Search results for Amiodarone

497 hits were found for Amiodarone

#	Family	MCID	Name	MIFTS	Score
1	P	ATR011	Atrial Fibrillation	66	0.622

2	c	GRV008	Graves Disease 1	56	0.547

3	P	HYP086	Hypothyroidism	69	0.535

4	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.493

5	P	HYP076	Hyperthyroidism	55	0.477

6		CNG034	Congestive Heart Failure	69	0.361

7	P	CRD119	Cardiac Arrest	67	0.315

8	P	PLM036	Pulmonary Fibrosis	65	0.310

9	c	FML001	Familial Atrial Fibrillation	65	0.293

10	P	NRP001	Neuropathy	56	0.293

11		CRD132	Cardiac Conduction Defect	58	0.292

12	P	THY032	Thyroiditis	52	0.266

13	c	DLT002	Dilated Cardiomyopathy	79	0.251

14	P	HRT032	Heart Disease	75	0.251

15		GTR002	Goiter	53	0.242

16	P	OPT006	Optic Nerve Disease	60	0.225

17		CRD223	Cardiac Arrhythmia	60	0.221

18		KRT008	Keratopathy	47	0.221

19	c	ATR087	Atrial Standstill 1	75	0.211

20		LNG099	Lung Disease	60	0.211

21		WLF001	Wolff-Parkinson-White Syndrome	66	0.204

22		SYN036	Syncope	45	0.184

23	P	MYC007	Myocardial Infarction	70	0.179

24		ATR057	Atrioventricular Block	55	0.179

25	P	HYP061	Hypertrophic Cardiomyopathy	70	0.169

26		LPP008	Lipoprotein Quantitative Trait Locus	62	0.169

27	P	PRP019	Peripheral Nervous System Disease	58	0.169

28	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.166

29		ANG054	Angina Pectoris	66	0.166

30	P	RSP003	Respiratory Failure	74	0.163

31	c	ACT075	Acute Myocardial Infarction	57	0.163

32	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.160

33	P	GRV001	Graves' Disease	55	0.158

34		ART140	Arteries, Anomalies of	52	0.158

35		CHG001	Chagas Disease	66	0.155

36	P	CRN300	Coronary Heart Disease 1	63	0.152

37	P	MYP004	Myopathy	70	0.146

38		LVR012	Liver Cirrhosis	62	0.143

39		48X005	48,xyyy	39	0.143

40	P	PNM007	Pneumonia	68	0.140

41		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	63	0.140

42		HYP005	Hypokalemia	55	0.140

43		ALL026	Allergic Hypersensitivity Disease	62	0.137

44		INT066	Interstitial Lung Disease	60	0.137

45	P	TRM003	Tremor	54	0.133

46	P	HPT021	Hepatitis	67	0.130

47		BRN002	Bronchiolitis	59	0.130

48	c	DWL002	Dowling-Degos Disease 1	58	0.130

49	P	SCK002	Sick Sinus Syndrome	55	0.130

50		CRB039	Cerebrovascular Disease	67	0.126

51	P	KDN018	Kidney Disease	72	0.123

52		BRN012	Bronchiolitis Obliterans	55	0.123

53		STR067	Stroke, Ischemic	81	0.119

54	P	LNG028	Long Qt Syndrome	66	0.119

55		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.119

56	P	LVR013	Liver Disease	68	0.115

57	P	EXN002	Exanthem	57	0.115

58		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.111

59	P	MLT008	Multinodular Goiter	42	0.111

60		HYD038	Hydrops Fetalis, Nonimmune	62	0.107

61		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.107

62		HYP645	Hyperthyroxinemia, Dystransthyretinemic	31	0.107

63		HYP029	Hyperthyroxinemia	31	0.107

64	c	CNG006	Congenital Hypothyroidism	64	0.103

65	c	ACT071	Acute Kidney Failure	60	0.103

66		NDL007	Nodular Goiter	47	0.103

67	P	ADL010	Adult Respiratory Distress Syndrome	65	0.099

68		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	62	0.099

69		TXC005	Toxic Shock Syndrome	62	0.099

70	P	MYC008	Myocarditis	59	0.099

71		CRY001	Cryptogenic Organizing Pneumonia	53	0.099

72		MYX004	Myxedema	43	0.099

73		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.094

74		LSH001	Leishmaniasis	63	0.094

75	P	ENC018	Encephalopathy	61	0.094

76	P	PNC044	Pancreatitis	61	0.094

77	c	ACT027	Acute Pancreatitis	60	0.094

78		PLM010	Pulmonary Edema	54	0.094

79		RHM028	Rheumatic Heart Disease	53	0.094

80		HRT012	Heart Valve Disease	53	0.094

81		THR016	Thrombophlebitis	51	0.094

82	P	KLZ004	Kala-Azar 1	41	0.094

83	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.089

84	P	HYP098	Hypereosinophilic Syndrome	67	0.089

85		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.089

86		CHL068	Cholestasis	61	0.089

87		ISC004	Ischemia	58	0.089

88		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.089

89		INT007	Intermediate Coronary Syndrome	55	0.089

90	c	SBC007	Subacute Thyroiditis	45	0.089

91	P	LNG032	Lung Cancer	98	0.084

92		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.084

93		HSH003	Hashimoto Thyroiditis	62	0.084

94		THY029	Thyroid Carcinoma	59	0.084

95	c	ACT134	Acute Liver Failure	56	0.084

96		THY030	Thyroid Gland Disease	52	0.084

97		OCL069	Ocular Motor Apraxia	51	0.084

98		47X002	47,xyy	49	0.084

99		ATX019	Ataxia with Vitamin E Deficiency	42	0.084

100		ACR008	Acrocallosal Syndrome	69	0.079

101	P	THR014	Thrombocytopenia	67	0.079

102	P	VSC011	Vasculitis	62	0.079

103	P	CRD246	Cardiovascular System Disease	57	0.079

104	P	MTR003	Mitral Valve Stenosis	50	0.079

105		SNT005	Sinoatrial Node Disease	49	0.079

106		RST023	Resting Heart Rate, Variation in	41	0.079

107	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.073

108	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.073

109	P	PLY019	Polyneuropathy	56	0.073

110	P	ESN008	Eosinophilic Pneumonia	50	0.073

111		HMP001	Hemopericardium	48	0.073

112		SBC016	Subacute Delirium	44	0.073

113		BCK006	Back Pain	42	0.073

114		DFF031	Diffuse Alveolar Hemorrhage	30	0.073

115		FBR012	Fabry Disease	72	0.067

116	P	BRG001	Brugada Syndrome	71	0.067

117		HYP056	Hypoglycemia	66	0.067

118	P	NTR004	Neutropenia	63	0.067

119	P	VSC007	Vascular Disease	63	0.067

120		DPR016	Depression	63	0.067

121		CTN007	Cutaneous Leishmaniasis	62	0.067

122		HYP066	Hyperglycemia	61	0.067

123	P	LPS004	Lupus Erythematosus	61	0.067

124		EXT034	Extrinsic Allergic Alveolitis	58	0.067

125		INT303	Intracranial Hypertension, Idiopathic	57	0.067

126	c	PRG043	Progressive Familial Heart Block, Type Ib	54	0.067

127		INT075	Intracranial Hypertension	53	0.067

128		NRT004	Neuritis	52	0.067

129	P	PRC012	Pericardial Effusion	51	0.067

130		PPL021	Papilledema	49	0.067

131		SYS003	Systolic Heart Failure	49	0.067

132		EBL001	Ebola Hemorrhagic Fever	49	0.067

133		CRD137	Cardiogenic Shock	47	0.067

134		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.067

135	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.067

136		49X006	49, Xxxxy Syndrome	41	0.067

137		TXC008	Toxic Optic Neuropathy	23	0.067

138	c	NRF023	Neurofibromatosis, Type Ii	80	0.060

139	c	HPT073	Hepatitis C Virus	72	0.060

140	P	TTR001	Tetralogy of Fallot	70	0.060

141	c	CHR684	Chronic Kidney Disease	70	0.060

142	P	PLM037	Pulmonary Hypertension	67	0.060

143		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.060

144		ATM095	Autoimmune Disease	62	0.060

145		IDP011	Idiopathic Interstitial Pneumonia	59	0.060

146		NNL006	Non-Alcoholic Steatohepatitis	54	0.060

147		PNC001	Pancytopenia	54	0.060

148		HRT011	Heart Septal Defect	50	0.060

149		HYP006	Hypertensive Heart Disease	49	0.060

150		LFT001	Left Bundle Branch Hemiblock	49	0.060

151	c	MTR002	Mitral Valve Insufficiency	48	0.060

152		LPD009	Lipid Storage Disease	46	0.060

153		HPT004	Hepatic Coma	45	0.060

154		GRN017	Granulocytopenia	44	0.060

155		DRG002	Drug-Induced Hepatitis	43	0.060

156		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.060

157		HYP344	Hyperthyroidism, Familial Gestational	39	0.060

158		MLT131	Multifocal Atrial Tachycardia	18	0.060

159	P	HPT023	Hepatocellular Carcinoma	100	0.052

160		MYL069	Myeloma, Multiple	85	0.052

161		MLR004	Malaria	81	0.052

162		CYS001	Cystic Fibrosis	81	0.052

163	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.052

164		AST005	Asthma	76	0.052

165	P	APL001	Aplastic Anemia	74	0.052

166	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.052

167	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.052

168		DFC004	Deficiency Anemia	70	0.052

169	P	AMY004	Amyloidosis	70	0.052

170		DWN001	Down Syndrome	70	0.052

171		ADL002	Adult Syndrome	70	0.052

172	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.052

173		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.052

174		TRN015	Transient Cerebral Ischemia	63	0.052

175	c	HPT001	Hepatitis C	62	0.052

176		FTT001	Fatty Liver Disease	61	0.052

177		ALC006	Alcoholic Hepatitis	61	0.052

178		HPT019	Hepatic Encephalopathy	60	0.052

179	P	URT039	Urticaria	58	0.052

180		NWB001	Newborn Respiratory Distress Syndrome	58	0.052

181		EYD002	Eye Disease	58	0.052

182	P	GLM007	Glomerulonephritis	57	0.052

183		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.052

184	P	ANG015	Angioedema	57	0.052

185	P	MYS005	Myositis	56	0.052

186	P	DRR001	Diarrhea	55	0.052

187	P	ALP008	Alopecia	54	0.052

188	c	VRL010	Viral Hepatitis	52	0.052

189		IMP005	Impotence	52	0.052

190		PTH003	Pathologic Nystagmus	52	0.052

191	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.052

192	c	ALM001	Al Amyloidosis	50	0.052

193		ACT029	Acute Interstitial Pneumonia	49	0.052

194		CRD001	Cardiac Tamponade	47	0.052

195		CYN002	Cyanosis, Transient Neonatal	45	0.052

196		CVD001	Covid-19	44	0.052

197		CRN322	Coronavirus Infectious Disease	40	0.052

198	c	ATM022	Autoimmune Myocarditis	35	0.052

199		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.052

200		ART110	Arteritic Anterior Ischemic Optic Neuropathy	33	0.052

201		THY001	Thyroid Crisis	31	0.052

202		ISC001	Ischemic Neuropathy	29	0.052

203		CHL079	Children's Interstitial Lung Disease	26	0.052

204		DFF002	Diffuse Pulmonary Fibrosis	25	0.052

205	P	CLR023	Colorectal Cancer	99	0.042

206	c	SYS001	Systemic Lupus Erythematosus	86	0.042

207	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.042

208	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.042

209	c	HMC039	Hemochromatosis, Type 1	74	0.042

210	P	PHC003	Pheochromocytoma	71	0.042

211	P	SRC025	Sarcoidosis 1	70	0.042

212	P	SLP006	Sleep Apnea	69	0.042

213		ART016	Aortic Aneurysm	69	0.042

214	c	BSL007	Basal Cell Carcinoma	68	0.042

215	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.042

216	P	TRN020	Turner Syndrome	67	0.042

217	c	RHB024	Rhabdomyosarcoma 2	67	0.042

218		ALC007	Alcohol Dependence	66	0.042

219	P	HML002	Hemolytic Anemia	63	0.042

220	c	ATM011	Autoimmune Hepatitis	63	0.042

221		LPD008	Lipid Metabolism Disorder	62	0.042

222	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.042

223	c	SVR001	Severe Acute Respiratory Syndrome	62	0.042

224	P	HYP750	Hypertriglyceridemia, Familial	62	0.042

225	P	ORT004	Orthostatic Intolerance	62	0.042

226		VRL011	Viral Infectious Disease	61	0.042

227	P	VNT002	Ventricular Septal Defect	60	0.042

228	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.042

229	P	CTR002	Cataract	60	0.042

230		CHL014	Cholera	59	0.042

231	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.042

232	P	SLP005	Sleep Disorder	59	0.042

233		PLM033	Pulmonary Embolism	59	0.042

234		PRT058	Pure Autonomic Failure	59	0.042

235		VSL002	Visual Epilepsy	59	0.042

236	P	MTR012	Mitral Valve Disease	58	0.042

237		CNS004	Constipation	58	0.042

238	P	OPT009	Optic Neuritis	57	0.042

239	P	PLY041	Polymyositis	57	0.042

240		THR024	Thrombosis	57	0.042

241	P	END033	Endocarditis	57	0.042

242		BLR008	Bilirubin Metabolic Disorder	57	0.042

243		HYP266	Hypoxia	57	0.042

244	P	SZR006	Seizure Disorder	56	0.042

245	P	ATR001	Atrioventricular Septal Defect	55	0.042

246		VSC003	Visceral Leishmaniasis	55	0.042

247		BRN014	Bronchopneumonia	54	0.042

248		SNS003	Sensory Peripheral Neuropathy	54	0.042

249	c	FML191	Familial Long Qt Syndrome	53	0.042

250	P	MSC003	Muscular Atrophy	52	0.042

251		PNG002	Pain Agnosia	51	0.042

252		END086	End Stage Renal Disease	51	0.042

253		CHR515	Chronic Atrial and Intestinal Dysrhythmia	50	0.042

254		STM007	Stomatitis	50	0.042

255		LRN003	Learning Disability	49	0.042

256		RGH001	Right Bundle Branch Block	48	0.042

257		DRG013	Drug-Induced Lupus Erythematosus	48	0.042

258		HYP025	Hyperphosphatemia	48	0.042

259		SXL003	Sexual Disorder	47	0.042

260		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.042

261	c	SHR030	Short Qt Syndrome	46	0.042

262		ANT039	Antisynthetase Syndrome	46	0.042

263		ADR040	Adrenal Gland Pheochromocytoma	46	0.042

264		CRN019	Coronary Artery Vasospasm	46	0.042

265	c	DRR009	Diarrhea 6	46	0.042

266		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	45	0.042

267	P	PRD021	Periodic Paralysis	45	0.042

268		PTT037	Pituitary Tumors	44	0.042

269		TST015	Testicular Disease	43	0.042

270	P	HYP265	Hypotonia	43	0.042

271		CYT002	Cytokine Deficiency	42	0.042

272	c	FML294	Familial Short Qt Syndrome	41	0.042

273		PLM068	Pulmonary Vein Stenosis	39	0.042

274		END028	Endemic Goiter	37	0.042

275		PLM011	Plummer's Disease	35	0.042

276		SBV001	Subvalvular Aortic Stenosis	33	0.042

277		IMM039	Immune Hydrops Fetalis	30	0.042

278	c	ACT053	Acute Thyroiditis	27	0.042

279		CHT001	Chaotic Atrial Tachycardia	10	0.042

280	P	PRS040	Prostate Cancer	97	0.030

281	P	BRS047	Breast Cancer	97	0.030

282	P	ALZ034	Alzheimer Disease	88	0.030

283	c	LKM061	Leukemia, Acute Myeloid	84	0.030

284	c	HYP595	Hypertension, Essential	84	0.030

285	P	BLD134	Bladder Cancer	79	0.030

286		CNN003	Conn's Syndrome	79	0.030

287	c	ART115	Aortic Valve Disease 1	75	0.030

288	P	OST002	Osteoporosis	74	0.030

289	c	BTT014	Beta-Thalassemia	74	0.030

290		PRP027	Peripheral Vascular Disease	71	0.030

291		MYL005	Myelofibrosis	70	0.030

292	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.030

293	P	LYM118	Lymphoma	68	0.030

294	P	TMP003	Temporal Arteritis	68	0.030

295	c	NMN015	Niemann-Pick Disease, Type C1	68	0.030

296	P	FRN006	Frontotemporal Dementia	68	0.030

297		GST092	Gastroesophageal Reflux	67	0.030

298	P	MLG056	Malignant Hyperthermia	67	0.030

299		THY121	Thyroid Gland Anaplastic Carcinoma	66	0.030

300	P	DMN002	Dementia	66	0.030

301	P	SKN015	Skin Carcinoma	66	0.030

302	c	LNG044	Long Qt Syndrome 1	66	0.030

303	c	SML038	Small Cell Cancer of the Lung	65	0.030

304		CRN036	Craniopharyngioma	65	0.030

305	P	CNJ013	Conjunctivitis	65	0.030

306		KRT019	Keratitis, Hereditary	65	0.030

307	P	MTR004	Maturity-Onset Diabetes of the Young	65	0.030

308	c	ART101	Aortic Valve Disease 2	65	0.030

309		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	65	0.030

310		PRT037	Pertussis	65	0.030

311		GRN037	Granulomatosis with Polyangiitis	65	0.030

312		ATH013	Atherosclerosis Susceptibility	65	0.030

313		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.030

314	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.030

315	P	DBT009	Diabetes Mellitus	64	0.030

316		APN008	Apnea, Obstructive Sleep	64	0.030

317		GT001	Gout	64	0.030

318		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.030

319		MSC007	Muscle Hypertrophy	64	0.030

320	P	ADN016	Adenocarcinoma	64	0.030

321	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	0.030

322	P	GLM045	Glioma	63	0.030

323	P	GCH001	Gaucher's Disease	63	0.030

324	c	PRC016	Pre-Eclampsia	63	0.030

325	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.030

326		SKN016	Skin Disease	63	0.030

327	P	HYP055	Hypoplastic Left Heart Syndrome	63	0.030

328	c	ACT068	Acute Cystitis	63	0.030

329	P	PSR002	Psoriasis	62	0.030

330	c	HPT003	Hepatitis a	62	0.030

331		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.030

332		DRM006	Dermatitis	61	0.030

333	P	MYL006	Myeloid Leukemia	60	0.030

334	P	NPH012	Nephrotic Syndrome	60	0.030

335		DPH001	Diphtheria	60	0.030

336		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.030

337		ACQ007	Acquired Immunodeficiency Syndrome	60	0.030

338		VRC005	Varicose Veins	60	0.030

339	P	GLY013	Glycogen Storage Disease	60	0.030

340	P	THL005	Thalassemia	60	0.030

341		PRT013	Portal Hypertension	59	0.030

342	P	BRN022	Bronchiectasis	59	0.030

343	P	LYM033	Lymphoproliferative Syndrome	59	0.030

344	P	NMN002	Niemann-Pick Disease	59	0.030

345	P	GLL022	Guillain-Barre Syndrome	59	0.030

346		ADN018	Adenoma	59	0.030

347		ANR040	Aneurysm	59	0.030

348		ANT024	Anthrax Disease	58	0.030

349	P	ALC033	Alcohol Use Disorder	58	0.030

350	P	CND004	Candidiasis	58	0.030

351		BRN056	Bronchopulmonary Dysplasia	57	0.030

352		MNR012	Meniere Disease	57	0.030

353		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.030

354		FRC011	Fructose Intolerance, Hereditary	57	0.030

355	P	PYL005	Pyelonephritis	56	0.030

356		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.030

357	P	HYP024	Hypoparathyroidism	56	0.030

358		BRN004	Brain Edema	56	0.030

359		AGN016	Aging	56	0.030

360	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.030

361	c	FML035	Familial Hyperlipidemia	55	0.030

362		MCL006	Macular Retinal Edema	55	0.030

363	P	DBT005	Diabetes Insipidus	55	0.030

364		HMP005	Hemiplegia	55	0.030

365		RSC001	Rosacea	54	0.030

366		GLC003	Glucose Intolerance	54	0.030

367	P	DXT004	Dextro-Looped Transposition of the Great Arteries	54	0.030

368	P	ART021	Arteriosclerosis	54	0.030

369		CLL003	Cellulitis	54	0.030

370		PRS045	Prostatic Hypertrophy	53	0.030

371	P	PLM006	Pulmonary Alveolar Proteinosis	53	0.030

372		INF034	Infective Endocarditis	53	0.030

373	P	PTS002	Ptosis	53	0.030

374		LYS002	Lysosomal Storage Disease	52	0.030

375	P	SML001	Small Cell Carcinoma	52	0.030

376		PST011	Pustulosis of Palm and Sole	52	0.030

377	P	DDN001	Duodenal Ulcer	52	0.030

378		HYP014	Hyperuricemia	52	0.030

379		LYM004	Lymphoid Interstitial Pneumonia	51	0.030

380	c	NMN014	Niemann-Pick Disease, Type C2	51	0.030

381		RYS001	Reye Syndrome	51	0.030

382		PRS021	Prostatic Adenoma	51	0.030

383		TRM010	Traumatic Brain Injury	51	0.030

384	P	CHL066	Cholangitis	51	0.030

385		PRT029	Parathyroid Adenoma	50	0.030

386	P	MMB011	Membranous Nephropathy	50	0.030

387		BLP005	Blepharitis	50	0.030

388		CRN030	Coronary Stenosis	50	0.030

389	c	SVR005	Severe Pre-Eclampsia	50	0.030

390	c	THY112	Thyroid Hormone Resistance, Generalized, Autosomal Dominant	50	0.030

391		TRY001	Trypanosomiasis	50	0.030

392	P	OBS001	Obstructive Jaundice	50	0.030

393		MTB004	Metabolic Acidosis	50	0.030

394		HYP748	Hypertelorism	50	0.030

395		DYS073	Dysphagia	50	0.030

396		HYP080	Hypogonadism	50	0.030

397		INP001	Inappropriate Adh Syndrome	49	0.030

398	P	ART018	Aortic Valve Insufficiency	49	0.030

399		GYN001	Gynecomastia	49	0.030

400		PRS129	Prostatic Hyperplasia, Benign	49	0.030

401		BRN071	Brain Injury	49	0.030

402	P	CMP008	Compartment Syndrome	49	0.030

403		HST010	Histiocytosis	48	0.030

404		WTH001	Withdrawal Disorder	48	0.030

405	P	CLR019	Color Blindness	48	0.030

406		RFR010	Refractory Anemia	48	0.030

407		VTM033	Vitamin K Deficiency Bleeding	48	0.030

408		CLS016	Clostridium Difficile Colitis	48	0.030

409		INT067	Interstitial Nephritis	48	0.030

410	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.030

411		PLM035	Pulmonary Eosinophilia	48	0.030

412		ASB001	Asbestosis	47	0.030

413		PPL002	Papillary Carcinoma	47	0.030

414		MCC002	Mucocutaneous Leishmaniasis	47	0.030

415	P	CRN028	Corneal Ulcer	47	0.030

416	P	RNL015	Renal Hypertension	47	0.030

417		CRN017	Coronary Thrombosis	47	0.030

418	c	INH020	Inherited Metabolic Disorder	47	0.030

419		SRT004	Serotonin Syndrome	47	0.030

420		ATN005	Autonomic Dysfunction	46	0.030

421	c	ACT076	Acute Myocarditis	46	0.030

422		ORC001	Orchitis	46	0.030

423	c	CHR037	Chronic Eosinophilic Pneumonia	46	0.030

424	P	BNG032	Benign Mesothelioma	46	0.030

425	P	MYC033	Myoclonus	46	0.030

426	c	ACT042	Acute Pyelonephritis	46	0.030

427		GLL048	Glial Tumor	45	0.030

428	P	HRN001	Horner's Syndrome	45	0.030

429		CRD231	Cardiomyopathy, Infantile Histiocytoid	45	0.030

430	c	TRC022	Tricuspid Valve Insufficiency	45	0.030

431		PLR022	Pleural Disease	45	0.030

432		CRB004	Cerebral Artery Occlusion	45	0.030

433		INT304	Interstitial Pneumonitis, Desquamative, Familial	45	0.030

434		TWN001	Twin-to-Twin Transfusion Syndrome	45	0.030

435		NNS002	Nonspecific Interstitial Pneumonia	45	0.030

436		THR099	Third-Degree Atrioventricular Block	45	0.030

437		ATN004	Autonomic Neuropathy	45	0.030

438		CRD003	Cardiac Sarcoidosis	44	0.030

439		SCT002	Scotoma	44	0.030

440		FBR054	Fibroma	44	0.030

441	P	MYG005	Myoglobinuria	44	0.030

442		CLL021	Collagenous Colitis	42	0.030

443		ALC010	Alcoholic Cardiomyopathy	42	0.030

444	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.030

445		TTT001	Tatton-Brown-Rahman Syndrome	41	0.030

446		DBT002	Diabetic Autonomic Neuropathy	41	0.030

447		LNR006	Linear Iga Disease	40	0.030

448	c	CRD081	Cardiomyopathy, Familial Hypertrophic, 12	39	0.030

449		WLL004	Wallerian Degeneration	39	0.030

450		FLL031	Follicular Adenoma	39	0.030

451		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.030

452		FRS012	First-Degree Atrioventricular Block	38	0.030

453		OPT010	Optic Papillitis	38	0.030

454		SCR039	Scorpion Envenomation	38	0.030

455		ACT167	Acute Generalized Exanthematous Pustulosis	37	0.030

456		FCL041	Focal Myositis	37	0.030

457	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	0.030

458		IND003	Indolent Myeloma	36	0.030

459	P	CNG024	Congenital Nystagmus	36	0.030

460	P	AXN001	Axonal Neuropathy	36	0.030

461		HRW001	Hair Whorl	36	0.030

462		BRK012	Broken Heart Syndrome	35	0.030

463		SRF006	Surfactant Dysfunction	35	0.030

464	c	ART068	Aortic Aneurysm, Familial Thoracic 2	34	0.030

465	c	ARR048	Arrhythmogenic Right Ventricular Dysplasia, Familial, 4	34	0.030

466	c	SHR032	Short Qt Syndrome 2	32	0.030

467		NNT010	Nontoxic Goiter	32	0.030

468		EPD018	Epididymo-Orchitis	32	0.030

469		CRT009	Critical Illness Polyneuropathy	32	0.030

470	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.030

471		INF021	Infant Gynecomastia	31	0.030

472		SNG003	Single Ventricular Heart	30	0.030

473		PLX004	Plexopathy	30	0.030

474	c	SHR033	Short Qt Syndrome 3	29	0.030

475		CRD220	Cardiac Valvular Defect, Developmental	29	0.030

476	c	ATR092	Atrial Fibrillation, Familial, 15	28	0.030

477	P	ATR081	Atrial Standstill	28	0.030

478		ANS021	Anisocoria	27	0.030

479		EXF003	Exfoliative Dermatitis	27	0.030

480		ACT038	Acute Retrobulbar Neuritis	27	0.030

481		IDN001	Iodine Hypothyroidism	26	0.030

482		ASB003	Asbestos Intoxication	26	0.030

483		VLK001	Volkmann Contracture	25	0.030

484		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.030

485	c	TRN047	Transient Congenital Hypothyroidism	23	0.030

486	P	PLM064	Pulmonary Sequestration	22	0.030

487		ATR024	Atrial Fibrillation and Stroke	22	0.030

488		PLR025	Pleuroparenchymal Fibroelastosis	22	0.030

489		CRN023	Corneal Deposit	22	0.030

490		CD4008	Cd4/cd8 T-Cell Ratio	20	0.030

491		ATR089	Atrioventricular Dissociation	20	0.030

492		BDR001	Bidirectional Tachycardia	19	0.030

493		ATM054	Autoimmune Disease 3	18	0.030

494		MYP026	Myopathy - Thyrotoxic	17	0.030

495		GRN059	Grn Frontotemporal Dementia	14	0.030

496		ETH013	Euthyroid Graves Orbitopathy	14	0.030

497		TXC006	Toxic Labyrinthitis	11	0.030