Search results for fas

1149 hits were found for fas

#	Family	MCID	Name	MIFTS	Score
1	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	11.675

2	c	FNC027	Fanconi Anemia, Complementation Group a	81	11.319

3		DNZ002	Dianzani Autoimmune Lymphoproliferative Disease	15	6.036

4	P	FRD001	Friedreich Ataxia	64	5.375

5	P	LNG032	Lung Cancer	98	4.420

6	P	CLR023	Colorectal Cancer	99	4.225

7	P	LYM033	Lymphoproliferative Syndrome	59	3.389

8	P	BRS047	Breast Cancer	97	3.281

9	P	PRS040	Prostate Cancer	97	3.227

10	P	OVR042	Ovarian Cancer	88	3.218

11	P	GST053	Gastric Cancer	83	3.215

12	c	HPT001	Hepatitis C	62	3.186

13	P	LYM118	Lymphoma	68	3.069

14	c	SYS001	Systemic Lupus Erythematosus	86	3.050

15		ATM095	Autoimmune Disease	62	3.034

16		SQM006	Squamous Cell Carcinoma	60	3.012

17	P	FTL001	Fetal Alcohol Syndrome	57	3.003

18	P	HPT023	Hepatocellular Carcinoma	100	2.959

19	P	LVR013	Liver Disease	68	2.953

20	P	PNC035	Pancreatic Cancer	84	2.825

21	P	SJG008	Sjogren Syndrome	61	2.813

22		FND001	Fundus Albipunctatus	60	2.672

23	P	GRF003	Graft-Versus-Host Disease	72	2.634

24	P	BCL017	B-Cell Lymphoma	58	2.588

25	P	RHM011	Rheumatoid Arthritis	80	2.550

26		HSH003	Hashimoto Thyroiditis	62	2.514

27	c	VRL010	Viral Hepatitis	52	2.503

28	P	GRV001	Graves' Disease	55	2.495

29		ESP021	Esophageal Cancer	90	2.479

30		MYL009	Myelodysplastic Syndrome	70	2.475

31		FTT001	Fatty Liver Disease	61	2.470

32		LYM027	Lymphopenia	58	2.466

33	P	APL001	Aplastic Anemia	74	2.462

34		SLC006	Silicosis	56	2.448

35		BRK010	Burkitt Lymphoma	67	2.443

36	P	CTN015	Cutaneous T Cell Lymphoma	49	2.443

37		CLN015	Colon Adenocarcinoma	65	2.423

38	c	ATM011	Autoimmune Hepatitis	63	2.413

39	P	ALZ034	Alzheimer Disease	88	2.407

40		SVR097	Severe Cutaneous Adverse Reaction	69	2.402

41		NNL005	Non-Alcoholic Fatty Liver Disease	61	2.402

42		GST040	Gastric Adenocarcinoma	70	2.378

43		SRC014	Sarcoma	65	2.364

44	P	THR014	Thrombocytopenia	67	2.350

45	P	MNC007	Monocytic Leukemia	53	2.342

46	P	DBT009	Diabetes Mellitus	64	2.334

47		MLR004	Malaria	81	2.317

48		AST005	Asthma	76	2.307

49		RNL114	Renal Cell Carcinoma, Nonpapillary	78	2.159

50		SPL018	Splenomegaly	48	2.145

51		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	2.138

52		IMM167	Immune Deficiency Disease	78	2.102

53	P	NRB001	Neuroblastoma	72	2.090

54		GLB015	Glioblastoma Multiforme	75	2.078

55		CRV035	Cervical Cancer	76	2.065

56	P	ADL017	Adult T-Cell Leukemia	56	2.042

57		HMN014	Human Immunodeficiency Virus Infectious Disease	55	2.027

58		LYM143	Lymphoma, Non-Hodgkin, Familial	72	2.017

59		CWP001	Cowpox	46	2.012

60		VRL011	Viral Infectious Disease	61	1.995

61	c	DLT002	Dilated Cardiomyopathy	79	1.989

62		ERY003	Erythema Multiforme	58	1.983

63	P	LNG064	Lung Cancer Susceptibility 3	78	1.976

64		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.956

65		VGT001	Vogt-Koyanagi-Harada Disease	55	1.949

66	P	BRS044	Breast Adenocarcinoma	59	1.941

67		ACT119	Acute Promyelocytic Leukemia	63	1.925

68	P	PNM006	Pneumoconiosis	56	1.925

69		LYM021	Lymphadenitis	57	1.916

70	P	HMP002	Hemophagocytic Lymphohistiocytosis	54	1.916

71		CMM004	Common Variable Immunodeficiency	68	1.906

72		NDL007	Nodular Goiter	47	1.906

73		LYM052	Lymphomatoid Papulosis	38	1.906

74	P	MDL005	Medulloblastoma	77	1.895

75		BRN032	Brain Glioma	45	1.895

76		BHC003	Behcet Syndrome	71	1.884

77		DGR001	Digeorge Syndrome	64	1.884

78	P	SYP003	Syphilis	58	1.884

79		CYT008	Cytomegalovirus Infection	57	1.884

80	P	ACT008	Actinic Keratosis	53	1.884

81	P	CRN025	Corneal Dystrophy	49	1.884

82	c	ACT076	Acute Myocarditis	46	1.884

83	P	CNR004	Cone-Rod Dystrophy 2	73	1.870

84		BLD131	Bladder Urothelial Carcinoma	62	1.870

85	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	1.855

86	P	ECT006	Ectodermal Dysplasia	62	1.855

87		PNN001	Panniculitis	51	1.855

88		TRY001	Trypanosomiasis	50	1.855

89		LYM015	Lymphocytic Gastritis	33	1.855

90	c	LKM061	Leukemia, Acute Myeloid	84	1.567

91		MYL069	Myeloma, Multiple	85	1.538

92	P	LKM071	Leukemia, Chronic Lymphocytic	79	1.505

93		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	1.478

94	P	FML364	Familial Thoracic Aortic Aneurysm and Aortic Dissection	66	1.426

95		MLT073	Multisystemic Smooth Muscle Dysfunction Syndrome	44	1.426

96	P	GLL022	Guillain-Barre Syndrome	59	1.393

97		AGG002	Aggressive Systemic Mastocytosis	49	1.361

98		KSH004	Kashin-Beck Disease	38	1.361

99	P	MLT008	Multinodular Goiter	42	1.348

100		PRS108	Persistent Polyclonal B-Cell Lymphocytosis	35	1.348

101	c	TYP024	Type Ii Mixed Cryoglobulinemia	34	1.348

102		CRT002	Cartilage-Hair Hypoplasia	59	1.332

103		CSP005	Caspase 8 Deficiency	55	1.332

104		EPS023	Epstein-Barr Virus-Associated Gastric Carcinoma	38	1.332

105		CPL004	Caplan's Syndrome	32	1.332

106		ACD003	Acid Sphingomyelinase Deficiency	32	1.332

107		SCL002	Scleredema Adultorum	46	1.311

108	P	HYP073	Hypersensitivity Reaction Type Iv Disease	44	1.311

109		CRN247	Corneal Dystrophy, Thiel-Behnke Type	38	1.311

110		MXD012	Mixed Oligodendroglioma-Astrocytoma	32	1.311

111		SBC005	Subacute Lymphocytic Thyroiditis	25	1.311

112		ESP016	Esophagus Melanoma	23	1.311

113		CRN023	Corneal Deposit	22	1.311

114		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.339

115		HYP060	Hyperinsulinism	54	0.255

116	P	GLM045	Glioma	63	0.231

117	P	LKM002	Leukemia	68	0.227

118	P	ADN016	Adenocarcinoma	64	0.213

119	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.209

120		GLL048	Glial Tumor	45	0.203

121	P	MLN008	Melanoma	69	0.198

122	P	GLM007	Glomerulonephritis	57	0.190

123	P	LPS004	Lupus Erythematosus	61	0.187

124	P	THY032	Thyroiditis	52	0.185

125		ALC001	Alcohol-Related Birth Defect	36	0.180

126		OST159	Osteogenic Sarcoma	66	0.175

127	P	MYL006	Myeloid Leukemia	60	0.175

128		SVR004	Severe Combined Immunodeficiency	73	0.173

129		CYT002	Cytokine Deficiency	42	0.173

130	P	BLD134	Bladder Cancer	79	0.172

131	P	PLM036	Pulmonary Fibrosis	65	0.172

132	c	LKM005	Leukemia, T-Cell, Chronic	34	0.168

133	c	PRC016	Pre-Eclampsia	63	0.164

134	c	FNC042	Fanconi Anemia, Complementation Group D2	56	0.164

135	c	ACT134	Acute Liver Failure	56	0.157

136	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.153

137		GNT167	Genetic Obesity	33	0.153

138	c	ACT135	Acute Graft Versus Host Disease	52	0.151

139		HYP066	Hyperglycemia	61	0.149

140		ALL014	Allergic Encephalomyelitis	38	0.149

141	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.147

142	c	HPT073	Hepatitis C Virus	72	0.142

143		HMN044	Human Immunodeficiency Virus Type 1	71	0.136

144		ISC004	Ischemia	58	0.136

145		CHL065	Cholangiocarcinoma	68	0.133

146		ALL026	Allergic Hypersensitivity Disease	62	0.133

147		INT079	Intrahepatic Cholangiocarcinoma	51	0.133

148		ORL015	Oral Squamous Cell Carcinoma	43	0.133

149		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.131

150		LVR012	Liver Cirrhosis	62	0.129

151		GLC003	Glucose Intolerance	54	0.129

152	P	HYP086	Hypothyroidism	69	0.126

153	P	HPT021	Hepatitis	67	0.126

154	P	MYC008	Myocarditis	59	0.126

155		THY029	Thyroid Carcinoma	59	0.126

156		ADN018	Adenoma	59	0.124

157	P	AST007	Astrocytoma	51	0.124

158	P	END044	Endometriosis	63	0.121

159	c	HPT016	Hepatitis B	59	0.121

160		LYM009	Lymphocytic Choriomeningitis	47	0.119

161	c	PCH010	Pachyonychia Congenita 3	44	0.119

162		DFC004	Deficiency Anemia	70	0.116

163		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.116

164	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.116

165		SYS071	Systemic Autoimmune Disease	37	0.116

166	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.114

167	c	LKM063	Leukemia, Chronic Myeloid	72	0.114

168		LPD008	Lipid Metabolism Disorder	62	0.114

169		ACQ007	Acquired Immunodeficiency Syndrome	60	0.114

170		48X005	48,xyyy	39	0.114

171	P	HYP750	Hypertriglyceridemia, Familial	62	0.111

172	c	SCL052	Scleroderma, Familial Progressive	61	0.111

173		LNG099	Lung Disease	60	0.111

174	P	NSP012	Nasopharyngeal Carcinoma	66	0.108

175	c	SML038	Small Cell Cancer of the Lung	65	0.108

176		SPN186	Spinal Cord Injury	60	0.108

177	P	UVT001	Uveitis	57	0.108

178	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.105

179	P	SPP010	Suppressor of Tumorigenicity 3	51	0.105

180		CNG034	Congestive Heart Failure	69	0.102

181	P	HYP098	Hypereosinophilic Syndrome	67	0.102

182	P	HRP006	Herpes Simplex	65	0.102

183	c	DBT099	Diabetes Mellitus, Type I	65	0.102

184		SKN016	Skin Disease	63	0.102

185	P	INF032	Infertility	57	0.102

186		BNR002	Bone Resorption Disease	48	0.102

187	c	MLG068	Malignant Glioma	46	0.102

188	c	FTL006	Fetal Alcohol Spectrum Disorder	43	0.102

189		OVR094	Ovarian Epithelial Cancer	38	0.102

190	P	KDN017	Kidney Cancer	60	0.099

191		BCT022	Bacterial Infectious Disease	56	0.099

192	c	FNC029	Fanconi Anemia, Complementation Group I	54	0.099

193		THY030	Thyroid Gland Disease	52	0.099

194		END086	End Stage Renal Disease	51	0.099

195	P	MLT020	Multiple Sclerosis	72	0.096

196		LYM133	Lymphoma, Hodgkin, Classic	69	0.096

197		MYC006	Mycosis Fungoides	66	0.096

198	P	SKN015	Skin Carcinoma	66	0.096

199	P	VSC007	Vascular Disease	63	0.096

200	P	PNC044	Pancreatitis	61	0.096

201		GTR002	Goiter	53	0.096

202		TRM010	Traumatic Brain Injury	51	0.096

203		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.096

204	P	KDN018	Kidney Disease	72	0.093

205	P	MYP004	Myopathy	70	0.093

206	P	GST044	Gastritis	56	0.093

207		KLD004	Keloid Disorder	40	0.093

208		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.093

209		HML018	Homologous Wasting Disease	22	0.093

210	P	GLM040	Glioma Susceptibility 1	81	0.089

211		END057	Endometrial Cancer	74	0.089

212	P	SRC025	Sarcoidosis 1	70	0.089

213	P	MYS003	Myasthenia Gravis	68	0.089

214		PRT037	Pertussis	65	0.089

215	P	NTR004	Neutropenia	63	0.089

216	P	DRM010	Dermatomyositis	61	0.089

217	c	ACT027	Acute Pancreatitis	60	0.089

218		INS001	Insulinoma	60	0.089

219		DFF005	Diffuse Large B-Cell Lymphoma	55	0.089

220	c	MCR113	Microvascular Complications of Diabetes 3	52	0.089

221	P	ECL001	Eclampsia	50	0.089

222		SLD003	Sialadenitis	49	0.089

223	c	MCR120	Microvascular Complications of Diabetes 7	47	0.089

224		CRB004	Cerebral Artery Occlusion	45	0.089

225	c	MCR130	Microvascular Complications of Diabetes 6	41	0.089

226	c	MCR133	Microvascular Complications of Diabetes 4	41	0.089

227		ERY066	Erythema Multiforme Major	30	0.089

228	c	ATR087	Atrial Standstill 1	75	0.086

229	P	RTN024	Retinoblastoma	73	0.086

230		ATH013	Atherosclerosis Susceptibility	65	0.086

231		CLT003	Colitis	62	0.086

232		TXC005	Toxic Shock Syndrome	62	0.086

233	c	ACT073	Acute Leukemia	58	0.086

234	P	FNC044	Fanconi Anemia, Complementation Group C	57	0.086

235	P	FBR017	Fibrosarcoma	56	0.086

236	P	NRP001	Neuropathy	56	0.086

237	P	ALP008	Alopecia	54	0.086

238	c	FML008	Familial Retinoblastoma	53	0.086

239		BRN071	Brain Injury	49	0.086

240		ATS010	Autosomal Recessive Disease	48	0.086

241		OST012	Osteoarthritis	78	0.082

242		PNC129	Pancreatic Adenocarcinoma	68	0.082

243	P	DRM053	Dermatitis, Atopic	66	0.082

244		DRM006	Dermatitis	61	0.082

245		CHL014	Cholera	59	0.082

246	P	PLY041	Polymyositis	57	0.082

247		ALL006	Allergic Asthma	56	0.082

248		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.082

249		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.082

250		ULC004	Ulcerative Colitis	73	0.078

251	c	BSL007	Basal Cell Carcinoma	68	0.078

252	P	MCR115	Microvascular Complications of Diabetes 5	66	0.078

253		KRT019	Keratitis, Hereditary	65	0.078

254		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.078

255		ORL011	Oral Cancer	60	0.078

256	P	MYM013	Moyamoya Disease 1	57	0.078

257		PNC001	Pancytopenia	54	0.078

258	P	LCH002	Lichen Planus	53	0.078

259		SPN035	Spindle Cell Sarcoma	53	0.078

260	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.078

261	c	FNC028	Fanconi Anemia, Complementation Group L	49	0.078

262	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.078

263	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.074

264		KPS004	Kaposi Sarcoma	75	0.074

265	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.074

266	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.074

267	P	ART022	Arthritis	69	0.074

268	P	THY023	Thymoma	65	0.074

269		LPP008	Lipoprotein Quantitative Trait Locus	62	0.074

270	P	ALP009	Alopecia Areata	60	0.074

271	P	MLN007	Male Infertility	55	0.074

272		SYN007	Synovitis	54	0.074

273	P	INF037	Inflammatory Bowel Disease	54	0.074

274	P	ART021	Arteriosclerosis	54	0.074

275	P	INS002	in Situ Carcinoma	53	0.074

276		ART140	Arteries, Anomalies of	52	0.074

277	c	THY107	Thymoma, Familial	52	0.074

278		DGN001	Degenerative Disc Disease	48	0.074

279		PLC002	Plica Syndrome	36	0.074

280		ALC002	Alcohol-Related Neurodevelopmental Disorder	30	0.074

281		CYS001	Cystic Fibrosis	81	0.070

282		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.070

283		INS024	Insulin-Like Growth Factor I	79	0.070

284	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.070

285	P	PHC003	Pheochromocytoma	71	0.070

286	c	RHB024	Rhabdomyosarcoma 2	67	0.070

287	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.070

288		LSH001	Leishmaniasis	63	0.070

289	P	CTR002	Cataract	60	0.070

290		HLC007	Helicobacter Pylori Infection	59	0.070

291		TRN018	Transitional Cell Carcinoma	56	0.070

292		PRP030	Purpura	54	0.070

293	P	LTR001	Lateral Sclerosis	54	0.070

294		NNL006	Non-Alcoholic Steatohepatitis	54	0.070

295		URM002	Uremia	49	0.070

296		RFR010	Refractory Anemia	48	0.070

297	P	BNG032	Benign Mesothelioma	46	0.070

298		ADR040	Adrenal Gland Pheochromocytoma	46	0.070

299	P	PRL003	Proliferative Glomerulonephritis	44	0.070

300	P	KLZ004	Kala-Azar 1	41	0.070

301		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.070

302	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.066

303		BRN028	Brain Cancer	74	0.066

304		LPT014	Leptin Deficiency or Dysfunction	74	0.066

305		ALC007	Alcohol Dependence	66	0.066

306		HYP056	Hypoglycemia	66	0.066

307	P	HYD006	Hydrocephalus	66	0.066

308		PRT036	Peritonitis	64	0.066

309	c	GLC092	Glaucoma, Primary Open Angle	62	0.066

310	P	VSC011	Vasculitis	62	0.066

311	P	PRM006	Primary Biliary Cirrhosis	62	0.066

312	c	ACT071	Acute Kidney Failure	60	0.066

313	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.066

314	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.066

315	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.066

316	P	PRP019	Peripheral Nervous System Disease	58	0.066

317	P	RHN004	Rhinitis	57	0.066

318		HYP266	Hypoxia	57	0.066

319		HPT022	Hepatoblastoma	56	0.066

320	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.066

321	P	DRR001	Diarrhea	55	0.066

322	P	HYP076	Hyperthyroidism	55	0.066

323	P	PMP001	Pemphigus	54	0.066

324		HLL004	Hellp Syndrome	54	0.066

325		DMY004	Demyelinating Disease	52	0.066

326	c	FNC025	Fanconi Anemia, Complementation Group J	52	0.066

327		NTR046	Neutrophil Migration	50	0.066

328		TRP002	Tropical Spastic Paraparesis	50	0.066

329		VRC001	Varicocele	49	0.066

330	P	OPN001	Open-Angle Glaucoma	49	0.066

331		VCC001	Vaccinia	49	0.066

332	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.066

333		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.066

334		GST010	Gestational Trophoblastic Neoplasm	46	0.066

335		ORL013	Oral Lichen Planus	45	0.066

336		MST004	Mast Cell Neoplasm	42	0.066

337	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.066

338		MYL057	Myelopathy, Htlv-1-Associated	39	0.066

339		EXT007	Extracutaneous Mastocytoma	38	0.066

340		SPS019	Spastic Paraparesis	38	0.066

341		HTL001	Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis	35	0.066

342	P	HRT032	Heart Disease	75	0.061

343	P	OST002	Osteoporosis	74	0.061

344		MNT001	Mantle Cell Lymphoma	69	0.061

345		ALL003	Allergic Rhinitis	67	0.061

346	P	BLD062	Bile Duct Cancer	67	0.061

347	P	CLC063	Celiac Disease 1	66	0.061

348		BRR014	Barrett Esophagus	65	0.061

349		CLR108	Colorectal Adenoma	64	0.061

350	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.061

351	P	PSR002	Psoriasis	62	0.061

352		CHL068	Cholestasis	61	0.061

353		HRP004	Herpes Zoster	60	0.061

354	c	JVN061	Juvenile Arthritis	60	0.061

355	P	SCL018	Scoliosis	60	0.061

356		BRN002	Bronchiolitis	59	0.061

357	P	ALC033	Alcohol Use Disorder	58	0.061

358		EXT034	Extrinsic Allergic Alveolitis	58	0.061

359	c	CHR417	Chronic Graft Versus Host Disease	57	0.061

360	c	ACT075	Acute Myocardial Infarction	57	0.061

361	P	MYS005	Myositis	56	0.061

362	P	PLY019	Polyneuropathy	56	0.061

363		IRD001	Iridocyclitis	53	0.061

364	c	FNC024	Fanconi Anemia, Complementation Group D1	52	0.061

365		PST011	Pustulosis of Palm and Sole	52	0.061

366	P	RCT021	Rectum Cancer	52	0.061

367		KRT009	Keratosis	51	0.061

368		LPT006	Leptin Receptor Deficiency	48	0.061

369		OPD006	Opioid Addiction	48	0.061

370		ANT018	Anthracosis	48	0.061

371		PPL002	Papillary Carcinoma	47	0.061

372		CHR074	Choriocarcinoma	47	0.061

373		LRY018	Laryngeal Squamous Cell Carcinoma	44	0.061

374		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.061

375		SMN007	Seminoma	43	0.061

376	c	MLG079	Malignant Pleural Mesothelioma	42	0.061

377		STR067	Stroke, Ischemic	81	0.055

378		PFF001	Pfeiffer Syndrome	79	0.055

379		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.055

380	P	FML018	Familial Mediterranean Fever	73	0.055

381		ADL002	Adult Syndrome	70	0.055

382		PLM001	Pulmonary Tuberculosis	69	0.055

383	P	SYS005	Systemic Scleroderma	68	0.055

384	P	FLL037	Follicular Lymphoma	67	0.055

385		BRC012	Brucellosis	64	0.055

386	P	PRD008	Periodontitis	64	0.055

387	P	RHB003	Rhabdomyosarcoma	63	0.055

388	P	HML002	Hemolytic Anemia	63	0.055

389	P	ART023	Arthropathy	62	0.055

390	P	ENC018	Encephalopathy	61	0.055

391		RTN017	Retinal Detachment	61	0.055

392		SZR001	Sezary's Disease	60	0.055

393	P	TXP001	Toxoplasmosis	60	0.055

394	P	BND020	Bone Disease	59	0.055

395	P	MLN069	Melanoma, Uveal	59	0.055

396		INC002	Inclusion Body Myositis	58	0.055

397		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.055

398	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.055

399		SCH014	Schistosomiasis	57	0.055

400		LST001	Listeriosis	56	0.055

401	P	PLY011	Polycystic Ovary Syndrome	56	0.055

402		BRN012	Bronchiolitis Obliterans	55	0.055

403	c	BCT007	Bacterial Meningitis	55	0.055

404	P	LRY044	Larynx Cancer	55	0.055

405		PRT082	Preterm Premature Rupture of the Membranes	54	0.055

406		HMS001	Hemosiderosis	54	0.055

407	P	CTN003	Cutaneous Lupus Erythematosus	53	0.055

408		HMC014	Homocysteinemia	53	0.055

409		SPN051	Spondylitis	51	0.055

410		PLR008	Pleurisy	50	0.055

411	P	FNC004	Fanconi Syndrome	50	0.055

412		AZS001	Azoospermia	50	0.055

413		STM007	Stomatitis	50	0.055

414		ENT004	Enthesopathy	49	0.055

415	P	BRS053	Breast Fibroadenoma	49	0.055

416	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.055

417		IGG001	Iga Glomerulonephritis	48	0.055

418	c	FNC023	Fanconi Anemia, Complementation Group N	48	0.055

419	P	HMN032	Human Herpesvirus 8	47	0.055

420		ORC001	Orchitis	46	0.055

421		TCL003	T Cell Deficiency	46	0.055

422	c	ATM099	Autoimmune Uveitis	45	0.055

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

424		IMM001	Immune-Complex Glomerulonephritis	40	0.055

425		HST016	Histiocytic Sarcoma	39	0.055

426		FLL031	Follicular Adenoma	39	0.055

427		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.055

428		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.055

429		INF009	Inflammatory Spondylopathy	31	0.055

430		INF158	Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations	30	0.055

431	c	HYP595	Hypertension, Essential	84	0.050

432	P	ATX030	Ataxia-Telangiectasia	82	0.050

433		CRH001	Crohn's Disease	74	0.050

434	c	SPN225	Spondyloarthropathy 1	73	0.050

435	P	MYC007	Myocardial Infarction	70	0.050

436		DWN001	Down Syndrome	70	0.050

437		ADN011	Adenoid Cystic Carcinoma	70	0.050

438	c	CHR684	Chronic Kidney Disease	70	0.050

439	P	SHW006	Shwachman-Diamond Syndrome 1	67	0.050

440	P	TRN020	Turner Syndrome	67	0.050

441	P	PLM037	Pulmonary Hypertension	67	0.050

442		ANG054	Angina Pectoris	66	0.050

443		CHG001	Chagas Disease	66	0.050

444	P	MNN013	Meningitis	66	0.050

445		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.050

446	P	CRN300	Coronary Heart Disease 1	63	0.050

447	P	LMY004	Leiomyosarcoma	63	0.050

448	c	HMP022	Hemophagocytic Lymphohistiocytosis, Familial, 1	63	0.050

449		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.050

450	P	PLY014	Polycystic Kidney Disease	62	0.050

451		CTN007	Cutaneous Leishmaniasis	62	0.050

452	P	ENC004	Encephalitis	61	0.050

453	P	TST021	Testicular Germ Cell Tumor	60	0.050

454	P	NMN002	Niemann-Pick Disease	59	0.050

455		PMP006	Pemphigus Vulgaris, Familial	57	0.050

456	P	EXN002	Exanthem	57	0.050

457	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.050

458	c	MST023	Mesothelioma, Malignant	57	0.050

459	P	CRD246	Cardiovascular System Disease	57	0.050

460		GST050	Gastrointestinal System Disease	56	0.050

461		AGN016	Aging	56	0.050

462		HRY003	Hairy Cell Leukemia	55	0.050

463		PLM010	Pulmonary Edema	54	0.050

464		LYM040	Lymphoblastic Lymphoma	54	0.050

465		CRY001	Cryptogenic Organizing Pneumonia	53	0.050

466	P	RTN018	Retinal Disease	53	0.050

467	P	DDN001	Duodenal Ulcer	52	0.050

468		TLN003	Telangiectasis	52	0.050

469	P	TRT010	Teratoma	52	0.050

470		PNG002	Pain Agnosia	51	0.050

471	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.050

472		CYS036	Cystinosis, Nephropathic	51	0.050

473	P	CHL066	Cholangitis	51	0.050

474		MLL001	Molluscum Contagiosum	50	0.050

475	P	KRT007	Keratoconus	50	0.050

476		HYP080	Hypogonadism	50	0.050

477		ERY004	Erysipelas	49	0.050

478		BKR002	Baker-Gordon Syndrome	49	0.050

479	c	BCT013	Bacterial Pneumonia	48	0.050

480		INT067	Interstitial Nephritis	48	0.050

481	c	FNC032	Fanconi Anemia, Complementation Group B	48	0.050

482		THY128	Thyroid Tumor	47	0.050

483	P	INN002	Inner Ear Disease	47	0.050

484		RNL077	Renal Fibrosis	47	0.050

485		RTN023	Retinitis	46	0.050

486		TST014	Testicular Cancer	46	0.050

487		HDN002	Head Injury	46	0.050

488		TST015	Testicular Disease	43	0.050

489	P	DMY001	Demyelinating Polyneuropathy	43	0.050

490		HYP457	Hypertrophic Scars	42	0.050

491		NRR001	Neuroretinitis	42	0.050

492	P	RRH023	Rare Hereditary Hemochromatosis	41	0.050

493	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.050

494	c	PRM301	Primary Cutaneous T-Cell Lymphoma	35	0.050

495		PRT086	Partial Hydatidiform Mole	27	0.050

496		RFR007	Refractory Anemia with Excess Blasts in Transformation	27	0.050

497		GST019	Gastrointestinal Stromal Tumor	78	0.043

498	P	PRK057	Parkinson Disease, Late-Onset	78	0.043

499	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.043

500	P	RSP003	Respiratory Failure	74	0.043

501	c	MNN043	Meningioma, Familial	74	0.043

502		MSC157	Muscular Dystrophy, Duchenne Type	72	0.043

503	P	HNT016	Huntington Disease	72	0.043

504	P	FML011	Familial Adenomatous Polyposis	72	0.043

505	P	AMY004	Amyloidosis	70	0.043

506	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.043

507	P	PNM007	Pneumonia	68	0.043

508	P	MYC084	Mycobacterium Tuberculosis 1	68	0.043

509		OBS002	Obsessive-Compulsive Disorder	68	0.043

510		SKN019	Skin Melanoma	68	0.043

511		FCT007	Factor Vii Deficiency	67	0.043

512	P	MSC005	Muscular Dystrophy	66	0.043

513	P	NRV007	Nervous System Disease	66	0.043

514	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.043

515	P	CNJ013	Conjunctivitis	65	0.043

516		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.043

517		KWS002	Kawasaki Disease	65	0.043

518	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.043

519	P	MST009	Mastocytosis	64	0.043

520		LYM017	Lyme Disease	64	0.043

521	c	SYS004	Systemic Mastocytosis	63	0.043

522		DPR016	Depression	63	0.043

523	c	HPT003	Hepatitis a	62	0.043

524	c	ANM038	Anemia, Autoimmune Hemolytic	62	0.043

525		MNN042	Meningioma, Radiation-Induced	62	0.043

526		ALC006	Alcoholic Hepatitis	61	0.043

527		ALV005	Alveolar Soft Part Sarcoma	61	0.043

528	c	WLM018	Wilms Tumor 5	61	0.043

529		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.043

530		DPH001	Diphtheria	60	0.043

531		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.043

532	P	SNS001	Sensorineural Hearing Loss	60	0.043

533	P	OPT006	Optic Nerve Disease	60	0.043

534		PNM001	Pneumocystosis	59	0.043

535		PPT005	Peptic Ulcer Disease	59	0.043

536		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.043

537		MNT002	Mental Depression	58	0.043

538	P	GLL018	Gallbladder Cancer	57	0.043

539		CHR070	Chronic Inflammatory Demyelinating Polyradiculoneuropathy	57	0.043

540		SKN022	Skin Squamous Cell Carcinoma	57	0.043

541	P	BPL003	Bipolar Disorder	56	0.043

542		PLS011	Plasmacytoma	56	0.043

543		ERY051	Erythroleukemia, Familial	56	0.043

544	P	SZR006	Seizure Disorder	56	0.043

545		SFT003	Soft Tissue Sarcoma	56	0.043

546		EMB004	Embryonal Carcinoma	56	0.043

547		MCS002	Mucositis	56	0.043

548		VSC003	Visceral Leishmaniasis	55	0.043

549		INT007	Intermediate Coronary Syndrome	55	0.043

550		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.043

551		CRY003	Cryptosporidiosis	54	0.043

552		HRT012	Heart Valve Disease	53	0.043

553		PLS016	Plasma Cell Leukemia	53	0.043

554	P	HML001	Hemolytic-Uremic Syndrome	53	0.043

555	P	PTS002	Ptosis	53	0.043

556		MRG003	Marginal Zone B-Cell Lymphoma	52	0.043

557		DYS015	Dysentery	52	0.043

558	P	MSC003	Muscular Atrophy	52	0.043

559		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.043

560		RSD004	Rosai-Dorfman Disease	51	0.043

561	P	MMB011	Membranous Nephropathy	50	0.043

562		SPN021	Spinal Meningioma	50	0.043

563	c	SVR005	Severe Pre-Eclampsia	50	0.043

564		CHR078	Chorioretinitis	50	0.043

565		PLC008	Placenta Disease	50	0.043

566	P	ATR005	Atrophic Gastritis	50	0.043

567	c	FNC048	Fanconi Anemia, Complementation Group O	49	0.043

568	P	MST002	Mast-Cell Leukemia	49	0.043

569	P	SCL009	Sclerosing Cholangitis	48	0.043

570		HLX001	Helix Syndrome	47	0.043

571		TST044	Testicular Torsion	47	0.043

572	P	OVR046	Ovarian Cyst	47	0.043

573		RTN020	Retinal Vascular Disease	46	0.043

574	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.043

575		MSN001	Mesangial Proliferative Glomerulonephritis	45	0.043

576		LYM126	Lymphoma Aids Related	44	0.043

577		TNG009	Tongue Squamous Cell Carcinoma	44	0.043

578	c	PRM038	Primary Agammaglobulinemia	44	0.043

579	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.043

580	P	CRN024	Corneal Disease	44	0.043

581	c	TCL001	T-Cell Adult Acute Lymphocytic Leukemia	43	0.043

582	P	TST026	Testicular Germ Cell Cancer	43	0.043

583		DSC009	Discoid Lupus Erythematosus	42	0.043

584	c	MJR024	Major Affective Disorder 9	41	0.043

585		SCR001	Secretory Meningioma	41	0.043

586		EXT006	Extrahepatic Cholestasis	39	0.043

587		LKP003	Leukoplakia	39	0.043

588		WLL004	Wallerian Degeneration	39	0.043

589		CRV045	Cervical Intraepithelial Neoplasia	39	0.043

590		OCL025	Ocular Toxoplasmosis	39	0.043

591		NDL024	Nodal Marginal Zone Lymphoma	38	0.043

592	c	MJR022	Major Affective Disorder 8	38	0.043

593	c	ATM045	Autoimmune Glomerulonephritis	36	0.043

594		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.043

595	c	ATM022	Autoimmune Myocarditis	35	0.043

596		PRM329	Premature Aging	35	0.043

597		GRM010	Germ Cells Tumors	34	0.043

598		CRB169	Cerebellar Atrophy, Developmental Delay, and Seizures	33	0.043

599		BWN006	Bowen's Disease	32	0.043

600		CHL079	Children's Interstitial Lung Disease	26	0.043

601		THY006	Thymus Lymphoma	26	0.043

602		MLG164	Malignant Epithelial Tumor of Ovary	26	0.043

603		PRT001	Partial Fetal Alcohol Syndrome	24	0.043

604		INT029	Interleukin-7 Receptor Alpha Deficiency	22	0.043

605		LYM053	Lymphomatous Thyroiditis	22	0.043

606	c	NRF023	Neurofibromatosis, Type Ii	80	0.035

607	P	LYN001	Lynch Syndrome	77	0.035

608		PHN003	Phenylketonuria	75	0.035

609		OTT002	Otitis Media	72	0.035

610		PRP027	Peripheral Vascular Disease	71	0.035

611		MYL005	Myelofibrosis	70	0.035

612	P	HYP061	Hypertrophic Cardiomyopathy	70	0.035

613		PLY001	Polycythemia Vera	69	0.035

614	P	LPR021	Leprosy 3	69	0.035

615		EWN003	Ewing Sarcoma	69	0.035

616	P	ESS003	Essential Thrombocythemia	68	0.035

617		BRN024	Bronchitis	68	0.035

618		CNN005	Connective Tissue Disease	68	0.035

619	P	MJR001	Major Depressive Disorder	68	0.035

620	P	CRD119	Cardiac Arrest	67	0.035

621		CRB039	Cerebrovascular Disease	67	0.035

622	P	CHR012	Chronic Granulomatous Disease	67	0.035

623		LPT001	Leptospirosis	66	0.035

624		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.035

625		TTN003	Tetanus	65	0.035

626	c	WLM013	Wilms Tumor 1	65	0.035

627	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.035

628		ART002	Arts Syndrome	64	0.035

629		END041	Endometrial Adenocarcinoma	63	0.035

630		HMT002	Hematologic Cancer	62	0.035

631		BRS099	Breast Ductal Carcinoma	62	0.035

632	P	HMN010	Hemangioma	61	0.035

633		SHG001	Shigellosis	60	0.035

634	P	CRB101	Cerebrooculofacioskeletal Syndrome 1	60	0.035

635		INT066	Interstitial Lung Disease	60	0.035

636		DNG002	Dengue Hemorrhagic Fever	60	0.035

637		CHC001	Chickenpox	60	0.035

638	P	MCR010	Microcephaly	59	0.035

639	c	DNG003	Dengue Disease	59	0.035

640		CHL123	Chlamydia	59	0.035

641		VSL002	Visual Epilepsy	59	0.035

642		DCT002	Ductal Carcinoma in Situ	59	0.035

643	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.035

644		GRD007	Grade Iii Astrocytoma	59	0.035

645	P	DNG005	Dengue Virus	59	0.035

646		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.035

647		ANR040	Aneurysm	59	0.035

648		ALP097	Alopecia Universalis Congenita	59	0.035

649		RBS001	Rabies	58	0.035

650		CNT047	Contact Dermatitis	58	0.035

651		ADR005	Adrenal Carcinoma	58	0.035

652	P	URT039	Urticaria	58	0.035

653		ADL030	Adult-Onset Still's Disease	58	0.035

654		EYD002	Eye Disease	58	0.035

655		CRV038	Cervical Squamous Cell Carcinoma	58	0.035

656		CHL028	Childhood Type Dermatomyositis	58	0.035

657	P	BNC003	Bone Cancer	58	0.035

658	P	CND004	Candidiasis	58	0.035

659		MXD005	Mixed Connective Tissue Disease	58	0.035

660		GLS018	Glass Syndrome	57	0.035

661		CHL067	Cholecystitis	57	0.035

662		BRN056	Bronchopulmonary Dysplasia	57	0.035

663		PLC005	Placental Insufficiency	57	0.035

664		AYM001	Ayme-Gripp Syndrome	57	0.035

665	P	PLY018	Polycythemia	56	0.035

666	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.035

667		EXF001	Exfoliation Syndrome	56	0.035

668		LMY014	Leiomyoma, Uterine	56	0.035

669		MCL006	Macular Retinal Edema	55	0.035

670		FDB001	Foodborne Botulism	55	0.035

671		MMB001	Membranoproliferative Glomerulonephritis	55	0.035

672	P	ANT006	Antiphospholipid Syndrome	55	0.035

673	P	SBS003	Substance Abuse	55	0.035

674		JVN009	Juvenile Pilocytic Astrocytoma	55	0.035

675		BRN014	Bronchopneumonia	54	0.035

676		DBT010	Diabetic Neuropathy	54	0.035

677	c	PST005	Posterior Uveitis	54	0.035

678		WST005	West Nile Virus	54	0.035

679		MYM001	Myoma	54	0.035

680	P	TRM003	Tremor	54	0.035

681		PRC002	Paracoccidioidomycosis	54	0.035

682		CLL003	Cellulitis	54	0.035

683		PRS045	Prostatic Hypertrophy	53	0.035

684		PLM012	Pulmonary Sarcoidosis	53	0.035

685	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.035

686	P	END047	Endophthalmitis	53	0.035

687		KRT006	Keratoconjunctivitis	53	0.035

688		PRP036	Peripheral T-Cell Lymphoma	53	0.035

689		CYS005	Cysticercosis	53	0.035

690		HYP063	Hypersplenism	53	0.035

691		GST023	Gastric Ulcer	53	0.035

692		DNT012	Dental Caries	53	0.035

693		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.035

694		PLM014	Pleomorphic Adenoma	52	0.035

695	P	HYP730	Hypogonadotropic Hypogonadism	52	0.035

696		PRV004	Periventricular Leukomalacia	52	0.035

697		LMY002	Leiomyoma	52	0.035

698		THR004	Thrombocytosis	51	0.035

699		FDL002	Food Allergy	51	0.035

700	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.035

701		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.035

702		CRN030	Coronary Stenosis	50	0.035

703		NPH010	Nephrosclerosis	50	0.035

704	c	FNC046	Fanconi Anemia, Complementation Group P	50	0.035

705	P	CRY007	Cryoglobulinemia, Familial Mixed	50	0.035

706		TCL002	T-Cell Large Granular Lymphocyte Leukemia	49	0.035

707		KRT001	Keratoconjunctivitis Sicca	49	0.035

708		PLR001	Pleural Tuberculosis	49	0.035

709		47X002	47,xyy	49	0.035

710		HST010	Histiocytosis	48	0.035

711		ADR016	Adrenal Cortical Carcinoma	48	0.035

712		HYP043	Hyperandrogenism	48	0.035

713		CRY004	Cryoglobulinemia	48	0.035

714		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.035

715		PNC013	Pancreatic Ductal Carcinoma	48	0.035

716		VLV034	Vulva Squamous Cell Carcinoma	48	0.035

717		PLC007	Placental Abruption	48	0.035

718		SYM002	Sympathetic Ophthalmia	47	0.035

719		ASB001	Asbestosis	47	0.035

720		PRD004	Prediabetes Syndrome	47	0.035

721		KRT008	Keratopathy	47	0.035

722		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.035

723		LYM019	Lymphosarcoma	46	0.035

724	c	FNC045	Fanconi Anemia, Complementation Group F	46	0.035

725		SGN002	Signet Ring Cell Adenocarcinoma	45	0.035

726		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	45	0.035

727		ACT003	Acute Kidney Tubular Necrosis	45	0.035

728		CLL014	Cll/sll	45	0.035

729	c	HMP012	Hemophagocytic Lymphohistiocytosis, Familial, 2	45	0.035

730	c	CHR086	Chronic Conjunctivitis	45	0.035

731		FCH001	Fuchs' Endothelial Dystrophy	44	0.035

732		SPN032	Spindle Cell Carcinoma	44	0.035

733	c	ATM101	Autoimmune Gastritis	43	0.035

734		CRS001	Crescentic Glomerulonephritis	43	0.035

735		PNM013	Pneumococcal Meningitis	42	0.035

736	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.035

737		IDP070	Idiopathic Scoliosis	42	0.035

738		MSN004	Mesenchymal Cell Neoplasm	41	0.035

739		LCH016	Lichen Sclerosus Et Atrophicus	41	0.035

740	c	FNC030	Fanconi Anemia, Complementation Group G	41	0.035

741		ADS004	Aids Dementia Complex	40	0.035

742	P	SPR119	Spermatogenic Failure, X-Linked, 1	39	0.035

743		CRN020	Coronary Restenosis	39	0.035

744		CTN004	Cutaneous Fibrous Histiocytoma	39	0.035

745		PCH007	Pouchitis	39	0.035

746		ADR004	Adrenal Cortical Adenocarcinoma	39	0.035

747	c	OVR114	Ovarian Cancer 1	38	0.035

748		ACR005	Acrodermatitis	38	0.035

749		SRC002	Sarcomatoid Renal Cell Carcinoma	38	0.035

750		SHW001	Shwartzman Phenomenon	37	0.035

751		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.035

752		GLM044	Glomerular Disease	37	0.035

753		KKC001	Kikuchi Disease	36	0.035

754		CRY036	Cryptogenic Cirrhosis	36	0.035

755	c	GLC078	Glaucoma 1, Open Angle, F	35	0.035

756		PLM011	Plummer's Disease	35	0.035

757		FXD003	Fixed Drug Eruption	35	0.035

758		SLL001	Sialolithiasis	35	0.035

759	c	ATM021	Autoimmune Inner Ear Disease	34	0.035

760		SPT007	Spitz Nevus	34	0.035

761		HNS001	Hansen's Disease	34	0.035

762		PLM028	Pulmonary Coin Lesion	33	0.035

763	c	LRG017	Large Intestine Cancer	32	0.035

764		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.035

765		GLL029	Gallbladder Adenoma	30	0.035

766		CRT069	Cortical Malformations, Occipital	30	0.035

767		ACR097	Acrodermatitis Chronica Atrophicans	27	0.035

768		CCH001	Cochlear Disease	26	0.035

769		ISL004	Isolated Gonadotropin-Releasing Hormone Deficiency	26	0.035

770		ASB003	Asbestos Intoxication	26	0.035

771		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.035

772		INT334	Intellectual Developmental Disorder and Retinitis Pigmentosa	19	0.035

773		LSS034	Lissencephaly Type Iii and Bone Dysplasia	16	0.035

774		CNG529	Congenital Femoral Deficiency	15	0.035

775		FRC013	Fructose Utilization	15	0.035

776		NRL016	Neural Tube Defects	82	0.025

777	c	TBR025	Tuberous Sclerosis 1	77	0.025

778		ADR007	Adrenoleukodystrophy	75	0.025

779	P	SCH015	Schizophrenia	74	0.025

780	c	BTT014	Beta-Thalassemia	74	0.025

781	c	TBR026	Tuberous Sclerosis 2	72	0.025

782	P	WSK001	Wiskott-Aldrich Syndrome	72	0.025

783	P	EPL164	Epilepsy	71	0.025

784		MLT157	Multiple System Atrophy 1	70	0.025

785	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	0.025

786	P	TTR001	Tetralogy of Fallot	70	0.025

787	P	TBR001	Tuberous Sclerosis	70	0.025

788	P	DMN001	Diamond-Blackfan Anemia	69	0.025

789		WRN001	Werner Syndrome	69	0.025

790	P	RTH006	Rothmund-Thomson Syndrome, Type 2	69	0.025

791		CRB037	Cerebral Palsy	69	0.025

792	P	SLP006	Sleep Apnea	69	0.025

793		ART016	Aortic Aneurysm	69	0.025

794		MST024	Mastocytosis, Cutaneous	69	0.025

795	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.025

796		RCK004	Rickets	68	0.025

797		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	68	0.025

798		PSY004	Psychotic Disorder	67	0.025

799	c	MGR028	Migraine with or Without Aura 1	67	0.025

800	P	DMN002	Dementia	66	0.025

801	c	MCR129	Microvascular Complications of Diabetes 1	66	0.025

802	P	ATR011	Atrial Fibrillation	66	0.025

803		MYL031	Myeloproliferative Neoplasm	66	0.025

804	P	ART005	Arteriovenous Malformation	65	0.025

805	P	AGM001	Agammaglobulinemia	65	0.025

806		ACR006	Aceruloplasminemia	65	0.025

807		IRR002	Irritable Bowel Syndrome	65	0.025

808		GRN037	Granulomatosis with Polyangiitis	65	0.025

809	P	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	65	0.025

810	P	PRS038	Personality Disorder	65	0.025

811	P	ADL010	Adult Respiratory Distress Syndrome	65	0.025

812		APN008	Apnea, Obstructive Sleep	64	0.025

813		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.025

814		ANG020	Angiosarcoma	64	0.025

815		CLF027	Cleft Palate, Isolated	64	0.025

816		TBC004	Tobacco Addiction	64	0.025

817		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.025

818		MSC007	Muscle Hypertrophy	64	0.025

819	P	HYP069	Hyperparathyroidism	63	0.025

820		PLG002	Plague	63	0.025

821	c	MLG084	Malignant Fibrous Histiocytoma	63	0.025

822	P	MVM001	Movement Disease	63	0.025

823		RHB001	Rhabdoid Cancer	63	0.025

824		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.025

825	c	BRN108	Branchiootic Syndrome 1	62	0.025

826	c	SVR001	Severe Acute Respiratory Syndrome	62	0.025

827		BLL006	Bullous Pemphigoid	62	0.025

828	P	BCK002	Beckwith-Wiedemann Syndrome	62	0.025

829	c	NMN013	Niemann-Pick Disease, Type a	62	0.025

830		HYP810	Hypereosinophilic Syndrome, Idiopathic	62	0.025

831		MSL001	Measles	62	0.025

832		PSR001	Psoriatic Arthritis	61	0.025

833	P	INT143	Interstitial Cystitis	61	0.025

834	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.025

835		YLL002	Yellow Fever	61	0.025

836		RCT015	Reactive Arthritis	61	0.025

837		SDD001	Sudden Infant Death Syndrome	61	0.025

838		APP008	Appendicitis	61	0.025

839		LBR030	Leber Optic Atrophy	60	0.025

840	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.025

841		HYD002	Hydronephrosis	60	0.025

842	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	60	0.025

843		ETN001	Eating Disorder	60	0.025

844	P	THL005	Thalassemia	60	0.025

845	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.025

846		VGN017	Vaginal Cancer	60	0.025

847		SPP011	Suppression of Tumorigenicity 12	59	0.025

848		PRT013	Portal Hypertension	59	0.025

849		IDP011	Idiopathic Interstitial Pneumonia	59	0.025

850		LGS001	Legius Syndrome	59	0.025

851		DBN001	Dubin-Johnson Syndrome	59	0.025

852	P	CYS018	Cystitis	59	0.025

853		AVN001	Avian Influenza	59	0.025

854		GLB001	Gilbert Syndrome	58	0.025

855		CRY005	Cryptococcosis	58	0.025

856	P	TYR004	Tyrosinemia	58	0.025

857		FBR047	Fibromyalgia	58	0.025

858		CHR072	Chordoma	58	0.025

859	c	PRM005	Primary Hyperparathyroidism	58	0.025

860	P	EPD083	Epidermodysplasia Verruciformis 1	58	0.025

861		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.025

862		BRS051	Breast Disease	58	0.025

863	c	DWL002	Dowling-Degos Disease 1	58	0.025

864		LNG108	Langerhans Cell Histiocytosis	58	0.025

865		CST005	Castleman Disease	57	0.025

866	c	CHL119	Cholangitis, Primary Sclerosing	57	0.025

867	P	SLV026	Salivary Gland Carcinoma	57	0.025

868		THY122	Thyroid Gland Cancer	57	0.025

869	P	PRN023	Prion Disease	57	0.025

870		THR024	Thrombosis	57	0.025

871		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.025

872		VSC002	Vascular Dementia	57	0.025

873		PHR003	Pharyngitis	57	0.025

874	P	PYL005	Pyelonephritis	56	0.025

875		CMR002	Coumarin Resistance	56	0.025

876	c	INT072	Intestinal Pseudo-Obstruction	56	0.025

877		ALL010	Allergic Contact Dermatitis	56	0.025

878		ANN002	Anencephaly	56	0.025

879		SML019	Smallpox	56	0.025

880	P	HYP838	Hyperlipidemia, Familial Combined, 3	56	0.025

881	c	FML035	Familial Hyperlipidemia	55	0.025

882	P	SCK002	Sick Sinus Syndrome	55	0.025

883		ORL004	Oral Submucous Fibrosis	55	0.025

884	P	PLM034	Pulmonary Emphysema	55	0.025

885		PRP009	Peripartum Cardiomyopathy	55	0.025

886		GNG005	Gangliocytoma	55	0.025

887		FLR002	Filariasis	55	0.025

888		END040	Endogenous Depression	55	0.025

889	P	SPN052	Spondyloarthropathy	54	0.025

890		RSC001	Rosacea	54	0.025

891		BRN015	Bronchiolo-Alveolar Adenocarcinoma	54	0.025

892		HMN009	Hemangioblastoma	54	0.025

893		GST037	Gastroparesis	54	0.025

894		PPL022	Papilloma	54	0.025

895		CLR030	Clear Cell Renal Cell Carcinoma	53	0.025

896	c	BRS111	Breast-Ovarian Cancer, Familial 2	53	0.025

897	P	RTN016	Retinal Degeneration	53	0.025

898		OCL006	Ocular Hypertension	53	0.025

899		MST005	Mastitis	53	0.025

900	c	PRD040	Periodontitis, Chronic	53	0.025

901		BRD004	Borderline Personality Disorder	53	0.025

902	P	CNT005	Central Nervous System Lymphoma	53	0.025

903		INT075	Intracranial Hypertension	53	0.025

904		INT051	Intussusception	53	0.025

905	P	RTN022	Retinal Vein Occlusion	53	0.025

906	c	HPT007	Hepatitis E	53	0.025

907		ALC009	Alcoholic Liver Cirrhosis	53	0.025

908		EXP004	Exophthalmos	52	0.025

909		GNG002	Ganglioneuroma	52	0.025

910		CHN054	Chondrodysplasia, Blomstrand Type	52	0.025

911		NRT004	Neuritis	52	0.025

912	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.025

913		PLS007	Plasmodium Falciparum Malaria	52	0.025

914		FLT011	Felty Syndrome	52	0.025

915	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.025

916		DFF036	Differentiated Thyroid Carcinoma	52	0.025

917	P	OVR049	Ovarian Disease	52	0.025

918	c	VRL005	Viral Pneumonia	52	0.025

919		SRS001	Serous Cystadenocarcinoma	52	0.025

920	P	HMP007	Hemophilia	51	0.025

921		TRC010	Trichotillomania	51	0.025

922		PLS009	Plasma Cell Neoplasm	51	0.025

923		ANK001	Ankylosis	51	0.025

924		CLR109	Colorectal Adenocarcinoma	51	0.025

925		CYS014	Cystadenocarcinoma	51	0.025

926		LNG031	Lung Benign Neoplasm	51	0.025

927	P	LSS002	Lissencephaly	51	0.025

928		SPN019	Spondylolisthesis	51	0.025

929		ACH005	Achalasia	51	0.025

930		TNG007	Tongue Carcinoma	51	0.025

931	P	HYP040	Hypospadias	51	0.025

932		PNM005	Pneumonic Plague	51	0.025

933		CHR005	Chorioamnionitis	51	0.025

934		PRT029	Parathyroid Adenoma	50	0.025

935		PLR007	Pleural Empyema	50	0.025

936		SCB001	Scabies	50	0.025

937	P	OVR082	Overgrowth Syndrome	50	0.025

938		RTN003	Retinal Ischemia	50	0.025

939	P	MYS079	Miyoshi Muscular Dystrophy	50	0.025

940		BLP005	Blepharitis	50	0.025

941	P	ESN008	Eosinophilic Pneumonia	50	0.025

942		CHL122	Cholesteatoma of Middle Ear	50	0.025

943		CRT013	Carotid Stenosis	50	0.025

944		HNT002	Hantavirus Pulmonary Syndrome	50	0.025

945	P	SCK005	Sickle Cell Disease	50	0.025

946	c	INF145	Infantile Liver Failure Syndrome 1	50	0.025

947		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.025

948		MCP006	Mucoepidermoid Carcinoma	50	0.025

949	P	PNV001	Panuveitis	50	0.025

950	P	AGG001	Aggressive Periodontitis	50	0.025

951		PRN009	Paranoid Schizophrenia	50	0.025

952		BLR001	Biliary Atresia	50	0.025

953		HMG002	Hemoglobinuria	50	0.025

954		ILT001	Ileitis	50	0.025

955		DYS073	Dysphagia	50	0.025

956	c	PSR021	Psoriasis 14, Pustular	50	0.025

957	P	MYT002	Myotonic Dystrophy	49	0.025

958		BLL004	Bullous Keratopathy	49	0.025

959	P	CRV039	Cervicitis	49	0.025

960		DFF035	Diffuse Cutaneous Systemic Sclerosis	49	0.025

961		CCN002	Cocaine Abuse	49	0.025

962	P	CRV031	Cervical Adenocarcinoma	49	0.025

963		MNN009	Meningoencephalitis	49	0.025

964	P	SDR003	Sideroblastic Anemia	49	0.025

965		FRN020	Frontal Fibrosing Alopecia	49	0.025

966		LRN003	Learning Disability	49	0.025

967		WTH001	Withdrawal Disorder	48	0.025

968		EVN001	Evans' Syndrome	48	0.025

969		PLM035	Pulmonary Eosinophilia	48	0.025

970		DBT006	Diabetic Macular Edema	48	0.025

971		GNG008	Ganglioneuroblastoma	48	0.025

972	c	VRL012	Viral Meningitis	48	0.025

973	c	PRM226	Primary Central Nervous System Lymphoma	48	0.025

974	c	HYD064	Hydrocephalus, Congenital, 1	48	0.025

975	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.025

976		SXL003	Sexual Disorder	47	0.025

977	c	PRM031	Primary Autosomal Recessive Microcephaly	47	0.025

978		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.025

979	P	PRR002	Pure Red-Cell Aplasia	47	0.025

980		PRC003	Proctitis	47	0.025

981		CRN027	Corneal Neovascularization	47	0.025

982	P	CLL015	Collagen Disease	47	0.025

983		KHN001	Kuhnt-Junius Degeneration	47	0.025

984	P	ENC008	Encephalocele	47	0.025

985		RTN001	Retinal Vasculitis	47	0.025

986	c	ADL052	Adult Acute Lymphocytic Leukemia	47	0.025

987	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.025

988		MLT113	Multicentric Castleman Disease	47	0.025

989		STR103	Streptococcus Pneumonia	47	0.025

990	P	VTR007	Vitreoretinopathy	46	0.025

991		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.025

992		ASP004	Asphyxia Neonatorum	46	0.025

993	c	CHR048	Chronic Rhinitis	46	0.025

994	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.025

995	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.025

996		CLN045	Colonic Benign Neoplasm	46	0.025

997		EXS001	Exostosis	46	0.025

998		PLL012	Pollen Allergy	46	0.025

999		KRT013	Keratolytic Winter Erythema	46	0.025

1000		EXT033	Extrapulmonary Tuberculosis	46	0.025

1001	c	FNC047	Fanconi Anemia, Complementation Group Q	46	0.025

1002		CHD004	Chudley-Mccullough Syndrome	46	0.025

1003		CHR008	Choroiditis	46	0.025

1004		GRW007	Growth Hormone Deficiency	46	0.025

1005		GST012	Gastroesophageal Junction Adenocarcinoma	46	0.025

1006		OBS004	Obstructive Hydrocephalus	46	0.025

1007		SQM002	Squamous Cell Papilloma	46	0.025

1008	c	EST002	Estrogen-Receptor Negative Breast Cancer	45	0.025

1009	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.025

1010		CNV002	Conversion Disorder	45	0.025

1011		URT010	Ureteral Obstruction	45	0.025

1012	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.025

1013	c	SBC007	Subacute Thyroiditis	45	0.025

1014	P	ATS406	Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2	45	0.025

1015		NNS002	Nonspecific Interstitial Pneumonia	45	0.025

1016	c	SPR009	Sporadic Breast Cancer	45	0.025

1017	c	MCR247	Microcephaly 1, Primary, Autosomal Recessive	45	0.025

1018	c	CLR017	Clear Cell Sarcoma	45	0.025

1019		CYS009	Cystadenoma	44	0.025

1020		CHL149	Childhood Acute Myeloid Leukemia	44	0.025

1021		DWR001	Dwarfism	44	0.025

1022	P	END039	Endodermal Sinus Tumor	44	0.025

1023		CNV018	Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis	44	0.025

1024	P	ATX024	Ataxia-Oculomotor Apraxia 3	44	0.025

1025		NDL001	Nodular Malignant Melanoma	44	0.025

1026	P	FBR003	Fibrous Histiocytoma	44	0.025

1027	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.025

1028		SPN040	Spinal Cancer	44	0.025

1029	P	BCT020	Bacteremia 2	44	0.025

1030		DYS018	Dysostosis	44	0.025

1031		CLN003	Clonorchiasis	44	0.025

1032		MTR010	Mature Teratoma	44	0.025

1033	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.025

1034	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.025

1035		CLN044	Colon Adenoma	44	0.025

1036	c	ATM097	Autoimmune Lymphoproliferative Syndrome, Type Iia	43	0.025

1037	P	ATX039	Ataxia-Pancytopenia Syndrome	43	0.025

1038		RDC006	Red Cell Aplasia	43	0.025

1039		DYS032	Dystrophinopathies	43	0.025

1040		MGS001	Megaesophagus	43	0.025

1041		BCL002	B Cell Deficiency	43	0.025

1042		MDD018	Middle East Respiratory Syndrome	43	0.025

1043		PRS042	Prostate Disease	43	0.025

1044		DNG001	Dengue Shock Syndrome	43	0.025

1045		HMP009	Haemophilus Influenzae	43	0.025

1046		DRG002	Drug-Induced Hepatitis	43	0.025

1047		PMP004	Pemphigus Foliaceus	43	0.025

1048		VRL003	Variola Major	42	0.025

1049		VCT001	Vacterl Association	42	0.025

1050		BLR013	Biliary Tract Cancer	42	0.025

1051	P	LBY004	Labyrinthitis	42	0.025

1052		ATX019	Ataxia with Vitamin E Deficiency	42	0.025

1053		THY009	Thyroid Lymphoma	42	0.025

1054	c	PRM212	Primary Microcephaly	42	0.025

1055		TND006	Tendinosis	42	0.025

1056		LRG008	Large Granular Lymphocyte Leukemia	41	0.025

1057		SLV003	Salivary Gland Disease	41	0.025

1058	c	MCR112	Microvascular Complications of Diabetes 2	41	0.025

1059		PST053	Postherpetic Neuralgia	40	0.025

1060	P	LTH003	Lethal Congenital Contracture Syndrome	40	0.025

1061		ANX004	Anoxia	40	0.025

1062		HYP784	Hypogonadism, Male	40	0.025

1063		MCL003	Macular Holes	40	0.025

1064		IDP064	Idiopathic Neutropenia	40	0.025

1065	c	FNC052	Fanconi Anemia, Complementation Group T	40	0.025

1066	P	ALK015	Alk-Positive Anaplastic Large Cell Lymphoma	40	0.025

1067		ALD013	Aldosterone-Producing Adenoma	39	0.025

1068		ORL012	Oral Leukoplakia	39	0.025

1069		KRK001	Krukenberg Carcinoma	39	0.025

1070		TST018	Testicular Yolk Sac Tumor	39	0.025

1071		AML001	Amelanotic Melanoma	39	0.025

1072		SCR011	Scrapie	39	0.025

1073		CRN288	Corneal Dystrophy, Band-Shaped	38	0.025

1074		ADR022	Adrenomyeloneuropathy	38	0.025

1075		PRP005	Parapsoriasis	38	0.025

1076		KDN002	Kidney Rhabdoid Cancer	38	0.025

1077		SMT002	Smooth Muscle Tumor	38	0.025

1078		HPT070	Hepatosplenic T-Cell Lymphoma	38	0.025

1079		PRS037	Periostitis	38	0.025

1080		KLD003	Keloid Formation	38	0.025

1081		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	0.025

1082	P	PST059	Pustular Psoriasis	37	0.025

1083	c	HMN022	Human T-Cell Leukemia Virus Type 2	37	0.025

1084		NPH113	Nephroma	37	0.025

1085		SCR003	Secretory Diarrhea	37	0.025

1086		MYC017	Mycobacterium Kansasii	36	0.025