Search results for Neurotransmitter Agents

2267 hits were found for Neurotransmitter Agents

#	Family	MCID	Name	MIFTS	Score
1	P	ALZ034	Alzheimer Disease	88	0.174

2	P	ENC018	Encephalopathy	61	0.164

3	P	NRB001	Neuroblastoma	72	0.160

4		HYP056	Hypoglycemia	66	0.157

5	P	LNG032	Lung Cancer	98	0.153

6	P	DRR001	Diarrhea	55	0.147

7	P	CLR023	Colorectal Cancer	99	0.140

8	P	OVR042	Ovarian Cancer	88	0.140

9	P	NTR004	Neutropenia	63	0.140

10		CNG034	Congestive Heart Failure	69	0.139

11		DPR016	Depression	63	0.138

12	P	LKM002	Leukemia	68	0.138

13		MYL069	Myeloma, Multiple	85	0.138

14		GLL048	Glial Tumor	45	0.137

15	P	GLM045	Glioma	63	0.136

16	P	BRS047	Breast Cancer	97	0.136

17		ALL026	Allergic Hypersensitivity Disease	62	0.136

18	P	KDN018	Kidney Disease	72	0.131

19		HYP266	Hypoxia	57	0.131

20		GLB015	Glioblastoma Multiforme	75	0.129

21	P	PNC035	Pancreatic Cancer	84	0.129

22	P	MYL006	Myeloid Leukemia	60	0.129

23	c	LKM061	Leukemia, Acute Myeloid	84	0.129

24		ISC004	Ischemia	58	0.128

25	P	PSR002	Psoriasis	62	0.126

26		PST011	Pustulosis of Palm and Sole	52	0.125

27		SCR011	Scrapie	39	0.125

28	c	SML038	Small Cell Cancer of the Lung	65	0.124

29		MYL009	Myelodysplastic Syndrome	70	0.123

30	P	PRS040	Prostate Cancer	97	0.123

31	P	TRM003	Tremor	54	0.121

32	P	SZR006	Seizure Disorder	56	0.119

33		ALC007	Alcohol Dependence	66	0.119

34		BCT022	Bacterial Infectious Disease	56	0.119

35	P	HRP006	Herpes Simplex	65	0.119

36	c	HYP595	Hypertension, Essential	84	0.118

37		ATM095	Autoimmune Disease	62	0.118

38		VSL002	Visual Epilepsy	59	0.117

39		48X005	48,xyyy	39	0.116

40		MNT002	Mental Depression	58	0.116

41	P	PHC003	Pheochromocytoma	71	0.114

42		ADR040	Adrenal Gland Pheochromocytoma	46	0.114

43	c	HPT073	Hepatitis C Virus	72	0.114

44	P	SCH015	Schizophrenia	74	0.114

45		ANX010	Anxiety	73	0.113

46	P	INF037	Inflammatory Bowel Disease	54	0.112

47	P	RHM011	Rheumatoid Arthritis	80	0.111

48	c	HPT001	Hepatitis C	62	0.111

49		PRT037	Pertussis	65	0.110

50		HRW001	Hair Whorl	36	0.110

51	c	MGR028	Migraine with or Without Aura 1	67	0.109

52		HMP009	Haemophilus Influenzae	43	0.108

53		LVR012	Liver Cirrhosis	62	0.108

54		DWN001	Down Syndrome	70	0.108

55	P	HNT016	Huntington Disease	72	0.108

56	c	SVR001	Severe Acute Respiratory Syndrome	62	0.108

57	P	NRP001	Neuropathy	56	0.108

58		TTN003	Tetanus	65	0.107

59		PNG002	Pain Agnosia	51	0.107

60	P	HRT032	Heart Disease	75	0.107

61		CYT002	Cytokine Deficiency	42	0.106

62	P	ADN016	Adenocarcinoma	64	0.106

63	P	MJR001	Major Depressive Disorder	68	0.105

64		HYP066	Hyperglycemia	61	0.104

65		CRH001	Crohn's Disease	74	0.104

66	c	PCH010	Pachyonychia Congenita 3	44	0.103

67		DRM006	Dermatitis	61	0.102

68		CNS004	Constipation	58	0.102

69		CHL014	Cholera	59	0.102

70		LSH001	Leishmaniasis	63	0.101

71	P	KLZ004	Kala-Azar 1	41	0.101

72		HMN044	Human Immunodeficiency Virus Type 1	71	0.101

73	P	LTR001	Lateral Sclerosis	54	0.101

74	P	DMN002	Dementia	66	0.101

75	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.100

76		OCL069	Ocular Motor Apraxia	51	0.099

77	P	BLD134	Bladder Cancer	79	0.099

78		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.099

79		AGN016	Aging	56	0.099

80		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.099

81		SPN186	Spinal Cord Injury	60	0.098

82	P	OST002	Osteoporosis	74	0.098

83		BRN071	Brain Injury	49	0.098

84	P	PRK057	Parkinson Disease, Late-Onset	78	0.098

85	P	LVR013	Liver Disease	68	0.098

86		TRM010	Traumatic Brain Injury	51	0.097

87	P	DBT009	Diabetes Mellitus	64	0.097

88	P	PNM007	Pneumonia	68	0.097

89	P	ART022	Arthritis	69	0.096

90	P	EXN002	Exanthem	57	0.096

91	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.096

92	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.096

93		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.096

94	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.096

95		LPD008	Lipid Metabolism Disorder	62	0.096

96	P	ENC004	Encephalitis	61	0.096

97		LYM017	Lyme Disease	64	0.095

98		ANG054	Angina Pectoris	66	0.095

99	P	VSC007	Vascular Disease	63	0.094

100	P	PRP019	Peripheral Nervous System Disease	58	0.094

101	P	CHR345	Chronic Pain	44	0.093

102	P	HPT021	Hepatitis	67	0.093

103		GST045	Gastroenteritis	59	0.093

104		MDD011	Mood Disorder	62	0.093

105	P	DYS154	Dystonia	65	0.093

106	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.092

107		SKN016	Skin Disease	63	0.092

108	P	BPL003	Bipolar Disorder	56	0.092

109	P	MVM001	Movement Disease	63	0.092

110		PLG002	Plague	63	0.092

111		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.092

112		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.092

113		CHG001	Chagas Disease	66	0.091

114		PPT005	Peptic Ulcer Disease	59	0.091

115	P	THR014	Thrombocytopenia	67	0.091

116	P	HDC001	Headache	57	0.090

117	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.090

118	P	MLT020	Multiple Sclerosis	72	0.090

119		OST159	Osteogenic Sarcoma	66	0.090

120		HPT004	Hepatic Coma	45	0.090

121	c	MJR024	Major Affective Disorder 9	41	0.090

122	c	MJR022	Major Affective Disorder 8	38	0.090

123		BNR002	Bone Resorption Disease	48	0.089

124		SRC014	Sarcoma	65	0.089

125		HPT019	Hepatic Encephalopathy	60	0.089

126		SPN035	Spindle Cell Sarcoma	53	0.089

127		ACQ007	Acquired Immunodeficiency Syndrome	60	0.088

128	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.088

129	P	BCL017	B-Cell Lymphoma	58	0.088

130		SQM006	Squamous Cell Carcinoma	60	0.088

131		SVR004	Severe Combined Immunodeficiency	73	0.087

132		IMP005	Impotence	52	0.087

133		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.087

134		ULC004	Ulcerative Colitis	73	0.087

135		AMN003	Amnestic Disorder	54	0.087

136	P	EPL164	Epilepsy	71	0.086

137		LYM133	Lymphoma, Hodgkin, Classic	69	0.086

138		CRB039	Cerebrovascular Disease	67	0.086

139		ATH013	Atherosclerosis Susceptibility	65	0.086

140	P	MNN013	Meningitis	66	0.086

141	c	NRF023	Neurofibromatosis, Type Ii	80	0.086

142	c	HPT016	Hepatitis B	59	0.085

143		ANX004	Anoxia	40	0.085

144	P	MLN008	Melanoma	69	0.085

145		CRB004	Cerebral Artery Occlusion	45	0.084

146		OST012	Osteoarthritis	78	0.084

147	P	ALP008	Alopecia	54	0.084

148		STT001	Status Epilepticus	60	0.084

149		PSR001	Psoriatic Arthritis	61	0.084

150	P	GST053	Gastric Cancer	83	0.084

151	P	ATR011	Atrial Fibrillation	66	0.084

152	P	KDN017	Kidney Cancer	60	0.083

153	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.083

154		STR067	Stroke, Ischemic	81	0.083

155		STM007	Stomatitis	50	0.083

156	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.083

157		IRN002	Iron Metabolism Disease	57	0.082

158	c	SPN225	Spondyloarthropathy 1	73	0.082

159		ADN018	Adenoma	59	0.082

160		LWC001	Low Compliance Bladder	43	0.082

161	P	SKN015	Skin Carcinoma	66	0.082

162		DNT012	Dental Caries	53	0.082

163		47X002	47,xyy	49	0.082

164		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.082

165		PLY150	Polykaryocytosis Inducer	31	0.081

166	P	ASP006	Aspergillosis	69	0.081

167		OBS002	Obsessive-Compulsive Disorder	68	0.081

168		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.081

169	P	HYP086	Hypothyroidism	69	0.081

170		DRM011	Dermatophytosis	52	0.081

171	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.081

172	P	PRD008	Periodontitis	64	0.080

173		PLM001	Pulmonary Tuberculosis	69	0.080

174	P	CTR002	Cataract	60	0.080

175		AST005	Asthma	76	0.080

176		CYS001	Cystic Fibrosis	81	0.080

177		GST023	Gastric Ulcer	53	0.079

178		BRN028	Brain Cancer	74	0.079

179		PLM033	Pulmonary Embolism	59	0.079

180	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.079

181		TRD006	Tardive Dyskinesia	54	0.079

182	P	INF038	Influenza	68	0.079

183	P	SLP005	Sleep Disorder	59	0.079

184	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.078

185		CHC001	Chickenpox	60	0.078

186	P	DRM053	Dermatitis, Atopic	66	0.078

187		PRT036	Peritonitis	64	0.078

188		IRR002	Irritable Bowel Syndrome	65	0.077

189	P	AST007	Astrocytoma	51	0.077

190	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.077

191	P	FBR017	Fibrosarcoma	56	0.076

192	P	ATS364	Autism	70	0.076

193		SPS057	Spasticity	45	0.076

194	P	HYP076	Hyperthyroidism	55	0.075

195		WTH001	Withdrawal Disorder	48	0.075

196		BRN004	Brain Edema	56	0.075

197	P	UVT001	Uveitis	57	0.075

198		CVD001	Covid-19	44	0.075

199	P	CRD119	Cardiac Arrest	67	0.075

200	P	END033	Endocarditis	57	0.075

201	P	AMY004	Amyloidosis	70	0.074

202	P	CYS018	Cystitis	59	0.074

203	P	VSC011	Vasculitis	62	0.074

204		MLR004	Malaria	81	0.074

205	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.074

206	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.074

207	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.074

208	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.074

209	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.074

210	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.074

211	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.074

212	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.074

213	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.074

214	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.074

215		END040	Endogenous Depression	55	0.074

216	P	URT039	Urticaria	58	0.074

217		END057	Endometrial Cancer	74	0.073

218	P	GLM007	Glomerulonephritis	57	0.073

219		SFT003	Soft Tissue Sarcoma	56	0.073

220	P	PLY011	Polycystic Ovary Syndrome	56	0.073

221	c	LKM063	Leukemia, Chronic Myeloid	72	0.072

222		ORL011	Oral Cancer	60	0.072

223	P	ALC033	Alcohol Use Disorder	58	0.072

224	P	MCR115	Microvascular Complications of Diabetes 5	66	0.072

225		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.072

226		OVR094	Ovarian Epithelial Cancer	38	0.072

227	P	MYS003	Myasthenia Gravis	68	0.072

228		PRT058	Pure Autonomic Failure	59	0.072

229	P	TRN020	Turner Syndrome	67	0.072

230	P	HYD006	Hydrocephalus	66	0.072

231		VSC002	Vascular Dementia	57	0.071

232	P	INF032	Infertility	57	0.071

233		VCC001	Vaccinia	49	0.071

234	c	MLG068	Malignant Glioma	46	0.071

235		HYP060	Hyperinsulinism	54	0.071

236		HLX001	Helix Syndrome	47	0.071

237	P	MYP004	Myopathy	70	0.071

238	c	VRL010	Viral Hepatitis	52	0.070

239		PLM010	Pulmonary Edema	54	0.070

240		GT001	Gout	64	0.070

241		ANT024	Anthrax Disease	58	0.070

242		FTT001	Fatty Liver Disease	61	0.070

243	c	HPT003	Hepatitis a	62	0.070

244		DYS015	Dysentery	52	0.070

245	P	BNG032	Benign Mesothelioma	46	0.070

246	c	ATS007	Autism Spectrum Disorder	67	0.070

247		PRT013	Portal Hypertension	59	0.070

248		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.070

249		CNT047	Contact Dermatitis	58	0.070

250	P	GRF003	Graft-Versus-Host Disease	72	0.069

251	P	BND020	Bone Disease	59	0.069

252		HDN002	Head Injury	46	0.069

253		PRS045	Prostatic Hypertrophy	53	0.069

254		SBC016	Subacute Delirium	44	0.069

255	P	SBS003	Substance Abuse	55	0.069

256	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.069

257		MSL001	Measles	62	0.069

258		THY029	Thyroid Carcinoma	59	0.069

259		SCH014	Schistosomiasis	57	0.069

260		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.069

261		ESP021	Esophageal Cancer	90	0.069

262	P	TXP001	Toxoplasmosis	60	0.069

263		HYP005	Hypokalemia	55	0.068

264	P	HYP098	Hypereosinophilic Syndrome	67	0.068

265		MCL006	Macular Retinal Edema	55	0.068

266	P	DDN001	Duodenal Ulcer	52	0.068

267	P	HYP069	Hyperparathyroidism	63	0.068

268		PHN003	Phenylketonuria	75	0.068

269	P	RTN024	Retinoblastoma	73	0.068

270	c	FML008	Familial Retinoblastoma	53	0.068

271	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.068

272		ACT119	Acute Promyelocytic Leukemia	63	0.068

273	P	END044	Endometriosis	63	0.068

274		CHL068	Cholestasis	61	0.067

275	c	DWL002	Dowling-Degos Disease 1	58	0.067

276	P	PLM036	Pulmonary Fibrosis	65	0.067

277		OST017	Osteomyelitis	64	0.067

278	P	RCT021	Rectum Cancer	52	0.067

279		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.067

280		PRS021	Prostatic Adenoma	51	0.067

281		TRN015	Transient Cerebral Ischemia	63	0.067

282		NRT001	Neurotic Disorder	53	0.067

283	c	CHR064	Chronic Monocytic Leukemia	33	0.067

284	P	SRC025	Sarcoidosis 1	70	0.066

285	P	GST044	Gastritis	56	0.066

286		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.066

287	P	GLM040	Glioma Susceptibility 1	81	0.066

288		SKN019	Skin Melanoma	68	0.066

289		OST003	Osteonecrosis	61	0.066

290	c	MCR113	Microvascular Complications of Diabetes 3	52	0.066

291	c	MCR120	Microvascular Complications of Diabetes 7	47	0.066

292	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.066

293	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.066

294	P	RSP003	Respiratory Failure	74	0.066

295	c	MCR130	Microvascular Complications of Diabetes 6	41	0.066

296	c	MCR133	Microvascular Complications of Diabetes 4	41	0.066

297		RCK004	Rickets	68	0.065

298		PRS129	Prostatic Hyperplasia, Benign	49	0.065

299		HRP004	Herpes Zoster	60	0.065

300		MNT001	Mantle Cell Lymphoma	69	0.065

301	P	HMN010	Hemangioma	61	0.065

302		PST028	Post-Traumatic Stress Disorder	58	0.065

303		VRC005	Varicose Veins	60	0.065

304	c	ACT027	Acute Pancreatitis	60	0.065

305	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.065

306		SXL003	Sexual Disorder	47	0.065

307	P	PRS038	Personality Disorder	65	0.065

308		CTN007	Cutaneous Leishmaniasis	62	0.064

309	P	SPP010	Suppressor of Tumorigenicity 3	51	0.064

310		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.064

311		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	47	0.064

312	P	OVR082	Overgrowth Syndrome	50	0.064

313	P	NSP012	Nasopharyngeal Carcinoma	66	0.064

314	P	NPH012	Nephrotic Syndrome	60	0.064

315	P	TCD001	Tic Disorder	53	0.064

316	P	HMP007	Hemophilia	51	0.064

317		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.064

318		CRD223	Cardiac Arrhythmia	60	0.064

319		TRN018	Transitional Cell Carcinoma	56	0.064

320		PRP030	Purpura	54	0.064

321	P	ART023	Arthropathy	62	0.063

322		CHL065	Cholangiocarcinoma	68	0.063

323		PNC129	Pancreatic Adenocarcinoma	68	0.063

324	P	PNC044	Pancreatitis	61	0.063

325	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.063

326	c	BCT007	Bacterial Meningitis	55	0.063

327	P	MSC005	Muscular Dystrophy	66	0.063

328	c	PRC016	Pre-Eclampsia	63	0.063

329		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.063

330	c	ACT134	Acute Liver Failure	56	0.063

331	P	MTR014	Motor Neuron Disease	65	0.063

332		CHR073	Choreatic Disease	52	0.063

333	P	RHB003	Rhabdomyosarcoma	63	0.063

334		GNG013	Gingivitis	59	0.063

335		HMS001	Hemosiderosis	54	0.063

336		PPL022	Papilloma	54	0.063

337	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.063

338	P	ART005	Arteriovenous Malformation	65	0.063

339		ACT084	Acute Stress Disorder	47	0.063

340	P	PRN023	Prion Disease	57	0.063

341		ENT004	Enthesopathy	49	0.063

342		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.063

343		ALL014	Allergic Encephalomyelitis	38	0.062

344		INT079	Intrahepatic Cholangiocarcinoma	51	0.062

345		KPS004	Kaposi Sarcoma	75	0.062

346		DPH001	Diphtheria	60	0.062

347		SLP001	Sleeping Sickness	54	0.062

348	P	MYC033	Myoclonus	46	0.062

349	P	NRC002	Narcolepsy	52	0.062

350	P	MYC008	Myocarditis	59	0.062

351		DFF005	Diffuse Large B-Cell Lymphoma	55	0.062

352		HNS001	Hansen's Disease	34	0.062

353	P	MSC003	Muscular Atrophy	52	0.062

354	P	SLP006	Sleep Apnea	69	0.062

355		VRL011	Viral Infectious Disease	61	0.062

356	P	HYP265	Hypotonia	43	0.062

357	P	LPR021	Leprosy 3	69	0.061

358	P	RRH023	Rare Hereditary Hemochromatosis	41	0.061

359		INS024	Insulin-Like Growth Factor I	79	0.061

360		OTT002	Otitis Media	72	0.061

361	c	OVR114	Ovarian Cancer 1	38	0.061

362	P	ART021	Arteriosclerosis	54	0.061

363		CRD132	Cardiac Conduction Defect	58	0.061

364		PLS009	Plasma Cell Neoplasm	51	0.061

365		GRN017	Granulocytopenia	44	0.061

366		ILS001	Ileus	51	0.061

367	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.061

368		GLC003	Glucose Intolerance	54	0.061

369	P	PRP029	Porphyria	62	0.060

370		CRB037	Cerebral Palsy	69	0.060

371	P	PNC025	Panic Disorder	53	0.060

372	P	MDL005	Medulloblastoma	77	0.060

373		BRK010	Burkitt Lymphoma	67	0.060

374		ATX019	Ataxia with Vitamin E Deficiency	42	0.060

375	P	MLG074	Malignant Mesenchymoma	40	0.060

376		KRT006	Keratoconjunctivitis	53	0.060

377	P	CTN015	Cutaneous T Cell Lymphoma	49	0.060

378		SQM002	Squamous Cell Papilloma	46	0.060

379	P	THL005	Thalassemia	60	0.060

380	P	ATX030	Ataxia-Telangiectasia	82	0.059

381		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.059

382		SYN007	Synovitis	54	0.059

383		PLC002	Plica Syndrome	36	0.059

384		URM002	Uremia	49	0.059

385		DSS008	Disease of Mental Health	58	0.059

386		VSC003	Visceral Leishmaniasis	55	0.059

387	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.059

388		GST033	Gestational Diabetes	61	0.059

389		EMB004	Embryonal Carcinoma	56	0.059

390	c	DLT002	Dilated Cardiomyopathy	79	0.059

391	P	SYS005	Systemic Scleroderma	68	0.059

392	P	MYC084	Mycobacterium Tuberculosis 1	68	0.059

393	c	JVN061	Juvenile Arthritis	60	0.059

394		ERY051	Erythroleukemia, Familial	56	0.059

395	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.058

396		HYP014	Hyperuricemia	52	0.058

397		INT075	Intracranial Hypertension	53	0.058

398		KRT009	Keratosis	51	0.058

399	P	ECL001	Eclampsia	50	0.058

400	c	INV001	Invasive Aspergillosis	49	0.058

401	P	NRV007	Nervous System Disease	66	0.058

402		CRC021	Carcinosarcoma	62	0.058

403		NNL006	Non-Alcoholic Steatohepatitis	54	0.057

404	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.057

405		PST092	Posttransplant Acute Limbic Encephalitis	29	0.057

406		DBT010	Diabetic Neuropathy	54	0.057

407	c	HMP029	Hemophilia a	67	0.057

408	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.057

409		MYL005	Myelofibrosis	70	0.056

410		KHN001	Kuhnt-Junius Degeneration	47	0.056

411		ADG002	Audiogenic Seizures	25	0.056

412	c	FML001	Familial Atrial Fibrillation	65	0.056

413	P	HYP750	Hypertriglyceridemia, Familial	62	0.056

414		INT066	Interstitial Lung Disease	60	0.056

415		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.056

416		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.056

417		GST050	Gastrointestinal System Disease	56	0.056

418		INF034	Infective Endocarditis	53	0.056

419		HYP020	Hyperprolactinemia	64	0.056

420	c	INF145	Infantile Liver Failure Syndrome 1	50	0.056

421	P	HML002	Hemolytic Anemia	63	0.056

422	c	MST023	Mesothelioma, Malignant	57	0.056

423	P	PYL005	Pyelonephritis	56	0.056

424	P	INT068	Intestinal Disease	53	0.056

425	P	PTS002	Ptosis	53	0.056

426	c	SCL052	Scleroderma, Familial Progressive	61	0.056

427		DYS073	Dysphagia	50	0.056

428		RTN017	Retinal Detachment	61	0.055

429	P	DNG005	Dengue Virus	59	0.055

430		LYM027	Lymphopenia	58	0.055

431		CRN030	Coronary Stenosis	50	0.055

432	P	MYP006	Myopia	55	0.055

433		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.055

434		FBR047	Fibromyalgia	58	0.055

435		CRY005	Cryptococcosis	58	0.055

436	c	GLL024	Gallbladder Disease 1	53	0.055

437		SPL018	Splenomegaly	48	0.055

438		MXD026	Mixed Glioma	45	0.055

439	P	HYP061	Hypertrophic Cardiomyopathy	70	0.055

440		ATN005	Autonomic Dysfunction	46	0.055

441		LMY002	Leiomyoma	52	0.055

442	c	MCR129	Microvascular Complications of Diabetes 1	66	0.055

443		CYT008	Cytomegalovirus Infection	57	0.055

444		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.054

445	P	ADL010	Adult Respiratory Distress Syndrome	65	0.054

446		HMT002	Hematologic Cancer	62	0.054

447		DRM009	Dermatomycosis	36	0.054

448		PHR003	Pharyngitis	57	0.054

449	P	INS002	in Situ Carcinoma	53	0.054

450		CRH005	Crohn's Colitis	53	0.054

451	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.054

452		ALL006	Allergic Asthma	56	0.054

453	c	BRN108	Branchiootic Syndrome 1	62	0.054

454		PST021	Postpartum Depression	50	0.054

455		GLL008	Gilles De La Tourette Syndrome	66	0.054

456		CNN005	Connective Tissue Disease	68	0.054

457	c	DBT099	Diabetes Mellitus, Type I	65	0.054

458		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.054

459		GLS001	Gliosarcoma	54	0.054

460	P	MJR007	Major Affective Disorder 1	43	0.054

461	P	NRF002	Neurofibromatosis	56	0.053

462		ART016	Aortic Aneurysm	69	0.053

463	P	ESP024	Esophagitis	62	0.053

464		CHR100	Chronic Ulcer of Skin	55	0.053

465		ORL015	Oral Squamous Cell Carcinoma	43	0.053

466		NRR001	Neuroretinitis	42	0.053

467		DRG003	Drug Dependence	47	0.053

468	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.053

469		EWN003	Ewing Sarcoma	69	0.053

470		PSY004	Psychotic Disorder	67	0.053

471	P	PLY018	Polycythemia	56	0.053

472		CRD137	Cardiogenic Shock	47	0.053

473		TRP009	Triple X Syndrome	42	0.053

474		CHR066	Chronic Fatigue Syndrome	61	0.053

475		ETN001	Eating Disorder	60	0.053

476	c	CNT035	Central Nervous System Disease	52	0.053

477	c	INH020	Inherited Metabolic Disorder	47	0.053

478		CHR178	Chromosomal Triplication	35	0.053

479		FDB001	Foodborne Botulism	55	0.053

480		GST019	Gastrointestinal Stromal Tumor	78	0.053

481		NTR005	Nutritional Deficiency Disease	62	0.053

482	c	PSR028	Psoriasis 7	42	0.053

483		RYN005	Raynaud Phenomenon	47	0.053

484		RTN023	Retinitis	46	0.053

485		ANR007	Anorexia Nervosa	63	0.052

486	c	PSR017	Psoriasis 2	53	0.052

487	c	PSR023	Psoriasis 1	52	0.052

488	c	PSR032	Psoriasis 11	47	0.052

489		CHR074	Choriocarcinoma	47	0.052

490	c	PSR018	Psoriasis 13	41	0.052

491	c	MCR112	Microvascular Complications of Diabetes 2	41	0.052

492	P	TMP001	Temporal Lobe Epilepsy	50	0.052

493	P	RTN016	Retinal Degeneration	53	0.052

494	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.052

495		PLS011	Plasmacytoma	56	0.052

496		CCN001	Cocaine Dependence	48	0.052

497		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.052

498		FLL027	Fallopian Tube Carcinoma	67	0.052

499	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.052

500	P	CHL066	Cholangitis	51	0.052

501		MCR004	Macroglobulinemia	49	0.052

502		NRM005	Neuromuscular Disease	64	0.052

503	c	WLM018	Wilms Tumor 5	61	0.052

504		TND005	Tendinitis	54	0.052

505		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.052

506	c	BSL007	Basal Cell Carcinoma	68	0.052

507		BRN002	Bronchiolitis	59	0.052

508		TXC002	Toxic Encephalopathy	53	0.052

509	c	BCT013	Bacterial Pneumonia	48	0.052

510		SYN036	Syncope	45	0.052

511		TBC004	Tobacco Addiction	64	0.052

512	P	PRM006	Primary Biliary Cirrhosis	62	0.051

513	P	BRN022	Bronchiectasis	59	0.051

514		IGR001	Ige Responsiveness, Atopic	59	0.051

515		EXT034	Extrinsic Allergic Alveolitis	58	0.051

516	c	FLL041	Follicular Lymphoma 1	49	0.051

517		TST014	Testicular Cancer	46	0.051

518		BCK006	Back Pain	42	0.051

519		PPL052	Papillomatosis, Confluent and Reticulated	33	0.051

520		RBS001	Rabies	58	0.051

521		BLR008	Bilirubin Metabolic Disorder	57	0.051

522		MTN003	Motion Sickness	53	0.051

523		ATS010	Autosomal Recessive Disease	48	0.051

524		MYL031	Myeloproliferative Neoplasm	66	0.051

525		MTH009	Mouth Disease	56	0.051

526	c	FML035	Familial Hyperlipidemia	55	0.051

527	P	PMP001	Pemphigus	54	0.051

528	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.051

529		HYP025	Hyperphosphatemia	48	0.051

530		TNP001	Tinea Pedis	46	0.051

531	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.051

532		CRC006	Carcinoid Syndrome	55	0.051

533	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.051

534		HLC007	Helicobacter Pylori Infection	59	0.051

535		CLL003	Cellulitis	54	0.051

536	c	PRD040	Periodontitis, Chronic	53	0.051

537	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.051

538		ANV001	Anovulation	47	0.051

539	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.051

540		GST037	Gastroparesis	54	0.050

541		HYP081	Hypolipoproteinemia	51	0.050

542		49X006	49, Xxxxy Syndrome	41	0.050

543		ANG049	Angioedema Induced by Ace Inhibitors	40	0.050

544		PRM020	Premenstrual Tension	40	0.050

545		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.050

546		PTH003	Pathologic Nystagmus	52	0.050

547	c	MNN043	Meningioma, Familial	74	0.050

548	P	LMY004	Leiomyosarcoma	63	0.050

549		MNN042	Meningioma, Radiation-Induced	62	0.050

550		SPP011	Suppression of Tumorigenicity 12	59	0.050

551	P	PLY019	Polyneuropathy	56	0.050

552	P	RTN022	Retinal Vein Occlusion	53	0.050

553		SPN021	Spinal Meningioma	50	0.050

554		NWC001	Newcastle Disease	45	0.050

555		SCR001	Secretory Meningioma	41	0.050

556		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.050

557		FDL002	Food Allergy	51	0.050

558		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.050

559	c	GLC092	Glaucoma, Primary Open Angle	62	0.050

560	c	PNS012	Paine Syndrome	61	0.050

561	P	BNG030	Benign Ependymoma	60	0.050

562	P	ALP009	Alopecia Areata	60	0.050

563		CLL010	Cellular Ependymoma	54	0.050

564		AMN001	Amenorrhea	54	0.050

565		MDD018	Middle East Respiratory Syndrome	43	0.050

566	P	SNS001	Sensorineural Hearing Loss	60	0.050

567		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.049

568	c	ATM011	Autoimmune Hepatitis	63	0.049

569	P	INT143	Interstitial Cystitis	61	0.049

570		ATR057	Atrioventricular Block	55	0.049

571		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.049

572		RTC005	Reticulosarcoma	47	0.049

573		CNT033	Central Nervous System Cancer	47	0.049

574	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.049

575	c	INF071	Inflammatory Bowel Disease 1	67	0.049

576	P	BNC003	Bone Cancer	58	0.049

577		DSS009	Disseminated Intravascular Coagulation	57	0.049

578		HRT012	Heart Valve Disease	53	0.049

579	P	PRR002	Pure Red-Cell Aplasia	47	0.049

580		MSC157	Muscular Dystrophy, Duchenne Type	72	0.049

581	P	OLG002	Oligodendroglioma	67	0.049

582		CRT015	Carotid Artery Occlusion	45	0.049

583	P	DRM010	Dermatomyositis	61	0.049

584		PRS047	Prostatitis	56	0.049

585	P	MNC007	Monocytic Leukemia	53	0.049

586	P	HMR005	Hemorrhoid	46	0.049

587	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.049

588		RDC006	Red Cell Aplasia	43	0.049

589		DRG024	Drug Allergy	42	0.049

590		GST020	Gastric Antral Vascular Ectasia	41	0.049

591	P	SJG008	Sjogren Syndrome	61	0.048

592		HYP043	Hyperandrogenism	48	0.048

593		CRN017	Coronary Thrombosis	47	0.048

594	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.048

595		ATM052	Autoimmune Disease 1	37	0.048

596		BLM002	Bulimia Nervosa	57	0.048

597	P	PLY014	Polycystic Kidney Disease	62	0.048

598		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.048

599		RDC002	Radiculopathy	50	0.048

600		TND004	Tendinopathy	43	0.048

601	P	ESS003	Essential Thrombocythemia	68	0.048

602	P	LNG028	Long Qt Syndrome	66	0.048

603		APN008	Apnea, Obstructive Sleep	64	0.048

604		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.048

605		NWB001	Newborn Respiratory Distress Syndrome	58	0.048

606	P	MMP001	Mumps	58	0.048

607	c	VSC019	Vesicoureteral Reflux 1	57	0.048

608		TNS005	Tonsillitis	57	0.048

609		HMR039	Hemorrhage, Intracerebral	57	0.048

610		AYM001	Ayme-Gripp Syndrome	57	0.048

611		ACR041	Acromelic Frontonasal Dysostosis	52	0.048

612		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.048

613		CRN322	Coronavirus Infectious Disease	40	0.048

614	c	ESS001	Essential Tremor	56	0.048

615		MLT157	Multiple System Atrophy 1	70	0.047

616		PRC013	Pericarditis	54	0.047

617		GST040	Gastric Adenocarcinoma	70	0.047

618		PLY001	Polycythemia Vera	69	0.047

619	c	JVN004	Juvenile Myelomonocytic Leukemia	67	0.047

620	c	MCL013	Mucolipidosis Iv	66	0.047

621		THY122	Thyroid Gland Cancer	57	0.047

622		MRG003	Marginal Zone B-Cell Lymphoma	52	0.047

623		THR004	Thrombocytosis	51	0.047

624		PPL001	Papillary Adenoma	44	0.047

625	c	MJR008	Major Affective Disorder 2	35	0.047

626	c	MJR023	Major Affective Disorder 7	33	0.047

627	c	MJR003	Major Affective Disorder 6	33	0.047

628	c	MJR006	Major Affective Disorder 5	33	0.047

629	c	MJR004	Major Affective Disorder 4	28	0.047

630		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.047

631		ANG020	Angiosarcoma	64	0.047

632	P	LYM033	Lymphoproliferative Syndrome	59	0.047

633		LMB062	Limb Ischemia	55	0.047

634		SNS003	Sensory Peripheral Neuropathy	54	0.047

635		PRP036	Peripheral T-Cell Lymphoma	53	0.047

636		CRY014	Cryptococcal Meningitis	48	0.047

637	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.047

638		PLY068	Polysubstance Abuse	43	0.047

639		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.047

640		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.047

641	c	DNG003	Dengue Disease	59	0.047

642	P	RNL015	Renal Hypertension	47	0.047

643		RFR003	Refractive Error	43	0.047

644	P	MYS005	Myositis	56	0.047

645	c	GRV008	Graves Disease 1	56	0.047

646		NRN004	Neuroendocrine Tumor	55	0.047

647		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.047

648	P	HMR003	Hemorrhagic Disease	53	0.047

649		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.047

650	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	0.047

651		CCN002	Cocaine Abuse	49	0.047

652	P	EPN001	Ependymoblastoma	44	0.047

653		SMN007	Seminoma	43	0.047

654		OPD006	Opioid Addiction	48	0.046

655		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.046

656		CLF027	Cleft Palate, Isolated	64	0.046

657	c	BTT014	Beta-Thalassemia	74	0.046

658	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.046

659		HRY003	Hairy Cell Leukemia	55	0.046

660	P	ACT008	Actinic Keratosis	53	0.046

661		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.046

662		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.046

663		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.046

664	P	PRV006	Pervasive Developmental Disorder	57	0.046

665		PRV004	Periventricular Leukomalacia	52	0.046

666		NRF007	Neurofibroma	64	0.046

667		GRD007	Grade Iii Astrocytoma	59	0.046

668		ERY003	Erythema Multiforme	58	0.046

669	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.046

670	c	PRM092	Primary Lateral Sclerosis, Adult, 1	53	0.046

671		GSG001	Gas Gangrene	53	0.046

672		PLC008	Placenta Disease	50	0.046

673	c	PRM226	Primary Central Nervous System Lymphoma	48	0.046

674		MYF001	Myofibroma	45	0.046

675		APP009	Appendix Adenocarcinoma	44	0.046

676		CRB086	Cerebral Aneurysms	40	0.046

677		HDG004	Hodgkin's Granuloma	23	0.046

678		HDG006	Hodgkin's Paragranuloma	22	0.046

679		INS001	Insulinoma	60	0.046

680		LMY014	Leiomyoma, Uterine	56	0.046

681	P	RST001	Restless Legs Syndrome	54	0.046

682		HYP080	Hypogonadism	50	0.046

683		ADR007	Adrenoleukodystrophy	75	0.045

684		BRR014	Barrett Esophagus	65	0.045

685	P	THY023	Thymoma	65	0.045

686		BRS099	Breast Ductal Carcinoma	62	0.045

687	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.045

688	P	MLN007	Male Infertility	55	0.045

689		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.045

690	c	THY107	Thymoma, Familial	52	0.045

691	c	ALM001	Al Amyloidosis	50	0.045

692		AZS001	Azoospermia	50	0.045

693		OPT003	Opiate Dependence	50	0.045

694	c	CHR418	Chronic Leukemia	49	0.045

695		GST049	Gastrointestinal System Cancer	49	0.045

696		BCT004	Bacteriuria	49	0.045

697		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.045

698		GST071	Gastrointestinal Carcinoma	47	0.045

699		MNN020	Meningococcal Infection	46	0.045

700		CLN045	Colonic Benign Neoplasm	46	0.045

701		URL001	Urolithiasis	45	0.045

702		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.045

703		CRV045	Cervical Intraepithelial Neoplasia	39	0.045

704		GRM010	Germ Cells Tumors	34	0.045

705	P	SPN046	Spinal Muscular Atrophy	62	0.045

706		AVD001	Avoidant Personality Disorder	51	0.045

707		SBS004	Substance Dependence	48	0.045

708		DFN270	Deafness, Dystonia, and Cerebral Hypomyelination	48	0.045

709	P	CLS010	Cluster Headache	42	0.045

710		HND015	Hand Skill, Relative	33	0.045

711		HYP141	Hyperphenylalaninemia	39	0.045

712		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.045

713		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.045

714		BRN056	Bronchopulmonary Dysplasia	57	0.045

715		TCK001	Tick-Borne Encephalitis	56	0.045

716		PLS016	Plasma Cell Leukemia	53	0.045

717	P	SML001	Small Cell Carcinoma	52	0.045

718		FCT001	Factor Viii Deficiency	51	0.045

719		THR016	Thrombophlebitis	51	0.045

720		CYS014	Cystadenocarcinoma	51	0.045

721		ESP002	Esophageal Varix	51	0.045

722		SKN013	Skin Benign Neoplasm	51	0.045

723		HYP781	Hypoascorbemia	51	0.045

724		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	45	0.045

725		RST023	Resting Heart Rate, Variation in	41	0.045

726		PRS063	Paresthesia	41	0.045

727		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	35	0.045

728		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.045

729		LNG015	Lingual-Facial-Buccal Dyskinesia	50	0.045

730	P	FRN006	Frontotemporal Dementia	68	0.045

731	c	EXD008	Exudative Vitreoretinopathy 1	71	0.045

732	P	LPS002	Liposarcoma	65	0.045

733	c	WLM013	Wilms Tumor 1	65	0.045

734		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.045

735	P	TST021	Testicular Germ Cell Tumor	60	0.045

736		PMP006	Pemphigus Vulgaris, Familial	57	0.045

737	c	LKM070	Leukemia, Acute Monocytic	57	0.045

738		PNM008	Pneumothorax	56	0.045

739	P	LRY044	Larynx Cancer	55	0.045

740		PRP016	Paraplegia	52	0.045

741	P	MMB011	Membranous Nephropathy	50	0.045

742		RSP006	Respiratory System Disease	50	0.045

743		KRT001	Keratoconjunctivitis Sicca	49	0.045

744		CHL004	Cholelithiasis	49	0.045

745		NSS002	Neisseria Meningitidis Infection	47	0.045

746		IMM136	Immune System Disease	45	0.045

747		PTT009	Pituitary Gland Disease	54	0.044

748	P	MLG056	Malignant Hyperthermia	67	0.044

749		WLD007	Waldenstroem's Macroglobulinemia	61	0.044

750	P	SCL018	Scoliosis	60	0.044

751		INT030	Intracranial Aneurysm	56	0.044

752		DMY004	Demyelinating Disease	52	0.044

753	c	VRL005	Viral Pneumonia	52	0.044

754	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.044

755		ADR016	Adrenal Cortical Carcinoma	48	0.044

756		GRM005	Germ Cell Cancer	47	0.044

757		PRD004	Prediabetes Syndrome	47	0.044

758	P	MTH007	Methemoglobinemia	46	0.044

759		ORB013	Orbital Disease	42	0.044

760		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.044

761	c	PLY105	Polycystic Ovary Syndrome 1	38	0.044

762		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.044

763		MLG164	Malignant Epithelial Tumor of Ovary	26	0.044

764		HRP008	Herpes Simiae	25	0.044

765	P	FRG001	Fragile X Syndrome	70	0.044

766	P	MTC069	Mitochondrial Disorders	56	0.044

767		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.044

768	P	VNS003	Venous Insufficiency	55	0.044

769		CLR030	Clear Cell Renal Cell Carcinoma	53	0.044

770	P	CRN028	Corneal Ulcer	47	0.044

771		GST010	Gestational Trophoblastic Neoplasm	46	0.044

772	P	SBR004	Seborrheic Dermatitis	45	0.044

773		ADR004	Adrenal Cortical Adenocarcinoma	39	0.044

774		TRP005	Trophoblastic Neoplasm	38	0.044

775	c	WLM011	Wilms Tumor 6	37	0.044

776		RSP007	Respiratory Distress Syndrome, Infant	30	0.044

777		HML018	Homologous Wasting Disease	22	0.044

778		CMP010	Complex Regional Pain Syndrome	58	0.044

779		NRL004	Neuroleptic Malignant Syndrome	56	0.044

780		FCL014	Focal Epilepsy	54	0.044

781		DCB001	Decubitus Ulcer	61	0.043

782		IDP011	Idiopathic Interstitial Pneumonia	59	0.043

783		PGM001	Pigmented Villonodular Synovitis	56	0.043

784	P	STR020	Strabismus	55	0.043

785	P	CNT005	Central Nervous System Lymphoma	53	0.043

786		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.043

787		SRS001	Serous Cystadenocarcinoma	52	0.043

788		FSC004	Fasciitis	50	0.043

789		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.043

790		DRY001	Dry Eye Syndrome	47	0.043

791		LYM012	Lymphoplasmacytic Lymphoma	47	0.043

792		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	45	0.043

793		BNM001	Bone Marrow Cancer	43	0.043

794		MCH006	Mechanical Strabismus	42	0.043

795		PTT037	Pituitary Tumors	44	0.043

796	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.043

797		PSD088	Pseudobulbar Affect	36	0.043

798	P	DBT005	Diabetes Insipidus	55	0.043

799		BRD004	Borderline Personality Disorder	53	0.043

800		RTN003	Retinal Ischemia	50	0.043

801		CRB090	Cerebral Hypoxia	44	0.043

802	c	HMC039	Hemochromatosis, Type 1	74	0.043

803		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	65	0.043

804		MGK001	Megakaryocytic Leukemia	64	0.043

805		BRS051	Breast Disease	58	0.043

806	P	GLL018	Gallbladder Cancer	57	0.043

807		BRN012	Bronchiolitis Obliterans	55	0.043

808		ORP003	Oropharynx Cancer	55	0.043

809		NTR018	Neutrophilia, Hereditary	52	0.043

810		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.043

811		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.043

812		LPT006	Leptin Receptor Deficiency	48	0.043

813		SRT004	Serotonin Syndrome	47	0.043

814		PLS025	Plasmablastic Lymphoma	47	0.043

815	P	TST026	Testicular Germ Cell Cancer	43	0.043

816		DFF003	Diffuse Scleroderma	41	0.043

817	P	DNT007	Dentin Sensitivity	36	0.043

818		TMR016	Tumor Suppressor Gene on Chromosome 11	28	0.043

819		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.043

820		TRG002	Trigeminal Neuralgia	60	0.043

821		MYM001	Myoma	54	0.043

822	P	OVR049	Ovarian Disease	52	0.043

823		ATN004	Autonomic Neuropathy	45	0.043

824		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.043

825	c	ALP101	Alpha-Thalassemia	62	0.042

826		CHL067	Cholecystitis	57	0.042

827	c	BSL024	Basal Cell Carcinoma 1	56	0.042

828		HMG005	Hemoglobinopathy	56	0.042

829		HPT022	Hepatoblastoma	56	0.042

830	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.042

831		GNT002	Giant Cell Glioblastoma	50	0.042

832		INT067	Interstitial Nephritis	48	0.042

833		SMT001	Somatization Disorder	46	0.042

834		OPD001	Opioid Abuse	46	0.042

835		IMM064	Immunodeficiency, Common Variable, 10	44	0.042

836		HYP344	Hyperthyroidism, Familial Gestational	39	0.042

837		ACH005	Achalasia	51	0.042

838		ONC002	Onchocerciasis	52	0.042

839		ASP004	Asphyxia Neonatorum	46	0.042

840	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	62	0.042

841		ALC006	Alcoholic Hepatitis	61	0.042

842		APH001	Aphthous Stomatitis	57	0.042

843	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.042

844	P	BRN035	Brain Stem Glioma	52	0.042

845	P	HYP040	Hypospadias	51	0.042

846		HPT014	Hepatorenal Syndrome	50	0.042

847		ACT029	Acute Interstitial Pneumonia	49	0.042

848	c	HPT015	Hepatitis D	49	0.042

849		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.042

850	P	HMN032	Human Herpesvirus 8	47	0.042

851		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.042

852	c	CNG216	Congenital Hydrocephalus	47	0.042

853		CYN002	Cyanosis, Transient Neonatal	45	0.042

854	P	OCY003	Oocyte Maturation Defect 1	45	0.042

855		ANP009	Anaplastic Oligodendroglioma	43	0.042

856		MYL074	Myelodysplastic Syndrome with Excess Blasts	38	0.042

857	P	RTN008	Retinitis Pigmentosa	79	0.042

858		LRN003	Learning Disability	49	0.042

859		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	0.042

860	P	FTL001	Fetal Alcohol Syndrome	57	0.042

861		ADN011	Adenoid Cystic Carcinoma	70	0.041

862		SVR097	Severe Cutaneous Adverse Reaction	69	0.041

863	c	ART101	Aortic Valve Disease 2	65	0.041

864	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.041

865		ING001	Inguinal Hernia	60	0.041

866		IRN001	Iron Deficiency Anemia	59	0.041

867		ADR005	Adrenal Carcinoma	58	0.041

868	P	GLL020	Gallbladder Disease	57	0.041

869		BRD001	Brody Myopathy	57	0.041

870		PLM012	Pulmonary Sarcoidosis	53	0.041

871	c	HRD202	Hereditary Lymphedema I	50	0.041

872		NTR046	Neutrophil Migration	50	0.041

873		PRL017	Prolymphocytic Leukemia	47	0.041

874		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.041

875	c	DRM054	Dermatitis, Atopic, 2	44	0.041

876	P	BCT020	Bacteremia 2	44	0.041

877	c	SRC023	Sarcoidosis 2	43	0.041

878		ENT001	Enterocele	39	0.041

879		ERY066	Erythema Multiforme Major	30	0.041

880	c	TST046	Testicular Germ Cell Tumor 1	29	0.041

881	P	RTT002	Rett Syndrome	80	0.041

882	P	BRB001	Beriberi	46	0.041

883	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.041

884	P	MST009	Mastocytosis	64	0.041

885		APP008	Appendicitis	61	0.041

886	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.041

887		SRC027	Sarcoma, Synovial	58	0.041

888	P	PLY041	Polymyositis	57	0.041

889	P	CHN012	Chondrosarcoma	56	0.041

890		CRT017	Cartilage Disease	54	0.041

891		MCN017	Meconium Ileus	52	0.041

892	c	PRM012	Primary Polycythemia	50	0.041

893	c	THR090	Thrombocythemia 1	49	0.041

894		RYN001	Raynaud Disease	48	0.041

895		CLS016	Clostridium Difficile Colitis	48	0.041

896		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	47	0.041

897		BRN032	Brain Glioma	45	0.041

898		PRT035	Peritoneum Cancer	44	0.041

899	P	AVS003	Avascular Necrosis	42	0.041

900	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.041

901		ENC065	Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization	33	0.041

902		CLS052	Classic Hairy Cell Leukemia	27	0.041

903	P	PRD037	Periodontal Ehlers-Danlos Syndrome	45	0.041

904	P	CNG001	Congenital Myasthenic Syndrome	66	0.041

905	P	BLD062	Bile Duct Cancer	67	0.041

906		ACR006	Aceruloplasminemia	65	0.041

907		CNG510	Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi	64	0.041

908	c	LPM012	Lipomatosis, Multiple	60	0.041

909		APL002	Aplasia of Lacrimal and Salivary Glands	57	0.041

910		NRT004	Neuritis	52	0.041

911		CRT016	Carotid Artery Disease	52	0.041

912		HPR003	Heparin-Induced Thrombocytopenia	48	0.041

913	P	BLD051	Blood Coagulation Disease	46	0.041

914		CLL014	Cll/sll	45	0.041

915		CYS009	Cystadenoma	44	0.041

916		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.041

917		RFR002	Refractory Hairy Cell Leukemia	33	0.041

918	P	VSC018	Visceral Steatosis	33	0.041

919		VLV047	Volvulus of Midgut	49	0.040

920		STF001	Stiff-Person Syndrome	60	0.040

921		MLN003	Melancholia	38	0.040

922	P	CLC063	Celiac Disease 1	66	0.040

923	c	CHR417	Chronic Graft Versus Host Disease	57	0.040

924		EPT010	Epithelial-Myoepithelial Carcinoma	55	0.040

925		URN010	Urinary Tract Obstruction	55	0.040

926		BRN014	Bronchopneumonia	54	0.040

927		ACT200	Acute Monoblastic Leukemia	52	0.040

928		SPL004	Splenic Marginal Zone Lymphoma	51	0.040

929		TNG007	Tongue Carcinoma	51	0.040

930		PNM005	Pneumonic Plague	51	0.040

931		LNG020	Lung Oat Cell Carcinoma	47	0.040

932		OBS003	Obsessive-Compulsive Personality Disorder	46	0.040

933		PST048	Postural Orthostatic Tachycardia Syndrome	45	0.040

934		HMR023	Hemorrhagic Cystitis	45	0.040

935		OVR112	Ovarian Germ Cell Cancer	45	0.040

936	P	ATX024	Ataxia-Oculomotor Apraxia 3	44	0.040

937	P	CRN024	Corneal Disease	44	0.040

938		SKN005	Skin Atrophy	43	0.040

939		BLR013	Biliary Tract Cancer	42	0.040

940		UTR043	Uterine Sarcoma	39	0.040

941	P	INT260	Intracranial Berry Aneurysm	39	0.040

942		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.040

943	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.040

944		MNR012	Meniere Disease	57	0.040

945		HPT046	Hepatic Veno-Occlusive Disease	56	0.040

946		SPN041	Spinal Cord Disease	56	0.040

947	P	ACT010	Acth-Secreting Pituitary Adenoma	55	0.040

948		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.040

949		IFP001	Ifap Syndrome with or Without Bresheck Syndrome	51	0.040

950		ACT017	Acute Chest Syndrome	51	0.040

951		CRT013	Carotid Stenosis	50	0.040

952		STT002	Status Asthmaticus	50	0.040

953		INT054	Intraocular Lymphoma	48	0.040

954		ACT098	Acute Erythroid Leukemia	48	0.040

955		PLL012	Pollen Allergy	46	0.040

956		EXT010	Extramedullary Plasmacytoma	45	0.040

957		CNT017	Central Nervous System Origin Vertigo	45	0.040

958		GNG003	Gingival Recession	44	0.040

959	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.040

960		IDP033	Idiopathic Edema	44	0.040

961	P	CRN026	Corneal Edema	43	0.040

962		URG005	Uruguay Faciocardiomusculoskeletal Syndrome	40	0.040

963		JVN026	Jeavons Syndrome	24	0.040

964		ADS004	Aids Dementia Complex	40	0.039

965	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.039

966	P	NJM001	Nijmegen Breakage Syndrome	74	0.039

967		THY111	Thyroid Carcinoma, Familial Medullary	67	0.039

968		PRT010	Parathyroid Carcinoma	67	0.039

969		MYX005	Myxoid Liposarcoma	66	0.039

970		CRN036	Craniopharyngioma	65	0.039

971		PRM126	Primary Peritoneal Carcinoma	62	0.039

972	P	ORT004	Orthostatic Intolerance	62	0.039

973		MSS001	Masa Syndrome	62	0.039

974	c	HRD002	Hereditary Angioedema	60	0.039

975	P	SLV026	Salivary Gland Carcinoma	57	0.039

976		NRG002	Neurogenic Bladder	55	0.039

977	P	ANT006	Antiphospholipid Syndrome	55	0.039

978	P	PTT006	Pituitary Adenoma	55	0.039

979		MYP159	Myopathy, Proximal, with Ophthalmoplegia	55	0.039

980	P	ORL007	Oral Cavity Cancer	53	0.039

981	P	PRC012	Pericardial Effusion	51	0.039

982	P	THR015	Thrombophilia	51	0.039

983		CHL018	Childhood Medulloblastoma	49	0.039

984		STP011	Stapes Ankylosis with Broad Thumbs and Toes	49	0.039

985		CHL061	Childhood Leukemia	48	0.039

986	P	SCL015	Scleritis	48	0.039

987		HMP001	Hemopericardium	48	0.039

988		KRT008	Keratopathy	47	0.039

989	c	ORT011	Orthostatic Hypotension 1	44	0.039

990		MCR011	Microinvasive Gastric Cancer	43	0.039

991		MCN008	Mucinous Cystadenocarcinoma	40	0.039

992		FML039	Female Reproductive System Disease	39	0.039

993	c	ADL008	Adult Oligodendroglioma	34	0.039

994		LRY047	Laryngeal Abductor Paralysis	28	0.039

995		LSC001	Lesch-Nyhan Syndrome	62	0.039

996		HYP264	Hypertonia	38	0.039

997	P	OLV001	Olivopontocerebellar Atrophy	51	0.039

998		CRP001	Carpal Tunnel Syndrome	67	0.039

999		HYD002	Hydronephrosis	60	0.039

1000		SPN027	Spinal Stenosis	59	0.039

1001		HMT008	Hematuria, Benign Familial	56	0.039

1002	P	DYS193	Dystonia 11, Myoclonic	55	0.039

1003	P	SPN052	Spondyloarthropathy	54	0.039

1004	P	CRB194	Cerebroretinal Microangiopathy with Calcifications and Cysts 1	53	0.039

1005	P	KRT007	Keratoconus	50	0.039

1006		HRT011	Heart Septal Defect	50	0.039

1007	c	INF023	Inflammatory Breast Carcinoma	50	0.039

1008		VRR004	Verrucous Carcinoma	49	0.039

1009		HDR003	Hidradenitis	49	0.039

1010		QDR001	Quadriplegia	48	0.039

1011		CRC014	Carcinoid Tumors, Intestinal	47	0.039

1012		MYC005	Myocardial Stunning	46	0.039

1013		ANP006	Anaplastic Ependymoma	46	0.039

1014		INT253	Intestinal Benign Neoplasm	45	0.039

1015		ORL013	Oral Lichen Planus	45	0.039

1016		CHL149	Childhood Acute Myeloid Leukemia	44	0.039

1017		SPR008	Supratentorial Primitive Neuroectodermal Tumor	43	0.039

1018		DBT002	Diabetic Autonomic Neuropathy	41	0.039

1019	P	ECT045	Ectodermal Dysplasia-Syndactyly Syndrome 1	39	0.039

1020		SWL001	Swallowing Disorders	38	0.039

1021		TST043	Testicular Seminoma	35	0.039

1022		PDT014	Pediatric Ependymoma	32	0.039

1023		TMP019	Temporomandibular Joint Anomaly	28	0.039

1024	P	CNT036	Central Nervous System Germ Cell Tumor	28	0.039

1025		HMP005	Hemiplegia	55	0.038

1026	c	DMN023	Diamond-Blackfan Anemia 1	53	0.038

1027	c	CRS016	Crisponi/cold-Induced Sweating Syndrome 1	52	0.038

1028		ADT003	Auditory System Disease	48	0.038

1029	c	ATM075	Autoimmune Encephalitis	38	0.038

1030	c	NRF024	Neurofibromatosis, Type I	77	0.038

1031	P	MLN066	Melanoma, Cutaneous Malignant 1	70	0.038

1032		INC002	Inclusion Body Myositis	58	0.038

1033		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.038

1034		ANG005	Anogenital Venereal Wart	55	0.038

1035		FLR002	Filariasis	55	0.038

1036		RHM028	Rheumatic Heart Disease	53	0.038

1037		LYS002	Lysosomal Storage Disease	52	0.038

1038		PPT001	Peptic Esophagitis	52	0.038

1039	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.038

1040		THY125	Thyroid Gland Medullary Carcinoma	50	0.038

1041		HMG002	Hemoglobinuria	50	0.038

1042		GYN001	Gynecomastia	49	0.038

1043	c	BPL002	Bipolar I Disorder	49	0.038

1044		MNN028	Mononeuropathy of the Median Nerve, Mild	46	0.038

1045		CRP002	Croup	44	0.038

1046		DMP001	Dumping Syndrome	44	0.038

1047	c	MLG064	Malignant Ependymoma	41	0.038

1048		KLD004	Keloid Disorder	40	0.038

1049		PLC009	Placenta Praevia	39	0.038

1050	P	CRN133	Coronary Artery Disease, Autosomal Dominant, 1	32	0.038

1051		INF021	Infant Gynecomastia	31	0.038

1052		STT009	Sutton Disease 2	30	0.038

1053	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.038

1054		FNT004	Fainting	30	0.038

1055		BRN049	Brain Tumor, Childhood	29	0.038

1056		FTL073	Fetal Anticonvulsant Syndrome	26	0.038

1057		CYS005	Cysticercosis	53	0.038

1058		MTC005	Mitochondrial Metabolism Disease	49	0.038

1059		HPT085	Hepatitis, Fulminant Viral	32	0.038

1060		NRL016	Neural Tube Defects	82	0.038

1061		MRF001	Marfan Syndrome	77	0.038

1062	c	TBR025	Tuberous Sclerosis 1	77	0.038

1063	P	ANR048	Aniridia 1	63	0.038

1064		CHN016	Cohen Syndrome	63	0.038

1065		PRG017	Paraganglioma and Gastric Stromal Sarcoma	61	0.038

1066		PNM010	Pneumothorax, Primary Spontaneous	60	0.038

1067		RHM001	Rheumatic Fever	60	0.038