Search results for Chloride ion

981 hits were found for Chloride ion

#	Family	MCID	Name	MIFTS	Score
1		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.874

2		CYS001	Cystic Fibrosis	84	0.468

3		HRW001	Hair Whorl	36	0.399

4		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.320

5		HLX001	Helix Syndrome	46	0.304

6	P	DRR001	Diarrhea	55	0.285

7	P	KDN018	Kidney Disease	73	0.262

8	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.258

9		MTB004	Metabolic Acidosis	48	0.255

10		48X005	48,xyyy	37	0.238

11	c	DNT047	Dentinogenesis Imperfecta Type 2	34	0.228

12	c	HYP595	Hypertension, Essential	87	0.224

13	P	NRB010	Neuroblastoma 1	66	0.223

14		HYP005	Hypokalemia	55	0.213

15		ALL026	Allergic Hypersensitivity Disease	65	0.212

16		MYT011	Myotonia	37	0.208

17		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.197

18	P	GLM045	Glioma	64	0.194

19		GLL048	Glial Tumor	48	0.194

20		PRT037	Pertussis	66	0.191

21	c	ACT071	Acute Kidney Failure	60	0.190

22		HYP266	Hypoxia	58	0.188

23		CHL014	Cholera	58	0.182

24		ANG020	Angiosarcoma	59	0.180

25		ANX004	Anoxia	44	0.179

26		ISC004	Ischemia	62	0.179

27		DRM006	Dermatitis	63	0.172

28		GLB002	Glioblastoma	74	0.171

29		GLB015	Glioblastoma Multiforme	60	0.171

30		LNG099	Lung Disease	62	0.170

31		CNG034	Congestive Heart Failure	69	0.169

32	P	LNG028	Long Qt Syndrome	68	0.166

33	P	HPT023	Hepatocellular Carcinoma	99	0.165

34	P	HRT032	Heart Disease	78	0.156

35		CNG064	Congenital Chloride Diarrhea	33	0.156

36		CNT047	Contact Dermatitis	58	0.156

37		LWC001	Low Compliance Bladder	45	0.155

38	P	CHR345	Chronic Pain	52	0.152

39		ATM095	Autoimmune Disease	62	0.152

40	P	ALZ034	Alzheimer Disease	90	0.150

41	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.150

42		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.150

43		PPL052	Papillomatosis, Confluent and Reticulated	34	0.149

44		47X002	47,xyy	49	0.146

45	P	MYT023	Myotonia Congenita	53	0.144

46		BNR002	Bone Resorption Disease	51	0.144

47	P	CRD119	Cardiac Arrest	71	0.141

48	P	PNC035	Pancreatic Cancer	86	0.139

49	P	SZR006	Seizure Disorder	59	0.138

50	P	LNG032	Lung Cancer	99	0.137

51	P	ADN016	Adenocarcinoma	65	0.137

52		PNG002	Pain Agnosia	52	0.135

53	P	PRS040	Prostate Cancer	97	0.135

54		VSL002	Visual Epilepsy	58	0.135

55		CYT002	Cytokine Deficiency	46	0.131

56		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	67	0.131

57	P	LVR013	Liver Disease	71	0.131

58		OST159	Osteogenic Sarcoma	67	0.131

59	P	PHC003	Pheochromocytoma	71	0.131

60		ADR040	Adrenal Gland Pheochromocytoma	51	0.131

61		LVR012	Liver Cirrhosis	67	0.130

62	c	MGR028	Migraine with or Without Aura 1	70	0.130

63		PLM017	Pulmonary Alveolar Microlithiasis	54	0.130

64	P	CRD132	Cardiac Conduction Defect	61	0.129

65	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	82	0.129

66	c	CHR684	Chronic Kidney Disease	68	0.129

67		BRN071	Brain Injury	51	0.128

68	P	CTR002	Cataract	62	0.127

69		DNT012	Dental Caries	52	0.125

70	c	BRN108	Branchiootic Syndrome 1	62	0.125

71		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.123

72		OST012	Osteoarthritis	80	0.122

73	P	PLY014	Polycystic Kidney Disease	61	0.122

74	P	ENC018	Encephalopathy	64	0.122

75		SPN186	Spinal Cord Injury	63	0.121

76		ALL010	Allergic Contact Dermatitis	56	0.121

77		CNS004	Constipation	59	0.121

78	P	EPL164	Epilepsy	73	0.121

79		PLM010	Pulmonary Edema	56	0.121

80		SCR003	Secretory Diarrhea	36	0.121

81	P	BPL003	Bipolar Disorder	59	0.120

82		GNG013	Gingivitis	60	0.119

83	P	CLR023	Colorectal Cancer	100	0.118

84		TRM010	Traumatic Brain Injury	54	0.118

85	P	VSC007	Vascular Disease	65	0.118

86	P	HYP069	Hyperparathyroidism	64	0.118

87	P	PRD021	Periodic Paralysis	47	0.118

88		TTN003	Tetanus	62	0.117

89		CRD223	Cardiac Arrhythmia	61	0.116

90		BRN004	Brain Edema	57	0.116

91	c	MJR024	Major Affective Disorder 9	42	0.116

92	c	MJR022	Major Affective Disorder 8	39	0.116

93	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.115

94		IRN002	Iron Metabolism Disease	58	0.115

95		DFC004	Deficiency Anemia	77	0.115

96	P	MRC003	Mercury Poisoning	47	0.115

97	P	INF037	Inflammatory Bowel Disease	57	0.115

98		MLN008	Melanoma	68	0.113

99		ATS010	Autosomal Recessive Disease	49	0.113

100		OCL069	Ocular Motor Apraxia	53	0.113

101	P	LTR001	Lateral Sclerosis	56	0.113

102	P	PLM037	Pulmonary Hypertension	69	0.112

103	P	MSC005	Muscular Dystrophy	68	0.112

104		HYP056	Hypoglycemia	68	0.109

105	P	MYC007	Myocardial Infarction	74	0.109

106		END030	End Stage Renal Failure	60	0.109

107		HYP066	Hyperglycemia	63	0.109

108		ADN018	Adenoma	60	0.108

109		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.108

110	P	BRT004	Bartter Disease	56	0.108

111	P	HRP006	Herpes Simplex	66	0.107

112	P	INF038	Influenza	69	0.107

113	P	ATR011	Atrial Fibrillation	67	0.107

114		AST005	Asthma	80	0.105

115		BRN024	Bronchitis	70	0.105

116		TXC005	Toxic Shock Syndrome	63	0.105

117	P	NRP001	Neuropathy	57	0.105

118	c	ACT210	Acute Respiratory Distress Syndrome	59	0.105

119	c	PNS012	Paine Syndrome	61	0.104

120		NPH003	Nephrocalcinosis	52	0.103

121		DPH001	Diphtheria	61	0.102

122	P	NSP012	Nasopharyngeal Carcinoma	67	0.102

123		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.102

124		DWN001	Down Syndrome	70	0.102

125		CLT003	Colitis	63	0.102

126		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.101

127		PST092	Posttransplant Acute Limbic Encephalitis	29	0.101

128	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	62	0.100

129		BND020	Bone Disease	60	0.100

130	P	GST044	Gastritis	58	0.100

131	P	MYS003	Myasthenia Gravis	68	0.100

132	P	TRN020	Turner Syndrome	66	0.100

133	P	GLM007	Glomerulonephritis	58	0.098

134	P	RNL007	Renal Tubular Acidosis	49	0.097

135		PPT005	Peptic Ulcer Disease	60	0.097

136		CRV035	Cervical Cancer	77	0.097

137		CRB004	Cerebral Artery Occlusion	38	0.097

138	c	PLM127	Pulmonary Hypertension, Primary, 3	33	0.096

139	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.096

140	c	SML038	Small Cell Cancer of the Lung	67	0.095

141	P	RHN004	Rhinitis	59	0.095

142	P	GST053	Gastric Cancer	85	0.094

143	P	DRM053	Dermatitis, Atopic	68	0.094

144		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.093

145		DPR016	Depression	64	0.092

146	P	INF032	Infertility	60	0.092

147		VCC001	Vaccinia	50	0.092

148	P	HYP086	Hypothyroidism	70	0.092

149		BRN028	Brain Cancer	75	0.092

150	P	LNG064	Lung Cancer Susceptibility 3	79	0.091

151	P	PRD008	Periodontitis	66	0.091

152	P	OVR042	Ovarian Cancer	89	0.091

153	P	HNT016	Huntington Disease	72	0.091

154	P	BRS047	Breast Cancer	99	0.090

155		RCK004	Rickets	70	0.090

156		GTL001	Gitelman Syndrome	62	0.090

157		MCS002	Mucositis	56	0.090

158		STR067	Stroke, Ischemic	82	0.089

159	c	HPT073	Hepatitis C Virus	74	0.089

160	P	VSC011	Vasculitis	64	0.089

161	P	AST007	Astrocytoma	52	0.088

162		ATH013	Atherosclerosis Susceptibility	68	0.088

163		SKN016	Skin Disease	64	0.088

164		BCT022	Bacterial Infectious Disease	57	0.088

165	P	RSP003	Respiratory Failure	75	0.088

166		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.088

167		SQM006	Squamous Cell Carcinoma	60	0.088

168	c	ACT068	Acute Cystitis	63	0.088

169		PLY150	Polykaryocytosis Inducer	31	0.087

170		ARG004	Argyria	28	0.087

171	c	PRC016	Pre-Eclampsia	63	0.087

172		CRB039	Cerebrovascular Disease	71	0.087

173		PLG002	Plague	54	0.087

174	c	HYP836	Hypercholesterolemia, Familial, 1	74	0.087

175	P	CHN012	Chondrosarcoma	57	0.086

176	P	CRN018	Coronary Artery Anomaly	67	0.086

177		ALC007	Alcohol Dependence	68	0.086

178	P	MNN013	Meningitis	67	0.085

179	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	61	0.085

180	c	ACT075	Acute Myocardial Infarction	59	0.084

181		HMS001	Hemosiderosis	54	0.084

182		LSH001	Leishmaniasis	64	0.084

183	P	PSD003	Pseudohypoaldosteronism	45	0.084

184	P	KLZ004	Kala-Azar 1	43	0.084

185		CRT084	Creatinine Clearance Quantitative Trait Locus	26	0.084

186	P	OST002	Osteoporosis	79	0.083

187		ALL003	Allergic Rhinitis	69	0.083

188	c	MCL042	Macular Degeneration, Age-Related, 1	88	0.083

189		SVR004	Severe Combined Immunodeficiency	74	0.083

190		AGN016	Aging	58	0.083

191		ANT024	Anthrax Disease	56	0.083

192	P	DBT009	Diabetes Mellitus	66	0.083

193	P	CRN300	Coronary Heart Disease 1	59	0.083

194	P	FBR017	Fibrosarcoma	57	0.082

195		SYN036	Syncope	46	0.082

196		HPT004	Hepatic Coma	42	0.082

197	P	MYP004	Myopathy	63	0.082

198	P	INT070	Intestinal Obstruction	60	0.082

199		GST045	Gastroenteritis	60	0.082

200	P	TRM003	Tremor	55	0.081

201	P	EPS003	Episodic Ataxia	60	0.081

202		PHN003	Phenylketonuria	73	0.081

203	P	RTN016	Retinal Degeneration	56	0.081

204		GTR002	Goiter	54	0.081

205		ALL014	Allergic Encephalomyelitis	40	0.081

206		SRC014	Sarcoma	67	0.081

207	P	DNT020	Dent Disease 1	60	0.081

208	c	ATR087	Atrial Standstill 1	76	0.080

209		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	0.080

210		IRR002	Irritable Bowel Syndrome	65	0.080

211		IDP011	Idiopathic Interstitial Pneumonia	65	0.079

212		SPN035	Spindle Cell Sarcoma	57	0.079

213	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	51	0.079

214	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	43	0.079

215		MDD011	Mood Disorder	62	0.079

216	P	MLN007	Male Infertility	57	0.079

217	P	MYT002	Myotonic Dystrophy	52	0.079

218	c	SVR001	Severe Acute Respiratory Syndrome	56	0.078

219		ATX019	Ataxia with Vitamin E Deficiency	46	0.078

220		THR024	Thrombosis	58	0.078

221		OCL006	Ocular Hypertension	52	0.078

222	P	PLM036	Pulmonary Fibrosis	66	0.078

223		MYT026	Myotonia Atrophica	25	0.077

224	P	OST001	Osteopetrosis	70	0.077

225	P	PRK057	Parkinson Disease, Late-Onset	77	0.077

226	P	LYM031	Lymphocytic Leukemia	56	0.077

227	P	DDN001	Duodenal Ulcer	50	0.077

228	c	MCR120	Microvascular Complications of Diabetes 7	48	0.077

229		LYS002	Lysosomal Storage Disease	52	0.077

230	P	SYS005	Systemic Scleroderma	68	0.077

231	P	DBT005	Diabetes Insipidus	54	0.076

232	P	OPN001	Open-Angle Glaucoma	50	0.076

233	P	HYP076	Hyperthyroidism	55	0.076

234		PRT036	Peritonitis	66	0.076

235		MSC157	Muscular Dystrophy, Duchenne Type	70	0.076

236	c	MCR113	Microvascular Complications of Diabetes 3	55	0.075

237	c	MCR130	Microvascular Complications of Diabetes 6	42	0.075

238	c	MCR133	Microvascular Complications of Diabetes 4	42	0.075

239	P	BRS044	Breast Adenocarcinoma	59	0.075

240		PLM001	Pulmonary Tuberculosis	72	0.075

241	c	ACT027	Acute Pancreatitis	60	0.075

242	c	LKM061	Leukemia, Acute Myeloid	84	0.075

243	P	TMP001	Temporal Lobe Epilepsy	53	0.075

244		HYP014	Hyperuricemia	52	0.075

245		URM002	Uremia	50	0.075

246	P	BRN022	Bronchiectasis	60	0.074

247	c	HPT001	Hepatitis C	62	0.074

248		ESP021	Esophageal Cancer	90	0.074

249	P	RCT021	Rectum Cancer	54	0.074

250		ART140	Arteries, Anomalies of	60	0.074

251	P	ECL001	Eclampsia	53	0.074

252		ULC004	Ulcerative Colitis	75	0.073

253		THY029	Thyroid Carcinoma	62	0.073

254	P	BLD134	Bladder Cancer	79	0.073

255	P	PRP019	Peripheral Nervous System Disease	64	0.073

256	P	THL005	Thalassemia	62	0.073

257	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.073

258		FTT001	Fatty Liver Disease	63	0.073

259		ANX010	Anxiety	75	0.072

260	P	PRP029	Porphyria	58	0.072

261	P	BCL017	B-Cell Lymphoma	61	0.072

262	P	HDC001	Headache	59	0.072

263	P	MLG056	Malignant Hyperthermia	60	0.072

264		HPT019	Hepatic Encephalopathy	60	0.072

265		ERY051	Erythroleukemia, Familial	58	0.072

266		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.072

267	P	AMY004	Amyloidosis	71	0.072

268	P	RRH023	Rare Hereditary Hemochromatosis	41	0.072

269		HMN044	Human Immunodeficiency Virus Type 1	73	0.071

270	c	SHR030	Short Qt Syndrome	47	0.071

271		KRT019	Keratitis, Hereditary	69	0.071

272		EYD002	Eye Disease	59	0.071

273	P	INT068	Intestinal Disease	56	0.071

274		TRY001	Trypanosomiasis	50	0.071

275	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	62	0.071

276	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.071

277		ATR057	Atrioventricular Block	56	0.071

278		OVR082	Overgrowth Syndrome	51	0.071

279	c	HPT016	Hepatitis B	63	0.071

280		PLM031	Poliomyelitis	58	0.071

281	P	PNC044	Pancreatitis	61	0.070

282		STM007	Stomatitis	51	0.070

283		IMP005	Impotence	53	0.070

284		GST023	Gastric Ulcer	53	0.070

285		OBS168	Obsolete: Atypical Teratoid/rhabdoid Tumor	25	0.070

286	P	PLY019	Polyneuropathy	55	0.070

287		ADL002	Adult Syndrome	62	0.070

288		RYN005	Raynaud Phenomenon	50	0.070

289		HVY002	Heavy Metal Poisoning	23	0.070

290		CTN007	Cutaneous Leishmaniasis	61	0.069

291	c	MNN043	Meningioma, Familial	74	0.069

292		MNN042	Meningioma, Radiation-Induced	64	0.069

293		MNT002	Mental Depression	60	0.069

294		SPN021	Spinal Meningioma	40	0.069

295		LYM002	Lymphoplasmacyte-Rich Meningioma	40	0.069

296		SCR001	Secretory Meningioma	38	0.069

297	P	MYC008	Myocarditis	60	0.069

298		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	56	0.069

299		RNL114	Renal Cell Carcinoma, Nonpapillary	79	0.069

300	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.069

301		ILS001	Ileus	51	0.069

302	P	MCR115	Microvascular Complications of Diabetes 5	67	0.068

303	c	SCN007	Secondary Hyperparathyroidism	52	0.068

304	P	ART022	Arthritis	71	0.068

305		DSS012	Disseminated Infection with Mycobacterium Avium Complex	21	0.068

306		BCT004	Bacteriuria	48	0.068

307	c	PRM005	Primary Hyperparathyroidism	60	0.068

308		BCT002	Bacterial Vaginosis	52	0.068

309		DYS073	Dysphagia	52	0.068

310	P	CYS018	Cystitis	59	0.067

311		SFT003	Soft Tissue Sarcoma	57	0.067

312		IMM064	Immunodeficiency, Common Variable, 10	51	0.067

313		DBT010	Diabetic Neuropathy	56	0.067

314		STT001	Status Epilepticus	61	0.066

315	P	MLT020	Multiple Sclerosis	73	0.066

316	P	ALP008	Alopecia	58	0.066

317		TLN003	Telangiectasis	53	0.066

318	c	RHB024	Rhabdomyosarcoma 2	64	0.066

319	P	NRF023	Neurofibromatosis, Type Ii	77	0.066

320	P	SNS001	Sensorineural Hearing Loss	62	0.066

321	P	SKN015	Skin Carcinoma	67	0.065

322		PNC129	Pancreatic Adenocarcinoma	69	0.065

323	c	PRS136	Prostate Cancer, Hereditary, 6	34	0.064

324	c	PRS130	Prostate Cancer, Hereditary, 8	33	0.064

325	P	NPH012	Nephrotic Syndrome	65	0.064

326	P	DST107	Distal Renal Tubular Acidosis	45	0.064

327	P	RHM011	Rheumatoid Arthritis	82	0.064

328		SCK003	Sickle Cell Anemia	74	0.064

329	P	HML002	Hemolytic Anemia	64	0.064

330	c	PRM038	Primary Agammaglobulinemia	45	0.064

331	c	MLG068	Malignant Glioma	46	0.064

332	P	RHB003	Rhabdomyosarcoma	62	0.064

333	P	EPL140	Epilepsy, Idiopathic Generalized	62	0.064

334		ALL006	Allergic Asthma	56	0.064

335		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	47	0.064

336	c	PLM164	Pulmonary Hypertension, Primary, 1	79	0.063

337	P	CNR004	Cone-Rod Dystrophy 2	72	0.062

338		SBC016	Subacute Delirium	43	0.062

339	P	LCT001	Lactic Acidosis	52	0.062

340	P	MYL006	Myeloid Leukemia	61	0.061

341		PTT037	Pituitary Tumors	47	0.061

342		GT001	Gout	63	0.061

343	c	MCL013	Mucolipidosis Iv	60	0.061

344		HYP060	Hyperinsulinism	55	0.061

345		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.061

346	P	BNG032	Benign Mesothelioma	47	0.061

347		DYS015	Dysentery	45	0.061

348	P	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.061

349		MYL069	Myeloma, Multiple	85	0.061

350	P	LYM118	Lymphoma	70	0.061

351		NWC001	Newcastle Disease	45	0.060

352		HND015	Hand Skill, Relative	33	0.060

353	P	NTR004	Neutropenia	64	0.060

354		NTR005	Nutritional Deficiency Disease	61	0.060

355		MLR004	Malaria	82	0.060

356		CHL123	Chlamydia	60	0.060

357		HYP025	Hyperphosphatemia	47	0.060

358		DMP001	Dumping Syndrome	44	0.060

359		INS024	Insulin-Like Growth Factor I	79	0.059

360	P	LKM002	Leukemia	69	0.058

361		CHL065	Cholangiocarcinoma	68	0.058

362		ANG054	Angina Pectoris	66	0.058

363		MST005	Mastitis	55	0.058

364		GLC003	Glucose Intolerance	55	0.058

365		INT079	Intrahepatic Cholangiocarcinoma	54	0.058

366	P	SCK005	Sickle Cell Disease	53	0.058

367	P	PNM007	Pneumonia	71	0.058

368	P	CNJ013	Conjunctivitis	67	0.058

369		TBR011	Tuberculous Meningitis	50	0.058

370		ACT003	Acute Kidney Tubular Necrosis	42	0.058

371		SPS057	Spasticity	38	0.058

372		GST050	Gastrointestinal System Disease	57	0.058

373		CHD004	Chudley-Mccullough Syndrome	44	0.058

374		MTH071	Methane Production	26	0.058

375		ORL011	Oral Cancer	62	0.058

376	P	CND004	Candidiasis	61	0.058

377		ANR040	Aneurysm	60	0.058

378	P	PYL005	Pyelonephritis	58	0.058

379	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.058

380	c	BDY021	Body Mass Index Quantitative Trait Locus 20	50	0.058

381	c	BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.058

382	c	BDY010	Body Mass Index Quantitative Trait Locus 4	48	0.058

383	c	BDY015	Body Mass Index Quantitative Trait Locus 12	48	0.058

384	c	BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.058

385	c	BDY011	Body Mass Index Quantitative Trait Locus 10	47	0.058

386	c	BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.058

387	c	BDY006	Body Mass Index Quantitative Trait Locus 8	45	0.058

388	c	BDY012	Body Mass Index Quantitative Trait Locus 7	45	0.058

389	P	RRT020	Rare Tumor	43	0.058

390		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	58	0.058

391	P	ATX030	Ataxia-Telangiectasia	83	0.057

392		CHR066	Chronic Fatigue Syndrome	61	0.057

393		OST011	Osteomalacia	51	0.057

394		CHR178	Chromosomal Triplication	36	0.057

395	P	THR014	Thrombocytopenia	67	0.057

396		KRT006	Keratoconjunctivitis	53	0.057

397		ENT011	Enterocolitis	51	0.057

398	c	DLT002	Dilated Cardiomyopathy	81	0.057

399	P	FBR031	Febrile Seizures	54	0.057

400	c	SPN225	Spondyloarthropathy 1	74	0.057

401		VGN023	Vaginitis	54	0.057

402		KRT001	Keratoconjunctivitis Sicca	53	0.057

403		CLN015	Colon Adenocarcinoma	65	0.056

404	P	ENC004	Encephalitis	64	0.056

405	P	ART023	Arthropathy	61	0.056

406		IRN001	Iron Deficiency Anemia	59	0.056

407		YLL002	Yellow Fever	58	0.056

408		PTH003	Pathologic Nystagmus	53	0.056

409	P	RTN018	Retinal Disease	53	0.056

410	c	RTN047	Retinitis Pigmentosa 18	40	0.056

411	P	KDN017	Kidney Cancer	60	0.055

412	P	ART021	Arteriosclerosis	56	0.055

413		HDN002	Head Injury	47	0.055

414		ORL015	Oral Squamous Cell Carcinoma	44	0.055

415		AMN006	Aminoaciduria	39	0.055

416		DMY004	Demyelinating Disease	54	0.055

417	P	PRD017	Periodic Paralyses	27	0.055

418		SPL018	Splenomegaly	48	0.055

419		CHL079	Children's Interstitial Lung Disease	27	0.055

420		OTT002	Otitis Media	71	0.055

421		OST003	Osteonecrosis	62	0.055

422	c	LNG047	Long Qt Syndrome 2	57	0.055

423	P	PSR002	Psoriasis	63	0.055

424		PPL022	Papilloma	56	0.055

425		PST011	Pustulosis of Palm and Sole	51	0.055

426		SQM002	Squamous Cell Papilloma	49	0.055

427	c	BRT024	Bartter Syndrome Type 4	26	0.055

428	P	DMN002	Dementia	68	0.054

429		GST092	Gastroesophageal Reflux	68	0.054

430		ANR007	Anorexia Nervosa	64	0.054

431		INT066	Interstitial Lung Disease	61	0.054

432	c	PCH010	Pachyonychia Congenita 3	43	0.054

433		ADG002	Audiogenic Seizures	25	0.054

434		MNK001	Menkes Disease	62	0.054

435		END040	Endogenous Depression	55	0.054

436		HMP009	Haemophilus Influenzae	46	0.054

437		ACR006	Aceruloplasminemia	74	0.053

438	P	SLP006	Sleep Apnea	71	0.053

439	P	ATS364	Autism	68	0.053

440	P	DYS154	Dystonia	65	0.053

441		PRS047	Prostatitis	57	0.053

442		CRD137	Cardiogenic Shock	50	0.053

443		HYP017	Hypophosphatemia	48	0.053

444		AVN001	Avian Influenza	56	0.053

445		CLF027	Cleft Palate, Isolated	67	0.053

446	P	HYP750	Hypertriglyceridemia, Familial	62	0.053

447		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.053

448		VRC005	Varicose Veins	61	0.053

449		NRT004	Neuritis	52	0.053

450		RRS014	Rare Surgical Neurologic Disease	33	0.053

451		SQM013	Squamous Cell Carcinoma, Head and Neck	81	0.053

452		OST017	Osteomyelitis	65	0.053

453		MSL001	Measles	61	0.053

454	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.053

455		CRH001	Crohn's Disease	75	0.052

456	c	FML001	Familial Atrial Fibrillation	67	0.052

457		MTH009	Mouth Disease	56	0.052

458	P	URT039	Urticaria	61	0.051

459	c	BRT053	Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness	34	0.051

460		INS001	Insulinoma	60	0.051

461		HYP052	Hyperkalemic Periodic Paralysis	59	0.051

462		MNR012	Meniere Disease	56	0.051

463		PRM057	Paramyotonia Congenita of Von Eulenburg	45	0.051

464	c	GLL024	Gallbladder Disease 1	53	0.051

465		DGN001	Degenerative Disc Disease	49	0.051

466	P	SCH015	Schizophrenia	76	0.050

467		MSC007	Muscle Hypertrophy	65	0.050

468		LKD001	Leukodystrophy	61	0.050

469	P	HYP097	Hyperekplexia	61	0.050

470	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	61	0.050

471	P	SJG008	Sjogren Syndrome	57	0.050

472		SNS003	Sensory Peripheral Neuropathy	56	0.050

473		LST001	Listeriosis	55	0.050

474		SPN051	Spondylitis	53	0.050

475		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	49	0.050

476	P	RNL015	Renal Hypertension	47	0.050

477	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.050

478		INF009	Inflammatory Spondylopathy	29	0.050

479		PRP027	Peripheral Vascular Disease	72	0.050

480		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.050

481		CHR073	Choreatic Disease	52	0.050

482		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	45	0.050

483	P	SRC025	Sarcoidosis 1	72	0.050

484		ERL001	Early Myoclonic Encephalopathy	60	0.050

485	c	LKM060	Leukemia, Acute Lymphoblastic 3	57	0.050

486	P	BNC003	Bone Cancer	56	0.050

487	c	ACT134	Acute Liver Failure	53	0.050

488		DYS014	Dyspepsia	51	0.050

489		NRL016	Neural Tube Defects	83	0.049

490	P	HYD006	Hydrocephalus	68	0.049

491	P	EPL198	Epilepsy, Myoclonic Juvenile	62	0.049

492	P	ESP024	Esophagitis	62	0.049

493		PLM033	Pulmonary Embolism	60	0.049

494		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	58	0.049

495	P	HYP024	Hypoparathyroidism	56	0.049

496	c	CNG216	Congenital Hydrocephalus	55	0.049

497	c	GRV008	Graves Disease 1	55	0.049

498		BLL006	Bullous Pemphigoid	63	0.049

499	c	MYT029	Myotonia Congenita, Autosomal Recessive	41	0.049

500	c	MYT027	Myotonia Congenita, Autosomal Dominant	35	0.049

501	P	END044	Endometriosis	63	0.049

502		RTR008	Root Resorption	44	0.049

503		HMG005	Hemoglobinopathy	57	0.048

504		SCR011	Scrapie	37	0.048

505	P	FML187	Familial Hypertension	35	0.048

506	P	EXN002	Exanthem	58	0.048

507		NNL006	Non-Alcoholic Steatohepatitis	53	0.048

508		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	34	0.048

509		ART016	Aortic Aneurysm	71	0.047

510	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	62	0.047

511	P	INT143	Interstitial Cystitis	62	0.047

512		CHL068	Cholestasis	61	0.047

513		AZS001	Azoospermia	51	0.047

514		THR013	Thoracic Outlet Syndrome	49	0.047

515		ANR004	Anuria	47	0.047

516	c	BDY007	Body Mass Index Quantitative Trait Locus 1	43	0.047

517		49X002	49,xxxxy Syndrome	39	0.047

518		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	0.047

519		END057	Endometrial Cancer	74	0.047

520		LYM133	Lymphoma, Hodgkin, Classic	70	0.047

521	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.047

522	P	MVM001	Movement Disease	63	0.047

523	P	LPS002	Liposarcoma	62	0.047

524	P	UVT001	Uveitis	58	0.047

525		PRP030	Purpura	56	0.047

526	c	PRD040	Periodontitis, Chronic	56	0.047

527		SPP010	Suppressor of Tumorigenicity 3	54	0.047

528	P	PNC025	Panic Disorder	53	0.047

529	P	MSC003	Muscular Atrophy	52	0.047

530		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	27	0.047

531		IMM167	Immune Deficiency Disease	79	0.047

532	P	DBT085	Diabetes Mellitus, Insulin-Dependent	68	0.047

533		UND005	Undifferentiated Pleomorphic Sarcoma	66	0.047

534		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.047

535		GRD007	Grade Iii Astrocytoma	59	0.047

536	P	SLP005	Sleep Disorder	58	0.047

537		SCH014	Schistosomiasis	57	0.047

538		ENH001	Enhanced S-Cone Syndrome	56	0.047

539	P	GLM044	Glomerular Disease	42	0.047

540		SCH060	Schistosoma Mansoni Infection, Susceptibility/	40	0.047

541		VGN019	Vaginal Discharge	35	0.047

542	P	RTN008	Retinitis Pigmentosa	77	0.046

543	P	HYP061	Hypertrophic Cardiomyopathy	68	0.046

544	P	SCK002	Sick Sinus Syndrome	56	0.046

545		MST021	Meester-Loeys Syndrome	32	0.046

546		STN013	Stenotrophomonas Maltophilia Infection	26	0.046

547		NRT001	Neurotic Disorder	53	0.046

548	c	INH020	Inherited Metabolic Disorder	51	0.046

549		CND006	Candida Glabrata	33	0.046

550		LPD008	Lipid Metabolism Disorder	64	0.045

551		CHL067	Cholecystitis	60	0.045

552		URN010	Urinary Tract Obstruction	59	0.045

553		RHM027	Rheumatic Disease	56	0.045

554		AMN003	Amnestic Disorder	55	0.045

555	P	INS002	in Situ Carcinoma	55	0.045

556		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	54	0.045

557		ATN005	Autonomic Dysfunction	48	0.045

558		CRN019	Coronary Artery Vasospasm	48	0.045

559	c	PSD092	Pseudohypoaldosteronism, Type Iie	45	0.045

560		CRT015	Carotid Artery Occlusion	44	0.045

561		INT052	Intestinal Volvulus	44	0.045

562		CLC006	Calcinosis	48	0.045

563		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	0.045

564		KRT008	Keratopathy	46	0.045

565		VGN020	Vaginal Disease	45	0.045

566	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.045

567		SYS071	Systemic Autoimmune Disease	38	0.045

568	P	ART005	Arteriovenous Malformation	63	0.044

569		ACQ007	Acquired Immunodeficiency Syndrome	61	0.044

570		HMC014	Homocysteinemia	54	0.044

571	P	MCL001	Mucolipidosis	46	0.044

572		RTN023	Retinitis	46	0.044

573		NRR001	Neuroretinitis	46	0.044

574		ACR007	Acromegaly	70	0.043

575	P	CLC063	Celiac Disease 1	66	0.043

576		CHG001	Chagas Disease	66	0.043

577		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	63	0.043

578		RTN017	Retinal Detachment	62	0.043

579		FBR047	Fibromyalgia	60	0.043

580		BLR008	Bilirubin Metabolic Disorder	58	0.043

581		RTN003	Retinal Ischemia	52	0.043

582		THY128	Thyroid Tumor	49	0.043

583	c	HNT004	Huntington Disease-Like 2	48	0.043

584		HST009	Histiocytoma	47	0.043

585	P	HMR005	Hemorrhoid	47	0.043

586		MLG065	Malignant Fibroxanthoma	45	0.043

587		FBR003	Fibrous Histiocytoma	43	0.043

588	P	HYP265	Hypotonia	43	0.043

589		GST040	Gastric Adenocarcinoma	67	0.043

590	P	SCL018	Scoliosis	61	0.043

591	P	RBL001	Rubella	56	0.043

592		HRT012	Heart Valve Disease	56	0.043

593	P	CHL066	Cholangitis	53	0.043

594	c	HNT011	Huntington Disease-Like 3	37	0.043

595	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	29	0.043

596		URT049	Urate Oxidase, Pseudogene	26	0.043

597	c	VRL010	Viral Hepatitis	56	0.043

598		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	56	0.043

599		PHR003	Pharyngitis	56	0.043

600		PRS045	Prostatic Hypertrophy	55	0.043

601	P	VTL001	Vitelliform Macular Dystrophy	43	0.043

602	P	MYG005	Myoglobinuria	43	0.043

603		BST007	Best Vitelliform Macular Dystrophy	34	0.043

604		CLC058	Clcn2-Related Leukoencephalopathy	17	0.043

605	c	BTT014	Beta-Thalassemia	73	0.042

606		HMR039	Hemorrhage, Intracerebral	59	0.042

607	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	58	0.042

608		KRT009	Keratosis	52	0.042

609		ONC002	Onchocerciasis	50	0.042

610	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	49	0.042

611		SCT005	Scott Syndrome	48	0.042

612		LCH001	Leech Infestation	40	0.042

613		CNT105	Central Core Disease of Muscle	61	0.041

614	P	SLV026	Salivary Gland Carcinoma	58	0.041

615	P	MTH008	Methylmalonic Acidemia	50	0.041

616		SLP001	Sleeping Sickness	47	0.041

617	c	SYS001	Systemic Lupus Erythematosus	88	0.040

618	P	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.040

619		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	65	0.040

620	P	LPS004	Lupus Erythematosus	62	0.040

621		PRT058	Pure Autonomic Failure	60	0.040

622	c	HPT003	Hepatitis a	60	0.040

623	P	SYP003	Syphilis	59	0.040

624		HYP081	Hypolipoproteinemia	51	0.040

625		BLD044	Bladder Disease	50	0.040

626		HYP781	Hypoascorbemia	48	0.040

627		PCD001	Pica Disease	33	0.040

628		EXN003	Exencephaly	32	0.040

629	c	PNC108	Pancreatitis, Hereditary	70	0.039

630	c	ATS007	Autism Spectrum Disorder	69	0.039

631		BRR014	Barrett Esophagus	67	0.039

632	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	64	0.039

633	P	PRM002	Primary Hyperoxaluria	60	0.039

634	P	HRD011	Hereditary Spherocytosis	59	0.039

635		RBS001	Rabies	57	0.039

636		HRY003	Hairy Cell Leukemia	57	0.039

637		RHM001	Rheumatic Fever	56	0.039

638	P	SML001	Small Cell Carcinoma	55	0.039

639		MSC190	Muscular Disease	54	0.039

640		CMB003	Combined T Cell and B Cell Immunodeficiency	53	0.039

641		FDB001	Foodborne Botulism	53	0.039

642	P	MNC007	Monocytic Leukemia	52	0.039

643	c	SVR005	Severe Pre-Eclampsia	50	0.039

644	P	NGH001	Night Blindness	48	0.039

645		PRS063	Paresthesia	46	0.039

646		IDP073	Idiopathic Hypercalciuria	43	0.039

647	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	0.039

648		HRD218	Hereditary Stomatocytosis	33	0.039

649		MTL005	Metal Allergy	32	0.039

650	c	PSD093	Pseudohypoaldosteronism, Type Iid	30	0.039

651	P	NRV007	Nervous System Disease	68	0.039

652	P	ANG001	Angelman Syndrome	65	0.039

653	P	CHR071	Charcot-Marie-Tooth Disease	65	0.039

654	P	MYP006	Myopia	58	0.039

655	P	LCH002	Lichen Planus	55	0.039

656	P	LMB006	Limb-Girdle Muscular Dystrophy	55	0.039

657	P	SLM003	Salmonellosis	54	0.039

658		LNG031	Lung Benign Neoplasm	52	0.039

659		HMN016	Hemangioendothelioma	41	0.039

660		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.039

661	c	RNL046	Renal Tubular Acidosis, Distal, Autosomal Dominant	34	0.039

662		EWN003	Ewing Sarcoma	69	0.038

663	P	THY023	Thymoma	64	0.038

664	P	HMP007	Hemophilia	58	0.038

665	c	THY107	Thymoma, Familial	55	0.038

666	P	ACT105	Acute Mountain Sickness	53	0.038

667		STT041	Stuttering	53	0.038

668	c	HPT007	Hepatitis E	53	0.038

669		PRP080	Peripheral Artery Disease	51	0.038

670		CHL004	Cholelithiasis	50	0.038

671	c	BCT013	Bacterial Pneumonia	49	0.038

672	c	FML036	Familial Periodic Paralysis	42	0.038

673		KLD004	Keloid Disorder	41	0.038

674		HRN029	Hearing Loss, Noise-Induced	38	0.038

675		ENM002	Enamel Erosion	28	0.038

676		OBS532	Obsolete: Ehlers-Danlos Syndrome, Fibronectinemic Type	15	0.038

677		CNN003	Conn's Syndrome	78	0.037

678	c	EXD008	Exudative Vitreoretinopathy 1	69	0.037

679	c	MCR129	Microvascular Complications of Diabetes 1	67	0.037

680		IGR001	Ige Responsiveness, Atopic	61	0.037

681	P	OPT006	Optic Nerve Disease	59	0.037

682		DSS009	Disseminated Intravascular Coagulation	58	0.037

683	c	FML035	Familial Hyperlipidemia	56	0.037

684	P	PLM034	Pulmonary Emphysema	55	0.037

685	P	OPT009	Optic Neuritis	55	0.037

686		URT010	Ureteral Obstruction	46	0.037

687		CHP002	Chops Syndrome	41	0.037

688	c	PLM128	Pulmonary Hypertension, Primary, 2	29	0.037

689	P	RTN024	Retinoblastoma	74	0.035

690	P	FCL005	Focal Segmental Glomerulosclerosis	63	0.035

691	c	DWL002	Dowling-Degos Disease 1	59	0.035

692	c	MST023	Mesothelioma, Malignant	59	0.035

693	P	LRY044	Larynx Cancer	59	0.035

694		PRM236	Primary Biliary Cholangitis	57	0.035

695	P	GRV001	Graves' Disease	57	0.035

696		FLR002	Filariasis	56	0.035

697	P	PRM006	Primary Biliary Cirrhosis	54	0.035

698		DRR016	Diarrhea 2, with Microvillus Atrophy	54	0.035

699		CLR030	Clear Cell Renal Cell Carcinoma	54	0.035

700		FRZ001	Frozen Shoulder	53	0.035

701		MCL006	Macular Retinal Edema	52	0.035

702	P	OBS001	Obstructive Jaundice	49	0.035

703		PRM020	Premenstrual Tension	48	0.035

704		VTR007	Vitreoretinopathy	48	0.035

705		CHR074	Choriocarcinoma	47	0.035

706	P	MTH007	Methemoglobinemia	47	0.035

707	c	FML008	Familial Retinoblastoma	46	0.035

708		ENT004	Enthesopathy	46	0.035

709	P	CRN025	Corneal Dystrophy	45	0.035

710		VSD002	Vas Deferens, Congenital Bilateral Aplasia of	45	0.035

711	P	SDR002	Siderosis	42	0.035

712		FNG016	Fungal Keratitis	42	0.035

713		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	41	0.035

714	P	HRD086	Hereditary Hypophosphatemic Rickets	41	0.035

715		KLB003	Klebsiella Pneumonia	36	0.035

716		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	26	0.035

717	P	FML011	Familial Adenomatous Polyposis	73	0.034

718	P	FRG001	Fragile X Syndrome	69	0.034

719	P	MPL001	Maple Syrup Urine Disease	68	0.034

720	P	PRP003	Porphyria Cutanea Tarda	66	0.034

721		NRM005	Neuromuscular Disease	62	0.034

722		HLC007	Helicobacter Pylori Infection	61	0.034

723		SPP011	Suppression of Tumorigenicity 12	61	0.034

724		MLT092	Multicentric Carpotarsal Osteolysis Syndrome	60	0.034

725		WST005	West Nile Virus	56	0.034

726		FCT001	Factor Viii Deficiency	54	0.034

727		THY030	Thyroid Gland Disease	53	0.034

728		CLR109	Colorectal Adenocarcinoma	51	0.034

729	P	SHR001	Short Bowel Syndrome	50	0.034

730	c	ACT078	Acute Porphyria	49	0.034

731	P	JVN007	Juvenile Absence Epilepsy	47	0.034

732		MYT030	Myotonia, Potassium-Aggravated	45	0.034

733		ISL099	Isolated Methylmalonic Acidemia	30	0.034

734	c	PLM121	Pulmonary Hypertension, Primary, 4	28	0.034

735	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	0.034

736	P	HYP098	Hypereosinophilic Syndrome	67	0.034

737		BRC012	Brucellosis	62	0.034

738	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.034

739	P	FCS002	Fucosidosis	58	0.034

740	P	ALC033	Alcohol Use Disorder	58	0.034

741		PNM008	Pneumothorax	56	0.034

742	c	BNG091	Benign Chronic Pemphigus	56	0.034

743	P	SBS003	Substance Abuse	56	0.034

744	P	CYS039	Cystic Kidney Disease	55	0.034

745	P	THY032	Thyroiditis	52	0.034

746	P	RNL017	Renal Oncocytoma	52	0.034

747	c	MGL009	Megalencephalic Leukoencephalopathy with Subcortical Cysts 1	51	0.034

748	c	INF145	Infantile Liver Failure Syndrome 1	50	0.034

749		PPT001	Peptic Esophagitis	47	0.034

750		CCC002	Coccidiosis	46	0.034

751		ART031	Aortic Coarctation	45	0.034

752		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.034

753	c	MCR112	Microvascular Complications of Diabetes 2	42	0.034

754	P	BRB001	Beriberi	41	0.034

755		STT004	Steatorrhea	39	0.034

756		DNT008	Denture Stomatitis	38	0.034

757		JMP002	Jumping Frenchmen of Maine	23	0.034

758		NND001	Nondystrophic Myotonia	20	0.034

759	P	RTT002	Rett Syndrome	81	0.030

760	P	CHR012	Chronic Granulomatous Disease	69	0.030

761		PSY004	Psychotic Disorder	68	0.030

762	P	GLM040	Glioma Susceptibility 1	68	0.030

763	c	BSL007	Basal Cell Carcinoma	68	0.030

764	P	FRD012	Friedreich Ataxia 1	65	0.030

765	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	63	0.030

766		MCR013	Microphthalmia	62	0.030

767	c	PRG042	Progressive Familial Heart Block, Type Ia	62	0.030

768		LSC001	Lesch-Nyhan Syndrome	61	0.030

769		CRV038	Cervical Squamous Cell Carcinoma	58	0.030

770		EMB004	Embryonal Carcinoma	57	0.030

771		RLP002	Relapsing-Remitting Multiple Sclerosis	57	0.030

772		GLS001	Gliosarcoma	56	0.030

773	P	PTT014	Pitt-Hopkins Syndrome	55	0.030

774	P	VNS003	Venous Insufficiency	55	0.030

775		ESP023	Esophageal Disease	55	0.030

776		VSC003	Visceral Leishmaniasis	55	0.030

777		HMT018	Hematopoietic Stem Cell Transplantation	54	0.030

778		AST006	Astigmatism	53	0.030

779		NPH018	Nephrogenic Systemic Fibrosis	51	0.030

780		LRN003	Learning Disability	51	0.030

781		FLR001	Filarial Elephantiasis	51	0.030

782	P	THY054	Thyrotoxic Periodic Paralysis	51	0.030

783		CRY003	Cryptosporidiosis	50	0.030

784		HMG002	Hemoglobinuria	49	0.030

785	c	PRG126	Progressive Familial Heart Block	49	0.030

786		CRN027	Corneal Neovascularization	48	0.030

787	c	CHR431	Chronic Venous Insufficiency	48	0.030

788		CCN002	Cocaine Abuse	48	0.030

789		CLS016	Clostridium Difficile Colitis	48	0.030

790		BRN014	Bronchopneumonia	47	0.030

791		VTM033	Vitamin K Deficiency Bleeding	47	0.030

792		MYC005	Myocardial Stunning	45	0.030

793		FBR054	Fibroma	45	0.030

794	c	SRC023	Sarcoidosis 2	43	0.030

795		STL007	Steel Syndrome	42	0.030

796	c	FML294	Familial Short Qt Syndrome	41	0.030

797	c	SPR086	Spermatogenic Failure 3	41	0.030

798		MNN028	Mononeuropathy of the Median Nerve, Mild	41	0.030

799		PLR006	Pleural Cancer	40	0.030

800		OVR093	Overhydrated Hereditary Stomatocytosis	40	0.030

801	c	EPL133	Epilepsy, Juvenile Absence 1	40	0.030

802		DSS010	Dissociative Disorder	35	0.030

803		BLR004	Biliary Dyskinesia	33	0.030

804		ISL119	Isolated Optic Neuritis	31	0.030

805		PRX097	Paroxysmal Dystonia	31	0.030

806	c	THY083	Thyrotoxic Periodic Paralysis 2	30	0.030

807	c	PRG019	Paragangliomas 2	30	0.030

808	c	FML159	Familial Periodic Paralyses	17	0.030

809		LYM143	Lymphoma, Non-Hodgkin, Familial	74	0.030

810	P	MYC084	Mycobacterium Tuberculosis 1	69	0.030

811	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	0.030

812		ACT119	Acute Promyelocytic Leukemia	63	0.030

813	P	MCH002	Machado-Joseph Disease	61	0.030

814		VTR013	Vitreoretinopathy, Neovascular Inflammatory	61	0.030

815	c	ACT073	Acute Leukemia	59	0.030

816	P	LDD007	Liddle Syndrome 1	58	0.030

817	P	HYP726	Hypercalcemia, Infantile, 1	58	0.030

818		INT007	Intermediate Coronary Syndrome	58	0.030

819		VSC002	Vascular Dementia	57	0.030

820		ORL005	Oral Candidiasis	56	0.030

821	c	BCT007	Bacterial Meningitis	56	0.030

822	P	ALP106	Alport Syndrome 1, X-Linked	55	0.030

823		CRC006	Carcinoid Syndrome	55	0.030

824		CHR100	Chronic Ulcer of Skin	53	0.030

825	P	PTT006	Pituitary Adenoma	53	0.030

826		STR008	Strongyloidiasis	53	0.030

827		FML063	Familial Glucocorticoid Deficiency	51	0.030

828		ACH005	Achalasia	50	0.030

829		HPT014	Hepatorenal Syndrome	49	0.030

830		MTN003	Motion Sickness	48	0.030

831	P	TCL004	T-Cell Leukemia	48	0.030

832		TTR011	Tetraploidy	47	0.030

833		WTH001	Withdrawal Disorder	47	0.030

834	c	VRL012	Viral Meningitis	47	0.030

835		ANH002	Anhidrosis	47	0.030

836	P	EPT020	Epithelioid Hemangioendothelioma	45	0.030

837		DWR001	Dwarfism	45	0.030

838		TND005	Tendinitis	45	0.030

839		CRB090	Cerebral Hypoxia	45	0.030

840		CRN017	Coronary Thrombosis	45	0.030

841		IDP033	Idiopathic Edema	44	0.030

842		SYN046	Syndrome of Inappropriate Antidiuretic Hormone	44	0.030

843		TND004	Tendinopathy	44	0.030

844		BRS064	Bursitis	42	0.030

845	P	CRV039	Cervicitis	42	0.030

846		PLY100	Polyploidy	41	0.030

847		AGR019	Age-Related Hearing Loss	40	0.030

848		BLN006	Blind Loop Syndrome	40	0.030

849	c	OVR114	Ovarian Cancer 1	39	0.030

850		HYP264	Hypertonia	39	0.030

851	c	ACT004	Acute Diarrhea	38	0.030

852	c	ELL005	Elliptocytosis 2	35	0.030

853	c	LKM005	Leukemia, T-Cell, Chronic	35	0.030

854	c	ELL006	Elliptocytosis 3	34	0.030

855	c	HYP600	Hyperaldosteronism, Familial, Type Ii	32	0.030

856		ANP008	Anaplastic Oligoastrocytoma	31	0.030

857		RRD056	Rare Disease in Surgical Orthopedic	29	0.030

858		NRM009	Normokalemic Periodic Paralysis	28	0.030

859		CYN003	Cyanide Poisoning	24	0.030

860		ETH012	Ethylene Glycol Poisoning	22	0.030

861		OBN001	Ouabain Resistance	19	0.030

862	c	LKM063	Leukemia, Chronic Myeloid	74	0.025

863		XRD010	Xeroderma Pigmentosum, Variant Type	72	0.025

864		ADR007	Adrenoleukodystrophy	72	0.025

865		MLT157	Multiple System Atrophy 1	71	0.025

866	P	ORT004	Orthostatic Intolerance	68	0.025

867	P	ASP006	Aspergillosis	67	0.025

868		ACR008	Acrocallosal Syndrome	66	0.025

869		MLD001	Melioidosis	66	0.025

870	P	ALP004	Alport Syndrome	66	0.025

871	P	MTR014	Motor Neuron Disease	66	0.025

872		WLF001	Wolff-Parkinson-White Syndrome	65	0.025

873		CLR108	Colorectal Adenoma	64	0.025

874		LYM017	Lyme Disease	64	0.025

875	P	VNW001	Von Willebrand's Disease	64	0.025

876		HSH003	Hashimoto Thyroiditis	63	0.025

877		OVR029	Ovarian Hyperstimulation Syndrome	63	0.025

878		CHY002	Chylomicron Retention Disease	63	0.025

879		BRS099	Breast Ductal Carcinoma	63	0.025

880		MRK001	Merkel Cell Carcinoma	62	0.025

881	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	62	0.025

882	P	ANP001	Anaplastic Large Cell Lymphoma	62	0.025

883		GRG001	Greig Cephalopolysyndactyly Syndrome	61	0.025

884		APP008	Appendicitis	61	0.025

885	P	TXP001	Toxoplasmosis	61	0.025

886	c	LPM012	Lipomatosis, Multiple	60	0.025

887		ALC006	Alcoholic Hepatitis	60	0.025

888	P	GLY013	Glycogen Storage Disease	59	0.025

889		ECT006	Ectodermal Dysplasia	58	0.025

890	c	HYP731	Hyperaldosteronism, Familial, Type I	57	0.025

891		DCT002	Ductal Carcinoma in Situ	57	0.025

892	P	PLY041	Polymyositis	57	0.025

893		FCL014	Focal Epilepsy	56	0.025

894		PRT038	Protein-Energy Malnutrition	56	0.025

895		HPT046	Hepatic Veno-Occlusive Disease	56	0.025

896	c	MSC170	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2	56	0.025

897		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.025

898	c	MYP132	Myopathy, Congenital	55	0.025

899		SLC006	Silicosis	55	0.025

900		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	55	0.025

901		HMP005	Hemiplegia	55	0.025

902		ORL004	Oral Submucous Fibrosis	55	0.025

903		TCK001	Tick-Borne Encephalitis	53	0.025

904		CYS036	Cystinosis, Nephropathic	53	0.025

905		HRT011	Heart Septal Defect	52	0.025

906		ASP003	Aseptic Meningitis	51	0.025

907		CRY005	Cryptococcosis	51	0.025

908	P	ANL018	Analbuminemia	51	0.025

909		ANK001	Ankylosis	51	0.025

910		ALP077	Alpha-Methylacetoacetic Aciduria	51	0.025

911		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	51	0.025

912	P	KRT007	Keratoconus	51	0.025

913	P	AGG001	Aggressive Periodontitis	50	0.025

914	P	ALL008	Allergic Bronchopulmonary Aspergillosis	50	0.025

915		MNN009	Meningoencephalitis	50	0.025

916		SXL003	Sexual Disorder	49	0.025

917	P	RNV001	Renovascular Hypertension	49	0.025

918		CRC014	Carcinoid Tumors, Intestinal	49	0.025

919		LPD009	Lipid Storage Disease	49	0.025

920	c	ANT034	Anterior Uveitis	48	0.025

921	P	TRT019	Torticollis	48	0.025

922		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	48	0.025

923		KRT002	Keratomalacia	47	0.025

924		MCR191	Microscopic Colitis	47	0.025

925	P	ENC008	Encephalocele	47	0.025

926		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	47	0.025

927		NDL007	Nodular Goiter	46	0.025

928		HRN026	Hernia, Hiatus	46	0.025

929		BST008	Bestrophinopathy, Autosomal Recessive	46	0.025

930		URN003	Urinary Schistosomiasis	45	0.025

931	c	ACT076	Acute Myocarditis	45	0.025

932		CRV043	Cervical Dystonia	45	0.025

933	c	LRG001	Large Cell Carcinoma	45	0.025

934		TNG009	Tongue Squamous Cell Carcinoma	44	0.025

935		AMB001	Amebiasis	44	0.025

936		URT001	Urethritis	44	0.025

937		PLR007	Pleural Empyema	44	0.025

938		DRG024	Drug Allergy	43	0.025

939		MCR011	Microinvasive Gastric Cancer	43	0.025

940		ISC015	Ischemic Colitis	43	0.025

941	c	MLG079	Malignant Pleural Mesothelioma	43	0.025

942	P	PRT026	Parotitis	43	0.025

943		PHY002	Physical Disorder	42	0.025

944		DBT007	Diabetic Cataract	42	0.025

945	P	STR092	Striatal Degeneration, Autosomal Dominant 2	42	0.025

946	P	DCR003	Dacryoadenitis	42	0.025

947		SCR015	Scarlet Fever	41	0.025

948		PLM005	Pleomorphic Lipoma	41	0.025

949	P	ANT061	Antenatal Bartter Syndrome	40	0.025

950		RHM035	Rheumatic Fever-Related Antigen	40	0.025

951		IDP070	Idiopathic Scoliosis	39	0.025

952		LYM042	Lymphocytic Colitis	39	0.025

953		CRT055	Creatine Deficiency Syndromes	39	0.025

954		RTC003	Root Caries	37	0.025

955		BKS003	Beukes Hip Dysplasia	37	0.025

956	P	MXL015	Maxillary Sinusitis	37	0.025

957		MXD026	Mixed Glioma	36	0.025

958	c	CHR020	Chronic Interstitial Cystitis	36	0.025

959		HNS001	Hansen's Disease	35	0.025

960		ACL001	Acalculous Cholecystitis	35	0.025

961		CRY019	Cryohydrocytosis	34	0.025

962	P	VSC018	Visceral Steatosis	34	0.025

963		TXC020	Toxic Oil Syndrome	34	0.025

964		VRS002	Virus-Associated Trichodysplasia Spinulosa	33	0.025

965		PLC006	Placental Choriocarcinoma	33	0.025

966		MYC014	Mycobacterium Chelonae	32	0.025

967		ISC001	Ischemic Neuropathy	32	0.025

968	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.025

969		TBL029	Tubulin, Beta	29	0.025

970		DNT010	Dentin Caries	27	0.025

971	c	RNG015	Ring Chromosome 2	27	0.025

972		EPL050	Epilepsy, Partial, with Pericentral Spikes	26	0.025

973	c	MYP127	Myopia 2, Autosomal Dominant	24	0.025

974		CRC034	Carcinoma Showing Thymus-Like Differentiation	23	0.025

975		FTL005	Fetal Adenoma	21	0.025

976		NPH026	Nephrotic Syndrome, Idiopathic, Steroid-Resistant	20	0.025

977		PST047	Post-Traumatic Epilepsy	20	0.025

978		SPN092	Spinal Shock	19	0.025

979		HMR014	Hemorrhagic Shock and Encephalopathy Syndrome	18	0.025

980		CNN008	Cinnamon Odor, Pleasantness of	14	0.025

981	P	ISL045	Isolated Focal Cortical Dysplasia Type I	12	0.025