Search results for mtor

1218 hits were found for mtor

#	Family	MCID	Name	MIFTS	Score
1	P	BRS047	Breast Cancer	97	3.625

2		SMT020	Smith-Kingsmore Syndrome	38	3.291

3		GLB015	Glioblastoma Multiforme	75	3.154

4	P	LNG032	Lung Cancer	98	3.097

5	P	CLR023	Colorectal Cancer	99	3.070

6		FCL081	Focal Cortical Dysplasia, Type Ii	58	3.068

7	P	HPT023	Hepatocellular Carcinoma	100	2.889

8	P	PNC035	Pancreatic Cancer	84	2.822

9	P	OVR042	Ovarian Cancer	88	2.804

10	P	PRS040	Prostate Cancer	97	2.776

11		END057	Endometrial Cancer	74	2.755

12	P	TBR001	Tuberous Sclerosis	70	2.617

13	P	KDN017	Kidney Cancer	60	2.542

14	P	GST053	Gastric Cancer	83	2.525

15		RNL114	Renal Cell Carcinoma, Nonpapillary	78	2.506

16		HYP266	Hypoxia	57	2.452

17	P	ALZ034	Alzheimer Disease	88	2.399

18	P	MLN008	Melanoma	69	2.381

19		SRC014	Sarcoma	65	2.373

20		CRV035	Cervical Cancer	76	2.194

21	P	KDN018	Kidney Disease	72	2.168

22		MSC007	Muscle Hypertrophy	64	2.143

23		RNL065	Renal Cell Carcinoma, Papillary, 1	73	2.115

24	P	EPL164	Epilepsy	71	2.112

25		CLR030	Clear Cell Renal Cell Carcinoma	53	2.089

26		SBP001	Subependymal Giant Cell Astrocytoma	49	2.077

27		KPS004	Kaposi Sarcoma	75	2.073

28		ESP021	Esophageal Cancer	90	2.068

29		NRN004	Neuroendocrine Tumor	55	2.064

30		HMM003	Hemimegalencephaly	48	2.059

31	P	HNT016	Huntington Disease	72	2.055

32		ANG018	Angiomyolipoma	46	2.045

33		LYM007	Lymphangioleiomyomatosis	69	2.041

34	c	SYS001	Systemic Lupus Erythematosus	86	2.031

35	P	DBT009	Diabetes Mellitus	64	1.990

36	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	1.970

37		ADN011	Adenoid Cystic Carcinoma	70	1.945

38	P	PLY014	Polycystic Kidney Disease	62	1.825

39	P	NRB001	Neuroblastoma	72	1.822

40		MNT001	Mantle Cell Lymphoma	69	1.799

41	P	NSP012	Nasopharyngeal Carcinoma	66	1.786

42		STM007	Stomatitis	50	1.786

43	c	TBR025	Tuberous Sclerosis 1	77	1.774

44		MCS002	Mucositis	56	1.771

45	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	1.764

46	P	ATS364	Autism	70	1.760

47	P	GLM040	Glioma Susceptibility 1	81	1.752

48		DFF005	Diffuse Large B-Cell Lymphoma	55	1.736

49		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	1.723

50	P	MSC003	Muscular Atrophy	52	1.714

51	P	RHB003	Rhabdomyosarcoma	63	1.709

52	P	THY023	Thymoma	65	1.704

53		GST040	Gastric Adenocarcinoma	70	1.694

54	c	TBR026	Tuberous Sclerosis 2	72	1.683

55		CYT008	Cytomegalovirus Infection	57	1.683

56	P	RRB004	Rare Breast Tumor	43	1.678

57		NNL006	Non-Alcoholic Steatohepatitis	54	1.666

58		RRC011	Rare Cancer of Corpus Uteri	36	1.666

59		BLD131	Bladder Urothelial Carcinoma	62	1.660

60	P	LYM033	Lymphoproliferative Syndrome	59	1.660

61		MYL005	Myelofibrosis	70	1.654

62	P	LMY004	Leiomyosarcoma	63	1.654

63	P	FRG001	Fragile X Syndrome	70	1.647

64	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	1.647

65		MCR004	Macroglobulinemia	49	1.640

66	c	NRF023	Neurofibromatosis, Type Ii	80	1.633

67	P	MDL005	Medulloblastoma	77	1.633

68	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	1.633

69		LGH007	Leigh Syndrome	70	1.633

70	P	HMN010	Hemangioma	61	1.633

71	P	SCH015	Schizophrenia	74	1.625

72		FCL014	Focal Epilepsy	54	1.625

73	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	1.617

74	P	RTT002	Rett Syndrome	80	1.608

75	c	CWD006	Cowden Syndrome 1	78	1.608

76	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	1.608

77		LNG039	Lung Squamous Cell Carcinoma	66	1.608

78		HMT002	Hematologic Cancer	62	1.608

79		END062	Endometrial Hyperplasia	48	1.608

80	P	OVR106	Ovarian Clear Cell Carcinoma	44	1.608

81		CHR072	Chordoma	58	1.599

82		OVR034	Ovarian Clear Cell Adenocarcinoma	38	1.599

83	P	RTN008	Retinitis Pigmentosa	79	1.588

84	P	PRK057	Parkinson Disease, Late-Onset	78	1.588

85	P	APL001	Aplastic Anemia	74	1.588

86	c	BSL007	Basal Cell Carcinoma	68	1.588

87		DRM014	Dermatofibrosarcoma Protuberans	65	1.588

88	P	SPN046	Spinal Muscular Atrophy	62	1.588

89	P	BRS044	Breast Adenocarcinoma	59	1.588

90		PRN014	Paronychia	49	1.588

91		HYP025	Hyperphosphatemia	48	1.588

92	c	HYP595	Hypertension, Essential	84	1.576

93	c	EXD008	Exudative Vitreoretinopathy 1	71	1.576

94		ALX003	Alexander Disease	59	1.576

95	P	INT070	Intestinal Obstruction	58	1.576

96	P	LNG035	Lung Large Cell Carcinoma	54	1.576

97	P	CRN025	Corneal Dystrophy	49	1.576

98		FBR012	Fabry Disease	72	1.562

99	P	ANG001	Angelman Syndrome	69	1.562

100	c	MCL013	Mucolipidosis Iv	66	1.562

101		ALV005	Alveolar Soft Part Sarcoma	61	1.562

102	P	NPH005	Nephronophthisis	59	1.562

103		OCL006	Ocular Hypertension	53	1.562

104	c	LRG001	Large Cell Carcinoma	50	1.562

105	P	MCL001	Mucolipidosis	48	1.562

106	c	LKM061	Leukemia, Acute Myeloid	84	1.416

107	P	LNG064	Lung Cancer Susceptibility 3	78	1.393

108		MYL069	Myeloma, Multiple	85	1.380

109	P	EXN002	Exanthem	57	1.293

110		CHL065	Cholangiocarcinoma	68	1.284

111		LYM143	Lymphoma, Non-Hodgkin, Familial	72	1.265

112		KDN015	Kidney Angiomyolipoma	45	1.221

113		BRT002	Birt-Hogg-Dube Syndrome	63	1.169

114		SPP011	Suppression of Tumorigenicity 12	59	1.169

115	P	CYS039	Cystic Kidney Disease	54	1.169

116	P	PRT008	Proteus Syndrome	64	1.160

117		KPS002	Kaposiform Hemangioendothelioma	43	1.160

118	P	CWD010	Cowden Syndrome	67	1.137

119		PLS025	Plasmablastic Lymphoma	47	1.137

120		LYM005	Lymphocele	35	1.137

121		PLY023	Polycystic Liver Disease	57	1.123

122	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	1.123

123		LRY029	Laryngomalacia	47	1.123

124		HPT006	Hepatic Angiomyolipoma	32	1.123

125		CHL044	Childhood Kidney Angiomyolipoma	10	1.123

126	P	BNG030	Benign Ependymoma	60	1.104

127		KRT071	Keratosis, Seborrheic	58	1.104

128		THY025	Thymus Cancer	58	1.104

129	P	PRV006	Pervasive Developmental Disorder	57	1.104

130		CRT033	Corticobasal Degeneration	57	1.104

131		SPN041	Spinal Cord Disease	56	1.104

132		PLM135	Palmoplantar Keratoderma, Bothnian Type	51	1.104

133		UMB002	Umbilical Hernia	46	1.104

134		CRN285	Corneal Dystrophy, Fleck	42	1.104

135		HRT007	Heart Cancer	42	1.104

136		CRD118	Cardiovascular Cancer	41	1.104

137		SBP002	Subependymal Glioma	40	1.104

138	c	MLG036	Malignant Spiradenoma	38	1.104

139		ACN010	Acanthoma	38	1.104

140		OVR015	Ovarian Mixed Germ Cell Neoplasm	35	1.104

141		ESP001	Esophageal Tuberculosis	34	1.104

142		DRM003	Dermatosis Papulosa Nigra	33	1.104

143	c	EXD010	Exudative Vitreoretinopathy 6	31	1.104

144		KDN016	Kidney Benign Neoplasm	29	1.104

145		CNT109	Central Nervous System Benign Neoplasm	28	1.104

146		THY026	Thymus Gland Disease	28	1.104

147	c	LRG002	Large Cell Acanthoma	26	1.104

148	c	ATS009	Autosomal Genetic Disease	25	1.104

149		VLV039	Vulvar Seborrheic Keratosis	25	1.104

150		MLN005	Melanoacanthoma	21	1.104

151		CLL012	Cell Type Benign Neoplasm	21	1.104

152	P	VGN018	Vaginal Carcinosarcoma	19	1.104

153		VGN012	Vaginal Adenosarcoma	19	1.104

154	P	GLM045	Glioma	63	0.235

155		GLL048	Glial Tumor	45	0.232

156	P	MYL006	Myeloid Leukemia	60	0.196

157	P	BCL017	B-Cell Lymphoma	58	0.195

158		SQM006	Squamous Cell Carcinoma	60	0.193

159	c	SML038	Small Cell Cancer of the Lung	65	0.185

160	P	BLD134	Bladder Cancer	79	0.181

161	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.180

162	P	LYM118	Lymphoma	68	0.178

163	P	ADN016	Adenocarcinoma	64	0.175

164		THY029	Thyroid Carcinoma	59	0.175

165		OST159	Osteogenic Sarcoma	66	0.170

166		HYP066	Hyperglycemia	61	0.168

167	c	MCR113	Microvascular Complications of Diabetes 3	52	0.159

168	c	MCR120	Microvascular Complications of Diabetes 7	47	0.159

169	c	MCR130	Microvascular Complications of Diabetes 6	41	0.159

170	c	MCR133	Microvascular Complications of Diabetes 4	41	0.159

171		ATM095	Autoimmune Disease	62	0.152

172	c	PCH010	Pachyonychia Congenita 3	44	0.151

173	c	ATS007	Autism Spectrum Disorder	67	0.142

174		AGN016	Aging	56	0.142

175	P	RTN024	Retinoblastoma	73	0.137

176	P	LKM002	Leukemia	68	0.137

177		FTT001	Fatty Liver Disease	61	0.137

178		ISC004	Ischemia	58	0.137

179	c	FML008	Familial Retinoblastoma	53	0.137

180		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.127

181		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.125

182		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.123

183	P	AST007	Astrocytoma	51	0.121

184		LYM133	Lymphoma, Hodgkin, Classic	69	0.119

185	P	NTR004	Neutropenia	63	0.119

186	P	NRF002	Neurofibromatosis	56	0.119

187		ORL015	Oral Squamous Cell Carcinoma	43	0.119

188		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.117

189		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.117

190		SPN035	Spindle Cell Sarcoma	53	0.117

191	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.112

192	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.112

193	P	OVR082	Overgrowth Syndrome	50	0.112

194	P	SKN015	Skin Carcinoma	66	0.110

195		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.110

196		SPN186	Spinal Cord Injury	60	0.110

197	P	SZR006	Seizure Disorder	56	0.110

198		INT079	Intrahepatic Cholangiocarcinoma	51	0.110

199		CRB004	Cerebral Artery Occlusion	45	0.110

200		SVR004	Severe Combined Immunodeficiency	73	0.108

201	P	LVR013	Liver Disease	68	0.108

202		VSL002	Visual Epilepsy	59	0.108

203	c	MLG068	Malignant Glioma	46	0.108

204	c	LKM063	Leukemia, Chronic Myeloid	72	0.105

205		ADN018	Adenoma	59	0.105

206		INS024	Insulin-Like Growth Factor I	79	0.103

207	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.103

208		OST012	Osteoarthritis	78	0.100

209		DWN001	Down Syndrome	70	0.100

210		OVR094	Ovarian Epithelial Cancer	38	0.100

211	c	THY107	Thymoma, Familial	52	0.098

212	c	CRT089	Cortical Dysplasia, Complex, with Other Brain Malformations 10	36	0.098

213	P	PLM036	Pulmonary Fibrosis	65	0.095

214		SKN016	Skin Disease	63	0.095

215		BRK010	Burkitt Lymphoma	67	0.093

216		ATH013	Atherosclerosis Susceptibility	65	0.093

217	P	HYP750	Hypertriglyceridemia, Familial	62	0.093

218		LNG099	Lung Disease	60	0.093

219		STT001	Status Epilepticus	60	0.093

220		HYP060	Hyperinsulinism	54	0.093

221		END086	End Stage Renal Disease	51	0.093

222		LYM019	Lymphosarcoma	46	0.093

223	P	MCR115	Microvascular Complications of Diabetes 5	66	0.090

224		ORL011	Oral Cancer	60	0.090

225	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.090

226	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.090

227	P	MGL013	Megalencephaly	45	0.090

228		MCR237	Macrocephaly/megalencephaly Syndrome, Autosomal Recessive	40	0.090

229	P	GRF003	Graft-Versus-Host Disease	72	0.087

230	P	END044	Endometriosis	63	0.087

231		GLC003	Glucose Intolerance	54	0.087

232	P	TMP001	Temporal Lobe Epilepsy	50	0.087

233		BRN071	Brain Injury	49	0.087

234	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.084

235	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.084

236	P	PSR002	Psoriasis	62	0.084

237		SFT003	Soft Tissue Sarcoma	56	0.084

238		PST011	Pustulosis of Palm and Sole	52	0.084

239		TLN003	Telangiectasis	52	0.084

240		RNL077	Renal Fibrosis	47	0.084

241	P	CHR345	Chronic Pain	44	0.084

242	c	HPT073	Hepatitis C Virus	72	0.081

243		SKN019	Skin Melanoma	68	0.081

244	P	LPS004	Lupus Erythematosus	61	0.081

245	P	ATX030	Ataxia-Telangiectasia	82	0.078

246	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.078

247		PTZ001	Peutz-Jeghers Syndrome	70	0.078

248	c	CHR684	Chronic Kidney Disease	70	0.078

249	P	THR014	Thrombocytopenia	67	0.078

250		DPR016	Depression	63	0.078

251		LPD008	Lipid Metabolism Disorder	62	0.078

252		MNT002	Mental Depression	58	0.078

253	P	BNG032	Benign Mesothelioma	46	0.078

254	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.075

255	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.075

256	P	MJR001	Major Depressive Disorder	68	0.075

257	P	FLL037	Follicular Lymphoma	67	0.075

258	c	PRC016	Pre-Eclampsia	63	0.075

259		CLT003	Colitis	62	0.075

260		INS001	Insulinoma	60	0.075

261	c	ACT073	Acute Leukemia	58	0.075

262	P	GLL018	Gallbladder Cancer	57	0.075

263	P	CHN012	Chondrosarcoma	56	0.075

264	P	LRY044	Larynx Cancer	55	0.075

265	P	LTR001	Lateral Sclerosis	54	0.075

266	P	SPP010	Suppressor of Tumorigenicity 3	51	0.075

267		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.075

268	c	LKM005	Leukemia, T-Cell, Chronic	34	0.075

269		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.075

270	P	PHC003	Pheochromocytoma	71	0.071

271	P	PLM037	Pulmonary Hypertension	67	0.071

272	P	VSC007	Vascular Disease	63	0.071

273	P	PLY011	Polycystic Ovary Syndrome	56	0.071

274		TRN018	Transitional Cell Carcinoma	56	0.071

275		ADR040	Adrenal Gland Pheochromocytoma	46	0.071

276		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.071

277		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.071

278	P	MYP004	Myopathy	70	0.067

279		EWN003	Ewing Sarcoma	69	0.067

280	P	PRD008	Periodontitis	64	0.067

281	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.067

282		ISL001	Islet Cell Tumor	56	0.067

283	c	MLG077	Malignant Peripheral Nerve Sheath Tumor	54	0.067

284		SPL018	Splenomegaly	48	0.067

285		NRN001	Neuroendocrine Carcinoma	47	0.067

286		CYT002	Cytokine Deficiency	42	0.067

287		ALL014	Allergic Encephalomyelitis	38	0.067

288		GST019	Gastrointestinal Stromal Tumor	78	0.064

289		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.064

290	c	ATR087	Atrial Standstill 1	75	0.064

291		FCT007	Factor Vii Deficiency	67	0.064

292		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.064

293		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.064

294		LVR012	Liver Cirrhosis	62	0.064

295	P	MYC008	Myocarditis	59	0.064

296	P	ADL017	Adult T-Cell Leukemia	56	0.064

297		HPT022	Hepatoblastoma	56	0.064

298	P	DRR001	Diarrhea	55	0.064

299	P	PTT006	Pituitary Adenoma	55	0.064

300		LNG031	Lung Benign Neoplasm	51	0.064

301	P	VTR007	Vitreoretinopathy	46	0.064

302		PTT037	Pituitary Tumors	44	0.064

303		LRY018	Laryngeal Squamous Cell Carcinoma	44	0.064

304		OVR063	Overnutrition	44	0.064

305		PRV003	Perivascular Epithelioid Cell Tumor	37	0.064

306	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.064

307	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.064

308		BRN028	Brain Cancer	74	0.059

309	c	MNN043	Meningioma, Familial	74	0.059

310		PNC129	Pancreatic Adenocarcinoma	68	0.059

311		MYC006	Mycosis Fungoides	66	0.059

312	P	MSC005	Muscular Dystrophy	66	0.059

313		CLN015	Colon Adenocarcinoma	65	0.059

314	c	HPT001	Hepatitis C	62	0.059

315	c	SVR001	Severe Acute Respiratory Syndrome	62	0.059

316		MNN042	Meningioma, Radiation-Induced	62	0.059

317		WLD007	Waldenstroem's Macroglobulinemia	61	0.059

318	P	FBR017	Fibrosarcoma	56	0.059

319		PST046	Post-Transplant Lymphoproliferative Disease	53	0.059

320	P	RTN016	Retinal Degeneration	53	0.059

321	P	RTN018	Retinal Disease	53	0.059

322		CLR109	Colorectal Adenocarcinoma	51	0.059

323		TRM010	Traumatic Brain Injury	51	0.059

324		SPN021	Spinal Meningioma	50	0.059

325	c	PRM038	Primary Agammaglobulinemia	44	0.059

326	c	MLG079	Malignant Pleural Mesothelioma	42	0.059

327		SCR001	Secretory Meningioma	41	0.059

328		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.059

329	c	DPD002	Depdc5-Related Epilepsy	13	0.059

330	P	RHM011	Rheumatoid Arthritis	80	0.055

331	c	NRF024	Neurofibromatosis, Type I	77	0.055

332		ULC004	Ulcerative Colitis	73	0.055

333	P	SRC025	Sarcoidosis 1	70	0.055

334		MYL009	Myelodysplastic Syndrome	70	0.055

335		ART016	Aortic Aneurysm	69	0.055

336		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.055

337		HYP056	Hypoglycemia	66	0.055

338		MYL031	Myeloproliferative Neoplasm	66	0.055

339		MRK001	Merkel Cell Carcinoma	65	0.055

340		ACT119	Acute Promyelocytic Leukemia	63	0.055

341		ALL026	Allergic Hypersensitivity Disease	62	0.055

342	c	SCL052	Scleroderma, Familial Progressive	61	0.055

343		WST001	West Syndrome	61	0.055

344	P	ENC018	Encephalopathy	61	0.055

345	P	BND020	Bone Disease	59	0.055

346		LYM027	Lymphopenia	58	0.055

347		VSC002	Vascular Dementia	57	0.055

348	c	ACT134	Acute Liver Failure	56	0.055

349	P	MTC069	Mitochondrial Disorders	56	0.055

350	P	NRP001	Neuropathy	56	0.055

351	c	FNC042	Fanconi Anemia, Complementation Group D2	56	0.055

352	P	INF037	Inflammatory Bowel Disease	54	0.055

353		LYM040	Lymphoblastic Lymphoma	54	0.055

354		PPL022	Papilloma	54	0.055

355		PLS009	Plasma Cell Neoplasm	51	0.055

356		HYP017	Hypophosphatemia	50	0.055

357	P	CTN015	Cutaneous T Cell Lymphoma	49	0.055

358		ADR016	Adrenal Cortical Carcinoma	48	0.055

359		BNR002	Bone Resorption Disease	48	0.055

360		LYM012	Lymphoplasmacytic Lymphoma	47	0.055

361		SQM002	Squamous Cell Papilloma	46	0.055

362		URT010	Ureteral Obstruction	45	0.055

363		LYM126	Lymphoma Aids Related	44	0.055

364	P	RRT020	Rare Tumor	41	0.055

365		ADR004	Adrenal Cortical Adenocarcinoma	39	0.055

366		PRM329	Premature Aging	35	0.055

367		HMN016	Hemangioendothelioma	34	0.055

368	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.055

369	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.050

370		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.050

371	P	MYC007	Myocardial Infarction	70	0.050

372		THY111	Thyroid Carcinoma, Familial Medullary	67	0.050

373	c	RHB024	Rhabdomyosarcoma 2	67	0.050

374		THY121	Thyroid Gland Anaplastic Carcinoma	66	0.050

375		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.050

376		ANG020	Angiosarcoma	64	0.050

377		NRM005	Neuromuscular Disease	64	0.050

378		NRF007	Neurofibroma	64	0.050

379		CLR108	Colorectal Adenoma	64	0.050

380		TXC005	Toxic Shock Syndrome	62	0.050

381		CHL068	Cholestasis	61	0.050

382		GST033	Gestational Diabetes	61	0.050

383		NRL005	Neurilemmoma	60	0.050

384		INT066	Interstitial Lung Disease	60	0.050

385	c	ACT027	Acute Pancreatitis	60	0.050

386		SRC027	Sarcoma, Synovial	58	0.050

387	P	GLM007	Glomerulonephritis	57	0.050

388		CST005	Castleman Disease	57	0.050

389	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.050

390		PLS011	Plasmacytoma	56	0.050

391		BRN004	Brain Edema	56	0.050

392	P	GST044	Gastritis	56	0.050

393		CRC006	Carcinoid Syndrome	55	0.050

394		GNG004	Ganglioglioma	54	0.050

395		LYM022	Lymphangioma	54	0.050

396	P	LCH002	Lichen Planus	53	0.050

397		FNG017	Fungal Infectious Disease	53	0.050

398	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.050

399	P	RCT021	Rectum Cancer	52	0.050

400	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.050

401	c	HRD202	Hereditary Lymphedema I	50	0.050

402		THY125	Thyroid Gland Medullary Carcinoma	50	0.050

403		DGN001	Degenerative Disc Disease	48	0.050

404	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.050

405	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.050

406	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.050

407	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.050

408	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.050

409		ORL013	Oral Lichen Planus	45	0.050

410	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.050

411		CRT015	Carotid Artery Occlusion	45	0.050

412		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.050

413	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.050

414		CVD001	Covid-19	44	0.050

415	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.050

416	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.050

417		MSN004	Mesenchymal Cell Neoplasm	41	0.050

418	P	MLG074	Malignant Mesenchymoma	40	0.050

419		ANX004	Anoxia	40	0.050

420		GLM044	Glomerular Disease	37	0.050

421		DFF039	Diffuse Midline Glioma, H3 K27m-Mutant	36	0.050

422		PLY150	Polykaryocytosis Inducer	31	0.050

423	P	RSP003	Respiratory Failure	74	0.045

424		CRH001	Crohn's Disease	74	0.045

425	P	MLN066	Melanoma, Cutaneous Malignant 1	70	0.045

426	P	ASP006	Aspergillosis	69	0.045

427		PLY001	Polycythemia Vera	69	0.045

428	P	SYS005	Systemic Scleroderma	68	0.045

429		RCK004	Rickets	68	0.045

430	P	HPT021	Hepatitis	67	0.045

431	P	OLG002	Oligodendroglioma	67	0.045

432		CRB039	Cerebrovascular Disease	67	0.045

433		FBR011	Fibrodysplasia Ossificans Progressiva	67	0.045

434	P	HYD006	Hydrocephalus	66	0.045

435	P	LPS002	Liposarcoma	65	0.045

436		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.045

437	P	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	64	0.045

438	P	HML002	Hemolytic Anemia	63	0.045

439		END041	Endometrial Adenocarcinoma	63	0.045

440		PSR001	Psoriatic Arthritis	61	0.045

441		OST003	Osteonecrosis	61	0.045

442		RTN017	Retinal Detachment	61	0.045

443		SZR001	Sezary's Disease	60	0.045

444	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.045

445		PRT013	Portal Hypertension	59	0.045

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

447	P	MLN069	Melanoma, Uveal	59	0.045

448	P	DNG005	Dengue Virus	59	0.045

449		PST028	Post-Traumatic Stress Disorder	58	0.045

450	P	PRP019	Peripheral Nervous System Disease	58	0.045

451	P	INF032	Infertility	57	0.045

452	P	UVT001	Uveitis	57	0.045

453	P	RHN004	Rhinitis	57	0.045

454	P	PRN023	Prion Disease	57	0.045

455	P	PLY018	Polycythemia	56	0.045

456	P	ANT006	Antiphospholipid Syndrome	55	0.045

457	P	ART021	Arteriosclerosis	54	0.045

458		DBT010	Diabetic Neuropathy	54	0.045

459		PNC001	Pancytopenia	54	0.045

460	P	INS002	in Situ Carcinoma	53	0.045

461		MST005	Mastitis	53	0.045

462		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.045

463		MRG003	Marginal Zone B-Cell Lymphoma	52	0.045

464		DSM007	Desmoplastic Small Round Cell Tumor	52	0.045

465	c	ACT135	Acute Graft Versus Host Disease	52	0.045

466		LMY002	Leiomyoma	52	0.045

467		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.045

468		47X002	47,xyy	49	0.045

469	c	FLL041	Follicular Lymphoma 1	49	0.045

470		MTC005	Mitochondrial Metabolism Disease	49	0.045

471		ACT084	Acute Stress Disorder	47	0.045

472		LYM009	Lymphocytic Choriomeningitis	47	0.045

473		MLT113	Multicentric Castleman Disease	47	0.045

474		GST071	Gastrointestinal Carcinoma	47	0.045

475		PLY100	Polyploidy	40	0.045

476		48X005	48,xyyy	39	0.045

477	P	PRP021	Peripheral Nervous System Neoplasm	39	0.045

478	c	PK3004	Pik3ca-Related Overgrowth Spectrum	26	0.045

479		BRN053	Bronchial Adenomas/carcinoids Childhood	25	0.045

480	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.039

481		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.039

482		MSC157	Muscular Dystrophy, Duchenne Type	72	0.039

483	P	FML011	Familial Adenomatous Polyposis	72	0.039

484		DFC004	Deficiency Anemia	70	0.039

485	c	GLY008	Glycogen Storage Disease Ii	70	0.039

486	P	HYP061	Hypertrophic Cardiomyopathy	70	0.039

487		ADL002	Adult Syndrome	70	0.039

488	P	PNM007	Pneumonia	68	0.039

489	P	INF038	Influenza	68	0.039

490	P	FRN006	Frontotemporal Dementia	68	0.039

491	P	CRD119	Cardiac Arrest	67	0.039

492		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.039

493	c	MCR129	Microvascular Complications of Diabetes 1	66	0.039

494		PRT037	Pertussis	65	0.039

495	P	HRP006	Herpes Simplex	65	0.039

496		PRT036	Peritonitis	64	0.039

497		LSH001	Leishmaniasis	63	0.039

498	c	MLG084	Malignant Fibrous Histiocytoma	63	0.039

499		TRN015	Transient Cerebral Ischemia	63	0.039

500		CHR619	Chromosome 2q35 Duplication Syndrome	62	0.039

501		MDD011	Mood Disorder	62	0.039

502		VRL011	Viral Infectious Disease	61	0.039

503	P	NPH012	Nephrotic Syndrome	60	0.039

504	P	MCR010	Microcephaly	59	0.039

505		GRD007	Grade Iii Astrocytoma	59	0.039

506	P	ALC033	Alcohol Use Disorder	58	0.039

507		SCC001	Succinic Semialdehyde Dehydrogenase Deficiency	58	0.039

508		EYD002	Eye Disease	58	0.039

509		CRV038	Cervical Squamous Cell Carcinoma	58	0.039

510	P	BNC003	Bone Cancer	58	0.039

511	P	CND004	Candidiasis	58	0.039

512	c	CHR417	Chronic Graft Versus Host Disease	57	0.039

513	P	PLY041	Polymyositis	57	0.039

514	c	MST023	Mesothelioma, Malignant	57	0.039

515		CMR002	Coumarin Resistance	56	0.039

516	P	PNL012	Penile Cancer	56	0.039

517	P	MLN007	Male Infertility	55	0.039

518		PRS045	Prostatic Hypertrophy	53	0.039

519	P	MNC007	Monocytic Leukemia	53	0.039

520	P	CNT005	Central Nervous System Lymphoma	53	0.039

521		ERD001	Erdheim-Chester Disease	53	0.039

522		DMY004	Demyelinating Disease	52	0.039

523	P	PRG013	Paraganglioma	52	0.039

524		LYS002	Lysosomal Storage Disease	52	0.039

525		IMP005	Impotence	52	0.039

526		FDL002	Food Allergy	51	0.039

527	P	LCT001	Lactic Acidosis	51	0.039

528		TNG007	Tongue Carcinoma	51	0.039

529		SKN013	Skin Benign Neoplasm	51	0.039

530	P	SCK005	Sickle Cell Disease	50	0.039

531		CLR003	Clear Cell Adenocarcinoma	50	0.039

532		GST049	Gastrointestinal System Cancer	49	0.039

533		URM002	Uremia	49	0.039

534		VCC001	Vaccinia	49	0.039

535	c	PRM226	Primary Central Nervous System Lymphoma	48	0.039

536	P	HMN032	Human Herpesvirus 8	47	0.039

537		RTC005	Reticulosarcoma	47	0.039

538	c	ADL052	Adult Acute Lymphocytic Leukemia	47	0.039

539		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.039

540	P	OVR046	Ovarian Cyst	47	0.039

541		RTN023	Retinitis	46	0.039

542		RTN020	Retinal Vascular Disease	46	0.039

543	P	LPM005	Lipomatosis	46	0.039

544	P	MGL030	Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1	46	0.039

545		PLY012	Polyhydramnios	46	0.039

546		END031	Endometrial Stromal Sarcoma	46	0.039

547		LTH001	Lethal Midline Granuloma	44	0.039

548		ACN001	Acinar Cell Carcinoma	44	0.039

549		CLP005	Ciliopathy	43	0.039

550		SMN007	Seminoma	43	0.039

551		NRF003	Neurofibrosarcoma	43	0.039

552	P	HYP265	Hypotonia	43	0.039

553		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.039

554		NRR001	Neuroretinitis	42	0.039

555	P	KLZ004	Kala-Azar 1	41	0.039

556	c	MCR112	Microvascular Complications of Diabetes 2	41	0.039

557		PLY062	Polyhydramnios, Megalencephaly, and Symptomatic Epilepsy	40	0.039

558		KLD004	Keloid Disorder	40	0.039

559		TRC005	Tracheal Stenosis	38	0.039

560		HRW001	Hair Whorl	36	0.039

561		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.039

562	c	CHR064	Chronic Monocytic Leukemia	33	0.039

563	P	RRL003	Rare Lymphatic Malformation	31	0.039

564		CLR137	Clear Cell Adenocarcinoma of the Ovary	31	0.039

565		MLG163	Malignant Tumor of Penis	29	0.039

566		HDG004	Hodgkin's Granuloma	23	0.039

567		HDG006	Hodgkin's Paragranuloma	22	0.039

568		MLR004	Malaria	81	0.032

569		CYS001	Cystic Fibrosis	81	0.032

570		STR067	Stroke, Ischemic	81	0.032

571	c	DLT002	Dilated Cardiomyopathy	79	0.032

572	P	HRT032	Heart Disease	75	0.032

573	P	OST002	Osteoporosis	74	0.032

574		ANX010	Anxiety	73	0.032

575	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.032

576	P	MLT020	Multiple Sclerosis	72	0.032

577		PRP027	Peripheral Vascular Disease	71	0.032

578		CNG034	Congestive Heart Failure	69	0.032

579	P	DMN001	Diamond-Blackfan Anemia	69	0.032

580	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.032

581	P	SLP006	Sleep Apnea	69	0.032

582	P	MYC084	Mycobacterium Tuberculosis 1	68	0.032

583	c	NMN015	Niemann-Pick Disease, Type C1	68	0.032

584	P	MYS003	Myasthenia Gravis	68	0.032

585	P	ESS003	Essential Thrombocythemia	68	0.032

586		BRN024	Bronchitis	68	0.032

587		CNN005	Connective Tissue Disease	68	0.032

588		HYL004	Hyaline Fibromatosis Syndrome	67	0.032

589	P	SHW006	Shwachman-Diamond Syndrome 1	67	0.032

590		FLL027	Fallopian Tube Carcinoma	67	0.032

591	P	HYP098	Hypereosinophilic Syndrome	67	0.032

592	P	DRM053	Dermatitis, Atopic	66	0.032

593	P	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	65	0.032

594		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.032

595		PTT048	Pituitary Adenoma, Prolactin-Secreting	65	0.032

596	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.032

597		OVR029	Ovarian Hyperstimulation Syndrome	64	0.032

598		CLF027	Cleft Palate, Isolated	64	0.032

599		CNG510	Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi	64	0.032

600	P	GCH001	Gaucher's Disease	63	0.032

601	P	PTT014	Pitt-Hopkins Syndrome	63	0.032

602	P	HRD008	Hereditary Hemorrhagic Telangiectasia	63	0.032

603		RHB001	Rhabdoid Cancer	63	0.032

604	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.032

605		NNN026	Noonan Syndrome with Multiple Lentigines	62	0.032

606		LPP008	Lipoprotein Quantitative Trait Locus	62	0.032

607	P	VSC011	Vasculitis	62	0.032

608		DRM006	Dermatitis	61	0.032

609	c	WLM018	Wilms Tumor 5	61	0.032

610	P	PNC044	Pancreatitis	61	0.032

611	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.032

612	P	SCL018	Scoliosis	60	0.032

613		ACQ007	Acquired Immunodeficiency Syndrome	60	0.032

614	c	ORF037	Orofaciodigital Syndrome I	60	0.032

615		CHC001	Chickenpox	60	0.032

616	P	CTR002	Cataract	60	0.032

617	c	ACT071	Acute Kidney Failure	60	0.032

618		PRG009	Progressive Multifocal Leukoencephalopathy	59	0.032

619		DCT002	Ductal Carcinoma in Situ	59	0.032

620	P	CYS018	Cystitis	59	0.032

621		AVN001	Avian Influenza	59	0.032

622	P	NMN002	Niemann-Pick Disease	59	0.032

623		CYS010	Cystinosis	59	0.032

624	P	PLY006	Polydactyly	59	0.032

625		PPT005	Peptic Ulcer Disease	59	0.032

626		BRS051	Breast Disease	58	0.032

627		CNS004	Constipation	58	0.032

628	c	DWL002	Dowling-Degos Disease 1	58	0.032

629		GLS018	Glass Syndrome	57	0.032

630		CHL067	Cholecystitis	57	0.032

631		IRN002	Iron Metabolism Disease	57	0.032

632		CHK001	Chikungunya	57	0.032

633		THY122	Thyroid Gland Cancer	57	0.032

634	c	ACT075	Acute Myocardial Infarction	57	0.032

635		THR024	Thrombosis	57	0.032

636		BLR008	Bilirubin Metabolic Disorder	57	0.032

637	c	LKM070	Leukemia, Acute Monocytic	57	0.032

638		ALL006	Allergic Asthma	56	0.032

639		LMY014	Leiomyoma, Uterine	56	0.032

640		BCT022	Bacterial Infectious Disease	56	0.032

641		ANS011	Anus Cancer	56	0.032

642		ACS001	Acoustic Neuroma	56	0.032

643		MTH009	Mouth Disease	56	0.032

644		EMB004	Embryonal Carcinoma	56	0.032

645		GST050	Gastrointestinal System Disease	56	0.032

646		MCL006	Macular Retinal Edema	55	0.032

647		ZLL002	Zollinger-Ellison Syndrome	55	0.032

648		VSC003	Visceral Leishmaniasis	55	0.032

649		ANG005	Anogenital Venereal Wart	55	0.032

650		HDR002	Hidradenitis Suppurativa	55	0.032

651		JVN009	Juvenile Pilocytic Astrocytoma	55	0.032

652	P	HYP050	Hyperinsulinemic Hypoglycemia	55	0.032

653		GST037	Gastroparesis	54	0.032

654	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.032

655		HMS001	Hemosiderosis	54	0.032

656	P	PRM051	Primary Pigmented Nodular Adrenocortical Disease	53	0.032

657		MMM001	Mammary Paget's Disease	53	0.032

658		PRP036	Peripheral T-Cell Lymphoma	53	0.032

659	P	ORL007	Oral Cavity Cancer	53	0.032

660	c	HPT007	Hepatitis E	53	0.032

661	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	53	0.032

662		PLM014	Pleomorphic Adenoma	52	0.032

663		ACR041	Acromelic Frontonasal Dysostosis	52	0.032

664		SMT003	Somatostatinoma	52	0.032

665		ART140	Arteries, Anomalies of	52	0.032

666		MTP025	Metaphyseal Chondrodysplasia, Schmid Type	52	0.032

667	P	NRC002	Narcolepsy	52	0.032

668		ACT200	Acute Monoblastic Leukemia	52	0.032

669		DFF036	Differentiated Thyroid Carcinoma	52	0.032

670	P	BRN035	Brain Stem Glioma	52	0.032

671		SRS001	Serous Cystadenocarcinoma	52	0.032

672		SPN051	Spondylitis	51	0.032

673		THR004	Thrombocytosis	51	0.032

674	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.032

675		PRS021	Prostatic Adenoma	51	0.032

676		VSC006	Vascular Cancer	51	0.032

677		SPL004	Splenic Marginal Zone Lymphoma	51	0.032

678		HND002	Hand, Foot and Mouth Disease	51	0.032

679		PTT041	Pituitary Stalk Interruption Syndrome	50	0.032

680		PST021	Postpartum Depression	50	0.032

681		CHR635	Chromosome 5q Deletion Syndrome	50	0.032

682	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	50	0.032

683	c	INF145	Infantile Liver Failure Syndrome 1	50	0.032

684		MCP006	Mucoepidermoid Carcinoma	50	0.032

685		OCL022	Ocular Melanoma	50	0.032

686	c	INF023	Inflammatory Breast Carcinoma	50	0.032

687		VRR004	Verrucous Carcinoma	49	0.032

688	P	MTC133	Mitochondrial Myopathy	49	0.032

689		PLY024	Polymicrogyria	49	0.032

690		HDR003	Hidradenitis	49	0.032

691		PRS129	Prostatic Hyperplasia, Benign	49	0.032

692		LRN003	Learning Disability	49	0.032

693	P	CPL014	Capillary Malformation-Arteriovenous Malformation 1	48	0.032

694	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.032

695		IGG001	Iga Glomerulonephritis	48	0.032

696		HLX001	Helix Syndrome	47	0.032

697		CRC014	Carcinoid Tumors, Intestinal	47	0.032

698	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.032

699		SRT004	Serotonin Syndrome	47	0.032

700		ANV001	Anovulation	47	0.032

701		CNT033	Central Nervous System Cancer	47	0.032

702		TST044	Testicular Torsion	47	0.032

703		CHR074	Choriocarcinoma	47	0.032

704		AML029	Ameloblastoma	46	0.032

705		LPD009	Lipid Storage Disease	46	0.032

706		MCS004	Mucosal Melanoma	46	0.032

707		OBS004	Obstructive Hydrocephalus	46	0.032

708		GST030	Gastrinoma	45	0.032

709		MXD026	Mixed Glioma	45	0.032

710		MSN001	Mesangial Proliferative Glomerulonephritis	45	0.032

711		LYM051	Lymphomatoid Granulomatosis	45	0.032

712		GLC036	Glucagonoma	45	0.032

713		BRN032	Brain Glioma	45	0.032

714	P	EPT012	Epithelioid Sarcoma	44	0.032

715		TNG009	Tongue Squamous Cell Carcinoma	44	0.032

716		PRT035	Peritoneum Cancer	44	0.032

717		PPL001	Papillary Adenoma	44	0.032

718		ANL017	Anal Squamous Cell Carcinoma	44	0.032

719		LRG014	Large Cell Neuroendocrine Carcinoma	44	0.032

720		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.032

721		MDD018	Middle East Respiratory Syndrome	43	0.032

722		BLR013	Biliary Tract Cancer	42	0.032

723	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.032

724	P	EPL196	Epilepsy, Familial Focal, with Variable Foci 1	41	0.032

725	P	RRH023	Rare Hereditary Hemochromatosis	41	0.032

726		PLY183	Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome	41	0.032

727		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.032

728	P	ALK015	Alk-Positive Anaplastic Large Cell Lymphoma	40	0.032

729	P	MCR364	Macrodactyly	40	0.032

730		CHL045	Choline Deficiency Disease	39	0.032

731		PNC008	Pancreatic Endocrine Carcinoma	39	0.032

732		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.032

733	c	MLG157	Malignant Pheochromocytoma	38	0.032

734		ANG065	Angioma, Tufted	38	0.032

735		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.032

736		DBT081	Diabetic Encephalopathy	37	0.032

737		LNG105	Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome	37	0.032

738		SYS070	Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood	36	0.032

739		TST043	Testicular Seminoma	35	0.032

740		CHR178	Chromosomal Triplication	35	0.032

741		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.032

742	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.032

743		PPL050	Papillary Tumor of the Pineal Region	33	0.032

744		INF009	Inflammatory Spondylopathy	31	0.032

745		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.032

746	c	CLB022	Coloboma, Ocular, Autosomal Recessive	28	0.032

747		NRF026	Neurofibromatosis, Type Iv, of Riccardi	26	0.032

748		PLY179	Polyomavirus-Associated Nephropathy	24	0.032

749		EPD052	Epidermolysis Bullosa Simplex Superficialis	24	0.032

750		AGG011	Aggressive B-Cell Non-Hodgkin Lymphoma	23	0.032

751		PST047	Post-Traumatic Epilepsy	22	0.032

752		HML018	Homologous Wasting Disease	22	0.032

753		RRS010	Rare Soft Tissue Tumor	18	0.032

754	P	LYN001	Lynch Syndrome	77	0.022

755	P	NNN008	Noonan Syndrome 1	76	0.022

756	P	NJM001	Nijmegen Breakage Syndrome	74	0.022

757		VNH007	Von Hippel-Lindau Syndrome	73	0.022

758	c	SPN225	Spondyloarthropathy 1	73	0.022

759		BSL036	Basal Cell Nevus Syndrome	73	0.022

760	P	FML018	Familial Mediterranean Fever	73	0.022

761		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.022

762		HMN044	Human Immunodeficiency Virus Type 1	71	0.022

763		WLS001	Wilson Disease	71	0.022

764	P	AMY004	Amyloidosis	70	0.022

765		MLT157	Multiple System Atrophy 1	70	0.022

766	c	GCH015	Gaucher Disease, Type I	70	0.022

767	P	OST001	Osteopetrosis	70	0.022

768		WRN001	Werner Syndrome	69	0.022

769	P	ART022	Arthritis	69	0.022

770		CRB037	Cerebral Palsy	69	0.022

771	P	LPR021	Leprosy 3	69	0.022

772	P	MPL001	Maple Syrup Urine Disease	69	0.022

773	P	CRN037	Craniosynostosis	68	0.022

774		CST001	Costello Syndrome	68	0.022

775	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.022

776	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.022

777	P	DYS007	Dyskeratosis Congenita	67	0.022

778	c	HMP029	Hemophilia a	67	0.022

779		PSY004	Psychotic Disorder	67	0.022

780	P	TRN020	Turner Syndrome	67	0.022

781	c	MGR028	Migraine with or Without Aura 1	67	0.022

782		ALC007	Alcohol Dependence	66	0.022

783		ANG054	Angina Pectoris	66	0.022

784		MYX005	Myxoid Liposarcoma	66	0.022

785	c	FML346	Familial Adenomatous Polyposis 1	66	0.022

786		AND002	Androgen Insensitivity Syndrome	66	0.022

787	P	ATR011	Atrial Fibrillation	66	0.022

788		CHG001	Chagas Disease	66	0.022

789	P	BRD002	Bardet-Biedl Syndrome	66	0.022

790	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	65	0.022

791	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.022

792	P	ART005	Arteriovenous Malformation	65	0.022

793		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.022

794	P	MTR014	Motor Neuron Disease	65	0.022

795		BRR014	Barrett Esophagus	65	0.022

796	P	CLD001	Cleidocranial Dysplasia	65	0.022

797	c	WLM013	Wilms Tumor 1	65	0.022

798	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.022

799		MYC079	Myoclonic Epilepsy of Lafora	64	0.022

800		GT001	Gout	64	0.022

801		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.022

802		BRC012	Brucellosis	64	0.022

803		DGR001	Digeorge Syndrome	64	0.022

804		DSM004	Desmoid Tumor	64	0.022

805		HYP020	Hyperprolactinemia	64	0.022

806	P	CRN300	Coronary Heart Disease 1	63	0.022

807	c	ACT068	Acute Cystitis	63	0.022

808	c	ATM011	Autoimmune Hepatitis	63	0.022

809		BDD001	Budd-Chiari Syndrome	63	0.022

810		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.022

811		ERL001	Early Myoclonic Encephalopathy	62	0.022

812	c	HPT003	Hepatitis a	62	0.022

813	c	BRN108	Branchiootic Syndrome 1	62	0.022

814		TKY002	Takayasu Arteritis	62	0.022

815	P	ESP024	Esophagitis	62	0.022

816	c	ANM038	Anemia, Autoimmune Hemolytic	62	0.022

817		BRS099	Breast Ductal Carcinoma	62	0.022

818		CTN007	Cutaneous Leishmaniasis	62	0.022

819		NTR005	Nutritional Deficiency Disease	62	0.022

820	P	CRN038	Carney Complex Variant	61	0.022

821		ATY005	Atypical Teratoid Rhabdoid Tumor	61	0.022

822	P	DRM010	Dermatomyositis	61	0.022

823	P	INT143	Interstitial Cystitis	61	0.022

824		ALC006	Alcoholic Hepatitis	61	0.022

825	P	SJG008	Sjogren Syndrome	61	0.022

826		APP008	Appendicitis	61	0.022

827		WLL001	Williams-Beuren Syndrome	60	0.022

828		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.022

829	P	TST021	Testicular Germ Cell Tumor	60	0.022

830		CRD223	Cardiac Arrhythmia	60	0.022

831	P	EMR001	Emery-Dreifuss Muscular Dystrophy	60	0.022

832	P	GLY013	Glycogen Storage Disease	60	0.022

833	P	THL005	Thalassemia	60	0.022

834		VGN017	Vaginal Cancer	60	0.022

835	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.022

836	P	OPT006	Optic Nerve Disease	60	0.022

837	c	HPT016	Hepatitis B	59	0.022

838	c	PCH015	Pachyonychia Congenita 1	59	0.022

839	P	SLP005	Sleep Disorder	59	0.022

840	P	PRD006	Prader-Willi Syndrome	59	0.022

841	c	HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	59	0.022

842		DNN001	Danon Disease	59	0.022

843	P	GLL022	Guillain-Barre Syndrome	59	0.022

844		GST045	Gastroenteritis	59	0.022

845		HLC007	Helicobacter Pylori Infection	59	0.022

846		ANR040	Aneurysm	59	0.022

847		INC002	Inclusion Body Myositis	58	0.022

848		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.022

849	P	SYP003	Syphilis	58	0.022

850		ANT024	Anthrax Disease	58	0.022

851		RBS001	Rabies	58	0.022

852		ERY029	Erythermalgia, Primary	58	0.022

853		CRD132	Cardiac Conduction Defect	58	0.022

854	c	PRG018	Paragangliomas 1	58	0.022

855		ADR005	Adrenal Carcinoma	58	0.022

856		PMP006	Pemphigus Vulgaris, Familial	57	0.022

857		MCR013	Microphthalmia	57	0.022

858		BRN056	Bronchopulmonary Dysplasia	57	0.022

859	P	SLV026	Salivary Gland Carcinoma	57	0.022

860		LYM021	Lymphadenitis	57	0.022

861		APH001	Aphthous Stomatitis	57	0.022

862		THY022	Thymic Carcinoma	57	0.022

863		TNS005	Tonsillitis	57	0.022

864		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.022

865	P	CRD246	Cardiovascular System Disease	57	0.022

866	P	FTL001	Fetal Alcohol Syndrome	57	0.022

867		SCH014	Schistosomiasis	57	0.022

868		SKN022	Skin Squamous Cell Carcinoma	57	0.022

869	P	ANG015	Angioedema	57	0.022

870	P	BPL003	Bipolar Disorder	56	0.022

871	P	PYL005	Pyelonephritis	56	0.022

872		PNM008	Pneumothorax	56	0.022

873	P	MYS005	Myositis	56	0.022

874	c	LSS005	Lissencephaly 1	56	0.022

875		ADN027	Adenomyosis	56	0.022

876		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.022

877		HMG005	Hemoglobinopathy	56	0.022

878	c	NPH055	Nephrotic Syndrome, Type 1	56	0.022

879	c	FML035	Familial Hyperlipidemia	55	0.022

880		HST011	Histoplasmosis	55	0.022

881		HYP005	Hypokalemia	55	0.022

882		ORP003	Oropharynx Cancer	55	0.022

883		ORL004	Oral Submucous Fibrosis	55	0.022

884		LMB062	Limb Ischemia	55	0.022

885	P	GRV001	Graves' Disease	55	0.022

886		CHR100	Chronic Ulcer of Skin	55	0.022

887		GNG005	Gangliocytoma	55	0.022

888	P	HYP076	Hyperthyroidism	55	0.022

889		EPT010	Epithelial-Myoepithelial Carcinoma	55	0.022

890	P	VNS003	Venous Insufficiency	55	0.022

891	c	XRD030	Xeroderma Pigmentosum, Complementation Group C	55	0.022

892		INT007	Intermediate Coronary Syndrome	55	0.022

893		GNT003	Genital Herpes	54	0.022

894	P	SPN052	Spondyloarthropathy	54	0.022

895		PRP030	Purpura	54	0.022

896		BRN015	Bronchiolo-Alveolar Adenocarcinoma	54	0.022

897	P	PMP001	Pemphigus	54	0.022

898	c	FNC029	Fanconi Anemia, Complementation Group I	54	0.022

899	P	MRN003	Marinesco-Sjogren Syndrome	54	0.022

900		SCH071	Schaaf-Yang Syndrome	54	0.022

901		VGN023	Vaginitis	54	0.022

902	P	ALP008	Alopecia	54	0.022

903		PRT038	Protein-Energy Malnutrition	54	0.022

904		TND005	Tendinitis	54	0.022

905		PLM010	Pulmonary Edema	54	0.022

906		PSD007	Pseudomyxoma Peritonei	54	0.022

907		WST005	West Nile Virus	54	0.022

908	P	FML012	Familial Partial Lipodystrophy	54	0.022

909	P	TRM003	Tremor	54	0.022

910	P	TCD001	Tic Disorder	53	0.022

911	P	RNL017	Renal Oncocytoma	53	0.022

912	P	HYP083	Hypopituitarism	53	0.022

913	P	HML001	Hemolytic-Uremic Syndrome	53	0.022

914	P	SHR001	Short Bowel Syndrome	53	0.022

915		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.022

916		HMC014	Homocysteinemia	53	0.022

917		OCL008	Oculopharyngeal Muscular Dystrophy	53	0.022

918	P	FBR031	Febrile Seizures	53	0.022

919		GST023	Gastric Ulcer	53	0.022

920		DNT012	Dental Caries	53	0.022

921		INT051	Intussusception	53	0.022

922	P	INT068	Intestinal Disease	53	0.022

923		EXP004	Exophthalmos	52	0.022

924		GNG002	Ganglioneuroma	52	0.022

925		CLB010	Coloboma of Macula	52	0.022

926	c	VRL010	Viral Hepatitis	52	0.022

927		MGL038	Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome	52	0.022

928		NRT004	Neuritis	52	0.022

929		PLS007	Plasmodium Falciparum Malaria	52	0.022

930	P	THY032	Thyroiditis	52	0.022

931	P	PRV002	Periventricular Nodular Heterotopia	52	0.022

932	P	OVR049	Ovarian Disease	52	0.022

933		THR009	Thrombocytopenia-Absent Radius Syndrome	52	0.022

934		INV006	Inverted Papilloma	52	0.022

935	P	HMP007	Hemophilia	51	0.022

936		NPH003	Nephrocalcinosis	51	0.022

937		OCL069	Ocular Motor Apraxia	51	0.022

938	c	NMN014	Niemann-Pick Disease, Type C2	51	0.022

939		MTP034	Metaphyseal Chondrodysplasia, Jansen Type	51	0.022

940	P	MND003	Mandibuloacral Dysplasia with Type a Lipodystrophy	51	0.022

941	P	LSS002	Lissencephaly	51	0.022

942	P	INT099	Intrahepatic Cholestasis of Pregnancy	51	0.022

943		FBR008	Fibrillary Astrocytoma	51	0.022

944	c	VRL007	Viral Encephalitis	51	0.022

945		TLR001	Tularemia	51	0.022

946	P	HYP040	Hypospadias	51	0.022

947		INC018	Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia	51	0.022

948		PNN001	Panniculitis	51	0.022

949		CRV040	Cervix Carcinoma	51	0.022

950	P	CHL066	Cholangitis	51	0.022

951	P	MMB011	Membranous Nephropathy	50	0.022

952		LNT004	Lentigines	50	0.022

953	P	FNC004	Fanconi Syndrome	50	0.022

954		RDC002	Radiculopathy	50	0.022

955		RTN003	Retinal Ischemia	50	0.022

956		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	0.022

957		HPT014	Hepatorenal Syndrome	50	0.022

958		FSC004	Fasciitis	50	0.022

959		PRT018	Portal Vein Thrombosis	50	0.022

960	P	PNV001	Panuveitis	50	0.022

961		NTR046	Neutrophil Migration	50	0.022

962		MTB004	Metabolic Acidosis	50	0.022

963	P	PNB001	Pineoblastoma	50	0.022

964		HYP080	Hypogonadism	50	0.022

965	P	ATR005	Atrophic Gastritis	50	0.022

966		ONC007	Oncocytoma	49	0.022

967	P	MYT002	Myotonic Dystrophy	49	0.022

968		ENT004	Enthesopathy	49	0.022

969		PPL021	Papilledema	49	0.022

970	P	CRV039	Cervicitis	49	0.022

971	c	CHR431	Chronic Venous Insufficiency	49	0.022

972		MCN001	Mucinous Adenocarcinoma	49	0.022

973		ERY004	Erysipelas	49	0.022

974		VRC001	Varicocele	49	0.022

975		ART017	Aortic Disease	49	0.022

976		SLD003	Sialadenitis	49	0.022

977		PLM041	Pulmonary Valve Stenosis	49	0.022

978	P	CRV031	Cervical Adenocarcinoma	49	0.022

979		FRN020	Frontal Fibrosing Alopecia	49	0.022

980		HST010	Histiocytosis	48	0.022

981		DDF001	Dedifferentiated Liposarcoma	48	0.022

982		HYP043	Hyperandrogenism	48	0.022

983		INT017	Intestinal Schistosomiasis	48	0.022

984		WTH001	Withdrawal Disorder	48	0.022

985		ATS010	Autosomal Recessive Disease	48	0.022

986		CHR563	Chronic Eosinophilic Leukemia	48	0.022

987	P	ATS011	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy	48	0.022

988	c	NPH049	Nephrotic Syndrome, Type 2	48	0.022

989	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.022

990		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.022

991		INT067	Interstitial Nephritis	48	0.022

992		DBT006	Diabetic Macular Edema	48	0.022

993		GNG008	Ganglioneuroblastoma	48	0.022

994		BLD044	Bladder Disease	48	0.022

995		GLC106	Glucocorticoid Resistance, Generalized	48	0.022

996		CYS002	Cystic Lymphangioma	48	0.022

997	c	MTR002	Mitral Valve Insufficiency	48	0.022

998		DSM003	Desmoid Disease, Hereditary	48	0.022

999		CHL056	Cheilitis	48	0.022

1000		FBR009	Fibrous Dysplasia	48	0.022

1001	c	CRD179	Ceroid Lipofuscinosis, Neuronal, 7	48	0.022

1002		PTT008	Pituitary Carcinoma	48	0.022

1003		ESN015	Eosinophilic Fasciitis	48	0.022

1004		MLK006	Milk Allergy	48	0.022

1005	P	KRT005	Keratoacanthoma	48	0.022

1006	c	HYD064	Hydrocephalus, Congenital, 1	48	0.022

1007		ART004	Aortic Atherosclerosis	47	0.022

1008	c	PRM031	Primary Autosomal Recessive Microcephaly	47	0.022

1009		ADN009	Adenosquamous Carcinoma	47	0.022

1010		MCR018	Microcytic Anemia	47	0.022

1011		ASB001	Asbestosis	47	0.022

1012		PPL002	Papillary Carcinoma	47	0.022

1013	c	HYD019	Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius	47	0.022

1014		THY128	Thyroid Tumor	47	0.022

1015		CRN027	Corneal Neovascularization	47	0.022

1016	c	CNG216	Congenital Hydrocephalus	47	0.022

1017		PHS021	Phosphoglycerate Dehydrogenase Deficiency	47	0.022

1018	P	PRC019	Precocious Puberty	46	0.022

1019		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.022

1020	c	ACT076	Acute Myocarditis	46	0.022

1021	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.022

1022		TST014	Testicular Cancer	46	0.022

1023	c	SCH079	Schizophrenia 1	46	0.022

1024		BRL010	Buruli Ulcer	46	0.022

1025		CWP001	Cowpox	46	0.022

1026	c	DRR009	Diarrhea 6	46	0.022

1027	c	ACT042	Acute Pyelonephritis	46	0.022

1028		BNS007	Bone Sarcoma	45	0.022

1029		INT253	Intestinal Benign Neoplasm	45	0.022

1030		CHR466	Chronic Thromboembolic Pulmonary Hypertension	45	0.022

1031		PNC056	Pineocytoma	45	0.022

1032		ACT003	Acute Kidney Tubular Necrosis	45	0.022

1033		NNS002	Nonspecific Interstitial Pneumonia	45	0.022

1034		URT051	Ureter, Cancer of	45	0.022

1035		CLL014	Cll/sll	45	0.022

1036	c	SPR009	Sporadic Breast Cancer	45	0.022

1037		LRN001	Laurence-Moon Syndrome	45	0.022

1038		MYF001	Myofibroma	45	0.022

1039		DBT090	Diabetes and Deafness, Maternally Inherited	44	0.022

1040		SBC016	Subacute Delirium	44	0.022

1041		DBT008	Diabetic Angiopathy	44	0.022

1042		APP009	Appendix Adenocarcinoma	44	0.022

1043		CRD043	Ceroid Storage Disease	44	0.022

1044	P	MTC004	Mitochondrial Encephalomyopathy	44	0.022

1045		DWR001	Dwarfism	44	0.022

1046	P	PRL003	Proliferative Glomerulonephritis	44	0.022

1047		CNV018	Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis	44	0.022

1048		PLX002	Plexiform Neurofibroma	44	0.022

1049		MCR096	Macrocephaly/autism Syndrome	44	0.022

1050	P	BNG095	Benign Giant Cell Tumor	44	0.022

1051		BCT021	Bacterial Sepsis	44	0.022

1052		MCR017	Macrocytic Anemia	44	0.022

1053		FBR054	Fibroma	44	0.022

1054	c	ALK016	Alk-Negative Anaplastic Large Cell Lymphoma	44	0.022

1055		END085	Endometrial Serous Adenocarcinoma	44	0.022

1056		ANP009	Anaplastic Oligodendroglioma	43	0.022

1057		CHN010	Chondroma	43	0.022

1058		TND004	Tendinopathy	43	0.022

1059		FRG010	Fragile X Tremor/ataxia Syndrome	43	0.022

1060	P	TST026	Testicular Germ Cell Cancer	43	0.022

1061	P	HYP078	Hypertrophy of Breast	43	0.022

1062		CRB016	Carbuncle	43	0.022

1063		TST015	Testicular Disease	43	0.022

1064		URT037	Urethral Stricture	43	0.022

1065		GLL017	Gallbladder Adenocarcinoma	43	0.022

1066		ECC004	Eccrine Porocarcinoma	43	0.022

1067		NSP002	Nasopharyngitis	43	0.022

1068		DNT001	Dental Fluorosis	43	0.022

1069	c	FTL006	Fetal Alcohol Spectrum Disorder	43	0.022

1070		PRS036	Parasitic Protozoa Infectious Disease	43	0.022

1071		FRG008	Fragile X-Associated Tremor/ataxia Syndrome	43	0.022

1072		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.022

1073		HYP457	Hypertrophic Scars	42	0.022

1074		TRP009	Triple X Syndrome	42	0.022

1075	P	AVS003	Avascular Necrosis	42	0.022

1076		PRG014	Progesterone Resistance	42	0.022

1077		TRC097	Tracheomalacia	42	0.022

1078		ALC010	Alcoholic Cardiomyopathy	42	0.022

1079		LRY017	Laryngeal Disease	42	0.022

1080		EXC002	Exocrine Pancreatic Insufficiency	42	0.022

1081		ATX019	Ataxia with Vitamin E Deficiency	42	0.022

1082	c	RTN041	Retinitis Pigmentosa 11	42	0.022

1083		OBS082	Obstructive Nephropathy	42	0.022

1084	c	VTL009