Search results for Atorvastatin

769 hits were found for Atorvastatin

#	Family	MCID	Name	MIFTS	Score
1		OBS306	Obsolete: Atorvastatin Toxicity	1	2.765

2	P	OBS339	Obsolete: Susceptibility to Adverse Reaction Due to Atorvastatin Treatment	1	2.765

3	c	HYP836	Hypercholesterolemia, Familial, 1	74	0.736

4		LPD008	Lipid Metabolism Disorder	64	0.579

5		ISC004	Ischemia	62	0.513

6	P	CRN300	Coronary Heart Disease 1	59	0.513

7	P	CRN018	Coronary Artery Anomaly	67	0.502

8	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.500

9	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.477

10		ART140	Arteries, Anomalies of	60	0.430

11		ATH013	Atherosclerosis Susceptibility	68	0.419

12	c	FML035	Familial Hyperlipidemia	56	0.388

13		HYP081	Hypolipoproteinemia	51	0.373

14	P	HRT032	Heart Disease	78	0.358

15	P	MYC007	Myocardial Infarction	74	0.323

16	P	DBT009	Diabetes Mellitus	66	0.310

17		CRB039	Cerebrovascular Disease	71	0.305

18	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	82	0.298

19	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.295

20	c	HYP595	Hypertension, Essential	87	0.293

21		STR067	Stroke, Ischemic	82	0.292

22	P	KDN018	Kidney Disease	73	0.284

23		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	54	0.267

24	c	FML021	Familial Hypercholesterolemia	67	0.260

25	P	VSC007	Vascular Disease	65	0.256

26	P	MYP004	Myopathy	63	0.252

27		INT007	Intermediate Coronary Syndrome	58	0.234

28		ANG054	Angina Pectoris	66	0.230

29	c	CHR684	Chronic Kidney Disease	68	0.227

30	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	61	0.225

31	P	HYP750	Hypertriglyceridemia, Familial	62	0.213

32	c	ACT075	Acute Myocardial Infarction	59	0.213

33		48X005	48,xyyy	37	0.207

34		CNG034	Congestive Heart Failure	69	0.200

35	P	ATR011	Atrial Fibrillation	67	0.192

36		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	0.183

37	P	LVR013	Liver Disease	71	0.179

38		ADL002	Adult Syndrome	62	0.171

39		FTT001	Fatty Liver Disease	63	0.169

40		PRP027	Peripheral Vascular Disease	72	0.167

41		OBS529	Obsolete: Combined Hyperlipidemia	22	0.167

42		THR024	Thrombosis	58	0.165

43	P	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.161

44	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	65	0.159

45		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	36	0.159

46	P	PRD008	Periodontitis	66	0.157

47	c	RHB024	Rhabdomyosarcoma 2	64	0.157

48		TRN015	Transient Cerebral Ischemia	62	0.157

49		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.157

50		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.157

51	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.153

52	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.151

53	c	BDY021	Body Mass Index Quantitative Trait Locus 20	50	0.151

54	c	BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.151

55	c	BDY010	Body Mass Index Quantitative Trait Locus 4	48	0.151

56	c	BDY015	Body Mass Index Quantitative Trait Locus 12	48	0.151

57	c	BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.151

58	c	BDY011	Body Mass Index Quantitative Trait Locus 10	47	0.151

59	c	BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.151

60	c	BDY006	Body Mass Index Quantitative Trait Locus 8	45	0.151

61	c	BDY012	Body Mass Index Quantitative Trait Locus 7	45	0.151

62	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	62	0.148

63	P	MLT020	Multiple Sclerosis	73	0.146

64	c	FML001	Familial Atrial Fibrillation	67	0.144

65	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.144

66	c	ACT071	Acute Kidney Failure	60	0.142

67	P	ART021	Arteriosclerosis	56	0.139

68	P	HYP838	Hyperlipidemia, Familial Combined, 3	54	0.139

69	c	PRD040	Periodontitis, Chronic	56	0.137

70	c	HYP740	Hyperlipoproteinemia, Type V	53	0.137

71	P	PRS040	Prostate Cancer	97	0.134

72	c	SYS001	Systemic Lupus Erythematosus	88	0.134

73	P	TRN020	Turner Syndrome	66	0.134

74	P	LPS004	Lupus Erythematosus	62	0.134

75	P	RHM011	Rheumatoid Arthritis	82	0.129

76		HMN044	Human Immunodeficiency Virus Type 1	73	0.129

77		HMZ003	Homozygous Familial Hypercholesterolemia	48	0.129

78	c	ATR087	Atrial Standstill 1	76	0.127

79	P	ART022	Arthritis	71	0.127

80		CYT002	Cytokine Deficiency	46	0.127

81		CRB004	Cerebral Artery Occlusion	38	0.127

82	P	DBT085	Diabetes Mellitus, Insulin-Dependent	68	0.124

83	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	58	0.124

84	P	PLM037	Pulmonary Hypertension	69	0.121

85		NNL006	Non-Alcoholic Steatohepatitis	53	0.121

86		BNR002	Bone Resorption Disease	51	0.121

87		END030	End Stage Renal Failure	60	0.118

88	P	MYS005	Myositis	54	0.118

89	P	CRD119	Cardiac Arrest	71	0.116

90		ATM095	Autoimmune Disease	62	0.116

91		ANR040	Aneurysm	60	0.116

92		RLP002	Relapsing-Remitting Multiple Sclerosis	57	0.116

93		CRT013	Carotid Stenosis	50	0.116

94	c	HYP555	Hypertriglyceridemia, Transient Infantile	38	0.116

95	c	PRS136	Prostate Cancer, Hereditary, 6	34	0.116

96	c	PRS130	Prostate Cancer, Hereditary, 8	33	0.116

97	P	BRS047	Breast Cancer	99	0.113

98		DWN001	Down Syndrome	70	0.113

99		HYP066	Hyperglycemia	63	0.113

100		PRP080	Peripheral Artery Disease	51	0.113

101		ALL026	Allergic Hypersensitivity Disease	65	0.110

102	P	PLY011	Polycystic Ovary Syndrome	58	0.110

103	c	MCR113	Microvascular Complications of Diabetes 3	55	0.110

104	c	MCR120	Microvascular Complications of Diabetes 7	48	0.110

105	c	MCR130	Microvascular Complications of Diabetes 6	42	0.110

106	c	MCR133	Microvascular Complications of Diabetes 4	42	0.110

107	c	HYP839	Hyperlipidemia, Familial Combined, 1	28	0.110

108	P	ALZ034	Alzheimer Disease	90	0.107

109		ACQ007	Acquired Immunodeficiency Syndrome	61	0.107

110		ALL014	Allergic Encephalomyelitis	40	0.107

111		CYT018	Cytochrome P450 2d6 Variant	28	0.107

112	P	CLR023	Colorectal Cancer	100	0.103

113		ART016	Aortic Aneurysm	71	0.103

114	P	HPT021	Hepatitis	69	0.103

115	P	PSR002	Psoriasis	63	0.103

116		IMP005	Impotence	53	0.103

117		PST011	Pustulosis of Palm and Sole	51	0.103

118	P	OST002	Osteoporosis	79	0.100

119	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.100

120		HMN014	Human Immunodeficiency Virus Infectious Disease	56	0.100

121		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	56	0.100

122		CRT016	Carotid Artery Disease	53	0.100

123	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	51	0.100

124		BRN071	Brain Injury	51	0.100

125	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	43	0.100

126	P	GRF003	Graft-Versus-Host Disease	71	0.097

127		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.097

128	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	62	0.097

129		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.097

130		TRM010	Traumatic Brain Injury	54	0.097

131		LPD009	Lipid Storage Disease	49	0.097

132		IMM167	Immune Deficiency Disease	79	0.093

133	P	LKM002	Leukemia	69	0.093

134		LVR012	Liver Cirrhosis	67	0.093

135		CHL068	Cholestasis	61	0.093

136	P	PNC044	Pancreatitis	61	0.093

137		AGN016	Aging	58	0.093

138		FML235	Familial Combined Hyperlipoproteinemia	29	0.093

139	c	PLM164	Pulmonary Hypertension, Primary, 1	79	0.089

140		KWS002	Kawasaki Disease	65	0.089

141		HYP266	Hypoxia	58	0.089

142		HMC014	Homocysteinemia	54	0.089

143	c	ACT135	Acute Graft Versus Host Disease	52	0.089

144	c	DLT002	Dilated Cardiomyopathy	81	0.086

145		LPT014	Leptin Deficiency or Dysfunction	72	0.086

146	P	LYM118	Lymphoma	70	0.086

147	P	THR014	Thrombocytopenia	67	0.086

148	P	PLM036	Pulmonary Fibrosis	66	0.086

149		IDP011	Idiopathic Interstitial Pneumonia	65	0.086

150	P	END044	Endometriosis	63	0.086

151		SPN186	Spinal Cord Injury	63	0.086

152		RHM027	Rheumatic Disease	56	0.086

153		HYP005	Hypokalemia	55	0.086

154		HMT018	Hematopoietic Stem Cell Transplantation	54	0.086

155		GSG001	Gas Gangrene	52	0.086

156		CRN030	Coronary Stenosis	49	0.086

157		LYM019	Lymphosarcoma	48	0.086

158		ATX019	Ataxia with Vitamin E Deficiency	46	0.086

159	c	PRM038	Primary Agammaglobulinemia	45	0.086

160	c	HPT073	Hepatitis C Virus	74	0.082

161	c	ART101	Aortic Valve Disease 2	67	0.082

162		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	63	0.082

163	c	HPT001	Hepatitis C	62	0.082

164	P	LYM031	Lymphocytic Leukemia	56	0.082

165	c	PSR017	Psoriasis 2	55	0.082

166	c	PSR023	Psoriasis 1	50	0.082

167	c	BDY007	Body Mass Index Quantitative Trait Locus 1	43	0.082

168	c	PSR028	Psoriasis 7	40	0.082

169	c	PSR018	Psoriasis 13	40	0.082

170	c	PSR032	Psoriasis 11	40	0.082

171		GLB002	Glioblastoma	74	0.078

172		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.078

173		SCK003	Sickle Cell Anemia	74	0.078

174	P	DMN002	Dementia	68	0.078

175	P	MCR115	Microvascular Complications of Diabetes 5	67	0.078

176	P	OCL013	Oculodentodigital Dysplasia	65	0.078

177	P	NPH012	Nephrotic Syndrome	65	0.078

178		GLB015	Glioblastoma Multiforme	60	0.078

179	c	ACT027	Acute Pancreatitis	60	0.078

180	c	HPT003	Hepatitis a	60	0.078

181		PRM236	Primary Biliary Cholangitis	57	0.078

182		PRP030	Purpura	56	0.078

183		MSC190	Muscular Disease	54	0.078

184		OCL069	Ocular Motor Apraxia	53	0.078

185	P	SCK005	Sickle Cell Disease	53	0.078

186		DYS014	Dyspepsia	51	0.078

187		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	45	0.078

188	P	VSC018	Visceral Steatosis	34	0.078

189		HML018	Homologous Wasting Disease	22	0.078

190	c	LKM061	Leukemia, Acute Myeloid	84	0.073

191		OST012	Osteoarthritis	80	0.073

192	P	SLP006	Sleep Apnea	71	0.073

193	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.073

194		INC002	Inclusion Body Myositis	66	0.073

195		KHL003	Kohlschutter-Tonz Syndrome	63	0.073

196		LNG099	Lung Disease	62	0.073

197	P	MYL006	Myeloid Leukemia	61	0.073

198	P	CRD132	Cardiac Conduction Defect	61	0.073

199	P	BRN022	Bronchiectasis	60	0.073

200	P	MYC008	Myocarditis	60	0.073

201	P	SZR006	Seizure Disorder	59	0.073

202		CNS004	Constipation	59	0.073

203		CMR002	Coumarin Resistance	56	0.073

204		HRT012	Heart Valve Disease	56	0.073

205	P	PRM006	Primary Biliary Cirrhosis	54	0.073

206	P	IDP024	Idiopathic Inflammatory Myopathy	49	0.073

207	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	49	0.073

208	c	CHR064	Chronic Monocytic Leukemia	43	0.073

209	c	SYS043	Systemic Lupus Erythematosus 1	39	0.073

210	P	OVR096	Overlap Myositis	28	0.073

211		CHL079	Children's Interstitial Lung Disease	27	0.073

212	c	ART115	Aortic Valve Disease 1	76	0.068

213		SVR004	Severe Combined Immunodeficiency	74	0.068

214	P	PNM007	Pneumonia	71	0.068

215		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	67	0.068

216	P	BLD124	Bleeding Disorder, Platelet-Type, 11	66	0.068

217	P	ADN016	Adenocarcinoma	65	0.068

218		APN008	Apnea, Obstructive Sleep	64	0.068

219		PRT013	Portal Hypertension	61	0.068

220	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	61	0.068

221		MNT002	Mental Depression	60	0.068

222		PLM033	Pulmonary Embolism	60	0.068

223	P	EXN002	Exanthem	58	0.068

224	P	PLY041	Polymyositis	57	0.068

225	P	DRR001	Diarrhea	55	0.068

226	P	INS002	in Situ Carcinoma	55	0.068

227	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	54	0.068

228		LYM040	Lymphoblastic Lymphoma	54	0.068

229		47X002	47,xyy	49	0.068

230	P	BLD051	Blood Coagulation Disease	48	0.068

231	P	CRN074	Coronary Artery Aneurysm	47	0.068

232		DST006	Diastolic Heart Failure	43	0.068

233	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.068

234		CLP006	Clopidogrel Resistance	41	0.068

235		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.068

236	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	28	0.068

237	P	PNC035	Pancreatic Cancer	86	0.063

238		MYL069	Myeloma, Multiple	85	0.063

239		CRH001	Crohn's Disease	75	0.063

240	P	HYP086	Hypothyroidism	70	0.063

241	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.063

242	c	MCR129	Microvascular Complications of Diabetes 1	67	0.063

243		MSC007	Muscle Hypertrophy	65	0.063

244	P	DRM010	Dermatomyositis	62	0.063

245		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.063

246	c	LKM060	Leukemia, Acute Lymphoblastic 3	57	0.063

247	P	NRP001	Neuropathy	57	0.063

248		HYP060	Hyperinsulinism	55	0.063

249		GLC003	Glucose Intolerance	55	0.063

250	c	SCN036	Secondary Progressive Multiple Sclerosis	54	0.063

251		DMY004	Demyelinating Disease	54	0.063

252	c	HYP739	Hyperlipoproteinemia, Type Iv	50	0.063

253		PRD004	Prediabetes Syndrome	49	0.063

254		GLL048	Glial Tumor	48	0.063

255	c	HNT004	Huntington Disease-Like 2	48	0.063

256		BHR001	Behr Syndrome	47	0.063

257		URT010	Ureteral Obstruction	46	0.063

258	c	PCH010	Pachyonychia Congenita 3	43	0.063

259	c	MCR112	Microvascular Complications of Diabetes 2	42	0.063

260	c	PLY105	Polycystic Ovary Syndrome 1	38	0.063

261	c	HNT011	Huntington Disease-Like 3	37	0.063

262		CYS001	Cystic Fibrosis	84	0.058

263		AST005	Asthma	80	0.058

264		DFC004	Deficiency Anemia	77	0.058

265	P	EPL164	Epilepsy	73	0.058

266	P	TBR001	Tuberous Sclerosis	72	0.058

267		MYL009	Myelodysplastic Syndrome	72	0.058

268		BRN024	Bronchitis	70	0.058

269		LYM133	Lymphoma, Hodgkin, Classic	70	0.058

270		HYP056	Hypoglycemia	68	0.058

271		SKN019	Skin Melanoma	68	0.058

272		MLN008	Melanoma	68	0.058

273	P	HYP098	Hypereosinophilic Syndrome	67	0.058

274		DPR016	Depression	64	0.058

275	P	VSC011	Vasculitis	64	0.058

276	c	FNC043	Fanconi Anemia, Complementation Group E	64	0.058

277	P	GLM045	Glioma	64	0.058

278	c	ATM011	Autoimmune Hepatitis	63	0.058

279		CLT003	Colitis	63	0.058

280		BRS099	Breast Ductal Carcinoma	63	0.058

281		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	62	0.058

282	c	SCL052	Scleroderma, Familial Progressive	62	0.058

283	P	CTR002	Cataract	62	0.058

284	P	BCL017	B-Cell Lymphoma	61	0.058

285		NTR005	Nutritional Deficiency Disease	61	0.058

286	P	HDC001	Headache	59	0.058

287	P	GLM007	Glomerulonephritis	58	0.058

288		IRN002	Iron Metabolism Disease	58	0.058

289		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	57	0.058

290		BRN004	Brain Edema	57	0.058

291	c	VRL010	Viral Hepatitis	56	0.058

292	P	CHL066	Cholangitis	53	0.058

293	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	53	0.058

294		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.058

295	c	LTN004	Late-Onset Retinal Degeneration	49	0.058

296		HYP043	Hyperandrogenism	48	0.058

297		ACT113	Acute Myeloblastic Leukemia with Maturation	48	0.058

298		HDN002	Head Injury	47	0.058

299		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	0.058

300		KRT013	Keratolytic Winter Erythema	45	0.058

301		SYS003	Systolic Heart Failure	43	0.058

302		TRP009	Triple X Syndrome	42	0.058

303	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.058

304	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	29	0.058

305	c	HYP163	Hyperlipidemia Type 3	23	0.058

306	P	HPT023	Hepatocellular Carcinoma	99	0.052

307	P	OVR042	Ovarian Cancer	89	0.052

308	c	LKM071	Leukemia, Chronic Lymphocytic	81	0.052

309		RNL114	Renal Cell Carcinoma, Nonpapillary	79	0.052

310	P	BLD134	Bladder Cancer	79	0.052

311		LYM143	Lymphoma, Non-Hodgkin, Familial	74	0.052

312	c	TBR025	Tuberous Sclerosis 1	74	0.052

313	P	SRC025	Sarcoidosis 1	72	0.052

314	P	SYS005	Systemic Scleroderma	68	0.052

315	P	HYP061	Hypertrophic Cardiomyopathy	68	0.052

316		ALC007	Alcohol Dependence	68	0.052

317		PRT036	Peritonitis	66	0.052

318		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	65	0.052

319		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.052

320		SKN016	Skin Disease	64	0.052

321	c	HPT016	Hepatitis B	63	0.052

322		GT001	Gout	63	0.052

323	c	PRC016	Pre-Eclampsia	63	0.052

324	P	HMN010	Hemangioma	62	0.052

325	P	INT143	Interstitial Cystitis	62	0.052

326	c	PNS012	Paine Syndrome	61	0.052

327	P	URT039	Urticaria	61	0.052

328		INT002	Intermittent Claudication	60	0.052

329	P	BPL003	Bipolar Disorder	59	0.052

330	P	ALC033	Alcohol Use Disorder	58	0.052

331		VSC002	Vascular Dementia	57	0.052

332		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.052

333		PLM010	Pulmonary Edema	56	0.052

334	P	DBT005	Diabetes Insipidus	54	0.052

335	P	ECL001	Eclampsia	53	0.052

336	P	CRB194	Cerebroretinal Microangiopathy with Calcifications and Cysts 1	53	0.052

337		RYN005	Raynaud Phenomenon	50	0.052

338	c	PRM108	Primary Progressive Multiple Sclerosis	49	0.052

339		RNL077	Renal Fibrosis	49	0.052

340		CLC006	Calcinosis	48	0.052

341		HYP025	Hyperphosphatemia	47	0.052

342		CRB008	Cerebral Atherosclerosis	47	0.052

343		ENT004	Enthesopathy	46	0.052

344		ART031	Aortic Coarctation	45	0.052

345		CRN017	Coronary Thrombosis	45	0.052

346	P	MYG005	Myoglobinuria	43	0.052

347	P	PRC031	Preeclampsia/eclampsia 1	42	0.052

348		ASP030	Aspirin Resistance	42	0.052

349	c	MJR024	Major Affective Disorder 9	42	0.052

350	P	GLM044	Glomerular Disease	42	0.052

351		ADS004	Aids Dementia Complex	41	0.052

352	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.052

353	c	HMG029	Hemoglobin Se Disease	40	0.052

354	P	ECT045	Ectodermal Dysplasia-Syndactyly Syndrome 1	39	0.052

355		49X002	49,xxxxy Syndrome	39	0.052

356		SPR126	Superior Semicircular Canal Dehiscence	39	0.052

357	c	MJR022	Major Affective Disorder 8	39	0.052

358	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	34	0.052

359	c	MYC058	Myocardial Infarction 2	30	0.052

360		CRT084	Creatinine Clearance Quantitative Trait Locus	26	0.052

361		INT074	Intracranial Arteriosclerosis	17	0.052

362		STT044	Statin Toxicity	12	0.052

363	P	LNG032	Lung Cancer	99	0.045

364		SQM013	Squamous Cell Carcinoma, Head and Neck	81	0.045

365		CNN003	Conn's Syndrome	78	0.045

366	P	RSP003	Respiratory Failure	75	0.045

367		RNL065	Renal Cell Carcinoma, Papillary, 1	75	0.045

368		END057	Endometrial Cancer	74	0.045

369	c	SPN225	Spondyloarthropathy 1	74	0.045

370		ADR007	Adrenoleukodystrophy	72	0.045

371		RCK004	Rickets	70	0.045

372	c	PNC108	Pancreatitis, Hereditary	70	0.045

373	P	MYS003	Myasthenia Gravis	68	0.045

374		WRN001	Werner Syndrome	68	0.045

375	P	GLM040	Glioma Susceptibility 1	68	0.045

376	P	NSP012	Nasopharyngeal Carcinoma	67	0.045

377		LYM007	Lymphangioleiomyomatosis	67	0.045

378	P	CNJ013	Conjunctivitis	67	0.045

379	c	MCL062	Mucolipidosis Ii Alpha/beta	67	0.045

380	P	SKN015	Skin Carcinoma	67	0.045

381	c	INF071	Inflammatory Bowel Disease 1	66	0.045

382		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	65	0.045

383	P	CRB048	Cerebral Cavernous Malformations	65	0.045

384	c	GCH015	Gaucher Disease, Type I	65	0.045

385		CLN015	Colon Adenocarcinoma	65	0.045

386	P	ENC018	Encephalopathy	64	0.045

387	P	GCH001	Gaucher's Disease	63	0.045

388		PSR001	Psoriatic Arthritis	63	0.045

389		PCK003	Pick Disease of Brain	63	0.045

390		TXC005	Toxic Shock Syndrome	63	0.045

391	P	FCL005	Focal Segmental Glomerulosclerosis	63	0.045

392	P	SNS001	Sensorineural Hearing Loss	62	0.045

393		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	62	0.045

394		CRD223	Cardiac Arrhythmia	61	0.045

395		STT001	Status Epilepticus	61	0.045

396	c	LCL006	Localized Scleroderma	61	0.045

397	P	CNT110	Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a	61	0.045

398	P	NMN002	Niemann-Pick Disease	60	0.045

399		ALC006	Alcoholic Hepatitis	60	0.045

400		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.045

401	P	KDN017	Kidney Cancer	60	0.045

402		HPT019	Hepatic Encephalopathy	60	0.045

403		HMR039	Hemorrhage, Intracerebral	59	0.045

404		EYD002	Eye Disease	59	0.045

405	P	BRS044	Breast Adenocarcinoma	59	0.045

406	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.045

407		VSL002	Visual Epilepsy	58	0.045

408	P	PRP029	Porphyria	58	0.045

409		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	58	0.045

410	P	ALP008	Alopecia	58	0.045

411	P	SLP005	Sleep Disorder	58	0.045

412	P	INF037	Inflammatory Bowel Disease	57	0.045

413		DCT002	Ductal Carcinoma in Situ	57	0.045

414	P	GRV001	Graves' Disease	57	0.045

415		APH002	Aphasia	56	0.045

416		ALL006	Allergic Asthma	56	0.045

417		CRH005	Crohn's Colitis	56	0.045

418	c	CHR417	Chronic Graft Versus Host Disease	56	0.045

419	P	SBS003	Substance Abuse	56	0.045

420	P	ACT010	Acth-Secreting Pituitary Adenoma	55	0.045

421		AMN003	Amnestic Disorder	55	0.045

422	P	HYP076	Hyperthyroidism	55	0.045

423	P	PLY019	Polyneuropathy	55	0.045

424		ANM046	Anemia, Sideroblastic, and Spinocerebellar Ataxia	55	0.045

425		PLM012	Pulmonary Sarcoidosis	54	0.045

426	P	HYP730	Hypogonadotropic Hypogonadism	54	0.045

427		PRC013	Pericarditis	54	0.045

428		HYP014	Hyperuricemia	52	0.045

429	P	CPL006	Capillary Hemangioma	52	0.045

430		NRT004	Neuritis	52	0.045

431		MCL006	Macular Retinal Edema	52	0.045

432	c	INF023	Inflammatory Breast Carcinoma	52	0.045

433	c	BRS049	Breast Carcinoma in Situ	51	0.045

434		IMM064	Immunodeficiency, Common Variable, 10	51	0.045

435		BLD053	Blood Platelet Disease	51	0.045

436	P	RTN022	Retinal Vein Occlusion	50	0.045

437		SCH012	Schizoaffective Disorder	50	0.045

438		CHL152	Childhood Acute Lymphocytic Leukemia	50	0.045

439		ACR041	Acromelic Frontonasal Dysostosis	50	0.045

440		IGG001	Iga Glomerulonephritis	50	0.045

441	c	INF145	Infantile Liver Failure Syndrome 1	50	0.045

442		HYP006	Hypertensive Heart Disease	49	0.045

443	c	MTR002	Mitral Valve Insufficiency	49	0.045

444	P	RNV001	Renovascular Hypertension	49	0.045

445	c	ACT078	Acute Porphyria	49	0.045

446		CVR006	Cavernous Hemangioma	49	0.045

447	c	CNT016	Central Retinal Vein Occlusion	48	0.045

448	c	PRG043	Progressive Familial Heart Block, Type Ib	48	0.045

449		DFF035	Diffuse Cutaneous Systemic Sclerosis	48	0.045

450	c	HYP837	Hypercholesterolemia, Familial, 2	48	0.045

451		RYN001	Raynaud Disease	48	0.045

452		ACT017	Acute Chest Syndrome	47	0.045

453		CRB027	Cerebellar Disease	47	0.045

454		NPH010	Nephrosclerosis	46	0.045

455		MYC005	Myocardial Stunning	45	0.045

456		BCK006	Back Pain	44	0.045

457	P	MJR007	Major Affective Disorder 1	44	0.045

458		ABD017	Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2	44	0.045

459		ATN004	Autonomic Neuropathy	43	0.045

460	c	SRC023	Sarcoidosis 2	43	0.045

461		DFF003	Diffuse Scleroderma	43	0.045

462	P	AVS003	Avascular Necrosis	43	0.045

463		MMM006	Mammographic Density	43	0.045

464		HPT004	Hepatic Coma	42	0.045

465		RTR011	Retroperitoneal Fibrosis	41	0.045

466		NSP002	Nasopharyngitis	41	0.045

467		AGR019	Age-Related Hearing Loss	40	0.045

468		DBT092	Diabetes Insipidus, Nephrogenic, X-Linked	37	0.045

469		FBR089	Fibrosclerosis, Multifocal	37	0.045

470	c	ATM022	Autoimmune Myocarditis	36	0.045

471		SHR109	Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities	36	0.045

472		47X003	47, Xxy	36	0.045

473		CVR010	Cavernous Malformation	36	0.045

474	c	MJR008	Major Affective Disorder 2	35	0.045

475		CRN006	Coronary Aneurysm	35	0.045

476		ACT011	Acute Contagious Conjunctivitis	35	0.045

477	c	MJR003	Major Affective Disorder 6	34	0.045

478	c	MJR006	Major Affective Disorder 5	34	0.045

479	c	MJR023	Major Affective Disorder 7	34	0.045

480		CRB031	Cerebral Arterial Disease	30	0.045

481	c	MJR004	Major Affective Disorder 4	29	0.045

482		PRQ002	Paraquat Poisoning	25	0.045

483		ACR039	Acromegaloid Hypertrichosis Syndrome	25	0.045

484		CNT023	Central Nervous System Hemangioma	13	0.045

485		MLR004	Malaria	82	0.037

486	P	RTN024	Retinoblastoma	74	0.037

487	c	LKM063	Leukemia, Chronic Myeloid	74	0.037

488	P	CNR004	Cone-Rod Dystrophy 2	72	0.037

489	c	MGR028	Migraine with or Without Aura 1	70	0.037

490		MNT001	Mantle Cell Lymphoma	69	0.037

491	P	MYC084	Mycobacterium Tuberculosis 1	69	0.037

492	P	INF038	Influenza	69	0.037

493	P	MJR001	Major Depressive Disorder	69	0.037

494		OBS002	Obsessive-Compulsive Disorder	69	0.037

495		CHL065	Cholangiocarcinoma	68	0.037

496	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.037

497		SRC014	Sarcoma	67	0.037

498		CHG001	Chagas Disease	66	0.037

499		MYL031	Myeloproliferative Neoplasm	66	0.037

500		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.037

501		MSM014	Mismatch Repair Cancer Syndrome	65	0.037

502		CLR108	Colorectal Adenoma	64	0.037

503		TNG002	Tangier Disease	64	0.037

504	P	HYP069	Hyperparathyroidism	64	0.037

505	P	VNW001	Von Willebrand's Disease	64	0.037

506		HMT002	Hematologic Cancer	64	0.037

507	P	NTR004	Neutropenia	64	0.037

508		DRM006	Dermatitis	63	0.037

509		HYP020	Hyperprolactinemia	62	0.037

510		OST003	Osteonecrosis	62	0.037

511		LYM012	Lymphoplasmacytic Lymphoma	62	0.037

512		VRL011	Viral Infectious Disease	62	0.037

513		IGR001	Ige Responsiveness, Atopic	61	0.037

514		PPT005	Peptic Ulcer Disease	60	0.037

515		PST028	Post-Traumatic Stress Disorder	60	0.037

516	c	ACT210	Acute Respiratory Distress Syndrome	59	0.037

517	P	MTR012	Mitral Valve Disease	59	0.037

518	P	MTC069	Mitochondrial Disorders	57	0.037

519		BCT022	Bacterial Infectious Disease	57	0.037

520		SFT003	Soft Tissue Sarcoma	57	0.037

521		SPN035	Spindle Cell Sarcoma	57	0.037

522		DBT010	Diabetic Neuropathy	56	0.037

523		SYN007	Synovitis	55	0.037

524		BRD001	Brody Myopathy	55	0.037

525		INT079	Intrahepatic Cholangiocarcinoma	54	0.037

526		PTT009	Pituitary Gland Disease	54	0.037

527		PRP016	Paraplegia	54	0.037

528	P	RCT021	Rectum Cancer	54	0.037

529	P	HYP083	Hypopituitarism	53	0.037

530	P	TMP001	Temporal Lobe Epilepsy	53	0.037

531		LNG031	Lung Benign Neoplasm	52	0.037

532	P	THY032	Thyroiditis	52	0.037

533	c	SCN007	Secondary Hyperparathyroidism	52	0.037

534	P	ANL018	Analbuminemia	51	0.037

535		GLS018	Glass Syndrome	51	0.037

536		HYP080	Hypogonadism	51	0.037

537	P	PST095	Post-Thrombotic Syndrome	50	0.037

538		MTC005	Mitochondrial Metabolism Disease	50	0.037

539		MYL075	Myelodysplastic/myeloproliferative Neoplasm	50	0.037

540		MCR004	Macroglobulinemia	50	0.037

541		CRD137	Cardiogenic Shock	50	0.037

542	c	HYP768	Hyperlipoproteinemia, Type I	50	0.037

543	c	MLG074	Malignant Mesenchymoma	50	0.037

544		SXL003	Sexual Disorder	49	0.037

545		HPT009	Hepatopulmonary Syndrome	49	0.037

546		ATS010	Autosomal Recessive Disease	49	0.037

547		GYN001	Gynecomastia	49	0.037

548		HPT014	Hepatorenal Syndrome	49	0.037

549		HYP781	Hypoascorbemia	48	0.037

550		EBL001	Ebola Hemorrhagic Fever	48	0.037

551		BNM001	Bone Marrow Cancer	48	0.037

552		CRN019	Coronary Artery Vasospasm	48	0.037

553		ADR038	Adermatoglyphia	48	0.037

554		WTH001	Withdrawal Disorder	47	0.037

555		LPT006	Leptin Receptor Deficiency	47	0.037

556	c	FCL025	Focal Segmental Glomerulosclerosis 1	47	0.037

557		ART004	Aortic Atherosclerosis	47	0.037

558		DBT006	Diabetic Macular Edema	46	0.037

559	c	FML008	Familial Retinoblastoma	46	0.037

560	P	CLL015	Collagen Disease	46	0.037

561		SYN036	Syncope	46	0.037

562		PRL017	Prolymphocytic Leukemia	45	0.037

563		ANG011	Angiodysplasia	45	0.037

564		TND005	Tendinitis	45	0.037

565		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	44	0.037

566		OBS082	Obstructive Nephropathy	44	0.037

567		DRG026	Drug Reaction with Eosinophilia and Systemic Symptoms	44	0.037

568		TND004	Tendinopathy	44	0.037

569		DRG024	Drug Allergy	43	0.037

570		SBC016	Subacute Delirium	43	0.037

571		ACT084	Acute Stress Disorder	42	0.037

572		GST020	Gastric Antral Vascular Ectasia	42	0.037

573		RDN001	Reading Disorder	42	0.037

574		HYP540	Hypertension, Diastolic	41	0.037

575		PLS016	Plasma Cell Leukemia	41	0.037

576		CRB086	Cerebral Aneurysms	41	0.037

577		CRD170	Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1	40	0.037

578		HYP064	Hypogonadotropism	40	0.037

579	c	OVR114	Ovarian Cancer 1	39	0.037

580		ANT039	Antisynthetase Syndrome	39	0.037

581	P	INT260	Intracranial Berry Aneurysm	38	0.037

582	c	LKM004	Leukemia, B-Cell, Chronic	35	0.037

583		RNL001	Renal Artery Obstruction	33	0.037

584		INF021	Infant Gynecomastia	32	0.037

585	c	CRN133	Coronary Artery Disease, Autosomal Dominant, 1	31	0.037

586		INF118	Inflammatory Myopathy with Abundant Macrophages	29	0.037

587	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	29	0.037

588		KDN013	Kidney Hypertrophy	27	0.037

589		HDG004	Hodgkin's Granuloma	27	0.037

590	c	CLB022	Coloboma, Ocular, Autosomal Recessive	27	0.037

591		FTL073	Fetal Anticonvulsant Syndrome	26	0.037

592		SCN001	Secondary Hyperparathyroidism of Renal Origin	23	0.037

593		HDG006	Hodgkin's Paragranuloma	23	0.037

594	c	CNG336	Congenital Analbuminemia	19	0.037

595		ESP021	Esophageal Cancer	90	0.026

596	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.026

597	c	MCL042	Macular Degeneration, Age-Related, 1	88	0.026

598	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.026

599	P	NRF023	Neurofibromatosis, Type Ii	77	0.026

600		ULC004	Ulcerative Colitis	75	0.026

601		BRN028	Brain Cancer	75	0.026

602		ANX010	Anxiety	75	0.026

603	P	FML011	Familial Adenomatous Polyposis	73	0.026

604	P	AMY004	Amyloidosis	71	0.026

605		LPD012	Lipoid Congenital Adrenal Hyperplasia	71	0.026

606		ACR007	Acromegaly	70	0.026

607	P	HYD006	Hydrocephalus	68	0.026

608		GST092	Gastroesophageal Reflux	68	0.026

609		CNN005	Connective Tissue Disease	68	0.026

610	c	HRD010	Hereditary Spastic Paraplegia	67	0.026

611	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	67	0.026

612	P	PSD087	Pseudoxanthoma Elasticum	67	0.026

613		OST159	Osteogenic Sarcoma	67	0.026

614	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	0.026

615	P	NRB010	Neuroblastoma 1	66	0.026

616		OST017	Osteomyelitis	65	0.026

617	P	HRD008	Hereditary Hemorrhagic Telangiectasia	64	0.026

618		KRN002	Kearns-Sayre Syndrome	64	0.026

619	c	GLC092	Glaucoma, Primary Open Angle	63	0.026

620	c	BRN108	Branchiootic Syndrome 1	62	0.026

621		TTN003	Tetanus	62	0.026

622		INT066	Interstitial Lung Disease	61	0.026

623	P	ART023	Arthropathy	61	0.026

624		HLC007	Helicobacter Pylori Infection	61	0.026

625		SPP011	Suppression of Tumorigenicity 12	61	0.026

626		SQM006	Squamous Cell Carcinoma	60	0.026

627		CHL067	Cholecystitis	60	0.026

628		BRN002	Bronchiolitis	60	0.026

629		ADN018	Adenoma	60	0.026

630	P	INT070	Intestinal Obstruction	60	0.026

631	P	INF032	Infertility	60	0.026

632	P	CYS018	Cystitis	59	0.026

633	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	59	0.026

634		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	58	0.026

635	P	UVT001	Uveitis	58	0.026

636		CYT008	Cytomegalovirus Infection	58	0.026

637		GST033	Gestational Diabetes	58	0.026

638		HYD002	Hydronephrosis	58	0.026

639		CHL014	Cholera	58	0.026

640		HPT022	Hepatoblastoma	58	0.026

641	P	GST044	Gastritis	58	0.026

642		SCH014	Schistosomiasis	57	0.026

643		TRN018	Transitional Cell Carcinoma	57	0.026

644	P	MLN007	Male Infertility	57	0.026

645		INT030	Intracranial Aneurysm	57	0.026

646	c	SPS222	Spastic Paraplegia 20, Autosomal Recessive	57	0.026

647	P	GLL022	Guillain-Barre Syndrome	56	0.026

648	c	SPS215	Spastic Paraplegia 3, Autosomal Dominant	56	0.026

649		ATR057	Atrioventricular Block	56	0.026

650	c	FNC042	Fanconi Anemia, Complementation Group D2	56	0.026

651		MCS002	Mucositis	56	0.026

652	P	PMP001	Pemphigus	56	0.026

653	P	LTR001	Lateral Sclerosis	56	0.026

654		GRN034	Grange Syndrome	55	0.026

655	c	CNG216	Congenital Hydrocephalus	55	0.026

656	P	PLM034	Pulmonary Emphysema	55	0.026

657		BRN012	Bronchiolitis Obliterans	55	0.026

658		ESP023	Esophageal Disease	55	0.026

659	P	LCH002	Lichen Planus	55	0.026

660	c	GRV008	Graves Disease 1	55	0.026

661		SPT004	Septic Arthritis	55	0.026

662		PRS045	Prostatic Hypertrophy	55	0.026

663		DCB001	Decubitus Ulcer	54	0.026

664		PLG002	Plague	54	0.026

665		INT075	Intracranial Hypertension	54	0.026

666		PLS007	Plasmodium Falciparum Malaria	53	0.026

667		TLN003	Telangiectasis	53	0.026

668		CMB003	Combined T Cell and B Cell Immunodeficiency	53	0.026

669	P	MYS079	Miyoshi Muscular Dystrophy	53	0.026

670	c	GLL024	Gallbladder Disease 1	53	0.026

671	c	ACT134	Acute Liver Failure	53	0.026

672		GST023	Gastric Ulcer	53	0.026

673		LMY002	Leiomyoma	52	0.026

674	P	MNC007	Monocytic Leukemia	52	0.026

675		PRS021	Prostatic Adenoma	52	0.026

676	P	TRT010	Teratoma	52	0.026

677		CRY005	Cryptococcosis	51	0.026

678		OVR082	Overgrowth Syndrome	51	0.026

679		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.026

680		QDR001	Quadriplegia	51	0.026

681		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.026

682		CRY003	Cryptosporidiosis	50	0.026

683	P	IGN003	Iga Nephropathy 1	50	0.026

684	P	OPN001	Open-Angle Glaucoma	50	0.026

685		PLR008	Pleurisy	50	0.026

686		MNN009	Meningoencephalitis	50	0.026

687		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	49	0.026

688		PRS129	Prostatic Hyperplasia, Benign	49	0.026

689		RTN020	Retinal Vascular Disease	49	0.026

690	c	BCT013	Bacterial Pneumonia	49	0.026

691		THR013	Thoracic Outlet Syndrome	49	0.026

692		MTB004	Metabolic Acidosis	48	0.026

693		BLP005	Blepharitis	48	0.026

694		ATN005	Autonomic Dysfunction	48	0.026

695		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	48	0.026

696		DBT004	Diabetic Polyneuropathy	48	0.026

697		ESN015	Eosinophilic Fasciitis	48	0.026

698		HDR003	Hidradenitis	48	0.026

699	P	HMR005	Hemorrhoid	47	0.026

700		INT010	Intracranial Embolism	47	0.026

701		HPT025	Hepatic Lipase Deficiency	47	0.026

702	P	MYC033	Myoclonus	47	0.026

703		FSC004	Fasciitis	47	0.026

704		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.026

705		MCR037	Macroglossia	46	0.026

706		HLX001	Helix Syndrome	46	0.026

707	c	RCR022	Recurrent Acute Pancreatitis	46	0.026

708		ASP007	Aspiration Pneumonia	46	0.026

709	P	CMP008	Compartment Syndrome	45	0.026

710	c	ATM099	Autoimmune Uveitis	45	0.026

711	c	DYS119	Dystonia 9	45	0.026

712		RTR008	Root Resorption	44	0.026

713		ORL015	Oral Squamous Cell Carcinoma	44	0.026

714		PLY068	Polysubstance Abuse	44	0.026

715		ANX004	Anoxia	44	0.026

716		CRT015	Carotid Artery Occlusion	44	0.026

717		INT052	Intestinal Volvulus	44	0.026

718		ANC002	Anca-Associated Vasculitis	43	0.026

719		PRS115	Prosthetic Joint Infection	43	0.026

720	P	CRB088	Cerebral Atrophy	43	0.026

721		CYS009	Cystadenoma	43	0.026

722		GLC086	Glucocorticoid-Induced Osteoporosis	42	0.026

723		CRS001	Crescentic Glomerulonephritis	42	0.026

724		ALC010	Alcoholic Cardiomyopathy	42	0.026

725		TND006	Tendinosis	42	0.026

726	P	CRC039	Coarctation of Aorta	42	0.026

727		CHR466	Chronic Thromboembolic Pulmonary Hypertension	41	0.026

728	P	SBR004	Seborrheic Dermatitis	41	0.026

729		DRG002	Drug-Induced Hepatitis	41	0.026

730		MYF001	Myofibroma	40	0.026

731	c	CHR096	Chronic Pulmonary Heart Disease	40	0.026

732		LNR006	Linear Iga Disease	40	0.026

733		SCH060	Schistosoma Mansoni Infection, Susceptibility/	40	0.026

734		HMR023	Hemorrhagic Cystitis	40	0.026

735		PLT015	Platelet Aggregation, Spontaneous	40	0.026

736		THR099	Third-Degree Atrioventricular Block	39	0.026

737		EXT006	Extrahepatic Cholestasis	38	0.026

738		SPS057	Spasticity	38	0.026

739		HRN029	Hearing Loss, Noise-Induced	38	0.026

740		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	38	0.026

741		RTR001	Retrograde Amnesia	38	0.026

742		BCK003	Background Diabetic Retinopathy	37	0.026

743	P	ANT001	Anterolateral Myocardial Infarction	37	0.026

744		AMR003	Amaurosis Fugax	36	0.026

745	c	PRG020	Paragangliomas 3	36	0.026

746		FXD003	Fixed Drug Eruption	36	0.026

747	c	CHR682	Chronic Bilirubin Encephalopathy	36	0.026

748		HMM004	Hamamy Syndrome	36	0.026

749		SBC014	Subclavian Steal Syndrome	36	0.026

750	P	PK3005	Pik3ca-Related Overgrowth Syndrome	35	0.026

751		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	34	0.026

752		MNN002	Mononeuritis Multiplex	33	0.026

753		LCH013	Lichen Planus Pemphigoides	33	0.026

754		RRS014	Rare Surgical Neurologic Disease	33	0.026

755	c	FTL070	Fetal Akinesia Deformation Sequence 2	33	0.026

756		ART012	Aortitis	33	0.026

757		ART010	Arteriolosclerosis	32	0.026

758	c	SPS036	Spastic Paraplegia 3	31	0.026

759		PMP009	Pemphigus Erythematosus	29	0.026

760	c	HRD138	Hereditary Motor and Sensory Neuropathy V	29	0.026

761		SLR005	Solar Urticaria	29	0.026

762		MDR006	Moderate and Severe Traumatic Brain Injury	27	0.026

763		PTN004	Patent Ductus Venosus	26	0.026

764		NCR015	Necrotizing Autoimmune Myopathy	26	0.026

765	P	CRT085	Carotid Intimal Medial Thickness 2	25	0.026

766		CNG092	Congenital Extrahepatic Portosystemic Shunt	24	0.026

767		TLM001	Telomere Length, Mean Leukocyte	19	0.026

768		NNC012	Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency	18	0.026

769		PRQ001	Paraquat Lung	17	0.026