Search results for Morphine

1560 hits were found for Morphine

#	Family	MCID	Name	MIFTS	Score
1		PNG002	Pain Agnosia	51	86.445

2		MRP001	Morphine Dependence	42	63.790

3	P	CHR345	Chronic Pain	50	33.578

4		WTH001	Withdrawal Disorder	48	31.142

5		OPT003	Opiate Dependence	49	27.600

6		OPD006	Opioid Addiction	48	23.973

7		CNS004	Constipation	56	23.593

8		48X005	48,xyyy	39	20.714

9		OPD001	Opioid Abuse	44	16.341

10		DRG003	Drug Dependence	46	15.028

11	c	PNS012	Paine Syndrome	60	14.285

12		PRT037	Pertussis	65	14.093

13		NNT008	Neonatal Abstinence Syndrome	40	13.869

14	P	SBS003	Substance Abuse	54	13.106

15	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	12.962

16		AMN003	Amnestic Disorder	54	12.706

17	P	TRM003	Tremor	48	12.434

18	P	NRB001	Neuroblastoma	66	12.337

19		BCK006	Back Pain	47	11.585

20	P	SCL018	Scoliosis	57	11.516

21	P	SCK005	Sickle Cell Disease	56	11.422

22	P	PTS002	Ptosis	52	11.068

23		ILS001	Ileus	50	10.889

24		SBC016	Subacute Delirium	43	10.666

25		ANX010	Anxiety	70	10.297

26		MCS002	Mucositis	56	9.934

27	P	MYC007	Myocardial Infarction	70	9.908

28	P	BNC003	Bone Cancer	58	9.655

29	P	SZR006	Seizure Disorder	70	9.623

30		ALL029	Allergic Disease	59	9.403

31	P	HDC001	Headache	57	9.298

32	P	SLP006	Sleep Apnea	69	9.008

33		IDP070	Idiopathic Scoliosis	42	8.884

34		ISC004	Ischemia	61	8.691

35	P	MYC033	Myoclonus	47	8.649

36	c	ACT075	Acute Myocardial Infarction	56	8.556

37	P	RSP003	Respiratory Failure	74	8.517

38		SPN186	Spinal Cord Injury	61	8.407

39		OST012	Osteoarthritis	77	8.295

40	P	DRR001	Diarrhea	55	8.199

41		PLM010	Pulmonary Edema	55	8.057

42		CHL067	Cholecystitis	60	7.969

43		PLM129	Pulmonary Disease, Chronic Obstructive	74	7.824

44		ALC007	Alcohol Dependence	66	7.579

45		CYT002	Cytokine Deficiency	43	7.561

46		HMN044	Human Immunodeficiency Virus Type 1	78	7.474

47		SPS057	Spasticity	42	7.446

48		DBT010	Diabetic Neuropathy	54	7.397

49		ACQ007	Acquired Immunodeficiency Syndrome	59	7.253

50		47X002	47,xyy	48	7.241

51		LNG099	Lung Disease	62	7.133

52		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	6.998

53	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	6.904

54	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	6.904

55	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	6.904

56	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	6.904

57	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	6.904

58	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	6.904

59	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	6.904

60	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	6.904

61	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	6.904

62	P	PRP019	Peripheral Nervous System Disease	58	6.761

63		CHL014	Cholera	62	6.730

64		LPT014	Leptin Deficiency or Dysfunction	78	6.616

65	P	ALC033	Alcohol Use Disorder	61	6.555

66		ING001	Inguinal Hernia	59	6.488

67		IMM167	Immune Deficiency Disease	78	6.478

68		APP008	Appendicitis	62	6.477

69		PRT036	Peritonitis	65	6.430

70	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	6.389

71		HYP056	Hypoglycemia	65	6.374

72		MNN017	Mononeuropathy	41	6.336

73	P	PNC044	Pancreatitis	61	6.267

74	P	NRP001	Neuropathy	60	6.222

75	c	MGR028	Migraine with or Without Aura 1	64	6.154

76		PST028	Post-Traumatic Stress Disorder	59	6.152

77		AGN016	Aging	54	5.925

78		HYP066	Hyperglycemia	61	5.909

79		DPR016	Depression	65	5.885

80		PST053	Postherpetic Neuralgia	40	5.707

81		VRS002	Virus-Associated Trichodysplasia Spinulosa	30	5.644

82		MNT002	Mental Depression	57	5.628

83	P	HRP006	Herpes Simplex	65	5.514

84		OCL069	Ocular Motor Apraxia	57	5.470

85		HDN002	Head Injury	44	5.344

86		LPP008	Lipoprotein Quantitative Trait Locus	65	5.321

87		FBR047	Fibromyalgia	58	5.296

88		SCK003	Sickle Cell Anemia	74	5.284

89	P	BRS047	Breast Cancer	98	5.206

90		ANG054	Angina Pectoris	66	5.158

91		ART016	Aortic Aneurysm	68	5.102

92		HRN003	Heroin Dependence	44	5.082

93		INT007	Intermediate Coronary Syndrome	54	5.080

94		ACT084	Acute Stress Disorder	54	5.077

95		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	5.075

96	P	ART022	Arthritis	71	4.960

97	c	ACT027	Acute Pancreatitis	60	4.960

98		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	4.899

99	P	CRD119	Cardiac Arrest	67	4.831

100		BLR004	Biliary Dyskinesia	37	4.790

101	P	PNC035	Pancreatic Cancer	86	4.756

102	P	CLR023	Colorectal Cancer	100	4.736

103		GLM045	Glioma	63	4.723

104	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	4.680

105		GLL048	Glial Tumor	52	4.662

106		PLC002	Plica Syndrome	35	4.662

107		SYN007	Synovitis	55	4.662

108	P	LNG032	Lung Cancer	98	4.606

109		APN008	Apnea, Obstructive Sleep	67	4.573

110		MDD011	Mood Disorder	62	4.563

111		TTN003	Tetanus	65	4.525

112	P	SLP005	Sleep Disorder	61	4.472

113		SPN354	Spinal Arachnoiditis	36	4.450

114		ARC002	Arachnoiditis	50	4.450

115	P	SCL057	Scoliosis, Isolated 1	40	4.450

116		INT066	Interstitial Lung Disease	60	4.444

117	P	EXN002	Exanthem	58	4.384

118		CRB037	Cerebral Palsy	67	4.358

119		ACT017	Acute Chest Syndrome	50	4.330

120		PRT058	Pure Autonomic Failure	58	4.328

121		TXC005	Toxic Shock Syndrome	62	4.324

122		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	4.318

123		STM007	Stomatitis	54	4.314

124		PNM008	Pneumothorax	54	4.310

125		PCT003	Pectus Excavatum	46	4.274

126		ANX004	Anoxia	40	4.252

127		PRP016	Paraplegia	52	4.250

128	P	ANR048	Aniridia 1	64	4.235

129		TRM010	Traumatic Brain Injury	51	4.234

130		NWB001	Newborn Respiratory Distress Syndrome	56	4.226

131		CMP010	Complex Regional Pain Syndrome	60	4.223

132		ART140	Arteries, Anomalies of	53	4.208

133		DFC004	Deficiency Anemia	74	4.148

134	P	ENC018	Encephalopathy	62	4.085

135	c	PRC016	Pre-Eclampsia	65	4.068

136	P	RST001	Restless Legs Syndrome	52	4.064

137		CNG034	Congestive Heart Failure	69	4.025

138	P	INT070	Intestinal Obstruction	57	4.022

139		DYS073	Dysphagia	53	4.010

140		RHB024	Rhabdomyosarcoma 2	67	4.007

141	P	TRN020	Turner Syndrome	67	3.979

142		GLB002	Glioblastoma	67	3.969

143	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	3.931

144		DMP001	Dumping Syndrome	43	3.917

145		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	3.898

146		MTN003	Motion Sickness	51	3.896

147		STT001	Status Epilepticus	59	3.865

148		ADL002	Adult Syndrome	70	3.863

149		INF118	Inflammatory Myopathy with Abundant Macrophages	27	3.839

150		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	3.828

151	P	CRN300	Coronary Heart Disease 1	73	3.825

152	c	PLM164	Pulmonary Hypertension, Primary, 1	76	3.825

153		IDP011	Idiopathic Interstitial Pneumonia	59	3.824

154	P	AGN002	Agnosia	54	3.808

155	P	LVR013	Liver Disease	69	3.805

156		BRN071	Brain Injury	50	3.803

157		HRP004	Herpes Zoster	61	3.789

158	P	ADL010	Adult Respiratory Distress Syndrome	71	3.777

159		PST021	Postpartum Depression	50	3.767

160		ANT039	Antisynthetase Syndrome	55	3.698

161		DWN001	Down Syndrome	70	3.675

162		RDC002	Radiculopathy	52	3.673

163	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	3.669

164		SBS004	Substance Dependence	47	3.639

165	P	RCT021	Rectum Cancer	54	3.637

166	P	PLM036	Pulmonary Fibrosis	66	3.569

167		RNL114	Renal Cell Carcinoma, Nonpapillary	80	3.562

168	P	PRS038	Personality Disorder	65	3.544

169		DGN001	Degenerative Disc Disease	49	3.531

170	P	CYS018	Cystitis	59	3.513

171		NPH009	Nephrolithiasis	54	3.510

172		PLM134	Pulmonary Fibrosis, Idiopathic	76	3.491

173		HLX001	Helix Syndrome	48	3.491

174		BNN005	Bunion	31	3.481

175	P	URT039	Urticaria	58	3.475

176		CHL068	Cholestasis	61	3.472

177		ESP021	Esophageal Cancer	83	3.464

178	P	BRS044	Breast Adenocarcinoma	58	3.464

179		PLY068	Polysubstance Abuse	41	3.433

180		HYP266	Hypoxia	57	3.431

181	c	ACT071	Acute Kidney Failure	60	3.426

182		CCN002	Cocaine Abuse	49	3.398

183		FTT001	Fatty Liver Disease	62	3.368

184	P	DDN001	Duodenal Ulcer	53	3.367

185	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	3.366

186	P	VSC007	Vascular Disease	63	3.359

187		SPN027	Spinal Stenosis	59	3.346

188		RSP019	Respiratory Distress Syndrome in Premature Infants	52	3.345

189		OBS002	Obsessive-Compulsive Disorder	68	3.345

190		NPH091	Nephrolithiasis, Calcium Oxalate	61	3.345

191		TRG002	Trigeminal Neuralgia	61	3.336

192		HYP080	Hypogonadism	50	3.336

193	c	HYP595	Hypertension, Essential	85	3.323

194		URL001	Urolithiasis	46	3.320

195	P	ART023	Arthropathy	61	3.305

196		SPS019	Spastic Paraparesis	38	3.275

197	P	KLZ004	Kala-Azar 1	41	3.222

198		CRD137	Cardiogenic Shock	56	3.222

199		LSH001	Leishmaniasis	64	3.222

200		SPN019	Spondylolisthesis	52	3.222

201	P	TTR001	Tetralogy of Fallot	69	3.218

202	P	PLM037	Pulmonary Hypertension	72	3.187

203	P	GST053	Gastric Cancer	83	3.176

204	P	HMR005	Hemorrhoid	49	3.176

205		SXL003	Sexual Disorder	49	3.172

206	P	MYS003	Myasthenia Gravis	68	3.145

207	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	3.145

208	P	DBT005	Diabetes Insipidus	54	3.131

209	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	3.129

210		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	3.116

211	P	PTN014	Patent Ductus Arteriosus 1	59	3.116

212		CHL004	Cholelithiasis	49	3.104

213	c	EXD008	Exudative Vitreoretinopathy 1	71	3.100

214	P	INF032	Infertility	57	3.099

215	P	HPT023	Hepatocellular Carcinoma	96	3.087

216		OST062	Osteoarthritis with Mild Chondrodysplasia	47	3.064

217	P	OST002	Osteoporosis	76	3.062

218	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	3.062

219	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	3.062

220		EXP004	Exophthalmos	51	3.058

221		SPL018	Splenomegaly	49	3.058

222	P	ECL001	Eclampsia	52	3.052

223	P	URN019	Urinary Tract Infection	49	3.051

224		INT146	Intervertebral Disc Disease	63	3.034

225	c	GLL024	Gallbladder Disease 1	52	3.030

226		NRT001	Neurotic Disorder	56	3.030

227	P	PHC003	Pheochromocytoma	69	3.029

228		ADR040	Adrenal Gland Pheochromocytoma	46	3.029

229		MYL069	Myeloma, Multiple	77	3.016

230	c	HPT073	Hepatitis C Virus	71	2.998

231		IRR002	Irritable Bowel Syndrome	65	2.975

232		HMN014	Human Immunodeficiency Virus Infectious Disease	54	2.974

233	P	DBT009	Diabetes Mellitus	67	2.974

234		CYN002	Cyanosis, Transient Neonatal	43	2.971

235	P	DMN002	Dementia	66	2.950

236	c	THY107	Thymoma, Familial	42	2.936

237	P	THY023	Thymoma	64	2.936

238	c	DNT047	Dentinogenesis Imperfecta Type 2	35	2.936

239		HRT012	Heart Valve Disease	53	2.918

240		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	2.897

241		SRT004	Serotonin Syndrome	54	2.882

242		PTH003	Pathologic Nystagmus	52	2.869

243		ANR040	Aneurysm	61	2.861

244	P	MYL006	Myeloid Leukemia	61	2.854

245	P	EPD016	Epidermolysis Bullosa	53	2.854

246	P	OVR082	Overgrowth Syndrome	49	2.851

247		NNL006	Non-Alcoholic Steatohepatitis	54	2.840

248		BRN056	Bronchopulmonary Dysplasia	56	2.840

249		MTB004	Metabolic Acidosis	48	2.839

250		ORL011	Oral Cancer	60	2.839

251		GST092	Gastroesophageal Reflux	61	2.820

252		END040	Endogenous Depression	55	2.816

253	P	NSP012	Nasopharyngeal Carcinoma	61	2.803

254	c	HPT001	Hepatitis C	62	2.788

255	P	HRT032	Heart Disease	81	2.788

256		RPD005	Rapidly Involuting Congenital Hemangioma	46	2.788

257		HRT011	Heart Septal Defect	49	2.788

258		PTT037	Pituitary Tumors	44	2.753

259		HPT004	Hepatic Coma	43	2.738

260	P	INF037	Inflammatory Bowel Disease	53	2.737

261		CNT047	Contact Dermatitis	57	2.733

262	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	2.720

263		CRB039	Cerebrovascular Disease	66	2.717

264		NNL005	Non-Alcoholic Fatty Liver Disease	63	2.713

265		ENT004	Enthesopathy	51	2.713

266	P	MJR001	Major Depressive Disorder	68	2.712

267		THR024	Thrombosis	56	2.708

268	c	FML116	Familial Cold Autoinflammatory Syndrome 1	55	2.690

269	P	HPT021	Hepatitis	69	2.677

270	c	TYP009	Type 2 Diabetes Mellitus	92	2.670

271		ATN005	Autonomic Dysfunction	46	2.667

272	P	ADN016	Adenocarcinoma	63	2.657

273		AND005	Androgen Insensitivity Syndrome, Mild	21	2.648

274	P	KDN018	Kidney Disease	72	2.646

275		RTR001	Retrograde Amnesia	41	2.644

276		CRB090	Cerebral Hypoxia	42	2.644

277		LMY002	Leiomyoma	51	2.641

278		HYD002	Hydronephrosis	58	2.622

279		LVR012	Liver Cirrhosis	63	2.622

280		PRS063	Paresthesia	39	2.622

281		LYM027	Lymphopenia	56	2.619

282		ETN001	Eating Disorder	59	2.618

283	P	BLD134	Bladder Cancer	79	2.609

284		BRN024	Bronchitis	67	2.609

285		DVR002	Diverticulitis	46	2.594

286	P	SKN015	Skin Carcinoma	71	2.594

287	P	HYP040	Hypospadias	51	2.587

288		ANR007	Anorexia Nervosa	60	2.556

289		RFL001	Reflex Sympathetic Dystrophy	51	2.539

290		ADG002	Audiogenic Seizures	25	2.539

291		ALG001	Algoneurodystrophy	38	2.539

292		CRV035	Cervical Cancer	73	2.537

293		CLF027	Cleft Palate, Isolated	64	2.537

294		OST159	Osteogenic Sarcoma	66	2.537

295		CRD223	Cardiac Arrhythmia	63	2.517

296	P	GLM040	Glioma Susceptibility 1	71	2.517

297		MLG169	Malignant Astrocytoma	57	2.517

298		PLM033	Pulmonary Embolism	58	2.515

299		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	46	2.485

300	P	PNM007	Pneumonia	67	2.484

301	P	BND020	Bone Disease	59	2.471

302		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	2.454

303	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	2.450

304		END086	End Stage Renal Disease	52	2.450

305		CRT015	Carotid Artery Occlusion	45	2.450

306	P	CNR004	Cone-Rod Dystrophy 2	74	2.442

307	P	VNT002	Ventricular Septal Defect	58	2.440

308	P	MLN007	Male Infertility	56	2.440

309		PRP027	Peripheral Vascular Disease	71	2.437

310	c	LKM061	Leukemia, Acute Myeloid	83	2.416

311	P	DYS154	Dystonia	64	2.414

312		NRM004	Neuroma	49	2.414

313	P	PLV020	Pelvic Organ Prolapse	58	2.409

314		CYS001	Cystic Fibrosis	78	2.395

315	c	MCL013	Mucolipidosis Iv	65	2.393

316	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	2.392

317	P	SCH015	Schizophrenia	74	2.388

318	P	PRK039	Parkinsonism	55	2.383

319	P	HNT016	Huntington Disease	73	2.379

320		PRL008	Paralytic Ileus	45	2.361

321	P	PLY019	Polyneuropathy	52	2.345

322		END057	Endometrial Cancer	72	2.342

323	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	2.340

324	P	LTR001	Lateral Sclerosis	58	2.340

325		SNG003	Single Ventricular Heart	30	2.320

326	c	DMN005	Diamond-Blackfan Anemia 2	28	2.320

327		ACL001	Acalculous Cholecystitis	38	2.320

328		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	2.320

329	c	LKM005	Leukemia, T-Cell, Chronic	34	2.320

330	c	HPT003	Hepatitis a	63	2.319

331		CLF001	Cleft Lip	53	2.317

332		ENT011	Enterocolitis	55	2.302

333		PPL052	Papillomatosis, Confluent and Reticulated	34	2.279

334	P	RHM011	Rheumatoid Arthritis	82	2.275

335	P	GLL020	Gallbladder Disease	56	2.275

336		PRV004	Periventricular Leukomalacia	52	2.270

337		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	2.268

338		CCN001	Cocaine Dependence	48	2.264

339	P	ATR010	Atrial Heart Septal Defect	58	2.263

340		PRN019	Perinatal Necrotizing Enterocolitis	60	2.263

341		CLF004	Cleft Lip/palate	57	2.261

342		HYP458	Hyper Ige Syndrome	60	2.261

343		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	36	2.257

344	P	BCL017	B-Cell Lymphoma	59	2.250

345		LPT006	Leptin Receptor Deficiency	50	2.242

346	c	VSC019	Vesicoureteral Reflux 1	57	2.236

347		BRN004	Brain Edema	54	2.236

348	c	RNG008	Ring Chromosome 13	30	2.236

349	P	LKM062	Leukemia, Acute Lymphoblastic	69	2.213

350	c	SML038	Small Cell Cancer of the Lung	69	2.213

351	c	CHR684	Chronic Kidney Disease	69	2.207

352	P	LKM002	Leukemia	67	2.205

353		NRG002	Neurogenic Bladder	55	2.204

354		PRD004	Prediabetes Syndrome	52	2.204

355		AVD001	Avoidant Personality Disorder	49	2.199

356		FML037	Female Breast Cancer	51	2.191

357		CYT018	Cytochrome P450 2d6 Variant	26	2.188

358		PRT013	Portal Hypertension	59	2.183

359	c	MJR022	Major Affective Disorder 8	38	2.167

360	c	MJR024	Major Affective Disorder 9	41	2.167

361	P	BPL003	Bipolar Disorder	56	2.167

362		MYF001	Myofibroma	42	2.167

363		KRT002	Keratomalacia	55	2.167

364		CLT003	Colitis	63	2.161

365		VGN023	Vaginitis	56	2.148

366	c	HYP836	Hypercholesterolemia, Familial, 1	73	2.145

367		BLR008	Bilirubin Metabolic Disorder	57	2.145

368	P	BNG032	Benign Mesothelioma	53	2.145

369	P	ENC004	Encephalitis	61	2.145

370		CDQ001	Cauda Equina Syndrome	37	2.141

371		SVR004	Severe Combined Immunodeficiency	72	2.141

372		GST037	Gastroparesis	52	2.141

373		HYP020	Hyperprolactinemia	63	2.123

374	P	MNN013	Meningitis	65	2.098

375		PLX004	Plexopathy	29	2.098

376		HPT019	Hepatic Encephalopathy	59	2.098

377		IMP005	Impotence	52	2.098

378		OCL010	Ocular Hypotension	37	2.098

379		SPR126	Superior Semicircular Canal Dehiscence	41	2.095

380	c	HMG029	Hemoglobin Se Disease	40	2.095

381	P	ATR011	Atrial Fibrillation	66	2.090

382		SDD001	Sudden Infant Death Syndrome	60	2.084

383	P	DRM053	Dermatitis, Atopic	65	2.084

384		HYP005	Hypokalemia	55	2.071

385		BCT021	Bacterial Sepsis	43	2.054

386	P	INT143	Interstitial Cystitis	60	2.025

387		SPN035	Spindle Cell Sarcoma	54	2.020

388		SRC014	Sarcoma	65	2.020

389		PNC129	Pancreatic Adenocarcinoma	65	2.009

390	c	PNC106	Pancreatic Agenesis 1	51	2.008

391		SPR004	Supravalvular Aortic Stenosis	57	2.008

392		BCT022	Bacterial Infectious Disease	56	2.008

393	P	FBR017	Fibrosarcoma	56	2.008

394	P	PYL005	Pyelonephritis	57	2.008

395		PNC034	Pancreas Disease	50	2.008

396	P	BLP003	Blepharospasm	46	2.005

397		TBC004	Tobacco Addiction	63	2.004

398		CLL003	Cellulitis	53	2.004

399		ATX019	Ataxia with Vitamin E Deficiency	44	2.003

400		UMB002	Umbilical Hernia	47	1.990

401		MYM001	Myoma	54	1.967

402		NRT004	Neuritis	53	1.967

403	P	RHN004	Rhinitis	57	1.962

404	P	STR020	Strabismus	56	1.960

405		HND015	Hand Skill, Relative	30	1.960

406		HRW001	Hair Whorl	35	1.960

407		MCH006	Mechanical Strabismus	40	1.960

408	P	MST009	Mastocytosis	64	1.960

409	P	LYM118	Lymphoma	67	1.956

410	P	CNJ013	Conjunctivitis	66	1.956

411		GLC003	Glucose Intolerance	54	1.948

412		CRB079	Cerebrospinal Fluid Leak	35	1.928

413		ART074	Aortic Dissection	53	1.919

414	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	1.919

415		URT049	Urate Oxidase, Pseudogene	24	1.911

416		INT051	Intussusception	52	1.911

417		PTC002	Potocki-Lupski Syndrome	48	1.911

418		VSC003	Visceral Leishmaniasis	55	1.911

419		CMM004	Common Variable Immunodeficiency	72	1.911

420		NWC001	Newcastle Disease	47	1.911

421		GST071	Gastrointestinal Carcinoma	46	1.904

422		ALL010	Allergic Contact Dermatitis	56	1.889

423		ARG004	Argyria	26	1.874

424		EPT021	Epithelial Recurrent Erosion Dystrophy	46	1.874

425		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	25	1.860

426		GRG001	Greig Cephalopolysyndactyly Syndrome	64	1.860

427	P	GLL022	Guillain-Barre Syndrome	60	1.851

428		VRL011	Viral Infectious Disease	61	1.843

429	P	KDN017	Kidney Cancer	61	1.843

430	P	THL005	Thalassemia	56	1.828

431	P	NRC002	Narcolepsy	56	1.828

432	P	THR014	Thrombocytopenia	66	1.828

433		DDN004	Duodenogastric Reflux	31	1.828

434		RTN003	Retinal Ischemia	49	1.828

435		SQM013	Squamous Cell Carcinoma, Head and Neck	73	1.819

436		ATR057	Atrioventricular Block	54	1.807

437		MYL001	Myelitis	50	1.807

438		CRB004	Cerebral Artery Occlusion	45	1.807

439		OTT002	Otitis Media	71	1.807

440	c	ACT073	Acute Leukemia	58	1.807

441	P	PLY018	Polycythemia	56	1.807

442		SPN369	Spinal Disease	44	1.802

443		SPN438	Spondyloepimetaphyseal Dysplasia, X-Linked, with Hypomyelinating Leukodystrophy	36	1.802

444		BRN028	Brain Cancer	74	1.785

445		SPS003	Spastic Diplegia	53	1.785

446		GLB001	Gilbert Syndrome	53	1.781

447		DSS032	Disease by Infectious Agent	55	1.781

448		PRP007	Priapism	47	1.781

449	P	AST005	Asthma	76	1.757

450	c	ACR088	Aicardi-Goutieres Syndrome 3	39	1.752

451		CTN007	Cutaneous Leishmaniasis	62	1.752

452		SNS003	Sensory Peripheral Neuropathy	52	1.752

453	P	END033	Endocarditis	58	1.752

454	P	MYT002	Myotonic Dystrophy	51	1.752

455	P	TXP001	Toxoplasmosis	60	1.752

456		PST030	Postcholecystectomy Syndrome	33	1.752

457		DSM003	Desmoid Disease, Hereditary	48	1.751

458	P	PRS040	Prostate Cancer	95	1.746

459	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	1.732

460	c	DPH024	Diaphragmatic Hernia, Congenital	64	1.732

461		DRG024	Drug Allergy	40	1.732

462	c	TYP008	Type 1 Diabetes Mellitus	70	1.725

463	c	ACT068	Acute Cystitis	61	1.725

464		WSR001	Was-Related Disorders	19	1.695

465	P	TRN034	Transverse Myelitis	47	1.693

466	P	CND004	Candidiasis	58	1.693

467		AMN001	Amenorrhea	54	1.693

468	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	1.681

469	c	LKM063	Leukemia, Chronic Myeloid	71	1.681

470	P	RRH023	Rare Hereditary Hemochromatosis	54	1.681

471	P	SYP003	Syphilis	59	1.681

472		HMS001	Hemosiderosis	48	1.681

473	P	MTR003	Mitral Valve Stenosis	53	1.681

474		TNS005	Tonsillitis	57	1.669

475	P	GRF003	Graft-Versus-Host Disease	71	1.654

476		DBT004	Diabetic Polyneuropathy	50	1.638

477		SPS007	Spastic Cerebral Palsy	46	1.636

478		CVD001	Covid-19	57	1.634

479	P	OVR046	Ovarian Cyst	46	1.634

480		PPT005	Peptic Ulcer Disease	58	1.632

481		NNT018	Neonatal Herpes	23	1.632

482		CHR100	Chronic Ulcer of Skin	57	1.632

483		MST024	Mastocytosis, Cutaneous	67	1.632

484	P	CRD246	Cardiovascular System Disease	56	1.632

485		VRC001	Varicocele	48	1.631

486	P	CMP008	Compartment Syndrome	50	1.631

487		NRL016	Neural Tube Defects	81	1.628

488		PNM010	Pneumothorax, Primary Spontaneous	58	1.628

489		GT001	Gout	64	1.628

490		SPN020	Spondylosis	46	1.628

491		DPH001	Diphtheria	59	1.628

492		DRM006	Dermatitis	62	1.587

493	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	60	1.577

494		VRC005	Varicose Veins	60	1.572

495		TST044	Testicular Torsion	45	1.572

496		URM002	Uremia	47	1.572

497		SYS004	Systemic Mastocytosis	63	1.572

498		PCD001	Pica Disease	38	1.572

499	P	HYP086	Hypothyroidism	69	1.572

500		ESP020	Esophageal Atresia	60	1.572

501		SQM006	Squamous Cell Carcinoma	60	1.572

502		HYP264	Hypertonia	36	1.572

503	c	RNG015	Ring Chromosome 2	22	1.572

504		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	1.564

505		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	1.564

506		PLS009	Plasma Cell Neoplasm	64	1.564

507		IGR001	Ige Responsiveness, Atopic	59	1.557

508		DCB001	Decubitus Ulcer	62	1.557

509		PNS018	Pain Sensitivity Quantitative Trait Locus 1	23	1.556

510		APN006	Apnea of Prematurity	24	1.514

511		CHR005	Chorioamnionitis	50	1.514

512		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.514

513		CHD001	Chediak-Higashi Syndrome	67	1.514

514	P	MYP004	Myopathy	67	1.514

515		ULC004	Ulcerative Colitis	74	1.514

516		SWL001	Swallowing Disorders	38	1.514

517		RHS001	Rh Isoimmunization	29	1.514

518		RCK004	Rickets	68	1.514

519	P	HYD006	Hydrocephalus	61	1.514

520		PRS045	Prostatic Hypertrophy	53	1.514

521		ANT013	Anterior Spinal Artery Syndrome	31	1.514

522	P	HYP076	Hyperthyroidism	53	1.514

523		BRS099	Breast Ductal Carcinoma	61	1.514

524		GST023	Gastric Ulcer	52	1.514

525	P	PRC019	Precocious Puberty	47	1.514

526		ETH012	Ethylene Glycol Poisoning	29	1.495

527	P	MLG056	Malignant Hyperthermia	66	1.495

528		PRC013	Pericarditis	53	1.495

529		HMP005	Hemiplegia	54	1.495

530		TYP007	Typhoid Fever	64	1.495

531		PTT009	Pituitary Gland Disease	53	1.492

532		URT014	Ureterolithiasis	43	1.492

533	P	END044	Endometriosis	62	1.486

534		CNT033	Central Nervous System Cancer	47	1.482

535	P	PRK057	Parkinson Disease, Late-Onset	80	1.478

536		CRH001	Crohn's Disease	80	1.478

537	P	ALZ034	Alzheimer Disease	87	1.472

538		GLC096	Galactorrhea	40	1.452

539		SCR039	Scorpion Envenomation	41	1.452

540	P	DXT004	Dextro-Looped Transposition of the Great Arteries	58	1.452

541		MWT001	Mowat-Wilson Syndrome	55	1.452

542		INF013	Inferior Myocardial Infarction	33	1.452

543	P	LNG064	Lung Cancer Susceptibility 3	70	1.452

544		EPD005	Epidural Abscess	31	1.452

545	P	MYC008	Myocarditis	59	1.452

546		FNT004	Fainting	29	1.452

547	P	CLS010	Cluster Headache	42	1.452

548		ANG049	Angioedema Induced by Ace Inhibitors	40	1.446

549		THR017	Thoracoabdominal Syndrome	40	1.446

550	c	THR090	Thrombocythemia 1	50	1.446

551	P	ANP001	Anaplastic Large Cell Lymphoma	61	1.446

552		SPL004	Splenic Marginal Zone Lymphoma	50	1.446

553	P	BLD124	Bleeding Disorder, Platelet-Type, 11	67	1.446

554		MYL009	Myelodysplastic Syndrome	67	1.446

555		CHR563	Chronic Eosinophilic Leukemia	48	1.446

556		MYL005	Myelofibrosis	71	1.446

557		PLY001	Polycythemia Vera	69	1.446

558		CHR286	Chronic Neutrophilic Leukemia	43	1.446

559	P	CHR285	Chronic Myelomonocytic Leukemia	60	1.446

560		BNM001	Bone Marrow Cancer	46	1.446

561		PRS047	Prostatitis	58	1.446

562		EXT010	Extramedullary Plasmacytoma	46	1.446

563		MNC006	Monoclonal Gammopathy of Uncertain Significance	47	1.446

564		PRL017	Prolymphocytic Leukemia	47	1.446

565		ACT029	Acute Interstitial Pneumonia	59	1.446

566	P	ESS003	Essential Thrombocythemia	69	1.446

567		MYL031	Myeloproliferative Neoplasm	66	1.446

568	c	PRM012	Primary Polycythemia	58	1.446

569		RFR002	Refractory Hairy Cell Leukemia	34	1.446

570		ACT011	Acute Contagious Conjunctivitis	42	1.446

571	c	ALM001	Al Amyloidosis	54	1.446

572		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	1.446

573		LYM019	Lymphosarcoma	46	1.446

574	c	THR092	Thrombophilia Due to Thrombin Defect	74	1.420

575	P	PLM034	Pulmonary Emphysema	58	1.418

576		CHR281	Chronic Hiccups	28	1.418

577		INS024	Insulin-Like Growth Factor I	78	1.396

578	c	SCN036	Secondary Progressive Multiple Sclerosis	55	1.396

579	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	1.396

580		INT075	Intracranial Hypertension	53	1.396

581		ACH005	Achalasia	55	1.396

582		BRN014	Bronchopneumonia	53	1.396

583		TRN018	Transitional Cell Carcinoma	56	1.396

584	P	HRN001	Horner's Syndrome	46	1.396

585		CLN045	Colonic Benign Neoplasm	48	1.393

586		ENT001	Enterocele	42	1.393

587	c	BLD140	Blood Group, I System	46	1.388

588	c	LKM070	Leukemia, Acute Monocytic	56	1.386

589		PLN026	Pilonidal Sinus	35	1.386

590		TRD006	Tardive Dyskinesia	53	1.386

591		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	42	1.386

592	P	VND001	Vein Disease	42	1.386

593		THY022	Thymic Carcinoma	57	1.386

594		MTS001	Mutism	44	1.386

595		CLR030	Clear Cell Renal Cell Carcinoma	54	1.386

596	P	MNC007	Monocytic Leukemia	47	1.386

597		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	1.386

598	P	SNS001	Sensorineural Hearing Loss	59	1.386

599	P	VNS003	Venous Insufficiency	55	1.386

600	P	PRP029	Porphyria	60	1.386

601		QDR001	Quadriplegia	50	1.386

602		ACT200	Acute Monoblastic Leukemia	41	1.386

603		ACT167	Acute Generalized Exanthematous Pustulosis	38	1.374

604		PLY150	Polykaryocytosis Inducer	29	1.348

605	P	CNG499	Congenital Anomalies of Kidney and Urinary Tract 2	52	1.348

606		CNT015	Central Sleep Apnea	46	1.348

607	P	MCR010	Microcephaly	60	1.348

608		HYP781	Hypoascorbemia	52	1.335

609		LWC001	Low Compliance Bladder	45	1.334

610		STT002	Status Asthmaticus	49	1.333

611		SCR015	Scarlet Fever	38	1.333

612		CHL079	Children's Interstitial Lung Disease	26	1.325

613		ACT171	Acute Opioid Poisoning	6	1.316

614		URM005	Uremic Pruritus	45	1.316

615		AMN014	Aminopterin Syndrome Sine Aminopterin	32	1.316

616		PLY028	Polycystic Bone Disease	17	1.316

617	P	ATR001	Atrioventricular Septal Defect	55	1.316

618		GLC106	Glucocorticoid Resistance, Generalized	48	1.316

619		INT304	Interstitial Pneumonitis, Desquamative, Familial	42	1.316

620		OST017	Osteomyelitis	63	1.316

621		CSL001	Causalgia	44	1.316

622	P	LCH002	Lichen Planus	54	1.316

623	c	BCT013	Bacterial Pneumonia	48	1.316

624		CHR066	Chronic Fatigue Syndrome	60	1.316

625	P	EPL164	Epilepsy	68	1.316

626	c	VRL007	Viral Encephalitis	50	1.316

627	c	ACT004	Acute Diarrhea	40	1.316

628		CMP006	Complex Partial Epilepsy	36	1.316

629		BRX001	Bruxism	51	1.316

630		BLR001	Biliary Atresia	55	1.316

631		FCL014	Focal Epilepsy	53	1.316

632		NNS002	Nonspecific Interstitial Pneumonia	42	1.316

633		CHL039	Choledocholithiasis	37	1.316

634	P	SHR001	Short Bowel Syndrome	53	1.316

635		ACT058	Active Peptic Ulcer Disease	56	1.316

636		SPT004	Septic Arthritis	58	1.316

637		PLG002	Plague	58	1.316

638	c	SVR005	Severe Pre-Eclampsia	50	1.316

639	P	MJR007	Major Affective Disorder 1	42	1.311

640	P	FNG006	Feingold Syndrome 1	62	1.293

641	c	RST012	Restless Legs Syndrome 1	33	1.276

642		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	1.276

643		PPL049	Papillon-Lefevre Syndrome	66	1.276

644	c	FNC043	Fanconi Anemia, Complementation Group E	62	1.276

645	c	DYS119	Dystonia 9	52	1.276

646	c	XNT010	Xanthinuria, Type I	52	1.276

647		LNG031	Lung Benign Neoplasm	51	1.276

648		HNT002	Hantavirus Pulmonary Syndrome	55	1.276

649		CRB009	Cerebritis	43	1.276

650		WHP002	Whiplash	36	1.248

651	P	CLC063	Celiac Disease 1	66	1.239

652	P	FML011	Familial Adenomatous Polyposis	71	1.239

653		INS001	Insulinoma	59	1.239

654		PLS011	Plasmacytoma	56	1.239

655		TRN015	Transient Cerebral Ischemia	63	1.239

656		IRN001	Iron Deficiency Anemia	58	1.239

657		MTR002	Mitral Valve Insufficiency	52	1.239

658		LYM017	Lyme Disease	62	1.239

659		DSC004	Discitis	34	1.239

660		DSS009	Disseminated Intravascular Coagulation	57	1.239

661		ANT019	Anterograde Amnesia	38	1.239

662		LST001	Listeriosis	59	1.239

663		IRN002	Iron Metabolism Disease	57	1.239

664	P	NRV007	Nervous System Disease	67	1.239

665		IDP022	Idiopathic Spinal Cord Herniation	17	1.239

666		ORL013	Oral Lichen Planus	46	1.239

667		CRC021	Carcinosarcoma	64	1.236

668		MCN017	Meconium Ileus	53	1.223

669		CRT084	Creatinine Clearance Quantitative Trait Locus	25	1.221

670		LMB062	Limb Ischemia	55	1.221

671	P	CHN012	Chondrosarcoma	57	1.221

672		STR067	Stroke, Ischemic	80	1.219

673	P	PRT026	Parotitis	42	1.219

674		IRR003	Irritant Dermatitis	47	1.195

675		MYC005	Myocardial Stunning	46	1.195

676	c	FRN037	Frontal Encephalocele	25	1.154

677	c	PRG042	Progressive Familial Heart Block, Type Ia	66	1.154

678		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	1.154

679		ACT119	Acute Promyelocytic Leukemia	62	1.154

680		ALL006	Allergic Asthma	56	1.154

681	P	CHL066	Cholangitis	52	1.154

682		ASY002	Asymptomatic Neurosyphilis	41	1.154

683		LFT001	Left Bundle Branch Hemiblock	47	1.154

684	P	UVT001	Uveitis	57	1.154

685	P	NPH012	Nephrotic Syndrome	60	1.154

686		CRD001	Cardiac Tamponade	43	1.154

687		THR012	Thoracic Cancer	44	1.154

688	P	TMP001	Temporal Lobe Epilepsy	49	1.154

689		HRP009	Herpes Simplex Encephalitis	58	1.154

690		CNG092	Congenital Extrahepatic Portosystemic Shunt	24	1.154

691	P	ENC008	Encephalocele	46	1.154

692		NRS003	Neurosyphilis	45	1.154

693		CNN001	Cannabis Dependence	38	1.146

694		DSS008	Disease of Mental Health	74	1.144

695		BNR002	Bone Resorption Disease	47	1.139

696	c	VRL010	Viral Hepatitis	53	1.139

697	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	1.122

698	c	MCL046	Mucolipidosis Iii Alpha/beta	60	1.122

699		PRG090	Progressive Relapsing Multiple Sclerosis	32	1.122

700	P	LYM033	Lymphoproliferative Syndrome	59	1.122

701		KHL003	Kohlschutter-Tonz Syndrome	59	1.122

702		VTM028	Vitamin E, Familial Isolated Deficiency of	53	1.122

703		RNL065	Renal Cell Carcinoma, Papillary, 1	79	1.122

704	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	55	1.122

705		STR081	Stormorken Syndrome	55	1.122

706	P	CMP005	Campomelic Dysplasia	65	1.122

707	c	HYP724	Hyperlipoproteinemia, Type Iii	67	1.122

708		SYS070	Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood	35	1.122

709		INT253	Intestinal Benign Neoplasm	46	1.122

710		MYL075	Myelodysplastic/myeloproliferative Neoplasm	51	1.122

711	P	MST002	Mast-Cell Leukemia	50	1.122

712		TXC002	Toxic Encephalopathy	52	1.122

713		INT054	Intraocular Lymphoma	48	1.122

714		NSP002	Nasopharyngitis	45	1.122

715		SML008	Small Intestine Lymphoma	33	1.122

716	P	NRV006	Nervous System Cancer	48	1.122

717		TRP009	Triple X Syndrome	41	1.122

718		HRT015	Heritable Pulmonary Arterial Hypertension	46	1.122

719		ACT113	Acute Myeloblastic Leukemia with Maturation	46	1.122

720		PST046	Post-Transplant Lymphoproliferative Disease	53	1.122

721		FBR012	Fabry Disease	70	1.122

722	P	STR092	Striatal Degeneration, Autosomal Dominant 2	47	1.122

723	P	ALP008	Alopecia	54	1.122

724		MYF002	Myofascial Pain Syndrome	46	1.112

725	P	AVS003	Avascular Necrosis	41	1.081

726		MYL020	Myelomeningocele	51	1.081

727	P	AMY004	Amyloidosis	70	1.081

728		DYS015	Dysentery	50	1.081

729		AMP007	Amphetamine Abuse	36	1.081

730	c	HRD039	Hereditary Amyloidosis	45	1.081

731	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	1.070

732		CHL013	Cholecystolithiasis	37	1.070

733		PHR003	Pharyngitis	58	1.070

734		CPL003	Capillary Leak Syndrome	54	1.070

735		MDR006	Moderate and Severe Traumatic Brain Injury	27	1.059

736		CMM005	Common Cold	56	1.059

737		PRP030	Purpura	54	1.059

738	c	TRN053	Transient Pseudohypoaldosteronism	24	1.057

739		INT072	Intestinal Pseudo-Obstruction	62	1.057

740	P	CRG003	Crigler-Najjar Syndrome, Type I	63	1.057

741	P	ORT004	Orthostatic Intolerance	63	1.057

742	c	CHL119	Cholangitis, Primary Sclerosing	58	1.057

743		PRP083	Porphyria, Acute Intermittent	65	1.057

744		CHL065	Cholangiocarcinoma	58	1.057

745		PST020	Postpoliomyelitis Syndrome	43	1.057

746	P	ERY008	Erythromelalgia	50	1.057

747	P	MSC005	Muscular Dystrophy	67	1.057

748	P	MGR001	Migraine Without Aura	49	1.057

749	P	ESP024	Esophagitis	60	1.057

750	P	SCL009	Sclerosing Cholangitis	48	1.057

751		NRG001	Neurogenic Bowel	31	1.057

752		RBS001	Rabies	58	1.057

753		INT079	Intrahepatic Cholangiocarcinoma	51	1.057

754		LPD008	Lipid Metabolism Disorder	62	1.057

755	P	LMY004	Leiomyosarcoma	62	1.057

756		FSC004	Fasciitis	49	1.057

757		EXN003	Exencephaly	30	1.057

758		LNP001	Loin Pain Hematuria Syndrome	17	1.057

759		CRD132	Cardiac Conduction Defect	60	1.019

760		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	1.019

761		NRM005	Neuromuscular Disease	63	1.019

762	P	CRN037	Craniosynostosis	68	1.019

763		OST160	Osteoid Osteoma	37	0.997

764		PHN003	Phenylketonuria	76	0.997

765		OBS082	Obstructive Nephropathy	41	0.997

766		SMT001	Somatization Disorder	50	0.997

767		VSL002	Visual Epilepsy	39	0.975

768		DNT012	Dental Caries	53	0.973

769	P	MLN008	Melanoma	76	0.963

770		BRD004	Borderline Personality Disorder	53	0.963

771		OST016	Osteochondrosis	52	0.963

772		RST023	Resting Heart Rate, Variation in	40	0.953

773	c	SCL052	Scleroderma, Familial Progressive	61	0.953

774	c	ATR087	Atrial Standstill 1	74	0.953

775		SKN016	Skin Disease	63	0.953

776		CRN019	Coronary Artery Vasospasm	47	0.953

777		THY020	Thyroid Hyalinizing Trabecular Adenoma	20	0.953

778	P	HYP055	Hypoplastic Left Heart Syndrome	65	0.953

779		MST020	Mast Cell Activation Syndrome	28	0.953

780	c	ACQ029	Acquired Porencephaly	27	0.943

781		GLM044	Glomerular Disease	35	0.943

782		ADN027	Adenomyosis	57	0.943

783		BLM002	Bulimia Nervosa	57	0.943

784		ATM095	Autoimmune Disease	61	0.943

785		OMN001	Omenn Syndrome	63	0.943

786		WLF001	Wolff-Parkinson-White Syndrome	65	0.943

787		CLR109	Colorectal Adenocarcinoma	50	0.943

788	P	PRN026	Porencephaly	55	0.943

789	P	NRD007	Neurodegeneration with Brain Iron Accumulation	52	0.943

790	c	CHR708	Chronic Urticaria	42	0.943

791		ANG016	Angiokeratoma	37	0.943

792		PRT009	Parotid Gland Cancer	33	0.943

793		SBV001	Subvalvular Aortic Stenosis	30	0.943

794		YLL002	Yellow Fever	61	0.943

795		MDN008	Median Arcuate Ligament Syndrome	37	0.943

796		HST010	Histiocytosis	49	0.943

797		SPN051	Spondylitis	51	0.943

798	P	CTR002	Cataract	60	0.943

799		INF009	Inflammatory Spondylopathy	30	0.943

800		ASP003	Aseptic Meningitis	50	0.943

801		TST014	Testicular Cancer	52	0.943

802		ANP005	Anaplastic Astrocytoma	57	0.943

803		FBR002	Fibrosarcoma of Bone	37	0.943

804		NCR007	Necrotizing Fasciitis	49	0.943

805		ADS006	Aids - Neurological Complications	11	0.943

806		LKP003	Leukoplakia	39	0.943

807		OGL001	Ogilvie Syndrome	24	0.943

808		BNG077	Benign Idiopathic Neonatal Seizures	23	0.883

809		PHS027	Phosphoglycoprotein 1	15	0.883

810	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.883

811		NRD100	Neurodevelopmental, Jaw, Eye, and Digital Syndrome	49	0.883

812		BLD130	Bladder Exstrophy	42	0.883

813	P	DRG020	Drug Metabolism, Poor, Cyp2d6-Related	21	0.883

814		CHR072	Chordoma	57	0.883

815		PST103	Postpartum Psychosis	31	0.883

816		THY029	Thyroid Carcinoma	51	0.883

817		INT002	Intermittent Claudication	61	0.883

818	P	SYS005	Systemic Scleroderma	74	0.883

819		SCR003	Secretory Diarrhea	35	0.883

820		SYN005	Synostosis	43	0.883

821		PRM236	Primary Biliary Cholangitis	60	0.883

822		HYP016	Hypochondriasis	47	0.883

823		ACR007	Acromegaly	70	0.883

824	P	EYD002	Eye Disease	57	0.883

825		GST050	Gastrointestinal System Disease	55	0.883

826	P	OBS001	Obstructive Jaundice	48	0.883

827	P	DYS021	Dysautonomia	38	0.883

828	c	EHL080	Ehlers-Danlos Syndrome, Musculocontractural Type, 1	52	0.863

829		BHR001	Behr Syndrome	51	0.863

830		DVR001	Diverticulitis of Colon	24	0.863

831	c	PNC108	Pancreatitis, Hereditary	69	0.848

832		MLR004	Malaria	80	0.848

833	P	RHB003	Rhabdomyosarcoma	66	0.848

834		TMP019	Temporomandibular Joint Anomaly	28	0.848

835	P	INF038	Influenza	68	0.848

836		ABD010	Abdominal Wall Defect	39	0.848

837	c	BCT007	Bacterial Meningitis	55	0.806

838	c	SCN052	Secondary Adrenal Insufficiency	36	0.806

839		PRS129	Prostatic Hyperplasia, Benign	49	0.806

840		RTN017	Retinal Detachment	60	0.806

841	P	MLT020	Multiple Sclerosis	79	0.806

842		RCR031	Rocuronium Allergy	12	0.806

843	P	FTL001	Fetal Alcohol Syndrome	55	0.806

844		HRN026	Hernia, Hiatus	47	0.806

845	P	HYP083	Hypopituitarism	52	0.806

846	P	VSC011	Vasculitis	61	0.806

847	P	MVM001	Movement Disease	61	0.806

848		PLR007	Pleural Empyema	51	0.806

849		PRS021	Prostatic Adenoma	43	0.806

850		CLB002	Clubfoot	51	0.806

851	P	ART021	Arteriosclerosis	54	0.806

852	P	ART005	Arteriovenous Malformation	65	0.806

853		GRN017	Granulocytopenia	42	0.806

854		HRS011	Horseshoe Kidney	31	0.806

855		ELC001	Elective Mutism	22	0.806

856		CHR178	Chromosomal Triplication	34	0.806

857		ACT159	Acute Transverse Myelitis	38	0.793

858		DYS140	Dyskinesia, Familial, with Facial Myokymia	37	0.793

859	c	SPR086	Spermatogenic Failure 3	46	0.793

860		LMY014	Leiomyoma, Uterine	56	0.793

861		KWS002	Kawasaki Disease	65	0.793

862	c	NRB010	Neuroblastoma 1	59	0.793

863		AKN002	Akinetic Mutism	36	0.793

864		ASP008	Aspiration Pneumonitis	42	0.793

865		CLL010	Cellular Ependymoma	57	0.793

866	P	HYP098	Hypereosinophilic Syndrome	66	0.793

867		MTR086	Motor Stereotypies	14	0.793

868		SPN043	Spinal Cord Glioma	31	0.793

869		CNV002	Conversion Disorder	47	0.793

870	P	GST044	Gastritis	55	0.793

871	P	PLL002	Pellagra	46	0.793

872	P	CRN028	Corneal Ulcer	47	0.793

873	P	BNG030	Benign Ependymoma	51	0.793

874		PLY021	Polyradiculopathy	34	0.793

875		RLP001	Relapsing Polychondritis	55	0.793

876	P	RNL015	Renal Hypertension	45	0.793

877	P	HYP265	Hypotonia	42	0.793

878		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	46	0.793

879		PNT023	Pontine Hemorrhage	17	0.793

880		SCR035	Sacral Agenesis with Vertebral Anomalies	38	0.783

881		PLM022	Pulmonary Valve Insufficiency	45	0.783

882		BRC010	Brachial Plexus Lesion	34	0.773

883	c	PCH015	Pachyonychia Congenita 1	60	0.751

884	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	59	0.751

885		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.751

886		ACR041	Acromelic Frontonasal Dysostosis	53	0.751

887	P	MCR129	Microvascular Complications of Diabetes 1	68	0.751

888	P	THY032	Thyroiditis	57	0.751

889		DBT002	Diabetic Autonomic Neuropathy	41	0.751

890		RFL002	Reflex Epilepsy	41	0.750

891		GNT167	Genetic Obesity	30	0.721

892		SHR107	Short Stature-Obesity Syndrome	25	0.721

893		ALL003	Allergic Rhinitis	67	0.721

894		VLV047	Volvulus of Midgut	52	0.721

895		ALC001	Alcohol-Related Birth Defect	36	0.721

896	c	BTT014	Beta-Thalassemia	72	0.721

897		EXR010	Exercise-Induced Bronchoconstriction	34	0.721

898		MYP159	Myopathy, Proximal, with Ophthalmoplegia	55	0.721

899		LGH019	Light Fixation Seizure Syndrome	27	0.721

900		ENC038	Encephalopathy, Progressive, with or Without Lipodystrophy	40	0.721

901	P	UTR058	Uterine Anomalies	46	0.721

902		MNN043	Meningioma, Familial	79	0.721

903		TNG007	Tongue Carcinoma	52	0.721

904	P	OPN001	Open-Angle Glaucoma	55	0.721

905	P	MSC003	Muscular Atrophy	52	0.721

906		URT010	Ureteral Obstruction	45	0.721

907	P	ART018	Aortic Valve Insufficiency	52	0.721

908		SCR001	Secretory Meningioma	40	0.721

909		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.721

910		CHR048	Chronic Rhinitis	46	0.721

911		MND031	Mandibuloacral Dysplasia Progeroid Syndrome	33	0.721

912		PLR008	Pleurisy	50	0.721

913	c	DLT002	Dilated Cardiomyopathy	78	0.721

914	P	NTR004	Neutropenia	63	0.721

915	P	SPN046	Spinal Muscular Atrophy	63	0.721

916		CLN015	Colon Adenocarcinoma	65	0.721

917		HMG005	Hemoglobinopathy	56	0.721

918		ALC005	Alcoholic Pancreatitis	38	0.721

919		ART008	Arteriosclerosis Obliterans	40	0.721

920	P	TCD001	Tic Disorder	49	0.721

921		NRL005	Neurilemmoma	60	0.721

922	P	SCK002	Sick Sinus Syndrome	55	0.721

923		SPN021	Spinal Meningioma	50	0.721

924		CHL122	Cholesteatoma of Middle Ear	51	0.721

925		GNR004	Generalized Anxiety Disorder	55	0.721

926		HYP060	Hyperinsulinism	54	0.721

927		PRS030	Persistent Fetal Circulation Syndrome	49	0.721

928		FTD001	Foot Drop	35	0.721

929		END072	Endotheliitis	36	0.709

930		DFN270	Deafness, Dystonia, and Cerebral Hypomyelination	41	0.709

931	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.709

932		AND020	Androgen Insensitivity, Partial	55	0.709

933		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	45	0.709

934		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.709

935		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.709

936		AGG012	Aggressive Nk-Cell Leukemia	46	0.709

937		BLD051	Blood Coagulation Disease	53	0.709

938		INF039	Infratentorial Cancer	38	0.709

939		SPR024	Supratentorial Cancer	39	0.709

940		IMM136	Immune System Disease	44	0.709

941		CRB196	Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome	47	0.709

942		AMD002	Amed Syndrome, Digenic	37	0.709

943		CRT017	Cartilage Disease	53	0.709

944		RDN001	Reading Disorder	40	0.709

945	P	CLL015	Collagen Disease	48	0.709

946	c	MST023	Mesothelioma, Malignant	56	0.699

947		LYM143	Lymphoma, Non-Hodgkin, Familial	75	0.699

948		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.699

949		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.699

950		SKN019	Skin Melanoma	71	0.699

951	P	PTT006	Pituitary Adenoma	55	0.699

952		PTH002	Pathological Gambling	48	0.699

953		CLN019	Colonic Disease	47	0.699

954	P	LRY019	Laryngitis	53	0.699

955	c	HTR021	Heterotaxy, Visceral, 5, Autosomal	38	0.636

956		BRN041	Bornholm Eye Disease	34	0.636

957		ASP030	Aspirin Resistance	40	0.636

958	c	MYS046	Myasthenic Syndrome, Congenital, 1a, Slow-Channel	44	0.636

959		PPL058	Papilloma of Choroid Plexus	55	0.636

960	c	DVL050	Developmental and Epileptic Encephalopathy 24	36	0.636

961		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	58