Search results for Morphine

1060 hits were found for Morphine

#	Family	MCID	Name	MIFTS	Score
1		MRP001	Morphine Dependence	41	8.086

2		PNG002	Pain Agnosia	51	1.306

3	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.492

4	c	PNS012	Paine Syndrome	61	0.485

5	P	CHR345	Chronic Pain	44	0.469

6		WTH001	Withdrawal Disorder	48	0.467

7		OPT003	Opiate Dependence	50	0.369

8		48X005	48,xyyy	39	0.336

9		CNS004	Constipation	58	0.324

10		OPD006	Opioid Addiction	48	0.322

11		DPR016	Depression	63	0.247

12		DRG003	Drug Dependence	47	0.209

13		OPD001	Opioid Abuse	46	0.203

14		PRT037	Pertussis	65	0.194

15	P	TRM003	Tremor	54	0.194

16		BCK006	Back Pain	42	0.194

17	P	DRR001	Diarrhea	55	0.192

18	P	NRB001	Neuroblastoma	72	0.183

19		AMN003	Amnestic Disorder	54	0.183

20		ANX010	Anxiety	73	0.180

21		MNT002	Mental Depression	58	0.177

22	P	PTS002	Ptosis	53	0.177

23	P	SZR006	Seizure Disorder	56	0.172

24		NNT008	Neonatal Abstinence Syndrome	41	0.172

25		VSL002	Visual Epilepsy	59	0.171

26		ALL026	Allergic Hypersensitivity Disease	62	0.165

27		SBC016	Subacute Delirium	44	0.164

28	P	SBS003	Substance Abuse	55	0.160

29	P	SCL018	Scoliosis	60	0.157

30	P	RSP003	Respiratory Failure	74	0.155

31		ISC004	Ischemia	58	0.155

32	P	HDC001	Headache	57	0.155

33	P	MYC007	Myocardial Infarction	70	0.152

34	P	TRN020	Turner Syndrome	67	0.151

35		CHL067	Cholecystitis	57	0.149

36	c	ACT075	Acute Myocardial Infarction	57	0.149

37	P	SCK005	Sickle Cell Disease	50	0.146

38		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.141

39		ILS001	Ileus	51	0.141

40	P	CNR004	Cone-Rod Dystrophy 2	73	0.136

41	P	KDN018	Kidney Disease	72	0.136

42	c	RHB024	Rhabdomyosarcoma 2	67	0.136

43	P	NRP001	Neuropathy	56	0.136

44	P	MYC033	Myoclonus	46	0.134

45		OST012	Osteoarthritis	78	0.133

46		ADL002	Adult Syndrome	70	0.133

47	P	SLP006	Sleep Apnea	69	0.131

48	P	BNC003	Bone Cancer	58	0.131

49		CHL079	Children's Interstitial Lung Disease	26	0.129

50		SPN186	Spinal Cord Injury	60	0.127

51		MCS002	Mucositis	56	0.127

52		LNG099	Lung Disease	60	0.124

53		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.122

54	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.120

55	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.120

56	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.120

57	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.120

58	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.120

59	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.120

60	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.120

61	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.120

62	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.120

63	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.120

64	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.120

65		IDP070	Idiopathic Scoliosis	42	0.120

66		HYP266	Hypoxia	57	0.118

67		PLM010	Pulmonary Edema	54	0.118

68		CYT002	Cytokine Deficiency	42	0.118

69		ATX019	Ataxia with Vitamin E Deficiency	42	0.118

70		HYP066	Hyperglycemia	61	0.116

71	P	AGN002	Agnosia	55	0.114

72		CNG034	Congestive Heart Failure	69	0.112

73		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.110

74		SPS057	Spasticity	45	0.108

75		MNN017	Mononeuropathy	42	0.108

76	P	HRT032	Heart Disease	75	0.105

77	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.105

78		SCK003	Sickle Cell Anemia	74	0.103

79		HYP056	Hypoglycemia	66	0.103

80		LPP008	Lipoprotein Quantitative Trait Locus	62	0.103

81	P	PRP019	Peripheral Nervous System Disease	58	0.103

82	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.099

83		DFC004	Deficiency Anemia	70	0.099

84	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.099

85	P	LVR013	Liver Disease	68	0.099

86		ACQ007	Acquired Immunodeficiency Syndrome	60	0.099

87		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.096

88		CHL014	Cholera	59	0.096

89		47X002	47,xyy	49	0.096

90		LPT014	Leptin Deficiency or Dysfunction	74	0.094

91		HMN044	Human Immunodeficiency Virus Type 1	71	0.094

92		APN008	Apnea, Obstructive Sleep	64	0.094

93	P	PNC044	Pancreatitis	61	0.094

94		DBT010	Diabetic Neuropathy	54	0.094

95		ALC007	Alcohol Dependence	66	0.091

96	P	HRP006	Herpes Simplex	65	0.091

97		PRT036	Peritonitis	64	0.091

98	P	GLM045	Glioma	63	0.091

99		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.091

100	c	MGR028	Migraine with or Without Aura 1	67	0.089

101		ANG054	Angina Pectoris	66	0.089

102	c	MCL013	Mucolipidosis Iv	66	0.089

103		GLL048	Glial Tumor	45	0.089

104	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.089

105	P	BRS047	Breast Cancer	97	0.083

106		TTN003	Tetanus	65	0.083

107		ING001	Inguinal Hernia	60	0.083

108		OCL069	Ocular Motor Apraxia	51	0.083

109		SPR126	Superior Semicircular Canal Dehiscence	40	0.083

110	c	HMG029	Hemoglobin Se Disease	39	0.083

111	P	CLR023	Colorectal Cancer	99	0.081

112	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.081

113		DWN001	Down Syndrome	70	0.081

114	P	PNM007	Pneumonia	68	0.081

115	c	ACT027	Acute Pancreatitis	60	0.081

116		PRP016	Paraplegia	52	0.081

117	P	LNG032	Lung Cancer	98	0.078

118	c	HYP595	Hypertension, Essential	84	0.078

119		IMM167	Immune Deficiency Disease	78	0.078

120	P	EXN002	Exanthem	57	0.078

121		INT007	Intermediate Coronary Syndrome	55	0.078

122	P	DDN001	Duodenal Ulcer	52	0.078

123		ART140	Arteries, Anomalies of	52	0.078

124		HLX001	Helix Syndrome	47	0.078

125		VRS002	Virus-Associated Trichodysplasia Spinulosa	32	0.078

126	P	CRD119	Cardiac Arrest	67	0.075

127	P	ENC018	Encephalopathy	61	0.075

128		SYN007	Synovitis	54	0.075

129		PST021	Postpartum Depression	50	0.075

130		PST053	Postherpetic Neuralgia	40	0.075

131		ANX004	Anoxia	40	0.075

132		PLC002	Plica Syndrome	36	0.075

133	P	ART022	Arthritis	69	0.071

134		ART016	Aortic Aneurysm	69	0.071

135		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.071

136		PST028	Post-Traumatic Stress Disorder	58	0.071

137		THR024	Thrombosis	57	0.071

138		PNM008	Pneumothorax	56	0.071

139		NPH009	Nephrolithiasis	55	0.071

140	P	RST001	Restless Legs Syndrome	54	0.071

141		MCN017	Meconium Ileus	52	0.071

142		ACT084	Acute Stress Disorder	47	0.071

143	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.071

144		BLR004	Biliary Dyskinesia	38	0.071

145		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.071

146		LVR012	Liver Cirrhosis	62	0.068

147		APP008	Appendicitis	61	0.068

148		INT066	Interstitial Lung Disease	60	0.068

149		STT001	Status Epilepticus	60	0.068

150	P	INT070	Intestinal Obstruction	58	0.068

151		NWB001	Newborn Respiratory Distress Syndrome	58	0.068

152		MTN003	Motion Sickness	53	0.068

153		BHR001	Behr Syndrome	51	0.068

154		BRN071	Brain Injury	49	0.068

155		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.068

156		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.068

157		BNN005	Bunion	33	0.068

158		INF118	Inflammatory Myopathy with Abundant Macrophages	28	0.068

159		CYT018	Cytochrome P450 2d6 Variant	27	0.068

160	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.065

161	P	DMN002	Dementia	66	0.065

162		MDD011	Mood Disorder	62	0.065

163		HRP004	Herpes Zoster	60	0.065

164		PRT058	Pure Autonomic Failure	59	0.065

165	P	ALC033	Alcohol Use Disorder	58	0.065

166	P	URT039	Urticaria	58	0.065

167		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.065

168		PTH003	Pathologic Nystagmus	52	0.065

169	P	ECL001	Eclampsia	50	0.065

170		STM007	Stomatitis	50	0.065

171		DYS073	Dysphagia	50	0.065

172		HDN002	Head Injury	46	0.065

173		URL001	Urolithiasis	45	0.065

174		ENT001	Enterocele	39	0.065

175		MYL069	Myeloma, Multiple	85	0.061

176	P	GST053	Gastric Cancer	83	0.061

177		AST005	Asthma	76	0.061

178		GLB015	Glioblastoma Multiforme	75	0.061

179	P	LKM002	Leukemia	68	0.061

180	P	VSC007	Vascular Disease	63	0.061

181	P	CRN300	Coronary Heart Disease 1	63	0.061

182	P	MYL006	Myeloid Leukemia	60	0.061

183		FBR047	Fibromyalgia	58	0.061

184		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.061

185	P	CRD246	Cardiovascular System Disease	57	0.061

186	P	DBT005	Diabetes Insipidus	55	0.061

187		END040	Endogenous Depression	55	0.061

188		HRT012	Heart Valve Disease	53	0.061

189	c	XNT010	Xanthinuria, Type I	53	0.061

190		TRM010	Traumatic Brain Injury	51	0.061

191		ACT017	Acute Chest Syndrome	51	0.061

192		DGN001	Degenerative Disc Disease	48	0.061

193		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.061

194		HRN003	Heroin Dependence	44	0.061

195		ARC002	Arachnoiditis	42	0.061

196		RDN001	Reading Disorder	40	0.061

197		SPN354	Spinal Arachnoiditis	36	0.061

198	c	LKM005	Leukemia, T-Cell, Chronic	34	0.061

199	c	LKM061	Leukemia, Acute Myeloid	84	0.057

200	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.057

201		KHL003	Kohlschutter-Tonz Syndrome	65	0.057

202	c	PRC016	Pre-Eclampsia	63	0.057

203		INT146	Intervertebral Disc Disease	63	0.057

204		TXC005	Toxic Shock Syndrome	62	0.057

205		PNM010	Pneumothorax, Primary Spontaneous	60	0.057

206	c	ACT071	Acute Kidney Failure	60	0.057

207	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.057

208		ANR040	Aneurysm	59	0.057

209	P	BCL017	B-Cell Lymphoma	58	0.057

210	P	GLL020	Gallbladder Disease	57	0.057

211		STR081	Stormorken Syndrome	57	0.057

212	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.057

213		AGN016	Aging	56	0.057

214		NRT001	Neurotic Disorder	53	0.057

215		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.057

216		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.057

217		CNT017	Central Nervous System Origin Vertigo	45	0.057

218		ESP021	Esophageal Cancer	90	0.053

219	P	PNC035	Pancreatic Cancer	84	0.053

220		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.053

221	c	LKM063	Leukemia, Chronic Myeloid	72	0.053

222		CRB037	Cerebral Palsy	69	0.053

223	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.053

224	P	LYM118	Lymphoma	68	0.053

225		OBS002	Obsessive-Compulsive Disorder	68	0.053

226	P	PLM037	Pulmonary Hypertension	67	0.053

227		PPL049	Papillon-Lefevre Syndrome	65	0.053

228	P	ADL010	Adult Respiratory Distress Syndrome	65	0.053

229	P	DBT009	Diabetes Mellitus	64	0.053

230		LSH001	Leishmaniasis	63	0.053

231		FTT001	Fatty Liver Disease	61	0.053

232		CMP010	Complex Regional Pain Syndrome	58	0.053

233		LYM027	Lymphopenia	58	0.053

234		PLS011	Plasmacytoma	56	0.053

235		RFL001	Reflex Sympathetic Dystrophy	54	0.053

236		PLS009	Plasma Cell Neoplasm	51	0.053

237		LNG031	Lung Benign Neoplasm	51	0.053

238		CHL004	Cholelithiasis	49	0.053

239		LPT006	Leptin Receptor Deficiency	48	0.053

240	P	BNG032	Benign Mesothelioma	46	0.053

241		DVR002	Diverticulitis	43	0.053

242		TRP009	Triple X Syndrome	42	0.053

243		GST020	Gastric Antral Vascular Ectasia	41	0.053

244	P	KLZ004	Kala-Azar 1	41	0.053

245	P	SCL057	Scoliosis, Isolated 1	41	0.053

246		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	0.053

247		CRB079	Cerebrospinal Fluid Leak	35	0.053

248	P	HPT023	Hepatocellular Carcinoma	100	0.048

249	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.048

250		CYS001	Cystic Fibrosis	81	0.048

251		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.048

252	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.048

253	P	OST002	Osteoporosis	74	0.048

254		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.048

255	c	HPT073	Hepatitis C Virus	72	0.048

256		OTT002	Otitis Media	72	0.048

257	c	EXD008	Exudative Vitreoretinopathy 1	71	0.048

258	P	EPL164	Epilepsy	71	0.048

259	P	AMY004	Amyloidosis	70	0.048

260		MYL009	Myelodysplastic Syndrome	70	0.048

261		MYL005	Myelofibrosis	70	0.048

262	P	TTR001	Tetralogy of Fallot	70	0.048

263		PLY001	Polycythemia Vera	69	0.048

264		LYM133	Lymphoma, Hodgkin, Classic	69	0.048

265		MNT001	Mantle Cell Lymphoma	69	0.048

266	P	ESS003	Essential Thrombocythemia	68	0.048

267		BRN024	Bronchitis	68	0.048

268		BRK010	Burkitt Lymphoma	67	0.048

269		CRB039	Cerebrovascular Disease	67	0.048

270	P	FLL037	Follicular Lymphoma	67	0.048

271		MYC006	Mycosis Fungoides	66	0.048

272	P	MNN013	Meningitis	66	0.048

273		MYL031	Myeloproliferative Neoplasm	66	0.048

274		IRR002	Irritable Bowel Syndrome	65	0.048

275	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.048

276		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.048

277		MSC007	Muscle Hypertrophy	64	0.048

278	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.048

279		ANR007	Anorexia Nervosa	63	0.048

280	P	ART023	Arthropathy	62	0.048

281		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.048

282		DRM006	Dermatitis	61	0.048

283	P	ENC004	Encephalitis	61	0.048

284		WLD007	Waldenstroem's Macroglobulinemia	61	0.048

285		SZR001	Sezary's Disease	60	0.048

286		CRD223	Cardiac Arrhythmia	60	0.048

287	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.048

288		IDP011	Idiopathic Interstitial Pneumonia	59	0.048

289		SPN027	Spinal Stenosis	59	0.048

290	P	SLP005	Sleep Disorder	59	0.048

291		PLM033	Pulmonary Embolism	59	0.048

292	P	BRS044	Breast Adenocarcinoma	59	0.048

293	P	GLL022	Guillain-Barre Syndrome	59	0.048

294		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.048

295	c	ACT073	Acute Leukemia	58	0.048

296	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.048

297		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.048

298		BRN056	Bronchopulmonary Dysplasia	57	0.048

299	P	PLY018	Polycythemia	56	0.048

300	P	ADL017	Adult T-Cell Leukemia	56	0.048

301	P	GST044	Gastritis	56	0.048

302		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.048

303		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.048

304		HRY003	Hairy Cell Leukemia	55	0.048

305		CRT017	Cartilage Disease	54	0.048

306		LYM040	Lymphoblastic Lymphoma	54	0.048

307		NNL006	Non-Alcoholic Steatohepatitis	54	0.048

308	P	CNT005	Central Nervous System Lymphoma	53	0.048

309		FNG017	Fungal Infectious Disease	53	0.048

310		TXC002	Toxic Encephalopathy	53	0.048

311	c	GLL024	Gallbladder Disease 1	53	0.048

312		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.048

313		MRG003	Marginal Zone B-Cell Lymphoma	52	0.048

314	P	RCT021	Rectum Cancer	52	0.048

315		SPL004	Splenic Marginal Zone Lymphoma	51	0.048

316		END086	End Stage Renal Disease	51	0.048

317	c	ALM001	Al Amyloidosis	50	0.048

318	c	PRM012	Primary Polycythemia	50	0.048

319		RDC002	Radiculopathy	50	0.048

320		HYP080	Hypogonadism	50	0.048

321		TCL002	T-Cell Large Granular Lymphocyte Leukemia	49	0.048

322	c	THR090	Thrombocythemia 1	49	0.048

323		PCT003	Pectus Excavatum	49	0.048

324		MCR004	Macroglobulinemia	49	0.048

325	c	FLL041	Follicular Lymphoma 1	49	0.048

326		CHR563	Chronic Eosinophilic Leukemia	48	0.048

327	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.048

328		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.048

329	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.048

330	c	PRM226	Primary Central Nervous System Lymphoma	48	0.048

331		PRL017	Prolymphocytic Leukemia	47	0.048

332		PLS025	Plasmablastic Lymphoma	47	0.048

333		CRD137	Cardiogenic Shock	47	0.048

334		LYM019	Lymphosarcoma	46	0.048

335		CLN045	Colonic Benign Neoplasm	46	0.048

336	P	HMR005	Hemorrhoid	46	0.048

337		EXT010	Extramedullary Plasmacytoma	45	0.048

338		LYM126	Lymphoma Aids Related	44	0.048

339		DMP001	Dumping Syndrome	44	0.048

340	c	PRM038	Primary Agammaglobulinemia	44	0.048

341		BNM001	Bone Marrow Cancer	43	0.048

342	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.048

343		DRG024	Drug Allergy	42	0.048

344		CHR286	Chronic Neutrophilic Leukemia	42	0.048

345		LRG008	Large Granular Lymphocyte Leukemia	41	0.048

346	c	PLM150	Pulmonary Alveolar Proteinosis, Acquired	40	0.048

347		ALG001	Algoneurodystrophy	39	0.048

348		SPS019	Spastic Paraparesis	38	0.048

349		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.048

350	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.048

351	c	RST012	Restless Legs Syndrome 1	34	0.048

352		RFR002	Refractory Hairy Cell Leukemia	33	0.048

353		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.048

354		CLS052	Classic Hairy Cell Leukemia	27	0.048

355		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.048

356		FTL073	Fetal Anticonvulsant Syndrome	26	0.048

357		ADG002	Audiogenic Seizures	25	0.048

358	P	PRS040	Prostate Cancer	97	0.043

359		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.043

360		BRN028	Brain Cancer	74	0.043

361		PRP027	Peripheral Vascular Disease	71	0.043

362		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.043

363	P	MYS003	Myasthenia Gravis	68	0.043

364	P	MJR001	Major Depressive Disorder	68	0.043

365	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.043

366	P	SKN015	Skin Carcinoma	66	0.043

367	P	NSP012	Nasopharyngeal Carcinoma	66	0.043

368	P	PLM036	Pulmonary Fibrosis	65	0.043

369	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.043

370	P	THY023	Thymoma	65	0.043

371		CLF027	Cleft Palate, Isolated	64	0.043

372	P	ADN016	Adenocarcinoma	64	0.043

373	P	ANR048	Aniridia 1	63	0.043

374	c	HPT001	Hepatitis C	62	0.043

375		VRL011	Viral Infectious Disease	61	0.043

376	P	KDN017	Kidney Cancer	60	0.043

377		TRG002	Trigeminal Neuralgia	60	0.043

378		SQM006	Squamous Cell Carcinoma	60	0.043

379	P	PTN014	Patent Ductus Arteriosus 1	60	0.043

380		ORL011	Oral Cancer	60	0.043

381	P	CYS018	Cystitis	59	0.043

382		CNT047	Contact Dermatitis	58	0.043

383		DSS008	Disease of Mental Health	58	0.043

384	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.043

385		HYP005	Hypokalemia	55	0.043

386		NRG002	Neurogenic Bladder	55	0.043

387	P	INF037	Inflammatory Bowel Disease	54	0.043

388		PRS045	Prostatic Hypertrophy	53	0.043

389	P	LCT002	Lactose Intolerance	53	0.043

390		GST023	Gastric Ulcer	53	0.043

391		EXP004	Exophthalmos	52	0.043

392	c	THY107	Thymoma, Familial	52	0.043

393		SPS003	Spastic Diplegia	51	0.043

394		NRM004	Neuroma	51	0.043

395		SPN019	Spondylolisthesis	51	0.043

396	P	AST007	Astrocytoma	51	0.043

397	P	OVR082	Overgrowth Syndrome	50	0.043

398	c	DYS119	Dystonia 9	50	0.043

399	P	CMP008	Compartment Syndrome	49	0.043

400		SPL018	Splenomegaly	48	0.043

401		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.043

402		ATN005	Autonomic Dysfunction	46	0.043

403		HPT004	Hepatic Coma	45	0.043

404		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.043

405		SPS007	Spastic Cerebral Palsy	45	0.043

406		RTR001	Retrograde Amnesia	44	0.043

407	P	BLP003	Blepharospasm	44	0.043

408		URT014	Ureterolithiasis	44	0.043

409		PLY068	Polysubstance Abuse	43	0.043

410		PRS063	Paresthesia	41	0.043

411		ANG049	Angioedema Induced by Ace Inhibitors	40	0.043

412		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.043

413	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.043

414	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.043

415	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.043

416	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.043

417		STR067	Stroke, Ischemic	81	0.037

418	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.037

419		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.037

420	P	PHC003	Pheochromocytoma	71	0.037

421	P	OCL013	Oculodentodigital Dysplasia	69	0.037

422	P	HYP086	Hypothyroidism	69	0.037

423		MST024	Mastocytosis, Cutaneous	69	0.037

424	P	THR014	Thrombocytopenia	67	0.037

425		GST092	Gastroesophageal Reflux	67	0.037

426		GRG001	Greig Cephalopolysyndactyly Syndrome	66	0.037

427	c	MCR129	Microvascular Complications of Diabetes 1	66	0.037

428	c	SML038	Small Cell Cancer of the Lung	65	0.037

429	P	PRS038	Personality Disorder	65	0.037

430	c	DBT099	Diabetes Mellitus, Type I	65	0.037

431		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.037

432	P	ESP024	Esophagitis	62	0.037

433		NTR005	Nutritional Deficiency Disease	62	0.037

434	P	INT143	Interstitial Cystitis	61	0.037

435	P	VNT002	Ventricular Septal Defect	60	0.037

436	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.037

437		HYD002	Hydronephrosis	60	0.037

438		ETN001	Eating Disorder	60	0.037

439	P	LYM033	Lymphoproliferative Syndrome	59	0.037

440		PPT005	Peptic Ulcer Disease	59	0.037

441		MNR012	Meniere Disease	57	0.037

442	c	VSC019	Vesicoureteral Reflux 1	57	0.037

443	c	MST023	Mesothelioma, Malignant	57	0.037

444		BLR008	Bilirubin Metabolic Disorder	57	0.037

445		GST050	Gastrointestinal System Disease	56	0.037

446		BRN004	Brain Edema	56	0.037

447	P	PLM034	Pulmonary Emphysema	55	0.037

448		CHR100	Chronic Ulcer of Skin	55	0.037

449		CLF004	Cleft Lip/palate	54	0.037

450	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.037

451		PST046	Post-Transplant Lymphoproliferative Disease	53	0.037

452	P	EPD016	Epidermolysis Bullosa	53	0.037

453		CLF001	Cleft Lip	53	0.037

454		INT075	Intracranial Hypertension	53	0.037

455		IMP005	Impotence	52	0.037

456	P	NRC002	Narcolepsy	52	0.037

457		FML037	Female Breast Cancer	52	0.037

458		LMY002	Leiomyoma	52	0.037

459	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.037

460		AVD001	Avoidant Personality Disorder	51	0.037

461		IFP001	Ifap Syndrome with or Without Bresheck Syndrome	51	0.037

462	P	HYP040	Hypospadias	51	0.037

463	c	INF145	Infantile Liver Failure Syndrome 1	50	0.037

464		NTR046	Neutrophil Migration	50	0.037

465		MTB004	Metabolic Acidosis	50	0.037

466		HRT011	Heart Septal Defect	50	0.037

467		ATY042	Atypical Chronic Myeloid Leukemia	49	0.037

468		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.037

469	P	MST002	Mast-Cell Leukemia	49	0.037

470		CCN002	Cocaine Abuse	49	0.037

471		ACT029	Acute Interstitial Pneumonia	49	0.037

472		INT054	Intraocular Lymphoma	48	0.037

473		SBS004	Substance Dependence	48	0.037

474		SXL003	Sexual Disorder	47	0.037

475		CRD001	Cardiac Tamponade	47	0.037

476		LYM012	Lymphoplasmacytic Lymphoma	47	0.037

477		GST071	Gastrointestinal Carcinoma	47	0.037

478		CNT033	Central Nervous System Cancer	47	0.037

479		HYD005	Hydrocele	46	0.037

480		ADR040	Adrenal Gland Pheochromocytoma	46	0.037

481		INT253	Intestinal Benign Neoplasm	45	0.037

482		PRL008	Paralytic Ileus	45	0.037

483		LYM051	Lymphomatoid Granulomatosis	45	0.037

484		LTH001	Lethal Midline Granuloma	44	0.037

485		HRT015	Heritable Pulmonary Arterial Hypertension	44	0.037

486		PTT037	Pituitary Tumors	44	0.037

487	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.037

488		CRB090	Cerebral Hypoxia	44	0.037

489	P	MJR007	Major Affective Disorder 1	43	0.037

490		URM005	Uremic Pruritus	42	0.037

491	P	CRN035	Cranial Nerve Palsy	42	0.037

492		49X006	49, Xxxxy Syndrome	41	0.037

493		RFL002	Reflex Epilepsy	40	0.037

494	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.037

495		ACT167	Acute Generalized Exanthematous Pustulosis	37	0.037

496		MYL067	Myeloproliferative Disorder, Chronic, with Eosinophilia	37	0.037

497		SYS070	Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood	36	0.037

498		HRW001	Hair Whorl	36	0.037

499		ACL001	Acalculous Cholecystitis	35	0.037

500		PPL052	Papillomatosis, Confluent and Reticulated	33	0.037

501		SML008	Small Intestine Lymphoma	33	0.037

502	c	RNG008	Ring Chromosome 13	31	0.037

503		SNG003	Single Ventricular Heart	30	0.037

504		DVR001	Diverticulitis of Colon	25	0.037

505	c	DMN005	Diamond-Blackfan Anemia 2	25	0.037

506		NNT018	Neonatal Herpes	24	0.037

507		PNS018	Pain Sensitivity Quantitative Trait Locus 1	23	0.037

508		HYP705	Hyperadrenalism	20	0.037

509	P	OVR042	Ovarian Cancer	88	0.030

510	P	ALZ034	Alzheimer Disease	88	0.030

511		MLR004	Malaria	81	0.030

512	P	RHM011	Rheumatoid Arthritis	80	0.030

513	P	BLD134	Bladder Cancer	79	0.030

514		INS024	Insulin-Like Growth Factor I	79	0.030

515		CRV035	Cervical Cancer	76	0.030

516		END057	Endometrial Cancer	74	0.030

517		CRH001	Crohn's Disease	74	0.030

518		SVR004	Severe Combined Immunodeficiency	73	0.030

519	c	SPN225	Spondyloarthropathy 1	73	0.030

520	P	MLT020	Multiple Sclerosis	72	0.030

521	P	HNT016	Huntington Disease	72	0.030

522	P	FML011	Familial Adenomatous Polyposis	72	0.030

523	P	GRF003	Graft-Versus-Host Disease	72	0.030

524		FBR012	Fabry Disease	72	0.030

525	P	BRG001	Brugada Syndrome	71	0.030

526	c	CHR684	Chronic Kidney Disease	70	0.030

527	P	MLN008	Melanoma	69	0.030

528		CHL065	Cholangiocarcinoma	68	0.030

529		CMM004	Common Variable Immunodeficiency	68	0.030

530		SKN019	Skin Melanoma	68	0.030

531		PNC129	Pancreatic Adenocarcinoma	68	0.030

532	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.030

533	P	HPT021	Hepatitis	67	0.030

534	c	PRD013	Periodic Fever, Familial, Autosomal Dominant	67	0.030

535		PSY004	Psychotic Disorder	67	0.030

536	P	MLG056	Malignant Hyperthermia	67	0.030

537		OST159	Osteogenic Sarcoma	66	0.030

538	P	DYS154	Dystonia	65	0.030

539		PRP001	Propionic Acidemia	65	0.030

540		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	65	0.030

541		KWS002	Kawasaki Disease	65	0.030

542	P	MST009	Mastocytosis	64	0.030

543	c	EPS035	Episodic Ataxia, Type 2	63	0.030

544	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.030

545	c	ACT068	Acute Cystitis	63	0.030

546		CTN007	Cutaneous Leishmaniasis	62	0.030

547		CRC021	Carcinosarcoma	62	0.030

548		CHL068	Cholestasis	61	0.030

549		DCB001	Decubitus Ulcer	61	0.030

550	c	LPM012	Lipomatosis, Multiple	60	0.030

551	P	TXP001	Toxoplasmosis	60	0.030

552		HPT019	Hepatic Encephalopathy	60	0.030

553	P	ATR010	Atrial Heart Septal Defect	60	0.030

554	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.030

555	P	CTR002	Cataract	60	0.030

556		PRT013	Portal Hypertension	59	0.030

557	c	PCH015	Pachyonychia Congenita 1	59	0.030

558		IGR001	Ige Responsiveness, Atopic	59	0.030

559		PRN019	Perinatal Necrotizing Enterocolitis	59	0.030

560		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.030

561		SPR004	Supravalvular Aortic Stenosis	58	0.030

562	P	MTR012	Mitral Valve Disease	58	0.030

563	P	CND004	Candidiasis	58	0.030

564	P	END033	Endocarditis	57	0.030

565		TNS005	Tonsillitis	57	0.030

566	P	BPL003	Bipolar Disorder	56	0.030

567	P	PYL005	Pyelonephritis	56	0.030

568	P	FBR017	Fibrosarcoma	56	0.030

569		HMT008	Hematuria, Benign Familial	56	0.030

570	c	INT072	Intestinal Pseudo-Obstruction	56	0.030

571		BCT022	Bacterial Infectious Disease	56	0.030

572		ALL010	Allergic Contact Dermatitis	56	0.030

573		INT030	Intracranial Aneurysm	56	0.030

574		ATR057	Atrioventricular Block	55	0.030

575	c	FML035	Familial Hyperlipidemia	55	0.030

576	P	MLN007	Male Infertility	55	0.030

577		VSC003	Visceral Leishmaniasis	55	0.030

578	P	DYS193	Dystonia 11, Myoclonic	55	0.030

579	P	STR020	Strabismus	55	0.030

580		HMP005	Hemiplegia	55	0.030

581		GLC003	Glucose Intolerance	54	0.030

582	P	ALP008	Alopecia	54	0.030

583	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.030

584		GST037	Gastroparesis	54	0.030

585		PRC013	Pericarditis	54	0.030

586		AMN001	Amenorrhea	54	0.030

587	P	LTR001	Lateral Sclerosis	54	0.030

588		MYM001	Myoma	54	0.030

589		SNS003	Sensory Peripheral Neuropathy	54	0.030

590		PTT009	Pituitary Gland Disease	54	0.030

591	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.030

592		BRN038	Bronchial Disease	53	0.030

593		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.030

594		DNT012	Dental Caries	53	0.030

595		INT051	Intussusception	53	0.030

596	P	SPN429	Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2	52	0.030

597	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.030

598		ACR041	Acromelic Frontonasal Dysostosis	52	0.030

599		NRT004	Neuritis	52	0.030

600		BWN001	Bowen-Conradi Syndrome	52	0.030

601		PPT001	Peptic Esophagitis	52	0.030

602		SPN051	Spondylitis	51	0.030

603	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.030

604		MYL001	Myelitis	51	0.030

605		ENT011	Enterocolitis	51	0.030

606	c	PNC106	Pancreatic Agenesis 1	51	0.030

607		HYP781	Hypoascorbemia	51	0.030

608		BRX001	Bruxism	50	0.030

609		STT002	Status Asthmaticus	50	0.030

610	P	MYT002	Myotonic Dystrophy	49	0.030

611		VRC001	Varicocele	49	0.030

612		CCN001	Cocaine Dependence	48	0.030

613		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.030

614		PTC002	Potocki-Lupski Syndrome	48	0.030

615		PNC034	Pancreas Disease	48	0.030

616		PRD004	Prediabetes Syndrome	47	0.030

617	P	CLL015	Collagen Disease	47	0.030

618		SRT004	Serotonin Syndrome	47	0.030

619	P	OVR046	Ovarian Cyst	47	0.030

620	P	BLD051	Blood Coagulation Disease	46	0.030

621		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	45	0.030

622	P	TRN034	Transverse Myelitis	45	0.030

623		CYN002	Cyanosis, Transient Neonatal	45	0.030

624		NWC001	Newcastle Disease	45	0.030

625		CRB004	Cerebral Artery Occlusion	45	0.030

626		IMM136	Immune System Disease	45	0.030

627		CRT015	Carotid Artery Occlusion	45	0.030

628		MYF001	Myofibroma	45	0.030

629		BCT021	Bacterial Sepsis	44	0.030

630		LWC001	Low Compliance Bladder	43	0.030

631		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.030

632		STL007	Steel Syndrome	43	0.030

633	P	PRT026	Parotitis	42	0.030

634		MYF002	Myofascial Pain Syndrome	42	0.030

635		MCH006	Mechanical Strabismus	42	0.030

636		DBT002	Diabetic Autonomic Neuropathy	41	0.030

637	c	MJR024	Major Affective Disorder 9	41	0.030

638		IMM080	Immunodeficiency 23	40	0.030

639		PLM005	Pleomorphic Lipoma	40	0.030

640		OCL010	Ocular Hypotension	39	0.030

641		PLC009	Placenta Praevia	39	0.030

642		SCR015	Scarlet Fever	39	0.030

643	c	ACR088	Aicardi-Goutieres Syndrome 3	39	0.030

644	c	PLM022	Pulmonary Valve Insufficiency	39	0.030

645		SPR024	Supratentorial Cancer	39	0.030

646		CDQ001	Cauda Equina Syndrome	38	0.030

647	c	MJR022	Major Affective Disorder 8	38	0.030

648		INF039	Infratentorial Cancer	38	0.030

649		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.030

650		CHL013	Cholecystolithiasis	37	0.030

651		PST030	Postcholecystectomy Syndrome	33	0.030

652		HND015	Hand Skill, Relative	33	0.030

653		SPN031	Supine Hypotensive Syndrome	32	0.030

654		INF009	Inflammatory Spondylopathy	31	0.030

655		CHR281	Chronic Hiccups	31	0.030

656		PLX004	Plexopathy	30	0.030

657		RSP007	Respiratory Distress Syndrome, Infant	30	0.030

658		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	26	0.030

659		URT049	Urate Oxidase, Pseudogene	25	0.030

660		HPS001	Hip Subluxation	20	0.030

661		OPD004	Opioid Dependence 1	16	0.030

662	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.022

663		NRL016	Neural Tube Defects	82	0.022

664	P	ATX030	Ataxia-Telangiectasia	82	0.022

665	P	GLM040	Glioma Susceptibility 1	81	0.022

666	P	RTT002	Rett Syndrome	80	0.022

667	P	LNG064	Lung Cancer Susceptibility 3	78	0.022

668	P	PRK057	Parkinson Disease, Late-Onset	78	0.022

669		PHN003	Phenylketonuria	75	0.022

670	P	SCH015	Schizophrenia	74	0.022

671		ULC004	Ulcerative Colitis	73	0.022

672		SCH036	Scheie Syndrome	72	0.022

673	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	0.022

674		APR006	Apert Syndrome	70	0.022

675	c	PNC108	Pancreatitis, Hereditary	70	0.022

676	P	MYP004	Myopathy	70	0.022

677	P	RTH006	Rothmund-Thomson Syndrome, Type 2	69	0.022

678		ACR008	Acrocallosal Syndrome	69	0.022

679	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.022

680	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.022

681		EWN003	Ewing Sarcoma	69	0.022

682	P	ANG001	Angelman Syndrome	69	0.022

683	P	INF038	Influenza	68	0.022

684		RCK004	Rickets	68	0.022

685		FCT007	Factor Vii Deficiency	67	0.022

686		OMN001	Omenn Syndrome	67	0.022

687	P	BLD062	Bile Duct Cancer	67	0.022

688		WLF001	Wolff-Parkinson-White Syndrome	66	0.022

689	P	CLC063	Celiac Disease 1	66	0.022

690		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.022

691		CHD001	Chediak-Higashi Syndrome	66	0.022

692	P	MSC005	Muscular Dystrophy	66	0.022

693		SPN209	Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations	66	0.022

694		ART001	Arterial Tortuosity Syndrome	66	0.022

695	c	FML346	Familial Adenomatous Polyposis 1	66	0.022

696	c	HRD010	Hereditary Spastic Paraplegia	66	0.022

697		AND002	Androgen Insensitivity Syndrome	66	0.022

698		CHR593	Chromosome 16p13.3 Deletion Syndrome, Proximal	66	0.022

699	P	ATR011	Atrial Fibrillation	66	0.022

700	P	HYD006	Hydrocephalus	66	0.022

701	P	DRM053	Dermatitis, Atopic	66	0.022

702	P	NRV007	Nervous System Disease	66	0.022

703		GTL001	Gitelman Syndrome	65	0.022

704	c	FML001	Familial Atrial Fibrillation	65	0.022

705		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.022

706		SRC014	Sarcoma	65	0.022

707		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.022

708		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.022

709		BRR014	Barrett Esophagus	65	0.022

710	c	ART101	Aortic Valve Disease 2	65	0.022

711		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.022

712		TBC004	Tobacco Addiction	64	0.022

713		GT001	Gout	64	0.022

714		DGR001	Digeorge Syndrome	64	0.022

715		PRP083	Porphyria, Acute Intermittent	64	0.022

716		LYM017	Lyme Disease	64	0.022

717		HYP020	Hyperprolactinemia	64	0.022

718		OST017	Osteomyelitis	64	0.022

719	P	RHB003	Rhabdomyosarcoma	63	0.022

720		TYP007	Typhoid Fever	63	0.022

721		PLG002	Plague	63	0.022

722	c	MLG084	Malignant Fibrous Histiocytoma	63	0.022

723	P	CRG003	Crigler-Najjar Syndrome, Type I	63	0.022

724		ACT119	Acute Promyelocytic Leukemia	63	0.022

725	P	SHR029	Short Syndrome	63	0.022

726	c	SYS004	Systemic Mastocytosis	63	0.022

727	P	LMY004	Leiomyosarcoma	63	0.022

728		TRN015	Transient Cerebral Ischemia	63	0.022

729	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.022

730		LPD008	Lipid Metabolism Disorder	62	0.022

731		CLT003	Colitis	62	0.022

732	c	HPT003	Hepatitis a	62	0.022

733	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.022

734	P	ORT004	Orthostatic Intolerance	62	0.022

735		ATM095	Autoimmune Disease	62	0.022

736	P	ACR001	Aicardi-Goutieres Syndrome	62	0.022

737		BRS099	Breast Ductal Carcinoma	62	0.022

738	P	PRP029	Porphyria	62	0.022

739		ESP020	Esophageal Atresia	62	0.022

740		SPN404	Spinal and Bulbar Muscular Atrophy, X-Linked 1	61	0.022

741	c	MCP047	Mucopolysaccharidosis, Type Iva	61	0.022

742		YLL002	Yellow Fever	61	0.022

743		CHR066	Chronic Fatigue Syndrome	61	0.022

744	P	SJG008	Sjogren Syndrome	61	0.022

745		SDD001	Sudden Infant Death Syndrome	61	0.022

746	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.022

747	P	NPH012	Nephrotic Syndrome	60	0.022

748		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.022

749		DPH001	Diphtheria	60	0.022

750	P	BNG030	Benign Ependymoma	60	0.022

751		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.022

752		ACN002	Acanthosis Nigricans	60	0.022

753	P	ALP009	Alopecia Areata	60	0.022

754	P	SNS001	Sensorineural Hearing Loss	60	0.022

755		VRC005	Varicose Veins	60	0.022

756		INS001	Insulinoma	60	0.022

757	P	THL005	Thalassemia	60	0.022

758	P	MYC008	Myocarditis	59	0.022

759	P	AXN002	Axenfeld-Rieger Syndrome	59	0.022

760	P	BND020	Bone Disease	59	0.022

761		GRD007	Grade Iii Astrocytoma	59	0.022

762		IRN001	Iron Deficiency Anemia	59	0.022

763		ADN018	Adenoma	59	0.022

764	P	SYP003	Syphilis	58	0.022

765		GLB001	Gilbert Syndrome	58	0.022

766		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	58	0.022

767		RBS001	Rabies	58	0.022

768		SPT004	Septic Arthritis	58	0.022

769		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.022

770		EYD002	Eye Disease	58	0.022

771	c	MCP004	Mucopolysaccharidosis Iv	57	0.022

772	P	GLL018	Gallbladder Cancer	57	0.022

773	P	INF032	Infertility	57	0.022

774	P	UVT001	Uveitis	57	0.022

775		BLM002	Bulimia Nervosa	57	0.022

776	c	CHL119	Cholangitis, Primary Sclerosing	57	0.022

777		IRN002	Iron Metabolism Disease	57	0.022

778	P	RHN004	Rhinitis	57	0.022

779		DSS009	Disseminated Intravascular Coagulation	57	0.022

780		THY022	Thymic Carcinoma	57	0.022

781	c	LKM070	Leukemia, Acute Monocytic	57	0.022

782	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.022

783		AYM001	Ayme-Gripp Syndrome	57	0.022

784		PPL058	Papilloma of Choroid Plexus	56	0.022

785	P	CHN012	Chondrosarcoma	56	0.022

786		CMR002	Coumarin Resistance	56	0.022

787		LST001	Listeriosis	56	0.022

788	P	MLT074	Multiple Endocrine Neoplasia	56	0.022

789		ALL006	Allergic Asthma	56	0.022

790		LMY014	Leiomyoma, Uterine	56	0.022

791		ADN027	Adenomyosis	56	0.022

792		SFT003	Soft Tissue Sarcoma	56	0.022

793		SCH003	Schizophreniform Disorder	56	0.022

794		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.022

795	P	PLY019	Polyneuropathy	56	0.022

796	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.022

797	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.022

798	P	ATR001	Atrioventricular Septal Defect	55	0.022

799		LMB062	Limb Ischemia	55	0.022

800	P	PTT006	Pituitary Adenoma	55	0.022

801		TRC109	Tracheoesophageal Fistula with or Without Esophageal Atresia	55	0.022

802		ACT058	Active Peptic Ulcer Disease	55	0.022

803	P	HYP076	Hyperthyroidism	55	0.022

804	P	ALP106	Alport Syndrome 1, X-Linked	55	0.022

805		BRN045	Brunner Syndrome	55	0.022

806	P	VNS003	Venous Insufficiency	55	0.022

807	P	FNG006	Feingold Syndrome 1	55	0.022

808	P	LRY044	Larynx Cancer	55	0.022

809		PRP030	Purpura	54	0.022

810		TRD006	Tardive Dyskinesia	54	0.022

811		PYD001	Pyoderma Gangrenosum	54	0.022

812		GLS001	Gliosarcoma	54	0.022

813		SCH071	Schaaf-Yang Syndrome	54	0.022

814	P	EPS030	Episodic Kinesigenic Dyskinesia 1	54	0.022

815	P	DXT004	Dextro-Looped Transposition of the Great Arteries	54	0.022

816		RLP001	Relapsing Polychondritis	54	0.022

817		FCL014	Focal Epilepsy	54	0.022

818		MWT001	Mowat-Wilson Syndrome	54	0.022

819		VLC001	Velocardiofacial Syndrome	54	0.022

820		CLL010	Cellular Ependymoma	54	0.022

821		THR013	Thoracic Outlet Syndrome	54	0.022

822		ANL018	Analbuminemia	54	0.022

823		HMS001	Hemosiderosis	54	0.022

824		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.022

825		CLL003	Cellulitis	54	0.022

826		CLR030	Clear Cell Renal Cell Carcinoma	53	0.022

827	P	LCH002	Lichen Planus	53	0.022

828		FRZ001	Frozen Shoulder	53	0.022

829		KRT006	Keratoconjunctivitis	53	0.022

830	P	MNC007	Monocytic Leukemia	53	0.022

831	P	EMB005	Embryonal Rhabdomyosarcoma	53	0.022

832		BRD004	Borderline Personality Disorder	53	0.022

833	P	SHR001	Short Bowel Syndrome	53	0.022

834	P	GRS003	Griscelli Syndrome	53	0.022

835		KNS001	Kniest Dysplasia	53	0.022

836		SPN035	Spindle Cell Sarcoma	53	0.022

837		ALC009	Alcoholic Liver Cirrhosis	53	0.022

838	c	CNT035	Central Nervous System Disease	52	0.022

839		DMY004	Demyelinating Disease	52	0.022

840		LYS002	Lysosomal Storage Disease	52	0.022

841		HRP009	Herpes Simplex Encephalitis	52	0.022

842	c	ACR116	Aicardi-Goutieres Syndrome 1	52	0.022

843		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.022

844	P	NRD007	Neurodegeneration with Brain Iron Accumulation	52	0.022

845		ACT200	Acute Monoblastic Leukemia	52	0.022

846		ART074	Aortic Dissection	52	0.022

847		PRV004	Periventricular Leukomalacia	52	0.022

848		CLR109	Colorectal Adenocarcinoma	51	0.022

849	P	LCT001	Lactic Acidosis	51	0.022

850	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.022

851		INT079	Intrahepatic Cholangiocarcinoma	51	0.022

852		PLS006	Plasmodium Vivax Malaria	51	0.022

853		ASP003	Aseptic Meningitis	51	0.022

854	c	VRL007	Viral Encephalitis	51	0.022

855	P	CHL066	Cholangitis	51	0.022

856		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.022

857		CHR005	Chorioamnionitis	51	0.022

858		GNT002	Giant Cell Glioblastoma	50	0.022

859		SCH012	Schizoaffective Disorder	50	0.022

860		RTN003	Retinal Ischemia	50	0.022

861		BLP005	Blepharitis	50	0.022

862	c	SVR005	Severe Pre-Eclampsia	50	0.022

863	P	MTR003	Mitral Valve Stenosis	50	0.022

864		FSC004	Fasciitis	50	0.022

865		PYD002	Pyoderma	50	0.022

866	P	TMP001	Temporal Lobe Epilepsy	50	0.022

867		BLR001	Biliary Atresia	50	0.022

868		DBT004	Diabetic Polyneuropathy	49	0.022

869		RBF001	Riboflavin Deficiency	49	0.022

870		ENT004	Enthesopathy	49	0.022

871		KRT001	Keratoconjunctivitis Sicca	49	0.022

872		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	49	0.022

873	c	NRB010	Neuroblastoma 1	49	0.022

874		LFT001	Left Bundle Branch Hemiblock	49	0.022

875		HDR003	Hidradenitis	49	0.022

876		GST049	Gastrointestinal System Cancer	49	0.022

877	P	MGR001	Migraine Without Aura	49	0.022

878		PTH002	Pathological Gambling	49	0.022

879		URM002	Uremia	49	0.022

880		HST010	Histiocytosis	48	0.022

881		QDR001	Quadriplegia	48	0.022

882	c	BCT013	Bacterial Pneumonia	48	0.022

883	c	DSB006	Desbuquois Dysplasia 1	48	0.022

884		NCR007	Necrotizing Fasciitis	48	0.022

885	P	SCL009	Sclerosing Cholangitis	48	0.022

886		VTM033	Vitamin K Deficiency Bleeding	48	0.022

887	P	PRN026	Porencephaly	48	0.022

888		GLC106	Glucocorticoid Resistance, Generalized	48	0.022

889		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.022

890	c	MTR002	Mitral Valve Insufficiency	48	0.022

891		HPR003	Heparin-Induced Thrombocytopenia	48	0.022

892		PRP007	Priapism	47	0.022

893		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.022

894		DRY001	Dry Eye Syndrome	47	0.022

895	P	CRN028	Corneal Ulcer	47	0.022

896	P	RNL015	Renal Hypertension	47	0.022

897	P	ERY008	Erythromelalgia	47	0.022

898		KRT002	Keratomalacia	47	0.022

899		ANT011	Antisocial Personality Disorder	47	0.022

900	P	ENC008	Encephalocele	47	0.022

901		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.022

902		TST044	Testicular Torsion	47	0.022

903	P	PRC019	Precocious Puberty	46	0.022

904	c	CNT075	Central Precocious Puberty	46	0.022

905		ASP004	Asphyxia Neonatorum	46	0.022

906		TST014	Testicular Cancer	46	0.022

907		SMT001	Somatization Disorder	46	0.022

908		MTS001	Mutism	46	0.022

909		SPN020	Spondylosis	46	0.022

910		KRT013	Keratolytic Winter Erythema	46	0.022

911		UMB002	Umbilical Hernia	46	0.022

912	P	PLL002	Pellagra	46	0.022

913		OBS003	Obsessive-Compulsive Personality Disorder	46	0.022

914	c	DRR009	Diarrhea 6	46	0.022

915	c	MLG068	Malignant Glioma	46	0.022

916		BNS007	Bone Sarcoma	45	0.022

917		MXD026	Mixed Glioma	45	0.022

918		PST048	Postural Orthostatic Tachycardia Syndrome	45	0.022

919		CNV002	Conversion Disorder	45	0.022

920		URT010	Ureteral Obstruction	45	0.022

921		NRS003	Neurosyphilis	45	0.022

922		ORL013	Oral Lichen Planus	45	0.022

923		STS002	Situs Inversus	45	0.022

924	c	SPN097	Spinocerebellar Ataxia 23	45	0.022

925		INT304	Interstitial Pneumonitis, Desquamative, Familial	45	0.022

926		NNS002	Nonspecific Interstitial Pneumonia	45	0.022

927		OVR112	Ovarian Germ Cell Cancer	45	0.022

928		ASP008	Aspiration Pneumonitis	45	0.022

929	c	CLR017	Clear Cell Sarcoma	45	0.022

930		GRN017	Granulocytopenia	44	0.022

931	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.022

932		OVR063	Overnutrition	44	0.022

933		VNC001	Von Economo's Disease	44	0.022

934		THR012	Thoracic Cancer	44	0.022

935	c	SPR086	Spermatogenic Failure 3	44	0.022

936		CHL109	Childhood Apraxia of Speech	44	0.022

937	c	RHB023	Rhabdomyosarcoma, Embryonal, 1	43	0.022

938		PST020	Postpoliomyelitis Syndrome	43	0.022

939		ORL015	Oral Squamous Cell Carcinoma	43	0.022

940	P	HYP265	Hypotonia	43	0.022

941	P	STR092	Striatal Degeneration, Autosomal Dominant 2	42	0.022

942	P	VND001	Vein Disease	42	0.022

943		TRC097	Tracheomalacia	42	0.022

944	P	CLS010	Cluster Headache	42	0.022

945		ORB013	Orbital Disease	42	0.022

946		GLC096	Galactorrhea	42	0.022

947		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.022

948		RST023	Resting Heart Rate, Variation in	41	0.022

949	P	RRH023	Rare Hereditary Hemochromatosis	41	0.022

950		PLY021	Polyradiculopathy	41	0.022

951		PCD001	Pica Disease	41	0.022

952		ACT088	Acute Insulin Response	41	0.022

953		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	41	0.022

954		ASY002	Asymptomatic Neurosyphilis	41	0.022

955	P	MLG074	Malignant Mesenchymoma	40	0.022

956		KDN007	Kidney Clear Cell Sarcoma	40	0.022

957		HYP030	Hypoactive Sexual Desire Disorder	40	0.022

958	P	TRC031	Trichorhinophalangeal Syndrome	40	0.022

959		UTR043	Uterine Sarcoma	39	0.022

960	P	INT260	Intracranial Berry Aneurysm	39	0.022

961	P	ARC016	Auriculocondylar Syndrome 1	39	0.022

962		LKP003	Leukoplakia	39	0.022

963	c	ACT004	Acute Diarrhea	39	0.022

964		FML039	Female Reproductive System Disease	39	0.022

965		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.022

966		ANT019	Anterograde Amnesia	38	0.022

967		CHL039	Choledocholithiasis	38	0.022

968		ANG016	Angiokeratoma	38	0.022

969		HYP264	Hypertonia	38	0.022

970	c	ACT159	Acute Transverse Myelitis	38	0.022

971		OVR094	Ovarian Epithelial Cancer	38	0.022

972		SCR039	Scorpion Envenomation	38	0.022

973		SWL001	Swallowing Disorders	38	0.022

974		MCP033	Mucopolysaccharidoses	38	0.022

975		CRB009	Cerebritis	37	0.022

976		AKN002	Akinetic Mutism	37	0.022

977		DDN027	Duodenum Disease	37	0.022

978	P	MRQ003	Morquio Syndrome	37	0.022

979		GLM044	Glomerular Disease	37	0.022

980	c	HTR021	Heterotaxy, Visceral, 5, Autosomal	37	0.022

981		GRS001	Gerstmann Syndrome	36	0.022

982		CMP006	Complex Partial Epilepsy	36	0.022

983		PRT009	Parotid Gland Cancer	36	0.022

984		TRG003	Trigeminal Nerve Disease	36	0.022

985		ABD010	Abdominal Wall Defect	36	0.022

986		CRY036	Cryptogenic Cirrhosis	36	0.022

987		ESP029	Esophageal Atresia/tracheoesophageal Fistula	36	0.022

988		MDN008	Median Arcuate Ligament Syndrome	35	0.022

989		EPD005	Epidural Abscess	35	0.022

990		PLN026	Pilonidal Sinus	35	0.022

991		TLS001	Tolosa-Hunt Syndrome	35	0.022

992		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	35	0.022

993	c	MJR008	Major Affective Disorder 2	35	0.022

994		ATX010	Ataxia Neuropathy Spectrum	34	0.022

995		FBR002	Fibrosarcoma of Bone	34	0.022

996		SPN043	Spinal Cord Glioma	34	0.022

997		GRM010	Germ Cells Tumors	34	0.022

998		BWN003	Bowenoid Papulosis	34	0.022

999	c	EPL125	Epileptic Encephalopathy, Early Infantile, 24	34	0.022

1000		GLC024	Glucose Transporter Type 1 Deficiency Syndrome	34	0.022

1001		BRN041	Bornholm Eye Disease	34	0.022

1002	c	MJR023	Major Affective Disorder 7	33	0.022

1003	c	CHR064	Chronic Monocytic Leukemia	33	0.022

1004		ALR002	Al-Raqad Syndrome	33	0.022

1005		PRS064	Persistent Vegetative State	33	0.022

1006		DDN004	Duodenogastric Reflux	33	0.022

1007		ACT064	Acute Necrotizing Encephalitis	33	0.022

1008	c	MJR003	Major Affective Disorder 6	33	0.022

1009	c	MJR006	Major Affective Disorder 5	33	0.022

1010		DYS140	Dyskinesia, Familial, with Facial Myokymia	33	0.022

1011		AMN014	Aminopterin Syndrome Sine Aminopterin	33	0.022

1012		SBV001	Subvalvular Aortic Stenosis	33	0.022

1013		INF013	Inferior Myocardial Infarction	33	0.022

1014	c	BLD140	Blood Group, I System	32	0.022

1015		FMR018	Femoral-Facial Syndrome	32	0.022

1016		NRN002	Neuronitis	32	0.022

1017		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.022

1018		PRX097	Paroxysmal Dystonia	32	0.022

1019		RHS001	Rh Isoimmunization	32	0.022

1020		SPC003	Specific Developmental Disorder	31	0.022

1021		EXN003	Exencephaly	31	0.022

1022		FMR003	Femoral Neuropathy	31	0.022

1023		NRG001	Neurogenic Bowel	31	0.022

1024		ASP036	Aspirin Allergy	30	0.022

1025		FNT004	Fainting	30	0.022

1026		MTY003	Mutyh Polyposis	30	0.022

1027		ACT228	Acute Radiation Syndrome	29	0.022

1028		ANT013	Anterior Spinal Artery Syndrome	29	0.022

1029		CRD220	Cardiac Valvular Defect, Developmental	29	0.022

1030		DSC004	Discitis	29	0.022

1031	c	MJR004	Major Affective Disorder 4	28	0.022

1032		TMP019	Temporomandibular Joint Anomaly	28	0.022

1033	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.022

1034		SPN185	Spinal Cord Infarction	28	0.022

1035		ARG004	Argyria	27	0.022

1036		BRB003	Barbiturate Abuse	27	0.022

1037		MDR006	Moderate and Severe Traumatic Brain Injury	27	0.022

1038		RHH001	Rohhad	27	0.022

1039	c	RNG015	Ring Chromosome 2	26	0.022

1040	c	ACQ029	Acquired Porencephaly	26	0.022

1041		ETH012	Ethylene Glycol Poisoning	26	0.022

1042		MLG164	Malignant Epithelial Tumor of Ovary	26	0.022

1043	c	FRN037	Frontal Encephalocele	26	0.022

1044		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.022

1045	c	TRN053	Transient Pseudohypoaldosteronism	25	0.022

1046		CPG001	Capgras Syndrome	24	0.022

1047		OGL001	Ogilvie Syndrome	24	0.022

1048		CNG092	Congenital Extrahepatic Portosystemic Shunt	23	0.022

1049		BLD165	Blood Group, Colton System	20	0.022

1050		LNP001	Loin Pain Hematuria Syndrome	18	0.022

1051		IDP022	Idiopathic Spinal Cord Herniation	17	0.022

1052		PNT023	Pontine Hemorrhage	17	0.022

1053		PLY028	Polycystic Bone Disease	17	0.022

1054		BLD137	Blood Group--Ahonen	16	0.022

1055		MTR086	Motor Stereotypies	16	0.022

1056		ADS006	Aids - Neurological Complications	15	0.022

1057	c	ADL020	Adult Malignant Mesenchymoma	11	0.022

1058		ERL051	Early Response to Neural Induction Gene	10	0.022

1059		CHL016	Childhood Malignant Mesenchymoma	8	0.022

1060		ACT171	Acute Opioid Poisoning	6	0.022