Search results for 15(S)-HETE

2177 hits were found for 15(S)-HETE

#	Family	MCID	Name	MIFTS	Score
1		PRT014	Protein S Deficiency	44	0.246

2	c	HPT016	Hepatitis B	59	0.168

3	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.167

4		SCH014	Schistosomiasis	57	0.164

5		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.163

6		HLX001	Helix Syndrome	47	0.161

7	P	LKM002	Leukemia	68	0.160

8		LYM133	Lymphoma, Hodgkin, Classic	69	0.159

9		47X002	47,xyy	49	0.156

10	P	DRR001	Diarrhea	55	0.155

11	P	MYL006	Myeloid Leukemia	60	0.155

12	P	LVR013	Liver Disease	68	0.152

13	P	BLD134	Bladder Cancer	79	0.152

14	P	NRB001	Neuroblastoma	72	0.150

15	P	THL005	Thalassemia	60	0.150

16		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.149

17	P	LYM118	Lymphoma	68	0.147

18		DPR016	Depression	63	0.144

19	P	ALZ034	Alzheimer Disease	88	0.143

20		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.141

21		CHR178	Chromosomal Triplication	35	0.140

22	P	ADN016	Adenocarcinoma	64	0.140

23		ACT119	Acute Promyelocytic Leukemia	63	0.140

24		BRK010	Burkitt Lymphoma	67	0.137

25		MNT002	Mental Depression	58	0.135

26	c	LKM061	Leukemia, Acute Myeloid	84	0.132

27	P	HPT023	Hepatocellular Carcinoma	100	0.131

28	P	OVR042	Ovarian Cancer	88	0.130

29	P	TRN020	Turner Syndrome	67	0.129

30		ATM095	Autoimmune Disease	62	0.129

31		CRH001	Crohn's Disease	74	0.128

32	P	SCK005	Sickle Cell Disease	50	0.127

33		THR024	Thrombosis	57	0.127

34		DWN001	Down Syndrome	70	0.126

35	P	UVT001	Uveitis	57	0.126

36	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.125

37		EWN003	Ewing Sarcoma	69	0.125

38	P	HRP006	Herpes Simplex	65	0.123

39	P	RTN024	Retinoblastoma	73	0.123

40		HMN044	Human Immunodeficiency Virus Type 1	71	0.121

41	c	FML008	Familial Retinoblastoma	53	0.120

42		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.120

43		HRW001	Hair Whorl	36	0.120

44		SCK003	Sickle Cell Anemia	74	0.120

45		ADL002	Adult Syndrome	70	0.118

46	P	MJR001	Major Depressive Disorder	68	0.118

47	P	GST053	Gastric Cancer	83	0.117

48	P	ATX030	Ataxia-Telangiectasia	82	0.116

49		TLN003	Telangiectasis	52	0.116

50		PNG002	Pain Agnosia	51	0.115

51		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.115

52		ISC004	Ischemia	58	0.115

53	c	SVR001	Severe Acute Respiratory Syndrome	62	0.114

54		DNT012	Dental Caries	53	0.114

55		ALL026	Allergic Hypersensitivity Disease	62	0.114

56	P	END033	Endocarditis	57	0.114

57	P	PRD006	Prader-Willi Syndrome	59	0.113

58	P	KDN018	Kidney Disease	72	0.113

59	P	THR015	Thrombophilia	51	0.112

60	P	VSC007	Vascular Disease	63	0.111

61	P	NTR004	Neutropenia	63	0.108

62		TYP007	Typhoid Fever	63	0.108

63		BRR014	Barrett Esophagus	65	0.108

64		OST012	Osteoarthritis	78	0.108

65		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.107

66	P	HPT021	Hepatitis	67	0.107

67		CRB039	Cerebrovascular Disease	67	0.107

68		DFC004	Deficiency Anemia	70	0.106

69		GLL048	Glial Tumor	45	0.106

70		SPN035	Spindle Cell Sarcoma	53	0.106

71	P	GLM045	Glioma	63	0.106

72	P	CTR002	Cataract	60	0.105

73	P	PRK057	Parkinson Disease, Late-Onset	78	0.105

74		CHL014	Cholera	59	0.105

75	c	SYS001	Systemic Lupus Erythematosus	86	0.105

76		SQM006	Squamous Cell Carcinoma	60	0.105

77	P	DBT009	Diabetes Mellitus	64	0.104

78		MLR004	Malaria	81	0.104

79		LPP008	Lipoprotein Quantitative Trait Locus	62	0.104

80		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.103

81	P	ANG001	Angelman Syndrome	69	0.103

82		MYL069	Myeloma, Multiple	85	0.102

83		SRC014	Sarcoma	65	0.102

84	c	PRC016	Pre-Eclampsia	63	0.101

85		PLM033	Pulmonary Embolism	59	0.101

86		TXC005	Toxic Shock Syndrome	62	0.101

87	c	PNS012	Paine Syndrome	61	0.100

88	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.100

89		PRP030	Purpura	54	0.100

90	c	SML038	Small Cell Cancer of the Lung	65	0.100

91		HMP009	Haemophilus Influenzae	43	0.099

92		HMG005	Hemoglobinopathy	56	0.099

93		THY029	Thyroid Carcinoma	59	0.099

94	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.098

95		CHL068	Cholestasis	61	0.098

96		CHC001	Chickenpox	60	0.098

97		PRT036	Peritonitis	64	0.098

98		AST005	Asthma	76	0.098

99	P	NRP001	Neuropathy	56	0.097

100	P	SZR006	Seizure Disorder	56	0.097

101		STR067	Stroke, Ischemic	81	0.097

102	P	INF032	Infertility	57	0.097

103		GLB015	Glioblastoma Multiforme	75	0.096

104	P	CHR345	Chronic Pain	44	0.096

105		OST159	Osteogenic Sarcoma	66	0.096

106	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.096

107	c	BTT014	Beta-Thalassemia	74	0.096

108		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.095

109	P	BCL017	B-Cell Lymphoma	58	0.095

110	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.095

111		CRV035	Cervical Cancer	76	0.095

112		ALC007	Alcohol Dependence	66	0.094

113		ULC004	Ulcerative Colitis	73	0.094

114		GST045	Gastroenteritis	59	0.094

115		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.094

116	P	CRN300	Coronary Heart Disease 1	63	0.094

117		CYS001	Cystic Fibrosis	81	0.094

118	P	TRM003	Tremor	54	0.093

119	P	LPS004	Lupus Erythematosus	61	0.092

120	P	VSC011	Vasculitis	62	0.092

121		CYT002	Cytokine Deficiency	42	0.092

122	P	MNN013	Meningitis	66	0.092

123	P	THR014	Thrombocytopenia	67	0.091

124		PST011	Pustulosis of Palm and Sole	52	0.091

125		ANX010	Anxiety	73	0.091

126		IMM167	Immune Deficiency Disease	78	0.091

127		ATX019	Ataxia with Vitamin E Deficiency	42	0.091

128	P	RHM011	Rheumatoid Arthritis	80	0.091

129		ENH001	Enhanced S-Cone Syndrome	57	0.090

130	P	PNM007	Pneumonia	68	0.090

131	P	SCL018	Scoliosis	60	0.089

132	P	SLM003	Salmonellosis	55	0.089

133		VSL002	Visual Epilepsy	59	0.089

134	P	INF038	Influenza	68	0.089

135	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.089

136	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.089

137		END086	End Stage Renal Disease	51	0.089

138		MSL001	Measles	62	0.088

139		ART140	Arteries, Anomalies of	52	0.088

140		TTN003	Tetanus	65	0.088

141		RTN023	Retinitis	46	0.087

142		NRR001	Neuroretinitis	42	0.087

143		MYL009	Myelodysplastic Syndrome	70	0.086

144		HYP056	Hypoglycemia	66	0.086

145	c	HPT073	Hepatitis C Virus	72	0.086

146	c	RHB024	Rhabdomyosarcoma 2	67	0.086

147	P	PLM037	Pulmonary Hypertension	67	0.086

148	c	HPT003	Hepatitis a	62	0.086

149	P	CRD119	Cardiac Arrest	67	0.086

150		DPH001	Diphtheria	60	0.085

151		HMC014	Homocysteinemia	53	0.085

152		BCT022	Bacterial Infectious Disease	56	0.085

153		END040	Endogenous Depression	55	0.085

154		SVR004	Severe Combined Immunodeficiency	73	0.085

155	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.085

156	P	HYP265	Hypotonia	43	0.085

157		HNS001	Hansen's Disease	34	0.085

158		CVD001	Covid-19	44	0.085

159	P	DMN002	Dementia	66	0.084

160	P	EXN002	Exanthem	57	0.084

161	c	PRM038	Primary Agammaglobulinemia	44	0.084

162	P	HYP086	Hypothyroidism	69	0.084

163		DSS009	Disseminated Intravascular Coagulation	57	0.084

164	c	CHR684	Chronic Kidney Disease	70	0.084

165	P	LPR021	Leprosy 3	69	0.083

166		HYP066	Hyperglycemia	61	0.083

167	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.082

168		LYM019	Lymphosarcoma	46	0.082

169	c	SPN225	Spondyloarthropathy 1	73	0.082

170		ANR007	Anorexia Nervosa	63	0.082

171		ACQ007	Acquired Immunodeficiency Syndrome	60	0.082

172		NRT001	Neurotic Disorder	53	0.082

173		FTT001	Fatty Liver Disease	61	0.082

174	c	ACT073	Acute Leukemia	58	0.081

175		ANR040	Aneurysm	59	0.081

176	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.081

177		ESP021	Esophageal Cancer	90	0.081

178		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.081

179		CLT003	Colitis	62	0.081

180		PRS045	Prostatic Hypertrophy	53	0.081

181	P	ENC018	Encephalopathy	61	0.081

182	P	NPH012	Nephrotic Syndrome	60	0.080

183		MST005	Mastitis	53	0.080

184		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.079

185	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.079

186	c	ACT075	Acute Myocardial Infarction	57	0.079

187	P	ATS364	Autism	70	0.079

188	P	ENC004	Encephalitis	61	0.079

189		SPL018	Splenomegaly	48	0.079

190		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.079

191	P	ALC033	Alcohol Use Disorder	58	0.079

192	P	RSP003	Respiratory Failure	74	0.079

193	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.079

194	P	LTR001	Lateral Sclerosis	54	0.078

195	P	HYP098	Hypereosinophilic Syndrome	67	0.078

196		ANG054	Angina Pectoris	66	0.078

197	P	RBL001	Rubella	59	0.078

198	P	MCR010	Microcephaly	59	0.078

199		OTT002	Otitis Media	72	0.078

200	P	DRM053	Dermatitis, Atopic	66	0.078

201	P	EPL164	Epilepsy	71	0.078

202	P	SKN015	Skin Carcinoma	66	0.077

203	P	HDC001	Headache	57	0.077

204	P	HRS035	Hirschsprung Disease 1	65	0.077

205		PRS021	Prostatic Adenoma	51	0.076

206	P	PHC003	Pheochromocytoma	71	0.076

207		GST092	Gastroesophageal Reflux	67	0.076

208		INF034	Infective Endocarditis	53	0.076

209		PRT011	Protein C Deficiency	44	0.076

210	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.076

211		PLM001	Pulmonary Tuberculosis	69	0.076

212	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.075

213	P	END044	Endometriosis	63	0.075

214		PLS011	Plasmacytoma	56	0.075

215	P	RNG032	Ring Chromosome	42	0.075

216		BCK006	Back Pain	42	0.075

217	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.075

218	P	RTN008	Retinitis Pigmentosa	79	0.075

219	P	MYP004	Myopathy	70	0.075

220	P	MLT020	Multiple Sclerosis	72	0.075

221		RSC001	Rosacea	54	0.075

222		VLV047	Volvulus of Midgut	49	0.074

223		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.074

224	P	ANR048	Aniridia 1	63	0.074

225		THR013	Thoracic Outlet Syndrome	54	0.074

226		FBR047	Fibromyalgia	58	0.074

227	P	SYP003	Syphilis	58	0.074

228	c	MGR028	Migraine with or Without Aura 1	67	0.074

229	P	PRD008	Periodontitis	64	0.074

230		LSH001	Leishmaniasis	63	0.073

231	P	KLZ004	Kala-Azar 1	41	0.073

232		IRN002	Iron Metabolism Disease	57	0.073

233		OST017	Osteomyelitis	64	0.073

234		TRN018	Transitional Cell Carcinoma	56	0.073

235		LPD008	Lipid Metabolism Disorder	62	0.073

236		IMP005	Impotence	52	0.073

237		ADR040	Adrenal Gland Pheochromocytoma	46	0.073

238		ORL011	Oral Cancer	60	0.073

239	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.073

240	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.073

241	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.073

242	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.073

243	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.073

244	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.073

245	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.073

246	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.073

247	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.073

248	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.073

249	c	HPT001	Hepatitis C	62	0.073

250	P	AST007	Astrocytoma	51	0.073

251		PLM031	Poliomyelitis	64	0.073

252	P	ECL001	Eclampsia	50	0.073

253		ACN002	Acanthosis Nigricans	60	0.073

254	c	ATR087	Atrial Standstill 1	75	0.073

255		PRS129	Prostatic Hyperplasia, Benign	49	0.073

256		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.072

257		OCL069	Ocular Motor Apraxia	51	0.072

258		DYS073	Dysphagia	50	0.072

259		HRT011	Heart Septal Defect	50	0.072

260		BRR002	Barrett's Adenocarcinoma	36	0.072

261		STM007	Stomatitis	50	0.072

262		END057	Endometrial Cancer	74	0.072

263		NTR005	Nutritional Deficiency Disease	62	0.072

264		AGN016	Aging	56	0.072

265	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.072

266	P	HNT016	Huntington Disease	72	0.072

267	c	BRN108	Branchiootic Syndrome 1	62	0.071

268		PPT005	Peptic Ulcer Disease	59	0.071

269	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.071

270		ATX010	Ataxia Neuropathy Spectrum	34	0.071

271		ACT064	Acute Necrotizing Encephalitis	33	0.071

272		BLD137	Blood Group--Ahonen	16	0.071

273	c	BSL007	Basal Cell Carcinoma	68	0.071

274	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.071

275	P	SRC025	Sarcoidosis 1	70	0.071

276	P	BPL003	Bipolar Disorder	56	0.070

277	P	RTN016	Retinal Degeneration	53	0.070

278	c	MCR113	Microvascular Complications of Diabetes 3	52	0.070

279	c	ACT068	Acute Cystitis	63	0.070

280	P	FBR017	Fibrosarcoma	56	0.070

281	c	ALP101	Alpha-Thalassemia	62	0.070

282	P	MCR115	Microvascular Complications of Diabetes 5	66	0.069

283	P	SCH015	Schizophrenia	74	0.069

284		DSS008	Disease of Mental Health	58	0.069

285	c	MJR024	Major Affective Disorder 9	41	0.069

286	c	MJR022	Major Affective Disorder 8	38	0.069

287	c	ACT027	Acute Pancreatitis	60	0.068

288		CHL079	Children's Interstitial Lung Disease	26	0.068

289		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.068

290	c	LKM005	Leukemia, T-Cell, Chronic	34	0.068

291	P	LNG064	Lung Cancer Susceptibility 3	78	0.068

292		PPL052	Papillomatosis, Confluent and Reticulated	33	0.068

293		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.068

294	P	PLM036	Pulmonary Fibrosis	65	0.068

295	c	MCR120	Microvascular Complications of Diabetes 7	47	0.068

296	c	MCR130	Microvascular Complications of Diabetes 6	41	0.068

297	c	MCR133	Microvascular Complications of Diabetes 4	41	0.068

298	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.068

299	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.068

300	P	THY032	Thyroiditis	52	0.067

301	P	MSC005	Muscular Dystrophy	66	0.067

302	P	HMP007	Hemophilia	51	0.067

303	P	RHN004	Rhinitis	57	0.067

304		KPS004	Kaposi Sarcoma	75	0.067

305	P	APL001	Aplastic Anemia	74	0.067

306		PPL022	Papilloma	54	0.066

307	P	NSP012	Nasopharyngeal Carcinoma	66	0.066

308		RHM001	Rheumatic Fever	60	0.066

309	c	DLT002	Dilated Cardiomyopathy	79	0.066

310		CRD132	Cardiac Conduction Defect	58	0.066

311	P	HYP076	Hyperthyroidism	55	0.066

312	c	ATS007	Autism Spectrum Disorder	67	0.066

313	P	ATR011	Atrial Fibrillation	66	0.066

314	P	PRS038	Personality Disorder	65	0.066

315		ADP007	Adie Pupil	39	0.065

316	P	OVR082	Overgrowth Syndrome	50	0.065

317		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.065

318		BNR002	Bone Resorption Disease	48	0.065

319		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.065

320		GST023	Gastric Ulcer	53	0.065

321	P	GRF003	Graft-Versus-Host Disease	72	0.065

322		SPN186	Spinal Cord Injury	60	0.065

323	c	ACT071	Acute Kidney Failure	60	0.065

324	P	HYP061	Hypertrophic Cardiomyopathy	70	0.065

325	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.065

326	P	HYP069	Hyperparathyroidism	63	0.065

327	P	PLY019	Polyneuropathy	56	0.065

328		DFF005	Diffuse Large B-Cell Lymphoma	55	0.064

329	P	OPN001	Open-Angle Glaucoma	49	0.064

330	P	GST044	Gastritis	56	0.064

331	P	CHL066	Cholangitis	51	0.064

332		PSY004	Psychotic Disorder	67	0.064

333		CHL123	Chlamydia	59	0.064

334	P	PRP034	Purpura Fulminans	43	0.064

335		AMN003	Amnestic Disorder	54	0.064

336		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.064

337		DYS015	Dysentery	52	0.064

338		CHL065	Cholangiocarcinoma	68	0.064

339		ORL015	Oral Squamous Cell Carcinoma	43	0.064

340	P	KDN017	Kidney Cancer	60	0.064

341		IGR001	Ige Responsiveness, Atopic	59	0.063

342		ATS010	Autosomal Recessive Disease	48	0.063

343	P	RHB003	Rhabdomyosarcoma	63	0.063

344	c	NRF023	Neurofibromatosis, Type Ii	80	0.063

345		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.063

346	P	MMP001	Mumps	58	0.063

347		HRP004	Herpes Zoster	60	0.063

348		CHG001	Chagas Disease	66	0.063

349		SQM002	Squamous Cell Papilloma	46	0.063

350		HNM002	Hinman Syndrome	27	0.063

351	P	HYD006	Hydrocephalus	66	0.062

352	P	FML011	Familial Adenomatous Polyposis	72	0.062

353		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.062

354	P	CNR004	Cone-Rod Dystrophy 2	73	0.062

355	P	DYS154	Dystonia	65	0.062

356		APH002	Aphasia	57	0.062

357	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.062

358	P	INS002	in Situ Carcinoma	53	0.062

359		CRH005	Crohn's Colitis	53	0.062

360	P	PRP019	Peripheral Nervous System Disease	58	0.062

361		HPT082	Hepatic Adenomas, Familial	44	0.062

362		VRC005	Varicose Veins	60	0.062

363		PHR003	Pharyngitis	57	0.062

364		INT079	Intrahepatic Cholangiocarcinoma	51	0.062

365	P	HMN010	Hemangioma	61	0.062

366		ONC002	Onchocerciasis	52	0.061

367		TBC004	Tobacco Addiction	64	0.061

368		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.061

369	P	MYS005	Myositis	56	0.061

370	P	VNT002	Ventricular Septal Defect	60	0.061

371		HDN002	Head Injury	46	0.061

372	P	MSC003	Muscular Atrophy	52	0.061

373	P	DDN001	Duodenal Ulcer	52	0.061

374		INT007	Intermediate Coronary Syndrome	55	0.061

375	c	VRL010	Viral Hepatitis	52	0.061

376	P	BNG032	Benign Mesothelioma	46	0.061

377	P	ANT006	Antiphospholipid Syndrome	55	0.061

378		OST003	Osteonecrosis	61	0.061

379	P	TXP001	Toxoplasmosis	60	0.061

380		CNS004	Constipation	58	0.061

381		INS024	Insulin-Like Growth Factor I	79	0.061

382		KHL003	Kohlschutter-Tonz Syndrome	65	0.061

383		OVR094	Ovarian Epithelial Cancer	38	0.061

384		MDD011	Mood Disorder	62	0.060

385		SFT003	Soft Tissue Sarcoma	56	0.060

386	P	AMY004	Amyloidosis	70	0.060

387		INT017	Intestinal Schistosomiasis	48	0.060

388		MDD018	Middle East Respiratory Syndrome	43	0.059

389		SPN051	Spondylitis	51	0.059

390	P	MYP006	Myopia	55	0.059

391		AMN001	Amenorrhea	54	0.059

392		HMS001	Hemosiderosis	54	0.059

393	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.059

394	P	MLN007	Male Infertility	55	0.059

395		RTN017	Retinal Detachment	61	0.059

396		EYD002	Eye Disease	58	0.059

397		IDP070	Idiopathic Scoliosis	42	0.059

398		CLF027	Cleft Palate, Isolated	64	0.059

399		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.059

400	P	TRT010	Teratoma	52	0.058

401	P	OST002	Osteoporosis	74	0.058

402		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.058

403	c	SCL052	Scleroderma, Familial Progressive	61	0.058

404		INF009	Inflammatory Spondylopathy	31	0.058

405	P	SLP006	Sleep Apnea	69	0.058

406		ALL003	Allergic Rhinitis	67	0.058

407		GST040	Gastric Adenocarcinoma	70	0.058

408		ART016	Aortic Aneurysm	69	0.058

409	P	AXN002	Axenfeld-Rieger Syndrome	59	0.058

410	P	HML002	Hemolytic Anemia	63	0.058

411	P	CYS018	Cystitis	59	0.058

412		ANT024	Anthrax Disease	58	0.058

413	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.057

414		PRT013	Portal Hypertension	59	0.057

415		CNN005	Connective Tissue Disease	68	0.057

416		RCK004	Rickets	68	0.057

417	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.057

418		ENT011	Enterocolitis	51	0.057

419	P	NRF002	Neurofibromatosis	56	0.057

420		SYN036	Syncope	45	0.057

421	P	RRH023	Rare Hereditary Hemochromatosis	41	0.057

422		HYP080	Hypogonadism	50	0.057

423		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.057

424		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.057

425	P	PNC044	Pancreatitis	61	0.057

426		ALL006	Allergic Asthma	56	0.057

427	P	SPP010	Suppressor of Tumorigenicity 3	51	0.057

428	P	CND004	Candidiasis	58	0.056

429	c	DBT099	Diabetes Mellitus, Type I	65	0.056

430	c	INF071	Inflammatory Bowel Disease 1	67	0.056

431		PLY150	Polykaryocytosis Inducer	31	0.056

432		ALP103	Alpha-1-Antitrypsin Deficiency	64	0.056

433		SMN007	Seminoma	43	0.056

434		AND002	Androgen Insensitivity Syndrome	66	0.056

435		PRT018	Portal Vein Thrombosis	50	0.056

436		WLL004	Wallerian Degeneration	39	0.056

437	P	SBS003	Substance Abuse	55	0.055

438	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.055

439		GT001	Gout	64	0.055

440		PNC001	Pancytopenia	54	0.055

441		NNL006	Non-Alcoholic Steatohepatitis	54	0.055

442		INT075	Intracranial Hypertension	53	0.055

443		PRP027	Peripheral Vascular Disease	71	0.055

444		CRB037	Cerebral Palsy	69	0.055

445	c	WLM018	Wilms Tumor 5	61	0.055

446		ALL014	Allergic Encephalomyelitis	38	0.055

447		PNM008	Pneumothorax	56	0.055

448	P	RCT021	Rectum Cancer	52	0.055

449	P	MYS003	Myasthenia Gravis	68	0.055

450		ALR002	Al-Raqad Syndrome	33	0.054

451		PST053	Postherpetic Neuralgia	40	0.054

452		ETN001	Eating Disorder	60	0.054

453		PTH003	Pathologic Nystagmus	52	0.054

454	P	MDL005	Medulloblastoma	77	0.054

455		ENT004	Enthesopathy	49	0.054

456	P	ASP006	Aspergillosis	69	0.054

457	P	ART023	Arthropathy	62	0.054

458	P	BRN022	Bronchiectasis	59	0.054

459		TRY001	Trypanosomiasis	50	0.053

460	P	NGH001	Night Blindness	48	0.053

461	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.053

462		CYT008	Cytomegalovirus Infection	57	0.053

463	P	INT070	Intestinal Obstruction	58	0.053

464	P	ALP106	Alport Syndrome 1, X-Linked	55	0.053

465		CLF001	Cleft Lip	53	0.053

466		SPT004	Septic Arthritis	58	0.053

467	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.053

468		HLC007	Helicobacter Pylori Infection	59	0.053

469		KRT019	Keratitis, Hereditary	65	0.053

470		RHM028	Rheumatic Heart Disease	53	0.053

471	c	MNN043	Meningioma, Familial	74	0.053

472		ANX004	Anoxia	40	0.053

473		TRN015	Transient Cerebral Ischemia	63	0.053

474	P	SML001	Small Cell Carcinoma	52	0.053

475	P	MYC008	Myocarditis	59	0.052

476	P	TBR001	Tuberous Sclerosis	70	0.052

477		FSC004	Fasciitis	50	0.052

478		CLN015	Colon Adenocarcinoma	65	0.052

479	P	LRY044	Larynx Cancer	55	0.052

480	P	PRP029	Porphyria	62	0.052

481		PST092	Posttransplant Acute Limbic Encephalitis	29	0.052

482	P	TTR001	Tetralogy of Fallot	70	0.052

483	P	SYS005	Systemic Scleroderma	68	0.052

484	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.052

485		PTT037	Pituitary Tumors	44	0.052

486		LPT014	Leptin Deficiency or Dysfunction	74	0.052

487		GST033	Gestational Diabetes	61	0.052

488		MCS002	Mucositis	56	0.052

489		LWC001	Low Compliance Bladder	43	0.052

490		MNN042	Meningioma, Radiation-Induced	62	0.051

491		SPN021	Spinal Meningioma	50	0.051

492		THR016	Thrombophlebitis	51	0.051

493		ERY003	Erythema Multiforme	58	0.051

494		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.051

495	P	ART021	Arteriosclerosis	54	0.051

496		URM002	Uremia	49	0.051

497	P	MYC084	Mycobacterium Tuberculosis 1	68	0.051

498	P	END047	Endophthalmitis	53	0.051

499	P	URT039	Urticaria	58	0.051

500	c	ACT134	Acute Liver Failure	56	0.051

501	P	PTS002	Ptosis	53	0.051

502	c	GLC092	Glaucoma, Primary Open Angle	62	0.051

503	P	PRM006	Primary Biliary Cirrhosis	62	0.051

504	P	PLY018	Polycythemia	56	0.051

505		GLC003	Glucose Intolerance	54	0.051

506		CLL003	Cellulitis	54	0.051

507		PPT001	Peptic Esophagitis	52	0.051

508		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.051

509		HYD002	Hydronephrosis	60	0.051

510	P	GLL022	Guillain-Barre Syndrome	59	0.051

511	c	DWL002	Dowling-Degos Disease 1	58	0.051

512		KRT009	Keratosis	51	0.050

513		INT066	Interstitial Lung Disease	60	0.050

514		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.050

515		SCR001	Secretory Meningioma	41	0.050

516		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.050

517		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.050

518		LYM017	Lyme Disease	64	0.050

519	P	MVM001	Movement Disease	63	0.050

520	P	RTN018	Retinal Disease	53	0.050

521	P	SCL057	Scoliosis, Isolated 1	41	0.050

522	c	EXD008	Exudative Vitreoretinopathy 1	71	0.050

523		ECH003	Echinococcosis	53	0.050

524		SVR097	Severe Cutaneous Adverse Reaction	69	0.050

525	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	35	0.050

526		PRP016	Paraplegia	52	0.050

527		FLR002	Filariasis	55	0.050

528		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.050

529	c	GLL024	Gallbladder Disease 1	53	0.050

530	P	FRD001	Friedreich Ataxia	64	0.049

531		NRL016	Neural Tube Defects	82	0.049

532		GTR002	Goiter	53	0.049

533		SKN019	Skin Melanoma	68	0.049

534	P	STR020	Strabismus	55	0.049

535		MCH006	Mechanical Strabismus	42	0.049

536		CRN030	Coronary Stenosis	50	0.049

537		SBC016	Subacute Delirium	44	0.049

538	P	HYP750	Hypertriglyceridemia, Familial	62	0.049

539	c	PST005	Posterior Uveitis	54	0.049

540		HRL004	Hurler-Scheie Syndrome	55	0.049

541		MYF002	Myofascial Pain Syndrome	42	0.049

542	P	ALP008	Alopecia	54	0.049

543		RYN005	Raynaud Phenomenon	47	0.049

544	P	CLC063	Celiac Disease 1	66	0.048

545		PLS009	Plasma Cell Neoplasm	51	0.048

546	P	PLY011	Polycystic Ovary Syndrome	56	0.048

547		WST005	West Nile Virus	54	0.048

548		CHL004	Cholelithiasis	49	0.048

549	c	ACT135	Acute Graft Versus Host Disease	52	0.048

550		ERY066	Erythema Multiforme Major	30	0.048

551		BRC012	Brucellosis	64	0.048

552	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.048

553		HPT022	Hepatoblastoma	56	0.048

554		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.048

555		LYM040	Lymphoblastic Lymphoma	54	0.048

556	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.048

557		PLG002	Plague	63	0.048

558	P	PLY014	Polycystic Kidney Disease	62	0.048

559	P	LMY004	Leiomyosarcoma	63	0.048

560		PSR001	Psoriatic Arthritis	61	0.048

561	P	ADL017	Adult T-Cell Leukemia	56	0.048

562		SCH036	Scheie Syndrome	72	0.047

563	P	HMC002	Homocystinuria	53	0.047

564	P	CNJ013	Conjunctivitis	65	0.047

565		ILS001	Ileus	51	0.047

566		PHN003	Phenylketonuria	75	0.047

567		APP008	Appendicitis	61	0.047

568		DBL002	Double Outlet Right Ventricle	56	0.047

569		ACT084	Acute Stress Disorder	47	0.047

570		KRT013	Keratolytic Winter Erythema	46	0.047

571	P	BND020	Bone Disease	59	0.047

572		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.047

573		ALB002	Albinism	46	0.047

574	P	AVS003	Avascular Necrosis	42	0.047

575	c	ATM011	Autoimmune Hepatitis	63	0.047

576	P	PNC025	Panic Disorder	53	0.047

577	P	THY023	Thymoma	65	0.047

578		CHL067	Cholecystitis	57	0.047

579	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.047

580	P	GRV001	Graves' Disease	55	0.047

581		HRT012	Heart Valve Disease	53	0.047

582	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.047

583		ING001	Inguinal Hernia	60	0.047

584		PLM010	Pulmonary Edema	54	0.047

585	P	GLL018	Gallbladder Cancer	57	0.047

586		CTN007	Cutaneous Leishmaniasis	62	0.047

587	P	MTR003	Mitral Valve Stenosis	50	0.047

588		ART001	Arterial Tortuosity Syndrome	66	0.047

589		NSS002	Neisseria Meningitidis Infection	47	0.047

590	P	DBT005	Diabetes Insipidus	55	0.047

591	P	FLL037	Follicular Lymphoma	67	0.046

592	c	MLG084	Malignant Fibrous Histiocytoma	63	0.046

593		NND010	Nondisjunction	34	0.046

594		PLS007	Plasmodium Falciparum Malaria	52	0.046

595		AZS001	Azoospermia	50	0.046

596		KWS002	Kawasaki Disease	65	0.046

597		CLR108	Colorectal Adenoma	64	0.046

598		PST028	Post-Traumatic Stress Disorder	58	0.046

599		HYP005	Hypokalemia	55	0.046

600		NRT004	Neuritis	52	0.046

601	P	MMB011	Membranous Nephropathy	50	0.046

602		GNG013	Gingivitis	59	0.046

603		RBS001	Rabies	58	0.046

604		MCL006	Macular Retinal Edema	55	0.046

605		IRD001	Iridocyclitis	53	0.046

606		YLL002	Yellow Fever	61	0.046

607		HND015	Hand Skill, Relative	33	0.046

608	P	DNG005	Dengue Virus	59	0.046

609	c	THY107	Thymoma, Familial	52	0.046

610		LMY002	Leiomyoma	52	0.046

611		49X006	49, Xxxxy Syndrome	41	0.046

612		SHG001	Shigellosis	60	0.046

613	P	INT099	Intrahepatic Cholestasis of Pregnancy	51	0.046

614	P	SLP005	Sleep Disorder	59	0.046

615	P	SNS001	Sensorineural Hearing Loss	60	0.046

616	P	PYL005	Pyelonephritis	56	0.046

617		PRC013	Pericarditis	54	0.046

618	c	HMP029	Hemophilia a	67	0.045

619		CCC001	Coccidioidomycosis	58	0.045

620		SYN007	Synovitis	54	0.045

621		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.045

622		PLC002	Plica Syndrome	36	0.045

623		HYP748	Hypertelorism	50	0.045

624		OBS002	Obsessive-Compulsive Disorder	68	0.045

625	P	NRV007	Nervous System Disease	66	0.045

626	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.045

627	P	GND004	Gonadal Dysgenesis	48	0.045

628		VSC002	Vascular Dementia	57	0.045

629		SLP001	Sleeping Sickness	54	0.045

630		PFF001	Pfeiffer Syndrome	79	0.045

631		PLY001	Polycythemia Vera	69	0.045

632		CRD137	Cardiogenic Shock	47	0.045

633		BLR008	Bilirubin Metabolic Disorder	57	0.045

634		FDL002	Food Allergy	51	0.045

635		VTM033	Vitamin K Deficiency Bleeding	48	0.045

636		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.045

637		SCB001	Scabies	50	0.045

638		TST014	Testicular Cancer	46	0.045

639	P	CRN037	Craniosynostosis	68	0.044

640		INS001	Insulinoma	60	0.044

641		MNN009	Meningoencephalitis	49	0.044

642		ART002	Arts Syndrome	64	0.044

643		BRN056	Bronchopulmonary Dysplasia	57	0.044

644		GRN017	Granulocytopenia	44	0.044

645	c	FML001	Familial Atrial Fibrillation	65	0.044

646	P	ART005	Arteriovenous Malformation	65	0.044

647		CHR074	Choriocarcinoma	47	0.044

648		RFR003	Refractive Error	43	0.044

649	c	FML035	Familial Hyperlipidemia	55	0.044

650		ART074	Aortic Dissection	52	0.044

651	c	HMP004	Hemophilia B	68	0.044

652		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.044

653		HST010	Histiocytosis	48	0.044

654		PRN019	Perinatal Necrotizing Enterocolitis	59	0.044

655		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.044

656		ATR057	Atrioventricular Block	55	0.044

657		PLC008	Placenta Disease	50	0.043

658		AST006	Astigmatism	47	0.043

659		KRT002	Keratomalacia	47	0.043

660		FCL012	Facial Paralysis	46	0.043

661	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.043

662	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.043

663		VRL011	Viral Infectious Disease	61	0.043

664		DCT002	Ductal Carcinoma in Situ	59	0.043

665		GST010	Gestational Trophoblastic Neoplasm	46	0.043

666	c	CHR064	Chronic Monocytic Leukemia	33	0.043

667		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.043

668		MYL005	Myelofibrosis	70	0.043

669		NRL005	Neurilemmoma	60	0.043

670		ANS003	Anisakiasis	40	0.043

671	P	RTN022	Retinal Vein Occlusion	53	0.043

672		VRC001	Varicocele	49	0.043

673		ACR007	Acromegaly	71	0.042

674		HMP005	Hemiplegia	55	0.042

675		HYP014	Hyperuricemia	52	0.042

676	P	CHN012	Chondrosarcoma	56	0.042

677	c	HMC039	Hemochromatosis, Type 1	74	0.042

678	P	OPT009	Optic Neuritis	57	0.042

679		HYP060	Hyperinsulinism	54	0.042

680	P	EPD016	Epidermolysis Bullosa	53	0.042

681	P	DVL012	Developmental Dysplasia of the Hip 1	38	0.042

682	P	ADL010	Adult Respiratory Distress Syndrome	65	0.042

683		BCT004	Bacteriuria	49	0.042

684	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.042

685	P	MTC069	Mitochondrial Disorders	56	0.042

686		TTR011	Tetraploidy	47	0.042

687		WRN001	Werner Syndrome	69	0.042

688		DCB001	Decubitus Ulcer	61	0.042

689	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.042

690		AVN001	Avian Influenza	59	0.042

691		PLR007	Pleural Empyema	50	0.042

692		SXL003	Sexual Disorder	47	0.042

693	P	SPN046	Spinal Muscular Atrophy	62	0.042

694		MRF001	Marfan Syndrome	77	0.042

695	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.042

696		STT001	Status Epilepticus	60	0.041

697	P	PMP001	Pemphigus	54	0.041

698		SPN019	Spondylolisthesis	51	0.041

699		NCR007	Necrotizing Fasciitis	48	0.041

700		PYD002	Pyoderma	50	0.041

701		NPH009	Nephrolithiasis	55	0.041

702		PPL002	Papillary Carcinoma	47	0.041

703		SPS057	Spasticity	45	0.041

704		MYC088	Mycobacterium Avium Complex Infections	29	0.041

705		AND005	Androgen Insensitivity Syndrome, Mild	19	0.041

706		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	58	0.041

707	c	HPT015	Hepatitis D	49	0.041

708		BDD001	Budd-Chiari Syndrome	63	0.041

709	P	SJG008	Sjogren Syndrome	61	0.041

710		EMB004	Embryonal Carcinoma	56	0.041

711		PLY100	Polyploidy	40	0.041

712	c	OVR114	Ovarian Cancer 1	38	0.041

713		PNC129	Pancreatic Adenocarcinoma	68	0.041

714	P	MLN069	Melanoma, Uveal	59	0.041

715	c	ART101	Aortic Valve Disease 2	65	0.040

716	c	WLM013	Wilms Tumor 1	65	0.040

717		LMB062	Limb Ischemia	55	0.040

718	P	DXT004	Dextro-Looped Transposition of the Great Arteries	54	0.040

719		DMY004	Demyelinating Disease	52	0.040

720		CRV045	Cervical Intraepithelial Neoplasia	39	0.040

721		KRN002	Kearns-Sayre Syndrome	63	0.040

722		CYN002	Cyanosis, Transient Neonatal	45	0.040

723	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.040

724	P	PLY006	Polydactyly	59	0.040

725	c	PRM005	Primary Hyperparathyroidism	58	0.040

726		FLR001	Filarial Elephantiasis	55	0.040

727	P	PLM034	Pulmonary Emphysema	55	0.040

728		KRT006	Keratoconjunctivitis	53	0.040

729	P	HYP040	Hypospadias	51	0.040

730	c	MLG068	Malignant Glioma	46	0.040

731	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.040

732	c	DNG003	Dengue Disease	59	0.040

733	c	FTL067	Fetal Hemoglobin Quantitative Trait Locus 6	28	0.040

734	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.040

735		MTH009	Mouth Disease	56	0.040

736	P	MNC007	Monocytic Leukemia	53	0.040

737		RTN001	Retinal Vasculitis	47	0.040

738		BNG077	Benign Idiopathic Neonatal Seizures	26	0.040

739		MSC157	Muscular Dystrophy, Duchenne Type	72	0.040

740	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.040

741	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.040

742		CRT013	Carotid Stenosis	50	0.039

743	P	TMP001	Temporal Lobe Epilepsy	50	0.039

744		FSC002	Fascioliasis	42	0.039

745	c	MST023	Mesothelioma, Malignant	57	0.039

746		VSC003	Visceral Leishmaniasis	55	0.039

747	c	BCT007	Bacterial Meningitis	55	0.039

748		PRP080	Peripheral Artery Disease	53	0.039

749		THR004	Thrombocytosis	51	0.039

750		HPT004	Hepatic Coma	45	0.039

751	P	MTR014	Motor Neuron Disease	65	0.039

752		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.039

753		CYS005	Cysticercosis	53	0.039

754	P	PRN023	Prion Disease	57	0.039

755	c	HMG029	Hemoglobin Se Disease	39	0.039

756		STN013	Stenotrophomonas Maltophilia Infection	25	0.039

757		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.039

758		THY111	Thyroid Carcinoma, Familial Medullary	67	0.039

759		THY030	Thyroid Gland Disease	52	0.039

760		SPS019	Spastic Paraparesis	38	0.039

761	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.039

762		HSH003	Hashimoto Thyroiditis	62	0.039

763		THY122	Thyroid Gland Cancer	57	0.039

764		TRC023	Trichinosis	53	0.039

765	c	SCN007	Secondary Hyperparathyroidism	51	0.039

766		CHR078	Chorioretinitis	50	0.039

767		LPR001	Lepromatous Leprosy	50	0.039

768	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.039

769		SCR015	Scarlet Fever	39	0.039

770		MTY003	Mutyh Polyposis	30	0.039

771		LYM009	Lymphocytic Choriomeningitis	47	0.038

772		LKP003	Leukoplakia	39	0.038

773	P	KRT007	Keratoconus	50	0.038

774	P	ART018	Aortic Valve Insufficiency	49	0.038

775		CMP010	Complex Regional Pain Syndrome	58	0.038

776		BRN002	Bronchiolitis	59	0.038

777		ANK001	Ankylosis	51	0.038

778	c	MTR002	Mitral Valve Insufficiency	48	0.038

779		NRG002	Neurogenic Bladder	55	0.038

780		INT051	Intussusception	53	0.038

781	P	PLV020	Pelvic Organ Prolapse	57	0.038

782	P	MYM013	Moyamoya Disease 1	57	0.038

783	P	HML001	Hemolytic-Uremic Syndrome	53	0.038

784	c	INH030	Inherited Retinal Disorder	51	0.038

785		DWR001	Dwarfism	44	0.038

786		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.038

787		MTB004	Metabolic Acidosis	50	0.037

788		MCR004	Macroglobulinemia	49	0.037

789	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.037

790		ALL010	Allergic Contact Dermatitis	56	0.037

791		OCL006	Ocular Hypertension	53	0.037

792		ACT017	Acute Chest Syndrome	51	0.037

793		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.037

794	P	FML018	Familial Mediterranean Fever	73	0.037

795	P	ORT004	Orthostatic Intolerance	62	0.037

796		INT002	Intermittent Claudication	61	0.037

797		IRN001	Iron Deficiency Anemia	59	0.037

798	P	PRC019	Precocious Puberty	46	0.037

799		TTH006	Tooth Disease	46	0.037

800	P	MYC033	Myoclonus	46	0.037

801		URL001	Urolithiasis	45	0.037

802	c	MCR129	Microvascular Complications of Diabetes 1	66	0.037

803	P	CCK001	Cockayne Syndrome	66	0.037

804		BRS099	Breast Ductal Carcinoma	62	0.037

805	P	EHL001	Ehlers-Danlos Syndrome	58	0.037

806		TNS005	Tonsillitis	57	0.037

807		AVD001	Avoidant Personality Disorder	51	0.037

808	c	SVR005	Severe Pre-Eclampsia	50	0.037

809		OPT003	Opiate Dependence	50	0.037

810		ADR016	Adrenal Cortical Carcinoma	48	0.037

811	c	INH020	Inherited Metabolic Disorder	47	0.037

812		CRT015	Carotid Artery Occlusion	45	0.037

813	c	BCT013	Bacterial Pneumonia	48	0.037

814	P	PRG013	Paraganglioma	52	0.037

815		FBR054	Fibroma	44	0.037

816	P	RRT020	Rare Tumor	41	0.037

817	P	MLT074	Multiple Endocrine Neoplasia	56	0.036

818	P	CRC039	Coarctation of Aorta	47	0.036

819	P	ATR010	Atrial Heart Septal Defect	60	0.036

820	c	ACR116	Aicardi-Goutieres Syndrome 1	52	0.036

821	P	GLM040	Glioma Susceptibility 1	81	0.036

822	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.036

823		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.036

824	P	HRD011	Hereditary Spherocytosis	60	0.036

825		INC002	Inclusion Body Myositis	58	0.036

826		VTM002	Vitamin B12 Deficiency	48	0.036

827	P	BNG030	Benign Ependymoma	60	0.036

828		HPT019	Hepatic Encephalopathy	60	0.036

829		SCH003	Schizophreniform Disorder	56	0.036

830		PRS047	Prostatitis	56	0.036

831		SLC006	Silicosis	56	0.036

832		NRN004	Neuroendocrine Tumor	55	0.036

833		CLL010	Cellular Ependymoma	54	0.036

834	P	RNL017	Renal Oncocytoma	53	0.036

835		CHR073	Choreatic Disease	52	0.036

836		OST011	Osteomalacia	52	0.036

837	P	CMP008	Compartment Syndrome	49	0.036

838		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	47	0.036

839		ATN005	Autonomic Dysfunction	46	0.036

840		IRR002	Irritable Bowel Syndrome	65	0.036

841		GLS018	Glass Syndrome	57	0.036

842		FND002	Fundus Dystrophy	55	0.036

843	P	FRG001	Fragile X Syndrome	70	0.036

844		MNT001	Mantle Cell Lymphoma	69	0.036

845		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.036

846		LGN006	Legionnaire Disease	52	0.036

847		THY125	Thyroid Gland Medullary Carcinoma	50	0.036

848		LRN003	Learning Disability	49	0.036

849		BNN003	Bone Inflammation Disease	48	0.036

850		KLD004	Keloid Disorder	40	0.036

851		CHL039	Choledocholithiasis	38	0.036

852		CLR030	Clear Cell Renal Cell Carcinoma	53	0.035

853		ALC009	Alcoholic Liver Cirrhosis	53	0.035

854		CLR109	Colorectal Adenocarcinoma	51	0.035

855		PST021	Postpartum Depression	50	0.035

856	P	FRN006	Frontotemporal Dementia	68	0.035

857		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.035

858		SDD001	Sudden Infant Death Syndrome	61	0.035

859		GRD007	Grade Iii Astrocytoma	59	0.035

860	c	CHL119	Cholangitis, Primary Sclerosing	57	0.035

861		JPN002	Japanese Encephalitis	57	0.035

862		LST001	Listeriosis	56	0.035

863		ESP002	Esophageal Varix	51	0.035

864	P	SCL009	Sclerosing Cholangitis	48	0.035

865		ANG020	Angiosarcoma	64	0.035

866		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	49	0.035

867		TBR011	Tuberculous Meningitis	48	0.035

868		MST019	Mastoiditis	43	0.035

869		GRM010	Germ Cells Tumors	34	0.035

870		NRM005	Neuromuscular Disease	64	0.035

871		MDS022	Mediastinitis	46	0.035

872		CYS009	Cystadenoma	44	0.035

873	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.035

874		EXP004	Exophthalmos	52	0.035

875		LNG108	Langerhans Cell Histiocytosis	58	0.035

876	P	NJM001	Nijmegen Breakage Syndrome	74	0.035

877	P	ESS003	Essential Thrombocythemia	68	0.035

878		BLD131	Bladder Urothelial Carcinoma	62	0.035

879	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.035

880		ALC006	Alcoholic Hepatitis	61	0.035

881		DBT010	Diabetic Neuropathy	54	0.035

882	P	ACT008	Actinic Keratosis	53	0.035

883		ADN001	Adenosine Deaminase Deficiency	47	0.035

884		NWB001	Newborn Respiratory Distress Syndrome	58	0.034

885		HPT046	Hepatic Veno-Occlusive Disease	56	0.034

886		HPR003	Heparin-Induced Thrombocytopenia	48	0.034

887		NWC001	Newcastle Disease	45	0.034

888		LPT001	Leptospirosis	66	0.034

889		NRF007	Neurofibroma	64	0.034

890		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.034

891		SBC001	Subacute Sclerosing Panencephalitis	56	0.034

892		MYL001	Myelitis	51	0.034

893		RGH001	Right Bundle Branch Block	48	0.034

894	P	MJR007	Major Affective Disorder 1	43	0.034

895		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.034

896	P	PLY041	Polymyositis	57	0.034

897		EXS001	Exostosis	46	0.034

898	P	GCH001	Gaucher's Disease	63	0.034

899	P	SHR029	Short Syndrome	63	0.034

900		CRC006	Carcinoid Syndrome	55	0.034

901		GNG003	Gingival Recession	44	0.034

902		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.034

903	P	CRB088	Cerebral Atrophy	37	0.034

904		WST001	West Syndrome	61	0.034

905		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	63	0.034

906		BLL006	Bullous Pemphigoid	62	0.034

907		LYM027	Lymphopenia	58	0.034

908		CHK001	Chikungunya	57	0.034

909		TCK001	Tick-Borne Encephalitis	56	0.034

910	P	PTT006	Pituitary Adenoma	55	0.034

911		FBR009	Fibrous Dysplasia	48	0.034

912	c	DRR009	Diarrhea 6	46	0.034

913		HRN029	Hearing Loss, Noise-Induced	37	0.034

914		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	26	0.034

915		HRP008	Herpes Simiae	25	0.034

916	P	LNG028	Long Qt Syndrome	66	0.034

917	P	AGM001	Agammaglobulinemia	65	0.034

918		PPL049	Papillon-Lefevre Syndrome	65	0.034

919		MSC007	Muscle Hypertrophy	64	0.034

920	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.034

921		DFF036	Differentiated Thyroid Carcinoma	52	0.034

922		SCH012	Schizoaffective Disorder	50	0.034

923	P	OPT006	Optic Nerve Disease	60	0.033

924	P	PSD015	Pseudohypoparathyroidism	56	0.033

925	P	MYT002	Myotonic Dystrophy	49	0.033

926		EPC002	Epicondylitis	41	0.033

927		ADR004	Adrenal Cortical Adenocarcinoma	39	0.033

928		PRM329	Premature Aging	35	0.033

929		BHC003	Behcet Syndrome	71	0.033

930		MCC012	Mccune-Albright Syndrome	70	0.033

931		VSC016	Vasculopathy, Retinal, with Cerebral Leukodystrophy	56	0.033

932		INT078	Intracranial Thrombosis	49	0.033

933	P	CHR071	Charcot-Marie-Tooth Disease	65	0.033

934	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.033

935		CND002	Conduct Disorder	51	0.033

936		MTR010	Mature Teratoma	44	0.033

937		TRP009	Triple X Syndrome	42	0.033

938		GST020	Gastric Antral Vascular Ectasia	41	0.033

939	P	DYS005	Dyslexia	40	0.033

940		CLF004	Cleft Lip/palate	54	0.033

941		ECT026	Ectopic Pregnancy	50	0.033

942	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.033

943	P	ACR001	Aicardi-Goutieres Syndrome	62	0.033

944		ANG005	Anogenital Venereal Wart	55	0.033

945	c	TBR025	Tuberous Sclerosis 1	77	0.032

946	P	CHR012	Chronic Granulomatous Disease	67	0.032

947	P	MLG056	Malignant Hyperthermia	67	0.032

948	c	FML021	Familial Hypercholesterolemia	66	0.032

949		MRK001	Merkel Cell Carcinoma	65	0.032

950		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.032

951	P	LYM033	Lymphoproliferative Syndrome	59	0.032

952		PLL012	Pollen Allergy	46	0.032

953		CRB079	Cerebrospinal Fluid Leak	35	0.032

954		BRN028	Brain Cancer	74	0.032

955		LNG039	Lung Squamous Cell Carcinoma	66	0.032

956		APN008	Apnea, Obstructive Sleep	64	0.032

957	c	PRG043	Progressive Familial Heart Block, Type Ib	54	0.032

958	P	TCD001	Tic Disorder	53	0.032

959	P	LCT001	Lactic Acidosis	51	0.032

960		CYS014	Cystadenocarcinoma	51	0.032

961		CRV040	Cervix Carcinoma	51	0.032

962		RTC005	Reticulosarcoma	47	0.032

963	c	GCH015	Gaucher Disease, Type I	70	0.032

964		PCK003	Pick Disease of Brain	68	0.032

965		BLM001	Bloom Syndrome	67	0.032

966		CRP001	Carpal Tunnel Syndrome	67	0.032

967		ALV005	Alveolar Soft Part Sarcoma	61	0.032

968		EXT034	Extrinsic Allergic Alveolitis	58	0.032

969	c	PSR023	Psoriasis 1	52	0.032

970	P	OBS001	Obstructive Jaundice	50	0.032

971		MTC005	Mitochondrial Metabolism Disease	49	0.032

972	P	CTN015	Cutaneous T Cell Lymphoma	49	0.032

973		IGG001	Iga Glomerulonephritis	48	0.032

974		CLF056	Cleft Lip with or Without Cleft Palate	47	0.032

975	P	CLL015	Collagen Disease	47	0.032

976		URT010	Ureteral Obstruction	45	0.032

977		FCT007	Factor Vii Deficiency	67	0.032

978		MXD005	Mixed Connective Tissue Disease	58	0.032

979		CHR100	Chronic Ulcer of Skin	55	0.032

980		HLL004	Hellp Syndrome	54	0.032

981	P	INT068	Intestinal Disease	53	0.032

982		STT041	Stuttering	52	0.032

983		CCN002	Cocaine Abuse	49	0.032

984		PLC007	Placental Abruption	48	0.032

985		EPD015	Epidemic Typhus	45	0.032

986		CND006	Candida Glabrata	32	0.032

987		PNM001	Pneumocystosis	59	0.032

988		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.032

989		BRT054	Brittle Bone Disorder	72	0.032

990		ADN011	Adenoid Cystic Carcinoma	70	0.032

991	P	DRM010	Dermatomyositis	61	0.032

992	c	LPM012	Lipomatosis, Multiple	60	0.032

993		PYD001	Pyoderma Gangrenosum	54	0.032

994		HMP001	Hemopericardium	48	0.032

995		CRT072	Creutzfeldt-Jakob Disease	70	0.032

996	P	USH001	Usher Syndrome	60	0.032

997	P	SPN052	Spondyloarthropathy	54	0.032

998		MRG003	Marginal Zone B-Cell Lymphoma	52	0.032

999		SPS003	Spastic Diplegia	51	0.032

1000		ANR004	Anuria	46	0.032

1001		MLD001	Melioidosis	68	0.031

1002		HYP020	Hyperprolactinemia	64	0.031

1003		PTN001	Patent Foramen Ovale	60	0.031

1004		MCR013	Microphthalmia	57	0.031

1005	P	PNM006	Pneumoconiosis	56	0.031

1006		AMB001	Amebiasis	55	0.031

1007		PLV003	Pelvic Inflammatory Disease	55	0.031

1008		HRY003	Hairy Cell Leukemia	55	0.031

1009		ACH005	Achalasia	51	0.031

1010		ASP003	Aseptic Meningitis	51	0.031

1011	P	ESN008	Eosinophilic Pneumonia	50	0.031

1012		AMB002	Amblyopia	49	0.031

1013		ANT018	Anthracosis	48	0.031

1014	P	VTR007	Vitreoretinopathy	46	0.031

1015		ACT003	Acute Kidney Tubular Necrosis	45	0.031

1016		CRN322	Coronavirus Infectious Disease	40	0.031

1017		HPR006	Heparin Cofactor Ii Deficiency	40	0.031

1018		SPP007	Suppression Amblyopia	39	0.031

1019		RHM035	Rheumatic Fever-Related Antigen	39	0.031

1020		LYM007	Lymphangioleiomyomatosis	69	0.031

1021		PLM070	Pulmonic Stenosis	57	0.031

1022		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.031

1023		CHR177	Chromophobe Renal Cell Carcinoma	57	0.031

1024		GST050	Gastrointestinal System Disease	56	0.031

1025		FCL014	Focal Epilepsy	54	0.031

1026		BCT002	Bacterial Vaginosis	53	0.031

1027	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.031

1028		PLR008	Pleurisy	50	0.031

1029		BLR001	Biliary Atresia	50	0.031

1030		URT001	Urethritis	49	0.031

1031		RNL077	Renal Fibrosis	47	0.031

1032		VSL013	Visual Impairment and Progressive Phthisis Bulbi	41	0.031

1033		RDN001	Reading Disorder	40	0.031

1034		GST019	Gastrointestinal Stromal Tumor	78	0.030

1035	P	TYS001	Tay-Sachs Disease	69	0.030

1036		PNM010	Pneumothorax, Primary Spontaneous	60	0.030

1037	P	LKD001	Leukodystrophy	59	0.030

1038		CRY005	Cryptococcosis	58	0.030

1039		HDR002	Hidradenitis Suppurativa	55	0.030

1040		MYL020	Myelomeningocele	51	0.030

1041		HDR003	Hidradenitis	49	0.030

1042		ANG018	Angiomyolipoma	46	0.030

1043		PLM005	Pleomorphic Lipoma	40	0.030

1044		RTR011	Retroperitoneal Fibrosis	40	0.030

1045		HRL003	Hurler Syndrome	65	0.030

1046		CLC001	Calciphylaxis	51	0.030

1047		STR008	Strongyloidiasis	51	0.030

1048	P	BCT020	Bacteremia 2	44	0.030

1049		SPC005	Speech Disorder	43	0.030

1050		ORL012	Oral Leukoplakia	39	0.030

1051		AYM001	Ayme-Gripp Syndrome	57	0.030

1052	P	VNS003	Venous Insufficiency	55	0.030

1053		GLS001	Gliosarcoma	54	0.030

1054	P	ICH004	Ichthyosis	54	0.030

1055		CRM001	Crimean-Congo Hemorrhagic Fever	53	0.030

1056		KRT001	Keratoconjunctivitis Sicca	49	0.030

1057	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.030

1058		CHL147	Chlamydia Pneumonia	48	0.030

1059		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.030

1060		PRP007	Priapism	47	0.030

1061		RTN020	Retinal Vascular Disease	46	0.030

1062	c	DRM054	Dermatitis, Atopic, 2	44	0.030

1063		DMP001	Dumping Syndrome	44	0.030

1064		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.030

1065		PRM020	Premenstrual Tension	40	0.030

1066		SCR011	Scrapie	39	0.030

1067		STR077	Streptococcal Toxic-Shock Syndrome	37	0.030

1068		LBR036	Leber Plus Disease	66	0.030

1069	P	MST009	Mastocytosis	64	0.030

1070		HMT002	Hematologic Cancer	62	0.030

1071		NRN001	Neuroendocrine Carcinoma	47	0.030

1072	c	TRC022	Tricuspid Valve Insufficiency	45	0.030

1073		MCR011	Microinvasive Gastric Cancer	43	0.030

1074		GRM004	Germinoma	40	0.030

1075		CYT018	Cytochrome P450 2d6 Variant	27	0.030

1076	c	HRD010	Hereditary Spastic Paraplegia	66	0.029

1077		CMM004	Common Variable Immunodeficiency	68	0.029

1078		MYL031	Myeloproliferative Neoplasm	66	0.029

1079	P	LPS002	Liposarcoma	65	0.029

1080	P	TST021	Testicular Germ Cell Tumor	60	0.029

1081		TRG002	Trigeminal Neuralgia	60	0.029

1082		LYM021	Lymphadenitis	57	0.029

1083		MCP006	Mucoepidermoid Carcinoma	50	0.029

1084	c	HRD026	Hereditary Ataxia	48	0.029

1085		GRW007	Growth Hormone Deficiency	46	0.029