Search results for Dopamine

2529 hits were found for Dopamine

#	Family	MCID	Name	MIFTS	Score
1		DPM001	Dopamine Beta-Hydroxylase Deficiency	53	43.815

2	P	PRK039	Parkinsonism	55	39.634

3	P	PRK057	Parkinson Disease, Late-Onset	80	36.657

4	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	30.978

5	P	PRK101	Parkinsonism-Dystonia, Infantile, 1	40	27.810

6	P	SCH015	Schizophrenia	74	26.572

7	c	ORT011	Orthostatic Hypotension 1	43	23.488

8	P	TRM003	Tremor	48	22.063

9		ALC007	Alcohol Dependence	66	20.769

10	P	DYS154	Dystonia	64	19.367

11		TRD006	Tardive Dyskinesia	53	19.321

12		HYP020	Hyperprolactinemia	63	19.302

13	P	MVM001	Movement Disease	61	18.812

14		PRT037	Pertussis	65	18.288

15	P	BPL003	Bipolar Disorder	56	17.900

16	P	PHC003	Pheochromocytoma	69	17.666

17		ADR040	Adrenal Gland Pheochromocytoma	46	17.624

18		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	17.563

19	P	NRB001	Neuroblastoma	66	17.258

20	P	HNT016	Huntington Disease	73	16.891

21	c	MJR022	Major Affective Disorder 8	38	16.817

22	c	MJR024	Major Affective Disorder 9	41	16.817

23	P	RST001	Restless Legs Syndrome	52	16.594

24		CCN002	Cocaine Abuse	49	16.274

25		BRN112	Brain Dopamine-Serotonin Vesicular Transport Disease	18	16.137

26	P	SBS003	Substance Abuse	54	15.841

27		PTT037	Pituitary Tumors	44	15.361

28	c	HYP595	Hypertension, Essential	85	15.108

29		ADN018	Adenoma	59	14.697

30		MNT002	Mental Depression	57	14.675

31		TXC005	Toxic Shock Syndrome	62	14.478

32		DPR016	Depression	65	14.196

33		SLC036	Slc6a3-Related Dopamine Transporter Deficiency Syndrome	8	13.907

34		PSY004	Psychotic Disorder	66	13.747

35	P	MJR001	Major Depressive Disorder	68	13.713

36		PRK102	Parkinsonism-Dystonia, Infantile, 2	26	13.538

37		TBC004	Tobacco Addiction	63	13.277

38	P	ALC033	Alcohol Use Disorder	61	12.957

39		MDD011	Mood Disorder	62	12.713

40		PTH002	Pathological Gambling	48	12.531

41	P	PTT006	Pituitary Adenoma	55	12.504

42		OBS002	Obsessive-Compulsive Disorder	68	12.208

43		CCN001	Cocaine Dependence	48	12.202

44		PRT058	Pure Autonomic Failure	58	12.142

45	c	ACT071	Acute Kidney Failure	60	12.004

46		GLL008	Gilles De La Tourette Syndrome	65	11.980

47	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	11.849

48		MLT157	Multiple System Atrophy 1	69	11.721

49		ACR007	Acromegaly	70	11.515

50		CHR073	Choreatic Disease	54	11.373

51		DPM008	Dopamine Beta-Hydroxylase, Plasma, Thermolability of	5	11.296

52		DRG003	Drug Dependence	46	10.679

53		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	10.657

54		ETN001	Eating Disorder	59	10.500

55		WTH001	Withdrawal Disorder	48	10.198

56		AGN016	Aging	54	10.141

57		CHL014	Cholera	62	10.016

58		PST028	Post-Traumatic Stress Disorder	59	9.878

59		TRM010	Traumatic Brain Injury	51	9.825

60	c	MGR028	Migraine with or Without Aura 1	64	9.730

61	P	TCD001	Tic Disorder	49	9.663

62		BRN071	Brain Injury	50	9.630

63		ANX010	Anxiety	70	9.591

64		CRD137	Cardiogenic Shock	56	9.334

65		HYP266	Hypoxia	57	9.314

66	P	MYP006	Myopia	56	9.298

67	P	KDN018	Kidney Disease	72	9.248

68	c	ATS007	Autism Spectrum Disorder	72	9.242

69		PNG002	Pain Agnosia	51	9.214

70		ALL029	Allergic Disease	59	9.163

71	P	SPR120	Supranuclear Palsy, Progressive, 1	69	9.095

72		48X005	48,xyyy	39	9.090

73	P	ATS364	Autism	69	9.041

74	c	ESS001	Essential Tremor	57	8.882

75		IRN002	Iron Metabolism Disease	57	8.717

76	P	ENC018	Encephalopathy	62	8.674

77	P	SLP005	Sleep Disorder	61	8.659

78	P	SZR006	Seizure Disorder	70	8.426

79	P	DMN002	Dementia	66	8.330

80	P	NRC002	Narcolepsy	56	8.320

81	P	CHR345	Chronic Pain	50	8.255

82		ACT084	Acute Stress Disorder	54	8.202

83		NRL004	Neuroleptic Malignant Syndrome	52	8.172

84		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	8.060

85	P	ALZ034	Alzheimer Disease	87	8.016

86	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	8.010

87	P	PRS038	Personality Disorder	65	7.984

88		ANR007	Anorexia Nervosa	60	7.874

89	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	7.779

90	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	7.779

91	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	7.779

92	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	7.779

93	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	7.779

94	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	7.779

95	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	7.779

96	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	7.779

97	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	7.779

98		CNG034	Congestive Heart Failure	69	7.685

99		HYP056	Hypoglycemia	65	7.684

100		HLX001	Helix Syndrome	48	7.596

101		OPD006	Opioid Addiction	48	7.558

102		PPL052	Papillomatosis, Confluent and Reticulated	34	7.557

103		ATN005	Autonomic Dysfunction	46	7.527

104		OPT003	Opiate Dependence	49	7.518

105		RMS001	Rem Sleep Behavior Disorder	47	7.457

106		SCH012	Schizoaffective Disorder	50	7.442

107		SBC016	Subacute Delirium	43	7.422

108		IMP006	Impulse Control Disorder	45	7.379

109		HYP066	Hyperglycemia	61	7.315

110	P	PTS002	Ptosis	52	7.088

111		IMP005	Impotence	52	7.041

112	P	HYP086	Hypothyroidism	69	7.041

113		GLC096	Galactorrhea	40	6.971

114		CNS004	Constipation	56	6.961

115		SXL003	Sexual Disorder	49	6.920

116	P	MJR007	Major Affective Disorder 1	42	6.899

117		HRT012	Heart Valve Disease	53	6.894

118		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	6.855

119		RPD005	Rapidly Involuting Congenital Hemangioma	46	6.822

120		END040	Endogenous Depression	55	6.797

121		AMN003	Amnestic Disorder	54	6.759

122		HYP060	Hyperinsulinism	54	6.560

123		ARM002	Aromatic L-Amino Acid Decarboxylase Deficiency	56	6.519

124		SBS004	Substance Dependence	47	6.498

125		PHN003	Phenylketonuria	76	6.472

126		AMN001	Amenorrhea	54	6.423

127	P	HRT032	Heart Disease	81	6.399

128	P	MYC033	Myoclonus	47	6.299

129		HPT004	Hepatic Coma	43	6.227

130	P	LTR001	Lateral Sclerosis	58	6.200

131		OVR029	Ovarian Hyperstimulation Syndrome	63	6.200

132		ANX004	Anoxia	40	6.168

133		HPT019	Hepatic Encephalopathy	59	6.168

134		HYP080	Hypogonadism	50	6.160

135		LSC001	Lesch-Nyhan Syndrome	62	6.141

136		FBR047	Fibromyalgia	58	6.141

137	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	6.138

138	P	HDC001	Headache	57	6.138

139		MLD018	Mild Cognitive Impairment	48	6.002

140	P	RSP003	Respiratory Failure	74	5.932

141	P	CRD119	Cardiac Arrest	67	5.876

142		GLM045	Glioma	63	5.775

143		GLL048	Glial Tumor	52	5.750

144	P	NRP001	Neuropathy	60	5.744

145		OCL069	Ocular Motor Apraxia	57	5.676

146	P	DDN001	Duodenal Ulcer	53	5.661

147	P	PRG013	Paraganglioma	57	5.502

148		BLM002	Bulimia Nervosa	57	5.469

149	P	HYP265	Hypotonia	42	5.424

150		CRB004	Cerebral Artery Occlusion	45	5.373

151		CRB039	Cerebrovascular Disease	66	5.336

152		MRP001	Morphine Dependence	42	5.331

153	P	HYP083	Hypopituitarism	52	5.325

154		SPN186	Spinal Cord Injury	61	5.323

155	P	PTN014	Patent Ductus Arteriosus 1	59	5.310

156		47X002	47,xyy	48	5.304

157	c	DYS191	Dystonia 1, Torsion, Autosomal Dominant	47	5.278

158		HRW001	Hair Whorl	35	5.277

159		HRN003	Heroin Dependence	44	5.266

160		CRT033	Corticobasal Degeneration	47	5.240

161		TTN003	Tetanus	65	5.237

162	P	DYS021	Dysautonomia	38	5.225

163		STR067	Stroke, Ischemic	80	5.224

164		PLY068	Polysubstance Abuse	41	5.211

165		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	5.207

166	c	TYP009	Type 2 Diabetes Mellitus	92	5.197

167		MNG007	Manganese Poisoning	28	5.194

168		ISC004	Ischemia	61	5.182

169		GLB002	Glioblastoma	67	5.153

170		CRB037	Cerebral Palsy	67	5.122

171	P	PLY011	Polycystic Ovary Syndrome	57	5.105

172		WLS001	Wilson Disease	70	5.089

173		DMN031	Dementia, Lewy Body	65	5.051

174	P	EPL164	Epilepsy	68	5.038

175		PLM010	Pulmonary Edema	55	5.037

176	P	FML187	Familial Hypertension	34	5.001

177		CYT002	Cytokine Deficiency	43	4.977

178		PRN009	Paranoid Schizophrenia	49	4.948

179		CND002	Conduct Disorder	51	4.909

180		OPD001	Opioid Abuse	44	4.895

181		RFR003	Refractive Error	41	4.853

182	c	ATR087	Atrial Standstill 1	74	4.813

183		GST037	Gastroparesis	52	4.801

184	c	BPL002	Bipolar I Disorder	47	4.790

185		LNG015	Lingual-Facial-Buccal Dyskinesia	47	4.725

186		TQP001	Taqi Polymorphism	29	4.712

187	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	4.699

188		INS024	Insulin-Like Growth Factor I	78	4.695

189		PST092	Posttransplant Acute Limbic Encephalitis	28	4.691

190	c	DLT002	Dilated Cardiomyopathy	78	4.685

191		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	4.669

192	P	PLM037	Pulmonary Hypertension	72	4.656

193		LVR012	Liver Cirrhosis	63	4.559

194	P	RTT002	Rett Syndrome	79	4.555

195		MTB004	Metabolic Acidosis	48	4.514

196	P	HYP076	Hyperthyroidism	53	4.512

197		BRN004	Brain Edema	54	4.501

198	c	SCH079	Schizophrenia 1	44	4.482

199		IMM167	Immune Deficiency Disease	78	4.469

200		VSC002	Vascular Dementia	60	4.452

201	P	ENC004	Encephalitis	61	4.441

202		GLC003	Glucose Intolerance	54	4.428

203	P	INF032	Infertility	57	4.404

204		SCH011	Schizotypal Personality Disorder	36	4.387

205		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	4.371

206	P	MGR001	Migraine Without Aura	49	4.350

207		AMP007	Amphetamine Abuse	36	4.334

208		SCH003	Schizophreniform Disorder	55	4.310

209		FCL022	Focal Dystonia	42	4.299

210	P	MGR003	Migraine with Aura	52	4.279

211		ANG054	Angina Pectoris	66	4.278

212	P	ADL010	Adult Respiratory Distress Syndrome	71	4.278

213		SRT004	Serotonin Syndrome	54	4.266

214	P	PNC025	Panic Disorder	52	4.232

215		PLM129	Pulmonary Disease, Chronic Obstructive	74	4.221

216		CRT015	Carotid Artery Occlusion	45	4.221

217		HYP005	Hypokalemia	55	4.212

218	P	DBT009	Diabetes Mellitus	67	4.202

219	c	ACT075	Acute Myocardial Infarction	56	4.199

220		FRN006	Frontotemporal Dementia	68	4.198

221		VSC064	Vascular Parkinsonism	21	4.187

222	P	PRM227	Primary Orthostatic Hypotension	24	4.184

223	P	SLP006	Sleep Apnea	69	4.184

224		STT041	Stuttering	52	4.173

225	c	MCR115	Microvascular Complications of Diabetes 5	65	4.170

226		IRR002	Irritable Bowel Syndrome	65	4.140

227	c	CHR684	Chronic Kidney Disease	69	4.110

228		SYN036	Syncope	45	4.109

229	c	ACT027	Acute Pancreatitis	60	4.102

230	c	TYP008	Type 1 Diabetes Mellitus	70	4.102

231		LPD008	Lipid Metabolism Disorder	62	4.090

232	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	4.070

233	c	ERL056	Early-Onset Parkinson's Disease	40	4.047

234		GTP002	Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia	18	4.038

235	c	CNT035	Central Nervous System Disease	54	4.031

236	P	END044	Endometriosis	62	4.025

237	P	GLM040	Glioma Susceptibility 1	71	4.010

238	c	PRC016	Pre-Eclampsia	65	4.010

239		ALL014	Allergic Encephalomyelitis	34	3.994

240		DFC004	Deficiency Anemia	74	3.978

241		CNN001	Cannabis Dependence	38	3.973

242		MLT116	Multiple System Atrophy, Parkinsonian Type	29	3.972

243	P	RTN016	Retinal Degeneration	52	3.971

244	P	RNL015	Renal Hypertension	45	3.971

245		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	3.963

246		NRR001	Neuroretinitis	42	3.958

247		RTN023	Retinitis	46	3.958

248		HPT014	Hepatorenal Syndrome	49	3.958

249	P	DRR001	Diarrhea	55	3.951

250	c	DNT047	Dentinogenesis Imperfecta Type 2	35	3.931

251	P	HYD006	Hydrocephalus	61	3.891

252		AVD001	Avoidant Personality Disorder	49	3.882

253		HND015	Hand Skill, Relative	30	3.872

254		END086	End Stage Renal Disease	52	3.863

255	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	3.858

256		PRT036	Peritonitis	65	3.853

257		DYS161	Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency	56	3.853

258		MLG169	Malignant Astrocytoma	57	3.846

259		DYS073	Dysphagia	53	3.833

260		RCK004	Rickets	68	3.825

261	P	FRG001	Fragile X Syndrome	70	3.819

262		HMN044	Human Immunodeficiency Virus Type 1	78	3.818

263		HDN002	Head Injury	44	3.798

264	P	TMP001	Temporal Lobe Epilepsy	49	3.785

265		NVL002	Novelty Seeking Personality Trait	15	3.769

266		CNN003	Conn's Syndrome	79	3.765

267		SPS057	Spasticity	42	3.735

268	P	VSC007	Vascular Disease	63	3.732

269	P	PRP019	Peripheral Nervous System Disease	58	3.731

270	P	MLT020	Multiple Sclerosis	79	3.720

271		DLS001	Delusional Disorder	45	3.715

272		HYP141	Hyperphenylalaninemia	42	3.709

273		ACT003	Acute Kidney Tubular Necrosis	46	3.698

274	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	3.680

275		ADG002	Audiogenic Seizures	25	3.641

276		ENT011	Enterocolitis	55	3.640

277		RBS001	Rabies	58	3.636

278	P	NRV007	Nervous System Disease	67	3.603

279	P	NRF002	Neurofibromatosis	57	3.602

280		FNC007	Functioning Pituitary Adenoma	42	3.592

281		TRN015	Transient Cerebral Ischemia	63	3.592

282	P	LCT001	Lactic Acidosis	51	3.588

283		INT075	Intracranial Hypertension	53	3.585

284	c	MCR130	Microvascular Complications of Diabetes 6	41	3.577

285	c	MCR120	Microvascular Complications of Diabetes 7	47	3.577

286	c	MCR113	Microvascular Complications of Diabetes 3	52	3.577

287	c	MCR133	Microvascular Complications of Diabetes 4	41	3.577

288	P	ECL001	Eclampsia	52	3.575

289		MNK001	Menkes Disease	64	3.561

290		MLG157	Malignant Pheochromocytoma	36	3.561

291	P	RTN024	Retinoblastoma	73	3.557

292	P	RHM011	Rheumatoid Arthritis	82	3.541

293		PTT009	Pituitary Gland Disease	53	3.539

294		PRT251	Proteinuria, Chronic Benign	57	3.516

295		ANT011	Antisocial Personality Disorder	47	3.495

296	c	CNG006	Congenital Hypothyroidism	63	3.494

297		STT001	Status Epilepticus	59	3.485

298		OCL006	Ocular Hypertension	53	3.483

299		SCL003	Social Phobia	48	3.480

300	c	EXD008	Exudative Vitreoretinopathy 1	71	3.477

301	P	RTN008	Retinitis Pigmentosa	80	3.476

302		BRD004	Borderline Personality Disorder	53	3.464

303	P	BLP003	Blepharospasm	46	3.440

304		GST023	Gastric Ulcer	52	3.424

305		NWB001	Newborn Respiratory Distress Syndrome	56	3.423

306		CNN002	Cannabis Abuse	45	3.423

307	P	STR001	Striatonigral Degeneration	37	3.411

308	P	INF037	Inflammatory Bowel Disease	53	3.397

309	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	3.381

310		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	42	3.378

311		SYD002	Sydenham Chorea	34	3.357

312		NRN004	Neuroendocrine Tumor	59	3.348

313		HRT011	Heart Septal Defect	49	3.346

314	P	PNC044	Pancreatitis	61	3.339

315	P	TXP001	Toxoplasmosis	60	3.339

316		PRN019	Perinatal Necrotizing Enterocolitis	60	3.339

317		OPP004	Oppositional Defiant Disorder	49	3.338

318	P	MLT074	Multiple Endocrine Neoplasia	59	3.323

319		ANV001	Anovulation	47	3.318

320	c	PNS012	Paine Syndrome	60	3.310

321		SVR004	Severe Combined Immunodeficiency	72	3.309

322		NRT001	Neurotic Disorder	56	3.294

323		CRV043	Cervical Dystonia	46	3.283

324	P	ORT004	Orthostatic Intolerance	63	3.278

325		ALD013	Aldosterone-Producing Adenoma	36	3.278

326		ARG004	Argyria	26	3.276

327		BSL008	Basal Ganglia Disease	41	3.272

328	P	HRP006	Herpes Simplex	65	3.271

329		ATN004	Autonomic Neuropathy	42	3.271

330		DSS008	Disease of Mental Health	74	3.253

331		APH002	Aphasia	56	3.240

332	P	LVR013	Liver Disease	69	3.234

333		DRG016	Drug Induced Dyskinesia	23	3.226

334		GNR004	Generalized Anxiety Disorder	55	3.214

335		BRX001	Bruxism	51	3.207

336		DBT010	Diabetic Neuropathy	54	3.189

337		IRN001	Iron Deficiency Anemia	58	3.183

338		PST021	Postpartum Depression	50	3.180

339		INT323	Intraocular Pressure Quantitative Trait Locus	64	3.175

340		PSD088	Pseudobulbar Affect	33	3.175

341		DWN001	Down Syndrome	70	3.163

342	P	DBT005	Diabetes Insipidus	54	3.151

343		NNF007	Non-Functioning Pituitary Adenoma	39	3.148

344		PRM003	Premature Ejaculation	44	3.147

345	P	OVR082	Overgrowth Syndrome	49	3.145

346		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	3.144

347	P	HYP605	Hyperphenylalaninemia, Bh4-Deficient, B	44	3.135

348		MNN043	Meningioma, Familial	79	3.125

349	P	EXN002	Exanthem	58	3.121

350	c	HRD198	Hereditary Dystonia	30	3.121

351		SCR001	Secretory Meningioma	40	3.102

352		LYM002	Lymphoplasmacyte-Rich Meningioma	35	3.102

353		SPN021	Spinal Meningioma	50	3.102

354	P	SPN301	Spinocerebellar Ataxia 2	59	3.100

355		GRN017	Granulocytopenia	42	3.098

356	c	NRP054	Neuropathy, Hereditary Sensory and Autonomic, Type Iii	66	3.082

357		CRD223	Cardiac Arrhythmia	63	3.049

358	c	INH020	Inherited Metabolic Disorder	48	3.037

359		MTR086	Motor Stereotypies	14	3.027

360		LRN003	Learning Disability	49	3.026

361		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	3.013

362		CRB090	Cerebral Hypoxia	42	3.012

363	P	PRS040	Prostate Cancer	95	3.011

364		RSP019	Respiratory Distress Syndrome in Premature Infants	52	2.994

365		MTR002	Mitral Valve Insufficiency	52	2.990

366	P	CRN300	Coronary Heart Disease 1	73	2.986

367	P	TRT019	Torticollis	47	2.981

368	P	OBS001	Obstructive Jaundice	48	2.967

369		GST092	Gastroesophageal Reflux	61	2.965

370		LPP008	Lipoprotein Quantitative Trait Locus	65	2.957

371	c	CHR056	Chronic Tic Disorder	36	2.939

372		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	2.937

373		GNG005	Gangliocytoma	55	2.912

374		GNG002	Ganglioneuroma	52	2.887

375	P	MLN008	Melanoma	76	2.883

376		CRH001	Crohn's Disease	80	2.872

377	c	ACT134	Acute Liver Failure	59	2.868

378		ACQ007	Acquired Immunodeficiency Syndrome	59	2.868

379		ATS010	Autosomal Recessive Disease	42	2.861

380		CRB009	Cerebritis	43	2.860

381		URM002	Uremia	47	2.852

382	c	HYP368	Hyperphenylalaninemia, Bh4-Deficient, C	37	2.851

383	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	2.850

384		PTH003	Pathologic Nystagmus	52	2.850

385	P	LNG032	Lung Cancer	98	2.842

386		DGR001	Digeorge Syndrome	62	2.838

387		LPT014	Leptin Deficiency or Dysfunction	78	2.836

388		FTL006	Fetal Alcohol Spectrum Disorder	43	2.836

389	P	STR092	Striatal Degeneration, Autosomal Dominant 2	47	2.821

390		CRC006	Carcinoid Syndrome	55	2.821

391	P	RNV001	Renovascular Hypertension	49	2.808

392	c	ERL020	Early-Onset Schizophrenia	44	2.808

393	P	MTR014	Motor Neuron Disease	65	2.802

394	P	BRS047	Breast Cancer	98	2.791

395		MLN003	Melancholia	41	2.789

396		RST023	Resting Heart Rate, Variation in	40	2.779

397		IGG001	Iga Glomerulonephritis	50	2.779

398	P	OLV001	Olivopontocerebellar Atrophy	51	2.779

399		CHR066	Chronic Fatigue Syndrome	60	2.770

400	P	PNM007	Pneumonia	67	2.764

401		PTT004	Pituitary Apoplexy	47	2.762

402		PST027	Postencephalitic Parkinson Disease	46	2.744

403	c	PLM164	Pulmonary Hypertension, Primary, 1	76	2.742

404	P	NPH012	Nephrotic Syndrome	60	2.738

405	P	MYC007	Myocardial Infarction	70	2.732

406	P	TRT010	Teratoma	51	2.728

407		HGH043	High Grade Glioma	45	2.720

408	P	PLY014	Polycystic Kidney Disease	69	2.707

409	P	HYP263	Hypersomnia	41	2.691

410		HMS001	Hemosiderosis	48	2.689

411		HGH001	High Pressure Neurological Syndrome	27	2.689

412		SPP007	Suppression Amblyopia	38	2.686

413		AMB002	Amblyopia	50	2.686

414		BCK006	Back Pain	47	2.686

415		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	2.680

416	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	2.680

417	P	GLM007	Glomerulonephritis	60	2.678

418		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	2.678

419		BRN056	Bronchopulmonary Dysplasia	56	2.673

420	P	PRV006	Pervasive Developmental Disorder	52	2.669

421	P	RRH023	Rare Hereditary Hemochromatosis	54	2.664

422	P	VNT002	Ventricular Septal Defect	58	2.664

423		SGW002	Segawa Syndrome, Autosomal Recessive	44	2.659

424	c	SML038	Small Cell Cancer of the Lung	69	2.650

425		BCT022	Bacterial Infectious Disease	56	2.639

426		MTS001	Mutism	44	2.639

427		HYP014	Hyperuricemia	51	2.625

428		ART140	Arteries, Anomalies of	53	2.612

429		ASP007	Aspiration Pneumonia	49	2.611

430	c	HYP331	Hyperphenylalaninemia, Bh4-Deficient, a	48	2.611

431		DBT002	Diabetic Autonomic Neuropathy	41	2.604

432		OCL010	Ocular Hypotension	37	2.597

433	P	HYP098	Hypereosinophilic Syndrome	66	2.595

434		ADL002	Adult Syndrome	70	2.592

435		CYN002	Cyanosis, Transient Neonatal	43	2.586

436		ERL001	Early Myoclonic Encephalopathy	62	2.575

437		DPH001	Diphtheria	59	2.568

438		ANR004	Anuria	44	2.562

439		ATM095	Autoimmune Disease	61	2.561

440	P	AMY004	Amyloidosis	70	2.555

441		PST103	Postpartum Psychosis	31	2.553

442	c	DYS056	Dystonia 12	63	2.548

443		NTR005	Nutritional Deficiency Disease	61	2.547

444		PPT005	Peptic Ulcer Disease	58	2.543

445		ATR057	Atrioventricular Block	54	2.537

446		DYS009	Dysthymic Disorder	52	2.537

447		HMC014	Homocysteinemia	52	2.536

448		GYN001	Gynecomastia	47	2.536

449		INF021	Infant Gynecomastia	30	2.536

450		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	2.535

451		TRC022	Tricuspid Valve Insufficiency	47	2.535

452		HYP030	Hypoactive Sexual Desire Disorder	41	2.527

453	P	CLS010	Cluster Headache	42	2.527

454		ANT039	Antisynthetase Syndrome	55	2.522

455		ALB002	Albinism	47	2.522

456		GRW007	Growth Hormone Deficiency	46	2.511

457	c	MJR006	Major Affective Disorder 5	32	2.509

458	c	MJR003	Major Affective Disorder 6	32	2.509

459	P	OPN001	Open-Angle Glaucoma	55	2.505

460	P	FTL001	Fetal Alcohol Syndrome	55	2.491

461	P	NRM002	Normal Pressure Hydrocephalus	49	2.485

462		APR001	Apraxia	52	2.481

463		DWR001	Dwarfism	44	2.478

464	P	MCH002	Machado-Joseph Disease	62	2.457

465	P	HPT023	Hepatocellular Carcinoma	96	2.456

466	c	BRN108	Branchiootic Syndrome 1	62	2.447

467		BRN028	Brain Cancer	74	2.439

468		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.431

469		IDP033	Idiopathic Edema	41	2.427

470		OST159	Osteogenic Sarcoma	66	2.426

471		ADS004	Aids Dementia Complex	40	2.410

472		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	2.409

473	P	RTN018	Retinal Disease	53	2.409

474	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	2.396

475		THY029	Thyroid Carcinoma	51	2.383

476		JPN002	Japanese Encephalitis	61	2.383

477	P	PLY019	Polyneuropathy	52	2.378

478		PRV004	Periventricular Leukomalacia	52	2.378

479		CRB033	Cerebral Degeneration	39	2.378

480		ART002	Arts Syndrome	66	2.377

481		OBS003	Obsessive-Compulsive Personality Disorder	43	2.370

482		CLB010	Coloboma of Macula	53	2.366

483	P	KDN017	Kidney Cancer	61	2.365

484		AND005	Androgen Insensitivity Syndrome, Mild	21	2.347

485	P	ATN002	Autonomic Nervous System Disease	51	2.343

486		SVR001	Severe Acute Respiratory Syndrome	67	2.335

487	P	PSR002	Psoriasis	63	2.334

488		PST011	Pustulosis of Palm and Sole	52	2.334

489		PRP009	Peripartum Cardiomyopathy	55	2.334

490	c	MJR008	Major Affective Disorder 2	34	2.330

491		LWC001	Low Compliance Bladder	45	2.322

492		INT007	Intermediate Coronary Syndrome	54	2.321

493		OST012	Osteoarthritis	77	2.319

494	P	MTR003	Mitral Valve Stenosis	53	2.317

495		EMP001	Empty Sella Syndrome	42	2.306

496	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	2.302

497	c	SYS001	Systemic Lupus Erythematosus	87	2.288

498	P	PLY018	Polycythemia	56	2.288

499		ART016	Aortic Aneurysm	68	2.283

500		HMP005	Hemiplegia	54	2.280

501		SDD001	Sudden Infant Death Syndrome	60	2.275

502	P	MLG056	Malignant Hyperthermia	66	2.275

503	P	ATR010	Atrial Heart Septal Defect	58	2.275

504		PRS030	Persistent Fetal Circulation Syndrome	49	2.275

505		BRN009	Burning Mouth Syndrome	51	2.268

506	P	OVR049	Ovarian Disease	52	2.263

507	P	ART022	Arthritis	71	2.260

508	P	NTR004	Neutropenia	63	2.260

509		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	2.242

510		PLY150	Polykaryocytosis Inducer	29	2.234

511	P	GRV001	Graves' Disease	55	2.234

512	P	MYC008	Myocarditis	59	2.228

513		ADR041	Adrenal Cortical Adenoma	49	2.225

514		FCL014	Focal Epilepsy	53	2.217

515	P	GST053	Gastric Cancer	83	2.214

516	P	CNJ013	Conjunctivitis	66	2.212

517	P	GRW001	Growth Hormone Secreting Pituitary Adenoma	47	2.210

518	P	ANG001	Angelman Syndrome	65	2.208

519	P	GCH001	Gaucher's Disease	70	2.208

520		LYM017	Lyme Disease	62	2.203

521		PLM033	Pulmonary Embolism	58	2.203

522	c	ACT249	Acute Asthma	40	2.200

523	P	BCL017	B-Cell Lymphoma	59	2.200

524		TTR005	Tetrahydrobiopterin Deficiency	48	2.200

525	c	SVR005	Severe Pre-Eclampsia	50	2.199

526		SPC005	Speech Disorder	45	2.180

527		DSS009	Disseminated Intravascular Coagulation	57	2.178

528	P	EYD002	Eye Disease	57	2.175

529		PCK003	Pick Disease of Brain	69	2.175

530	c	RST012	Restless Legs Syndrome 1	33	2.174

531	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	2.172

532	P	TTR001	Tetralogy of Fallot	69	2.172

533		PRD002	Periodic Limb Movement Disorder	34	2.172

534	P	VSC011	Vasculitis	61	2.172

535	P	PNC035	Pancreatic Cancer	86	2.171

536	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	2.171

537		PRX097	Paroxysmal Dystonia	32	2.171

538	c	THY107	Thymoma, Familial	42	2.163

539	P	THY023	Thymoma	64	2.163

540	P	LPS004	Lupus Erythematosus	61	2.157

541		PRP016	Paraplegia	52	2.152

542		PPL001	Papillary Adenoma	44	2.150

543	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	2.148

544	c	SCH085	Schizophrenia 2	27	2.143

545	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	2.143

546		ETH004	Euthyroid Sick Syndrome	38	2.142

547	P	OPT006	Optic Nerve Disease	58	2.139

548		ESP021	Esophageal Cancer	83	2.138

549		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	2.131

550	P	MTC069	Mitochondrial Disorders	57	2.120

551	c	HRD173	Hereditary Late-Onset Parkinson Disease	49	2.108

552	P	TRN020	Turner Syndrome	67	2.108

553	P	HYP730	Hypogonadotropic Hypogonadism	53	2.108

554		PRT013	Portal Hypertension	59	2.108

555		RTR011	Retroperitoneal Fibrosis	47	2.108

556	c	BCT007	Bacterial Meningitis	55	2.101

557	P	MNN013	Meningitis	65	2.101

558		CVD001	Covid-19	57	2.096

559		MTC005	Mitochondrial Metabolism Disease	45	2.095

560		BRN045	Brunner Syndrome	52	2.081

561		CHR682	Chronic Bilirubin Encephalopathy	37	2.071

562		PRP027	Peripheral Vascular Disease	71	2.050

563		KRN002	Kearns-Sayre Syndrome	63	2.050

564	P	HML002	Hemolytic Anemia	62	2.050

565		ATY001	Atypical Depressive Disorder	45	2.049

566	P	ACT010	Acth-Secreting Pituitary Adenoma	61	2.049

567		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	2.041

568	c	PRK089	Parkinson Disease 2, Autosomal Recessive Juvenile	58	2.039

569	P	GST044	Gastritis	55	2.036

570	P	DYS005	Dyslexia	41	2.027

571		LTN004	Late-Onset Retinal Degeneration	60	2.021

572		HYP722	Hyperphenylalaninemia, Mild, Non-Bh4-Deficient	23	2.019

573	c	ORT012	Orthostatic Hypotension 2	20	2.019

574	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	2.018

575		VRC005	Varicose Veins	60	2.015

576	P	ATX030	Ataxia-Telangiectasia	80	2.012

577		THY111	Thyroid Carcinoma, Familial Medullary	67	2.012

578		THY125	Thyroid Gland Medullary Carcinoma	48	2.012

579		TLN003	Telangiectasis	51	2.012

580		CRB036	Cerebral Meningioma	35	2.009

581		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	58	2.006

582		YLL002	Yellow Fever	61	2.006

583		PCD001	Pica Disease	38	2.006

584		HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	60	1.999

585	c	SCH052	Schizophrenia 14	19	1.986

586	P	SHR121	Short Sleep, Familial Natural, 1	18	1.986

587	P	PRN023	Prion Disease	60	1.986

588		DPR002	Depersonalization Disorder	41	1.986

589	P	CRD246	Cardiovascular System Disease	56	1.984

590		HYP264	Hypertonia	36	1.983

591		ATH004	Athetosis	25	1.983

592	c	NRB010	Neuroblastoma 1	59	1.982

593	P	OVR042	Ovarian Cancer	88	1.979

594		TRT001	Teratocarcinoma	42	1.970

595		PNK001	Pink1 Type of Young-Onset Parkinson Disease	8	1.970

596		CHR178	Chromosomal Triplication	34	1.970

597		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.966

598	P	ESP024	Esophagitis	60	1.963

599		STN005	St Anthony's Fire	18	1.960

600	c	HYP836	Hypercholesterolemia, Familial, 1	73	1.953

601	P	MYP004	Myopathy	67	1.953

602	P	PRD006	Prader-Willi Syndrome	61	1.953

603	P	ART018	Aortic Valve Insufficiency	52	1.953

604		GNG008	Ganglioneuroblastoma	47	1.953

605		GTR002	Goiter	53	1.953

606	c	PRG018	Paragangliomas 1	59	1.952

607		BLP048	Blepharospasm, Benign Essential	37	1.933

608		HYP085	Hypothalamic Disease	38	1.933

609		DYS192	Dystonia, Dopa-Responsive	55	1.922

610	c	ATM075	Autoimmune Encephalitis	40	1.922

611	c	THR092	Thrombophilia Due to Thrombin Defect	74	1.919

612	P	MST009	Mastocytosis	64	1.919

613	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	1.918

614		PRC013	Pericarditis	53	1.918

615		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	1.915

616	P	SCK005	Sickle Cell Disease	56	1.904

617		ANR040	Aneurysm	61	1.895

618	c	SCH080	Schizophrenia 3	28	1.895

619	c	DMN005	Diamond-Blackfan Anemia 2	28	1.895

620		RTN003	Retinal Ischemia	49	1.895

621		PLG002	Plague	58	1.895

622	c	VPS003	Vps35-Related Parkinson Disease	12	1.895

623		KLP001	Kleptomania	36	1.890

624	P	BRB001	Beriberi	44	1.884

625		CHL068	Cholestasis	61	1.884

626		CRN036	Craniopharyngioma	64	1.873

627	P	THY032	Thyroiditis	57	1.861

628		PLY138	Polymerase Proofreading-Related Adenomatous Polyposis	29	1.860

629		MCR379	Microcystic Stromal Tumor	29	1.856

630		CLT003	Colitis	63	1.848

631		PRS021	Prostatic Adenoma	43	1.848

632		PRS045	Prostatic Hypertrophy	53	1.848

633		MYC005	Myocardial Stunning	46	1.848

634		CLR030	Clear Cell Renal Cell Carcinoma	54	1.847

635		AGR002	Agoraphobia	45	1.843

636	P	EPL198	Epilepsy, Myoclonic Juvenile	61	1.831

637		HYP017	Hypophosphatemia	49	1.827

638		SPS003	Spastic Diplegia	53	1.822

639		TRC010	Trichotillomania	50	1.820

640	c	INH030	Inherited Retinal Disorder	28	1.816

641		FND002	Fundus Dystrophy	55	1.816

642		ABT001	Abetalipoproteinemia	68	1.811

643	P	INT068	Intestinal Disease	53	1.809

644		DST006	Diastolic Heart Failure	45	1.799

645		ISL135	Isolated Dystonia	22	1.794

646	c	GRV008	Graves Disease 1	54	1.794

647		LCH001	Leech Infestation	38	1.794

648		ABD010	Abdominal Wall Defect	39	1.793

649		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	26	1.792

650		SMT006	Somatoform Disorder	50	1.786

651	P	EPL140	Epilepsy, Idiopathic Generalized	62	1.782

652		ADR008	Adrenal Adenoma	55	1.781

653	P	SNS001	Sensorineural Hearing Loss	59	1.774

654		CHL065	Cholangiocarcinoma	58	1.773

655		AKN002	Akinetic Mutism	36	1.773

656		INT079	Intrahepatic Cholangiocarcinoma	51	1.773

657	P	PRC019	Precocious Puberty	47	1.760

658		LNG099	Lung Disease	62	1.759

659	c	SPN309	Spinocerebellar Ataxia 6	58	1.754

660		MTN003	Motion Sickness	51	1.741

661	P	ART023	Arthropathy	61	1.740

662		PTT003	Pituitary-Dependent Cushing's Disease	39	1.740

663	P	DYS193	Dystonia 11, Myoclonic	55	1.740

664		QDR001	Quadriplegia	50	1.740

665		PRS129	Prostatic Hyperplasia, Benign	49	1.734

666		NRG002	Neurogenic Bladder	55	1.734

667		CCN009	Cocaine Intoxication	30	1.730

668		ALC001	Alcohol-Related Birth Defect	36	1.730

669		VCC001	Vaccinia	47	1.730

670		OCL066	Oculogyric Crisis	35	1.725

671		DSS032	Disease by Infectious Agent	55	1.725

672		GT001	Gout	64	1.725

673	P	HYP061	Hypertrophic Cardiomyopathy	69	1.725

674	P	ART021	Arteriosclerosis	54	1.725

675		ADN027	Adenomyosis	57	1.717

676	P	INF038	Influenza	68	1.717

677	P	MLN007	Male Infertility	56	1.704

678		HMN014	Human Immunodeficiency Virus Infectious Disease	54	1.703

679		CYS001	Cystic Fibrosis	78	1.694

680		NNL005	Non-Alcoholic Fatty Liver Disease	63	1.694

681	P	SCL018	Scoliosis	57	1.694

682		CHR074	Choriocarcinoma	46	1.694

683	P	SHR001	Short Bowel Syndrome	53	1.694

684		DYT003	Dyt-Gnal	16	1.694

685		BNS003	Binswanger's Disease	41	1.694

686	P	ANR048	Aniridia 1	64	1.692

687	P	DRM053	Dermatitis, Atopic	65	1.689

688	c	PRG011	Progressive Myoclonus Epilepsy	41	1.684

689	P	HMN010	Hemangioma	62	1.684

690		DMP001	Dumping Syndrome	43	1.684

691		GST050	Gastrointestinal System Disease	55	1.684

692	P	MYC026	Myoclonus Epilepsy	35	1.684

693		BRN024	Bronchitis	67	1.652

694		BRK012	Broken Heart Syndrome	42	1.652

695		GST045	Gastroenteritis	58	1.638

696		MDD018	Middle East Respiratory Syndrome	44	1.637

697		DSS002	Dissociative Amnesia	28	1.637

698	P	URN019	Urinary Tract Infection	49	1.628

699	P	AST005	Asthma	76	1.627

700	P	SML001	Small Cell Carcinoma	52	1.624

701	c	LKM061	Leukemia, Acute Myeloid	83	1.624

702	c	NRF024	Neurofibromatosis, Type I	72	1.624

703		PLM022	Pulmonary Valve Insufficiency	45	1.624

704	P	LNG028	Long Qt Syndrome	64	1.624

705		ATH013	Atherosclerosis Susceptibility	63	1.615

706	P	OCL001	Ocular Albinism	48	1.615

707		LMB062	Limb Ischemia	55	1.615

708		RHM035	Rheumatic Fever-Related Antigen	37	1.615

709		OVR063	Overnutrition	42	1.615

710		RHM001	Rheumatic Fever	59	1.615

711		CRT072	Creutzfeldt-Jakob Disease	68	1.608

712	c	DYS151	Dystonia 25	40	1.608

713	P	ALP008	Alopecia	54	1.608

714		PLC005	Placental Insufficiency	56	1.608

715	P	CMP008	Compartment Syndrome	50	1.608

716		FRG008	Fragile X-Associated Tremor/ataxia Syndrome	44	1.595

717		VRL011	Viral Infectious Disease	61	1.595

718		END057	Endometrial Cancer	72	1.587

719	c	SCH082	Schizophrenia 5	23	1.587

720		ULC004	Ulcerative Colitis	74	1.587

721		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	1.587

722	P	HYP750	Hypertriglyceridemia, Familial	62	1.575

723		RNL077	Renal Fibrosis	46	1.575

724		MCP006	Mucoepidermoid Carcinoma	48	1.575

725	P	TBR001	Tuberous Sclerosis	69	1.575

726		PST048	Postural Orthostatic Tachycardia Syndrome	46	1.575

727		KFR001	Kufor-Rakeb Syndrome	59	1.563

728		HYD002	Hydronephrosis	58	1.563

729		RYN005	Raynaud Phenomenon	45	1.563

730	c	RNG015	Ring Chromosome 2	22	1.563

731		SPC010	Speech and Communication Disorders	48	1.558

732	P	STR020	Strabismus	56	1.558

733		MCH006	Mechanical Strabismus	40	1.558

734		RSP007	Respiratory Distress Syndrome, Infant	40	1.558

735		VLC001	Velocardiofacial Syndrome	57	1.551

736		RHB024	Rhabdomyosarcoma 2	67	1.541

737	c	WLF013	Wolfram Syndrome 1	60	1.535

738		PRX035	Paroxysmal Dyskinesia	30	1.535

739		CRT084	Creatinine Clearance Quantitative Trait Locus	25	1.535

740	c	OPT053	Optic Atrophy 1	62	1.535

741	P	ANP001	Anaplastic Large Cell Lymphoma	61	1.535

742		PRP080	Peripheral Artery Disease	54	1.535

743	P	DXT004	Dextro-Looped Transposition of the Great Arteries	58	1.535

744		PRP015	Paraphilia Disorder	31	1.535

745	P	MSC003	Muscular Atrophy	52	1.535

746	P	CHL066	Cholangitis	52	1.535

747	P	PLM036	Pulmonary Fibrosis	66	1.535

748	P	ACN011	Acne	57	1.535

749		CRD001	Cardiac Tamponade	43	1.535

750		NPH010	Nephrosclerosis	50	1.535

751	P	FML018	Familial Mediterranean Fever	73	1.535

752	P	MDL005	Medulloblastoma	75	1.535

753		BRC012	Brucellosis	66	1.535

754		FRG010	Fragile X Tremor/ataxia Syndrome	44	1.534

755		WSR001	Was-Related Disorders	19	1.532

756		PHR003	Pharyngitis	58	1.531

757		PRT019	Protein-Losing Enteropathy	45	1.528

758	c	MCL013	Mucolipidosis Iv	65	1.528

759		KRT002	Keratomalacia	55	1.524

760		CLS049	Classic Phenylketonuria	41	1.516

761		THR024	Thrombosis	56	1.516

762	c	PRG020	Paragangliomas 3	39	1.516

763		URT049	Urate Oxidase, Pseudogene	24	1.516

764		TLG001	Telogen Effluvium	31	1.516

765		AML001	Amelanotic Melanoma	37	1.516

766		PTT008	Pituitary Carcinoma	46	1.508

767		CRD132	Cardiac Conduction Defect	60	1.507

768		INS001	Insulinoma	59	1.507

769	P	MYS003	Myasthenia Gravis	68	1.493

770		MSC007	Muscle Hypertrophy	64	1.493

771		EWN003	Ewing Sarcoma	70	1.493

772		TRG002	Trigeminal Neuralgia	61	1.493

773	P	THR014	Thrombocytopenia	66	1.493

774		NSP002	Nasopharyngitis	45	1.493

775	P	NSP012	Nasopharyngeal Carcinoma	61	1.485

776	P	MYC084	Mycobacterium Tuberculosis 1	68	1.485

777		CYC001	Cycloplegia	34	1.485

778	P	PRD037	Periodontal Ehlers-Danlos Syndrome	49	1.485

779	c	ACR088	Aicardi-Goutieres Syndrome 3	39	1.478

780	P	ASP001	Asperger Syndrome	48	1.478

781	P	HPT021	Hepatitis	69	1.478

782		BDY001	Body Dysmorphic Disorder	41	1.469

783		AGR019	Age-Related Hearing Loss	41	1.469

784	c	PRK100	Parkinson Disease 23, Autosomal Recessive Early-Onset	25	1.466

785		ISL001	Islet Cell Tumor	56	1.466

786	P	INT070	Intestinal Obstruction	57	1.460

787	c	SPN294	Spinocerebellar Ataxia 1	53	1.455

788	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	67	1.450

789		DSR074	Disorder of Purine Metabolism	23	1.450

790		CHR005	Chorioamnionitis	50	1.450

791		MLR004	Malaria	80	1.450

792		WST001	West Syndrome	59	1.450

793		BCT021	Bacterial Sepsis	43	1.450

794		HLC007	Helicobacter Pylori Infection	67	1.450

795	c	PRG043	Progressive Familial Heart Block, Type Ib	54	1.449

796		MYF002	Myofascial Pain Syndrome	46	1.448

797	P	MCR129	Microvascular Complications of Diabetes 1	68	1.447

798		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	46	1.446

799		ORM002	Oromandibular Dystonia	40	1.444

800		PRM020	Premenstrual Tension	39	1.444

801		HRT015	Heritable Pulmonary Arterial Hypertension	46	1.439

802		KLN009	Kleine-Levin Hibernation Syndrome	41	1.418

803		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	57	1.416

804		CHD004	Chudley-Mccullough Syndrome	48	1.413

805		CRN030	Coronary Stenosis	50	1.413

806		GST033	Gestational Diabetes	61	1.413

807		INT030	Intracranial Aneurysm	55	1.413

808		ILS001	Ileus	50	1.410

809	c	SCL052	Scleroderma, Familial Progressive	61	1.410

810		BNR002	Bone Resorption Disease	47	1.410

811		ASP008	Aspiration Pneumonitis	42	1.410

812		BRK010	Burkitt Lymphoma	66	1.404

813	P	APL001	Aplastic Anemia	73	1.404

814		ALX002	Alexithymia	37	1.404

815	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	1.404

816		TST044	Testicular Torsion	45	1.404

817	P	FML340	Familial Episodic Pain Syndrome	50	1.404

818	P	HYP077	Hypertrichosis	46	1.404

819		FTT001	Fatty Liver Disease	62	1.404

820		DSR031	Disorder of Copper Metabolism	25	1.404

821	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	1.404

822	P	HYP069	Hyperparathyroidism	62	1.404

823		KLV001	Kluver-Bucy Syndrome	34	1.404

824		LYM133	Lymphoma, Hodgkin, Classic	74	1.403

825		HYP781	Hypoascorbemia	52	1.403

826		ALV005	Alveolar Soft Part Sarcoma	61	1.403

827	P	MYL006	Myeloid Leukemia	61	1.403

828	P	MYT002	Myotonic Dystrophy	51	1.403

829		CLL010	Cellular Ependymoma	57	1.396

830	P	BNG030	Benign Ependymoma	51	1.396

831		NRM022	Neurometabolic Disease	24	1.389

832		OCC006	Occipital Horn Syndrome	54	1.389

833	P	LYM118	Lymphoma	67	1.380

834		LPT006	Leptin Receptor Deficiency	50	1.380

835		SKN019	Skin Melanoma	71	1.380

836		AMD002	Amed Syndrome, Digenic	37	1.380

837	P	CLR023	Colorectal Cancer	100	1.376

838		HYP025	Hyperphosphatemia	48	1.376

839		LKN025	Leukoencephalopathy, Hereditary Diffuse, with Spheroids	66	1.376

840	P	LKM002	Leukemia	67	1.376

841		THY030	Thyroid Gland Disease	50	1.375

842	c	BLD140	Blood Group, I System	46	1.371

843		MLD017	Mal De Debarquement Syndrome	29	1.371

844		SQM013	Squamous Cell Carcinoma, Head and Neck	73	1.363

845	c	DRR009	Diarrhea 6	45	1.363

846	P	ATR011	Atrial Fibrillation	66	1.357

847		ACH005	Achalasia	55	1.357

848		NRR002	Norrie Disease	61	1.357

849		RTN017	Retinal Detachment	60	1.357

850	P	FML023	Familial Hemiplegic Migraine	53	1.357

851	c	PRK021	Parkinson Disease 7, Autosomal Recessive Early-Onset	39	1.357

852	c	MYP018	Myopia 6	27	1.357

853	c	PRK085	Parkinson Disease 1, Autosomal Dominant	49	1.357

854		GST019	Gastrointestinal Stromal Tumor	78	1.357

855		SCR011	Scrapie	39	1.357

856		OBS004	Obstructive Hydrocephalus	45	1.357

857	c	SCH087	Schizophrenia 18	28	1.357

858		WST005	West Nile Virus	57	1.357

859		LMY002	Leiomyoma	51	1.357

860		HRP009	Herpes Simplex Encephalitis	58	1.357

861		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	1.342

862		SCH014	Schistosomiasis	56	1.342

863		WLM014	Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome	52	1.326

864	c	HPT073	Hepatitis C Virus	71	1.320

865	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	51	1.320

866	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	53	1.320

867		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	1.316

868	c	ACT068	Acute Cystitis	61	1.315

869	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	63	1.307

870		CHR100	Chronic Ulcer of Skin	57	1.307

871		FCL049	Focal Hand Dystonia	31	1.307

872	c	TBR025	Tuberous Sclerosis 1	84	1.307

873		OCL052	Ocular Dominance	40	1.307

874	P	CRN249	Cornea Plana	30	1.307

875		BRN018	Borna Disease	36	1.307

876	c	BCT013	Bacterial Pneumonia	48	1.307

877		FCT008	Factitious Disorder	34	1.307

878	P	GRF003	Graft-Versus-Host Disease	71	1.307

879		SNS003	Sensory Peripheral Neuropathy	52	1.307

880		KLB003	Klebsiella Pneumonia	50	1.307

881		CHL078	Childhood-Onset Schizophrenia	29	1.307

882		HMD003	Hemidystonia	28	1.306

883	P	MCR010	Microcephaly	60	1.306

884		PRS063	Paresthesia	39	1.306

885		GGN002	Gigantism	33	1.306

886	P	BLD134	Bladder Cancer	79	1.305

887	c	CTR110	Cataract 26, Multiple Types	26	1.305

888		LYM143	Lymphoma, Non-Hodgkin, Familial	75	1.305

889		NRN002	Neuronitis	31	1.305

890	c	GLL024	Gallbladder Disease 1	52	1.301

891		FML035	Familial Hyperlipidemia	55	1.298

892		NRL016	Neural Tube Defects	81	1.296

893		MLT105	Multiple System Atrophy, Cerebellar Type	25	1.296

894		SYS003	Systolic Heart Failure	49	1.296

895		PTT001	Pituitary Hypoplasia	34	1.280

896	c	MJR023	Major Affective Disorder 7	33	1.255

897	c	MJR004	Major Affective Disorder 4	28	1.255

898	P	STR035	Streptococcal Group a Invasive Disease	24	1.254

899		RNL113	Renal Failure, Progressive, with Hypertension	31	1.254

900		NRN005	Neuronal Ceroid-Lipofuscinoses	61	1.254

901		CST001	Costello Syndrome	68	1.254

902		AMN015	Amenorrhea-Galactorrhea Syndrome	21	1.254

903		ORL015	Oral Squamous Cell Carcinoma	43	1.254

904	P	WLF004	Wolfram Syndrome	61	1.254

905		HMP027	Hemiparkinsonism-Hemiatrophy Syndrome	21	1.254

906	P	RHB003	Rhabdomyosarcoma	66	1.254

907		ECH002	Echolalia	33	1.254

908		VRC001	Varicocele	48	1.254

909		BLR008	Bilirubin Metabolic Disorder	57	1.254

910		RTN020	Retinal Vascular Disease	46	1.254

911	P	SCK002	Sick Sinus Syndrome	55	1.254

912	P	BNC003	Bone Cancer	58	1.254

913		HYP835	Hypothalamic Obesity	38	1.254

914		SGC002	Sgce Myoclonus-Dystonia	24	1.254

915		MYL069	Myeloma, Multiple	77	1.250

916		APN008	Apnea, Obstructive Sleep	67	1.250

917		TXC002	Toxic Encephalopathy	52	1.240

918		PLM001	Pulmonary Tuberculosis	69	1.240

919	P	CTR002	Cataract	60	1.240

920		CHL004	Cholelithiasis	49	1.240

921		ADJ001	Adjustment Disorder	47	1.240

922		PPT001	Peptic Esophagitis	52	1.240

923	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	1.234

924		ACT011	Acute Contagious Conjunctivitis	42	1.234

925	c	DPH024	Diaphragmatic Hernia, Congenital	64	1.231

926		SKN016	Skin Disease	63	1.231

927		ASP004	Asphyxia Neonatorum	50	1.231

928		HYP043	Hyperandrogenism	48	1.231

929	P	URT039	Urticaria	58	1.231

930	P	UVT001	Uveitis	57	1.230

931		BCT002	Bacterial Vaginosis	53	1.230

932		PPL049	Papillon-Lefevre Syndrome	66	1.229

933	c	HPT001	Hepatitis C	62	1.211

934		BNG077	Benign Idiopathic Neonatal Seizures	23	1.198

935		GLM044	Glomerular Disease	35	1.198

936		DYS064	Dystonia 3, Torsion, X-Linked	45	1.198

937	c	MJR014	Major Depressive Disorder 2	13	1.198

938		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	37	1.198

939	P	ATR001	Atrioventricular Septal Defect	55	1.198

940	c	ART101	Aortic Valve Disease 2	66	1.198

941	c	SCH075	Schizophrenia 19	27	1.198

942	c	GLC092	Glaucoma, Primary Open Angle	62	1.198

943		BSL009	Basal Ganglia Calcification	45	1.198

944	c	PRM316	Primary Congenital Hypothyroidism	32	1.198

945	c	ACT076	Acute Myocarditis	47	1.198

946	P	FBR017	Fibrosarcoma	56	1.198

947		TRY001	Trypanosomiasis	50	1.198

948		CHG001	Chagas Disease	66	1.198

949		CPG001	Capgras Syndrome	26	1.198

950		ALC005	Alcoholic Pancreatitis	38	1.198

951		STM006	Stomach Disease	47	1.198

952		PRT029	Parathyroid Adenoma	51	1.198

953		CNG021	Congenital Toxoplasmosis	55	1.198