency Bleeding	47	0.058

710	c	PNC106	Pancreatic Agenesis 1	50	0.058

711		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.058

712	c	CHR682	Chronic Bilirubin Encephalopathy	36	0.058

713		RSP021	Respiratory Allergy	45	0.057

714	P	SCH015	Schizophrenia	76	0.057

715	c	ACT036	Acute Cholangitis	37	0.057

716		CHK001	Chikungunya	55	0.057

717		UND005	Undifferentiated Pleomorphic Sarcoma	66	0.057

718		DVR002	Diverticulitis	44	0.057

719		CNT025	Central Pontine Myelinolysis	45	0.057

720		OCL022	Ocular Melanoma	54	0.057

721		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	33	0.057

722		CRT015	Carotid Artery Occlusion	44	0.057

723	c	HNT011	Huntington Disease-Like 3	37	0.057

724		PLC008	Placenta Disease	51	0.056

725	c	TYR012	Tyrosinemia, Type I	61	0.056

726	P	BPL003	Bipolar Disorder	59	0.056

727		PLM005	Pleomorphic Lipoma	41	0.056

728	c	DPH024	Diaphragmatic Hernia, Congenital	66	0.056

729		CRY035	Cryptorchidism, Unilateral or Bilateral	61	0.056

730	P	PTS002	Ptosis	53	0.056

731		CRY003	Cryptosporidiosis	50	0.056

732	P	GRV001	Graves' Disease	57	0.056

733		ATN004	Autonomic Neuropathy	43	0.056

734		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.056

735		ERY051	Erythroleukemia, Familial	58	0.056

736		STT004	Steatorrhea	39	0.056

737	c	ALM001	Al Amyloidosis	50	0.055

738	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	62	0.055

739	P	HYP024	Hypoparathyroidism	56	0.055

740		TRY001	Trypanosomiasis	50	0.055

741		PRM020	Premenstrual Tension	48	0.055

742		PRD004	Prediabetes Syndrome	49	0.055

743		SCB001	Scabies	50	0.055

744		TRN018	Transitional Cell Carcinoma	57	0.055

745		MDS022	Mediastinitis	42	0.055

746		LYM021	Lymphadenitis	58	0.055

747		PRP083	Porphyria, Acute Intermittent	62	0.055

748		HST009	Histiocytoma	47	0.055

749		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	49	0.055

750	P	MRC003	Mercury Poisoning	47	0.055

751	c	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	62	0.054

752		THR123	Thrombotic Microangiopathy	41	0.054

753		MCR017	Macrocytic Anemia	41	0.054

754		PHN003	Phenylketonuria	73	0.054

755	P	HYP730	Hypogonadotropic Hypogonadism	54	0.054

756		GST030	Gastrinoma	43	0.054

757		ACT162	Acute Sensory Ataxic Neuropathy	27	0.054

758	P	BLD051	Blood Coagulation Disease	48	0.054

759	c	CNG216	Congenital Hydrocephalus	55	0.054

760		RYN005	Raynaud Phenomenon	50	0.054

761	P	RTN018	Retinal Disease	53	0.054

762		THY111	Thyroid Carcinoma, Familial Medullary	68	0.054

763		SYN036	Syncope	46	0.054

764		RDN001	Reading Disorder	42	0.054

765	P	THR015	Thrombophilia	51	0.054

766		MXD005	Mixed Connective Tissue Disease	55	0.054

767	P	LPS002	Liposarcoma	62	0.054

768	P	HMR003	Hemorrhagic Disease	54	0.054

769	c	CHR417	Chronic Graft Versus Host Disease	56	0.054

770		JPN002	Japanese Encephalitis	56	0.054

771		DSS008	Disease of Mental Health	66	0.054

772		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	58	0.054

773		THY125	Thyroid Gland Medullary Carcinoma	52	0.053

774	P	HYD006	Hydrocephalus	68	0.053

775		PSY004	Psychotic Disorder	68	0.053

776		LMB062	Limb Ischemia	50	0.053

777		BCT021	Bacterial Sepsis	44	0.053

778		FBR003	Fibrous Histiocytoma	43	0.053

779		LYS012	Lysosomal Acid Lipase Deficiency	63	0.053

780	P	CRY007	Cryoglobulinemia, Familial Mixed	50	0.053

781	c	HNT004	Huntington Disease-Like 2	48	0.053

782		NRF026	Neurofibromatosis, Type Iv, of Riccardi	65	0.053

783		DRM011	Dermatophytosis	49	0.053

784	c	MJR024	Major Affective Disorder 9	42	0.053

785	c	MJR022	Major Affective Disorder 8	39	0.053

786		PLS007	Plasmodium Falciparum Malaria	53	0.053

787		MCR011	Microinvasive Gastric Cancer	43	0.053

788		TRN015	Transient Cerebral Ischemia	62	0.053

789	P	MYS003	Myasthenia Gravis	68	0.052

790	P	HYP083	Hypopituitarism	53	0.052

791		ATR057	Atrioventricular Block	56	0.052

792	P	MNC007	Monocytic Leukemia	52	0.052

793	P	TBR001	Tuberous Sclerosis	72	0.052

794	P	HML001	Hemolytic-Uremic Syndrome	54	0.052

795		MSN004	Mesenchymal Cell Neoplasm	45	0.052

796	P	BRB001	Beriberi	41	0.052

797		LYS002	Lysosomal Storage Disease	52	0.052

798		SMN007	Seminoma	43	0.052

799	P	HMP002	Hemophagocytic Lymphohistiocytosis	68	0.052

800		KLT001	Klatskin's Tumor	50	0.052

801		BLR028	Biliary Atresia, Extrahepatic	35	0.052

802		GST020	Gastric Antral Vascular Ectasia	42	0.052

803		HYP017	Hypophosphatemia	48	0.052

804	P	TCD001	Tic Disorder	55	0.052

805	P	TRC086	Trichohepatoenteric Syndrome 1	57	0.052

806	P	MTH008	Methylmalonic Acidemia	50	0.052

807		BLR013	Biliary Tract Cancer	44	0.052

808		GRD001	Giardiasis	42	0.052

809		PRP001	Propionic Acidemia	63	0.052

810		MLG065	Malignant Fibroxanthoma	45	0.052

811		GYN001	Gynecomastia	49	0.052

812		INF021	Infant Gynecomastia	32	0.052

813		ING001	Inguinal Hernia	61	0.052

814		PNT038	Peanut Allergy	45	0.052

815		LNG031	Lung Benign Neoplasm	52	0.052

816	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	29	0.051

817		TNS005	Tonsillitis	58	0.051

818		FRC011	Fructose Intolerance, Hereditary	52	0.051

819		BLD063	Bile Duct Cysts	42	0.051

820		CRN030	Coronary Stenosis	49	0.051

821	P	HYP058	Hypervitaminosis a	45	0.051

822		ANR004	Anuria	47	0.051

823		DBN001	Dubin-Johnson Syndrome	58	0.051

824	P	AGM001	Agammaglobulinemia	66	0.051

825		HRT012	Heart Valve Disease	56	0.051

826		ADR016	Adrenal Cortical Carcinoma	51	0.051

827	c	MLG074	Malignant Mesenchymoma	50	0.051

828		ACN002	Acanthosis Nigricans	62	0.051

829		NRT001	Neurotic Disorder	53	0.051

830	c	WLM013	Wilms Tumor 1	69	0.051

831		ADR054	Adrenocortical Carcinoma, Hereditary	68	0.051

832		CCC001	Coccidioidomycosis	54	0.051

833	P	SPR119	Spermatogenic Failure, X-Linked, 1	38	0.051

834		EXP004	Exophthalmos	53	0.051

835	P	DRM010	Dermatomyositis	62	0.051

836	P	MYS005	Myositis	54	0.051

837	P	CNR004	Cone-Rod Dystrophy 2	72	0.050

838	c	JVN010	Juvenile Rheumatoid Arthritis	67	0.050

839		HYP020	Hyperprolactinemia	62	0.050

840		PPL001	Papillary Adenoma	42	0.050

841		CLN045	Colonic Benign Neoplasm	52	0.050

842		ORN008	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to	60	0.050

843	c	ATM006	Autoimmune Lymphoproliferative Syndrome	73	0.050

844	P	MMP001	Mumps	57	0.050

845	c	BRN108	Branchiootic Syndrome 1	62	0.050

846		PRM329	Premature Aging	41	0.050

847	c	HYP555	Hypertriglyceridemia, Transient Infantile	38	0.050

848		ACR007	Acromegaly	70	0.050

849		VTM002	Vitamin B12 Deficiency	48	0.050

850		CHR178	Chromosomal Triplication	36	0.050

851		CHR100	Chronic Ulcer of Skin	53	0.050

852	c	ATS007	Autism Spectrum Disorder	69	0.050

853		DMP001	Dumping Syndrome	44	0.050

854		INT002	Intermittent Claudication	60	0.050

855		SYN007	Synovitis	55	0.050

856		EMB004	Embryonal Carcinoma	57	0.050

857	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.050

858		BRR014	Barrett Esophagus	67	0.050

859	P	CHN012	Chondrosarcoma	57	0.050

860	c	MNN043	Meningioma, Familial	74	0.049

861		MNN042	Meningioma, Radiation-Induced	64	0.049

862		SPN021	Spinal Meningioma	40	0.049

863		END040	Endogenous Depression	55	0.049

864	P	GND004	Gonadal Dysgenesis	47	0.049

865		PSR001	Psoriatic Arthritis	63	0.049

866		CLF027	Cleft Palate, Isolated	67	0.049

867	P	OVR046	Ovarian Cyst	50	0.049

868		PRM024	Primary Angle-Closure Glaucoma	39	0.049

869		INT071	Intestinal Perforation	45	0.049

870	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	62	0.049

871		PTN001	Patent Foramen Ovale	57	0.049

872	P	ACT008	Actinic Keratosis	50	0.049

873		SCR011	Scrapie	37	0.049

874		BRN028	Brain Cancer	75	0.049

875		SPS057	Spasticity	38	0.049

876	P	BRN022	Bronchiectasis	60	0.048

877		SCR001	Secretory Meningioma	38	0.048

878		ADR007	Adrenoleukodystrophy	72	0.048

879		RRS014	Rare Surgical Neurologic Disease	33	0.048

880		EXT007	Extracutaneous Mastocytoma	39	0.048

881		STN013	Stenotrophomonas Maltophilia Infection	26	0.048

882	c	BSL007	Basal Cell Carcinoma	68	0.048

883	c	ANM038	Anemia, Autoimmune Hemolytic	61	0.048

884		PNC119	Pancreatic Neuroendocrine Tumor	48	0.048

885		PRT019	Protein-Losing Enteropathy	41	0.048

886	P	RTN016	Retinal Degeneration	56	0.048

887		ART004	Aortic Atherosclerosis	47	0.048

888		LYM002	Lymphoplasmacyte-Rich Meningioma	40	0.048

889	P	ZLL001	Zellweger Syndrome	56	0.048

890		ETN001	Eating Disorder	61	0.048

891		EXC002	Exocrine Pancreatic Insufficiency	41	0.048

892	c	LVR030	Liver Failure, Infantile, Transient	33	0.048

893		ERY003	Erythema Multiforme	57	0.048

894		PRX001	Peroxisomal Disease	45	0.048

895		DST016	Distomatosis	27	0.048

896		CHR066	Chronic Fatigue Syndrome	61	0.048

897		SPP011	Suppression of Tumorigenicity 12	61	0.048

898		WST005	West Nile Virus	56	0.048

899	P	LRY044	Larynx Cancer	59	0.047

900	P	ATR010	Atrial Heart Septal Defect	61	0.047

901		ISL099	Isolated Methylmalonic Acidemia	30	0.047

902		BNG077	Benign Idiopathic Neonatal Seizures	27	0.047

903		PRC001	Pericoronitis	40	0.047

904		UMB002	Umbilical Hernia	45	0.047

905	P	PLY041	Polymyositis	57	0.047

906		OTT002	Otitis Media	71	0.047

907	P	PTN014	Patent Ductus Arteriosus 1	60	0.047

908		NRT004	Neuritis	52	0.047

909	P	ALP061	Alopecia, Androgenetic, 1	51	0.047

910	c	NMN015	Niemann-Pick Disease, Type C1	67	0.047

911		SLC006	Silicosis	55	0.047

912	c	SCN007	Secondary Hyperparathyroidism	52	0.047

913	P	CLL015	Collagen Disease	46	0.047

914	P	MPL001	Maple Syrup Urine Disease	68	0.047

915		PRS034	Parasitic Helminthiasis Infectious Disease	48	0.047

916		ART002	Arts Syndrome	63	0.047

917	c	PRG020	Paragangliomas 3	36	0.047

918		DBT007	Diabetic Cataract	42	0.047

919		CRH005	Crohn's Colitis	56	0.047

920		SQM013	Squamous Cell Carcinoma, Head and Neck	81	0.047

921		MSC157	Muscular Dystrophy, Duchenne Type	70	0.047

922		KWS002	Kawasaki Disease	65	0.047

923		BRN002	Bronchiolitis	60	0.047

924		ADR004	Adrenal Cortical Adenocarcinoma	44	0.047

925		MYL005	Myelofibrosis	69	0.047

926		MCP006	Mucoepidermoid Carcinoma	53	0.047

927		SPN051	Spondylitis	53	0.046

928		EPD015	Epidemic Typhus	47	0.046

929		PTH003	Pathologic Nystagmus	53	0.046

930		FLR001	Filarial Elephantiasis	51	0.046

931		GLC036	Glucagonoma	45	0.046

932		LNG073	Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.046

933		VRC001	Varicocele	51	0.046

934		KLD004	Keloid Disorder	41	0.046

935		INT007	Intermediate Coronary Syndrome	58	0.046

936	P	ICH004	Ichthyosis	55	0.046

937	P	ATR005	Atrophic Gastritis	49	0.046

938		TBC004	Tobacco Addiction	65	0.046

939		MST004	Mast Cell Neoplasm	40	0.046

940		KHL003	Kohlschutter-Tonz Syndrome	63	0.046

941		STM006	Stomach Disease	50	0.046

942		CNN003	Conn's Syndrome	78	0.046

943		MMB001	Membranoproliferative Glomerulonephritis	54	0.046

944	c	HYP511	Hypogonadotropic Hypogonadism 15 with or Without Anosmia	29	0.046

945		GNG003	Gingival Recession	43	0.046

946		OBS168	Obsolete: Atypical Teratoid/rhabdoid Tumor	25	0.046

947		BRN014	Bronchopneumonia	47	0.046

948	P	HMN036	Hemangiopericytoma, Malignant	57	0.045

949	P	TTR001	Tetralogy of Fallot	70	0.045

950	P	MGL001	Megaloblastic Anemia	54	0.045

951		INT051	Intussusception	48	0.045

952	c	PSR017	Psoriasis 2	55	0.045

953	c	PSR023	Psoriasis 1	50	0.045

954	c	PSR028	Psoriasis 7	40	0.045

955	c	PSR018	Psoriasis 13	40	0.045

956	c	PSR032	Psoriasis 11	40	0.045

957		49X002	49,xxxxy Syndrome	39	0.045

958	P	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.045

959		APN008	Apnea, Obstructive Sleep	64	0.045

960		MYM001	Myoma	52	0.045

961		URT010	Ureteral Obstruction	46	0.045

962	c	PLY105	Polycystic Ovary Syndrome 1	38	0.045

963	P	CRV031	Cervical Adenocarcinoma	49	0.045

964		ARG002	Argininosuccinic Aciduria	59	0.045

965	P	ANL018	Analbuminemia	51	0.045

966		INF058	Inflammatory Myofibroblastic Tumor	44	0.045

967		ANT078	Antipyrine Metabolism	24	0.045

968		RBS001	Rabies	57	0.045

969		IRD001	Iridocyclitis	42	0.045

970		IRT001	Iritis	37	0.045

971		MCN017	Meconium Ileus	54	0.045

972		CHL013	Cholecystolithiasis	37	0.045

973		CMM004	Common Variable Immunodeficiency	69	0.045

974		NRL005	Neurilemmoma	62	0.045

975		HMZ003	Homozygous Familial Hypercholesterolemia	48	0.045

976	P	HYP265	Hypotonia	43	0.045

977		HPT066	Hepatoportal Sclerosis	24	0.045

978		THY030	Thyroid Gland Disease	53	0.045

979		SHW001	Shwartzman Phenomenon	35	0.045

980		INF009	Inflammatory Spondylopathy	29	0.045

981		ADN011	Adenoid Cystic Carcinoma	71	0.044

982		MLD001	Melioidosis	66	0.044

983		GLS018	Glass Syndrome	51	0.044

984		MNN009	Meningoencephalitis	50	0.044

985		BRN056	Bronchopulmonary Dysplasia	57	0.044

986		PPT001	Peptic Esophagitis	47	0.044

987		GNR004	Generalized Anxiety Disorder	55	0.044

988	P	GNG009	Gangliosidosis	45	0.044

989		PYR016	Pyridoxine Deficiency	31	0.044

990		HYP084	Hypopyon	39	0.044

991		HMG002	Hemoglobinuria	49	0.044

992	P	AVS003	Avascular Necrosis	43	0.044

993		CYT018	Cytochrome P450 2d6 Variant	28	0.044

994		ORL004	Oral Submucous Fibrosis	55	0.044

995	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.044

996		LYM017	Lyme Disease	64	0.044

997		CRT013	Carotid Stenosis	50	0.044

998		OVR094	Ovarian Epithelial Cancer	39	0.044

999	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	64	0.044

1000	P	HRD207	Hereditary Transthyretin Amyloidosis	26	0.044

1001		VNT037	Ventral Hernia	31	0.044

1002		OCL006	Ocular Hypertension	52	0.044

1003	P	STR020	Strabismus	57	0.044

1004		MCH006	Mechanical Strabismus	31	0.044

1005		PRT058	Pure Autonomic Failure	60	0.044

1006	P	RNV001	Renovascular Hypertension	49	0.043

1007		BCT004	Bacteriuria	48	0.043

1008		CTS005	Catastrophic Antiphospholipid Syndrome	44	0.043

1009		GRM010	Germ Cells Tumors	35	0.043

1010	c	CHL132	Cholestasis, Progressive Familial Intrahepatic, 1	54	0.043

1011	c	CHL136	Cholestasis, Progressive Familial Intrahepatic, 2	54	0.043

1012	P	MVM001	Movement Disease	63	0.043

1013		SRC027	Sarcoma, Synovial	60	0.043

1014		EXT034	Extrinsic Allergic Alveolitis	58	0.043

1015	P	FLL037	Follicular Lymphoma	67	0.043

1016		ADR022	Adrenomyeloneuropathy	39	0.043

1017		MYF001	Myofibroma	40	0.043

1018	P	CHR012	Chronic Granulomatous Disease	69	0.043

1019	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	44	0.043

1020	c	VSC053	Visceral Steatosis, Congenital	22	0.043

1021	P	SNS001	Sensorineural Hearing Loss	62	0.043

1022		IRR003	Irritant Dermatitis	46	0.043

1023		LKP003	Leukoplakia	40	0.043

1024		ABT001	Abetalipoproteinemia	68	0.043

1025		MYS004	Myiasis	39	0.043

1026		CRV040	Cervix Carcinoma	52	0.043

1027	P	RTN008	Retinitis Pigmentosa	77	0.042

1028		FBR047	Fibromyalgia	60	0.042

1029		MYX004	Myxedema	41	0.042

1030	P	MTC069	Mitochondrial Disorders	57	0.042

1031	c	MCL062	Mucolipidosis Ii Alpha/beta	67	0.042

1032		NWB001	Newborn Respiratory Distress Syndrome	58	0.042

1033		NPH003	Nephrocalcinosis	52	0.042

1034		ISL001	Islet Cell Tumor	47	0.042

1035		GLC008	Glucose Metabolism Disease	47	0.042

1036		CRT084	Creatinine Clearance Quantitative Trait Locus	26	0.042

1037	c	ADL017	Adult T-Cell Leukemia	59	0.042

1038		ORL013	Oral Lichen Planus	47	0.042

1039	P	DYS154	Dystonia	65	0.042

1040		FBR054	Fibroma	45	0.042

1041	P	PRS038	Personality Disorder	66	0.042

1042		GRW007	Growth Hormone Deficiency	48	0.042

1043		GST071	Gastrointestinal Carcinoma	42	0.042

1044		ATP014	Atp8b1 Deficiency	25	0.042

1045		CRB037	Cerebral Palsy	69	0.042

1046		ANT024	Anthrax Disease	56	0.042

1047	P	KRT007	Keratoconus	51	0.042

1048		LTX001	Latex Allergy	42	0.042

1049		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.042

1050	P	END039	Endodermal Sinus Tumor	44	0.042

1051		LPR001	Lepromatous Leprosy	50	0.042

1052		NCR004	Nocardiosis	44	0.042

1053		BRS099	Breast Ductal Carcinoma	63	0.042

1054		CHP002	Chops Syndrome	41	0.042

1055	P	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	65	0.041

1056	c	CHL134	Cholestasis, Benign Recurrent Intrahepatic, 1	56	0.041

1057	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	50	0.041

1058		DXT002	Dextrocardia with Situs Inversus	44	0.041

1059		SNG003	Single Ventricular Heart	31	0.041

1060		PST028	Post-Traumatic Stress Disorder	60	0.041

1061		ACT084	Acute Stress Disorder	42	0.041

1062	c	ART101	Aortic Valve Disease 2	67	0.041

1063	c	ALP101	Alpha-Thalassemia	63	0.041

1064		MCP033	Mucopolysaccharidoses	39	0.041

1065		SVR097	Severe Cutaneous Adverse Reaction	66	0.041

1066		HYD002	Hydronephrosis	58	0.041

1067		HYP043	Hyperandrogenism	48	0.041

1068		LYM009	Lymphocytic Choriomeningitis	45	0.041

1069		INT066	Interstitial Lung Disease	61	0.041

1070	P	MMB011	Membranous Nephropathy	54	0.041

1071		INT067	Interstitial Nephritis	46	0.041

1072	c	MST023	Mesothelioma, Malignant	59	0.041

1073	P	MYT002	Myotonic Dystrophy	52	0.041

1074		RHB001	Rhabdoid Cancer	62	0.041

1075		SLP001	Sleeping Sickness	47	0.041

1076		RHM001	Rheumatic Fever	56	0.041

1077		ATM052	Autoimmune Disease 1	38	0.041

1078	c	BCT013	Bacterial Pneumonia	49	0.041

1079		HPR003	Heparin-Induced Thrombocytopenia	49	0.041

1080		BLR004	Biliary Dyskinesia	33	0.041

1081