Search results for smad4

869 hits were found for smad4

#	Family	MCID	Name	MIFTS	Score
1	P	TMR010	Tumor Predisposition Syndrome	69	102.535

2		CTN028	Cutaneous Telangiectasia and Cancer Syndrome, Familial	70	99.869

3		INH023	Inherited Cancer-Predisposing Syndrome	53	99.869

4	P	JVN014	Juvenile Polyposis Syndrome	65	80.363

5		GNR035	Generalized Juvenile Polyposis/juvenile Polyposis Coli	41	57.019

6		MYH012	Myhre Syndrome	43	51.803

7		JVN012	Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome	48	50.311

8	P	PNC035	Pancreatic Cancer	86	47.673

9	P	CLR023	Colorectal Cancer	100	41.307

10	P	HRD008	Hereditary Hemorrhagic Telangiectasia	65	33.970

11	P	LNG032	Lung Cancer	98	24.828

12	P	BRS047	Breast Cancer	97	23.233

13		GST040	Gastric Adenocarcinoma	66	21.165

14		PNC129	Pancreatic Adenocarcinoma	65	20.840

15	P	GST053	Gastric Cancer	82	20.777

16		ESP021	Esophageal Cancer	84	19.840

17	P	ADN016	Adenocarcinoma	63	19.480

18	P	LNG064	Lung Cancer Susceptibility 3	70	18.734

19	P	PRS040	Prostate Cancer	95	18.578

20	P	THR014	Thrombocytopenia	66	18.253

21		END057	Endometrial Cancer	71	17.492

22	P	FML364	Familial Thoracic Aortic Aneurysm and Aortic Dissection	71	17.373

23	P	OVR042	Ovarian Cancer	88	16.858

24		CRV035	Cervical Cancer	72	16.656

25		CLN015	Colon Adenocarcinoma	64	16.107

26	P	HPT023	Hepatocellular Carcinoma	95	15.860

27		SQM006	Squamous Cell Carcinoma	59	15.280

28		SQM013	Squamous Cell Carcinoma, Head and Neck	75	15.095

29		ADN018	Adenoma	58	15.044

30	P	BLD062	Bile Duct Cancer	68	14.739

31		DSS008	Disease of Mental Health	74	14.477

32		PNC041	Pancreatic Ductal Adenocarcinoma	51	14.348

33		BRS099	Breast Ductal Carcinoma	61	13.569

34	P	FML011	Familial Adenomatous Polyposis	71	13.511

35	P	PLM037	Pulmonary Hypertension	69	13.383

36		TLN003	Telangiectasis	51	13.169

37		GST103	Gastric Cancer, Hereditary Diffuse	68	13.167

38		CLT003	Colitis	63	12.941

39		ART016	Aortic Aneurysm	69	12.033

40	P	ART005	Arteriovenous Malformation	65	11.652

41		PNC013	Pancreatic Ductal Carcinoma	48	11.582

42		ART074	Aortic Dissection	53	11.573

43		ART017	Aortic Disease	49	11.563

44	P	RHB003	Rhabdomyosarcoma	66	11.362

45		SPP011	Suppression of Tumorigenicity 12	61	11.350

46	P	PNC044	Pancreatitis	61	11.215

47		ULC004	Ulcerative Colitis	74	11.152

48	P	CWD010	Cowden Syndrome	71	11.019

49	P	NSP012	Nasopharyngeal Carcinoma	60	11.019

50	P	HRT032	Heart Disease	84	10.973

51		HRT036	Heritable Thoracic Aortic Disease	36	10.519

52		CLR003	Clear Cell Adenocarcinoma	50	10.413

53		CHL065	Cholangiocarcinoma	58	10.250

54		INT079	Intrahepatic Cholangiocarcinoma	51	10.250

55		ANR040	Aneurysm	60	10.130

56		BRR014	Barrett Esophagus	66	10.044

57		DFC004	Deficiency Anemia	74	9.651

58		PTZ001	Peutz-Jeghers Syndrome	69	9.579

59		BLR013	Biliary Tract Cancer	43	9.570

60		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	9.566

61	P	BRC006	Brachydactyly	52	9.291

62	P	HMR003	Hemorrhagic Disease	59	9.261

63	c	ART115	Aortic Valve Disease 1	72	9.248

64		CLN044	Colon Adenoma	44	9.172

65	c	CWD006	Cowden Syndrome 1	79	9.158

66		ACT119	Acute Promyelocytic Leukemia	62	9.038

67		VPM001	Vipoma	49	8.889

68	c	TLN006	Telangiectasia, Hereditary Hemorrhagic, Type 1	56	8.820

69		ACN001	Acinar Cell Carcinoma	44	8.571

70		PYR010	Peyronie's Disease	50	8.553

71	P	MLN069	Melanoma, Uveal	59	8.510

72		ADN009	Adenosquamous Carcinoma	49	8.510

73		AMP013	Ampulla of Vater Cancer	41	8.486

74	c	LCL006	Localized Scleroderma	64	8.458

75	P	TTR001	Tetralogy of Fallot	69	8.425

76		OCL022	Ocular Melanoma	54	8.425

77	P	SML016	Small Intestine Cancer	47	8.383

78	P	LRG016	Large Intestine Adenocarcinoma	34	8.280

79	P	MCR010	Microcephaly	59	8.280

80		MCN008	Mucinous Cystadenocarcinoma	39	8.280

81	c	PLM164	Pulmonary Hypertension, Primary, 1	80	8.133

82	c	ART067	Aortic Aneurysm, Familial Thoracic 1	61	7.362

83	P	LYN001	Lynch Syndrome	76	7.154

84		PLM134	Pulmonary Fibrosis, Idiopathic	76	7.126

85	P	LYS001	Loeys-Dietz Syndrome	65	6.956

86		OVR059	Ovary Adenocarcinoma	49	6.928

87		APP009	Appendix Adenocarcinoma	47	6.747

88		SML009	Small Intestine Adenocarcinoma	57	6.732

89	P	HRD144	Hereditary Mixed Polyposis Syndrome	54	6.703

90	P	LFR001	Li-Fraumeni Syndrome	73	6.634

91	c	CLR087	Colorectal Cancer 12	34	6.419

92	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	60	6.419

93		APP010	Appendix Cancer	44	6.000

94	c	FML311	Familial Colorectal Cancer Type X	37	6.000

95		NPH018	Nephrogenic Systemic Fibrosis	49	6.000

96	c	SPN395	Spinal Muscular Atrophy, Type Ii	55	5.958

97	c	SPN398	Spinal Muscular Atrophy, Type Iv	44	5.958

98		URT024	Urethra Clear Cell Adenocarcinoma	26	5.958

99		MCN005	Mucinous Intrahepatic Cholangiocarcinoma	23	5.958

100		DDN010	Duodenum Cancer	52	5.855

101		CLL012	Cell Type Benign Neoplasm	21	5.855

102		CRD007	Cardiovascular Organ Benign Neoplasm	25	5.855

103		ALB025	Albinism, Ocular, with Late-Onset Sensorineural Deafness	49	5.855

104	c	HMC009	Hemochromatosis Type 2	58	5.855

105	c	ATS417	Autosomal Dominant Non-Syndromic Intellectual Disability 19	28	5.855

106		APP018	Appendix Disease	31	5.855

107		MLG168	Malignant Exocrine Pancreas Neoplasm	30	5.855

108		BRT013	Baritosis	32	5.855

109		OVR047	Ovarian Cystadenocarcinoma	38	5.855

110		GST038	Gastrointestinal Adenoma	21	5.855

111		DDN027	Duodenum Disease	36	5.855

112		INT253	Intestinal Benign Neoplasm	46	5.855

113	P	ART028	Aortic Aneurysm, Familial Thoracic 4	61	4.190

114		ADN011	Adenoid Cystic Carcinoma	68	3.699

115		LNG039	Lung Squamous Cell Carcinoma	57	3.625

116	P	BLD134	Bladder Cancer	79	3.367

117	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	3.019

118		BLD173	Bladder Small Cell Carcinoma	44	2.999

119	P	SKN015	Skin Carcinoma	71	2.897

120		GLM045	Glioma	62	2.617

121		ADN089	Adenosquamous Lung Carcinoma	49	2.611

122		BRN015	Bronchiolo-Alveolar Adenocarcinoma	55	2.611

123	c	SML038	Small Cell Cancer of the Lung	69	2.487

124		ORL015	Oral Squamous Cell Carcinoma	43	2.447

125		DST001	Distal Biliary Tract Carcinoma	24	2.379

126	P	SPP010	Suppressor of Tumorigenicity 3	51	2.270

127		RNL077	Renal Fibrosis	46	2.268

128	P	PLM036	Pulmonary Fibrosis	65	2.143

129		IDP092	Idiopathic/heritable Pulmonary Arterial Hypertension	43	2.060

130	c	MCR133	Microvascular Complications of Diabetes 4	41	1.998

131	c	MCR113	Microvascular Complications of Diabetes 3	52	1.998

132	c	MCR130	Microvascular Complications of Diabetes 6	41	1.998

133	c	MCR120	Microvascular Complications of Diabetes 7	47	1.998

134		THY029	Thyroid Carcinoma	54	1.962

135		GLL048	Glial Tumor	52	1.957

136	c	BSL007	Basal Cell Carcinoma	68	1.921

137		SKN022	Skin Squamous Cell Carcinoma	54	1.910

138	c	BRN108	Branchiootic Syndrome 1	63	1.884

139		HYP266	Hypoxia	56	1.861

140	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	1.751

141		NNL005	Non-Alcoholic Fatty Liver Disease	63	1.748

142		IRN002	Iron Metabolism Disease	56	1.716

143		OST159	Osteogenic Sarcoma	66	1.716

144		RNL114	Renal Cell Carcinoma, Nonpapillary	79	1.697

145	P	RCT021	Rectum Cancer	54	1.614

146		MRF001	Marfan Syndrome	76	1.538

147		HLX001	Helix Syndrome	47	1.513

148		URT010	Ureteral Obstruction	45	1.513

149	P	INF037	Inflammatory Bowel Disease	53	1.504

150		CRH001	Crohn's Disease	80	1.478

151	c	HPT073	Hepatitis C Virus	71	1.475

152		OVR011	Ovarian Mucinous Adenocarcinoma	34	1.475

153		CLF027	Cleft Palate, Isolated	64	1.470

154		OVR094	Ovarian Epithelial Cancer	39	1.460

155		MNN043	Meningioma, Familial	79	1.419

156	P	ALP008	Alopecia	53	1.403

157	c	WLM013	Wilms Tumor 1	65	1.396

158		CLR109	Colorectal Adenocarcinoma	50	1.385

159		HMS001	Hemosiderosis	48	1.352

160	P	RRH023	Rare Hereditary Hemochromatosis	53	1.352

161		ORL011	Oral Cancer	60	1.337

162		HRD224	Hereditary Nonpolyposis Colon Cancer	51	1.326

163	c	TLN010	Telangiectasia, Hereditary Hemorrhagic, Type 4	21	1.321

164		HRW001	Hair Whorl	35	1.315

165		MCR013	Microphthalmia	60	1.302

166		THY123	Thyroid Gland Follicular Carcinoma	53	1.298

167	c	WLM018	Wilms Tumor 5	54	1.293

168	P	MYM016	Moyamoya Angiopathy	22	1.293

169		PRS129	Prostatic Hyperplasia, Benign	48	1.289

170		PRS045	Prostatic Hypertrophy	52	1.289

171		THY124	Thyroid Gland Papillary Carcinoma	38	1.263

172		SQM016	Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract	16	1.263

173		CRC045	Carcinoma of Gallbladder and Extrahepatic Biliary Tract	20	1.263

174	P	NRB001	Neuroblastoma	66	1.252

175		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.232

176		LKP003	Leukoplakia	39	1.232

177		SRR001	Serrated Polyposis Syndrome	42	1.220

178		ORL012	Oral Leukoplakia	35	1.211

179	P	BND020	Bone Disease	60	1.203

180	P	END044	Endometriosis	62	1.200

181	c	LKM061	Leukemia, Acute Myeloid	83	1.200

182	P	RRT020	Rare Tumor	39	1.200

183		BNR002	Bone Resorption Disease	47	1.189

184	c	PNC103	Pancreatic Cancer 4	25	1.177

185		PLM151	Pulmonary Arteriovenous Fistulas	35	1.169

186	P	MLN008	Melanoma	75	1.166

187		TRM010	Traumatic Brain Injury	50	1.166

188		47X002	47,xyy	48	1.166

189		THR100	Thrombocytopenic Purpura, Autoimmune	60	1.154

190	P	INF032	Infertility	60	1.115

191		TRN018	Transitional Cell Carcinoma	56	1.115

192	P	INS002	in Situ Carcinoma	53	1.115

193	c	PRC016	Pre-Eclampsia	64	1.102

194		PPL052	Papillomatosis, Confluent and Reticulated	34	1.102

195		PRS047	Prostatitis	58	1.102

196		CHR074	Choriocarcinoma	46	1.102

197		RPD005	Rapidly Involuting Congenital Hemangioma	48	1.088

198		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	1.088

199		END041	Endometrial Adenocarcinoma	63	1.079

200		PLM173	Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal	34	1.077

201		PSD011	Pseudovascular Skin Squamous Cell Carcinoma	16	1.077

202	c	TLN011	Telangiectasia, Hereditary Hemorrhagic, Type 2	45	1.071

203		ISC004	Ischemia	61	1.058

204	c	BSL024	Basal Cell Carcinoma 1	54	1.058

205		SKN013	Skin Benign Neoplasm	49	1.058

206		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	1.058

207		MCR011	Microinvasive Gastric Cancer	41	1.042

208		PRS021	Prostatic Adenoma	43	1.042

209		PPL002	Papillary Carcinoma	46	1.042

210		LNG099	Lung Disease	62	1.032

211		SHP005	Shprintzen-Goldberg Craniosynostosis Syndrome	46	1.025

212		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	1.025

213	P	EMB005	Embryonal Rhabdomyosarcoma	53	1.025

214		IRN001	Iron Deficiency Anemia	58	1.025

215	c	FML053	Familial Colorectal Cancer	47	1.009

216		LBL001	Lobular Neoplasia	55	1.008

217	P	SCH015	Schizophrenia	74	1.008

218		LPD008	Lipid Metabolism Disorder	61	1.008

219		SGN002	Signet Ring Cell Adenocarcinoma	46	1.008

220		HYP457	Hypertrophic Scars	42	1.001

221		KLD004	Keloid Disorder	39	0.990

222	P	RTN024	Retinoblastoma	72	0.979

223		GLB002	Glioblastoma	67	0.979

224	P	ART023	Arthropathy	60	0.979

225		THR004	Thrombocytosis	52	0.969

226		PRP030	Purpura	54	0.969

227		PLM052	Pulmonary Arteriovenous Malformation	42	0.969

228	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.947

229	P	OST002	Osteoporosis	77	0.944

230		SVR004	Severe Combined Immunodeficiency	71	0.944

231	c	MSM022	Mismatch Repair Cancer Syndrome 1	69	0.933

232	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	0.932

233	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.932

234		PRC013	Pericarditis	53	0.932

235		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	0.919

236		NRN004	Neuroendocrine Tumor	55	0.919

237		CNS004	Constipation	56	0.919

238		SKN019	Skin Melanoma	70	0.913

239	c	PRG020	Paragangliomas 3	39	0.906

240		CLR030	Clear Cell Renal Cell Carcinoma	54	0.906

241		MCN001	Mucinous Adenocarcinoma	49	0.892

242	P	PLY011	Polycystic Ovary Syndrome	57	0.892

243		MTY003	Mutyh Polyposis	38	0.892

244	c	PCH010	Pachyonychia Congenita 3	43	0.878

245	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.878

246		GST071	Gastrointestinal Carcinoma	46	0.878

247	P	GLL018	Gallbladder Cancer	53	0.878

248	c	CLR077	Colorectal Cancer 10	32	0.865

249		HLC007	Helicobacter Pylori Infection	67	0.864

250		HYD002	Hydronephrosis	58	0.864

251	c	HPT016	Hepatitis B	62	0.864

252	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	79	0.864

253	P	ART022	Arthritis	70	0.864

254		FTT001	Fatty Liver Disease	61	0.864

255	P	NRF002	Neurofibromatosis	60	0.864

256		INT358	Intestinal Polyposis Syndrome	25	0.864

257		LNG012	Lung Occult Squamous Cell Carcinoma	20	0.852

258		PPL004	Papillary Squamous Carcinoma	39	0.852

259		LNG007	Lung Mixed Small Cell and Squamous Cell Carcinoma	20	0.852

260	c	ACT027	Acute Pancreatitis	60	0.851

261	c	HMC039	Hemochromatosis, Type 1	73	0.848

262		END062	Endometrial Hyperplasia	48	0.848

263		RVL002	Ruvalcaba Syndrome	42	0.848

264	P	HPT021	Hepatitis	68	0.848

265		FRZ001	Frozen Shoulder	54	0.848

266		SFT003	Soft Tissue Sarcoma	57	0.848

267		THY128	Thyroid Tumor	33	0.848

268	P	ANT088	Anterior Segment Dysgenesis	53	0.832

269	c	VRL010	Viral Hepatitis	52	0.832

270		KRT009	Keratosis	52	0.832

271		GST033	Gestational Diabetes	61	0.832

272		PTR032	Peters-Plus Syndrome	63	0.832

273	P	CTR002	Cataract	59	0.832

274		MYH016	Myh-Associated Polyposis	38	0.832

275		ECH003	Echinococcosis	52	0.819

276		NNL006	Non-Alcoholic Steatohepatitis	54	0.816

277	P	CLD001	Cleidocranial Dysplasia	64	0.816

278	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	0.816

279	c	HPT001	Hepatitis C	61	0.816

280	P	VSC007	Vascular Disease	62	0.816

281	P	TRT010	Teratoma	50	0.816

282		CRV002	Cervix Uteri Carcinoma in Situ	48	0.816

283		CRV045	Cervical Intraepithelial Neoplasia	38	0.816

284		ANT024	Anthrax Disease	58	0.816

285	c	CLD019	Cleidocranial Dysplasia Spectrum Disorder	20	0.816

286		DWR001	Dwarfism	45	0.816

287	P	ACT008	Actinic Keratosis	54	0.816

288		MCN019	Mucinous Adenocarcinoma of Ovary	16	0.816

289		WRN001	Werner Syndrome	69	0.798

290		MSC007	Muscle Hypertrophy	64	0.798

291		GLC003	Glucose Intolerance	53	0.798

292	c	FML347	Familial Adenomatous Polyposis 2	56	0.798

293	P	MYC007	Myocardial Infarction	69	0.798

294		BRT054	Brittle Bone Disorder	74	0.798

295		OSS012	Osseous Heteroplasia, Progressive	61	0.798

296		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.798

297	P	CRN300	Coronary Heart Disease 1	73	0.798

298	P	ATT003	Attenuated Familial Adenomatous Polyposis	57	0.798

299	P	NRP001	Neuropathy	59	0.798

300	P	PRG139	Progeroid Syndrome	29	0.798

301		PRM013	Premature Menopause	57	0.779

302		RTN017	Retinal Detachment	60	0.779

303		TNG009	Tongue Squamous Cell Carcinoma	43	0.779

304		TRT017	Teratoma, Ovarian	28	0.779

305		IGG001	Iga Glomerulonephritis	50	0.779

306	P	HML002	Hemolytic Anemia	62	0.779

307		OVR109	Ovarian Germ Cell Teratoma	32	0.779

308		HRT011	Heart Septal Defect	49	0.779

309	P	HYP086	Hypothyroidism	69	0.779

310		HYP066	Hyperglycemia	60	0.779

311		CRV038	Cervical Squamous Cell Carcinoma	56	0.779

312	c	HMP012	Hemophagocytic Lymphohistiocytosis, Familial, 2	47	0.779

313		BRN056	Bronchopulmonary Dysplasia	57	0.779

314	P	GLM040	Glioma Susceptibility 1	70	0.763

315	P	OLG002	Oligodendroglioma	66	0.763

316	c	CLR085	Colorectal Cancer 1	42	0.762

317	c	CLR075	Colorectal Cancer 3	31	0.762

318		MLN065	Melanocytic Nevus Syndrome, Congenital	61	0.762

319		MYP002	Myoepithelial Carcinoma	46	0.762

320		EPT010	Epithelial-Myoepithelial Carcinoma	55	0.762

321	P	SNS001	Sensorineural Hearing Loss	59	0.759

322	P	PNM006	Pneumoconiosis	55	0.759

323		INT395	Intracranial Meningioma	48	0.759

324		CRY035	Cryptorchidism, Unilateral or Bilateral	57	0.759

325		ERM002	Ear Malformation	35	0.759

326	P	VNT002	Ventricular Septal Defect	58	0.759

327	P	NPH012	Nephrotic Syndrome	62	0.759

328		ANT018	Anthracosis	51	0.759

329	P	RST002	Restrictive Cardiomyopathy	54	0.759

330	P	FBR017	Fibrosarcoma	55	0.759

331		VLV034	Vulva Squamous Cell Carcinoma	49	0.759

332	P	MYP004	Myopathy	67	0.759

333		SCR001	Secretory Meningioma	40	0.759

334		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.759

335	P	ADT009	Auditory Neuropathy Spectrum Disorder	33	0.759

336		THR123	Thrombotic Microangiopathy	40	0.759

337		VLL006	Villous Adenoma	40	0.737

338	P	CRC039	Coarctation of Aorta	46	0.737

339	c	PNC108	Pancreatitis, Hereditary	68	0.737

340		RTN020	Retinal Vascular Disease	45	0.737

341	P	GLM007	Glomerulonephritis	59	0.737

342		PLS011	Plasmacytoma	56	0.737

343		SMN007	Seminoma	42	0.737

344		ALL006	Allergic Asthma	56	0.737

345		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.713

346		IMM167	Immune Deficiency Disease	77	0.713

347	P	EXN002	Exanthem	58	0.713

348	c	LFR007	Li-Fraumeni Syndrome 2	44	0.713

349	P	DFF019	Diffuse Gastric Cancer	50	0.713

350		ACT098	Acute Erythroid Leukemia	55	0.713

351		DBL002	Double Outlet Right Ventricle	57	0.713

352		DFF002	Diffuse Pulmonary Fibrosis	27	0.713

353		SNS003	Sensory Peripheral Neuropathy	51	0.713

354	P	KDN017	Kidney Cancer	60	0.713

355		SLC006	Silicosis	55	0.713

356		LNG031	Lung Benign Neoplasm	51	0.713

357	P	BRS044	Breast Adenocarcinoma	58	0.713

358		NNS035	Nonsyndromic 46,xx Testicular Disorders of Sex Development	10	0.713

359	P	HYP730	Hypogonadotropic Hypogonadism	54	0.685

360		PRT019	Protein-Losing Enteropathy	44	0.685

361	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	0.685

362	c	DWL002	Dowling-Degos Disease 1	58	0.685

363		GRG001	Greig Cephalopolysyndactyly Syndrome	64	0.685

364		HYP060	Hyperinsulinism	53	0.685

365		LRY018	Laryngeal Squamous Cell Carcinoma	47	0.685

366		LYM027	Lymphopenia	56	0.685

367		GNG002	Ganglioneuroma	52	0.685

368		HYP080	Hypogonadism	49	0.685

369		GNG005	Gangliocytoma	54	0.685

370	P	PLY006	Polydactyly	58	0.685

371	P	HRP006	Herpes Simplex	65	0.685

372	c	JVN010	Juvenile Rheumatoid Arthritis	66	0.685

373	P	PRC019	Precocious Puberty	49	0.685

374		MCR004	Macroglobulinemia	48	0.685

375		IRN008	Iron Overload in Africa	51	0.660

376		RJS001	Ruijs-Aalfs Syndrome	47	0.660

377		LMN016	Luminal Breast Carcinoma B	28	0.660

378	P	LMN015	Luminal Breast Carcinoma a	34	0.660

379		HPT079	Hepatoid Adenocarcinoma	39	0.660

380	c	CHL136	Cholestasis, Progressive Familial Intrahepatic, 2	57	0.660

381	c	PRS070	Prostate Cancer, Hereditary, 12	22	0.660

382	c	PRS071	Prostate Cancer, Hereditary, 13	25	0.660

383	c	PRS117	Prostate Cancer, Hereditary, 11	24	0.660

384	c	PRS114	Prostate Cancer, Hereditary, 2	33	0.660

385	c	PRS097	Prostate Cancer, Hereditary, 1	38	0.660

386		ADL096	Adult Hepatocellular Carcinoma	60	0.660

387		PRS015	Prostate Signet Ring Cell Adenocarcinoma	25	0.660

388	c	PRG047	Progressive Familial Intrahepatic Cholestasis	64	0.660

389		PDT042	Pediatric Hepatocellular Carcinoma	50	0.660

390		PTY007	Pityriasis Rotunda	26	0.660

391		FBR086	Fibrolamellar Carcinoma	59	0.660

392		HPT011	Hepatocellular Clear Cell Carcinoma	45	0.660

393		OVR062	Ovary Serous Adenocarcinoma	25	0.660

394		MCP006	Mucoepidermoid Carcinoma	48	0.654

395	P	DRM010	Dermatomyositis	61	0.652

396		HNC001	Henoch-Schoenlein Purpura	56	0.652

397		PLC006	Placental Choriocarcinoma	38	0.652

398		ALL029	Allergic Disease	61	0.652

399		PNC034	Pancreas Disease	49	0.652

400		CRN006	Coronary Aneurysm	41	0.652

401	P	MSC003	Muscular Atrophy	52	0.652

402		CHL078	Childhood-Onset Schizophrenia	29	0.652

403	P	CRN074	Coronary Artery Aneurysm	41	0.652

404	c	DNT047	Dentinogenesis Imperfecta Type 2	35	0.652

405		MRK001	Merkel Cell Carcinoma	65	0.642

406		CRC021	Carcinosarcoma	62	0.634

407		CYN002	Cyanosis, Transient Neonatal	43	0.609

408	P	ASP006	Aspergillosis	71	0.609

409	P	ALL008	Allergic Bronchopulmonary Aspergillosis	53	0.609

410		CYS008	Cystic Echinococcosis	57	0.609

411		INS001	Insulinoma	59	0.609

412		VCC001	Vaccinia	49	0.609

413	c	PNC106	Pancreatic Agenesis 1	51	0.609

414		GST030	Gastrinoma	45	0.609

415		EXT034	Extrinsic Allergic Alveolitis	56	0.609

416		THY121	Thyroid Gland Anaplastic Carcinoma	66	0.560

417		CHR072	Chordoma	57	0.544

418		MYL005	Myelofibrosis	70	0.544

419	P	LKM071	Leukemia, Chronic Lymphocytic	74	0.544

420	c	GLM043	Glioma Susceptibility 9	30	0.539

421	c	GLM047	Glioma Susceptibility 3	32	0.539

422	c	GLM025	Glioma Susceptibility 2	29	0.539

423		THY127	Thyroid Gland Hurthle Cell Carcinoma	19	0.539

424		THY027	Thymus Squamous Cell Carcinoma	24	0.539

425		PRM126	Primary Peritoneal Carcinoma	61	0.539

426	P	SLV026	Salivary Gland Carcinoma	60	0.527

427		ALV002	Alveolar Echinococcosis	56	0.506

428		48X005	48,xyyy	39	0.506

429	P	FLL037	Follicular Lymphoma	73	0.484

430		THY022	Thymic Carcinoma	56	0.484

431		TCL027	T-Cell Acute Lymphoblastic Leukemia	52	0.441

432	P	LKM002	Leukemia	66	0.413

433		CLR108	Colorectal Adenoma	63	0.400

434	P	SYS005	Systemic Scleroderma	73	0.386

435		LYM143	Lymphoma, Non-Hodgkin, Familial	79	0.381

436		PLS025	Plasmablastic Lymphoma	56	0.381

437		END032	Endometrial Clear Cell Adenocarcinoma	33	0.381

438		FLL027	Fallopian Tube Carcinoma	66	0.381

439		THY025	Thymus Cancer	56	0.381

440		KRK001	Krukenberg Carcinoma	39	0.381

441		PNS010	Penis Squamous Cell Carcinoma	45	0.381

442	P	LNG035	Lung Large Cell Carcinoma	53	0.381

443	c	TYP010	Type C Thymoma	25	0.381

444		SCL043	Sclerosing Mucoepidermoid Carcinoma with Eosinophilia	18	0.381

445		LNG006	Lung Occult Large Cell Carcinoma	14	0.381

446		PNS005	Penis Mixed Squamous Cell Carcinoma	12	0.381

447		LYM018	Lymphoepithelioma-Like Thymic Carcinoma	26	0.381

448	P	LYM118	Lymphoma	69	0.358

449		NRN001	Neuroendocrine Carcinoma	47	0.358

450		ATM095	Autoimmune Disease	61	0.342

451		TRC005	Tracheal Stenosis	43	0.326

452		OST003	Osteonecrosis	61	0.310

453		LYN004	Lynch Syndrome I	60	0.310

454		KLD003	Keloid Formation	34	0.310

455	c	FML346	Familial Adenomatous Polyposis 1	65	0.310

456		LVR012	Liver Cirrhosis	62	0.310

457		END086	End Stage Renal Disease	54	0.310

458		HRT015	Heritable Pulmonary Arterial Hypertension	46	0.310

459		SZR028	Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome	36	0.292

460	P	ANP001	Anaplastic Large Cell Lymphoma	61	0.292

461	c	SCL052	Scleroderma, Familial Progressive	60	0.292

462		GST029	Gastric Cardia Adenocarcinoma	29	0.292

463	P	BCL017	B-Cell Lymphoma	57	0.292

464	c	46X071	46,xy Disorder of Sexual Development Due to Dihydrotestosterone Backdoor Pathway Biosynthesis Defect	42	0.292

465	c	LKM063	Leukemia, Chronic Myeloid	71	0.273

466		TNG007	Tongue Carcinoma	55	0.273

467	c	SPN225	Spondyloarthropathy 1	70	0.273

468		GST086	Gastric Adenocarcinoma and Proximal Polyposis of the Stomach	30	0.273

469	c	AVS006	Avascular Necrosis of Femoral Head, Primary, 1	42	0.273

470		SPN051	Spondylitis	51	0.273

471		INF009	Inflammatory Spondylopathy	30	0.273

472		SKN016	Skin Disease	62	0.273

473	P	MLT074	Multiple Endocrine Neoplasia	58	0.273

474	P	GST044	Gastritis	55	0.273

475	P	KDN018	Kidney Disease	72	0.273

476	P	HRD200	Hereditary Breast Ovarian Cancer Syndrome	68	0.273

477		GRN022	Granulosa Cell Tumor of the Ovary	34	0.273

478	c	MLT156	Multiple Endocrine Neoplasia, Type I	71	0.253

479	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.253

480	P	MLT020	Multiple Sclerosis	79	0.253

481		BRN032	Brain Glioma	45	0.253

482		CNV018	Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis	42	0.253

483		KPS004	Kaposi Sarcoma	76	0.253

484		PNM010	Pneumothorax, Primary Spontaneous	58	0.253

485		LMY002	Leiomyoma	51	0.253

486		PLM009	Pleomorphic Adenoma Carcinoma	33	0.253

487		PNM008	Pneumothorax	54	0.253

488	P	OBS001	Obstructive Jaundice	49	0.253

489		INT066	Interstitial Lung Disease	60	0.253

490		PSD007	Pseudomyxoma Peritonei	52	0.253

491	c	TLN009	Telangiectasia, Hereditary Hemorrhagic, Type 3	18	0.253

492		HRT012	Heart Valve Disease	53	0.253

493		LYM126	Lymphoma Aids Related	44	0.253

494	P	MYL006	Myeloid Leukemia	60	0.253

495		PLM014	Pleomorphic Adenoma	51	0.253

496		VRS002	Virus-Associated Trichodysplasia Spinulosa	30	0.253

497		ACR121	Acromelic Dysplasia	11	0.253

498	P	AST005	Asthma	76	0.231

499		OSS014	Ossification of the Posterior Longitudinal Ligament of Spine	48	0.231

500		PRT251	Proteinuria, Chronic Benign	58	0.231

501	P	GLP001	Geleophysic Dysplasia	46	0.231

502		ACR043	Acromicric Dysplasia	49	0.231

503	P	RHM011	Rheumatoid Arthritis	81	0.231

504	P	WLL002	Weill-Marchesani Syndrome	55	0.231

505	c	PLM128	Pulmonary Hypertension, Primary, 2	28	0.231

506	c	VSC019	Vesicoureteral Reflux 1	56	0.231

507		SVR001	Severe Acute Respiratory Syndrome	68	0.231

508		UTR024	Uterine Carcinosarcoma	58	0.231

509		PPL022	Papilloma	53	0.231

510		SQM002	Squamous Cell Papilloma	45	0.231

511		KHN001	Kuhnt-Junius Degeneration	48	0.231

512	P	LPS002	Liposarcoma	64	0.231

513	P	DNT011	Dentinogenesis Imperfecta	52	0.231

514		SPN035	Spindle Cell Sarcoma	51	0.231

515		ACT058	Active Peptic Ulcer Disease	55	0.231

516	c	CHR684	Chronic Kidney Disease	74	0.231

517		BRN071	Brain Injury	50	0.231

518		APC006	Apc-Associated Polyposis Conditions	22	0.231

519		PRQ002	Paraquat Poisoning	28	0.231

520		CLR137	Clear Cell Adenocarcinoma of the Ovary	31	0.231

521		AGN016	Aging	54	0.206

522	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.206

523		CRT069	Cortical Malformations, Occipital	31	0.206

524	P	MLT008	Multinodular Goiter	42	0.206

525		PRT013	Portal Hypertension	59	0.206

526		DST033	Distichiasis	35	0.206

527	P	SCL057	Scoliosis, Isolated 1	40	0.206

528	P	SCL018	Scoliosis	57	0.206

529		IDP070	Idiopathic Scoliosis	41	0.206

530	P	CNG499	Congenital Anomalies of Kidney and Urinary Tract 2	52	0.206

531		LYM029	Lymphedema-Distichiasis Syndrome	52	0.206

532	P	PYR039	Peyronie Disease	39	0.206

533	P	HMN032	Human Herpesvirus 8	47	0.206

534		SRC014	Sarcoma	64	0.206

535	c	HRD202	Hereditary Lymphedema I	55	0.206

536		OPS001	Opisthorchiasis	41	0.206

537		FLL031	Follicular Adenoma	40	0.206

538		PRG009	Progressive Multifocal Leukoencephalopathy	58	0.206

539		TBL003	Tubular Adenocarcinoma	40	0.206

540		OVR034	Ovarian Clear Cell Adenocarcinoma	39	0.206

541		PNC015	Pancreatic Acinar Cell Adenocarcinoma	39	0.206

542		GTR002	Goiter	52	0.206

543		PLM010	Pulmonary Edema	54	0.206

544	P	THY023	Thymoma	64	0.206

545	c	THY107	Thymoma, Familial	42	0.206

546	P	MSC005	Muscular Dystrophy	66	0.206

547	c	ACT075	Acute Myocardial Infarction	55	0.206

548	P	ATR005	Atrophic Gastritis	50	0.206

549		ACN026	Acinar Cell Carcinoma of Pancreas	27	0.206

550		PRM334	Primary Bone Dysplasia with Increased Bone Density	15	0.206

551		RNL078	Renal Dysplasia	46	0.206

552		INT381	Intraductal Tubulopapillary Neoplasm of Pancreas	12	0.206

553		ART140	Arteries, Anomalies of	52	0.179

554	c	FRS014	Fraser Syndrome 1	56	0.179

555		MYL069	Myeloma, Multiple	77	0.179

556		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.179

557	P	RTN008	Retinitis Pigmentosa	79	0.179

558	c	MCR115	Microvascular Complications of Diabetes 5	65	0.179

559		LPP008	Lipoprotein Quantitative Trait Locus	65	0.179

560	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.179

561	P	SML001	Small Cell Carcinoma	52	0.179

562		DSS032	Disease by Infectious Agent	55	0.179

563		NRR001	Neuroretinitis	42	0.179

564	P	OPN001	Open-Angle Glaucoma	55	0.179

565	P	CRB045	Cerebellar Hypoplasia	40	0.179

566		GST105	Gastroesophageal Adenocarcinoma	42	0.179

567		CKT002	Cakut	48	0.179

568	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	0.179

569		ATH013	Atherosclerosis Susceptibility	63	0.179

570		BRK010	Burkitt Lymphoma	66	0.179

571	c	ATS007	Autism Spectrum Disorder	72	0.179

572		ADR040	Adrenal Gland Pheochromocytoma	45	0.179

573	P	APL001	Aplastic Anemia	73	0.179

574		CHD004	Chudley-Mccullough Syndrome	47	0.179

575		ALL003	Allergic Rhinitis	66	0.179

576	P	CPL014	Capillary Malformation-Arteriovenous Malformation 1	53	0.179

577	P	PHC003	Pheochromocytoma	70	0.179

578	c	TLN008	Telangiectasia, Hereditary Hemorrhagic, Type 5	24	0.179

579	c	GLC092	Glaucoma, Primary Open Angle	61	0.179

580	P	ATS364	Autism	72	0.179

581		BRN012	Bronchiolitis Obliterans	56	0.179

582		BRN002	Bronchiolitis	57	0.179

583		DNT012	Dental Caries	53	0.179

584		CYS009	Cystadenoma	43	0.179

585		ISL001	Islet Cell Tumor	55	0.179

586	P	CRV031	Cervical Adenocarcinoma	48	0.179

587		RTN023	Retinitis	45	0.179

588		BLD039	Bladder Adenocarcinoma	32	0.179

589		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	0.179

590		STR067	Stroke, Ischemic	79	0.179

591		GST019	Gastrointestinal Stromal Tumor	78	0.179

592		URC003	Urachal Adenocarcinoma	30	0.179

593		OBS082	Obstructive Nephropathy	41	0.179

594		CYT002	Cytokine Deficiency	43	0.179

595		FRS019	Farsightedness	35	0.179

596		PTT037	Pituitary Tumors	44	0.179

597		ANL017	Anal Squamous Cell Carcinoma	44	0.179

598		SPL018	Splenomegaly	47	0.179

599		PNC019	Pancreatoblastoma	39	0.179

600	P	INT070	Intestinal Obstruction	57	0.179

601	P	DBT009	Diabetes Mellitus	67	0.179

602	c	MNS014	Monosomy 22	34	0.179

603	P	VTR007	Vitreoretinopathy	45	0.179

604	c	FNC042	Fanconi Anemia, Complementation Group D2	54	0.146

605		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.146

606		ADN027	Adenomyosis	59	0.146

607		RHB024	Rhabdomyosarcoma 2	65	0.146

608	P	ATX030	Ataxia-Telangiectasia	80	0.146

609		INS024	Insulin-Like Growth Factor I	77	0.146

610	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	0.146

611	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.146

612	c	BDY012	Body Mass Index Quantitative Trait Locus 7	43	0.146

613	c	HMP013	Hemophagocytic Lymphohistiocytosis, Familial, 3	47	0.146

614	c	FNC025	Fanconi Anemia, Complementation Group J	52	0.146

615		WST005	West Nile Virus	55	0.146

616	c	BRS098	Breast-Ovarian Cancer, Familial 4	29	0.146

617	c	ATM024	Autoimmune Pancreatitis	52	0.146

618	c	NPH096	Nephrotic Syndrome, Type 12	28	0.146

619		CMB007	Combined Immunodeficiency	56	0.146

620		CRB004	Cerebral Artery Occlusion	46	0.146

621		OTT002	Otitis Media	71	0.146

622	c	ATR087	Atrial Standstill 1	74	0.146

623	c	MCR247	Microcephaly 1, Primary, Autosomal Recessive	42	0.146

624	c	TYP008	Type 1 Diabetes Mellitus	77	0.146

625		CNT061	Conotruncal Heart Malformations	66	0.146

626		CRH005	Crohn's Colitis	53	0.146

627		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.146

628	c	NPH093	Nephrotic Syndrome, Type 13	21	0.146

629	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.146

630	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	0.146

631	c	BDY006	Body Mass Index Quantitative Trait Locus 8	43	0.146

632	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	0.146

633	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.146

634		ECT009	Ectopia Pupillae	13	0.146

635	P	CMR001	Camurati-Engelmann Disease	59	0.146

636	c	NRF024	Neurofibromatosis, Type I	76	0.146

637	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.146

638	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.146

639		HND015	Hand Skill, Relative	29	0.146

640		CRC014	Carcinoid Tumors, Intestinal	46	0.146

641		WTS001	Watson Syndrome	30	0.146

642		PYL006	Pyloric Stenosis	48	0.146

643	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.146

644		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	0.146

645		NRD100	Neurodevelopmental, Jaw, Eye, and Digital Syndrome	49	0.146

646		CHL068	Cholestasis	61	0.146

647		CNG034	Congestive Heart Failure	69	0.146

648	P	ACN011	Acne	55	0.146

649		PNC127	Pancreatic Adenosquamous Carcinoma	34	0.146

650	P	PRP019	Peripheral Nervous System Disease	57	0.146

651	P	ATR010	Atrial Heart Septal Defect	58	0.146

652		RCT020	Rectum Adenocarcinoma	48	0.146

653		ANG011	Angiodysplasia	42	0.146

654	P	HMN010	Hemangioma	61	0.146

655	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.146

656	P	HYP069	Hyperparathyroidism	62	0.146

657		DDN003	Duodenum Adenocarcinoma	37	0.146

658		END011	Endometriosis of Ovary	40	0.146

659		CNS002	Constrictive Pericarditis	39	0.146

660		HMP001	Hemopericardium	47	0.146

661	P	PRC012	Pericardial Effusion	50	0.146

662	P	ADL010	Adult Respiratory Distress Syndrome	71	0.146

663	P	LVR013	Liver Disease	68	0.146

664		OLF005	Olfactory Neuroblastoma	46	0.146

665		HGH043	High Grade Glioma	46	0.146

666	P	PTT006	Pituitary Adenoma	55	0.146

667	P	RHN004	Rhinitis	57	0.146

668		ASC004	Ascending Colon Cancer	42	0.146

669	P	AML002	Amelogenesis Imperfecta	56	0.146

670	P	ART021	Arteriosclerosis	53	0.146

671		GST049	Gastrointestinal System Cancer	49	0.146

672		BLD063	Bile Duct Cysts	42	0.146

673		THY042	Thymic Epithelial Tumor	26	0.146

674		BNG036	Bone Giant Cell Tumor	48	0.146

675	c	CLR039	Colorectal Cancer, Hereditary Nonpolyposis, Type 4	40	0.146

676		GBL002	Goblet Cell Carcinoid	32	0.146

677	P	THL005	Thalassemia	56	0.146

678		WBR001	Weber Syndrome	38	0.146

679		DYS073	Dysphagia	53	0.146

680		DGN001	Degenerative Disc Disease	48	0.146

681		CLF001	Cleft Lip	54	0.146

682		OVR012	Ovarian Serous Cystadenocarcinoma	55	0.146

683		ORL004	Oral Submucous Fibrosis	56	0.146

684		VNF001	Vein of Galen Aneurysm	18	0.146

685		PPT005	Peptic Ulcer Disease	58	0.146

686		CHL040	Cholangiolocellular Carcinoma	30	0.146

687	c	SPR009	Sporadic Breast Cancer	42	0.146

688		PLC008	Placenta Disease	49	0.146

689		PST021	Postpartum Depression	50	0.146

690		DFF035	Diffuse Cutaneous Systemic Sclerosis	45	0.146

691		GNT179	Genetic Steroid-Resistant Nephrotic Syndrome	40	0.146

692		GRM010	Germ Cells Tumors	33	0.146

693		PRT009	Parotid Gland Cancer	32	0.146

694	P	HYP658	Hypoplastic Amelogenesis Imperfecta	30	0.146

695		DFF036	Differentiated Thyroid Carcinoma	51	0.146

696		THY089	Thymic Epithelial Neoplasm	27	0.146

697		PLY100	Polyploidy	36	0.146

698	P	ALZ034	Alzheimer Disease	87	0.103

699	c	TYP009	Type 2 Diabetes Mellitus	92	0.103

700		CYS001	Cystic Fibrosis	77	0.103

701	P	FNC044	Fanconi Anemia, Complementation Group C	56	0.103

702		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.103

703	c	GLL024	Gallbladder Disease 1	53	0.103

704		XRD010	Xeroderma Pigmentosum, Variant Type	72	0.103

705	P	MYS003	Myasthenia Gravis	68	0.103

706	P	PRS083	Prostate Cancer, Hereditary, X-Linked 1	12	0.103

707		AST006	Astigmatism	46	0.103

708		ANX010	Anxiety	70	0.103

709		MYL009	Myelodysplastic Syndrome	67	0.103

710		ADR016	Adrenal Cortical Carcinoma	61	0.103

711	P	CLR037	Colorectal Cancer, Hereditary Nonpolyposis, Type 5	48	0.103

712	c	DVL078	Developmental and Epileptic Encephalopathy 54	26	0.103

713		CPL015	Capillary Malformation-Arteriovenous Malformation 2	29	0.103

714		KSH004	Kashin-Beck Disease	37	0.103

715		HYP020	Hyperprolactinemia	63	0.103

716		ZLL002	Zollinger-Ellison Syndrome	55	0.103

717		LNG111	Lung Non-Squamous Non-Small Cell Carcinoma	56	0.103

718	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.103

719		DSM004	Desmoid Tumor	65	0.103

720		THY111	Thyroid Carcinoma, Familial Medullary	67	0.103

721		MLT092	Multicentric Carpotarsal Osteolysis Syndrome	64	0.103

722		PLY150	Polykaryocytosis Inducer	29	0.103

723	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.103

724	P	EPD083	Epidermodysplasia Verruciformis 1	57	0.103

725	P	CLC063	Celiac Disease 1	66	0.103

726		ENT011	Enterocolitis	55	0.103

727		VNH007	Von Hippel-Lindau Syndrome	73	0.103

728	P	OVR106	Ovarian Clear Cell Carcinoma	43	0.103

729	P	SLP006	Sleep Apnea	69	0.103

730		MTR088	Mature T-Cell and Nk-Cell Lymphoma	42	0.103

731		CHL147	Chlamydia Pneumonia	47	0.103

732	P	SCL048	Sclerosteosis	58	0.103

733		PLL012	Pollen Allergy	44	0.103

734		LRG014	Large Cell Neuroendocrine Carcinoma	44	0.103

735		HYP114	Hypertensive Nephropathy	35	0.103

736	P	DRM053	Dermatitis, Atopic	65	0.103

737		OVR112	Ovarian Germ Cell Cancer	41	0.103

738		HMN044	Human Immunodeficiency Virus Type 1	76	0.103

739		MND020	Mandibulofacial Dysostosis, Guion-Almeida Type	50	0.103

740	c	BNM016	Bone Mineral Density Quantitative Trait Locus 1	24	0.103

741		PKL001	Poikiloderma with Neutropenia	43	0.103

742	P	KLZ004	Kala-Azar 1	41	0.103

743	c	MLT086	Multiple Endocrine Neoplasia, Type Iv	50	0.103

744	c	HYP595	Hypertension, Essential	84	0.103

745	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.103

746		INT051	Intussusception	53	0.103

747		EPC005	Epicanthus	36	0.103

748		NRL016	Neural Tube Defects	81	0.103

749	c	CHL119	Cholangitis, Primary Sclerosing	57	0.103

750	P	CNG436	Congenital Disorder of Deglycosylation	51	0.103

751	P	WSK001	Wiskott-Aldrich Syndrome	72	0.103

752		CHR610	Chromosome 10q22.3-Q23.2 Deletion Syndrome	22	0.103

753	P	RTH006	Rothmund-Thomson Syndrome, Type 2	67	0.103

754	c	CLR041	Colorectal Cancer, Hereditary Nonpolyposis, Type 2	36	0.103

755		ADR054	Adrenocortical Carcinoma, Hereditary	47	0.103

756	P	CRD224	Cardiofaciocutaneous Syndrome 1	71	0.103

757		CRD223	Cardiac Arrhythmia	63	0.103

758		DGR001	Digeorge Syndrome	62	0.103

759	c	DPH024	Diaphragmatic Hernia, Congenital	64	0.103

760	c	TBR025	Tuberous Sclerosis 1	84	0.103

761		APP003	Appendiceal Neoplasm	36	0.103

762	P	ALC033	Alcohol Use Disorder	67	0.103

763	P	PTS002	Ptosis	52	0.103

764	P	PRG013	Paraganglioma	57	0.103

765		RHM028	Rheumatic Heart Disease	56	0.103

766		CMP034	Complete Androgen Insensitivity Syndrome	55	0.103

767		MLC004	Mulchandani-Bhoj-Conlin Syndrome	51	0.103

768		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	58	0.103

769	c	ACT073	Acute Leukemia	59	0.103

770		PTN001	Patent Foramen Ovale	62	0.103

771	P	MYP006	Myopia	55	0.103

772		CLN003	Clonorchiasis	42	0.103

773	P	TBR001	Tuberous Sclerosis	69	0.103

774		MLG169	Malignant Astrocytoma	57	0.103

775		OVR015	Ovarian Mixed Germ Cell Neoplasm	35	0.103

776		CRB039	Cerebrovascular Disease	65	0.103

777		BLD050	Bladder Urachal Carcinoma	24	0.103

778		ACR014	Acral Lentiginous Melanoma	52	0.103

779		ANP006	Anaplastic Ependymoma	46	0.103

780		BRN024	Bronchitis	67	0.103

781	P	BNG030	Benign Ependymoma	51	0.103

782	P	INT068	Intestinal Disease	53	0.103

783		GST041	Gastric Cardia Carcinoma	20	0.103

784	c	INF023	Inflammatory Breast Carcinoma	48	0.103

785		THY030	Thyroid Gland Disease	50	0.103

786		CMD001	Comedo Carcinoma	37	0.103

787	P	HYP040	Hypospadias	51	0.103

788		KRT002	Keratomalacia	54	0.103

789	P	LTR001	Lateral Sclerosis	58	0.103

790		URT037	Urethral Stricture	42	0.103

791		IMP005	Impotence	52	0.103

792		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.103

793		TST015	Testicular Disease	42	0.103

794		THY122	Thyroid Gland Cancer	59	0.103

795		AZS001	Azoospermia	45	0.103

796	P	SCL009	Sclerosing Cholangitis	46	0.103

797	P	GND004	Gonadal Dysgenesis	46	0.103

798	c	DLT002	Dilated Cardiomyopathy	79	0.103

799	P	DMN001	Diamond-Blackfan Anemia	73	0.103

800	P	HYD006	Hydrocephalus	63	0.103

801	c	PRM005	Primary Hyperparathyroidism	59	0.103

802		CHL123	Chlamydia	58	0.103

803	P	ESP024	Esophagitis	60	0.103

804	P	PLM006	Pulmonary Alveolar Proteinosis	53	0.103

805		LYM009	Lymphocytic Choriomeningitis	46	0.103

806	P	NTR004	Neutropenia	62	0.103

807		CRT017	Cartilage Disease	52	0.103

808		BLP004	Blepharophimosis	36	0.103

809		PNL012	Penile Cancer	57	0.103

810		PLC005	Placental Insufficiency	56	0.103

811	P	TCD001	Tic Disorder	50	0.103

812		TST014	Testicular Cancer	51	0.103

813		AMP009	Ampulla of Vater Adenocarcinoma	36	0.103

814		ADR004	Adrenal Cortical Adenocarcinoma	38	0.103

815		EMB004	Embryonal Carcinoma	55	0.103

816		MMM001	Mammary Paget's Disease	53	0.103

817		PPL018	Papillary Adenocarcinoma	44	0.103

818		DMY004	Demyelinating Disease	50	0.103

819		MCN003	Mucinous Ovarian Cystadenoma	21	0.103

820		THY125	Thyroid Gland Medullary Carcinoma	48	0.103

821	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.103

822	P	PTN014	Patent Ductus Arteriosus 1	59	0.103

823		PRM014	Periampullary Adenocarcinoma	39	0.103

824	P	MYC008	Myocarditis	59	0.103

825		NRM005	Neuromuscular Disease	63	0.103

826		DRM006	Dermatitis	62	0.103

827		CNG608	Congenital Hypopituitarism	29	0.103

828	P	INH011	Inherited Bone Marrow Failure Syndromes	34	0.103

829		NRN006	Neuroendocrine Carcinoma of the Cervix	19	0.103

830		BCK006	Back Pain	43	0.103

831	P	ENC018	Encephalopathy	62	0.103

832		TST043	Testicular Seminoma	31	0.103

833		SRF006	Surfactant Dysfunction	33	0.103

834	P	HYP265	Hypotonia	42	0.103

835		VSC003	Visceral Leishmaniasis	54	0.103

836		NGL006	Ngly1-Related Congenital Disorder of Deglycosylation	15	0.103

837		CLL010	Cellular Ependymoma	58	0.103

838		AVN001	Avian Influenza	61	0.103

839	c	LRG001	Large Cell Carcinoma	48	0.103

840		WST010	West Nile Virus Infection	32	0.103

841		ALL014	Allergic Encephalomyelitis	34	0.103

842		HPT022	Hepatoblastoma	54	0.103

843		LSH001	Leishmaniasis	63	0.103

844		OST012	Osteoarthritis	77	0.103

845	P	INF038	Influenza	68	0.103

846		DVR002	Diverticulitis	46	0.103

847		PTT001	Pituitary Hypoplasia	34	0.103

848		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.103

849		PRT029	Parathyroid Adenoma	51	0.103

850		GST050	Gastrointestinal System Disease	55	0.103

851		IRF001	Irf6-Related Disorders	11	0.103

852		DST006	Diastolic Heart Failure	45	0.103

853	P	CHL066	Cholangitis	51	0.103

854		NRF007	Neurofibroma	64	0.103

855		PRN019	Perinatal Necrotizing Enterocolitis	60	0.103

856		GRW007	Growth Hormone Deficiency	47	0.103

857		FXG001	Foxg1 Syndrome	27	0.103

858	P	HYP083	Hypopituitarism	52	0.103

859		ERY069	Erythrokeratoderma ''en Cocardes''	26	0.103

860		NTH004	Nthl1 Tumor Syndrome	9	0.103

861		PRT063	Proteus-Like Syndrome	27	0.103

862		CLF056	Cleft Lip with or Without Cleft Palate	43	0.103

863		MXD032	Mixed Germ Cell Tumor	24	0.103

864		CLF004	Cleft Lip/palate	57	0.103

865		MLG163	Malignant Tumor of Penis	29	0.103

866		SLD011	Solid Pseudopapillary Carcinoma of Pancreas	29	0.103

867		HRD215	Hereditary Gastric Cancer	21	0.103

868		EXT062	Extracranial Carotid Artery Aneurysm	19	0.103

869		ATR055	Atrial Septal Aneurysm	22	0.103