Search results for Dopamine

1642 hits were found for Dopamine

#	Family	MCID	Name	MIFTS	Score
1		DPM001	Dopamine Beta-Hydroxylase Deficiency	47	7.997

2	P	PRK101	Parkinsonism-Dystonia, Infantile, 1	39	5.617

3	c	ORT011	Orthostatic Hypotension 1	43	4.067

4		BRN112	Brain Dopamine-Serotonin Vesicular Transport Disease	18	3.259

5		SLC036	Slc6a3-Related Dopamine Transporter Deficiency Syndrome	8	2.373

6	c	PRK102	Parkinsonism-Dystonia, Infantile, 2	27	2.328

7		DPM008	Dopamine Beta-Hydroxylase, Plasma, Thermolability of	5	2.308

8	P	PRK057	Parkinson Disease, Late-Onset	76	0.472

9	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.467

10	P	SCH015	Schizophrenia	75	0.440

11		ALC007	Alcohol Dependence	66	0.345

12		PRT037	Pertussis	65	0.305

13	P	TRM003	Tremor	53	0.285

14	P	NRB001	Neuroblastoma	71	0.274

15		TRD006	Tardive Dyskinesia	55	0.274

16		HYP020	Hyperprolactinemia	64	0.264

17	P	PHC003	Pheochromocytoma	71	0.264

18	P	BPL003	Bipolar Disorder	56	0.263

19		ADR040	Adrenal Gland Pheochromocytoma	46	0.263

20	c	MJR024	Major Affective Disorder 9	41	0.251

21	c	MJR022	Major Affective Disorder 8	38	0.251

22	P	DYS154	Dystonia	65	0.247

23		ADN018	Adenoma	58	0.245

24	P	MVM001	Movement Disease	61	0.240

25	P	HNT016	Huntington Disease	71	0.239

26		CCN002	Cocaine Abuse	48	0.238

27		DPR016	Depression	63	0.231

28	P	SBS003	Substance Abuse	54	0.231

29	c	HYP595	Hypertension, Essential	84	0.223

30		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	0.220

31		PTT037	Pituitary Tumors	44	0.212

32	P	RST001	Restless Legs Syndrome	54	0.209

33		CNG034	Congestive Heart Failure	70	0.206

34		PSY004	Psychotic Disorder	67	0.203

35		TBC004	Tobacco Addiction	64	0.193

36		MNT002	Mental Depression	57	0.193

37	P	MJR001	Major Depressive Disorder	68	0.191

38	P	ALC033	Alcohol Use Disorder	58	0.183

39	c	ACT071	Acute Kidney Failure	59	0.181

40		CCN001	Cocaine Dependence	48	0.181

41		MDD011	Mood Disorder	62	0.181

42		TXC005	Toxic Shock Syndrome	61	0.180

43		HYP266	Hypoxia	56	0.179

44	P	KDN018	Kidney Disease	70	0.178

45		PTH002	Pathological Gambling	48	0.177

46	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.174

47		GLL008	Gilles De La Tourette Syndrome	66	0.165

48		OBS002	Obsessive-Compulsive Disorder	68	0.163

49		DRG003	Drug Dependence	47	0.163

50		MLT157	Multiple System Atrophy 1	70	0.159

51		ALL026	Allergic Hypersensitivity Disease	64	0.159

52		ANX010	Anxiety	72	0.158

53	P	PTT006	Pituitary Adenoma	54	0.157

54		48X005	48,xyyy	39	0.154

55	P	HRT032	Heart Disease	75	0.152

56		PRT058	Pure Autonomic Failure	59	0.152

57	c	MGR028	Migraine with or Without Aura 1	69	0.151

58		WTH001	Withdrawal Disorder	48	0.150

59		TRM010	Traumatic Brain Injury	53	0.148

60	P	ALZ034	Alzheimer Disease	88	0.142

61		ETN001	Eating Disorder	59	0.142

62		HLX001	Helix Syndrome	47	0.142

63		BRN071	Brain Injury	49	0.140

64		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	46	0.140

65		CHR073	Choreatic Disease	52	0.139

66		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.139

67		ACR007	Acromegaly	71	0.138

68		PNG002	Pain Agnosia	51	0.138

69	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.136

70	P	ATS364	Autism	65	0.136

71		CHL014	Cholera	55	0.136

72		CRD137	Cardiogenic Shock	48	0.136

73	P	SZR006	Seizure Disorder	58	0.135

74	P	DMN002	Dementia	67	0.134

75		HYP056	Hypoglycemia	66	0.134

76	c	ESS001	Essential Tremor	56	0.134

77		VSL002	Visual Epilepsy	58	0.133

78		PPL052	Papillomatosis, Confluent and Reticulated	34	0.131

79	P	PRS038	Personality Disorder	65	0.130

80	P	ENC018	Encephalopathy	61	0.130

81		OPD006	Opioid Addiction	48	0.130

82	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.129

83	P	MYP006	Myopia	55	0.128

84	P	TCD001	Tic Disorder	54	0.125

85	c	ATS007	Autism Spectrum Disorder	67	0.122

86		ISC004	Ischemia	60	0.121

87		PST028	Post-Traumatic Stress Disorder	58	0.120

88		OPT003	Opiate Dependence	50	0.120

89		ANR007	Anorexia Nervosa	63	0.118

90		ATX038	Ataxia and Polyneuropathy, Adult-Onset	44	0.117

91	P	MJR007	Major Affective Disorder 1	43	0.117

92	P	HYP086	Hypothyroidism	68	0.114

93		AGN016	Aging	56	0.114

94	P	NRC002	Narcolepsy	51	0.114

95		AMN003	Amnestic Disorder	54	0.113

96		HRT012	Heart Valve Disease	53	0.113

97		SCH012	Schizoaffective Disorder	50	0.113

98		ACT084	Acute Stress Disorder	48	0.113

99	P	SLP005	Sleep Disorder	59	0.110

100	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.110

101	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.110

102	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.110

103	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.110

104	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.110

105	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.110

106	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.110

107	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.110

108	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.110

109	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.110

110		SBC016	Subacute Delirium	44	0.108

111	P	GLM045	Glioma	63	0.105

112		OVR029	Ovarian Hyperstimulation Syndrome	63	0.105

113		IRN002	Iron Metabolism Disease	57	0.105

114		ANX004	Anoxia	42	0.104

115		HPT019	Hepatic Encephalopathy	60	0.102

116		NRL004	Neuroleptic Malignant Syndrome	55	0.102

117		HPT004	Hepatic Coma	43	0.102

118		END040	Endogenous Depression	54	0.101

119	P	CHR345	Chronic Pain	50	0.099

120		IMP006	Impulse Control Disorder	45	0.099

121	P	PTS002	Ptosis	52	0.097

122		47X002	47,xyy	49	0.097

123	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.097

124		TQP001	Taqi Polymorphism	32	0.097

125		HYP066	Hyperglycemia	61	0.096

126		RRS014	Rare Surgical Neurologic Disease	32	0.096

127		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.094

128		AMN001	Amenorrhea	54	0.094

129	P	RSP003	Respiratory Failure	74	0.092

130		HYP060	Hyperinsulinism	54	0.092

131	P	DDN001	Duodenal Ulcer	50	0.092

132		SBS004	Substance Dependence	48	0.092

133		PLY068	Polysubstance Abuse	43	0.092

134		PHN003	Phenylketonuria	75	0.090

135		GLL048	Glial Tumor	45	0.090

136	P	CRD119	Cardiac Arrest	67	0.088

137		LSC001	Lesch-Nyhan Syndrome	62	0.088

138		FBR047	Fibromyalgia	59	0.088

139		OCL069	Ocular Motor Apraxia	51	0.088

140	P	MYC033	Myoclonus	46	0.088

141		LVR012	Liver Cirrhosis	63	0.087

142		CRT033	Corticobasal Degeneration	55	0.087

143		CND002	Conduct Disorder	51	0.087

144		MRP001	Morphine Dependence	41	0.087

145		CRB039	Cerebrovascular Disease	69	0.085

146	c	ACT075	Acute Myocardial Infarction	56	0.085

147		IMP005	Impotence	52	0.085

148	c	DYS191	Dystonia 1, Torsion, Autosomal Dominant	50	0.085

149		ATN005	Autonomic Dysfunction	47	0.085

150		RMS001	Rem Sleep Behavior Disorder	44	0.085

151	P	EPL164	Epilepsy	71	0.083

152		HRN003	Heroin Dependence	44	0.083

153		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.081

154		DMN031	Dementia, Lewy Body	65	0.081

155		TTN003	Tetanus	64	0.081

156		CNS004	Constipation	57	0.081

157	P	PLY011	Polycystic Ovary Syndrome	56	0.081

158		SXL003	Sexual Disorder	48	0.081

159	P	MGR001	Migraine Without Aura	48	0.081

160		CRB004	Cerebral Artery Occlusion	44	0.081

161	P	FML187	Familial Hypertension	37	0.081

162		SPN186	Spinal Cord Injury	60	0.079

163		BLM002	Bulimia Nervosa	57	0.079

164	P	HDC001	Headache	57	0.079

165	P	NRP001	Neuropathy	56	0.079

166		HYP005	Hypokalemia	55	0.079

167	P	MGR003	Migraine with Aura	50	0.079

168		HYP080	Hypogonadism	50	0.079

169		HYP064	Hypogonadotropism	40	0.079

170		STR067	Stroke, Ischemic	80	0.077

171		GLB015	Glioblastoma Multiforme	75	0.077

172	P	PLM037	Pulmonary Hypertension	68	0.077

173	c	CHR684	Chronic Kidney Disease	66	0.077

174		SCH003	Schizophreniform Disorder	56	0.077

175	P	PRG013	Paraganglioma	52	0.077

176		PRN009	Paranoid Schizophrenia	49	0.077

177		OPD001	Opioid Abuse	45	0.077

178		GLC096	Galactorrhea	42	0.077

179		HRW001	Hair Whorl	36	0.077

180		MNG007	Manganese Poisoning	29	0.077

181	P	MYC007	Myocardial Infarction	70	0.074

182		DWN001	Down Syndrome	70	0.074

183	P	PTN014	Patent Ductus Arteriosus 1	60	0.074

184	P	HYP076	Hyperthyroidism	55	0.074

185		PLM010	Pulmonary Edema	55	0.074

186		GLC003	Glucose Intolerance	54	0.074

187		AVD001	Avoidant Personality Disorder	54	0.074

188	c	SCH079	Schizophrenia 1	48	0.074

189		CYT002	Cytokine Deficiency	44	0.074

190		PST092	Posttransplant Acute Limbic Encephalitis	29	0.074

191	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	89	0.072

192	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.072

193		WLS001	Wilson Disease	70	0.072

194	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	0.072

195		END030	End Stage Renal Failure	58	0.072

196	P	LTR001	Lateral Sclerosis	53	0.072

197		DLS001	Delusional Disorder	48	0.072

198		SCH011	Schizotypal Personality Disorder	39	0.072

199	P	SLP006	Sleep Apnea	69	0.070

200		CRB037	Cerebral Palsy	68	0.070

201		ANG054	Angina Pectoris	66	0.070

202		DSS008	Disease of Mental Health	57	0.070

203		NRT001	Neurotic Disorder	52	0.070

204		LNG015	Lingual-Facial-Buccal Dyskinesia	47	0.070

205		SYN036	Syncope	45	0.070

206		CRT015	Carotid Artery Occlusion	44	0.070

207		HND015	Hand Skill, Relative	33	0.070

208		INS024	Insulin-Like Growth Factor I	79	0.068

209		SVR004	Severe Combined Immunodeficiency	73	0.068

210	P	LVR013	Liver Disease	68	0.068

211	P	NRV007	Nervous System Disease	66	0.068

212		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.068

213	P	VSC007	Vascular Disease	63	0.068

214		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.068

215	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.068

216		VSC002	Vascular Dementia	57	0.068

217	c	SVR001	Severe Acute Respiratory Syndrome	55	0.068

218		GST037	Gastroparesis	53	0.068

219	P	RTN016	Retinal Degeneration	53	0.068

220	P	PNC025	Panic Disorder	53	0.068

221	c	BPL002	Bipolar I Disorder	49	0.068

222	P	HYP265	Hypotonia	42	0.068

223		AMP007	Amphetamine Abuse	40	0.068

224		ALL014	Allergic Encephalomyelitis	39	0.068

225		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.068

226	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.065

227		HMN044	Human Immunodeficiency Virus Type 1	71	0.065

228		MLN008	Melanoma	69	0.065

229	P	FRG001	Fragile X Syndrome	68	0.065

230	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	66	0.065

231		LPD008	Lipid Metabolism Disorder	62	0.065

232		ATM095	Autoimmune Disease	61	0.065

233	P	HYP083	Hypopituitarism	53	0.065

234		GST023	Gastric Ulcer	53	0.065

235		HPT014	Hepatorenal Syndrome	50	0.065

236		SCL003	Social Phobia	48	0.065

237		ANT011	Antisocial Personality Disorder	46	0.065

238		RFR003	Refractive Error	44	0.065

239		CNN001	Cannabis Dependence	38	0.065

240		MLT116	Multiple System Atrophy, Parkinsonian Type	31	0.065

241	c	ATR087	Atrial Standstill 1	74	0.063

242	P	TRN020	Turner Syndrome	65	0.063

243		PRT036	Peritonitis	65	0.063

244	c	PRC016	Pre-Eclampsia	63	0.063

245	P	CRN300	Coronary Heart Disease 1	63	0.063

246	P	END044	Endometriosis	62	0.063

247		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.063

248	P	BLD124	Bleeding Disorder, Platelet-Type, 11	61	0.063

249	c	PNS012	Paine Syndrome	61	0.063

250	P	PNC044	Pancreatitis	61	0.063

251	P	DRR001	Diarrhea	57	0.063

252		BRN004	Brain Edema	55	0.063

253		PTT009	Pituitary Gland Disease	54	0.063

254	c	CNT035	Central Nervous System Disease	54	0.063

255		OCL006	Ocular Hypertension	53	0.063

256	P	LCT001	Lactic Acidosis	51	0.063

257	P	ECL001	Eclampsia	51	0.063

258		ENT011	Enterocolitis	50	0.063

259		MTB004	Metabolic Acidosis	50	0.063

260		ATX019	Ataxia with Vitamin E Deficiency	48	0.063

261		PPL001	Papillary Adenoma	45	0.063

262	P	CLR023	Colorectal Cancer	98	0.060

263	P	RTT002	Rett Syndrome	80	0.060

264	c	DLT002	Dilated Cardiomyopathy	79	0.060

265		IMM167	Immune Deficiency Disease	78	0.060

266		RCK004	Rickets	69	0.060

267		GNR004	Generalized Anxiety Disorder	56	0.060

268		PRN019	Perinatal Necrotizing Enterocolitis	54	0.060

269		INT075	Intracranial Hypertension	53	0.060

270		BRD004	Borderline Personality Disorder	53	0.060

271	P	AST007	Astrocytoma	50	0.060

272		BSL008	Basal Ganglia Disease	43	0.060

273	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.060

274	c	ERL056	Early-Onset Parkinson's Disease	39	0.060

275	P	STR001	Striatonigral Degeneration	38	0.060

276		NVL002	Novelty Seeking Personality Trait	16	0.060

277		LPT014	Leptin Deficiency or Dysfunction	73	0.057

278	P	HYP724	Hyperlipoproteinemia, Type Iii	72	0.057

279	P	RTN024	Retinoblastoma	72	0.057

280	P	MLT020	Multiple Sclerosis	72	0.057

281	c	EXD008	Exudative Vitreoretinopathy 1	69	0.057

282	P	DBT085	Diabetes Mellitus, Insulin-Dependent	67	0.057

283	P	MCR115	Microvascular Complications of Diabetes 5	66	0.057

284	P	DBT009	Diabetes Mellitus	64	0.057

285		KHL003	Kohlschutter-Tonz Syndrome	64	0.057

286	P	CRN018	Coronary Artery Anomaly	63	0.057

287	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.057

288		TRN015	Transient Cerebral Ischemia	62	0.057

289	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.057

290		RBS001	Rabies	58	0.057

291	P	INF032	Infertility	57	0.057

292	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	56	0.057

293		NRN004	Neuroendocrine Tumor	55	0.057

294	c	FML008	Familial Retinoblastoma	53	0.057

295	c	MCR113	Microvascular Complications of Diabetes 3	52	0.057

296		PRV004	Periventricular Leukomalacia	51	0.057

297	P	TMP001	Temporal Lobe Epilepsy	50	0.057

298		OPP004	Oppositional Defiant Disorder	49	0.057

299	P	RNL015	Renal Hypertension	48	0.057

300		ANV001	Anovulation	47	0.057

301	c	MCR120	Microvascular Complications of Diabetes 7	47	0.057

302		CNN002	Cannabis Abuse	44	0.057

303		FCL022	Focal Dystonia	42	0.057

304		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	42	0.057

305	c	MCR130	Microvascular Complications of Diabetes 6	41	0.057

306	c	MCR133	Microvascular Complications of Diabetes 4	41	0.057

307	P	DYS021	Dysautonomia	39	0.057

308		ALD013	Aldosterone-Producing Adenoma	38	0.057

309	c	RST012	Restless Legs Syndrome 1	34	0.057

310	c	DNT047	Dentinogenesis Imperfecta Type 2	33	0.057

311		CHL079	Children's Interstitial Lung Disease	27	0.057

312		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.057

313	P	PRM227	Primary Orthostatic Hypotension	25	0.057

314		HGH001	High Pressure Neurological Syndrome	24	0.057

315		DRG016	Drug Induced Dyskinesia	24	0.057

316	P	PRS040	Prostate Cancer	97	0.054

317		OST012	Osteoarthritis	78	0.054

318	P	RTN008	Retinitis Pigmentosa	77	0.054

319		DFC004	Deficiency Anemia	75	0.054

320	c	MNN043	Meningioma, Familial	74	0.054

321		ACR006	Aceruloplasminemia	73	0.054

322	P	FRN006	Frontotemporal Dementia	70	0.054

323	P	HPT021	Hepatitis	67	0.054

324	P	LKM002	Leukemia	66	0.054

325	c	CNG006	Congenital Hypothyroidism	65	0.054

326		NRF026	Neurofibromatosis, Type Iv, of Riccardi	63	0.054

327	P	ADL010	Adult Respiratory Distress Syndrome	63	0.054

328		PPL049	Papillon-Lefevre Syndrome	63	0.054

329		MNN042	Meningioma, Radiation-Induced	62	0.054

330		CRD223	Cardiac Arrhythmia	60	0.054

331		ACQ007	Acquired Immunodeficiency Syndrome	60	0.054

332	c	ACT027	Acute Pancreatitis	59	0.054

333		PPT005	Peptic Ulcer Disease	58	0.054

334	P	CRD246	Cardiovascular System Disease	56	0.054

335	P	INF037	Inflammatory Bowel Disease	56	0.054

336	P	ATN002	Autonomic Nervous System Disease	52	0.054

337		ARM002	Aromatic L-Amino Acid Decarboxylase Deficiency	51	0.054

338		PST021	Postpartum Depression	50	0.054

339		SPN021	Spinal Meningioma	47	0.054

340		RTN023	Retinitis	46	0.054

341		HDN002	Head Injury	45	0.054

342		SYD002	Sydenham Chorea	44	0.054

343		GRN017	Granulocytopenia	44	0.054

344		PRM003	Premature Ejaculation	44	0.054

345		OBS003	Obsessive-Compulsive Personality Disorder	44	0.054

346		NRR001	Neuroretinitis	43	0.054

347	c	FTL006	Fetal Alcohol Spectrum Disorder	42	0.054

348		TRP009	Triple X Syndrome	42	0.054

349	c	SCH082	Schizophrenia 5	38	0.054

350		SCR001	Secretory Meningioma	37	0.054

351		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.054

352		GTP002	Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia	19	0.054

353	P	LNG032	Lung Cancer	97	0.051

354	P	GST053	Gastric Cancer	83	0.051

355		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.051

356		CNN003	Conn's Syndrome	79	0.051

357		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.051

358	P	CNR004	Cone-Rod Dystrophy 2	71	0.051

359	P	OCL013	Oculodentodigital Dysplasia	69	0.051

360	P	PNM007	Pneumonia	68	0.051

361	P	ATR011	Atrial Fibrillation	66	0.051

362	P	HYP098	Hypereosinophilic Syndrome	66	0.051

363	c	RHB024	Rhabdomyosarcoma 2	65	0.051

364		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.051

365	P	ADN016	Adenocarcinoma	64	0.051

366		DGR001	Digeorge Syndrome	63	0.051

367	P	ORT004	Orthostatic Intolerance	63	0.051

368	P	NTR004	Neutropenia	63	0.051

369	P	EPL198	Epilepsy, Myoclonic Juvenile	62	0.051

370	P	ENC004	Encephalitis	61	0.051

371		ERL001	Early Myoclonic Encephalopathy	61	0.051

372	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	60	0.051

373		NWB001	Newborn Respiratory Distress Syndrome	58	0.051

374	P	EXN002	Exanthem	57	0.051

375		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.051

376		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.051

377		HRT011	Heart Septal Defect	50	0.051

378		LRN003	Learning Disability	49	0.051

379		GYN001	Gynecomastia	49	0.051

380		ATS010	Autosomal Recessive Disease	48	0.051

381		SRT004	Serotonin Syndrome	46	0.051

382		ACT003	Acute Kidney Tubular Necrosis	45	0.051

383		ATN004	Autonomic Neuropathy	44	0.051

384	c	CHR056	Chronic Tic Disorder	43	0.051

385		NNF007	Non-Functioning Pituitary Adenoma	42	0.051

386		RST023	Resting Heart Rate, Variation in	41	0.051

387		RTR011	Retroperitoneal Fibrosis	40	0.051

388	c	CHR682	Chronic Bilirubin Encephalopathy	38	0.051

389	c	SCH080	Schizophrenia 3	37	0.051

390	c	MJR008	Major Affective Disorder 2	34	0.051

391		INF021	Infant Gynecomastia	31	0.051

392		ADG002	Audiogenic Seizures	26	0.051

393	P	HPT023	Hepatocellular Carcinoma	100	0.048

394	P	BRS047	Breast Cancer	96	0.048

395	P	RHM011	Rheumatoid Arthritis	80	0.048

396		AST005	Asthma	77	0.048

397		CRH001	Crohn's Disease	74	0.048

398	P	OST002	Osteoporosis	73	0.048

399	P	ART022	Arthritis	70	0.048

400	P	LYM118	Lymphoma	68	0.048

401	P	ANG001	Angelman Syndrome	67	0.048

402		OST159	Osteogenic Sarcoma	66	0.048

403		GST092	Gastroesophageal Reflux	65	0.048

404		IRR002	Irritable Bowel Syndrome	63	0.048

405	P	MCH002	Machado-Joseph Disease	63	0.048

406		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	62	0.048

407	P	VNT002	Ventricular Septal Defect	60	0.048

408		DPH001	Diphtheria	60	0.048

409		STT001	Status Epilepticus	59	0.048

410	c	HPT016	Hepatitis B	59	0.048

411		PLM033	Pulmonary Embolism	59	0.048

412	P	PRV006	Pervasive Developmental Disorder	57	0.048

413		PLG002	Plague	57	0.048

414		RSP019	Respiratory Distress Syndrome in Premature Infants	57	0.048

415	P	PRP019	Peripheral Nervous System Disease	57	0.048

416	P	DYS193	Dystonia 11, Myoclonic	56	0.048

417	P	FTL001	Fetal Alcohol Syndrome	55	0.048

418		DBT010	Diabetic Neuropathy	55	0.048

419		DYS161	Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency	53	0.048

420		ART140	Arteries, Anomalies of	53	0.048

421		STT041	Stuttering	52	0.048

422		PTH003	Pathologic Nystagmus	51	0.048

423	P	TRT010	Teratoma	51	0.048

424		SMT006	Somatoform Disorder	51	0.048

425		SPS003	Spastic Diplegia	50	0.048

426	P	OVR082	Overgrowth Syndrome	50	0.048

427		TRC010	Trichotillomania	50	0.048

428	P	ASP001	Asperger Syndrome	48	0.048

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

430		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.048

431	c	INH020	Inherited Metabolic Disorder	46	0.048

432		CYN002	Cyanosis, Transient Neonatal	45	0.048

433		AGR002	Agoraphobia	44	0.048

434	c	ERL020	Early-Onset Schizophrenia	44	0.048

435		ATN011	Autoinflammation with Infantile Enterocolitis	43	0.048

436		CRB090	Cerebral Hypoxia	43	0.048

437	c	PRM038	Primary Agammaglobulinemia	43	0.048

438	P	STR092	Striatal Degeneration, Autosomal Dominant 2	43	0.048

439		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.048

440	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	41	0.048

441		GST020	Gastric Antral Vascular Ectasia	41	0.048

442		49X006	49, Xxxxy Syndrome	41	0.048

443		SPS057	Spasticity	41	0.048

444		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	38	0.048

445		HYP141	Hyperphenylalaninemia	38	0.048

446		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	37	0.048

447		PSD088	Pseudobulbar Affect	36	0.048

448	c	SCH056	Schizophrenia 15	34	0.048

449	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.048

450	c	MJR003	Major Affective Disorder 6	33	0.048

451	c	MJR006	Major Affective Disorder 5	33	0.048

452		PST103	Postpartum Psychosis	33	0.048

453		CGN007	Cognitive Function 1, Social	28	0.048

454	P	PNC035	Pancreatic Cancer	84	0.044

455		END057	Endometrial Cancer	74	0.044

456	c	HYP836	Hypercholesterolemia, Familial, 1	72	0.044

457		PRP027	Peripheral Vascular Disease	71	0.044

458	c	GCH015	Gaucher Disease, Type I	70	0.044

459		ADL002	Adult Syndrome	69	0.044

460	c	FML001	Familial Atrial Fibrillation	66	0.044

461		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.044

462	P	LNG028	Long Qt Syndrome	65	0.044

463	c	SML038	Small Cell Cancer of the Lung	65	0.044

464	P	MTR014	Motor Neuron Disease	64	0.044

465	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.044

466	P	GCH001	Gaucher's Disease	64	0.044

467	P	ANR048	Aniridia 1	63	0.044

468	c	HPT001	Hepatitis C	63	0.044

469	P	PSR002	Psoriasis	62	0.044

470		NTR005	Nutritional Deficiency Disease	61	0.044

471		INT002	Intermittent Claudication	61	0.044

472	P	KDN017	Kidney Cancer	61	0.044

473	P	CTR002	Cataract	60	0.044

474	c	PRK089	Parkinson Disease 2, Autosomal Recessive Juvenile	60	0.044

475	P	PLY014	Polycystic Kidney Disease	59	0.044

476	P	TRC086	Trichohepatoenteric Syndrome 1	59	0.044

477	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	59	0.044

478		GST033	Gestational Diabetes	57	0.044

479		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	57	0.044

480	P	STR020	Strabismus	56	0.044

481	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.044

482	c	FML035	Familial Hyperlipidemia	55	0.044

483	P	GRV001	Graves' Disease	55	0.044

484		GNG005	Gangliocytoma	55	0.044

485		CRC006	Carcinoid Syndrome	55	0.044

486		INT007	Intermediate Coronary Syndrome	55	0.044

487		JPN002	Japanese Encephalitis	54	0.044

488		FCL014	Focal Epilepsy	54	0.044

489		BRN045	Brunner Syndrome	53	0.044

490		GLS018	Glass Syndrome	53	0.044

491		GNG002	Ganglioneuroma	53	0.044

492	P	INT068	Intestinal Disease	52	0.044

493	c	SPN294	Spinocerebellar Ataxia 1	52	0.044

494		PST011	Pustulosis of Palm and Sole	52	0.044

495		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.044

496		HYP081	Hypolipoproteinemia	50	0.044

497		TRT020	Tritanopia	50	0.044

498		BRX001	Bruxism	50	0.044

499	P	SCK005	Sickle Cell Disease	50	0.044

500	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	50	0.044

501	P	OPN001	Open-Angle Glaucoma	49	0.044

502		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	49	0.044

503		QDR001	Quadriplegia	48	0.044

504		SMT001	Somatization Disorder	48	0.044

505	c	OPT050	Opitz Gbbb Syndrome, Type Ii	47	0.044

506	P	TRT019	Torticollis	47	0.044

507		LPT006	Leptin Receptor Deficiency	47	0.044

508	c	MTR002	Mitral Valve Insufficiency	47	0.044

509		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.044

510	c	MLG068	Malignant Glioma	45	0.044

511		CRV043	Cervical Dystonia	45	0.044

512		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	45	0.044

513	P	BRB001	Beriberi	44	0.044

514		CHL012	Childhood Disintegrative Disease	44	0.044

515		DWR001	Dwarfism	44	0.044

516		BCK006	Back Pain	42	0.044

517	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.044

518		CLR033	Color Vision Deficiency	41	0.044

519	P	DYS005	Dyslexia	40	0.044

520		ADS004	Aids Dementia Complex	40	0.044

521		ANG049	Angioedema Induced by Ace Inhibitors	40	0.044

522		MCH006	Mechanical Strabismus	39	0.044

523		OCL010	Ocular Hypotension	38	0.044

524	c	PLY105	Polycystic Ovary Syndrome 1	38	0.044

525	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.044

526	c	MJR023	Major Affective Disorder 7	33	0.044

527	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.044

528	c	HRD198	Hereditary Dystonia	31	0.044

529	c	MJR004	Major Affective Disorder 4	28	0.044

530		ARG004	Argyria	28	0.044

531	c	ORT012	Orthostatic Hypotension 2	27	0.044

532		SDD004	Sudden Arrhythmia Death Syndrome	23	0.044

533		MTR086	Motor Stereotypies	16	0.044

534		ESP021	Esophageal Cancer	90	0.040

535	P	OVR042	Ovarian Cancer	89	0.040

536	c	LKM061	Leukemia, Acute Myeloid	83	0.040

537		CYS001	Cystic Fibrosis	80	0.040

538	P	BLD134	Bladder Cancer	78	0.040

539	P	NRF023	Neurofibromatosis, Type Ii	76	0.040

540	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.040

541		BRN028	Brain Cancer	73	0.040

542		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.040

543		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.040

544	P	SYS005	Systemic Scleroderma	70	0.040

545		LYM133	Lymphoma, Hodgkin, Classic	69	0.040

546		SKN019	Skin Melanoma	67	0.040

547		CHL065	Cholangiocarcinoma	67	0.040

548	c	NRP054	Neuropathy, Hereditary Sensory and Autonomic, Type Iii	66	0.040

549	c	MCR129	Microvascular Complications of Diabetes 1	66	0.040

550	P	HYD006	Hydrocephalus	65	0.040

551		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	65	0.040

552		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.040

553		APN008	Apnea, Obstructive Sleep	65	0.040

554		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	64	0.040

555	c	DYS056	Dystonia 12	64	0.040

556		IDP011	Idiopathic Interstitial Pneumonia	63	0.040

557	P	NRN021	Neuronal Ceroid Lipofuscinosis	63	0.040

558		CLT003	Colitis	62	0.040

559	P	EPL140	Epilepsy, Idiopathic Generalized	61	0.040

560	P	PLM036	Pulmonary Fibrosis	61	0.040

561		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.040

562		CHR066	Chronic Fatigue Syndrome	61	0.040

563	c	BRN108	Branchiootic Syndrome 1	61	0.040

564		LNG099	Lung Disease	61	0.040

565	P	MYL006	Myeloid Leukemia	60	0.040

566		ORL011	Oral Cancer	60	0.040

567	P	MYC008	Myocarditis	59	0.040

568		THY029	Thyroid Carcinoma	59	0.040

569		DBT084	Diabetes Mellitus, Ketosis-Prone	59	0.040

570		CRD132	Cardiac Conduction Defect	59	0.040

571	c	SPN301	Spinocerebellar Ataxia 2	59	0.040

572		EYD002	Eye Disease	58	0.040

573	P	GLL020	Gallbladder Disease	58	0.040

574	P	ACT010	Acth-Secreting Pituitary Adenoma	57	0.040

575		APH002	Aphasia	57	0.040

576	P	GLM007	Glomerulonephritis	57	0.040

577		ADN027	Adenomyosis	57	0.040

578		HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	56	0.040

579	P	ALP008	Alopecia	56	0.040

580		GST050	Gastrointestinal System Disease	56	0.040

581		PRP009	Peripartum Cardiomyopathy	55	0.040

582		RLP002	Relapsing-Remitting Multiple Sclerosis	55	0.040

583	P	MLT074	Multiple Endocrine Neoplasia	55	0.040

584	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	53	0.040

585		IMM102	Immunodeficiency 14	53	0.040

586	c	LTN004	Late-Onset Retinal Degeneration	52	0.040

587		ESP023	Esophageal Disease	52	0.040

588	c	PRM092	Primary Lateral Sclerosis, Adult, 1	52	0.040

589	P	OLV001	Olivopontocerebellar Atrophy	52	0.040

590	P	SPN429	Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2	51	0.040

591		PPT001	Peptic Esophagitis	51	0.040

592		THY030	Thyroid Gland Disease	51	0.040

593	P	MTR003	Mitral Valve Stenosis	50	0.040

594		DYS073	Dysphagia	50	0.040

595		INT079	Intrahepatic Cholangiocarcinoma	50	0.040

596		AMB002	Amblyopia	50	0.040

597	c	ACH020	Achromatopsia 2	50	0.040

598		BRN009	Burning Mouth Syndrome	49	0.040

599	c	SVR005	Severe Pre-Eclampsia	49	0.040

600		BHR001	Behr Syndrome	49	0.040

601		URM002	Uremia	49	0.040

602	P	OBS001	Obstructive Jaundice	48	0.040

603	P	CLR019	Color Blindness	48	0.040

604		ASP007	Aspiration Pneumonia	48	0.040

605		IGG001	Iga Glomerulonephritis	48	0.040

606		PLC007	Placental Abruption	48	0.040

607		STM006	Stomach Disease	48	0.040

608		SPC010	Speech and Communication Disorders	47	0.040

609	c	LRG017	Large Intestine Cancer	47	0.040

610		HYP082	Hypopharynx Cancer	47	0.040

611		LYM019	Lymphosarcoma	47	0.040

612		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	46	0.040

613		PST048	Postural Orthostatic Tachycardia Syndrome	45	0.040

614		CNV002	Conversion Disorder	45	0.040

615		ATY001	Atypical Depressive Disorder	45	0.040

616		IMM064	Immunodeficiency, Common Variable, 10	44	0.040

617		FNC007	Functioning Pituitary Adenoma	44	0.040

618	c	HYP272	Hypercholesterolemia, Familial, 3	43	0.040

619		IDP033	Idiopathic Edema	43	0.040

620	P	CLS010	Cluster Headache	43	0.040

621		LWC001	Low Compliance Bladder	42	0.040

622		PHY002	Physical Disorder	42	0.040

623		RDN001	Reading Disorder	40	0.040

624		JWD001	Jawad Syndrome	40	0.040

625		MLN003	Melancholia	39	0.040

626		SPP007	Suppression Amblyopia	39	0.040

627		DSS010	Dissociative Disorder	38	0.040

628		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.040

629		FBR089	Fibrosclerosis, Multifocal	38	0.040

630		PLC009	Placenta Praevia	37	0.040

631		OBS015	Obesity, Hyperphagia, and Developmental Delay	35	0.040

632		CHR178	Chromosomal Triplication	35	0.040

633		CRB036	Cerebral Meningioma	34	0.040

634		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	33	0.040

635	c	SCH064	Schizophrenia 10	31	0.040

636		MLT105	Multiple System Atrophy, Cerebellar Type	29	0.040

637		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.040

638		GLC025	Galactorrhoea-Hyperprolactinaemia	21	0.040

639	P	ATX030	Ataxia-Telangiectasia	83	0.036

640		MLR004	Malaria	80	0.036

641		CRV035	Cervical Cancer	76	0.036

642		MRF001	Marfan Syndrome	75	0.036

643		PLM134	Pulmonary Fibrosis, Idiopathic	75	0.036

644	c	NRF024	Neurofibromatosis, Type I	71	0.036

645	c	MLT156	Multiple Endocrine Neoplasia, Type I	71	0.036

646	P	AMY004	Amyloidosis	70	0.036

647		BRN024	Bronchitis	68	0.036

648	P	CRN037	Craniosynostosis	68	0.036

649		PCK003	Pick Disease of Brain	68	0.036

650	P	MLG056	Malignant Hyperthermia	67	0.036

651	P	NSP012	Nasopharyngeal Carcinoma	67	0.036

652	P	SKN015	Skin Carcinoma	67	0.036

653	c	MCL062	Mucolipidosis Ii Alpha/beta	66	0.036

654	P	MSC005	Muscular Dystrophy	66	0.036

655		ATH013	Atherosclerosis Susceptibility	66	0.036

656	P	THY023	Thymoma	65	0.036

657	P	MYP004	Myopathy	64	0.036

658	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	63	0.036

659		SKN016	Skin Disease	63	0.036

660	P	NPH012	Nephrotic Syndrome	63	0.036

661	c	SCL052	Scleroderma, Familial Progressive	62	0.036

662	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.036

663	P	ART023	Arthropathy	62	0.036

664	P	HML002	Hemolytic Anemia	62	0.036

665		WLL001	Williams-Beuren Syndrome	62	0.036

666	P	FRN044	Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1	62	0.036

667	P	VSC011	Vasculitis	62	0.036

668	P	ESP024	Esophagitis	62	0.036

669		SDD001	Sudden Infant Death Syndrome	61	0.036

670		VRL011	Viral Infectious Disease	61	0.036

671		RHM001	Rheumatic Fever	61	0.036

672	P	ATR010	Atrial Heart Septal Defect	60	0.036

673		ING001	Inguinal Hernia	60	0.036

674	P	TXP001	Toxoplasmosis	60	0.036

675	P	BNG030	Benign Ependymoma	60	0.036

676	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	60	0.036

677		DCB001	Decubitus Ulcer	60	0.036

678		RTN017	Retinal Detachment	60	0.036

679	P	SCL018	Scoliosis	60	0.036

680	P	CNT110	Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a	60	0.036

681	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	59	0.036

682		GST045	Gastroenteritis	59	0.036

683	P	INT070	Intestinal Obstruction	58	0.036

684		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	58	0.036

685	P	OPT006	Optic Nerve Disease	57	0.036

686		LYM027	Lymphopenia	57	0.036

687		TNS005	Tonsillitis	57	0.036

688		HMR039	Hemorrhage, Intracerebral	57	0.036

689		DYS192	Dystonia, Dopa-Responsive	57	0.036

690		THR024	Thrombosis	56	0.036

691		ISL001	Islet Cell Tumor	56	0.036

692		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	56	0.036

693		CMM005	Common Cold	56	0.036

694		ADR008	Adrenal Adenoma	56	0.036

695	P	GST044	Gastritis	55	0.036

696	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.036

697		ACT058	Active Peptic Ulcer Disease	55	0.036

698		MRD002	Marden-Walker Syndrome	55	0.036

699	P	DBT005	Diabetes Insipidus	55	0.036

700	P	LYM031	Lymphocytic Leukemia	55	0.036

701		HMP005	Hemiplegia	54	0.036

702		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	54	0.036

703		VLC001	Velocardiofacial Syndrome	54	0.036

704		HMS001	Hemosiderosis	54	0.036

705		PRC013	Pericarditis	54	0.036

706		GST009	Gastroschisis	54	0.036

707	c	THY107	Thymoma, Familial	54	0.036

708	c	LBR014	Leber Congenital Amaurosis 4	53	0.036

709		HYP815	Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome	53	0.036

710		CLB010	Coloboma of Macula	53	0.036

711		CLL010	Cellular Ependymoma	53	0.036

712		PRP080	Peripheral Artery Disease	53	0.036

713		PRS030	Persistent Fetal Circulation Syndrome	52	0.036

714		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	52	0.036

715	P	ACT105	Acute Mountain Sickness	52	0.036

716	c	GLL024	Gallbladder Disease 1	52	0.036

717		TXC002	Toxic Encephalopathy	52	0.036

718		MTN003	Motion Sickness	52	0.036

719		HYP014	Hyperuricemia	51	0.036

720	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.036

721		TLN003	Telangiectasis	51	0.036

722		APL002	Aplasia of Lacrimal and Salivary Glands	50	0.036

723		HYP781	Hypoascorbemia	50	0.036

724		PNM005	Pneumonic Plague	50	0.036

725		NTR046	Neutrophil Migration	50	0.036

726	P	MYT002	Myotonic Dystrophy	49	0.036

727		CHL004	Cholelithiasis	49	0.036

728	c	NRC009	Narcolepsy 1	49	0.036

729		SLP001	Sleeping Sickness	48	0.036

730		PLC003	Placental Site Trophoblastic Tumor	48	0.036

731	c	HYP331	Hyperphenylalaninemia, Bh4-Deficient, a	47	0.036

732		WRN003	Wernicke Encephalopathy	47	0.036

733	P	CRC039	Coarctation of Aorta	47	0.036

734	c	PRK092	Parkinson Disease 6, Autosomal Recessive Early-Onset	47	0.036

735		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.036

736		ANR004	Anuria	46	0.036

737		PRT019	Protein-Losing Enteropathy	46	0.036

738	P	PRD037	Periodontal Ehlers-Danlos Syndrome	46	0.036

739		PST027	Postencephalitic Parkinson Disease	45	0.036

740	c	TRC022	Tricuspid Valve Insufficiency	45	0.036

741		IMM003	Immunoglobulin Alpha Deficiency	45	0.036

742		CHR466	Chronic Thromboembolic Pulmonary Hypertension	45	0.036

743	P	HYP605	Hyperphenylalaninemia, Bh4-Deficient, B	45	0.036

744	P	BLP003	Blepharospasm	44	0.036

745		DST006	Diastolic Heart Failure	44	0.036

746	P	PHR004	Pharynx Cancer	44	0.036

747		EMP001	Empty Sella Syndrome	44	0.036

748		CNT017	Central Nervous System Origin Vertigo	44	0.036

749		DMP001	Dumping Syndrome	44	0.036

750		OVR063	Overnutrition	43	0.036

751		CRB196	Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome	43	0.036

752		DRG024	Drug Allergy	43	0.036

753		ADR041	Adrenal Cortical Adenoma	43	0.036

754	c	ADV003	Advanced Sleep Phase Syndrome, Familial, 1	43	0.036

755	c	HRD173	Hereditary Late-Onset Parkinson Disease	43	0.036

756		ASP008	Aspiration Pneumonitis	42	0.036

757	c	PRG011	Progressive Myoclonus Epilepsy	42	0.036

758		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	42	0.036

759		ALX001	Alexia	42	0.036

760		SPC005	Speech Disorder	42	0.036

761		BP1002	Bap1 Tumor Predisposition Syndrome	41	0.036

762	P	CRN035	Cranial Nerve Palsy	41	0.036

763		DBT002	Diabetic Autonomic Neuropathy	41	0.036

764	P	HYP263	Hypersomnia	41	0.036

765	P	RRH023	Rare Hereditary Hemochromatosis	41	0.036

766		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.036

767		BKR002	Baker-Gordon Syndrome	40	0.036

768	c	PLM022	Pulmonary Valve Insufficiency	40	0.036

769		PTT003	Pituitary-Dependent Cushing's Disease	39	0.036

770	P	ECT045	Ectodermal Dysplasia-Syndactyly Syndrome 1	39	0.036

771	c	MLG157	Malignant Pheochromocytoma	39	0.036

772		ENT001	Enterocele	39	0.036

773		HYP030	Hypoactive Sexual Desire Disorder	39	0.036

774		BLR002	Bile Reflux	39	0.036

775		CGN005	Cognitive Impairment with or Without Cerebellar Ataxia	39	0.036

776		NNT008	Neonatal Abstinence Syndrome	38	0.036

777	P	CRB088	Cerebral Atrophy	38	0.036

778		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.036

779		CHL013	Cholecystolithiasis	37	0.036

780	c	PRK085	Parkinson Disease 1, Autosomal Dominant	37	0.036

781		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	37	0.036

782		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	36	0.036

783		MYT011	Myotonia	35	0.036

784		ABD010	Abdominal Wall Defect	35	0.036

785	P	MYC026	Myoclonus Epilepsy	35	0.036

786		DDN009	Duodenal Obstruction	34	0.036

787		BNN005	Bunion	33	0.036

788	c	SCH083	Schizophrenia 7	33	0.036

789	c	SCH085	Schizophrenia 2	33	0.036

790	c	SCH081	Schizophrenia 6	32	0.036

791		CHR281	Chronic Hiccups	31	0.036

792		MCL057	Macular Dystrophy with Central Cone Involvement	31	0.036

793		CHL078	Childhood-Onset Schizophrenia	31	0.036

794		CLS047	Classic Progressive Supranuclear Palsy Syndrome	30	0.036

795		IDP093	Idiopathic Gastroparesis	30	0.036

796		RSP007	Respiratory Distress Syndrome, Infant	30	0.036

797		PYL002	Pylorospasm	28	0.036

798		PRR019	Perioral Myoclonia with Absences	28	0.036

799	c	PRK098	Parkinson Disease 5, Autosomal Dominant	26	0.036

800		FTL073	Fetal Anticonvulsant Syndrome	26	0.036

801	c	RST020	Restless Legs Syndrome 6	25	0.036

802		BRR004	Baroreflex Failure	25	0.036

803		JVN026	Jeavons Syndrome	24	0.036

804		DSC013	Discrimination, Two-Point, Reduction in	23	0.036

805	c	DRG020	Drug Metabolism, Poor, Cyp2d6-Related	22	0.036

806	c	TYP027	Type 1 Diabetes Mellitus 10	22	0.036

807		DSS012	Disseminated Infection with Mycobacterium Avium Complex	20	0.036

808		CRB089	Cerebral Beriberi	20	0.036

809	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	0.036

810		FBR090	Fibro-Adipose Vascular Anomaly	17	0.036

811	c	SYS001	Systemic Lupus Erythematosus	86	0.031

812		MYL069	Myeloma, Multiple	85	0.031

813	P	GLM040	Glioma Susceptibility 1	81	0.031

814	c	LKM071	Leukemia, Chronic Lymphocytic	79	0.031

815	P	LNG064	Lung Cancer Susceptibility 3	77	0.031

816	P	MDL005	Medulloblastoma	77	0.031

817		GST019	Gastrointestinal Stromal Tumor	76	0.031

818		ADR007	Adrenoleukodystrophy	74	0.031

819		ULC004	Ulcerative Colitis	73	0.031

820		SCK003	Sickle Cell Anemia	72	0.031

821	P	FML018	Familial Mediterranean Fever	72	0.031

822		MSC157	Muscular Dystrophy, Duchenne Type	71	0.031

823	P	SRC025	Sarcoidosis 1	70	0.031

824		PLM001	Pulmonary Tuberculosis	70	0.031

825	P	TTR001	Tetralogy of Fallot	69	0.031

826	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	69	0.031

827	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.031

828	P	MYC084	Mycobacterium Tuberculosis 1	68	0.031

829	P	INF038	Influenza	68	0.031

830	c	INF071	Inflammatory Bowel Disease 1	68	0.031

831		ACR008	Acrocallosal Syndrome	68	0.031

832	P	KBK002	Kabuki Syndrome 1	67	0.031

833	P	OLG002	Oligodendroglioma	67	0.031

834	c	PRG042	Progressive Familial Heart Block, Type Ia	67	0.031

835		THY111	Thyroid Carcinoma, Familial Medullary	67	0.031

836		FLL027	Fallopian Tube Carcinoma	67	0.031

837	P	MTR004	Maturity-Onset Diabetes of the Young	66	0.031

838	c	LNG044	Long Qt Syndrome 1	66	0.031

839		FCT007	Factor Vii Deficiency	66	0.031

840		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.031

841	c	MYT021	Myotonic Dystrophy 1	66	0.031

842		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.031

843		CRN036	Craniopharyngioma	65	0.031

844		MSM014	Mismatch Repair Cancer Syndrome	65	0.031

845	P	HRP006	Herpes Simplex	65	0.031

846		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	64	0.031

847	c	MCL013	Mucolipidosis Iv	64	0.031

848		LYS012	Lysosomal Acid Lipase Deficiency	64	0.031

849		MNK001	Menkes Disease	64	0.031

850		CRN296	Carnitine Palmitoyltransferase Ii Deficiency, Infantile	64	0.031

851		NRF007	Neurofibroma	64	0.031

852		PRP083	Porphyria, Acute Intermittent	63	0.031

853		LYM017	Lyme Disease	63	0.031

854		NRM005	Neuromuscular Disease	63	0.031

855		ART002	Arts Syndrome	63	0.031

856		MSC152	Muscular Dystrophy, Becker Type	63	0.031

857	P	FRD001	Friedreich Ataxia	63	0.031

858	P	PRD008	Periodontitis	62	0.031

859	P	HYP055	Hypoplastic Left Heart Syndrome	62	0.031

860		MSS001	Masa Syndrome	62	0.031

861	P	PRP029	Porphyria	62	0.031

862		TTH002	Tooth Agenesis	61	0.031

863	P	INT143	Interstitial Cystitis	61	0.031

864	P	LPS004	Lupus Erythematosus	61	0.031

865		OST003	Osteonecrosis	61	0.031

866	P	SNS001	Sensorineural Hearing Loss	61	0.031

867		PRT013	Portal Hypertension	60	0.031

868	P	CHL002	Childhood Absence Epilepsy	60	0.031

869		ACN002	Acanthosis Nigricans	60	0.031

870		YLL002	Yellow Fever	60	0.031

871	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.031

872		CYS010	Cystinosis	60	0.031

873		SQM006	Squamous Cell Carcinoma	60	0.031

874	P	ALP009	Alopecia Areata	60	0.031

875		INT066	Interstitial Lung Disease	59	0.031

876		GNG013	Gingivitis	59	0.031

877	P	SPN309	Spinocerebellar Ataxia 6	59	0.031

878	P	BND020	Bone Disease	59	0.031

879		GRD007	Grade Iii Astrocytoma	59	0.031

880	P	SYP003	Syphilis	59	0.031

881		CHL123	Chlamydia	59	0.031

882		SPN027	Spinal Stenosis	59	0.031

883		VLV032	Vulva Cancer	59	0.031

884		ANR040	Aneurysm	58	0.031

885		IRN001	Iron Deficiency Anemia	58	0.031

886	c	PRG126	Progressive Familial Heart Block	58	0.031

887		ADR005	Adrenal Carcinoma	58	0.031

888	c	PRG018	Paragangliomas 1	57	0.031

889		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.031

890	P	BNC003	Bone Cancer	57	0.031

891	P	EHL001	Ehlers-Danlos Syndrome	57	0.031

892		DNT005	Dentatorubral-Pallidoluysian Atrophy	57	0.031

893	P	SJG008	Sjogren Syndrome	56	0.031

894		PLS011	Plasmacytoma	56	0.031

895	P	ORL007	Oral Cavity Cancer	56	0.031

896	P	OPT009	Optic Neuritis	56	0.031

897		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.031

898		INT303	Intracranial Hypertension, Idiopathic	56	0.031

899		BCT022	Bacterial Infectious Disease	56	0.031

900	P	MLN007	Male Infertility	56	0.031

901	c	INT072	Intestinal Pseudo-Obstruction	56	0.031

902		RHM027	Rheumatic Disease	56	0.031

903		VGN017	Vaginal Cancer	55	0.031

904		MCS002	Mucositis	55	0.031

905		BRD001	Brody Myopathy	55	0.031

906		JVN009	Juvenile Pilocytic Astrocytoma	55	0.031

907	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.031

908		LMB002	Lambert-Eaton Myasthenic Syndrome	54	0.031

909		GLS001	Gliosarcoma	54	0.031

910		ORP003	Oropharynx Cancer	54	0.031

911	c	PRD040	Periodontitis, Chronic	54	0.031

912	P	LRY044	Larynx Cancer	54	0.031

913		UNV001	Unverricht-Lundborg Syndrome	54	0.031

914		LYM040	Lymphoblastic Lymphoma	54	0.031

915		PRT082	Preterm Premature Rupture of the Membranes	54	0.031

916		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	53	0.031

917		PRP016	Paraplegia	53	0.031

918		CLR030	Clear Cell Renal Cell Carcinoma	53	0.031

919		MYP139	Myopathy, Proximal, and Ophthalmoplegia	53	0.031

920		NRT004	Neuritis	53	0.031

921		RHM028	Rheumatic Heart Disease	53	0.031

922		SNS003	Sensory Peripheral Neuropathy	53	0.031

923		BRN038	Bronchial Disease	53	0.031

924	P	HYP730	Hypogonadotropic Hypogonadism	53	0.031

925		HMC014	Homocysteinemia	53	0.031

926		KRT006	Keratoconjunctivitis	53	0.031

927		ANM046	Anemia, Sideroblastic, and Spinocerebellar Ataxia	53	0.031

928		KRT009	Keratosis	53	0.031

929	P	OVR049	Ovarian Disease	53	0.031

930		THR013	Thoracic Outlet Syndrome	53	0.031

931		CRH005	Crohn's Colitis	52	0.031

932		EXP004	Exophthalmos	52	0.031

933	c	DMN023	Diamond-Blackfan Anemia 1	52	0.031

934		ACR041	Acromelic Frontonasal Dysostosis	52	0.031

935		DMY004	Demyelinating Disease	52	0.031

936	P	ACT008	Actinic Keratosis	52	0.031

937		GNT002	Giant Cell Glioblastoma	52	0.031

938	c	PSR017	Psoriasis 2	52	0.031

939		MYC080	Myoclonic Epilepsy of Unverricht and Lundborg	52	0.031

940		VSC044	Visceral Myopathy	51	0.031

941	P	BRN035	Brain Stem Glioma	51	0.031

942		FND002	Fundus Dystrophy	51	0.031

943		CYS036	Cystinosis, Nephropathic	51	0.031

944		PLS009	Plasma Cell Neoplasm	51	0.031

945		MSC190	Muscular Disease	51	0.031

946	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	51	0.031

947		SCR020	Sacral Defect with Anterior Meningocele	51	0.031

948		DNT012	Dental Caries	51	0.031

949	c	PTT057	Pituitary Adenoma 4, Acth-Secreting	51	0.031

950		APR001	Apraxia	51	0.031

951		PRS021	Prostatic Adenoma	51	0.031

952		THY125	Thyroid Gland Medullary Carcinoma	51	0.031

953		SGW002	Segawa Syndrome, Autosomal Recessive	51	0.031

954		BWN001	Bowen-Conradi Syndrome	51	0.031

955	c	ACT134	Acute Liver Failure	51	0.031

956		RTN003	Retinal Ischemia	50	0.031

957		ACH005	Achalasia	50	0.031

958		CHL061	Childhood Leukemia	50	0.031

959	c	INF145	Infantile Liver Failure Syndrome 1	50	0.031

960	P	ESN008	Eosinophilic Pneumonia	50	0.031

961		HYL004	Hyaline Fibromatosis Syndrome	50	0.031

962		KRT001	Keratoconjunctivitis Sicca	50	0.031

963	c	INF023	Inflammatory Breast Carcinoma	49	0.031

964	c	PSR023	Psoriasis 1	49	0.031

965		VCC001	Vaccinia	49	0.031

966		LFT001	Left Bundle Branch Hemiblock	49	0.031

967	c	DYS119	Dystonia 9	49	0.031

968	P	RNV001	Renovascular Hypertension	49	0.031

969		GST049	Gastrointestinal System Cancer	49	0.031

970		ALN001	Aland Island Eye Disease	49	0.031

971		BNR002	Bone Resorption Disease	48	0.031

972		END021	Endomyocardial Fibrosis	48	0.031

973		KRT002	Keratomalacia	48	0.031

974		ENT004	Enthesopathy	48	0.031

975		PLP001	Pulpitis	48	0.031

976		FBR009	Fibrous Dysplasia	48	0.031

977	c	DSB006	Desbuquois Dysplasia 1	48	0.031

978		HYP043	Hyperandrogenism	48	0.031

979		STP011	Stapes Ankylosis with Broad Thumbs and Toes	48	0.031

980	c	BNG023	Benign Familial Infantile Epilepsy	48	0.031

981		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.031

982		KHN001	Kuhnt-Junius Degeneration	48	0.031

983	P	JVN007	Juvenile Absence Epilepsy	48	0.031

984		PLM035	Pulmonary Eosinophilia	48	0.031

985	P	NRV006	Nervous System Cancer	48	0.031

986		CRC014	Carcinoid Tumors, Intestinal	48	0.031

987	P	UTR058	Uterine Anomalies	48	0.031

988	P	PRR002	Pure Red-Cell Aplasia	48	0.031

989		ADR016	Adrenal Cortical Carcinoma	48	0.031

990	P	NGH001	Night Blindness	47	0.031

991		DRY001	Dry Eye Syndrome	47	0.031

992		AST006	Astigmatism	47	0.031

993		NRN001	Neuroendocrine Carcinoma	47	0.031

994		SMN008	Semantic Dementia	47	0.031

995	c	HYP795	Hypothyroidism, Congenital, Nongoitrous, 4	47	0.031

996	c	INH030	Inherited Retinal Disorder	47	0.031

997		CYC008	Cyclic Vomiting Syndrome	47	0.031

998		HST009	Histiocytoma	46	0.031

999		TTH006	Tooth Disease	46	0.031

1000	c	ALP104	Alport Syndrome 3, Autosomal Dominant	46	0.031

1001	c	CNT033	Central Nervous System Cancer	46	0.031

1002		ALB002	Albinism	46	0.031

1003		KRT013	Keratolytic Winter Erythema	46	0.031

1004		CNG028	Congenital Hypoplastic Anemia	46	0.031

1005		ANP006	Anaplastic Ependymoma	46	0.031

1006		LCK001	Locked-in Syndrome	46	0.031

1007		TTR005	Tetrahydrobiopterin Deficiency	46	0.031

1008		DFF006	Diffuse Idiopathic Skeletal Hyperostosis	46	0.031

1009		TRT001	Teratocarcinoma	46	0.031

1010		SBP004	Subependymoma	46	0.031

1011		GST071	Gastrointestinal Carcinoma	45	0.031

1012	P	EPN001	Ependymoblastoma	45	0.031

1013		MXD026	Mixed Glioma	45	0.031

1014	P	OCY003	Oocyte Maturation Defect 1	45	0.031

1015		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.031

1016		MYX001	Myxopapillary Ependymoma	45	0.031

1017		MTS001	Mutism	45	0.031

1018	P	END084	Endocrine System Disease	44	0.031

1019		ACT029	Acute Interstitial Pneumonia	44	0.031

1020		CHN010	Chondroma	44	0.031

1021	P	GNT008	Giant Cell Tumor	44	0.031

1022		PRT035	Peritoneum Cancer	44	0.031

1023		GNG003	Gingival Recession	44	0.031

1024	P	CRB154	Cerebrocostomandibular Syndrome	44	0.031

1025		FRG010	Fragile X Tremor/ataxia Syndrome	43	0.031

1026		MGS001	Megaesophagus	43	0.031

1027		RNL097	Renal Artery Disease	43	0.031

1028		GRW007	Growth Hormone Deficiency	43	0.031

1029		EST005	Esotropia	43	0.031

1030		ACH015	Achalasia, Familial Esophageal	43	0.031

1031	c	SRC023	Sarcoidosis 2	43	0.031

1032		CYS009	Cystadenoma	43	0.031

1033		NRP045	Neuropathy, Ataxia, and Retinitis Pigmentosa	43	0.031

1034		MCR011	Microinvasive Gastric Cancer	43	0.031

1035		ANP009	Anaplastic Oligodendroglioma	43	0.031

1036		RDC006	Red Cell Aplasia	42	0.031

1037		AND001	Anodontia	42	0.031

1038		MYF002	Myofascial Pain Syndrome	42	0.031

1039		HYP085	Hypothalamic Disease	42	0.031

1040		EXT022	Exotropia	42	0.031

1041		FRG008	Fragile X-Associated Tremor/ataxia Syndrome	42	0.031

1042	P	RNG032	Ring Chromosome	42	0.031

1043	c	ADN012	Adenocarcinoma in Situ	42	0.031

1044		DFF003	Diffuse Scleroderma	42	0.031

1045		OCL011	Ocular Motility Disease	41	0.031

1046		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.031

1047		CTN004	Cutaneous Fibrous Histiocytoma	41	0.031

1048		FBR003	Fibrous Histiocytoma	41	0.031

1049	c	MLG064	Malignant Ependymoma	41	0.031

1050		ADJ001	Adjustment Disorder	41	0.031

1051		INT319	Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked	41	0.031

1052		CRN212	Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome	41	0.031

1053	c	CNG413	Congenital Short Bowel Syndrome	41	0.031

1054	c	MYT029	Myotonia Congenita, Autosomal Recessive	41	0.031

1055		CYC005	Cyclothymic Disorder	40	0.031

1056	P	NSL008	Nasal Cavity Cancer	40	0.031

1057		PHB003	Phobia, Specific	40	0.031

1058		KLN009	Kleine-Levin Hibernation Syndrome	40	0.031

1059		GLC008	Glucose Metabolism Disease	40	0.031

1060		PRD002	Periodic Limb Movement Disorder	40	0.031

1061		SLT009	Solitary Bone Cyst	40	0.031

1062	c	HYP543	Hypoplastic Left Heart Syndrome 1	40	0.031

1063	c	HMG001	Hemoglobin C Disease	40	0.031

1064		SPR126	Superior Semicircular Canal Dehiscence	40	0.031

1065		ART103	Arthrogryposis, Mental Retardation, and Seizures	40	0.031

1066		URG005	Uruguay Faciocardiomusculoskeletal Syndrome	39	0.031

1067	c	EPL133	Epilepsy, Juvenile Absence 1	39	0.031

1068	c	PRK093	Parkinson Disease 8, Autosomal Dominant	39	0.031

1069		BDY001	Body Dysmorphic Disorder	39	0.031

1070		AGR019	Age-Related Hearing Loss	39	0.031

1071		ALX002	Alexithymia	39	0.031

1072		RHM035	Rheumatic Fever-Related Antigen	39	0.031

1073	c	PSR028	Psoriasis 7	39	0.031

1074		NMN001	Nominal Aphasia	39	0.031

1075	c	PSR032	Psoriasis 11	38	0.031

1076	c	PSR018	Psoriasis 13	38	0.031

1077	c	OVR114	Ovarian Cancer 1	38	0.031