Search results for Chloride ion

989 hits were found for Chloride ion

#	Family	MCID	Name	MIFTS	Score
1		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.851

2		CYS001	Cystic Fibrosis	81	0.437

3		HRW001	Hair Whorl	36	0.390

4		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.321

5		HLX001	Helix Syndrome	47	0.292

6	P	DRR001	Diarrhea	55	0.279

7	P	KDN018	Kidney Disease	72	0.253

8		MTB004	Metabolic Acidosis	50	0.249

9	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.224

10		48X005	48,xyyy	39	0.223

11	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.220

12	c	HYP595	Hypertension, Essential	84	0.216

13	P	NRB001	Neuroblastoma	72	0.213

14	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.209

15		HYP005	Hypokalemia	55	0.209

16		MYT011	Myotonia	34	0.201

17		ALL026	Allergic Hypersensitivity Disease	62	0.199

18		PRT037	Pertussis	65	0.185

19	P	GLM045	Glioma	63	0.184

20		GLL048	Glial Tumor	45	0.183

21	c	ACT071	Acute Kidney Failure	60	0.183

22		HYP266	Hypoxia	57	0.179

23		ANG020	Angiosarcoma	64	0.179

24		CHL014	Cholera	59	0.177

25		ANX004	Anoxia	40	0.173

26		CNG034	Congestive Heart Failure	69	0.170

27	P	HPT023	Hepatocellular Carcinoma	100	0.166

28		DRM006	Dermatitis	61	0.164

29	P	LNG028	Long Qt Syndrome	66	0.163

30		ISC004	Ischemia	58	0.162

31		LNG099	Lung Disease	60	0.161

32		GLB015	Glioblastoma Multiforme	75	0.160

33	P	HRT032	Heart Disease	75	0.154

34		CNG064	Congenital Chloride Diarrhea	32	0.154

35		CNT047	Contact Dermatitis	58	0.153

36		LWC001	Low Compliance Bladder	43	0.149

37		ATM095	Autoimmune Disease	62	0.148

38	P	ALZ034	Alzheimer Disease	88	0.147

39	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.147

40		PPL052	Papillomatosis, Confluent and Reticulated	33	0.146

41		47X002	47,xyy	49	0.144

42		NPH009	Nephrolithiasis	55	0.143

43	P	CHR345	Chronic Pain	44	0.142

44	P	MYT023	Myotonia Congenita	56	0.140

45		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.139

46		BNR002	Bone Resorption Disease	48	0.139

47	P	CRD119	Cardiac Arrest	67	0.137

48	P	PNC035	Pancreatic Cancer	84	0.136

49	P	ADN016	Adenocarcinoma	64	0.136

50	P	LNG032	Lung Cancer	98	0.135

51		PNG002	Pain Agnosia	51	0.133

52	P	SZR006	Seizure Disorder	56	0.133

53		VSL002	Visual Epilepsy	59	0.130

54		OST159	Osteogenic Sarcoma	66	0.129

55		CYT002	Cytokine Deficiency	42	0.129

56	c	CHR684	Chronic Kidney Disease	70	0.128

57	P	LVR013	Liver Disease	68	0.127

58		DNT012	Dental Caries	53	0.127

59		LVR012	Liver Cirrhosis	62	0.126

60		CRD132	Cardiac Conduction Defect	58	0.125

61	P	PHC003	Pheochromocytoma	71	0.125

62		ADR040	Adrenal Gland Pheochromocytoma	46	0.125

63	P	PRS040	Prostate Cancer	97	0.124

64	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.124

65		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.124

66	P	BPL003	Bipolar Disorder	56	0.124

67	c	MGR028	Migraine with or Without Aura 1	67	0.123

68		CRD223	Cardiac Arrhythmia	60	0.122

69	c	BRN108	Branchiootic Syndrome 1	62	0.122

70	c	MJR024	Major Affective Disorder 9	41	0.120

71	c	MJR022	Major Affective Disorder 8	38	0.120

72		ALL010	Allergic Contact Dermatitis	56	0.119

73		SCR003	Secretory Diarrhea	37	0.119

74		SPN186	Spinal Cord Injury	60	0.118

75	P	PLY014	Polycystic Kidney Disease	62	0.118

76		URL001	Urolithiasis	45	0.117

77		CNS004	Constipation	58	0.116

78		PLM010	Pulmonary Edema	54	0.116

79	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.116

80	P	CTR002	Cataract	60	0.116

81		BRN071	Brain Injury	49	0.115

82	P	ENC018	Encephalopathy	61	0.115

83	P	EPL164	Epilepsy	71	0.115

84		GNG013	Gingivitis	59	0.115

85	P	CLR023	Colorectal Cancer	99	0.114

86	P	LTR001	Lateral Sclerosis	54	0.114

87		ATS010	Autosomal Recessive Disease	48	0.114

88		BRN004	Brain Edema	56	0.113

89	P	VSC007	Vascular Disease	63	0.113

90	P	HYP069	Hyperparathyroidism	63	0.113

91		OST012	Osteoarthritis	78	0.113

92		TTN003	Tetanus	65	0.113

93	P	PRD021	Periodic Paralysis	45	0.111

94		IRN002	Iron Metabolism Disease	57	0.111

95	P	MYC007	Myocardial Infarction	70	0.111

96	P	MRC003	Mercury Poisoning	48	0.110

97		OCL069	Ocular Motor Apraxia	51	0.110

98	P	HRP006	Herpes Simplex	65	0.109

99		DFC004	Deficiency Anemia	70	0.108

100	P	MSC005	Muscular Dystrophy	66	0.108

101		TRM010	Traumatic Brain Injury	51	0.107

102		BRN024	Bronchitis	68	0.107

103	P	NSP012	Nasopharyngeal Carcinoma	66	0.107

104		TXC005	Toxic Shock Syndrome	62	0.106

105		PST092	Posttransplant Acute Limbic Encephalitis	29	0.106

106		HYP056	Hypoglycemia	66	0.105

107		AST005	Asthma	76	0.105

108	P	PLM037	Pulmonary Hypertension	67	0.105

109	P	BRT004	Bartter Disease	52	0.104

110	P	MLN008	Melanoma	69	0.104

111		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.104

112		HYP066	Hyperglycemia	61	0.103

113		ADN018	Adenoma	59	0.103

114		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.103

115	P	ATR011	Atrial Fibrillation	66	0.101

116		DPH001	Diphtheria	60	0.101

117		NPH003	Nephrocalcinosis	51	0.100

118	P	TRN020	Turner Syndrome	67	0.099

119	P	INF037	Inflammatory Bowel Disease	54	0.099

120		END086	End Stage Renal Disease	51	0.099

121		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.098

122	P	GST044	Gastritis	56	0.098

123	P	BND020	Bone Disease	59	0.098

124	P	NRP001	Neuropathy	56	0.098

125	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.098

126		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.097

127	P	GLM007	Glomerulonephritis	57	0.097

128	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.096

129		CLT003	Colitis	62	0.096

130		CRV035	Cervical Cancer	76	0.096

131		CRB004	Cerebral Artery Occlusion	45	0.096

132	c	PLM127	Pulmonary Hypertension, Primary, 3	34	0.096

133	P	MYS003	Myasthenia Gravis	68	0.096

134	P	RNL007	Renal Tubular Acidosis	51	0.095

135	c	PNS012	Paine Syndrome	61	0.094

136		DWN001	Down Syndrome	70	0.093

137		PPT005	Peptic Ulcer Disease	59	0.093

138	c	SVR001	Severe Acute Respiratory Syndrome	62	0.093

139	P	PRD008	Periodontitis	64	0.092

140		RCK004	Rickets	68	0.092

141		MCS002	Mucositis	56	0.092

142	P	HYP086	Hypothyroidism	69	0.092

143		BRN028	Brain Cancer	74	0.091

144	P	RHN004	Rhinitis	57	0.091

145		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.091

146	P	RSP003	Respiratory Failure	74	0.090

147	P	DRM053	Dermatitis, Atopic	66	0.090

148		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.090

149	P	LNG064	Lung Cancer Susceptibility 3	78	0.089

150	P	GST053	Gastric Cancer	83	0.089

151		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.089

152	c	SML038	Small Cell Cancer of the Lung	65	0.089

153	P	CHN012	Chondrosarcoma	56	0.089

154		ATH013	Atherosclerosis Susceptibility	65	0.088

155		VCC001	Vaccinia	49	0.088

156		BCT022	Bacterial Infectious Disease	56	0.088

157	P	INF038	Influenza	68	0.088

158	c	PRC016	Pre-Eclampsia	63	0.088

159	c	ACT068	Acute Cystitis	63	0.088

160	P	HNT016	Huntington Disease	72	0.088

161		DPR016	Depression	63	0.088

162	P	OVR042	Ovarian Cancer	88	0.088

163		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.088

164	c	ACT075	Acute Myocardial Infarction	57	0.088

165	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.087

166		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.087

167		PLG002	Plague	63	0.086

168	P	BRS047	Breast Cancer	97	0.086

169		PLY150	Polykaryocytosis Inducer	31	0.086

170		GTL001	Gitelman Syndrome	65	0.085

171	P	AST007	Astrocytoma	51	0.085

172		SKN016	Skin Disease	63	0.085

173		STR067	Stroke, Ischemic	81	0.084

174	c	HPT073	Hepatitis C Virus	72	0.084

175		MDD018	Middle East Respiratory Syndrome	43	0.084

176		SQM006	Squamous Cell Carcinoma	60	0.084

177		ARG004	Argyria	27	0.084

178	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.083

179		MDD011	Mood Disorder	62	0.083

180		HMS001	Hemosiderosis	54	0.083

181		ALC007	Alcohol Dependence	66	0.083

182		LSH001	Leishmaniasis	63	0.082

183	P	PSD003	Pseudohypoaldosteronism	44	0.082

184	P	KLZ004	Kala-Azar 1	41	0.082

185	P	MNN013	Meningitis	66	0.082

186	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.082

187	P	INF032	Infertility	57	0.082

188		ALL003	Allergic Rhinitis	67	0.081

189		SRC014	Sarcoma	65	0.081

190		THR024	Thrombosis	57	0.080

191	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.080

192		SVR004	Severe Combined Immunodeficiency	73	0.080

193		ANT024	Anthrax Disease	58	0.080

194	P	TRM003	Tremor	54	0.080

195		LPP008	Lipoprotein Quantitative Trait Locus	62	0.080

196	P	VSC011	Vasculitis	62	0.080

197	P	FBR017	Fibrosarcoma	56	0.079

198		SPN035	Spindle Cell Sarcoma	53	0.079

199	P	OST001	Osteopetrosis	70	0.079

200		HPT004	Hepatic Coma	45	0.079

201	P	MYP004	Myopathy	70	0.079

202	P	INT070	Intestinal Obstruction	58	0.079

203		GST045	Gastroenteritis	59	0.079

204	P	EPS003	Episodic Ataxia	59	0.078

205		PHN003	Phenylketonuria	75	0.078

206		GTR002	Goiter	53	0.078

207		ALL014	Allergic Encephalomyelitis	38	0.078

208	P	MLN007	Male Infertility	55	0.078

209	P	PRK057	Parkinson Disease, Late-Onset	78	0.078

210	P	DBT009	Diabetes Mellitus	64	0.078

211	c	ACT027	Acute Pancreatitis	60	0.078

212	P	DNT020	Dent Disease 1	62	0.077

213	c	ATR087	Atrial Standstill 1	75	0.077

214		SYN036	Syncope	45	0.077

215		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.077

216		IRR002	Irritable Bowel Syndrome	65	0.077

217	P	DBT005	Diabetes Insipidus	55	0.077

218	P	CRN300	Coronary Heart Disease 1	63	0.077

219		OCL006	Ocular Hypertension	53	0.076

220	P	RTN016	Retinal Degeneration	53	0.076

221	c	LKM061	Leukemia, Acute Myeloid	84	0.076

222		AGN016	Aging	56	0.076

223	P	OST002	Osteoporosis	74	0.076

224	P	MYT002	Myotonic Dystrophy	49	0.076

225		FTT001	Fatty Liver Disease	61	0.076

226		KRT019	Keratitis, Hereditary	65	0.076

227	P	PLM036	Pulmonary Fibrosis	65	0.075

228	P	BRN022	Bronchiectasis	59	0.074

229	P	OVR082	Overgrowth Syndrome	50	0.074

230	P	THL005	Thalassemia	60	0.074

231		THY029	Thyroid Carcinoma	59	0.074

232	P	DDN001	Duodenal Ulcer	52	0.074

233		LYS002	Lysosomal Storage Disease	52	0.074

234	P	SYS005	Systemic Scleroderma	68	0.074

235	P	BCL017	B-Cell Lymphoma	58	0.074

236	P	RCT021	Rectum Cancer	52	0.074

237	P	OPN001	Open-Angle Glaucoma	49	0.074

238	P	HYP076	Hyperthyroidism	55	0.073

239	P	ECL001	Eclampsia	50	0.073

240		EYD002	Eye Disease	58	0.073

241		MSC157	Muscular Dystrophy, Duchenne Type	72	0.073

242	c	MCR120	Microvascular Complications of Diabetes 7	47	0.072

243		MNT002	Mental Depression	58	0.072

244	P	BRS044	Breast Adenocarcinoma	59	0.072

245		HYP014	Hyperuricemia	52	0.072

246	P	TMP001	Temporal Lobe Epilepsy	50	0.072

247		URM002	Uremia	49	0.072

248		PLM001	Pulmonary Tuberculosis	69	0.072

249		ATX019	Ataxia with Vitamin E Deficiency	42	0.072

250	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.072

251	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.072

252	c	HPT001	Hepatitis C	62	0.071

253		ESP021	Esophageal Cancer	90	0.071

254		ADL002	Adult Syndrome	70	0.071

255	c	MCR113	Microvascular Complications of Diabetes 3	52	0.071

256	c	MCR130	Microvascular Complications of Diabetes 6	41	0.071

257	c	MCR133	Microvascular Complications of Diabetes 4	41	0.071

258		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.071

259		HVY002	Heavy Metal Poisoning	22	0.071

260	P	RRH023	Rare Hereditary Hemochromatosis	41	0.071

261		ALL006	Allergic Asthma	56	0.070

262	P	PRP019	Peripheral Nervous System Disease	58	0.070

263		GST050	Gastrointestinal System Disease	56	0.070

264	P	PRP029	Porphyria	62	0.070

265		HMN044	Human Immunodeficiency Virus Type 1	71	0.070

266	P	MLG056	Malignant Hyperthermia	67	0.070

267		ANX010	Anxiety	73	0.069

268	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.069

269		HPT019	Hepatic Encephalopathy	60	0.069

270		ERY051	Erythroleukemia, Familial	56	0.069

271		DYS073	Dysphagia	50	0.069

272		PRT036	Peritonitis	64	0.068

273	c	SHR030	Short Qt Syndrome	46	0.068

274	c	MNN043	Meningioma, Familial	74	0.068

275	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	0.068

276		MNN042	Meningioma, Radiation-Induced	62	0.068

277		SPN021	Spinal Meningioma	50	0.068

278		SCR001	Secretory Meningioma	41	0.068

279		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.068

280		CTN007	Cutaneous Leishmaniasis	62	0.068

281	P	MYC008	Myocarditis	59	0.068

282	P	INT068	Intestinal Disease	53	0.068

283		TRY001	Trypanosomiasis	50	0.068

284	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.068

285		PLM031	Poliomyelitis	64	0.068

286	c	HPT016	Hepatitis B	59	0.068

287	P	PNC044	Pancreatitis	61	0.068

288		STM007	Stomatitis	50	0.068

289		DSS012	Disseminated Infection with Mycobacterium Avium Complex	20	0.068

290		GST023	Gastric Ulcer	53	0.068

291		TLN003	Telangiectasis	52	0.068

292	P	AMY004	Amyloidosis	70	0.068

293		SFT003	Soft Tissue Sarcoma	56	0.068

294	P	PLY019	Polyneuropathy	56	0.067

295		IMP005	Impotence	52	0.067

296		RYN005	Raynaud Phenomenon	47	0.067

297		CRB039	Cerebrovascular Disease	67	0.067

298	P	HDC001	Headache	57	0.067

299	c	PRM038	Primary Agammaglobulinemia	44	0.067

300	P	SKN015	Skin Carcinoma	66	0.066

301		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.066

302	c	MLG068	Malignant Glioma	46	0.066

303		ATR057	Atrioventricular Block	55	0.066

304	c	SCN007	Secondary Hyperparathyroidism	51	0.066

305	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.066

306		ILS001	Ileus	51	0.066

307		ULC004	Ulcerative Colitis	73	0.066

308	P	MYL006	Myeloid Leukemia	60	0.066

309		ART140	Arteries, Anomalies of	52	0.066

310	P	MLT020	Multiple Sclerosis	72	0.066

311		BCT004	Bacteriuria	49	0.066

312	c	PRM005	Primary Hyperparathyroidism	58	0.065

313		BCT002	Bacterial Vaginosis	53	0.065

314	P	CYS018	Cystitis	59	0.065

315		PNC129	Pancreatic Adenocarcinoma	68	0.064

316		DBT010	Diabetic Neuropathy	54	0.064

317		STT001	Status Epilepticus	60	0.064

318	P	MCR115	Microvascular Complications of Diabetes 5	66	0.064

319	P	HML002	Hemolytic Anemia	63	0.064

320	P	ALP008	Alopecia	54	0.064

321	P	DST107	Distal Renal Tubular Acidosis	42	0.064

322	c	NRF023	Neurofibromatosis, Type Ii	80	0.063

323	P	SNS001	Sensorineural Hearing Loss	60	0.063

324	P	LCT001	Lactic Acidosis	51	0.063

325	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.063

326	P	PNM007	Pneumonia	68	0.062

327	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.062

328	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.062

329	P	NPH012	Nephrotic Syndrome	60	0.062

330		SCK003	Sickle Cell Anemia	74	0.061

331	P	RHB003	Rhabdomyosarcoma	63	0.061

332	P	EPL140	Epilepsy, Idiopathic Generalized	62	0.061

333		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	56	0.061

334	P	CNR004	Cone-Rod Dystrophy 2	73	0.061

335	P	NTR004	Neutropenia	63	0.061

336	P	CRD246	Cardiovascular System Disease	57	0.061

337		HYP025	Hyperphosphatemia	48	0.061

338	c	RHB024	Rhabdomyosarcoma 2	67	0.060

339	P	THR014	Thrombocytopenia	67	0.060

340		NWC001	Newcastle Disease	45	0.060

341		SBC016	Subacute Delirium	44	0.060

342	c	DLT002	Dilated Cardiomyopathy	79	0.059

343	P	ATX030	Ataxia-Telangiectasia	82	0.059

344		NTR005	Nutritional Deficiency Disease	62	0.059

345		INS024	Insulin-Like Growth Factor I	79	0.059

346	P	ART022	Arthritis	69	0.059

347		PTT037	Pituitary Tumors	44	0.059

348	c	MCL013	Mucolipidosis Iv	66	0.059

349		GT001	Gout	64	0.059

350		HYP060	Hyperinsulinism	54	0.059

351		DYS015	Dysentery	52	0.059

352		PTH003	Pathologic Nystagmus	52	0.059

353		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.059

354	P	BNG032	Benign Mesothelioma	46	0.059

355		MTH071	Methane Production	26	0.059

356	P	LKM002	Leukemia	68	0.059

357		ANG054	Angina Pectoris	66	0.059

358		GLC003	Glucose Intolerance	54	0.059

359	P	SCK005	Sickle Cell Disease	50	0.059

360		CVD001	Covid-19	44	0.059

361	P	RRT020	Rare Tumor	41	0.059

362		MYL069	Myeloma, Multiple	85	0.058

363	P	PSR002	Psoriasis	62	0.058

364		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.058

365		PST011	Pustulosis of Palm and Sole	52	0.058

366	P	BLD134	Bladder Cancer	79	0.058

367	P	RTN018	Retinal Disease	53	0.058

368		CHD004	Chudley-Mccullough Syndrome	46	0.058

369		HND015	Hand Skill, Relative	33	0.058

370	P	CNJ013	Conjunctivitis	65	0.058

371		SPL018	Splenomegaly	48	0.058

372		ACT003	Acute Kidney Tubular Necrosis	45	0.058

373	P	SCH015	Schizophrenia	74	0.058

374		ORL011	Oral Cancer	60	0.058

375		SPS057	Spasticity	45	0.058

376		MLR004	Malaria	81	0.058

377		CHR066	Chronic Fatigue Syndrome	61	0.057

378		CHL123	Chlamydia	59	0.057

379		DMY004	Demyelinating Disease	52	0.057

380		DMP001	Dumping Syndrome	44	0.057

381		PPL022	Papilloma	54	0.057

382		ENT011	Enterocolitis	51	0.057

383		SQM002	Squamous Cell Papilloma	46	0.057

384	P	ENC004	Encephalitis	61	0.056

385	P	FBR031	Febrile Seizures	53	0.056

386		CHL065	Cholangiocarcinoma	68	0.056

387		MST005	Mastitis	53	0.056

388		INT079	Intrahepatic Cholangiocarcinoma	51	0.056

389		TBR011	Tuberculous Meningitis	48	0.056

390		IRN001	Iron Deficiency Anemia	59	0.056

391		INT066	Interstitial Lung Disease	60	0.056

392	P	CND004	Candidiasis	58	0.056

393	P	PYL005	Pyelonephritis	56	0.056

394		ORL015	Oral Squamous Cell Carcinoma	43	0.056

395		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.056

396		END040	Endogenous Depression	55	0.055

397		OST011	Osteomalacia	52	0.055

398	P	FML187	Familial Hypertension	37	0.055

399		CHR178	Chromosomal Triplication	35	0.055

400	P	DMN002	Dementia	66	0.055

401	P	HYP750	Hypertriglyceridemia, Familial	62	0.055

402	P	LKD001	Leukodystrophy	59	0.055

403		KRT006	Keratoconjunctivitis	53	0.055

404	c	SPN225	Spondyloarthropathy 1	73	0.054

405		VGN023	Vaginitis	54	0.054

406		KRT001	Keratoconjunctivitis Sicca	49	0.054

407	P	ART023	Arthropathy	62	0.054

408		CLN015	Colon Adenocarcinoma	65	0.054

409		YLL002	Yellow Fever	61	0.054

410		MNK001	Menkes Disease	64	0.054

411	c	RTN047	Retinitis Pigmentosa 18	42	0.054

412	P	KDN017	Kidney Cancer	60	0.053

413		ANR040	Aneurysm	59	0.053

414	P	EXN002	Exanthem	57	0.053

415		MTH009	Mouth Disease	56	0.053

416	P	ART021	Arteriosclerosis	54	0.053

417		HDN002	Head Injury	46	0.053

418		AMN006	Aminoaciduria	38	0.053

419		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.053

420		OST017	Osteomyelitis	64	0.053

421		PRM057	Paramyotonia Congenita of Von Eulenburg	58	0.053

422	P	PRD017	Periodic Paralyses	25	0.053

423		OTT002	Otitis Media	72	0.053

424	c	LNG047	Long Qt Syndrome 2	58	0.053

425	c	BRT024	Bartter Syndrome Type 4	20	0.053

426	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.052

427		GST092	Gastroesophageal Reflux	67	0.052

428		ANR007	Anorexia Nervosa	63	0.052

429		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.052

430		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.052

431	c	PCH010	Pachyonychia Congenita 3	44	0.052

432		ADG002	Audiogenic Seizures	25	0.052

433		INS001	Insulinoma	60	0.052

434		HMP009	Haemophilus Influenzae	43	0.052

435	P	SLP006	Sleep Apnea	69	0.051

436	P	DYS154	Dystonia	65	0.051

437		PRS047	Prostatitis	56	0.051

438		CHR073	Choreatic Disease	52	0.051

439		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	47	0.051

440	P	HYD006	Hydrocephalus	66	0.051

441		HYP017	Hypophosphatemia	50	0.051

442		CRD137	Cardiogenic Shock	47	0.051

443		OST003	Osteonecrosis	61	0.051

444		AVN001	Avian Influenza	59	0.051

445		DGN001	Degenerative Disc Disease	48	0.051

446		MSL001	Measles	62	0.051

447	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.051

448		CLF027	Cleft Palate, Isolated	64	0.051

449		MSC007	Muscle Hypertrophy	64	0.051

450		CHL068	Cholestasis	61	0.051

451		VRC005	Varicose Veins	60	0.051

452	c	FML001	Familial Atrial Fibrillation	65	0.050

453	P	URT039	Urticaria	58	0.049

454	P	BRT053	Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness	46	0.049

455		CHL079	Children's Interstitial Lung Disease	26	0.049

456	P	LYM118	Lymphoma	68	0.049

457	P	END044	Endometriosis	63	0.049

458		HYP052	Hyperkalemic Periodic Paralysis	61	0.049

459		MNR012	Meniere Disease	57	0.049

460		HMG005	Hemoglobinopathy	56	0.049

461	c	GLL024	Gallbladder Disease 1	53	0.049

462	P	HYP097	Hyperekplexia	61	0.048

463	P	SJG008	Sjogren Syndrome	61	0.048

464	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.048

465		LST001	Listeriosis	56	0.048

466		SNS003	Sensory Peripheral Neuropathy	54	0.048

467	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.048

468	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.048

469		SPN051	Spondylitis	51	0.048

470		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.048

471	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.048

472	P	RNL015	Renal Hypertension	47	0.048

473	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.048

474	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.048

475	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.048

476	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.048

477	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.048

478	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.048

479	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.048

480	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.048

481		INF009	Inflammatory Spondylopathy	31	0.048

482		IMM167	Immune Deficiency Disease	78	0.048

483		END057	Endometrial Cancer	74	0.048

484		PRP027	Peripheral Vascular Disease	71	0.048

485		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.048

486		GLM044	Glomerular Disease	37	0.048

487	P	SRC025	Sarcoidosis 1	70	0.048

488		ERL001	Early Myoclonic Encephalopathy	62	0.048

489	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.048

490	c	ACT134	Acute Liver Failure	56	0.048

491	c	PRD040	Periodontitis, Chronic	53	0.048

492		NRT001	Neurotic Disorder	53	0.048

493	P	SPP010	Suppressor of Tumorigenicity 3	51	0.048

494		CND006	Candida Glabrata	32	0.048

495		NRL016	Neural Tube Defects	82	0.048

496		CRH001	Crohn's Disease	74	0.048

497	c	DBT099	Diabetes Mellitus, Type I	65	0.048

498	P	EPL198	Epilepsy, Myoclonic Juvenile	62	0.048

499		PLM033	Pulmonary Embolism	59	0.048

500	c	GRV008	Graves Disease 1	56	0.048

501	P	INS002	in Situ Carcinoma	53	0.048

502		BLL006	Bullous Pemphigoid	62	0.047

503	c	MYT029	Myotonia Congenita, Autosomal Recessive	41	0.047

504	c	MYT027	Myotonia Congenita, Autosomal Dominant	34	0.047

505	P	ART005	Arteriovenous Malformation	65	0.047

506	P	SCL018	Scoliosis	60	0.047

507		RTR008	Root Resorption	45	0.047

508	P	MJR007	Major Affective Disorder 1	43	0.047

509	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.047

510		SCR011	Scrapie	39	0.047

511	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.046

512		AMN003	Amnestic Disorder	54	0.046

513		VLV047	Volvulus of Midgut	49	0.046

514	P	INT143	Interstitial Cystitis	61	0.045

515		NRT004	Neuritis	52	0.045

516		AZS001	Azoospermia	50	0.045

517		CLC006	Calcinosis	48	0.045

518		ANR004	Anuria	46	0.045

519	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.045

520		49X006	49, Xxxxy Syndrome	41	0.045

521	P	ATS364	Autism	70	0.045

522		LYM133	Lymphoma, Hodgkin, Classic	69	0.045

523	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.045

524	P	LPS002	Liposarcoma	65	0.045

525	P	MVM001	Movement Disease	63	0.045

526		FBR047	Fibromyalgia	58	0.045

527	P	UVT001	Uveitis	57	0.045

528	P	MYP006	Myopia	55	0.045

529		PRP030	Purpura	54	0.045

530	P	PNC025	Panic Disorder	53	0.045

531	P	MSC003	Muscular Atrophy	52	0.045

532		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.045

533		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	26	0.045

534		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.045

535	c	MLG084	Malignant Fibrous Histiocytoma	63	0.045

536	P	ESP024	Esophagitis	62	0.045

537	P	SLP005	Sleep Disorder	59	0.045

538		GRD007	Grade Iii Astrocytoma	59	0.045

539		SCH014	Schistosomiasis	57	0.045

540	P	HYP024	Hypoparathyroidism	56	0.045

541	P	HMR005	Hemorrhoid	46	0.045

542		VGN019	Vaginal Discharge	46	0.045

543	P	HYP265	Hypotonia	43	0.045

544		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.045

545	P	RTN008	Retinitis Pigmentosa	79	0.044

546		MST021	Meester-Loeys Syndrome	35	0.044

547		STN013	Stenotrophomonas Maltophilia Infection	25	0.044

548	c	INH020	Inherited Metabolic Disorder	47	0.044

549	c	MJR003	Major Affective Disorder 6	33	0.044

550	c	MJR006	Major Affective Disorder 5	33	0.044

551	c	BTT014	Beta-Thalassemia	74	0.044

552		LPD008	Lipid Metabolism Disorder	62	0.044

553		CHL067	Cholecystitis	57	0.044

554		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.044

555		URN010	Urinary Tract Obstruction	55	0.044

556		ATN005	Autonomic Dysfunction	46	0.044

557		CRN019	Coronary Artery Vasospasm	46	0.044

558		CRT015	Carotid Artery Occlusion	45	0.044

559	c	PSD092	Pseudohypoaldosteronism, Type Iie	39	0.044

560		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.044

561		ART016	Aortic Aneurysm	69	0.043

562	c	DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.043

563	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.043

564		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.043

565		GLS018	Glass Syndrome	57	0.043

566		KRT008	Keratopathy	47	0.043

567	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.043

568		SYS071	Systemic Autoimmune Disease	37	0.043

569		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.043

570	P	CNG001	Congenital Myasthenic Syndrome	66	0.042

571		ACQ007	Acquired Immunodeficiency Syndrome	60	0.042

572		HMC014	Homocysteinemia	53	0.042

573	P	MCL001	Mucolipidosis	48	0.042

574		RTN023	Retinitis	46	0.042

575		NRR001	Neuroretinitis	42	0.042

576	P	RHM011	Rheumatoid Arthritis	80	0.042

577		ACR007	Acromegaly	71	0.042

578	P	CLC063	Celiac Disease 1	66	0.042

579		CHG001	Chagas Disease	66	0.042

580		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.042

581		RTN017	Retinal Detachment	61	0.042

582		BLR008	Bilirubin Metabolic Disorder	57	0.042

583	c	HNT004	Huntington Disease-Like 2	50	0.042

584		RTN003	Retinal Ischemia	50	0.042

585		THY128	Thyroid Tumor	47	0.042

586	P	FBR003	Fibrous Histiocytoma	44	0.042

587		GST040	Gastric Adenocarcinoma	70	0.041

588	P	RBL001	Rubella	59	0.041

589	P	CHL066	Cholangitis	51	0.041

590	c	HNT011	Huntington Disease-Like 3	38	0.041

591		URT049	Urate Oxidase, Pseudogene	25	0.041

592		PHR003	Pharyngitis	57	0.041

593		PRS045	Prostatic Hypertrophy	53	0.041

594		PRP016	Paraplegia	52	0.041

595	c	VRL010	Viral Hepatitis	52	0.041

596		VGN020	Vaginal Disease	49	0.041

597	P	MYG005	Myoglobinuria	44	0.041

598	P	VTL001	Vitelliform Macular Dystrophy	42	0.041

599		BST007	Best Vitelliform Macular Dystrophy	34	0.041

600		CLC058	Clcn2-Related Leukoencephalopathy	17	0.041

601		VRL011	Viral Infectious Disease	61	0.041

602		HMR039	Hemorrhage, Intracerebral	57	0.041

603		ONC002	Onchocerciasis	52	0.041

604		KRT009	Keratosis	51	0.041

605		SCT005	Scott Syndrome	49	0.041

606		LCH001	Leech Infestation	35	0.041

607		CNT105	Central Core Disease of Muscle	60	0.039

608		SPP011	Suppression of Tumorigenicity 12	59	0.039

609	P	BNC003	Bone Cancer	58	0.039

610	P	SLV026	Salivary Gland Carcinoma	57	0.039

611		SLP001	Sleeping Sickness	54	0.039

612		CLR109	Colorectal Adenocarcinoma	51	0.039

613	P	MTH008	Methylmalonic Acidemia	50	0.039

614		DDN004	Duodenogastric Reflux	33	0.039

615	c	HPT003	Hepatitis a	62	0.039

616	P	LPS004	Lupus Erythematosus	61	0.039

617		PRT058	Pure Autonomic Failure	59	0.039

618	P	SYP003	Syphilis	58	0.039

619		HYP781	Hypoascorbemia	51	0.039

620		HYP081	Hypolipoproteinemia	51	0.039

621		BLD044	Bladder Disease	48	0.039

622		PCD001	Pica Disease	41	0.039

623		EXN003	Exencephaly	31	0.039

624	c	PLM128	Pulmonary Hypertension, Primary, 2	29	0.039

625	c	PNC108	Pancreatitis, Hereditary	70	0.038

626	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.038

627	c	ATS007	Autism Spectrum Disorder	67	0.038

628		BRR014	Barrett Esophagus	65	0.038

629		NRM005	Neuromuscular Disease	64	0.038

630	P	PRM002	Primary Hyperoxaluria	62	0.038

631		RHM001	Rheumatic Fever	60	0.038

632	P	HRD011	Hereditary Spherocytosis	60	0.038

633		RBS001	Rabies	58	0.038

634		FDB001	Foodborne Botulism	55	0.038

635		HRY003	Hairy Cell Leukemia	55	0.038

636	P	MNC007	Monocytic Leukemia	53	0.038

637	P	SML001	Small Cell Carcinoma	52	0.038

638	c	SVR005	Severe Pre-Eclampsia	50	0.038

639	P	OBS001	Obstructive Jaundice	50	0.038

640	P	NGH001	Night Blindness	48	0.038

641		IDP073	Idiopathic Hypercalciuria	43	0.038

642		MTL005	Metal Allergy	41	0.038

643		PRS063	Paresthesia	41	0.038

644	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	35	0.038

645	c	MJR008	Major Affective Disorder 2	35	0.038

646	c	MJR023	Major Affective Disorder 7	33	0.038

647		HRD218	Hereditary Stomatocytosis	32	0.038

648	c	PSD093	Pseudohypoaldosteronism, Type Iid	31	0.038

649	c	MJR004	Major Affective Disorder 4	28	0.038

650		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	26	0.038

651	P	ANG001	Angelman Syndrome	69	0.038

652	P	NRV007	Nervous System Disease	66	0.038

653	P	CHR071	Charcot-Marie-Tooth Disease	65	0.038

654	P	SBS003	Substance Abuse	55	0.038

655	P	SLM003	Salmonellosis	55	0.038

656		NNL006	Non-Alcoholic Steatohepatitis	54	0.038

657	P	LCH002	Lichen Planus	53	0.038

658	P	LMB006	Limb-Girdle Muscular Dystrophy	53	0.038

659		LNG031	Lung Benign Neoplasm	51	0.038

660		CHR074	Choriocarcinoma	47	0.038

661		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.038

662		HMN016	Hemangioendothelioma	34	0.038

663	P	FRG001	Fragile X Syndrome	70	0.036

664		EWN003	Ewing Sarcoma	69	0.036

665	P	THY023	Thymoma	65	0.036

666		HRT012	Heart Valve Disease	53	0.036

667	c	HPT007	Hepatitis E	53	0.036

668		PRP080	Peripheral Artery Disease	53	0.036

669		STT041	Stuttering	52	0.036

670		THY030	Thyroid Gland Disease	52	0.036

671	c	THY107	Thymoma, Familial	52	0.036

672	P	ACT105	Acute Mountain Sickness	52	0.036

673	P	HMP007	Hemophilia	51	0.036

674		CHL004	Cholelithiasis	49	0.036

675	c	BCT013	Bacterial Pneumonia	48	0.036

676	c	FML036	Familial Periodic Paralysis	44	0.036

677		KLD004	Keloid Disorder	40	0.036

678		HRN029	Hearing Loss, Noise-Induced	37	0.036

679		ENM002	Enamel Erosion	26	0.036

680	c	SYS001	Systemic Lupus Erythematosus	86	0.036

681		CNN003	Conn's Syndrome	79	0.036

682	c	EXD008	Exudative Vitreoretinopathy 1	71	0.036

683	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.036

684	P	OPT006	Optic Nerve Disease	60	0.036

685		IGR001	Ige Responsiveness, Atopic	59	0.036

686		DSS009	Disseminated Intravascular Coagulation	57	0.036

687	c	FML035	Familial Hyperlipidemia	55	0.036

688	P	PLM034	Pulmonary Emphysema	55	0.036

689		PLS009	Plasma Cell Neoplasm	51	0.036

690		ALB002	Albinism	46	0.036

691		URT010	Ureteral Obstruction	45	0.036

692		CHP002	Chops Syndrome	44	0.036

693	P	RTN024	Retinoblastoma	73	0.034

694	c	BSL007	Basal Cell Carcinoma	68	0.034

695	P	PRM006	Primary Biliary Cirrhosis	62	0.034

696		DRR016	Diarrhea 2, with Microvillus Atrophy	60	0.034

697	c	DWL002	Dowling-Degos Disease 1	58	0.034

698	c	MST023	Mesothelioma, Malignant	57	0.034

699	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.034

700		MCL006	Macular Retinal Edema	55	0.034

701	P	GRV001	Graves' Disease	55	0.034

702		CHR100	Chronic Ulcer of Skin	55	0.034

703		FLR002	Filariasis	55	0.034

704	P	LRY044	Larynx Cancer	55	0.034

705		CLR030	Clear Cell Renal Cell Carcinoma	53	0.034

706		FRZ001	Frozen Shoulder	53	0.034

707	c	FML008	Familial Retinoblastoma	53	0.034

708		ESP023	Esophageal Disease	52	0.034

709	P	CRN025	Corneal Dystrophy	49	0.034

710		ENT004	Enthesopathy	49	0.034

711	P	VTR007	Vitreoretinopathy	46	0.034

712	P	MTH007	Methemoglobinemia	46	0.034

713		VSD002	Vas Deferens, Congenital Bilateral Aplasia of	45	0.034

714	P	SDR002	Siderosis	44	0.034

715		KLB003	Klebsiella Pneumonia	41	0.034

716	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.034

717		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.034

718		FNG016	Fungal Keratitis	40	0.034

719		PRM020	Premenstrual Tension	40	0.034

720		BLR004	Biliary Dyskinesia	38	0.034

721		ANP008	Anaplastic Oligoastrocytoma	30	0.034

722	P	GLM040	Glioma Susceptibility 1	81	0.033

723	P	FML011	Familial Adenomatous Polyposis	72	0.033

724	P	MPL001	Maple Syrup Urine Disease	69	0.033

725	P	PRP003	Porphyria Cutanea Tarda	67	0.033

726		MLT092	Multicentric Carpotarsal Osteolysis Syndrome	65	0.033

727		HLC007	Helicobacter Pylori Infection	59	0.033

728		CRV038	Cervical Squamous Cell Carcinoma	58	0.033

729		WST005	West Nile Virus	54	0.033

730	P	SHR001	Short Bowel Syndrome	53	0.033

731	c	ACT078	Acute Porphyria	51	0.033

732	P	JVN007	Juvenile Absence Epilepsy	47	0.033

733		MYT030	Myotonia, Potassium-Aggravated	45	0.033

734		STL007	Steel Syndrome	43	0.033

735		DSS010	Dissociative Disorder	39	0.033

736		ISL099	Isolated Methylmalonic Acidemia	29	0.033

737	c	PLM121	Pulmonary Hypertension, Primary, 4	28	0.033

738	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	0.033

739		SKN019	Skin Melanoma	68	0.033

740	P	HYP098	Hypereosinophilic Syndrome	67	0.033

741	c	MCR129	Microvascular Complications of Diabetes 1	66	0.033

742		BRC012	Brucellosis	64	0.033

743		FCS002	Fucosidosis	61	0.033

744	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.033

745	c	BNG091	Benign Chronic Pemphigus	58	0.033

746	P	ALC033	Alcohol Use Disorder	58	0.033

747	P	GLL018	Gallbladder Cancer	57	0.033

748		PNM008	Pneumothorax	56	0.033

749	P	CYS039	Cystic Kidney Disease	54	0.033

750		CRH005	Crohn's Colitis	53	0.033

751	P	RNL017	Renal Oncocytoma	53	0.033

752	P	THY032	Thyroiditis	52	0.033

753		CCC002	Coccidiosis	51	0.033

754	c	INF145	Infantile Liver Failure Syndrome 1	50	0.033

755	c	MGL009	Megalencephalic Leukoencephalopathy with Subcortical Cysts 1	50	0.033

756		WTH001	Withdrawal Disorder	48	0.033

757		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.033

758	P	BRB001	Beriberi	46	0.033

759		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.033

760		HYP264	Hypertonia	38	0.033

761		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.033

762		DNT008	Denture Stomatitis	35	0.033

763	c	LKM005	Leukemia, T-Cell, Chronic	34	0.033

764		JMP002	Jumping Frenchmen of Maine	22	0.033

765		NND001	Nondystrophic Myotonia	20	0.033

766	P	RTT002	Rett Syndrome	80	0.029

767	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.029

768	P	CHR012	Chronic Granulomatous Disease	67	0.029

769		PSY004	Psychotic Disorder	67	0.029

770	P	FRD001	Friedreich Ataxia	64	0.029

771	P	PTT014	Pitt-Hopkins Syndrome	63	0.029

772	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	62	0.029

773		LSC001	Lesch-Nyhan Syndrome	62	0.029

774		DCT002	Ductal Carcinoma in Situ	59	0.029

775		MCR013	Microphthalmia	57	0.029

776		CHK001	Chikungunya	57	0.029

777		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.029

778		SBC001	Subacute Sclerosing Panencephalitis	56	0.029

779		EMB004	Embryonal Carcinoma	56	0.029

780		FLR001	Filarial Elephantiasis	55	0.029

781	c	PRG126	Progressive Familial Heart Block	55	0.029

782		VSC003	Visceral Leishmaniasis	55	0.029

783	P	VNS003	Venous Insufficiency	55	0.029

784		GLS001	Gliosarcoma	54	0.029

785		CRY003	Cryptosporidiosis	54	0.029

786		BRN014	Bronchopneumonia	54	0.029

787	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.029

788		NPH018	Nephrogenic Systemic Fibrosis	50	0.029

789		HMG002	Hemoglobinuria	50	0.029

790	c	CHR431	Chronic Venous Insufficiency	49	0.029

791		CCN002	Cocaine Abuse	49	0.029

792		LRN003	Learning Disability	49	0.029

793		VTM033	Vitamin K Deficiency Bleeding	48	0.029

794		CLS016	Clostridium Difficile Colitis	48	0.029

795		CRN027	Corneal Neovascularization	47	0.029

796		AST006	Astigmatism	47	0.029

797		MNN028	Mononeuropathy of the Median Nerve, Mild	46	0.029

798	P	THY054	Thyrotoxic Periodic Paralysis	46	0.029

799		MYC005	Myocardial Stunning	46	0.029

800		TNG009	Tongue Squamous Cell Carcinoma	44	0.029

801	c	SPR086	Spermatogenic Failure 3	44	0.029

802		FBR054	Fibroma	44	0.029

803	c	EPL133	Epilepsy, Juvenile Absence 1	43	0.029

804		OVR093	Overhydrated Hereditary Stomatocytosis	43	0.029

805	c	SRC023	Sarcoidosis 2	43	0.029

806		IDP070	Idiopathic Scoliosis	42	0.029

807	c	FML294	Familial Short Qt Syndrome	41	0.029

808		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.029

809		PLR006	Pleural Cancer	38	0.029

810		PRX097	Paroxysmal Dystonia	32	0.029

811	c	THY083	Thyrotoxic Periodic Paralysis 2	31	0.029

812	c	PRG019	Paragangliomas 2	31	0.029

813	c	FML159	Familial Periodic Paralyses	16	0.029

814		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.029

815		MYL009	Myelodysplastic Syndrome	70	0.029

816	P	MYC084	Mycobacterium Tuberculosis 1	68	0.029

817		ACT119	Acute Promyelocytic Leukemia	63	0.029

818		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.029

819	P	MCH002	Machado-Joseph Disease	62	0.029

820	P	LDD007	Liddle Syndrome 1	59	0.029

821	c	ACT073	Acute Leukemia	58	0.029

822		FML063	Familial Glucocorticoid Deficiency	58	0.029

823		VSC002	Vascular Dementia	57	0.029

824		HPT046	Hepatic Veno-Occlusive Disease	56	0.029

825		ORL005	Oral Candidiasis	56	0.029

826	c	BCT007	Bacterial Meningitis	55	0.029

827	P	PTT006	Pituitary Adenoma	55	0.029

828		CRC006	Carcinoid Syndrome	55	0.029

829	P	ALP106	Alport Syndrome 1, X-Linked	55	0.029

830		INT007	Intermediate Coronary Syndrome	55	0.029

831		TND005	Tendinitis	54	0.029

832		ANL018	Analbuminemia	54	0.029

833		MTN003	Motion Sickness	53	0.029

834		RYS001	Reye Syndrome	51	0.029

835		STR008	Strongyloidiasis	51	0.029

836		INT071	Intestinal Perforation	51	0.029

837		HPT014	Hepatorenal Syndrome	50	0.029

838	P	CRV039	Cervicitis	49	0.029

839		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	49	0.029

840		BRS064	Bursitis	48	0.029

841	c	VRL012	Viral Meningitis	48	0.029

842		ANH002	Anhidrosis	47	0.029

843		CRN017	Coronary Thrombosis	47	0.029

844		TTR011	Tetraploidy	47	0.029

845	P	CRC039	Coarctation of Aorta	47	0.029

846	c	ACT076	Acute Myocarditis	46	0.029

847		DWR001	Dwarfism	44	0.029

848		IDP033	Idiopathic Edema	44	0.029

849		CRB090	Cerebral Hypoxia	44	0.029

850		TND004	Tendinopathy	43	0.029

851	P	EPT020	Epithelioid Hemangioendothelioma	43	0.029

852	c	AGR019	Age-Related Hearing Loss	42	0.029

853	c	MCR112	Microvascular Complications of Diabetes 2	41	0.029

854		CRN322	Coronavirus Infectious Disease	40	0.029

855		PLY100	Polyploidy	40	0.029

856	c	ACT004	Acute Diarrhea	39	0.029

857	c	OVR114	Ovarian Cancer 1	38	0.029

858	c	ELL005	Elliptocytosis 2	38	0.029

859		BLN006	Blind Loop Syndrome	37	0.029

860	c	RNL046	Renal Tubular Acidosis, Distal, Autosomal Dominant	37	0.029

861	c	ELL006	Elliptocytosis 3	36	0.029

862		VRS002	Virus-Associated Trichodysplasia Spinulosa	32	0.029

863	c	HYP600	Hyperaldosteronism, Familial, Type Ii	32	0.029

864		NRM009	Normokalemic Periodic Paralysis	28	0.029

865		ETH012	Ethylene Glycol Poisoning	26	0.029

866		CYN003	Cyanide Poisoning	24	0.029

867	c	RRH015	Rare Hemorrhagic Disorder	23	0.029

868		OBN001	Ouabain Resistance	18	0.029

869		ADR007	Adrenoleukodystrophy	75	0.024

870		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.024

871		MLT157	Multiple System Atrophy 1	70	0.024

872	P	ASP006	Aspergillosis	69	0.024

873		ACR008	Acrocallosal Syndrome	69	0.024

874	P	ALP004	Alport Syndrome	68	0.024

875		MLD001	Melioidosis	68	0.024

876		GRG001	Greig Cephalopolysyndactyly Syndrome	66	0.024

877	P	VNW001	Von Willebrand's Disease	65	0.024

878	P	MTR014	Motor Neuron Disease	65	0.024

879		CHY002	Chylomicron Retention Disease	65	0.024

880		MRK001	Merkel Cell Carcinoma	65	0.024

881		OVR029	Ovarian Hyperstimulation Syndrome	64	0.024

882		CLR108	Colorectal Adenoma	64	0.024

883	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	64	0.024

884		LYM017	Lyme Disease	64	0.024

885		TRN015	Transient Cerebral Ischemia	63	0.024

886	c	OPT053	Optic Atrophy 1	63	0.024

887	P	ECT006	Ectodermal Dysplasia	62	0.024

888	P	ORT004	Orthostatic Intolerance	62	0.024

889		HSH003	Hashimoto Thyroiditis	62	0.024

890		BRS099	Breast Ductal Carcinoma	62	0.024

891		ALC006	Alcoholic Hepatitis	61	0.024

892		APP008	Appendicitis	61	0.024

893	c	LPM012	Lipomatosis, Multiple	60	0.024

894	P	TXP001	Toxoplasmosis	60	0.024

895	c	MSC170	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2	60	0.024

896	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	60	0.024

897	c	HYP731	Hyperaldosteronism, Familial, Type I	60	0.024

898	P	GLY013	Glycogen Storage Disease	60	0.024

899		CRY005	Cryptococcosis	58	0.024

900	P	HYP726	Hypercalcemia, Infantile, 1	58	0.024

901	P	PLY041	Polymyositis	57	0.024

902		TCK001	Tick-Borne Encephalitis	56	0.024

903		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.024

904		SLC006	Silicosis	56	0.024

905		ORL004	Oral Submucous Fibrosis	55	0.024

906		AMB001	Amebiasis	55	0.024

907		ALP077	Alpha-Methylacetoacetic Aciduria	55	0.024

908	c	MYP132	Myopathy, Congenital	55	0.024

909	P	XRD029	Xeroderma Pigmentosum, Complementation Group a	55	0.024

910		HMP005	Hemiplegia	55	0.024

911		FCL014	Focal Epilepsy	54	0.024

912		PRT038	Protein-Energy Malnutrition	54	0.024

913		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.024

914	P	LCT002	Lactose Intolerance	53	0.024

915	P	ALL008	Allergic Bronchopulmonary Aspergillosis	53	0.024

916		IRD001	Iridocyclitis	53	0.024

917	c	NMN014	Niemann-Pick Disease, Type C2	51	0.024

918		ANK001	Ankylosis	51	0.024

919		CYS036	Cystinosis, Nephropathic	51	0.024

920		ACH005	Achalasia	51	0.024

921		ASP003	Aseptic Meningitis	51	0.024

922		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	0.024

923		PLR007	Pleural Empyema	50	0.024

924	P	AGG001	Aggressive Periodontitis	50	0.024

925	P	KRT007	Keratoconus	50	0.024

926	c	LRG001	Large Cell Carcinoma	50	0.024

927		HRT011	Heart Septal Defect	50	0.024

928		OPT003	Opiate Dependence	50	0.024

929		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	49	0.024

930		URT001	Urethritis	49	0.024

931		BLD053	Blood Platelet Disease	49	0.024

932		MNN009	Meningoencephalitis	49	0.024

933	P	RNV001	Renovascular Hypertension	48	0.024

934	P	TRT019	Torticollis	48	0.024

935		VTM002	Vitamin B12 Deficiency	48	0.024

936		SXL003	Sexual Disorder	47	0.024

937		HRN026	Hernia, Hiatus	47	0.024

938		MCR018	Microcytic Anemia	47	0.024

939		CRC014	Carcinoid Tumors, Intestinal	47	0.024

940		PPL002	Papillary Carcinoma	47	0.024

941		NDL007	Nodular Goiter	47	0.024

942		KRT002	Keratomalacia	47	0.024

943	P	ENC008	Encephalocele	47	0.024

944		BST008	Bestrophinopathy, Autosomal Recessive	46	0.024

945		URN003	Urinary Schistosomiasis	46	0.024

946		MXD026	Mixed Glioma	45	0.024

947	P	DCR003	Dacryoadenitis	45	0.024

948		ISC015	Ischemic Colitis	44	0.024

949		MCR011	Microinvasive Gastric Cancer	43	0.024

950	P	STR092	Striatal Degeneration, Autosomal Dominant 2	42	0.024

951		PHY002	Physical Disorder	42	0.024

952		CRV043	Cervical Dystonia	42	0.024

953	P	PRT026	Parotitis	42	0.024

954	c	MLG079	Malignant Pleural Mesothelioma	42	0.024

955		LYM042	Lymphocytic Colitis	41	0.024

956		BKS003	Beukes Hip Dysplasia	41	0.024

957		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	41	0.024

958		PLM005	Pleomorphic Lipoma	40	0.024

959		SCR015	Scarlet Fever	39	0.024

960		RHM035	Rheumatic Fever-Related Antigen	39	0.024

961		DBT007	Diabetic Cataract	38	0.024

962		CRT055	Creatine Deficiency Syndromes	38	0.024

963	P	ANT061	Antenatal Bartter Syndrome	37	0.024

964	c	CHR020	Chronic Interstitial Cystitis	37	0.024

965		PLC006	Placental Choriocarcinoma	36	0.024

966	P	MXL015	Maxillary Sinusitis	36	0.024

967		ACL001	Acalculous Cholecystitis	35	0.024

968		CRY019	Cryohydrocytosis	34	0.024

969		HNS001	Hansen's Disease	34	0.024

970		RTC003	Root Caries	33	0.024

971	P	VSC018	Visceral Steatosis	33	0.024

972		TXC020	Toxic Oil Syndrome	33	0.024

973		HPT081	Hepatic Infarction	33	0.024

974		DNT010	Dentin Caries	32	0.024

975		MYC014	Mycobacterium Chelonae	31	0.024

976		GST007	Gastric Dilatation	31	0.024

977		ISL119	Isolated Optic Neuritis	30	0.024

978	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.024

979	c	MYP127	Myopia 2, Autosomal Dominant	28	0.024

980		TBL029	Tubulin, Beta	28	0.024

981	c	RNG015	Ring Chromosome 2	26	0.024

982		EPL050	Epilepsy, Partial, with Pericentral Spikes	25	0.024

983		CRC034	Carcinoma Showing Thymus-Like Differentiation	23	0.024

984		PST047	Post-Traumatic Epilepsy	22	0.024

985		FTL005	Fetal Adenoma	20	0.024

986		SPN092	Spinal Shock	19	0.024

987		HMR014	Hemorrhagic Shock and Encephalopathy Syndrome	17	0.024

988		CNN008	Cinnamon Odor, Pleasantness of	14	0.024

989	P	ISL045	Isolated Focal Cortical Dysplasia Type I	11	0.024