Search results for Calcium

2819 hits were found for Calcium

#	Family	MCID	Name	MIFTS	Score
1	c	CHN022	Chondrocalcinosis 2	35	8.354

2		NPH091	Nephrolithiasis, Calcium Oxalate	54	7.104

3		IMM066	Immunodeficiency 9	25	5.887

4		IMM065	Immunodeficiency 10	29	5.883

5		FML307	Familial Calcium Pyrophosphate Deposition	36	5.294

6		NPH009	Nephrolithiasis	58	3.447

7	P	CHN059	Chondrocalcinosis	48	3.131

8	c	BLD126	Bleeding Disorder, Platelet-Type, 18	20	2.938

9	c	AML006	Amelogenesis Imperfecta Hypoplastic Type, Ig	22	2.095

10		CMB055	Combined Immunodeficiency Due to Crac Channel Dysfunction	14	2.077

11	P	HYP069	Hyperparathyroidism	59	0.244

12	P	OST002	Osteoporosis	74	0.239

13	P	CLR023	Colorectal Cancer	99	0.211

14		GST049	Gastrointestinal System Cancer	62	0.208

15		GST071	Gastrointestinal Carcinoma	45	0.208

16	P	ADN016	Adenocarcinoma	70	0.190

17	c	LRG017	Large Intestine Cancer	63	0.189

18	P	INT068	Intestinal Disease	62	0.185

19		INT253	Intestinal Benign Neoplasm	57	0.185

20		BND020	Bone Disease	64	0.184

21		RCT017	Rectal Disease	43	0.183

22		CLN019	Colonic Disease	62	0.182

23	P	KDN018	Kidney Disease	71	0.170

24		RCK004	Rickets	66	0.164

25	c	SCN007	Secondary Hyperparathyroidism	55	0.163

26		BNR002	Bone Resorption Disease	54	0.163

27	P	RCT021	Rectum Cancer	58	0.159

28	c	PRM005	Primary Hyperparathyroidism	60	0.154

29		ISC004	Ischemia	67	0.153

30	c	HYP595	Hypertension, Essential	81	0.150

31	P	LKM002	Leukemia	72	0.150

32	P	HYP024	Hypoparathyroidism	55	0.145

33	c	CHR089	Chronic Kidney Failure	73	0.142

34	P	BRS047	Breast Cancer	100	0.142

35	P	LYM118	Lymphoma	69	0.141

36		CLC006	Calcinosis	53	0.132

37	P	MLG056	Malignant Hyperthermia	60	0.130

38		LYM024	Lymphatic System Disease	54	0.129

39	P	LYM033	Lymphoproliferative Syndrome	63	0.129

40		LYM019	Lymphosarcoma	53	0.129

41	P	HYP073	Hypersensitivity Reaction Type Iv Disease	50	0.128

42		CLN015	Colon Adenocarcinoma	57	0.126

43		RCT020	Rectum Adenocarcinoma	40	0.125

44	P	ALZ034	Alzheimer Disease	87	0.125

45		HYP025	Hyperphosphatemia	49	0.125

46	P	HRT032	Heart Disease	76	0.123

47	P	CRN018	Coronary Artery Anomaly	75	0.123

48		ANG054	Angina Pectoris	69	0.123

49	P	MYC007	Myocardial Infarction	78	0.121

50	P	ART022	Arthritis	77	0.121

51		RRR001	Rere-Related Disorders	59	0.120

52	P	PRS040	Prostate Cancer	93	0.120

53	P	LYM031	Lymphocytic Leukemia	61	0.120

54		URN009	Urinary System Disease	59	0.119

55	P	DBT009	Diabetes Mellitus	67	0.118

56	P	CRN300	Coronary Heart Disease 1	61	0.117

57		BNF002	Bone Fracture	48	0.117

58	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.116

59		ART140	Arteries, Anomalies of	66	0.116

60		LYM040	Lymphoblastic Lymphoma	57	0.114

61	c	ACT074	Acute Lymphocytic Leukemia	63	0.113

62		IMM136	Immune System Disease	57	0.113

63		VSC007	Vascular Disease	72	0.112

64		IDP073	Idiopathic Hypercalciuria	48	0.112

65		INS001	Insulinoma	64	0.112

66		LYM067	Lymphoid Leukemia	47	0.111

67	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	29	0.110

68	c	PRC016	Pre-Eclampsia	61	0.109

69		ISC006	Ischemic Heart Disease	72	0.108

70	P	ART021	Arteriosclerosis	61	0.108

71		LMB002	Lambert-Eaton Myasthenic Syndrome	58	0.108

72	P	OVR042	Ovarian Cancer	83	0.105

73		ALL026	Allergic Hypersensitivity Disease	68	0.105

74	P	HYP802	Hypocalcemia, Autosomal Dominant 1	66	0.105

75		END030	End Stage Renal Failure	60	0.105

76		BRK010	Burkitt Lymphoma	69	0.101

77		ACQ007	Acquired Immunodeficiency Syndrome	66	0.101

78		ADN018	Adenoma	64	0.101

79		HMN014	Human Immunodeficiency Virus Infectious Disease	62	0.101

80	P	LNG032	Lung Cancer	99	0.100

81	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	92	0.100

82	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	63	0.100

83	P	FML068	Familial Hypocalciuric Hypercalcemia	50	0.098

84		MYL069	Myeloma, Multiple	85	0.098

85		LYM133	Lymphoma, Hodgkin, Classic	72	0.097

86	c	GLL024	Gallbladder Disease 1	45	0.097

87		OCL033	Oculocerebral Syndrome with Hypopigmentation	45	0.097

88		HYP266	Hypoxia	63	0.096

89	P	ECL001	Eclampsia	58	0.095

90		SPS003	Spastic Diplegia	55	0.095

91	c	PRS136	Prostate Cancer, Hereditary, 6	40	0.095

92	c	PRS130	Prostate Cancer, Hereditary, 8	37	0.095

93		ESP021	Esophageal Cancer	82	0.094

94		GST053	Gastric Cancer	78	0.094

95	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	40	0.094

96	P	ART023	Arthropathy	68	0.094

97		URM002	Uremia	53	0.094

98		CLN045	Colonic Benign Neoplasm	48	0.094

99	P	RHM011	Rheumatoid Arthritis	81	0.093

100	P	EPL164	Epilepsy	72	0.093

101		AGN016	Aging	63	0.093

102	c	BNM029	Bone Mineral Density Quantitative Trait Locus 15	46	0.093

103	P	PRD008	Periodontitis	66	0.091

104		JNT002	Joint Disorders	64	0.091

105		TTH006	Tooth Disease	54	0.091

106		CNG034	Congestive Heart Failure	70	0.090

107	P	NRP001	Neuropathy	63	0.090

108		ISL119	Isolated Optic Neuritis	34	0.090

109		THY028	Thyroid Cancer	72	0.089

110	P	ATR011	Atrial Fibrillation	69	0.089

111		OST011	Osteomalacia	52	0.089

112		NTR005	Nutritional Deficiency Disease	59	0.088

113	P	PNC044	Pancreatitis	62	0.087

114		ACT103	Acute Lymphoblastic Leukemia, Childhood	55	0.087

115		DNT012	Dental Caries	52	0.087

116		NPH003	Nephrocalcinosis	50	0.087

117	P	PNC035	Pancreatic Cancer	82	0.086

118		LPD008	Lipid Metabolism Disorder	65	0.086

119		END035	Endocrine Gland Cancer	57	0.086

120	P	GLM045	Glioma	55	0.085

121		CYS001	Cystic Fibrosis	82	0.084

122		OST017	Osteomyelitis	64	0.083

123	P	DRR001	Diarrhea	58	0.083

124		GST050	Gastrointestinal System Disease	67	0.082

125		HYP060	Hyperinsulinism	57	0.082

126	P	MSC005	Muscular Dystrophy	66	0.081

127		CLR108	Colorectal Adenoma	64	0.081

128		BRR014	Barrett Esophagus	70	0.080

129		GT001	Gout	62	0.080

130		PNC034	Pancreas Disease	59	0.079

131	c	PNC106	Pancreatic Agenesis 1	51	0.079

132		PRT030	Parathyroid Gland Disease	50	0.079

133		LYM143	Lymphoma, Non-Hodgkin, Familial	73	0.078

134		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.078

135	P	PSD015	Pseudohypoparathyroidism	51	0.078

136		RTR008	Root Resorption	46	0.078

137	P	INF032	Infertility	60	0.077

138	P	SCH015	Schizophrenia	73	0.076

139		DPR016	Depression	72	0.076

140		STM006	Stomach Disease	55	0.076

141		OST012	Osteoarthritis	80	0.075

142	P	LVR013	Liver Disease	76	0.075

143		ESP023	Esophageal Disease	59	0.075

144	c	ADL052	Adult Acute Lymphocytic Leukemia	45	0.075

145		SKN016	Skin Disease	68	0.074

146		RNL011	Renal Osteodystrophy	49	0.074

147		FSH001	Fish-Eye Disease	50	0.073

148	P	HPT023	Hepatocellular Carcinoma	96	0.072

149		CRB039	Cerebrovascular Disease	70	0.072

150	P	AST007	Astrocytoma	52	0.072

151		SKN027	Skin Conditions	51	0.072

152		TRP008	Tropical Calcific Pancreatitis	50	0.072

153	P	ENC018	Encephalopathy	65	0.071

154		FXF002	Fox-Fordyce Disease	40	0.071

155		OST097	Osteoporotic Fracture	36	0.071

156	P	MLT020	Multiple Sclerosis	75	0.070

157		SRC014	Sarcoma	70	0.070

158		THR024	Thrombosis	64	0.070

159		GND003	Gonadal Disease	49	0.070

160	c	AMY091	Amyotrophic Lateral Sclerosis 1	90	0.069

161	P	PLM037	Pulmonary Hypertension	77	0.069

162		PNC033	Pancreas Adenocarcinoma	67	0.069

163		PRD007	Periodontal Disease	66	0.069

164		MLN008	Melanoma	63	0.069

165	P	CRD132	Cardiac Conduction Defect	63	0.069

166		ZLL002	Zollinger-Ellison Syndrome	58	0.069

167		PRM020	Premenstrual Tension	53	0.069

168		MTB004	Metabolic Acidosis	50	0.069

169	P	HMP006	Hemiplegic Migraine	49	0.069

170	P	LTR001	Lateral Sclerosis	60	0.068

171	c	SML038	Small Cell Cancer of the Lung	68	0.067

172		ATM095	Autoimmune Disease	68	0.067

173		GST040	Gastric Adenocarcinoma	66	0.067

174	c	ACT027	Acute Pancreatitis	59	0.067

175	c	HYP752	Hypocalciuric Hypercalcemia, Familial, Type I	46	0.067

176	P	MSC007	Muscle Hypertrophy	64	0.066

177		ATH013	Atherosclerosis Susceptibility	60	0.066

178		RTC009	Reticulum Cell Sarcoma	55	0.066

179		GNG012	Gingival Overgrowth	53	0.066

180		PLM017	Pulmonary Alveolar Microlithiasis	52	0.066

181		RTC005	Reticulosarcoma	48	0.066

182		INT038	Interdigitating Dendritic Cell Sarcoma	43	0.066

183		PHS001	Phosphorus Metabolism Disease	40	0.066

184		STR067	Stroke, Ischemic	82	0.064

185	P	DLT002	Dilated Cardiomyopathy	75	0.064

186	P	PNM007	Pneumonia	72	0.064

187		PRT037	Pertussis	70	0.064

188		THY111	Thyroid Carcinoma, Familial Medullary	70	0.064

189		CNN005	Connective Tissue Disease	67	0.064

190	P	PRP019	Peripheral Nervous System Disease	66	0.064

191		RHM027	Rheumatic Disease	65	0.064

192		HYP056	Hypoglycemia	64	0.064

193	P	OVR049	Ovarian Disease	63	0.064

194	P	HYP061	Hypertrophic Cardiomyopathy	59	0.064

195		PLC008	Placenta Disease	59	0.064

196		HMT018	Hematopoietic Stem Cell Transplantation	59	0.064

197		CRN030	Coronary Stenosis	52	0.064

198	c	ATR087	Atrial Standstill 1	70	0.063

199		DMN002	Dementia	69	0.063

200		BRS051	Breast Disease	66	0.063

201		OST159	Osteogenic Sarcoma	66	0.063

202	P	CRD119	Cardiac Arrest	66	0.063

203		GLC003	Glucose Intolerance	59	0.063

204		SQM006	Squamous Cell Carcinoma	58	0.063

205		BRN080	Brain Ischemia	43	0.063

206	c	SYS001	Systemic Lupus Erythematosus	88	0.062

207		AST005	Asthma	81	0.062

208	P	PHC003	Pheochromocytoma	72	0.062

209	P	LPS004	Lupus Erythematosus	69	0.062

210	P	HYP086	Hypothyroidism	66	0.062

211		MSC157	Muscular Dystrophy, Duchenne Type	65	0.062

212		MTH009	Mouth Disease	64	0.062

213		MYC005	Myocardial Stunning	47	0.062

214	P	HYP776	Hyperparathyroidism, Neonatal Severe	42	0.062

215		INS024	Insulin-Like Growth Factor I	82	0.061

216		GLB002	Glioblastoma	74	0.061

217	P	PLY011	Polycystic Ovary Syndrome	64	0.061

218	P	BNC003	Bone Cancer	62	0.061

219	P	CTR002	Cataract	59	0.061

220		CNS004	Constipation	58	0.061

221		BRN071	Brain Injury	55	0.061

222	P	ATS308	Autosomal Dominant Cerebellar Ataxia	55	0.061

223		MLR006	Male Reproductive Organ Cancer	49	0.061

224		HMN044	Human Immunodeficiency Virus Type 1	75	0.059

225	P	MYL006	Myeloid Leukemia	67	0.059

226		HYP066	Hyperglycemia	64	0.059

227		ERY003	Erythema Multiforme	62	0.059

228	P	EXN002	Exanthem	62	0.059

229	P	TRC086	Trichohepatoenteric Syndrome 1	60	0.059

230	P	PRM002	Primary Hyperoxaluria	58	0.059

231	c	MCR113	Microvascular Complications of Diabetes 3	58	0.059

232	c	ACT075	Acute Myocardial Infarction	57	0.059

233		GLC008	Glucose Metabolism Disease	53	0.059

234		CLC001	Calciphylaxis	52	0.059

235	c	FML023	Familial Hemiplegic Migraine	50	0.059

236	c	MCR120	Microvascular Complications of Diabetes 7	46	0.059

237	c	MCR130	Microvascular Complications of Diabetes 6	43	0.059

238	c	MCR133	Microvascular Complications of Diabetes 4	43	0.059

239		INT323	Intraocular Pressure Quantitative Trait Locus	38	0.059

240	c	TRC078	Trichohepatoenteric Syndrome 2	35	0.059

241	P	BPL003	Bipolar Disorder	61	0.058

242		DFF005	Diffuse Large B-Cell Lymphoma	58	0.058

243	P	RNL007	Renal Tubular Acidosis	51	0.058

244		PRP017	Periapical Periodontitis	48	0.058

245		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	34	0.058

246		CRH001	Crohn's Disease	79	0.057

247	P	HPT021	Hepatitis	73	0.057

248	P	HNT016	Huntington Disease	73	0.057

249	P	PLY014	Polycystic Kidney Disease	62	0.057

250		MCS002	Mucositis	60	0.057

251		SFT003	Soft Tissue Sarcoma	59	0.057

252	c	MLG074	Malignant Mesenchymoma	54	0.057

253	P	CLL015	Collagen Disease	52	0.057

254	c	BDY007	Body Mass Index Quantitative Trait Locus 1	48	0.057

255	c	PLM164	Pulmonary Hypertension, Primary, 1	70	0.055

256	P	ATS364	Autism	67	0.055

257	P	PSR002	Psoriasis	67	0.055

258		PRT010	Parathyroid Carcinoma	64	0.055

259		STT001	Status Epilepticus	60	0.055

260		BRN106	Burns	59	0.055

261		TXC002	Toxic Encephalopathy	57	0.055

262		NTR046	Neutrophil Migration	56	0.055

263		MCN001	Mucinous Adenocarcinoma	54	0.055

264		CYS014	Cystadenocarcinoma	53	0.055

265		PRS042	Prostate Disease	47	0.055

266		GLC086	Glucocorticoid-Induced Osteoporosis	46	0.055

267	P	HRD086	Hereditary Hypophosphatemic Rickets	45	0.055

268		ESP025	Esophagus Adenocarcinoma	43	0.055

269		APP009	Appendix Adenocarcinoma	43	0.055

270		ATX038	Ataxia and Polyneuropathy, Adult-Onset	42	0.055

271		DNT014	Dental Pulp Disease	41	0.055

272		SCK003	Sickle Cell Anemia	74	0.054

273		PRP027	Peripheral Vascular Disease	72	0.054

274		LVR012	Liver Cirrhosis	67	0.054

275	P	ENC004	Encephalitis	66	0.054

276	P	LNG028	Long Qt Syndrome	66	0.054

277		SPN186	Spinal Cord Injury	66	0.054

278		GST045	Gastroenteritis	65	0.054

279	P	BCL006	B-Cell Lymphomas	64	0.054

280	c	ADL017	Adult T-Cell Leukemia	62	0.054

281		HDC001	Headache	62	0.054

282	c	ACT073	Acute Leukemia	62	0.054

283		WVR001	Weaver Syndrome	60	0.054

284		TRN015	Transient Cerebral Ischemia	59	0.054

285		NRT004	Neuritis	58	0.054

286		PNM001	Pneumocystosis	58	0.054

287		MMM001	Mammary Paget's Disease	56	0.054

288	P	TCL004	T-Cell Leukemia	53	0.054

289	P	SCL057	Scoliosis, Isolated 1	45	0.054

290		BCL008	B-Cell Childhood Acute Lymphoblastic Leukemia	35	0.054

291		ENM002	Enamel Erosion	29	0.054

292		DSS008	Disease of Mental Health	71	0.053

293		LPT014	Leptin Deficiency or Dysfunction	70	0.053

294		DRM006	Dermatitis	69	0.053

295		FTT001	Fatty Liver Disease	66	0.053

296	P	MYP004	Myopathy	64	0.053

297		OVR029	Ovarian Hyperstimulation Syndrome	64	0.053

298		RNL114	Renal Cell Carcinoma, Nonpapillary	63	0.053

299	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	61	0.053

300		NRM005	Neuromuscular Disease	61	0.053

301	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	60	0.053

302	P	MSC033	Muscle Disorders	57	0.053

303	P	INF037	Inflammatory Bowel Disease	56	0.053

304		CRD223	Cardiac Arrhythmia	55	0.053

305		CYS039	Cystic Kidney Disease	55	0.053

306		PLS025	Plasmablastic Lymphoma	53	0.053

307	P	DDN001	Duodenal Ulcer	51	0.053

308		HYP017	Hypophosphatemia	49	0.053

309	P	FML187	Familial Hypertension	42	0.053

310		LYM048	Lymphoma, Large-Cell, Immunoblastic	34	0.053

311		BLD165	Blood Group, Colton System	34	0.053

312		CRY024	Crystal Arthropathies	27	0.053

313		RPD005	Rapidly Involuting Congenital Hemangioma	25	0.053

314	P	HYP607	Hypercholesterolemia, Familial	81	0.051

315	P	MCR115	Microvascular Complications of Diabetes 5	70	0.051

316		GST092	Gastroesophageal Reflux	66	0.051

317	P	THL005	Thalassemia	65	0.051

318		CHL065	Cholangiocarcinoma	64	0.051

319	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	60	0.051

320	P	HYP076	Hyperthyroidism	55	0.051

321	P	MYT002	Myotonic Dystrophy	52	0.051

322		GRN017	Granulocytopenia	51	0.051

323		WTH001	Withdrawal Disorder	50	0.051

324		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	49	0.051

325	c	PRC031	Preeclampsia/eclampsia 1	41	0.051

326		SPN125	Spondyloenchondrodysplasia	31	0.051

327		MYT026	Myotonia Atrophica	28	0.051

328	c	LKM061	Leukemia, Acute Myeloid	81	0.050

329	c	LKM071	Leukemia, Chronic Lymphocytic	78	0.050

330	c	LKM063	Leukemia, Chronic Myeloid	73	0.050

331		ANX010	Anxiety	73	0.050

332		MNT002	Mental Depression	65	0.050

333	P	THR014	Thrombocytopenia	64	0.050

334		BCT022	Bacterial Infectious Disease	62	0.050

335	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	62	0.050

336		DBT010	Diabetic Neuropathy	60	0.050

337	P	PGT001	Paget's Disease of Bone	59	0.050

338		EWN002	Ewing's Family of Tumors	57	0.050

339		LNG031	Lung Benign Neoplasm	56	0.050

340		OBS082	Obstructive Nephropathy	52	0.050

341	c	MTR002	Mitral Valve Insufficiency	50	0.050

342		CNN004	Connective Tissue Cancer	45	0.050

343		GST012	Gastroesophageal Junction Adenocarcinoma	42	0.050

344	c	LKM004	Leukemia, B-Cell, Chronic	38	0.050

345		ACT118	Acute Non Lymphoblastic Leukemia	32	0.050

346		NTR027	Neutrophil Actin Dysfunction	32	0.050

347	P	SRC025	Sarcoidosis 1	76	0.048

348		MRF001	Marfan Syndrome	75	0.048

349	P	NRV007	Nervous System Disease	71	0.048

350		DWN001	Down Syndrome	71	0.048

351		ART016	Aortic Aneurysm	71	0.048

352		ACR007	Acromegaly	70	0.048

353		VRL011	Viral Infectious Disease	68	0.048

354		THR100	Thrombocytopenic Purpura, Autoimmune	67	0.048

355		OST003	Osteonecrosis	67	0.048

356	c	ACT210	Acute Respiratory Distress Syndrome	66	0.048

357	P	NTR004	Neutropenia	60	0.048

358		PTT009	Pituitary Gland Disease	59	0.048

359	P	SCL018	Scoliosis	58	0.048

360		TRM010	Traumatic Brain Injury	56	0.048

361		HYP005	Hypokalemia	55	0.048

362	c	OVR114	Ovarian Cancer 1	51	0.048

363	P	NRB010	Neuroblastoma 1	51	0.048

364		THY030	Thyroid Gland Disease	50	0.048

365		ADR040	Adrenal Gland Pheochromocytoma	49	0.048

366	c	CHR579	Chiari Malformation Type Ii	49	0.048

367	c	CRN243	Carney Complex, Type 1	45	0.048

368		TND005	Tendinitis	45	0.048

369		BNS001	Bone Osteosarcoma	39	0.048

370		HDG004	Hodgkin's Granuloma	30	0.048

371		HDG006	Hodgkin's Paragranuloma	22	0.048

372		TCL018	T-Cell Childhood Acute Lymphocytic Leukemia	21	0.048

373		CRN167	Caronte	19	0.048

374		ETH012	Ethylene Glycol Poisoning	18	0.048

375		RCT006	Rectum Mucinous Adenocarcinoma	15	0.048

376	P	INF038	Influenza	75	0.046

377		PLM129	Pulmonary Disease, Chronic Obstructive	75	0.046

378		MNT001	Mantle Cell Lymphoma	73	0.046

379		ACR006	Aceruloplasminemia	73	0.046

380		MYL009	Myelodysplastic Syndrome	70	0.046

381		LNG099	Lung Disease	70	0.046

382		ACH004	Achondroplasia	68	0.046

383	c	SCL052	Scleroderma, Familial Progressive	67	0.046

384	P	NRV006	Nervous System Cancer	60	0.046

385		CHL014	Cholera	60	0.046

386	P	ANP001	Anaplastic Large Cell Lymphoma	60	0.046

387		CHL068	Cholestasis	60	0.046

388		TRD006	Tardive Dyskinesia	60	0.046

389	c	PRD040	Periodontitis, Chronic	59	0.046

390		RTN018	Retinal Disease	58	0.046

391		PRP080	Peripheral Artery Disease	56	0.046

392		BLR006	Biliary Tract Disease	52	0.046

393		PLP001	Pulpitis	50	0.046

394		CRB004	Cerebral Artery Occlusion	47	0.046

395		GST030	Gastrinoma	43	0.046

396	c	TCL001	T-Cell Adult Acute Lymphocytic Leukemia	41	0.046

397		IDP070	Idiopathic Scoliosis	40	0.046

398		LYM049	Lymphoma, Small Cleaved-Cell, Diffuse	37	0.046

399		CLN002	Colon Mucinous Adenocarcinoma	32	0.046

400		SML025	Small Non-Cleaved Cell Lymphoma	25	0.046

401		RCT013	Rectum Signet Ring Adenocarcinoma	17	0.046

402		LRG015	Large Intestine Adenoma	17	0.046

403	c	JVN010	Juvenile Rheumatoid Arthritis	70	0.045

404		BRT054	Brittle Bone Disorder	70	0.045

405	c	THR092	Thrombophilia Due to Thrombin Defect	69	0.045

406		TTN003	Tetanus	66	0.045

407	P	TXP001	Toxoplasmosis	66	0.045

408	c	CNT035	Central Nervous System Disease	65	0.045

409		INT002	Intermittent Claudication	64	0.045

410		PPT005	Peptic Ulcer Disease	63	0.045

411	c	ART101	Aortic Valve Disease 2	63	0.045

412		HYP020	Hyperprolactinemia	63	0.045

413	P	SZR006	Seizure Disorder	61	0.045

414	P	HMR003	Hemorrhagic Disease	59	0.045

415	P	TRM003	Tremor	55	0.045

416		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	55	0.045

417		PRT029	Parathyroid Adenoma	52	0.045

418	P	BLD051	Blood Coagulation Disease	52	0.045

419		PRD004	Prediabetes Syndrome	51	0.045

420	c	SPN309	Spinocerebellar Ataxia 6	49	0.045

421		CHR074	Choriocarcinoma	49	0.045

422	P	LCT002	Lactose Intolerance	47	0.045

423		RST023	Resting Heart Rate, Variation in	44	0.045

424		STT004	Steatorrhea	43	0.045

425		VSC008	Vascular Hemostatic Disease	43	0.045

426		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	38	0.045

427		DNT006	Dental Pulp Necrosis	34	0.045

428		MYT011	Myotonia	34	0.045

429		CL1004	Col1a1/2-Related Osteogenesis Imperfecta	31	0.045

430		MNS002	Mini Stroke	25	0.045

431		HRN028	Horns in Sheep	24	0.045

432	P	RTN008	Retinitis Pigmentosa	80	0.043

433	P	GRF003	Graft-Versus-Host Disease	71	0.043

434	P	BLD134	Bladder Cancer	70	0.043

435	P	TTR001	Tetralogy of Fallot	70	0.043

436		CNN003	Conn's Syndrome	70	0.043

437	c	HPT016	Hepatitis B	70	0.043

438	P	PSD087	Pseudoxanthoma Elasticum	68	0.043

439	P	FLL037	Follicular Lymphoma	67	0.043

440	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	66	0.043

441		GLB015	Glioblastoma Multiforme	64	0.043

442		IRR002	Irritable Bowel Syndrome	64	0.043

443		RSP006	Respiratory System Disease	64	0.043

444	P	BLD062	Bile Duct Cancer	64	0.043

445		MYL031	Myeloproliferative Neoplasm	64	0.043

446	P	NPH012	Nephrotic Syndrome	63	0.043

447	P	GLL020	Gallbladder Disease	62	0.043

448	c	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.043

449	P	EPS003	Episodic Ataxia	59	0.043

450	P	CHL002	Childhood Absence Epilepsy	59	0.043

451		GLM004	Gliomatosis Cerebri	58	0.043

452	P	RTN016	Retinal Degeneration	56	0.043

453		NRN004	Neuroendocrine Tumor	56	0.043

454		PRS036	Parasitic Protozoa Infectious Disease	52	0.043

455	P	SLL003	Salla Disease	52	0.043

456	P	BLD036	Bile Duct Disease	51	0.043

457		INT007	Intermediate Coronary Syndrome	50	0.043

458		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	48	0.043

459		BRN041	Bornholm Eye Disease	45	0.043

460		PRS063	Paresthesia	45	0.043

461		OVR094	Ovarian Epithelial Cancer	41	0.043

462	c	MGR032	Migraine, Familial Hemiplegic, 1	40	0.043

463	c	PGT007	Paget Disease of Bone 3	39	0.043

464		DNT007	Dentin Sensitivity	39	0.043

465		HML018	Homologous Wasting Disease	24	0.043

466		NRL016	Neural Tube Defects	79	0.041

467		BRN028	Brain Cancer	72	0.041

468	c	JVN004	Juvenile Myelomonocytic Leukemia	70	0.041

469		ALC007	Alcohol Dependence	69	0.041

470		ANR007	Anorexia Nervosa	68	0.041

471		CLT003	Colitis	65	0.041

472	P	CHR285	Chronic Myelomonocytic Leukemia	64	0.041

473		PLM033	Pulmonary Embolism	64	0.041

474	P	OST001	Osteopetrosis	63	0.041

475		ANT024	Anthrax Disease	61	0.041

476	c	VSC019	Vesicoureteral Reflux 1	58	0.041

477	P	CNT005	Central Nervous System Lymphoma	57	0.041

478	c	ACT068	Acute Cystitis	56	0.041

479	P	NNL004	Nonalcoholic Fatty Liver Disease	56	0.041

480		SNS003	Sensory Peripheral Neuropathy	56	0.041

481	P	MSC003	Muscular Atrophy	56	0.041

482		GLL018	Gallbladder Cancer	55	0.041

483		THR004	Thrombocytosis	55	0.041

484		PRP016	Paraplegia	54	0.041

485		HPR003	Heparin-Induced Thrombocytopenia	53	0.041

486	c	PRM226	Primary Central Nervous System Lymphoma	52	0.041

487	c	PNC128	Pain - Chronic	49	0.041

488		PRT035	Peritoneum Cancer	47	0.041

489	c	HYP794	Hyperoxaluria, Primary, Type I	45	0.041

490		OST004	Osteitis Fibrosa	45	0.041

491	P	RNL045	Renal Tubular Acidosis, Distal	45	0.041

492		BLD054	Blood Protein Disease	43	0.041

493		CRB085	Cerebral Hemorrhage	42	0.041

494	P	CRB059	Cerebellar Degeneration	40	0.041

495	c	BST008	Bestrophinopathy, Autosomal Recessive	33	0.041

496	c	MCL042	Macular Degeneration, Age-Related, 1	83	0.039

497	P	RTT002	Rett Syndrome	82	0.039

498		PLY001	Polycythemia Vera	75	0.039

499		MYL005	Myelofibrosis	69	0.039

500	P	SYS005	Systemic Scleroderma	67	0.039

501	P	DRM010	Dermatomyositis	65	0.039

502	P	ADL010	Adult Respiratory Distress Syndrome	64	0.039

503	P	RHN004	Rhinitis	64	0.039

504		HMT002	Hematologic Cancer	64	0.039

505		GST033	Gestational Diabetes	63	0.039

506		GTL001	Gitelman Syndrome	62	0.039

507		HMR039	Hemorrhage, Intracerebral	62	0.039

508	P	BRG001	Brugada Syndrome	61	0.039

509		CCC001	Coccidioidomycosis	61	0.039

510		EMB004	Embryonal Carcinoma	59	0.039

511		NWB001	Newborn Respiratory Distress Syndrome	59	0.039

512	P	DNT020	Dent Disease 1	59	0.039

513		PLM010	Pulmonary Edema	59	0.039

514	P	KDN017	Kidney Cancer	59	0.039

515		ILT001	Ileitis	59	0.039

516		GST023	Gastric Ulcer	58	0.039

517	c	ACT020	Acute T Cell Leukemia	57	0.039

518		SCK005	Sickle Cell Disease	57	0.039

519	P	PMP001	Pemphigus	56	0.039

520	P	VNS003	Venous Insufficiency	54	0.039

521		SPN041	Spinal Cord Disease	54	0.039

522		ACT058	Active Peptic Ulcer Disease	53	0.039

523		MSC190	Muscular Disease	53	0.039

524	P	LCT001	Lactic Acidosis	52	0.039

525		HYD002	Hydronephrosis	52	0.039

526		HMS001	Hemosiderosis	52	0.039

527	P	RNV001	Renovascular Hypertension	52	0.039

528		CRN019	Coronary Artery Vasospasm	50	0.039

529	c	CHR431	Chronic Venous Insufficiency	50	0.039

530		KRT008	Keratopathy	48	0.039

531		EPD070	Epidermoid Cysts	48	0.039

532		NRR001	Neuroretinitis	47	0.039

533		MRG013	Mirage Syndrome	45	0.039

534	P	JVN024	Juvenile Hereditary Hemochromatosis	44	0.039

535		BRN039	Bronchial Neoplasm	43	0.039

536	c	PLY105	Polycystic Ovary Syndrome 1	42	0.039

537	P	CHR084	Chromosomal Disease	42	0.039

538		BNG018	Benign Paroxysmal Positional Nystagmus	40	0.039

539	c	APL023	Aplasia Cutis Congenita, Nonsyndromic	40	0.039

540		MSC004	Muscle Tissue Disease	39	0.039

541		RSP007	Respiratory Distress Syndrome, Infant	37	0.039

542	P	VRT013	Vertigo, Benign Recurrent	37	0.039

543		GRM010	Germ Cells Tumors	35	0.039

544	c	LKM005	Leukemia, T-Cell, Chronic	31	0.039

545	P	LNG064	Lung Cancer Susceptibility 3	79	0.037

546	c	SPN225	Spondyloarthropathy 1	75	0.037

547	c	HMC039	Hemochromatosis, Type 1	74	0.037

548	c	BTT014	Beta-Thalassemia	72	0.037

549	P	RTN024	Retinoblastoma	72	0.037

550		CRP001	Carpal Tunnel Syndrome	71	0.037

551		BRC012	Brucellosis	70	0.037

552	P	SLP006	Sleep Apnea	70	0.037

553		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	69	0.037

554	c	MGR028	Migraine with or Without Aura 1	69	0.037

555		PRT036	Peritonitis	66	0.037

556		VRC005	Varicose Veins	66	0.037

557	P	END044	Endometriosis	65	0.037

558		MDD011	Mood Disorder	65	0.037

559		INT066	Interstitial Lung Disease	65	0.037

560	P	AMY004	Amyloidosis	64	0.037

561		WLL001	Williams-Beuren Syndrome	63	0.037

562		GNG013	Gingivitis	63	0.037

563	P	MYS005	Myositis	61	0.037

564	P	GLM007	Glomerulonephritis	61	0.037

565		CRH005	Crohn's Colitis	61	0.037

566	P	GRV001	Graves' Disease	61	0.037

567	P	SJG008	Sjogren Syndrome	60	0.037

568	P	SML001	Small Cell Carcinoma	60	0.037

569		IRN002	Iron Metabolism Disease	60	0.037

570	c	INF071	Inflammatory Bowel Disease 1	60	0.037

571	c	PRG042	Progressive Familial Heart Block, Type Ia	59	0.037

572	P	CYS018	Cystitis	58	0.037

573		MRG003	Marginal Zone B-Cell Lymphoma	58	0.037

574	P	ANG015	Angioedema	57	0.037

575	c	GRV008	Graves Disease 1	57	0.037

576	P	MLT074	Multiple Endocrine Neoplasia	56	0.037

577	P	DBT005	Diabetes Insipidus	55	0.037

578		TST014	Testicular Cancer	54	0.037

579		GTR002	Goiter	54	0.037

580		LMB062	Limb Ischemia	54	0.037

581		PNC041	Pancreatic Ductal Adenocarcinoma	54	0.037

582		ATR057	Atrioventricular Block	54	0.037

583		STM007	Stomatitis	53	0.037

584		OVR063	Overnutrition	53	0.037

585		CRT013	Carotid Stenosis	53	0.037

586	P	OVR046	Ovarian Cyst	52	0.037

587		CHL061	Childhood Leukemia	52	0.037

588		KLD001	Keloids	51	0.037

589		MTR003	Mitral Valve Stenosis	51	0.037

590		SPL004	Splenic Marginal Zone Lymphoma	50	0.037

591		CCC002	Coccidiosis	50	0.037

592		GRW007	Growth Hormone Deficiency	49	0.037

593		BNN003	Bone Inflammation Disease	48	0.037

594		MMM006	Mammographic Density	47	0.037

595	c	MLG068	Malignant Glioma	47	0.037

596		PRP056	Porphyria, Acute Hepatic	47	0.037

597		SPN369	Spinal Disease	47	0.037

598		SYS003	Systolic Heart Failure	46	0.037

599		NDL024	Nodal Marginal Zone Lymphoma	43	0.037

600		MLG086	Malignant Hyperthermia Susceptibility	41	0.037

601		SCR035	Sacral Agenesis with Vertebral Anomalies	41	0.037

602		PRM050	Primary Orthostatic Tremor	33	0.037

603		CRC034	Carcinoma Showing Thymus-Like Differentiation	28	0.037

604		MLR004	Malaria	84	0.035

605		KPS004	Kaposi Sarcoma	77	0.035

606		PHN003	Phenylketonuria	74	0.035

607	P	DBT085	Diabetes Mellitus, Insulin-Dependent	73	0.035

608	c	MLT156	Multiple Endocrine Neoplasia, Type I	71	0.035

609		CMM004	Common Variable Immunodeficiency	71	0.035

610	P	DRM053	Dermatitis, Atopic	71	0.035

611		ALL003	Allergic Rhinitis	70	0.035

612		BRN024	Bronchitis	70	0.035

613	P	ESS003	Essential Thrombocythemia	69	0.035

614		LSH001	Leishmaniasis	69	0.035

615	P	INT143	Interstitial Cystitis	66	0.035

616	P	VSC011	Vasculitis	66	0.035

617	P	SKN015	Skin Carcinoma	65	0.035

618	P	THY023	Thymoma	63	0.035

619	P	UVT001	Uveitis	62	0.035

620	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	61	0.035

621	P	EPL140	Epilepsy, Idiopathic Generalized	61	0.035

622	P	CMR001	Camurati-Engelmann Disease	61	0.035

623		HRY003	Hairy Cell Leukemia	60	0.035

624	P	PNS012	Paine Syndrome	60	0.035

625	c	INS002	in Situ Carcinoma	60	0.035

626	c	SVR001	Severe Acute Respiratory Syndrome	60	0.035

627		PRP030	Purpura	60	0.035

628	P	PLY018	Polycythemia	60	0.035

629		CFF002	Coffin-Lowry Syndrome	59	0.035

630	c	ACT135	Acute Graft Versus Host Disease	58	0.035

631	c	EPS035	Episodic Ataxia, Type 2	57	0.035

632	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	56	0.035

633		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.035

634	P	CTN015	Cutaneous T Cell Lymphoma	56	0.035

635		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	55	0.035

636		CLR109	Colorectal Adenocarcinoma	54	0.035

637		MYL004	Myelodysplastic Myeloproliferative Cancer	54	0.035

638		PNG002	Pain Agnosia	54	0.035

639		ENT011	Enterocolitis	54	0.035

640	P	INN002	Inner Ear Disease	54	0.035

641	P	BRT004	Bartter Disease	53	0.035

642		HYP080	Hypogonadism	53	0.035

643		TST015	Testicular Disease	52	0.035

644	P	SHR001	Short Bowel Syndrome	52	0.035

645		TMT001	Timothy Syndrome	52	0.035

646		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.035

647		ADT003	Auditory System Disease	52	0.035

648		KRT002	Keratomalacia	51	0.035

649		CHL004	Cholelithiasis	51	0.035

650	c	BPL002	Bipolar I Disorder	49	0.035

651	P	ART018	Aortic Valve Insufficiency	49	0.035

652		MLK006	Milk Allergy	48	0.035

653	P	ART084	Arteriovenous Fistula	48	0.035

654		HRT007	Heart Cancer	47	0.035

655		BLR013	Biliary Tract Cancer	47	0.035

656		VST004	Vestibular Disease	45	0.035

657		CRB086	Cerebral Aneurysms	45	0.035

658		MCC013	Mucocutaneous Ulceration, Chronic	45	0.035

659	P	MJR007	Major Affective Disorder 1	45	0.035

660		FML075	Familial Isolated Hyperparathyroidism	45	0.035

661		HRT008	Heart Conduction Disease	44	0.035

662		ANG025	Angioimmunoblastic Lymphadenopathy with Dysproteinemia	43	0.035

663		HYP064	Hypogonadotropism	42	0.035

664		CHL149	Childhood Acute Myeloid Leukemia	42	0.035

665	c	HYP608	Hypocalciuric Hypercalcemia, Familial, Type Iii	40	0.035

666	P	LBY004	Labyrinthitis	40	0.035

667	c	MJR023	Major Affective Disorder 7	39	0.035

668		CYT002	Cytokine Deficiency	39	0.035

669		CGN005	Cognitive Impairment with or Without Cerebellar Ataxia	38	0.035

670	P	HYP733	Hypercalciuria, Absorptive, 2	37	0.035

671	c	MJR022	Major Affective Disorder 8	36	0.035

672	c	MJR024	Major Affective Disorder 9	36	0.035

673	P	AST055	Asthma-Related Traits 1	34	0.035

674	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	31	0.035

675		CRN288	Corneal Dystrophy, Band-Shaped	31	0.035

676		ENM001	Enamel Caries	30	0.035

677		TRD008	Triiodothyronine Receptor Auxiliary Protein	27	0.035

678	c	HYP831	Hyperparathyroidism, Transient Neonatal	20	0.035

679	P	MDL005	Medulloblastoma	76	0.033

680		PLM001	Pulmonary Tuberculosis	74	0.033

681		WRN001	Werner Syndrome	73	0.033

682		MYC006	Mycosis Fungoides	73	0.033

683		CRB037	Cerebral Palsy	71	0.033

684	P	FRN006	Frontotemporal Dementia	69	0.033

685	P	ALC004	Alcohol Abuse	68	0.033

686		END057	Endometrial Cancer	68	0.033

687	c	ATS007	Autism Spectrum Disorder	67	0.033

688	c	HPT003	Hepatitis a	66	0.033

689		FBR047	Fibromyalgia	66	0.033

690		SZR001	Sezary's Disease	66	0.033

691		LWC002	Lowe Oculocerebrorenal Syndrome	66	0.033

692	P	LYN001	Lynch Syndrome	66	0.033

693	P	DYS154	Dystonia	65	0.033

694	P	HML002	Hemolytic Anemia	64	0.033

695	P	ANR048	Aniridia 1	64	0.033

696	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	64	0.033

697	P	GLM040	Glioma Susceptibility 1	63	0.033

698	c	PNC108	Pancreatitis, Hereditary	62	0.033

699		PLS011	Plasmacytoma	62	0.033

700		RHM001	Rheumatic Fever	61	0.033

701	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	61	0.033

702	P	FBR017	Fibrosarcoma	61	0.033

703	P	SBS003	Substance Abuse	60	0.033

704		URT039	Urticaria	60	0.033

705	P	LRY044	Larynx Cancer	60	0.033

706		DMY004	Demyelinating Disease	60	0.033

707	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	60	0.033

708		DBT062	Diabetic Foot Ulcers	58	0.033

709		IGG001	Iga Glomerulonephritis	58	0.033

710		HRT012	Heart Valve Disease	58	0.033

711		DSS009	Disseminated Intravascular Coagulation	58	0.033

712	P	PLY041	Polymyositis	58	0.033

713		CRT016	Carotid Artery Disease	58	0.033

714		OST016	Osteochondrosis	58	0.033

715		VSC002	Vascular Dementia	57	0.033

716		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	57	0.033

717		IMP005	Impotence	56	0.033

718		MYM001	Myoma	56	0.033

719		ANK001	Ankylosis	56	0.033

720		AMN001	Amenorrhea	55	0.033

721	c	SVR005	Severe Pre-Eclampsia	55	0.033

722	P	HYP050	Hyperinsulinemic Hypoglycemia	55	0.033

723		PRS021	Prostatic Adenoma	55	0.033

724		SPN051	Spondylitis	55	0.033

725		THR016	Thrombophlebitis	54	0.033

726		PRS129	Prostatic Hyperplasia, Benign	53	0.033

727		MCL006	Macular Retinal Edema	53	0.033

728	P	MLN007	Male Infertility	52	0.033

729		HDN002	Head Injury	52	0.033

730	P	CMP008	Compartment Syndrome	52	0.033

731	c	RTN162	Retinitis Pigmentosa 2	51	0.033

732	P	NGH001	Night Blindness	50	0.033

733		ACN001	Acinar Cell Carcinoma	49	0.033

734		GNG011	Gingival Disease	49	0.033

735		HYP789	Hypophosphatemic Rickets with Hypercalciuria, Hereditary	49	0.033

736		VND001	Vein Disease	49	0.033

737	P	RNL015	Renal Hypertension	49	0.033

738		SYN036	Syncope	49	0.033

739		URT010	Ureteral Obstruction	49	0.033

740		DYS073	Dysphagia	48	0.033

741		DBT008	Diabetic Angiopathy	48	0.033

742		RYN001	Raynaud Disease	48	0.033

743		DFF003	Diffuse Scleroderma	46	0.033

744		MNN028	Mononeuropathy of the Median Nerve, Mild	46	0.033

745		THR035	Thrombasthenia	46	0.033

746		GST105	Gastroesophageal Adenocarcinoma	45	0.033

747	P	CLS010	Cluster Headache	45	0.033

748		LFT001	Left Bundle Branch Hemiblock	44	0.033

749	P	TST026	Testicular Germ Cell Cancer	44	0.033

750		ACT003	Acute Kidney Tubular Necrosis	44	0.033

751		SLT001	Solitary Osseous Plasmacytoma	44	0.033

752		RHM035	Rheumatic Fever-Related Antigen	44	0.033

753	P	HYP265	Hypotonia	43	0.033

754	c	HYP057	Hypervitaminosis D	43	0.033

755		MST004	Mast Cell Neoplasm	42	0.033

756		EXT007	Extracutaneous Mastocytoma	41	0.033

757		CHR178	Chromosomal Triplication	41	0.033

758		EXC002	Exocrine Pancreatic Insufficiency	41	0.033

759	c	HYP753	Hypocalciuric Hypercalcemia, Familial, Type Ii	40	0.033

760		ATX010	Ataxia Neuropathy Spectrum	39	0.033

761		CLC004	Calcific Tendinitis	38	0.033

762	c	TST017	Testicular Malignant Germ Cell Cancer	38	0.033

763		CRD220	Cardiac Valvular Defect, Developmental	36	0.033

764		ESP027	Esophagus Squamous Cell Carcinoma	35	0.033

765		PRN032	Paraneoplastic Cerebellar Degeneration	35	0.033

766		PNC015	Pancreatic Acinar Cell Adenocarcinoma	34	0.033

767		HRW001	Hair Whorl	33	0.033

768		IDP085	Idiopathic Infantile Hypercalcemia	28	0.033

769		BRN055	Bronchogenic Cyst	27	0.033

770	c	RTN181	Retinitis Pigmentosa 2, X-Linked	21	0.033

771		CRV035	Cervical Cancer	76	0.030

772	P	PRK057	Parkinson Disease, Late-Onset	76	0.030

773	P	WSK001	Wiskott-Aldrich Syndrome	76	0.030

774	P	NRF023	Neurofibromatosis, Type Ii	75	0.030

775		PSY004	Psychotic Disorder	74	0.030

776	c	HPT073	Hepatitis C Virus	72	0.030

777	P	RSP003	Respiratory Failure	72	0.030

778	P	HRP006	Herpes Simplex	71	0.030

779	P	CLC063	Celiac Disease 1	71	0.030

780	c	HPT001	Hepatitis C	69	0.030

781		OBS002	Obsessive-Compulsive Disorder	68	0.030

782	c	PRM196	Premature Ovarian Failure 1	68	0.030

783		GLN010	Glanzmann Thrombasthenia	67	0.030

784	P	MJR001	Major Depressive Disorder	67	0.030

785		SKN019	Skin Melanoma	67	0.030

786		DFC004	Deficiency Anemia	66	0.030

787	P	GCH001	Gaucher's Disease	66	0.030

788		ART005	Arteriovenous Malformation	66	0.030

789	P	NSP012	Nasopharyngeal Carcinoma	65	0.030

790	P	SNS014	Sinusitis	65	0.030

791		ETN001	Eating Disorder	65	0.030

792		CNT047	Contact Dermatitis	64	0.030

793		CYS013	Cystinuria	64	0.030

794	P	TST021	Testicular Germ Cell Tumor	63	0.030

795		HRP004	Herpes Zoster	63	0.030

796		PRM236	Primary Biliary Cholangitis	63	0.030

797	P	EPN002	Ependymoma	62	0.030

798		TRN018	Transitional Cell Carcinoma	62	0.030

799		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	62	0.030

800		MSC152	Muscular Dystrophy, Becker Type	62	0.030

801	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	62	0.030

802		SPN027	Spinal Stenosis	61	0.030

803		RSC001	Rosacea	61	0.030

804	P	PTN014	Patent Ductus Arteriosus 1	61	0.030

805		SPT004	Septic Arthritis	61	0.030

806	P	PRT013	Portal Hypertension	61	0.030

807	P	GST044	Gastritis	60	0.030

808		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.030

809	P	ESP024	Esophagitis	60	0.030

810	P	UTR058	Uterine Anomalies	60	0.030

811		BRN056	Bronchopulmonary Dysplasia	60	0.030

812		CLL003	Cellulitis	60	0.030

813		OPT006	Optic Nerve Disease	60	0.030

814		SLP005	Sleep Disorder	60	0.030

815		CNT061	Conotruncal Heart Malformations	60	0.030

816		INT030	Intracranial Aneurysm	59	0.030

817	c	THY109	Thyroid Cancer, Nonmedullary, 1	59	0.030

818		PLG002	Plague	59	0.030

819	P	MYC008	Myocarditis	59	0.030

820	P	SPN301	Spinocerebellar Ataxia 2	59	0.030

821		CHL028	Childhood Type Dermatomyositis	59	0.030

822	c	ESS001	Essential Tremor	59	0.030

823		BRN004	Brain Edema	59	0.030

824	P	HYP750	Hypertriglyceridemia, Familial	58	0.030

825		RLP002	Relapsing-Remitting Multiple Sclerosis	58	0.030

826		CHL067	Cholecystitis	58	0.030

827		PRN019	Perinatal Necrotizing Enterocolitis	58	0.030

828	P	TMP001	Temporal Lobe Epilepsy	58	0.030

829		DCT002	Ductal Carcinoma in Situ	58	0.030

830		PRM042	Primary Effusion Lymphoma	58	0.030

831		GLS001	Gliosarcoma	57	0.030

832		HLL004	Hellp Syndrome	57	0.030

833		PRS047	Prostatitis	56	0.030

834		MCN017	Meconium Ileus	56	0.030

835	c	PRM012	Primary Polycythemia	56	0.030

836		PST021	Postpartum Depression	56	0.030

837	P	ALP008	Alopecia	56	0.030

838	c	OST164	Osteoporosis, Juvenile	56	0.030

839		TLN003	Telangiectasis	56	0.030

840		GNT002	Giant Cell Glioblastoma	56	0.030

841	P	OPT009	Optic Neuritis	55	0.030

842		RDC002	Radiculopathy	55	0.030

843	c	BNG091	Benign Chronic Pemphigus	54	0.030

844	c	ACT071	Acute Kidney Failure	54	0.030

845	P	PRM006	Primary Biliary Cirrhosis	54	0.030

846	P	PTT006	Pituitary Adenoma	54	0.030

847		MCR004	Macroglobulinemia	54	0.030

848		ERY017	Erythema Elevatum Diutinum	54	0.030

849	c	BNG030	Benign Ependymoma	53	0.030

850	P	OBS001	Obstructive Jaundice	53	0.030

851		FRZ001	Frozen Shoulder	53	0.030

852		BSC001	Buschke-Ollendorff Syndrome	53	0.030

853	P	MTC069	Mitochondrial Disorders	53	0.030

854		CHN016	Cohen Syndrome	53	0.030

855		SXL003	Sexual Disorder	53	0.030

856		PLR008	Pleurisy	53	0.030

857		CRT049	Critical Limb Ischemia	53	0.030

858	P	SML016	Small Intestine Cancer	53	0.030

859	c	CNG027	Congenital Hemolytic Anemia	53	0.030

860		LKC003	Leukocyte Disease	52	0.030

861		INT067	Interstitial Nephritis	52	0.030

862	P	PRC019	Precocious Puberty	52	0.030

863	P	FNC004	Fanconi Syndrome	52	0.030

864	P	PLG001	Pelger-Huet Anomaly	52	0.030

865		RYN005	Raynaud Phenomenon	52	0.030

866		PST095	Post-Thrombotic Syndrome	51	0.030

867		SMT003	Somatostatinoma	51	0.030

868		DRG003	Drug Dependence	51	0.030

869		PRT018	Portal Vein Thrombosis	50	0.030

870		ACT088	Acute Insulin Response	50	0.030

871		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.030

872	c	PRG126	Progressive Familial Heart Block	50	0.030

873	c	THY107	Thymoma, Familial	50	0.030

874		NWC001	Newcastle Disease	50	0.030

875		PRL017	Prolymphocytic Leukemia	49	0.030

876		PGM003	Pigmentation Disease	49	0.030

877		DNT001	Dental Fluorosis	48	0.030

878	c	HMC010	Hemochromatosis, Type 3	47	0.030

879	P	HYP058	Hypervitaminosis a	47	0.030

880		DCB001	Decubitus Ulcer	47	0.030

881		PMP004	Pemphigus Foliaceus	46	0.030

882		DBT002	Diabetic Autonomic Neuropathy	46	0.030

883		HYP085	Hypothalamic Disease	46	0.030

884		DST006	Diastolic Heart Failure	46	0.030

885		SML008	Small Intestine Lymphoma	46	0.030

886	P	HRT035	Heart Block, Congenital	45	0.030

887		PPT001	Peptic Esophagitis	45	0.030

888		NPH010	Nephrosclerosis	45	0.030

889		HMP001	Hemopericardium	45	0.030

890		CRB008	Cerebral Atherosclerosis	44	0.030

891		BRS064	Bursitis	44	0.030

892		MNN017	Mononeuropathy	44	0.030

893		HYP082	Hypopharynx Cancer	43	0.030

894		BCL014	B-Cell Growth Factor	43	0.030

895		SPR008	Supratentorial Primitive Neuroectodermal Tumor	43	0.030

896		CLN044	Colon Adenoma	43	0.030

897	c	AVS006	Avascular Necrosis of Femoral Head, Primary, 1	43	0.030

898		DYS011	Dyskinesia of Esophagus	42	0.030

899		CRD137	Cardiogenic Shock	42	0.030

900		BWN003	Bowenoid Papulosis	42	0.030

901		OVR112	Ovarian Germ Cell Cancer	42	0.030

902	P	LRG016	Large Intestine Adenocarcinoma	42	0.030

903		HYP070	Hyperpituitarism	42	0.030

904		GNT050	Genitourinary Tract Anomalies	40	0.030

905		LWT001	Low Tension Glaucoma	40	0.030

906		HYD003	Hydrarthrosis	40	0.030

907		RGD002	Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal	40	0.030

908	P	HYP599	Hypoparathyroidism, Familial Isolated	40	0.030

909		EXC003	Excessive Tearing	38	0.030

910	c	HYP602	Hyperoxaluria, Primary, Type Ii	38	0.030

911	c	BLR024	Biliary Cirrhosis, Primary, 1	38	0.030

912		CRD245	Cardiac-Urogenital Syndrome	38	0.030

913	P	VSC018	Visceral Steatosis	37	0.030

914	c	HYP534	Hypomagnesemia 3, Renal	37	0.030

915		SWL001	Swallowing Disorders	36	0.030

916	c	BSL038	Basal Ganglia Calcification, Idiopathic, 1	36	0.030

917		FNT004	Fainting	36	0.030

918		EXT025	Extragonadal Germ Cell Cancer	35	0.030

919	c	TST046	Testicular Germ Cell Tumor 1	35	0.030

920		URN022	Urinary Tract Infections, Recurrent	34	0.030

921		MSC012	Muscular Dystrophy, Duchenne and Becker Type	33	0.030

922		PPL052	Papillomatosis, Confluent and Reticulated	33	0.030

923		SNG003	Single Ventricular Heart	31	0.030

924		ENP001	Enophthalmos	30	0.030

925		RDN004	Radin Blood Group Antigen	28	0.030

926		MTH071	Methane Production	27	0.030

927		CHR476	Chronic Angina	27	0.030

928		DNT010	Dentin Caries	26	0.030

929		DGS002	Degos 'en Cocarde' Erythrokeratoderma	25	0.030

930		PRR001	Periarthritis	25	0.030

931		HYP705	Hyperadrenalism	23	0.030

932		GLC025	Galactorrhoea-Hyperprolactinaemia	23	0.030

933		LYM126	Lymphoma Aids Related	23	0.030

934		INT074	Intracranial Arteriosclerosis	16	0.030

935		EWN003	Ewing Sarcoma	74	0.028

936		MLT157	Multiple System Atrophy 1	72	0.028

937		MLD001	Melioidosis	72	0.028

938		CHG001	Chagas Disease	72	0.028

939		LPD012	Lipoid Congenital Adrenal Hyperplasia	71	0.028

940	P	FML011	Familial Adenomatous Polyposis	71	0.028

941	P	MNN013	Meningitis	69	0.028

942	P	WLD002	Waldenstrom Macroglobulinemia	69	0.028

943	c	WLM013	Wilms Tumor 1	68	0.028

944		APN008	Apnea, Obstructive Sleep	68	0.028

945		CTN007	Cutaneous Leishmaniasis	68	0.028

946	P	HYP098	Hypereosinophilic Syndrome	67	0.028

947		HSH003	Hashimoto Thyroiditis	67	0.028

948		GLL008	Gilles De La Tourette Syndrome	67	0.028

949		MVM001	Movement Disease	67	0.028

950		CHL123	Chlamydia	66	0.028

951	c	HMP004	Hemophilia B	66	0.028

952	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	66	0.028

953	P	CNJ013	Conjunctivitis	65	0.028

954		BLL006	Bullous Pemphigoid	64	0.028

955	P	ANG001	Angelman Syndrome	64	0.028

956	c	WLM018	Wilms Tumor 5	64	0.028

957		FLL027	Fallopian Tube Carcinoma	64	0.028

958	c	CNR004	Cone-Rod Dystrophy 2	63	0.028

959		APH001	Aphthous Stomatitis	63	0.028

960		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	63	0.028

961		CMP010	Complex Regional Pain Syndrome	63	0.028

962		DPH001	Diphtheria	63	0.028

963		ALC006	Alcoholic Hepatitis	62	0.028

964		KRT001	Keratoconjunctivitis Sicca	62	0.028

965	P	GLY013	Glycogen Storage Disease	61	0.028

966		HNC001	Henoch-Schoenlein Purpura	61	0.028

967		CRY035	Cryptorchidism, Unilateral or Bilateral	61	0.028

968		GRD007	Grade Iii Astrocytoma	61	0.028

969	P	HST010	Histiocytosis	60	0.028

970		SPP010	Suppressor of Tumorigenicity 3	60	0.028

971		ORP003	Oropharynx Cancer	60	0.028

972		HPT019	Hepatic Encephalopathy	60	0.028

973	c	VRL010	Viral Hepatitis	60	0.028

974	P	SPN052	Spondyloarthropathy	59	0.028

975	P	RST001	Restless Legs Syndrome	59	0.028

976		END040	Endogenous Depression	59	0.028

977		SYN007	Synovitis	59	0.028

978	c	MYT020	Myotonic Dystrophy 2	58	0.028

979		LMY002	Leiomyoma	58	0.028

980		BLD044	Bladder Disease	57	0.028

981	P	RHB003	Rhabdomyosarcoma	57	0.028

982		INT075	Intracranial Hypertension	57	0.028

983	P	PLY019	Polyneuropathy	57	0.028

984		LYS002	Lysosomal Storage Disease	56	0.028

985		ART017	Aortic Disease	56	0.028

986		BLD053	Blood Platelet Disease	56	0.028

987		CRC006	Carcinoid Syndrome	56	0.028

988	P	THR015	Thrombophilia	56	0.028

989	c	ALM001	Al Amyloidosis	55	0.028

990	P	INT070	Intestinal Obstruction	55	0.028

991		INT079	Intrahepatic Cholangiocarcinoma	55	0.028

992		HYP014	Hyperuricemia	55	0.028

993		OPT003	Opiate Dependence	55	0.028

994		PSD014	Pseudopseudohypoparathyroidism	55	0.028

995	P	MCR010	Microcephaly	55	0.028

996	P	PMP005	Pemphigus Vulgaris	54	0.028

997	P	LPC002	Lip Cancer	54	0.028

998	P	HMR005	Hemorrhoid	54	0.028

999	P	RTN022	Retinal Vein Occlusion	54	0.028

1000		NNL002	Nonalcoholic Steatohepatitis	54	0.028

1001	c	LBR014	Leber Congenital Amaurosis 4	54	0.028

1002		HMG005	Hemoglobinopathy	54	0.028

1003	P	PRC012	Pericardial Effusion	53	0.028

1004	P	CNG010	Congenital Stationary Night Blindness	53	0.028

1005		CHR563	Chronic Eosinophilic Leukemia	53	0.028

1006	P	OPN001	Open-Angle Glaucoma	53	0.028

1007		DRY001	Dry Eye Syndrome	53	0.028

1008		ISL003	Isolated Growth Hormone Deficiency	52	0.028

1009		LPD009	Lipid Storage Disease	52	0.028

1010		SNS008	Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis	52	0.028

1011		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	52	0.028

1012	P	BRN035	Brain Stem Glioma	52	0.028

1013		CLS016	Clostridium Difficile Colitis	52	0.028

1014		NSD001	Nose Disease	52	0.028

1015	P	PTY003	Pityriasis Rubra Pilaris	51	0.028

1016		LRY017	Laryngeal Disease	51	0.028

1017		RNL077	Renal Fibrosis	51	0.028

1018	P	CHL066	Cholangitis	51	0.028

1019		CRC014	Carcinoid Tumors, Intestinal	51	0.028

1020		ISL001	Islet Cell Tumor	51	0.028

1021		EXT010	Extramedullary Plasmacytoma	51	0.028

1022		ACT011	Acute Contagious Conjunctivitis	51	0.028

1023		PTH003	Pathologic Nystagmus	50	0.028

1024		CHR073	Choreatic Disease	50	0.028

1025		GLC036	Glucagonoma	50	0.028

1026		SPH010	Sphingolipidosis	50	0.028

1027		CHL018	Childhood Medulloblastoma	50	0.028

1028		LRG008	Large Granular Lymphocyte Leukemia	49	0.028

1029		HYP006	Hypertensive Heart Disease	49	0.028

1030		NTR003	Natural Killer Cell Leukemia	49	0.028

1031		MST002	Mast-Cell Leukemia	49	0.028

1032		PRV004	Periventricular Leukomalacia	49	0.028

1033		PRN014	Paronychia	49	0.028

1034	c	PSR017	Psoriasis 2	49	0.028

1035		SXD002	Sex Development Disorder	49	0.028

1036		HYP457	Hypertrophic Scars	48	0.028

1037		HYP741	Hyperparathyroidism 2 with Jaw Tumors	48	0.028

1038		RTN023	Retinitis	48	0.028

1039		PTT037	Pituitary Tumors	48	0.028

1040		TCL002	T-Cell Large Granular Lymphocyte Leukemia	47	0.028

1041		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	47	0.028

1042	P	BRB001	Beriberi	46	0.028

1043		APP010	Appendix Cancer	46	0.028

1044		MDL009	Medullary Sponge Kidney	46	0.028

1045		SKL017	Skeletal Dysplasias	46	0.028

1046		RGH001	Right Bundle Branch Block	46	0.028

1047		ATN004	Autonomic Neuropathy	46	0.028

1048		PST053	Postherpetic Neuralgia	45	0.028

1049		ART004	Aortic Atherosclerosis	45	0.028

1050		HPT004	Hepatic Coma	45	0.028

1051		CRN024	Corneal Disease	45	0.028

1052		SGN002	Signet Ring Cell Adenocarcinoma	45	0.028

1053		GRM004	Germinoma	45	0.028

1054		PRM175	Primary Familial Brain Calcification	44	0.028

1055		FDL002	Food Allergy	44	0.028

1056		PHT003	Phototoxic Dermatitis	44	0.028

1057		HYP030	Hypoactive Sexual Desire Disorder	44	0.028

1058		SPS057	Spasticity	44	0.028

1059	c	PSR028	Psoriasis 7	43	0.028

1060	c	PSR032	Psoriasis 11	43	0.028

1061	c	SRC023	Sarcoidosis 2	43	0.028

1062		LCR008	Lacrimal Apparatus Disease	43	0.028

1063	P	OCY003	Oocyte Maturation Defect 1	42	0.028

1064	c	PSR018	Psoriasis 13	42	0.028

1065		MTR007	Motor Peripheral Neuropathy	41	0.028

1066	c	PMP006	Pemphigus Vulgaris, Familial	41	0.028

1067		TRT001	Teratocarcinoma	41	0.028

1068		LKM006	Leukomalacia	41	0.028

1069		PRN039	Paraneoplastic Syndromes	40	0.028

1070		HLX001	Helix Syndrome	40	0.028

1071	c	CHR020	Chronic Interstitial Cystitis	39	0.028

1072		URT014	Ureterolithiasis	39	0.028

1073		PDT014	Pediatric Ependymoma	38	0.028

1074		CHR286	Chronic Neutrophilic Leukemia	38	0.028

1075	P	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	37	0.028

1076		OLC001	Olecranon Bursitis	36	0.028

1077	P	BCL013	B-Cell Adult Acute Lymphocytic Leukemia	35	0.028

1078		CNT018	Central Nervous System Leukemia	35	0.028

1079		TTH007	Tooth Erosion	34	0.028

1080		RFR002	Refractory Hairy Cell Leukemia	34	0.028

1081	c	HYP603	Hyperoxaluria, Primary, Type Iii	33	0.028

1082		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	32	0.028

1083	P	PRX010	Paroxysmal Ventricular Fibrillation	32	0.028

1084		RNL001	Renal Artery Obstruction	31	0.028

1085	c	ANR047	Aniridia 2	31	0.028

1086		HYP827	Hypomagnesemia 5, Renal, with or Without Ocular Involvement	29	0.028

1087	P	STR035	Streptococcal Group a Invasive Disease	29	0.028

1088		FNC005	Functional Colonic Disease	29	0.028

1089		PDT040	Pediatric Hypertension	29	0.028

1090