Search results for Epinephrine

2006 hits were found for Epinephrine

#	Family	MCID	Name	MIFTS	Score
1	P	CRD119	Cardiac Arrest	67	30.911

2	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	22.846

3		PNG002	Pain Agnosia	51	20.038

4		HYP056	Hypoglycemia	65	18.734

5		FDL002	Food Allergy	47	14.027

6	P	PHC003	Pheochromocytoma	69	13.875

7		BRN002	Bronchiolitis	57	13.143

8		ADR040	Adrenal Gland Pheochromocytoma	46	12.457

9		TXC005	Toxic Shock Syndrome	62	12.144

10		HYP066	Hyperglycemia	61	11.468

11		PLP001	Pulpitis	48	10.452

12		PPT005	Peptic Ulcer Disease	58	10.188

13		CRP002	Croup	42	10.160

14	c	HYP595	Hypertension, Essential	85	9.643

15		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	9.240

16		HYP060	Hyperinsulinism	54	9.121

17		PRT037	Pertussis	65	9.002

18		PLM010	Pulmonary Edema	55	8.512

19	P	LNG028	Long Qt Syndrome	64	8.120

20	P	OPN001	Open-Angle Glaucoma	55	7.953

21		CRD137	Cardiogenic Shock	56	7.948

22	c	TYP008	Type 1 Diabetes Mellitus	70	7.852

23	P	ANG015	Angioedema	56	7.803

24		HYP005	Hypokalemia	55	7.781

25	P	AST005	Asthma	76	7.578

26	c	ATR087	Atrial Standstill 1	74	7.183

27		SYN036	Syncope	45	7.160

28	c	ACT249	Acute Asthma	40	6.870

29		ALL029	Allergic Disease	59	6.750

30	P	PNC044	Pancreatitis	61	6.672

31		ISC004	Ischemia	61	6.621

32	P	RHN004	Rhinitis	57	6.465

33	P	URT039	Urticaria	58	6.445

34	c	ACT075	Acute Myocardial Infarction	56	6.285

35		PNT038	Peanut Allergy	46	6.225

36	P	MYC007	Myocardial Infarction	70	6.199

37		ACR008	Acrocallosal Syndrome	70	6.010

38		CRD223	Cardiac Arrhythmia	63	6.003

39	P	CTR002	Cataract	60	5.952

40		PRT058	Pure Autonomic Failure	58	5.903

41		MTB004	Metabolic Acidosis	48	5.888

42		INT323	Intraocular Pressure Quantitative Trait Locus	64	5.860

43		ALL003	Allergic Rhinitis	67	5.846

44		48X005	48,xyyy	39	5.802

45		OCL006	Ocular Hypertension	53	5.799

46		CHL014	Cholera	62	5.722

47	c	FML191	Familial Long Qt Syndrome	55	5.664

48	P	LCT001	Lactic Acidosis	51	5.514

49		CRD132	Cardiac Conduction Defect	60	5.511

50		LPP008	Lipoprotein Quantitative Trait Locus	65	5.508

51		ATN004	Autonomic Neuropathy	42	5.420

52		ATN005	Autonomic Dysfunction	46	5.391

53		BRK012	Broken Heart Syndrome	42	5.332

54	c	ACT027	Acute Pancreatitis	60	5.274

55	P	DDN001	Duodenal Ulcer	53	5.214

56	P	HYP086	Hypothyroidism	69	5.210

57	P	HYP076	Hyperthyroidism	53	5.115

58		HYP266	Hypoxia	57	5.094

59		ACT058	Active Peptic Ulcer Disease	56	4.823

60		47X002	47,xyy	48	4.814

61	c	GLC092	Glaucoma, Primary Open Angle	62	4.705

62	P	BRS047	Breast Cancer	98	4.704

63	c	PNS012	Paine Syndrome	60	4.671

64	c	ACT071	Acute Kidney Failure	60	4.626

65	P	EXN002	Exanthem	58	4.589

66		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	4.523

67	c	LNG047	Long Qt Syndrome 2	59	4.498

68		ART140	Arteries, Anomalies of	53	4.465

69		CNG034	Congestive Heart Failure	69	4.441

70	P	TRM003	Tremor	48	4.426

71	c	DLT002	Dilated Cardiomyopathy	78	4.426

72	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	4.369

73	P	NRP001	Neuropathy	60	4.350

74		GLC003	Glucose Intolerance	54	4.274

75	P	DBT009	Diabetes Mellitus	67	4.259

76	P	ANR048	Aniridia 1	64	4.199

77		OCL069	Ocular Motor Apraxia	57	4.186

78	P	RSP003	Respiratory Failure	74	4.073

79	c	LNG048	Long Qt Syndrome 3	53	4.036

80		AMN003	Amnestic Disorder	54	4.022

81		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	4.014

82		ANG054	Angina Pectoris	66	3.993

83		AGN016	Aging	54	3.964

84	P	NRB001	Neuroblastoma	66	3.937

85	P	PTS002	Ptosis	52	3.922

86	P	HRT032	Heart Disease	81	3.902

87		PST028	Post-Traumatic Stress Disorder	59	3.893

88		ADN018	Adenoma	59	3.876

89	c	TYP009	Type 2 Diabetes Mellitus	92	3.858

90		CYT002	Cytokine Deficiency	43	3.831

91	c	HYP836	Hypercholesterolemia, Familial, 1	73	3.807

92		THR024	Thrombosis	56	3.804

93	P	HYP040	Hypospadias	51	3.796

94		CRN019	Coronary Artery Vasospasm	47	3.765

95		MCL006	Macular Retinal Edema	57	3.763

96	P	MLT074	Multiple Endocrine Neoplasia	59	3.760

97		GST023	Gastric Ulcer	52	3.759

98		ASP030	Aspirin Resistance	40	3.730

99	P	SCK005	Sickle Cell Disease	56	3.720

100		MYM001	Myoma	54	3.694

101	P	PRG013	Paraganglioma	57	3.680

102	P	PLM037	Pulmonary Hypertension	72	3.638

103		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	3.582

104		RST023	Resting Heart Rate, Variation in	40	3.572

105	P	ORT004	Orthostatic Intolerance	63	3.542

106	P	PNC025	Panic Disorder	52	3.531

107	P	DRM053	Dermatitis, Atopic	65	3.509

108		ANX004	Anoxia	40	3.496

109		DYS073	Dysphagia	53	3.492

110		PRS045	Prostatic Hypertrophy	53	3.464

111	P	HRP006	Herpes Simplex	65	3.456

112		PLM033	Pulmonary Embolism	58	3.434

113		PRS129	Prostatic Hyperplasia, Benign	49	3.384

114		PRS021	Prostatic Adenoma	43	3.384

115	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	63	3.368

116	P	VSC007	Vascular Disease	63	3.335

117	P	SLP006	Sleep Apnea	69	3.332

118	P	VNW001	Von Willebrand's Disease	65	3.306

119	P	MST009	Mastocytosis	64	3.302

120		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	3.261

121		PRT036	Peritonitis	65	3.261

122	P	THY032	Thyroiditis	57	3.244

123		MNT002	Mental Depression	57	3.241

124		TTN003	Tetanus	65	3.241

125		ATR057	Atrioventricular Block	54	3.210

126		END086	End Stage Renal Disease	52	3.202

127	P	PRD008	Periodontitis	64	3.197

128		OST012	Osteoarthritis	77	3.180

129	P	MYC008	Myocarditis	59	3.168

130		PNM008	Pneumothorax	54	3.164

131		LPD008	Lipid Metabolism Disorder	62	3.163

132		LMY002	Leiomyoma	51	3.155

133		NTL004	Nut Allergy	37	3.143

134		ALC007	Alcohol Dependence	66	3.140

135		INT007	Intermediate Coronary Syndrome	54	3.135

136	P	HDC001	Headache	57	3.127

137	P	KDN018	Kidney Disease	72	3.122

138	P	BLD124	Bleeding Disorder, Platelet-Type, 11	67	3.120

139		PRS063	Paresthesia	39	3.112

140		IGR001	Ige Responsiveness, Atopic	59	3.103

141		TRM010	Traumatic Brain Injury	51	3.099

142		ACT084	Acute Stress Disorder	54	3.099

143		URM002	Uremia	47	3.091

144		ANX010	Anxiety	70	3.091

145	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	67	3.079

146	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	3.071

147		RPD005	Rapidly Involuting Congenital Hemangioma	46	3.038

148		MYC005	Myocardial Stunning	46	3.034

149	P	SCL018	Scoliosis	57	3.010

150		MLG157	Malignant Pheochromocytoma	36	3.006

151	P	THR014	Thrombocytopenia	66	2.991

152	P	CRP001	Carpal Tunnel Syndrome	66	2.978

153		DBT002	Diabetic Autonomic Neuropathy	41	2.976

154		HRW001	Hair Whorl	35	2.954

155	c	MGR028	Migraine with or Without Aura 1	64	2.953

156		CRN017	Coronary Thrombosis	46	2.946

157		CRB039	Cerebrovascular Disease	66	2.944

158	P	ATR011	Atrial Fibrillation	66	2.924

159		MYF001	Myofibroma	42	2.916

160		VRC005	Varicose Veins	60	2.913

161		GLM045	Glioma	63	2.902

162		HDN002	Head Injury	44	2.897

163	P	TRN020	Turner Syndrome	67	2.887

164		CYN002	Cyanosis, Transient Neonatal	43	2.886

165		ESP021	Esophageal Cancer	83	2.885

166		DRM006	Dermatitis	62	2.885

167		EGG001	Egg Allergy	41	2.880

168		GLL048	Glial Tumor	52	2.876

169	c	PRC016	Pre-Eclampsia	65	2.869

170		ALL006	Allergic Asthma	56	2.861

171		BRN071	Brain Injury	50	2.861

172	P	ADL010	Adult Respiratory Distress Syndrome	71	2.848

173		STT002	Status Asthmaticus	49	2.846

174		ACT088	Acute Insulin Response	39	2.839

175		CRN030	Coronary Stenosis	50	2.839

176	P	SZR006	Seizure Disorder	70	2.836

177	c	THR092	Thrombophilia Due to Thrombin Defect	74	2.822

178		LRY004	Laryngotracheitis	33	2.814

179		LVR012	Liver Cirrhosis	63	2.810

180		RYN005	Raynaud Phenomenon	45	2.810

181		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	2.748

182		PRP007	Priapism	47	2.742

183	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	2.738

184	P	ECL001	Eclampsia	52	2.730

185		ENT011	Enterocolitis	55	2.714

186		DSS009	Disseminated Intravascular Coagulation	57	2.714

187		THR035	Thrombasthenia	48	2.714

188	P	HYP050	Hyperinsulinemic Hypoglycemia	57	2.709

189		CLF027	Cleft Palate, Isolated	64	2.708

190		MCR011	Microinvasive Gastric Cancer	41	2.708

191	P	DBT005	Diabetes Insipidus	54	2.695

192		PTT037	Pituitary Tumors	44	2.695

193		RHB024	Rhabdomyosarcoma 2	67	2.685

194	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	2.667

195		THY030	Thyroid Gland Disease	50	2.667

196	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	2.652

197		DWN001	Down Syndrome	70	2.652

198		EXR007	Exercise-Induced Anaphylaxis	23	2.632

199		THY029	Thyroid Carcinoma	51	2.631

200	P	CNJ013	Conjunctivitis	66	2.622

201	P	ENC018	Encephalopathy	62	2.591

202		MLK006	Milk Allergy	47	2.589

203	P	LRY019	Laryngitis	53	2.585

204		ING001	Inguinal Hernia	59	2.554

205	P	CYS018	Cystitis	59	2.548

206	P	DYS154	Dystonia	64	2.533

207	P	OVR042	Ovarian Cancer	88	2.529

208		IMP005	Impotence	52	2.520

209		PRP030	Purpura	54	2.515

210		PST092	Posttransplant Acute Limbic Encephalitis	28	2.514

211	P	ART021	Arteriosclerosis	54	2.499

212		NNL005	Non-Alcoholic Fatty Liver Disease	63	2.483

213		LYM027	Lymphopenia	56	2.483

214		CRC021	Carcinosarcoma	64	2.481

215		QBC001	Quebec Platelet Disorder	44	2.473

216	P	NTR004	Neutropenia	63	2.467

217	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	2.461

218	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	2.461

219	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	2.461

220	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	2.461

221	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	2.461

222	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	2.461

223	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	2.461

224	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	2.461

225	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	2.461

226		SYS004	Systemic Mastocytosis	63	2.452

227		PRN019	Perinatal Necrotizing Enterocolitis	60	2.452

228		MLL004	Mallory-Weiss Syndrome	22	2.449

229		HMN044	Human Immunodeficiency Virus Type 1	78	2.447

230		PLM129	Pulmonary Disease, Chronic Obstructive	74	2.447

231	c	GRV008	Graves Disease 1	54	2.433

232	c	CHR684	Chronic Kidney Disease	69	2.433

233		HRT011	Heart Septal Defect	49	2.431

234		STR067	Stroke, Ischemic	80	2.427

235	P	ART022	Arthritis	71	2.427

236	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	2.421

237		EPG003	Epiglottitis	33	2.421

238	P	MYP004	Myopathy	67	2.421

239		PRT013	Portal Hypertension	59	2.421

240	c	PRG043	Progressive Familial Heart Block, Type Ib	54	2.419

241		CRH001	Crohn's Disease	80	2.412

242		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	2.411

243		CHL068	Cholestasis	61	2.356

244	P	FML187	Familial Hypertension	34	2.356

245		BRN056	Bronchopulmonary Dysplasia	56	2.356

246	P	ESS003	Essential Thrombocythemia	69	2.355

247		SQM006	Squamous Cell Carcinoma	60	2.340

248		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	2.335

249	c	ORT011	Orthostatic Hypotension 1	43	2.332

250		STC016	Sticky Platelet Syndrome	23	2.325

251		SPN186	Spinal Cord Injury	61	2.312

252	P	CRN300	Coronary Heart Disease 1	73	2.312

253		ART016	Aortic Aneurysm	68	2.291

254		TRN015	Transient Cerebral Ischemia	63	2.289

255	c	ORT012	Orthostatic Hypotension 2	20	2.286

256		ACR007	Acromegaly	70	2.283

257		DPR016	Depression	65	2.273

258	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	2.264

259	c	HRD002	Hereditary Angioedema	62	2.254

260		HYP020	Hyperprolactinemia	63	2.253

261		CRC006	Carcinoid Syndrome	55	2.253

262		BLP006	Blepharoconjunctivitis	33	2.253

263		SKN016	Skin Disease	63	2.240

264		VNH007	Von Hippel-Lindau Syndrome	73	2.233

265		BLD053	Blood Platelet Disease	51	2.233

266	P	NRF002	Neurofibromatosis	57	2.233

267		GNG013	Gingivitis	59	2.233

268		PRS030	Persistent Fetal Circulation Syndrome	49	2.219

269		VRS002	Virus-Associated Trichodysplasia Spinulosa	30	2.218

270	P	CRC039	Coarctation of Aorta	46	2.215

271		DPM001	Dopamine Beta-Hydroxylase Deficiency	53	2.205

272		DLF001	Dieulafoy Lesion	31	2.200

273		CNS004	Constipation	56	2.200

274	P	INF037	Inflammatory Bowel Disease	53	2.186

275	P	BRG001	Brugada Syndrome	69	2.176

276	P	GLM040	Glioma Susceptibility 1	71	2.176

277		CRB037	Cerebral Palsy	67	2.176

278	c	PRG042	Progressive Familial Heart Block, Type Ia	66	2.173

279		OST062	Osteoarthritis with Mild Chondrodysplasia	47	2.172

280		PPL052	Papillomatosis, Confluent and Reticulated	34	2.168

281		DSS032	Disease by Infectious Agent	55	2.168

282		EXT054	Extra-Adrenal Pheochromocytoma	32	2.168

283		HYP014	Hyperuricemia	51	2.166

284		THR004	Thrombocytosis	53	2.152

285	P	SNS001	Sensorineural Hearing Loss	59	2.145

286		HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	60	2.143

287	P	THL005	Thalassemia	56	2.136

288		PST011	Pustulosis of Palm and Sole	52	2.136

289		ACQ007	Acquired Immunodeficiency Syndrome	59	2.136

290		THY111	Thyroid Carcinoma, Familial Medullary	67	2.135

291	P	VNT002	Ventricular Septal Defect	58	2.135

292		THY125	Thyroid Gland Medullary Carcinoma	48	2.135

293	P	HYP061	Hypertrophic Cardiomyopathy	69	2.131

294		SQM013	Squamous Cell Carcinoma, Head and Neck	73	2.123

295		SCK003	Sickle Cell Anemia	74	2.120

296		RTR001	Retrograde Amnesia	41	2.120

297	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	2.107

298		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	2.107

299	P	SCK002	Sick Sinus Syndrome	55	2.107

300	P	ATR010	Atrial Heart Septal Defect	58	2.095

301		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	2.091

302		GSG001	Gas Gangrene	52	2.089

303		BRN038	Bronchial Disease	51	2.082

304	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	2.068

305	P	PLY018	Polycythemia	56	2.068

306		CYS001	Cystic Fibrosis	78	2.066

307		DBT084	Diabetes Mellitus, Ketosis-Prone	60	2.066

308		TRC020	Tracheitis	43	2.066

309	P	VSC011	Vasculitis	61	2.066

310	P	MLG056	Malignant Hyperthermia	66	2.066

311	P	ALC033	Alcohol Use Disorder	61	2.056

312		ANR007	Anorexia Nervosa	60	2.052

313		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	2.052

314		PNC085	Penicillin Allergy	43	2.052

315	P	MJR001	Major Depressive Disorder	68	2.052

316	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	2.052

317	P	SLP005	Sleep Disorder	61	2.052

318		AND005	Androgen Insensitivity Syndrome, Mild	21	2.049

319	P	HMR005	Hemorrhoid	49	2.044

320		MTR002	Mitral Valve Insufficiency	52	2.042

321		CCN002	Cocaine Abuse	49	2.042

322	P	CHR345	Chronic Pain	50	2.042

323		MCS002	Mucositis	56	2.034

324	P	PLY011	Polycystic Ovary Syndrome	57	2.031

325	P	ACT105	Acute Mountain Sickness	52	2.031

326		WTH001	Withdrawal Disorder	48	2.028

327		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	2.028

328	P	PRS040	Prostate Cancer	95	2.008

329	P	HMN010	Hemangioma	62	2.008

330	P	ART005	Arteriovenous Malformation	65	2.008

331		ANT039	Antisynthetase Syndrome	55	1.996

332	P	PRK039	Parkinsonism	55	1.994

333		ANG049	Angioedema Induced by Ace Inhibitors	40	1.993

334		AGG012	Aggressive Nk-Cell Leukemia	46	1.992

335	P	CHL066	Cholangitis	52	1.987

336		GLN010	Glanzmann Thrombasthenia	66	1.967

337		INT075	Intracranial Hypertension	53	1.962

338		CHR066	Chronic Fatigue Syndrome	60	1.962

339		END040	Endogenous Depression	55	1.962

340		CMM005	Common Cold	56	1.962

341	c	THR090	Thrombocythemia 1	50	1.961

342	P	PTN014	Patent Ductus Arteriosus 1	59	1.957

343		ATR089	Atrioventricular Dissociation	21	1.951

344		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	1.934

345		PRP027	Peripheral Vascular Disease	71	1.930

346	P	ATS364	Autism	69	1.919

347		DFC004	Deficiency Anemia	74	1.919

348	P	PTT006	Pituitary Adenoma	55	1.915

349		MDD011	Mood Disorder	62	1.915

350		INS024	Insulin-Like Growth Factor I	78	1.901

351	P	CRN026	Corneal Edema	42	1.900

352		GST039	Gastroduodenitis	37	1.883

353		MLG169	Malignant Astrocytoma	57	1.880

354		SBC016	Subacute Delirium	43	1.872

355		RNL114	Renal Cell Carcinoma, Nonpapillary	80	1.865

356		CLF001	Cleft Lip	53	1.865

357		STT001	Status Epilepticus	59	1.865

358	c	EXD008	Exudative Vitreoretinopathy 1	71	1.854

359		HMR023	Hemorrhagic Cystitis	43	1.854

360		ART074	Aortic Dissection	53	1.854

361		SHW001	Shwartzman Phenomenon	36	1.854

362		RGH001	Right Bundle Branch Block	47	1.854

363		CLT003	Colitis	63	1.850

364		INS001	Insulinoma	59	1.840

365	P	THR015	Thrombophilia	51	1.840

366		BRN004	Brain Edema	54	1.830

367	P	NPH012	Nephrotic Syndrome	60	1.828

368		ADL002	Adult Syndrome	70	1.818

369	P	BRN019	Bernard-Soulier Syndrome	61	1.818

370		ATH013	Atherosclerosis Susceptibility	63	1.813

371	P	RHM011	Rheumatoid Arthritis	82	1.813

372		MSC007	Muscle Hypertrophy	64	1.813

373		BRR014	Barrett Esophagus	66	1.813

374	P	EYD002	Eye Disease	57	1.813

375		ENT004	Enthesopathy	51	1.813

376		FBR047	Fibromyalgia	58	1.810

377		SNT005	Sinoatrial Node Disease	47	1.807

378		CNT047	Contact Dermatitis	57	1.807

379		BCK006	Back Pain	47	1.805

380		HPT014	Hepatorenal Syndrome	49	1.803

381	P	ART023	Arthropathy	61	1.803

382	P	PRP019	Peripheral Nervous System Disease	58	1.799

383	P	HYP098	Hypereosinophilic Syndrome	66	1.799

384		QDR001	Quadriplegia	50	1.799

385		NRT001	Neurotic Disorder	56	1.793

386		CNN003	Conn's Syndrome	79	1.761

387		SNG003	Single Ventricular Heart	30	1.759

388	P	ADN016	Adenocarcinoma	63	1.759

389		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	1.756

390		BRN024	Bronchitis	67	1.756

391		DDN006	Duodenitis	50	1.752

392		DRG024	Drug Allergy	40	1.746

393		ULC004	Ulcerative Colitis	74	1.738

394	c	ATS383	Autosomal Dominant Non-Syndromic Intellectual Disability 1	37	1.738

395		C1N001	C1 Inhibitor Deficiency	43	1.723

396		AYM001	Ayme-Gripp Syndrome	56	1.723

397	P	CRV039	Cervicitis	52	1.723

398	P	LNG032	Lung Cancer	98	1.712

399		CRT069	Cortical Malformations, Occipital	30	1.712

400		INF034	Infective Endocarditis	54	1.712

401	P	END033	Endocarditis	58	1.705

402		SCL003	Social Phobia	48	1.705

403	c	SCN052	Secondary Adrenal Insufficiency	36	1.701

404	P	ALZ034	Alzheimer Disease	87	1.701

405	P	PNC035	Pancreatic Cancer	86	1.701

406		LPT014	Leptin Deficiency or Dysfunction	78	1.701

407		APN008	Apnea, Obstructive Sleep	67	1.701

408		SDD001	Sudden Infant Death Syndrome	60	1.666

409		PLY001	Polycythemia Vera	69	1.666

410		CRN036	Craniopharyngioma	64	1.666

411		PPT002	Peptic Ulcer Perforation	34	1.666

412		HLX001	Helix Syndrome	48	1.666

413		CLN015	Colon Adenocarcinoma	65	1.666

414	P	EPL164	Epilepsy	68	1.666

415		HYP063	Hypersplenism	52	1.651

416	P	PRD037	Periodontal Ehlers-Danlos Syndrome	49	1.651

417		ACT098	Acute Erythroid Leukemia	55	1.646

418		LTX001	Latex Allergy	42	1.646

419	P	HRN001	Horner's Syndrome	46	1.646

420		ANR040	Aneurysm	61	1.640

421		BHR001	Behr Syndrome	51	1.630

422		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	36	1.630

423	c	DWL002	Dowling-Degos Disease 1	58	1.618

424		HYP540	Hypertension, Diastolic	37	1.618

425		MYL005	Myelofibrosis	71	1.618

426		FML063	Familial Glucocorticoid Deficiency	58	1.618

427		HRT012	Heart Valve Disease	53	1.618

428	c	LNG044	Long Qt Syndrome 1	66	1.614

429	c	PNC106	Pancreatic Agenesis 1	51	1.610

430		PNC034	Pancreas Disease	50	1.610

431		PPL001	Papillary Adenoma	44	1.610

432		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	1.604

433	c	PRM093	Premature Ovarian Failure 7	48	1.598

434	P	HYP083	Hypopituitarism	52	1.598

435	P	PSR002	Psoriasis	63	1.598

436		MTN003	Motion Sickness	51	1.576

437		SPN035	Spindle Cell Sarcoma	54	1.574

438		SRC014	Sarcoma	65	1.574

439		MNN028	Mononeuropathy of the Median Nerve, Mild	46	1.573

440		GLC084	Glaucoma, Normal Tension	45	1.569

441		SCN049	Second-Degree Atrioventricular Block	33	1.569

442		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	1.569

443		PLT016	Platelet Adenylate Cyclase Activity	16	1.569

444		PLT031	Platelet Membrane Fluidity	28	1.569

445		CRT015	Carotid Artery Occlusion	45	1.569

446		IRR002	Irritable Bowel Syndrome	65	1.569

447	P	PHC019	Pheochromocytoma-Paraganglioma	35	1.554

448	P	MLT020	Multiple Sclerosis	79	1.554

449	P	ART018	Aortic Valve Insufficiency	52	1.554

450	P	LVR013	Liver Disease	69	1.554

451	P	CRD246	Cardiovascular System Disease	56	1.554

452		URT037	Urethral Stricture	42	1.547

453		OTT002	Otitis Media	71	1.543

454	P	SKN015	Skin Carcinoma	71	1.539

455	P	LPR021	Leprosy 3	71	1.517

456		LPM012	Lipomatosis, Multiple	60	1.517

457		ADR016	Adrenal Cortical Carcinoma	62	1.517

458		ADR054	Adrenocortical Carcinoma, Hereditary	47	1.517

459	P	RTN024	Retinoblastoma	73	1.517

460		OST159	Osteogenic Sarcoma	66	1.517

461		ADR004	Adrenal Cortical Adenocarcinoma	38	1.517

462		PLM005	Pleomorphic Lipoma	40	1.517

463		HYP080	Hypogonadism	50	1.517

464		HNS001	Hansen's Disease	32	1.517

465		BDR001	Bidirectional Tachycardia	14	1.517

466	c	ACT134	Acute Liver Failure	59	1.508

467	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	1.508

468	P	ALP008	Alopecia	54	1.508

469	P	ACN011	Acne	57	1.508

470		HYP835	Hypothalamic Obesity	38	1.503

471		PLY150	Polykaryocytosis Inducer	29	1.502

472	P	PLV020	Pelvic Organ Prolapse	58	1.502

473	P	END044	Endometriosis	62	1.502

474	c	CNG513	Congenital Ptosis	42	1.502

475		PRT010	Parathyroid Carcinoma	68	1.471

476	P	GST053	Gastric Cancer	83	1.467

477		INT030	Intracranial Aneurysm	55	1.467

478	P	RRT020	Rare Tumor	39	1.466

479		KRT019	Keratitis, Hereditary	66	1.466

480		THR100	Thrombocytopenic Purpura, Autoimmune	61	1.466

481		FST010	Fasting Hypoglycemia	33	1.465

482	P	HML001	Hemolytic-Uremic Syndrome	52	1.463

483	P	RBL001	Rubella	58	1.463

484		PRN009	Paranoid Schizophrenia	49	1.463

485	c	MLG069	Malignant Hypertension	46	1.463

486	P	BNG032	Benign Mesothelioma	53	1.463

487	c	ACQ012	Acquired Angioedema	38	1.463

488		CNT060	Central Serous Chorioretinopathy	38	1.463

489		MSL001	Measles	61	1.463

490	P	BPL003	Bipolar Disorder	56	1.460

491	P	ESP024	Esophagitis	60	1.460

492		FSH003	Fish Allergy	30	1.451

493		BNR002	Bone Resorption Disease	47	1.426

494	P	HYP069	Hyperparathyroidism	62	1.426

495		PLM001	Pulmonary Tuberculosis	69	1.423

496		PLM022	Pulmonary Valve Insufficiency	45	1.423

497	c	NNS018	Nonsyndromic Paraganglioma	33	1.411

498		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	1.405

499		PRT251	Proteinuria, Chronic Benign	57	1.405

500		ALL010	Allergic Contact Dermatitis	56	1.405

501	P	MMP001	Mumps	57	1.405

502	c	MLT159	Multiple Endocrine Neoplasia, Type Iib	61	1.404

503		PLT033	Platelet Signal Processing Defect	9	1.404

504	P	MSC005	Muscular Dystrophy	67	1.394

505		GST013	Gastrojejunal Ulcer	41	1.394

506		PRM024	Primary Angle-Closure Glaucoma	39	1.394

507		ART006	Arthus Reaction	40	1.394

508		SPL018	Splenomegaly	49	1.394

509		SPN019	Spondylolisthesis	52	1.387

510		EXR010	Exercise-Induced Bronchoconstriction	34	1.385

511	P	TTR001	Tetralogy of Fallot	69	1.385

512		MLT073	Multisystemic Smooth Muscle Dysfunction Syndrome	44	1.384

513		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	64	1.384

514		SWL001	Swallowing Disorders	38	1.384

515		HNT002	Hantavirus Pulmonary Syndrome	55	1.384

516		ATX019	Ataxia with Vitamin E Deficiency	44	1.384

517		LNG099	Lung Disease	62	1.370

518		SHL001	Shoulder Impingement Syndrome	35	1.364

519		GRW007	Growth Hormone Deficiency	46	1.359

520	P	LKM002	Leukemia	67	1.359

521		URT001	Urethritis	53	1.358

522		DBT010	Diabetic Neuropathy	54	1.344

523		EPL050	Epilepsy, Partial, with Pericentral Spikes	26	1.343

524	P	PRK057	Parkinson Disease, Late-Onset	80	1.343

525		CHR100	Chronic Ulcer of Skin	57	1.343

526	P	PLY006	Polydactyly	59	1.343

527		MLD001	Melioidosis	67	1.343

528	P	LCT002	Lactose Intolerance	52	1.343

529	c	ACT072	Acute Laryngitis	29	1.343

530		MCL003	Macular Holes	44	1.343

531	c	ACT076	Acute Myocarditis	47	1.343

532		PLC005	Placental Insufficiency	56	1.343

533		GTR002	Goiter	53	1.343

534		FCL012	Facial Paralysis	49	1.343

535	P	OVR046	Ovarian Cyst	46	1.343

536		MCP033	Mucopolysaccharidoses	44	1.343

537	c	CNT101	Central Congenital Hypothyroidism	36	1.343

538		DVR002	Diverticulitis	46	1.333

539		TYP007	Typhoid Fever	64	1.315

540	c	SCL052	Scleroderma, Familial Progressive	61	1.304

541	c	ART101	Aortic Valve Disease 2	66	1.304

542		NRN004	Neuroendocrine Tumor	59	1.304

543	P	CLS010	Cluster Headache	42	1.304

544		MNR012	Meniere Disease	56	1.301

545		FTT001	Fatty Liver Disease	62	1.301

546		CDQ001	Cauda Equina Syndrome	37	1.301

547		IRN002	Iron Metabolism Disease	57	1.301

548	c	SML038	Small Cell Cancer of the Lung	69	1.297

549	P	MTH007	Methemoglobinemia	46	1.297

550		ORL011	Oral Cancer	60	1.297

551	c	MCP049	Mucopolysaccharidosis, Type Vii	63	1.278

552	c	ATS007	Autism Spectrum Disorder	72	1.278

553	P	STR092	Striatal Degeneration, Autosomal Dominant 2	47	1.278

554	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	70	1.278

555		PHN003	Phenylketonuria	76	1.278

556	P	MYP006	Myopia	56	1.278

557	P	PRT096	Peritoneal Mesothelioma	49	1.278

558	P	FBR017	Fibrosarcoma	56	1.278

559		PRC001	Pericoronitis	26	1.278

560	P	PSD015	Pseudohypoparathyroidism	55	1.278

561		DYS009	Dysthymic Disorder	52	1.278

562		PRV004	Periventricular Leukomalacia	52	1.278

563		DMP001	Dumping Syndrome	43	1.278

564		ACC002	Accommodative Spasm	25	1.278

565		PLN005	Palindromic Rheumatism	43	1.278

566		CHL122	Cholesteatoma of Middle Ear	51	1.278

567		NRM004	Neuroma	49	1.278

568	P	INS002	in Situ Carcinoma	53	1.278

569		GRN017	Granulocytopenia	42	1.278

570		CRB090	Cerebral Hypoxia	42	1.278

571	P	HPT023	Hepatocellular Carcinoma	96	1.267

572	P	DXT004	Dextro-Looped Transposition of the Great Arteries	58	1.257

573	P	RNV001	Renovascular Hypertension	49	1.257

574		PRP016	Paraplegia	52	1.257

575		OCL010	Ocular Hypotension	37	1.257

576	P	HYP265	Hypotonia	42	1.257

577	P	ESP035	Esophagitis, Eosinophilic, 1	58	1.247

578		DNT012	Dental Caries	53	1.247

579		SPN027	Spinal Stenosis	59	1.247

580		LYM019	Lymphosarcoma	46	1.247

581	c	PRD040	Periodontitis, Chronic	52	1.226

582		STM007	Stomatitis	54	1.226

583	P	VNS003	Venous Insufficiency	55	1.225

584	c	PSD108	Pseudohypoparathyroidism, Type Ia	65	1.225

585		URT049	Urate Oxidase, Pseudogene	24	1.225

586		ANG018	Angiomyolipoma	46	1.225

587		NRD001	Neurodermatitis	39	1.225

588		ILS001	Ileus	50	1.212

589	P	RNL015	Renal Hypertension	45	1.212

590		HMP009	Haemophilus Influenzae	41	1.212

591	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	1.211

592	P	CNR004	Cone-Rod Dystrophy 2	74	1.211

593	P	MCR129	Microvascular Complications of Diabetes 1	68	1.211

594		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	38	1.211

595		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	40	1.211

596		THY122	Thyroid Gland Cancer	59	1.211

597		CTS005	Catastrophic Antiphospholipid Syndrome	43	1.211

598		CRY008	Cryopyrin-Associated Periodic Syndrome	48	1.211

599	P	NRV007	Nervous System Disease	67	1.211

600		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	31	1.206

601		ACT235	Acute Macular Neuroretinopathy	16	1.206

602		NTR018	Neutrophilia, Hereditary	50	1.206

603		PNM010	Pneumothorax, Primary Spontaneous	58	1.206

604		CHR048	Chronic Rhinitis	46	1.206

605		CRY005	Cryptococcosis	60	1.206

606		SPS004	Spastic Quadriplegia	40	1.206

607		MNN009	Meningoencephalitis	48	1.206

608		VSC002	Vascular Dementia	60	1.206

609		INT146	Intervertebral Disc Disease	63	1.191

610		GST071	Gastrointestinal Carcinoma	46	1.191

611	P	MLN008	Melanoma	76	1.191

612	c	BSL007	Basal Cell Carcinoma	68	1.191

613		GST050	Gastrointestinal System Disease	55	1.191

614		ALD013	Aldosterone-Producing Adenoma	36	1.185

615	c	DPH024	Diaphragmatic Hernia, Congenital	64	1.185

616		ADR041	Adrenal Cortical Adenoma	49	1.185

617	P	OPT006	Optic Nerve Disease	58	1.185

618	P	MTR012	Mitral Valve Disease	57	1.185

619	P	DRR001	Diarrhea	55	1.185

620	P	HYP055	Hypoplastic Left Heart Syndrome	65	1.185

621	P	HYP750	Hypertriglyceridemia, Familial	62	1.164

622		HPT004	Hepatic Coma	43	1.164

623		CRD001	Cardiac Tamponade	43	1.164

624	c	PRM005	Primary Hyperparathyroidism	59	1.164

625		CHL035	Cholinergic Urticaria	29	1.164

626	P	HMP007	Hemophilia	52	1.164

627		CRB086	Cerebral Aneurysms	40	1.164

628	P	DYS021	Dysautonomia	38	1.164

629		CRV002	Cervix Uteri Carcinoma in Situ	47	1.127

630		CRV045	Cervical Intraepithelial Neoplasia	39	1.127

631	P	MYS003	Myasthenia Gravis	68	1.126

632		RTN017	Retinal Detachment	60	1.126

633		TNG007	Tongue Carcinoma	52	1.126

634		ACT003	Acute Kidney Tubular Necrosis	46	1.126

635		EXP004	Exophthalmos	51	1.126

636	P	ANT001	Anterolateral Myocardial Infarction	34	1.126

637	P	RRH023	Rare Hereditary Hemochromatosis	54	1.126

638		ADR005	Adrenal Carcinoma	62	1.126

639		HMS001	Hemosiderosis	48	1.126

640		CCC002	Coccidiosis	50	1.126

641		NPH010	Nephrosclerosis	50	1.126

642	P	TCD001	Tic Disorder	49	1.126

643		GLM008	Glomus Tumor	50	1.126

644		PST053	Postherpetic Neuralgia	40	1.126

645		CLS040	Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency	37	1.126

646		PRS115	Prosthetic Joint Infection	42	1.126

647	c	SYS001	Systemic Lupus Erythematosus	87	1.119

648	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	1.119

649	c	MJR022	Major Affective Disorder 8	38	1.119

650	P	LKM062	Leukemia, Acute Lymphoblastic	69	1.119

651	c	MJR024	Major Affective Disorder 9	41	1.119

652	P	ACT092	Acth-Independent Macronodular Adrenal Hyperplasia	56	1.119

653	P	STR020	Strabismus	56	1.119

654		CMP010	Complex Regional Pain Syndrome	60	1.119

655		MCH006	Mechanical Strabismus	40	1.119

656	P	MYL006	Myeloid Leukemia	61	1.119

657	P	PRS038	Personality Disorder	65	1.119

658		DSS008	Disease of Mental Health	74	1.119

659		ISL003	Isolated Growth Hormone Deficiency	57	1.119

660	P	BND020	Bone Disease	59	1.119

661	P	SBS003	Substance Abuse	54	1.119

662		AMN001	Amenorrhea	54	1.119

663	P	HYP120	Hypoaldosteronism	35	1.119

664		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	61	1.118

665		FML159	Familial Periodic Paralyses	16	1.115

666		HYP017	Hypophosphatemia	49	1.114

667		NRL016	Neural Tube Defects	81	1.114

668		CHG001	Chagas Disease	66	1.114

669		HPT019	Hepatic Encephalopathy	59	1.114

670		ANG011	Angiodysplasia	42	1.114

671		GST033	Gestational Diabetes	61	1.114

672		HYP026	Hypoglycemic Coma	37	1.114

673		FNT004	Fainting	29	1.114

674		MCR359	Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss	44	1.091

675		TNS005	Tonsillitis	57	1.087

676		NNF008	Non-Functioning Paraganglioma	19	1.068

677		SPR068	Sporadic Pheochromocytoma/secreting Paraganglioma	29	1.068

678	c	ERL020	Early-Onset Schizophrenia	44	1.063

679		ATS010	Autosomal Recessive Disease	42	1.063

680		IMM167	Immune Deficiency Disease	78	1.063

681		BCT022	Bacterial Infectious Disease	56	1.063

682		PST048	Postural Orthostatic Tachycardia Syndrome	46	1.063

683	c	CHR708	Chronic Urticaria	42	1.063

684		GNG002	Ganglioneuroma	52	1.063

685		GNG005	Gangliocytoma	55	1.063

686		IDP070	Idiopathic Scoliosis	42	1.063

687		GNR004	Generalized Anxiety Disorder	55	1.063

688	P	MYT002	Myotonic Dystrophy	51	1.063

689		APP008	Appendicitis	62	1.051

690		OPT003	Opiate Dependence	49	1.051

691	P	INT068	Intestinal Disease	53	1.051

692	P	BLD134	Bladder Cancer	79	1.048

693	P	OST002	Osteoporosis	76	1.048

694		ATM095	Autoimmune Disease	61	1.048

695	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	1.048

696	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	1.048

697		CVD001	Covid-19	57	1.048

698		URL001	Urolithiasis	46	1.048

699	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	1.048

700		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.048

701		GYN001	Gynecomastia	47	1.048

702	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	1.048

703		SVR001	Severe Acute Respiratory Syndrome	67	1.048

704		PSY004	Psychotic Disorder	66	1.048

705		INF021	Infant Gynecomastia	30	1.048

706	P	INF032	Infertility	57	1.048

707	P	GLM007	Glomerulonephritis	60	1.048

708	c	BRT042	Bartter Syndrome, Type 3	46	1.036

709		DBT092	Diabetes Insipidus, Nephrogenic, X-Linked	38	1.036

710		RYN001	Raynaud Disease	50	1.036

711		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	1.036

712		LNG105	Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome	35	1.036

713	P	AMY004	Amyloidosis	70	1.036

714		EXT007	Extracutaneous Mastocytoma	38	1.036

715		VLK001	Volkmann Contracture	23	1.036

716		HMG002	Hemoglobinuria	50	1.036

717		MST004	Mast Cell Neoplasm	42	1.036

718	P	SYP003	Syphilis	59	1.036

719	c	SCN006	Secondary Syphilis	36	1.036

720		SPL006	Splenic Infarction	37	1.036

721		LFT001	Left Bundle Branch Hemiblock	47	1.036

722	P	TBR001	Tuberous Sclerosis	69	1.036

723	P	GLY013	Glycogen Storage Disease	60	1.036

724		DPH001	Diphtheria	59	1.036

725		DDN009	Duodenal Obstruction	34	1.036

726		RCT020	Rectum Adenocarcinoma	48	1.036

727	P	CLL015	Collagen Disease	48	1.036

728		CRH005	Crohn's Colitis	53	1.022

729	c	INF071	Inflammatory Bowel Disease 1	65	1.022

730		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	1.022

731		VGN023	Vaginitis	56	1.022

732	c	LKM063	Leukemia, Chronic Myeloid	71	1.008

733		CMP040	Complement Component 4, Partial Deficiency of	34	1.008

734	P	MSC003	Muscular Atrophy	52	1.008

735		WHT017	Wheat Allergy	31	1.008

736		RTN020	Retinal Vascular Disease	46	1.008

737		IRN001	Iron Deficiency Anemia	58	1.008

738	P	PYL005	Pyelonephritis	57	1.008

739		ESP002	Esophageal Varix	51	1.008

740	P	MYC033	Myoclonus	47	1.008

741		PMP014	Pemphigoid	51	0.979

742	P	PLM034	Pulmonary Emphysema	58	0.979

743		CHR008	Choroiditis	48	0.979

744		SPS057	Spasticity	42	0.968

745	P	PLY014	Polycystic Kidney Disease	69	0.968

746		RHM028	Rheumatic Heart Disease	56	0.968

747		RCK004	Rickets	68	0.968

748		LWC001	Low Compliance Bladder	45	0.968

749	P	INT143	Interstitial Cystitis	60	0.968

750		ADR008	Adrenal Adenoma	55	0.968

751	P	SCH015	Schizophrenia	74	0.950

752		GST092	Gastroesophageal Reflux	61	0.950

753		PRP080	Peripheral Artery Disease	54	0.950

754		PLL012	Pollen Allergy	45	0.950

755		ZLL002	Zollinger-Ellison Syndrome	55	0.950

756	c	ACQ017	Acquired Von Willebrand Syndrome	48	0.950

757		GST030	Gastrinoma	45	0.950

758	P	MVM001	Movement Disease	61	0.950

759	P	HML002	Hemolytic Anemia	62	0.950

760		CHL067	Cholecystitis	60	0.950

761		CLL003	Cellulitis	53	0.950

762	P	HRM001	Hermansky-Pudlak Syndrome	65	0.950

763		QLT001	Qualitative Platelet Defect	29	0.950

764		ASP004	Asphyxia Neonatorum	50	0.950

765		CRT004	Carotid Artery Thrombosis	39	0.950

766	P	PLY019	Polyneuropathy	52	0.950

767	P	MTR003	Mitral Valve Stenosis	53	0.950

768		CLP006	Clopidogrel Resistance	44	0.950

769		MLT131	Multifocal Atrial Tachycardia	17	0.930

770		CLR108	Colorectal Adenoma	64	0.930

771		DBN001	Dubin-Johnson Syndrome	57	0.930

772		TRC109	Tracheoesophageal Fistula with or Without Esophageal Atresia	54	0.930

773	c	TBR025	Tuberous Sclerosis 1	84	0.930

774		MDD018	Middle East Respiratory Syndrome	44	0.930

775		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	43	0.930

776		SBV001	Subvalvular Aortic Stenosis	30	0.930

777		KDN015	Kidney Angiomyolipoma	46	0.930

778		TRN018	Transitional Cell Carcinoma	56	0.930

779		AMP007	Amphetamine Abuse	36	0.930

780		PDP001	Pedophilia	29	0.930

781		PTT004	Pituitary Apoplexy	47	0.930

782		ANG005	Anogenital Venereal Wart	56	0.930

783		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	64	0.914

784		LWF001	Low-Flow Priapism	16	0.889

785	c	PLM164	Pulmonary Hypertension, Primary, 1	76	0.889

786	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.889

787		FCT001	Factor Viii Deficiency	60	0.889

788	c	MCR115	Microvascular Complications of Diabetes 5	65	0.889

789	c	MCR130	Microvascular Complications of Diabetes 6	41	0.889

790		MYL009	Myelodysplastic Syndrome	67	0.889

791		LMB062	Limb Ischemia	55	0.889

792	c	CHR711	Chronic Asthma	41	0.889

793		HLC007	Helicobacter Pylori Infection	67	0.889

794	c	MCR120	Microvascular Complications of Diabetes 7	47	0.889

795	c	HMP029	Hemophilia a	68	0.889

796		MLT157	Multiple System Atrophy 1	69	0.889

797		MST024	Mastocytosis, Cutaneous	67	0.889

798		CLR109	Colorectal Adenocarcinoma	50	0.889

799		INT002	Intermittent Claudication	61	0.889

800		ANR004	Anuria	44	0.889

801		AGR002	Agoraphobia	45	0.889

802		CRB004	Cerebral Artery Occlusion	45	0.889

803	c	MCR113	Microvascular Complications of Diabetes 3	52	0.889

804	c	MCR133	Microvascular Complications of Diabetes 4	41	0.889

805		CRT013	Carotid Stenosis	51	0.889

806	P	HYD006	Hydrocephalus	61	0.889

807		SVR004	Severe Combined Immunodeficiency	72	0.889

808	c	FML021	Familial Hypercholesterolemia	72	0.889

809		HYP141	Hyperphenylalaninemia	42	0.889

810	P	MNN013	Meningitis	65	0.889

811		HRP004	Herpes Zoster	61	0.889

812		ORL012	Oral Leukoplakia	36	0.889

813		LKP003	Leukoplakia	39	0.889

814		CHR178	Chromosomal Triplication	34	0.889

815	P	CRD224	Cardiofaciocutaneous Syndrome 1	71	0.889

816	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	0.889

817		NTR005	Nutritional Deficiency Disease	61	0.889

818		NWB001	Newborn Respiratory Distress Syndrome	56	0.889

819		SKN013	Skin Benign Neoplasm	50	0.889

820		DNT014	Dental Pulp Disease	43	0.889

821	c	BTT014	Beta-Thalassemia	72	0.878

822		HYP780	Hypoadrenocorticism, Familial	61	0.878

823	P	MJR007	Major Affective Disorder 1	42	0.878

824		GST040	Gastric Adenocarcinoma	67	0.878

825		TRC022	Tricuspid Valve Insufficiency	47	0.878

826	P	DMN002	Dementia	66	0.878

827	P	GRV001	Graves' Disease	55	0.878

828		EPC002	Epicondylitis	44	0.878

829	c	INH020	Inherited Metabolic Disorder	48	0.878

830	P	PNM007	Pneumonia	67	0.878

831		FSC004	Fasciitis	49	0.878

832		TNS014	Tenosynovitis	46	0.878

833	P	PRC019	Precocious Puberty	47	0.878

834		CHR344	Chronic Orthostatic Intolerance	14	0.878

835		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	44	0.861

836		CCN009	Cocaine Intoxication	30	0.823

837		PLM061	Pulmonary Edema of Mountaineers	26	0.823

838	P	FML018	Familial Mediterranean Fever	73	0.823

839		OBS002	Obsessive-Compulsive Disorder	68	0.823

840		FCL074	Facial Spasm	19	0.823

841		ANS021	Anisocoria	25	0.823

842	c	BRN108	Branchiootic Syndrome 1	62	0.823

843		ARM002	Aromatic L-Amino Acid Decarboxylase Deficiency	56	0.823

844		TRG002	Trigeminal Neuralgia	61	0.823

845		PTT046	Pituitary Hormone Deficiency, Combined, 2	62	0.823

846	P	HNT016	Huntington Disease	73	0.823

847	c	DMN023	Diamond-Blackfan Anemia 1	66	0.823

848	c	AST034	Asthma-Related Traits 4	28	0.823

849		INT394	Intermittent Asthma	21	0.823

850		INF118	Inflammatory Myopathy with Abundant Macrophages	27	0.823

851		WHP002	Whiplash	36	0.823

852		GNG008	Ganglioneuroblastoma	47	0.823

853		PRL008	Paralytic Ileus	45	0.823

854	P	GRF003	Graft-Versus-Host Disease	71	0.823

855		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.823

856		MYL031	Myeloproliferative Neoplasm	66	0.823

857		BRC012	Brucellosis	66	0.823

858		PLC009	Placenta Praevia	38	0.823

859		HMP001	Hemopericardium	47	0.823

860		ANH002	Anhidrosis	46	0.823

861		HYP043	Hyperandrogenism	48	0.823

862	P	PRC012	Pericardial Effusion	50	0.823

863		EHR002	Ehrlichiosis	39	0.823

864	P	RTN018	Retinal Disease	53	0.823

865		PTN001	Patent Foramen Ovale	62	0.823

866		GST037	Gastroparesis	52	0.823

867		MST020	Mast Cell Activation Syndrome	28	0.823

868		BRT037	Brittle Diabetes	24	0.823

869	c	BLD140	Blood Group, I System	46	0.791

870		LGH007	Leigh Syndrome	70	0.791

871	c	HYP272	Hypercholesterolemia, Familial, 3	45	0.791

872	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	0.791

873		MTC112	Mitochondrial Dna-Associated Leigh Syndrome	32	0.791

874		LCR013	Lacrimal Duct Defect	40	0.790

875	c	DMN005	Diamond-Blackfan Anemia 2	28	0.790

876	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	55	0.790

877		CHR072	Chordoma	57	0.790

878		INT067	Interstitial Nephritis	46	0.790

879	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	64	0.790

880	c	PSD117	Pseudohypoparathyroidism, Type Ic	37	0.790

881	P	TYR004	Tyrosinemia	50	0.790

882	P	CND004	Candidiasis	58	0.790

883	P	SYS005	Systemic Scleroderma	74	0.790

884		MRS001	Marasmus	42	0.790

885		CRB016	Carbuncle	39	0.790

886		GST045	Gastroenteritis	58	0.790

887		KWS001	Kwashiorkor	45	0.790

888		NCR001	Necrotizing Ulcerative Gingivitis	26	0.790

889		CLS032	Clostridium Perfringens Infection	16	0.790

890		AMR003	Amaurosis Fugax	33	0.790

891		ALL014	Allergic Encephalomyelitis	34	0.790

892		BRN045	Brunner Syndrome	52	0.779

893	P	PRD017	Periodic Paralyses	24	0.779

894		PST021	Postpartum Depression	50	0.771

895		APN006	Apnea of Prematurity	24	0.771

896	P	ACT244	Acth-Independent Cushing Syndrome	38	0.771

897		CNG506	Congenital Amyoplasia	27	0.771

898	P	VTR007	Vitreoretinopathy	46	0.771

899	P	MYC084	Mycobacterium Tuberculosis 1	68	0.771

900	P	CLR023	Colorectal Cancer	100	0.771

901	P	URN019	Urinary Tract Infection	49	0.771

902	P	LYM118	Lymphoma	67	0.771

903	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.771

904		RFL001	Reflex Sympathetic Dystrophy	51	0.771

905		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.771

906		NRR001	Neuroretinitis	42	0.771

907	c	PRM340	Primary Adrenal Insufficiency	38	0.771

908	c	HPT003	Hepatitis a	63	0.771

909	P	LPS004	Lupus Erythematosus	61	0.771

910	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	0.771

911		RTN023	Retinitis	46	0.771

912	c	ACT068	Acute Cystitis	61	0.771

913		ALG001	Algoneurodystrophy	38	0.771

914		HGH043	High Grade Glioma	45	0.771

915		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.771

916		CPL003	Capillary Leak Syndrome	54	0.771

917		LGP001	Lagophthalmos	30	0.771

918		PLT032	Platelet Responsiveness to Adrenaline, Depressed	7	0.755

919		PLY100	Polyploidy	36	0.751

920		SCR039	Scorpion Envenomation	41	0.751

921		CHR005	Chorioamnionitis	50	0.751

922	P	ANP001	Anaplastic Large Cell Lymphoma	61	0.751

923		PHY008	Physical Urticaria	33	0.751

924		MYL020	Myelomeningocele	51	0.751

925		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	61	0.751

926	P	FTL001	Fetal Alcohol Syndrome	55	0.751

927		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	0.751

928	c	BRS111	Breast-Ovarian Cancer, Familial 2	53	0.751

929	P	SCL057	Scoliosis, Isolated 1	40	0.751

930		GST019	Gastrointestinal Stromal Tumor	78	0.751

931		PTC002	Potocki-Lupski Syndrome	48	0.751

932	c	ACT042	Acute Pyelonephritis	45	0.751

933		INT040	Intrinsic Asthma	36	0.751

934		CHR074	Choriocarcinoma	46	0.751

935	P	PRD021	Periodic Paralysis	41	0.751

936	P	ANT006	Antiphospholipid Syndrome	55	0.751

937		NPH009	Nephrolithiasis	54	0.751

938	P	INT070	Intestinal Obstruction	57	0.751

939	P	RTN014	Retinal Artery Occlusion	47	0.751

940		ERY003	Erythema Multiforme	56	0.751

941		BRN026	Branch Retinal Artery Occlusion	41	0.751

942	P	HMR003	Hemorrhagic Disease	59	0.751

943		CRS013	Crustacean Allergy	21	0.751

944		RBS001	Rabies	58	0.751

945		PRT029	Parathyroid Adenoma	51	0.751

946		PHR003	Pharyngitis	58	0.751

947	c	BNG021	Benign Essential Hypertension	35	0.751

948	P	CMP008	Compartment Syndrome	50	0.751

949		SYS003	Systolic Heart Failure	49	0.751

950		END051	Endolymphatic Sac Tumor	24	0.751

951	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.715

952	c	MCL013	Mucolipidosis Iv	65	0.715

953		AND020	Androgen Insensitivity, Partial	55