Search results for Potassium

2133 hits were found for Potassium

#	Family	MCID	Name	MIFTS	Score
1		MYT030	Myotonia, Potassium-Aggravated	46	6.211

2		HYP005	Hypokalemia	55	5.751

3		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	4.183

4		OVR093	Overhydrated Hereditary Stomatocytosis	44	3.725

5		GTL001	Gitelman Syndrome	66	3.307

6		HYP052	Hyperkalemic Periodic Paralysis	59	2.014

7	P	BRT004	Bartter Disease	55	1.965

8		KND001	Kindler Syndrome	63	1.935

9		SDM004	Sodium-Potassium-Atpase Activity of Red Cell	7	1.883

10		PTS020	Potassium Dichromate Allergic Contact Dermatitis	4	1.883

11	c	OBS577	Obsolete: Channelopathy Due to a Voltage-Gated Potassium Channel Defect	3	1.876

12	c	OBS578	Obsolete: Channelopathy Due to an Inwardly Rectifying Potassium Channel Defect	3	1.876

13	c	OBS582	Obsolete: Channelopathy Due to a Calcium-Activated Potassium Channel Defect	3	1.876

14	c	NRL029	Neurological Muscular Channelopathy Due to a Genetic Potassium Channel Defect	3	1.876

15	c	OBS758	Obsolete: Autoimmune Neurological Channelopathy Due to a Potassium Channel Defect	2	1.876

16	c	NRL037	Neurological Channelopathy of the Central Nervous System Due to a Genetic Potassium Channel Defect	2	1.876

17		NRM009	Normokalemic Periodic Paralysis	28	1.867

18		ALP077	Alpha-Methylacetoacetic Aciduria	56	1.857

19	c	PRG143	Progressive Myoclonus Epilepsy 7	12	1.857

20	c	EPL134	Epilepsy, Progressive Myoclonic 7	27	1.844

21	c	HYP595	Hypertension, Essential	84	0.311

22	P	KDN018	Kidney Disease	70	0.250

23	P	LNG028	Long Qt Syndrome	65	0.236

24	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	0.212

25	P	CRD119	Cardiac Arrest	67	0.208

26		HRW001	Hair Whorl	36	0.205

27	c	ACT075	Acute Myocardial Infarction	56	0.204

28		ALL026	Allergic Hypersensitivity Disease	64	0.200

29		CNG034	Congestive Heart Failure	70	0.198

30		PRT037	Pertussis	65	0.189

31	c	CHR684	Chronic Kidney Disease	66	0.183

32		HLX001	Helix Syndrome	47	0.180

33		MTB004	Metabolic Acidosis	50	0.177

34		ISC004	Ischemia	60	0.169

35		ANX004	Anoxia	42	0.169

36	P	HRT032	Heart Disease	75	0.167

37		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.163

38	P	PRD021	Periodic Paralysis	46	0.163

39		HYP266	Hypoxia	56	0.162

40	P	ENC004	Encephalitis	61	0.161

41	P	NRB001	Neuroblastoma	71	0.152

42	P	MYC007	Myocardial Infarction	70	0.151

43	P	DRR001	Diarrhea	57	0.150

44		CRD223	Cardiac Arrhythmia	60	0.147

45		48X005	48,xyyy	39	0.147

46		HYP056	Hypoglycemia	66	0.146

47		CRD132	Cardiac Conduction Defect	59	0.145

48	P	SZR006	Seizure Disorder	58	0.144

49		END030	End Stage Renal Failure	58	0.144

50		ATX038	Ataxia and Polyneuropathy, Adult-Onset	44	0.144

51		VSL002	Visual Epilepsy	58	0.143

52		LMB024	Limbic Encephalitis	41	0.142

53		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.137

54	P	HYP076	Hyperthyroidism	55	0.134

55		LVR012	Liver Cirrhosis	63	0.132

56	c	MGR028	Migraine with or Without Aura 1	69	0.128

57	P	GLM045	Glioma	63	0.128

58		GLL048	Glial Tumor	45	0.128

59		HYP066	Hyperglycemia	61	0.125

60	c	GRV008	Graves Disease 1	55	0.124

61	P	ATR011	Atrial Fibrillation	66	0.123

62	P	HYP086	Hypothyroidism	68	0.122

63	P	EPL164	Epilepsy	71	0.121

64	P	ENC018	Encephalopathy	61	0.121

65		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.120

66	P	EPS003	Episodic Ataxia	60	0.119

67		ATM095	Autoimmune Disease	61	0.114

68	P	CYS018	Cystitis	59	0.112

69		ANG054	Angina Pectoris	66	0.110

70		HYP060	Hyperinsulinism	54	0.110

71	P	LVR013	Liver Disease	68	0.109

72		OCL069	Ocular Motor Apraxia	51	0.109

73		PRS021	Prostatic Adenoma	51	0.108

74		PRS045	Prostatic Hypertrophy	52	0.107

75		PRS129	Prostatic Hyperplasia, Benign	49	0.107

76	P	CRN018	Coronary Artery Anomaly	63	0.106

77	c	BRN108	Branchiootic Syndrome 1	61	0.106

78		DRM006	Dermatitis	61	0.105

79	P	INT143	Interstitial Cystitis	61	0.105

80		ADN018	Adenoma	58	0.105

81		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	57	0.105

82	c	ACT071	Acute Kidney Failure	59	0.103

83	P	DBT009	Diabetes Mellitus	64	0.102

84	P	VSC007	Vascular Disease	63	0.102

85		DWN001	Down Syndrome	70	0.101

86		CRB039	Cerebrovascular Disease	69	0.101

87	c	FML191	Familial Long Qt Syndrome	53	0.101

88		GTR002	Goiter	52	0.101

89		CRB004	Cerebral Artery Occlusion	44	0.101

90		STR067	Stroke, Ischemic	80	0.100

91		URM002	Uremia	49	0.100

92		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.098

93	P	PLM037	Pulmonary Hypertension	68	0.098

94	P	RNL007	Renal Tubular Acidosis	50	0.098

95		BNR002	Bone Resorption Disease	48	0.098

96	P	GST053	Gastric Cancer	83	0.096

97	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	0.096

98	P	TMP001	Temporal Lobe Epilepsy	50	0.096

99		CYS001	Cystic Fibrosis	80	0.093

100	P	TRN020	Turner Syndrome	65	0.093

101	P	DNT007	Dentin Sensitivity	35	0.093

102		TXC005	Toxic Shock Syndrome	61	0.092

103		ATR057	Atrioventricular Block	55	0.092

104	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.090

105		ADL002	Adult Syndrome	69	0.090

106		TTN003	Tetanus	64	0.090

107		PPT005	Peptic Ulcer Disease	58	0.090

108	P	PYL005	Pyelonephritis	56	0.090

109	P	CRD246	Cardiovascular System Disease	56	0.090

110		HYP014	Hyperuricemia	51	0.090

111		SPN186	Spinal Cord Injury	60	0.087

112		DBT084	Diabetes Mellitus, Ketosis-Prone	59	0.087

113		CHL014	Cholera	55	0.087

114	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.087

115	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.087

116	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.087

117	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.087

118	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.087

119	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.087

120	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.087

121	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.087

122	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.087

123	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.087

124		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.086

125	P	MYP004	Myopathy	64	0.086

126	P	CRN300	Coronary Heart Disease 1	63	0.086

127	c	LNG047	Long Qt Syndrome 2	58	0.086

128		SPR010	Sporotrichosis	48	0.086

129	P	THY054	Thyrotoxic Periodic Paralysis	47	0.086

130	P	OST002	Osteoporosis	73	0.084

131	P	ADN016	Adenocarcinoma	64	0.084

132	c	PRC016	Pre-Eclampsia	63	0.084

133	c	PNS012	Paine Syndrome	61	0.084

134		STT001	Status Epilepticus	59	0.084

135	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.084

136	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.084

137		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.083

138	P	GRV001	Graves' Disease	55	0.083

139	P	TRM003	Tremor	53	0.083

140		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.083

141	P	MSC005	Muscular Dystrophy	66	0.081

142	c	EPS042	Episodic Ataxia, Type 1	58	0.081

143		CNS004	Constipation	57	0.081

144		BRN004	Brain Edema	55	0.081

145	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.081

146		LWC001	Low Compliance Bladder	42	0.081

147	c	SZR022	Seizures, Benign Familial Neonatal, 1	42	0.081

148	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	41	0.081

149		MYT011	Myotonia	35	0.081

150		CYN003	Cyanide Poisoning	24	0.081

151	c	FML001	Familial Atrial Fibrillation	66	0.080

152		PRT036	Peritonitis	65	0.080

153		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.080

154	c	ACT068	Acute Cystitis	63	0.080

155		CLT003	Colitis	62	0.080

156	P	NRP001	Neuropathy	56	0.080

157	P	PHC003	Pheochromocytoma	71	0.078

158	P	CHR345	Chronic Pain	50	0.078

159		MLL001	Molluscum Contagiosum	49	0.078

160		BRN071	Brain Injury	49	0.078

161		ADR040	Adrenal Gland Pheochromocytoma	46	0.078

162	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	89	0.076

163		ULC004	Ulcerative Colitis	73	0.076

164	P	HYP724	Hyperlipoproteinemia, Type Iii	72	0.076

165	P	MYS003	Myasthenia Gravis	68	0.076

166		ATH013	Atherosclerosis Susceptibility	66	0.076

167		HLC007	Helicobacter Pylori Infection	59	0.076

168	P	GLM007	Glomerulonephritis	57	0.076

169	P	DST107	Distal Renal Tubular Acidosis	41	0.076

170		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.076

171		ALC007	Alcohol Dependence	66	0.075

172	c	FML036	Familial Periodic Paralysis	44	0.075

173	P	BRS047	Breast Cancer	96	0.073

174	P	ALZ034	Alzheimer Disease	88	0.073

175		GLB015	Glioblastoma Multiforme	75	0.073

176	c	RHB024	Rhabdomyosarcoma 2	65	0.073

177	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.073

178		GLC003	Glucose Intolerance	54	0.073

179		ILS001	Ileus	51	0.073

180		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.073

181	P	CLR023	Colorectal Cancer	98	0.071

182	P	RSP003	Respiratory Failure	74	0.071

183	c	HYP836	Hypercholesterolemia, Familial, 1	72	0.071

184		OTT002	Otitis Media	71	0.071

185	P	NPH012	Nephrotic Syndrome	63	0.071

186	P	PRD008	Periodontitis	62	0.071

187		CNT047	Contact Dermatitis	57	0.071

188	P	DBT005	Diabetes Insipidus	55	0.071

189		PLM010	Pulmonary Edema	55	0.071

190		TRM010	Traumatic Brain Injury	53	0.071

191		ART140	Arteries, Anomalies of	53	0.071

192		NPH003	Nephrocalcinosis	51	0.071

193		PLP001	Pulpitis	48	0.071

194	P	RNL015	Renal Hypertension	48	0.071

195		HYP189	Hypoadrenalism	37	0.071

196	P	HYP120	Hypoaldosteronism	37	0.071

197	P	BRG001	Brugada Syndrome	70	0.069

198		PLM001	Pulmonary Tuberculosis	70	0.069

199	P	ESP024	Esophagitis	62	0.069

200		NTR005	Nutritional Deficiency Disease	61	0.069

201	P	CTR002	Cataract	60	0.069

202		INS001	Insulinoma	60	0.069

203		DNT012	Dental Caries	51	0.069

204	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.068

205		ANX010	Anxiety	72	0.068

206		RCK004	Rickets	69	0.068

207	P	PNM007	Pneumonia	68	0.068

208	P	PSR002	Psoriasis	62	0.068

209	P	HDC001	Headache	57	0.068

210		PST011	Pustulosis of Palm and Sole	52	0.068

211		HYP017	Hypophosphatemia	49	0.068

212		ATX019	Ataxia with Vitamin E Deficiency	48	0.068

213	P	PSD003	Pseudohypoaldosteronism	45	0.068

214		ALL014	Allergic Encephalomyelitis	39	0.068

215	c	ATM075	Autoimmune Encephalitis	38	0.068

216		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	36	0.068

217	c	FML159	Familial Periodic Paralyses	17	0.068

218	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.066

219		HMN044	Human Immunodeficiency Virus Type 1	71	0.066

220	P	LKM002	Leukemia	66	0.066

221		DPR016	Depression	63	0.066

222	P	BND020	Bone Disease	59	0.066

223		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.066

224		AMN003	Amnestic Disorder	54	0.066

225	P	LTR001	Lateral Sclerosis	53	0.066

226		PNG002	Pain Agnosia	51	0.066

227	P	DDN001	Duodenal Ulcer	50	0.066

228	P	BNG026	Benign Neonatal Seizures	48	0.066

229		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	34	0.066

230	P	MLT020	Multiple Sclerosis	72	0.064

231	P	AMY004	Amyloidosis	70	0.064

232		GST092	Gastroesophageal Reflux	65	0.064

233		IRN002	Iron Metabolism Disease	57	0.064

234	P	RHN004	Rhinitis	57	0.064

235	P	GST044	Gastritis	55	0.064

236		IMP005	Impotence	52	0.064

237	c	SHR030	Short Qt Syndrome	48	0.064

238		MYC005	Myocardial Stunning	46	0.064

239	P	MYC033	Myoclonus	46	0.064

240	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.062

241	c	LKM071	Leukemia, Chronic Lymphocytic	79	0.062

242		AST005	Asthma	77	0.062

243	c	ATR087	Atrial Standstill 1	74	0.062

244	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.062

245	P	EXN002	Exanthem	57	0.062

246		SCH014	Schistosomiasis	56	0.062

247	P	BPL003	Bipolar Disorder	56	0.062

248		INT007	Intermediate Coronary Syndrome	55	0.062

249	P	LYM031	Lymphocytic Leukemia	55	0.062

250		PPL022	Papilloma	54	0.062

251		GLS018	Glass Syndrome	53	0.062

252	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	52	0.062

253	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	48	0.062

254	c	MCR120	Microvascular Complications of Diabetes 7	47	0.062

255	P	HMR005	Hemorrhoid	46	0.062

256	c	MJR024	Major Affective Disorder 9	41	0.062

257		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.062

258	c	MJR022	Major Affective Disorder 8	38	0.062

259		CHL079	Children's Interstitial Lung Disease	27	0.062

260	P	LYM118	Lymphoma	68	0.060

261		OST159	Osteogenic Sarcoma	66	0.060

262	P	MNN013	Meningitis	65	0.060

263	P	THY023	Thymoma	65	0.060

264		GT001	Gout	63	0.060

265	P	PLY014	Polycystic Kidney Disease	59	0.060

266	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.060

267	c	THY107	Thymoma, Familial	54	0.060

268		GST023	Gastric Ulcer	53	0.060

269	P	LCT001	Lactic Acidosis	51	0.060

270	P	ECL001	Eclampsia	51	0.060

271	P	RNV001	Renovascular Hypertension	49	0.060

272		SYN036	Syncope	45	0.060

273		HDN002	Head Injury	45	0.060

274		PPL052	Papillomatosis, Confluent and Reticulated	34	0.060

275		DFC004	Deficiency Anemia	75	0.057

276	P	FRG001	Fragile X Syndrome	68	0.057

277		NRM005	Neuromuscular Disease	63	0.057

278		ANR007	Anorexia Nervosa	63	0.057

279	P	SNS001	Sensorineural Hearing Loss	61	0.057

280		BCT022	Bacterial Infectious Disease	56	0.057

281		HRT012	Heart Valve Disease	53	0.057

282	c	MCR113	Microvascular Complications of Diabetes 3	52	0.057

283		DRM011	Dermatophytosis	52	0.057

284		DMY004	Demyelinating Disease	52	0.057

285		47X002	47,xyy	49	0.057

286		ANR004	Anuria	46	0.057

287		PRM057	Paramyotonia Congenita of Von Eulenburg	46	0.057

288	P	BNG032	Benign Mesothelioma	45	0.057

289		IDP073	Idiopathic Hypercalciuria	43	0.057

290		DHY016	Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema	43	0.057

291		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	42	0.057

292	c	MCR130	Microvascular Complications of Diabetes 6	41	0.057

293	c	MCR133	Microvascular Complications of Diabetes 4	41	0.057

294		KCN010	Kcnq2-Related Disorders	27	0.057

295	P	LNG032	Lung Cancer	97	0.055

296	P	RHM011	Rheumatoid Arthritis	80	0.055

297	P	SCH015	Schizophrenia	75	0.055

298		CRH001	Crohn's Disease	74	0.055

299		SCK003	Sickle Cell Anemia	72	0.055

300		BRN024	Bronchitis	68	0.055

301	P	ATS364	Autism	65	0.055

302	P	HYP069	Hyperparathyroidism	62	0.055

303	P	VSC011	Vasculitis	62	0.055

304	P	EPL140	Epilepsy, Idiopathic Generalized	61	0.055

305		LNG099	Lung Disease	61	0.055

306		ACQ007	Acquired Immunodeficiency Syndrome	60	0.055

307		SQM006	Squamous Cell Carcinoma	60	0.055

308		GST045	Gastroenteritis	59	0.055

309	P	ALC033	Alcohol Use Disorder	58	0.055

310	P	PRP019	Peripheral Nervous System Disease	57	0.055

311		PRS047	Prostatitis	56	0.055

312	P	INF037	Inflammatory Bowel Disease	56	0.055

313		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.055

314		FCL014	Focal Epilepsy	54	0.055

315	P	MSC003	Muscular Atrophy	52	0.055

316	c	VRL010	Viral Hepatitis	51	0.055

317		THR004	Thrombocytosis	51	0.055

318	P	SCK005	Sickle Cell Disease	50	0.055

319		LYM019	Lymphosarcoma	47	0.055

320	P	HYP733	Hypercalciuria, Absorptive, 2	46	0.055

321		HPT004	Hepatic Coma	43	0.055

322	c	PRM038	Primary Agammaglobulinemia	43	0.055

323		HMP009	Haemophilus Influenzae	42	0.055

324	c	CHR098	Chronic Pyelonephritis	35	0.055

325	c	INT059	Internal Hemorrhoid	33	0.055

326		KCN014	Kcnq3-Related Disorders	9	0.055

327		OST012	Osteoarthritis	78	0.053

328	P	PRK057	Parkinson Disease, Late-Onset	76	0.053

329		ACR006	Aceruloplasminemia	73	0.053

330	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	64	0.053

331	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.053

332	P	NTR004	Neutropenia	63	0.053

333		TRN015	Transient Cerebral Ischemia	62	0.053

334		HPT019	Hepatic Encephalopathy	60	0.053

335		THY029	Thyroid Carcinoma	59	0.053

336	P	LDD007	Liddle Syndrome 1	59	0.053

337	P	INT070	Intestinal Obstruction	58	0.053

338		TNS005	Tonsillitis	57	0.053

339		PLM031	Poliomyelitis	57	0.053

340	P	JRV004	Jervell and Lange-Nielsen Syndrome 1	56	0.053

341		PHR003	Pharyngitis	56	0.053

342		AGN016	Aging	56	0.053

343	P	AST007	Astrocytoma	50	0.053

344		HYP025	Hyperphosphatemia	47	0.053

345		SQM002	Squamous Cell Papilloma	42	0.053

346		SPS057	Spasticity	41	0.053

347		MST020	Mast Cell Activation Syndrome	27	0.053

348		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.050

349		IMM167	Immune Deficiency Disease	78	0.050

350	P	GRF003	Graft-Versus-Host Disease	71	0.050

351	P	SYS005	Systemic Scleroderma	70	0.050

352		CRT072	Creutzfeldt-Jakob Disease	69	0.050

353	P	DBT085	Diabetes Mellitus, Insulin-Dependent	67	0.050

354	P	MCR115	Microvascular Complications of Diabetes 5	66	0.050

355	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	66	0.050

356		LPD008	Lipid Metabolism Disorder	62	0.050

357	P	MVM001	Movement Disease	61	0.050

358		ERL001	Early Myoclonic Encephalopathy	61	0.050

359	P	BCL017	B-Cell Lymphoma	58	0.050

360	P	URT039	Urticaria	58	0.050

361	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.050

362		GST050	Gastrointestinal System Disease	56	0.050

363		DBT010	Diabetic Neuropathy	55	0.050

364	P	ART021	Arteriosclerosis	54	0.050

365	c	XNT010	Xanthinuria, Type I	50	0.050

366		STM007	Stomatitis	49	0.050

367		ECT026	Ectopic Pregnancy	49	0.050

368		INT067	Interstitial Nephritis	46	0.050

369		CRN019	Coronary Artery Vasospasm	46	0.050

370		PTT037	Pituitary Tumors	44	0.050

371		GNG003	Gingival Recession	44	0.050

372		ALD013	Aldosterone-Producing Adenoma	38	0.050

373		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.050

374	c	SYS001	Systemic Lupus Erythematosus	86	0.048

375		INS024	Insulin-Like Growth Factor I	79	0.048

376		CNN003	Conn's Syndrome	79	0.048

377	P	HNT016	Huntington Disease	71	0.048

378	c	LNG044	Long Qt Syndrome 1	66	0.048

379	P	DYS154	Dystonia	65	0.048

380		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.048

381	P	END044	Endometriosis	62	0.048

382		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.048

383		FTT001	Fatty Liver Disease	61	0.048

384		CHL068	Cholestasis	60	0.048

385	P	MYC008	Myocarditis	59	0.048

386	P	SYP003	Syphilis	59	0.048

387	P	END033	Endocarditis	57	0.048

388		RHM027	Rheumatic Disease	56	0.048

389		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.048

390		ALL010	Allergic Contact Dermatitis	55	0.048

391		PRT038	Protein-Energy Malnutrition	54	0.048

392		PRP016	Paraplegia	53	0.048

393		SZR026	Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance	53	0.048

394		TLN003	Telangiectasis	51	0.048

395		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.048

396	P	MGR003	Migraine with Aura	50	0.048

397		DYS015	Dysentery	50	0.048

398	P	OVR082	Overgrowth Syndrome	50	0.048

399	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	50	0.048

400		NTR046	Neutrophil Migration	50	0.048

401		QDR001	Quadriplegia	48	0.048

402		CRD137	Cardiogenic Shock	48	0.048

403		TBR011	Tuberculous Meningitis	48	0.048

404		RNL077	Renal Fibrosis	47	0.048

405		SBC016	Subacute Delirium	44	0.048

406		CYT002	Cytokine Deficiency	44	0.048

407		CRB090	Cerebral Hypoxia	43	0.048

408	P	HYP265	Hypotonia	42	0.048

409	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.048

410		HYP540	Hypertension, Diastolic	40	0.048

411	P	FML187	Familial Hypertension	37	0.048

412		RRS014	Rare Surgical Neurologic Disease	32	0.048

413	P	HPT023	Hepatocellular Carcinoma	100	0.045

414	c	LKM061	Leukemia, Acute Myeloid	83	0.045

415		CRV035	Cervical Cancer	76	0.045

416		PRP027	Peripheral Vascular Disease	71	0.045

417		LYM133	Lymphoma, Hodgkin, Classic	69	0.045

418	P	SLP006	Sleep Apnea	69	0.045

419	P	MYC084	Mycobacterium Tuberculosis 1	68	0.045

420		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.045

421		DBT083	Diabetes Mellitus, Permanent Neonatal	64	0.045

422		OST017	Osteomyelitis	64	0.045

423		MDD011	Mood Disorder	62	0.045

424	P	HMN010	Hemangioma	61	0.045

425	c	HYP731	Hyperaldosteronism, Familial, Type I	60	0.045

426		DPH001	Diphtheria	60	0.045

427	c	ACT073	Acute Leukemia	58	0.045

428		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	57	0.045

429		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	56	0.045

430		CMM005	Common Cold	56	0.045

431	P	HYP050	Hyperinsulinemic Hypoglycemia	54	0.045

432	P	RNL017	Renal Oncocytoma	53	0.045

433	P	THY032	Thyroiditis	53	0.045

434		THR013	Thoracic Outlet Syndrome	53	0.045

435		PYD002	Pyoderma	51	0.045

436		THY030	Thyroid Gland Disease	51	0.045

437		ENT011	Enterocolitis	50	0.045

438	c	PYR010	Peyronie's Disease	50	0.045

439	P	NNT009	Neonatal Diabetes Mellitus	50	0.045

440	P	MYT002	Myotonic Dystrophy	49	0.045

441	c	SPN311	Spinocerebellar Ataxia 13	49	0.045

442		PYL006	Pyloric Stenosis	48	0.045

443	c	BNG006	Benign Familial Neonatal Epilepsy	47	0.045

444		CLS016	Clostridium Difficile Colitis	46	0.045

445	c	BRT050	Bartter Syndrome, Type 2, Antenatal	45	0.045

446	c	MLG068	Malignant Glioma	45	0.045

447		KWS001	Kwashiorkor	45	0.045

448		49X006	49, Xxxxy Syndrome	41	0.045

449	c	KCN020	Kcnt1-Related Epilepsy	14	0.045

450	P	PRS040	Prostate Cancer	97	0.042

451	P	PNC035	Pancreatic Cancer	84	0.042

452	P	BLD134	Bladder Cancer	78	0.042

453		LPT014	Leptin Deficiency or Dysfunction	73	0.042

454	P	OCL013	Oculodentodigital Dysplasia	69	0.042

455	P	INF038	Influenza	68	0.042

456		CRB037	Cerebral Palsy	68	0.042

457	c	ATS007	Autism Spectrum Disorder	67	0.042

458	P	MLG056	Malignant Hyperthermia	67	0.042

459		CNN005	Connective Tissue Disease	66	0.042

460	P	CNJ013	Conjunctivitis	65	0.042

461		WLF001	Wolff-Parkinson-White Syndrome	65	0.042

462		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.042

463	P	MTR014	Motor Neuron Disease	64	0.042

464		IRR002	Irritable Bowel Syndrome	63	0.042

465		MSC007	Muscle Hypertrophy	63	0.042

466		SKN016	Skin Disease	63	0.042

467	P	HML002	Hemolytic Anemia	62	0.042

468	P	HYP750	Hypertriglyceridemia, Familial	61	0.042

469	P	MYL006	Myeloid Leukemia	60	0.042

470	P	SLP005	Sleep Disorder	59	0.042

471		MNR012	Meniere Disease	57	0.042

472		MNT002	Mental Depression	57	0.042

473	P	MYT023	Myotonia Congenita	55	0.042

474	P	SCK002	Sick Sinus Syndrome	55	0.042

475	P	PMP001	Pemphigus	55	0.042

476	P	RTN016	Retinal Degeneration	53	0.042

477		MRG003	Marginal Zone B-Cell Lymphoma	53	0.042

478	P	RCT021	Rectum Cancer	53	0.042

479		KRT009	Keratosis	53	0.042

480		PTH003	Pathologic Nystagmus	51	0.042

481		PPT001	Peptic Esophagitis	51	0.042

482		DYS073	Dysphagia	50	0.042

483		TRY001	Trypanosomiasis	50	0.042

484		PNN001	Panniculitis	49	0.042

485		ATN005	Autonomic Dysfunction	47	0.042

486	c	BRT042	Bartter Syndrome, Type 3	46	0.042

487		ACT003	Acute Kidney Tubular Necrosis	45	0.042

488	P	DYS021	Dysautonomia	39	0.042

489		VLK001	Volkmann Contracture	32	0.042

490	P	PRD017	Periodic Paralyses	25	0.042

491		OBN001	Ouabain Resistance	18	0.042

492	P	OVR042	Ovarian Cancer	89	0.039

493		MYL069	Myeloma, Multiple	85	0.039

494		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.039

495	P	ART022	Arthritis	70	0.039

496	P	HPT021	Hepatitis	67	0.039

497	P	DMN002	Dementia	67	0.039

498	P	NSP012	Nasopharyngeal Carcinoma	67	0.039

499		MNT001	Mantle Cell Lymphoma	66	0.039

500	P	HYP098	Hypereosinophilic Syndrome	66	0.039

501		CHG001	Chagas Disease	66	0.039

502	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.039

503	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.039

504		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.039

505	P	LPS004	Lupus Erythematosus	61	0.039

506		SDD001	Sudden Infant Death Syndrome	61	0.039

507	P	PNC044	Pancreatitis	61	0.039

508		VRC005	Varicose Veins	60	0.039

509		ACN002	Acanthosis Nigricans	60	0.039

510		ETN001	Eating Disorder	59	0.039

511	c	DWL002	Dowling-Degos Disease 1	58	0.039

512	P	BNC003	Bone Cancer	57	0.039

513	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	57	0.039

514		CMR002	Coumarin Resistance	56	0.039

515	c	SVR001	Severe Acute Respiratory Syndrome	55	0.039

516	P	ANG015	Angioedema	54	0.039

517	P	ESP035	Esophagitis, Eosinophilic, 1	54	0.039

518		AMN001	Amenorrhea	54	0.039

519		SNS003	Sensory Peripheral Neuropathy	53	0.039

520		INF034	Infective Endocarditis	52	0.039

521		NNL006	Non-Alcoholic Steatohepatitis	51	0.039

522		CRN030	Coronary Stenosis	50	0.039

523		ENT004	Enthesopathy	48	0.039

524		WTH001	Withdrawal Disorder	48	0.039

525	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.039

526		ASP007	Aspiration Pneumonia	48	0.039

527		RTN020	Retinal Vascular Disease	48	0.039

528	c	MLG069	Malignant Hypertension	47	0.039

529		RTN023	Retinitis	46	0.039

530		ATN011	Autoinflammation with Infantile Enterocolitis	43	0.039

531		BRN032	Brain Glioma	43	0.039

532	c	BRT052	Bartter Syndrome, Type 1, Antenatal	43	0.039

533		NRR001	Neuroretinitis	43	0.039

534		TRP009	Triple X Syndrome	42	0.039

535	P	BRT053	Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness	42	0.039

536		SNL007	Senile Cataract	42	0.039

537		MDL009	Medullary Sponge Kidney	42	0.039

538		PRM020	Premenstrual Tension	39	0.039

539	c	PSD092	Pseudohypoaldosteronism, Type Iie	38	0.039

540	c	THY084	Thyrotoxic Periodic Paralysis 1	35	0.039

541	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.039

542	c	HYP438	Hyperaldosteronism, Familial, Type Iii	32	0.039

543		ADG002	Audiogenic Seizures	26	0.039

544		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.039

545		URT049	Urate Oxidase, Pseudogene	25	0.039

546		PRN068	Paraneoplastic Limbic Encephalitis	21	0.039

547		CNV009	Convulsions Benign Familial Neonatal Dominant Form	17	0.039

548	c	DLT002	Dilated Cardiomyopathy	79	0.036

549	P	LNG064	Lung Cancer Susceptibility 3	77	0.036

550	P	RTN008	Retinitis Pigmentosa	77	0.036

551		END057	Endometrial Cancer	74	0.036

552		BRN028	Brain Cancer	73	0.036

553		MSC157	Muscular Dystrophy, Duchenne Type	71	0.036

554	P	SRC025	Sarcoidosis 1	70	0.036

555		WLS001	Wilson Disease	70	0.036

556		GST040	Gastric Adenocarcinoma	70	0.036

557		MLN008	Melanoma	69	0.036

558		KRT019	Keratitis, Hereditary	67	0.036

559		BRK010	Burkitt Lymphoma	67	0.036

560		ALL003	Allergic Rhinitis	67	0.036

561	P	LPR021	Leprosy 3	67	0.036

562		PSY004	Psychotic Disorder	67	0.036

563	P	FLL037	Follicular Lymphoma	66	0.036

564	c	MCR129	Microvascular Complications of Diabetes 1	66	0.036

565		SRC014	Sarcoma	65	0.036

566		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.036

567	c	ART101	Aortic Valve Disease 2	63	0.036

568		IDP011	Idiopathic Interstitial Pneumonia	63	0.036

569	P	ANR048	Aniridia 1	63	0.036

570	P	ADL010	Adult Respiratory Distress Syndrome	63	0.036

571	c	EPS035	Episodic Ataxia, Type 2	63	0.036

572	c	HPT001	Hepatitis C	63	0.036

573	c	HPT003	Hepatitis a	63	0.036

574	P	PLM036	Pulmonary Fibrosis	61	0.036

575		APP008	Appendicitis	60	0.036

576	c	VSC019	Vesicoureteral Reflux 1	59	0.036

577	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	59	0.036

578		GNG013	Gingivitis	59	0.036

579	c	ACT027	Acute Pancreatitis	59	0.036

580		HYD002	Hydronephrosis	59	0.036

581		CHL123	Chlamydia	59	0.036

582		BRN002	Bronchiolitis	59	0.036

583		CHL067	Cholecystitis	58	0.036

584		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.036

585		BNG009	Benign Epilepsy with Centrotemporal Spikes	58	0.036

586	P	CND004	Candidiasis	57	0.036

587	P	INF032	Infertility	57	0.036

588		VSC002	Vascular Dementia	57	0.036

589		THR024	Thrombosis	56	0.036

590		ANG005	Anogenital Venereal Wart	56	0.036

591	c	INT072	Intestinal Pseudo-Obstruction	56	0.036

592		CHR177	Chromophobe Renal Cell Carcinoma	56	0.036

593		ALL006	Allergic Asthma	56	0.036

594		LYM040	Lymphoblastic Lymphoma	54	0.036

595		INT075	Intracranial Hypertension	53	0.036

596	c	LNG048	Long Qt Syndrome 3	52	0.036

597		MCN017	Meconium Ileus	52	0.036

598		MCR141	Mucormycosis	51	0.036

599		SPL004	Splenic Marginal Zone Lymphoma	51	0.036

600		SPN035	Spindle Cell Sarcoma	51	0.036

601	c	ALM001	Al Amyloidosis	50	0.036

602		HYP781	Hypoascorbemia	50	0.036

603		ALL009	Allergic Conjunctivitis	50	0.036

604		VLV047	Volvulus of Midgut	50	0.036

605	c	SVR005	Severe Pre-Eclampsia	49	0.036

606		VCC001	Vaccinia	49	0.036

607	c	FLL041	Follicular Lymphoma 1	49	0.036

608		KRT002	Keratomalacia	48	0.036

609	c	PRM093	Premature Ovarian Failure 7	47	0.036

610	c	LRG017	Large Intestine Cancer	47	0.036

611		PLS025	Plasmablastic Lymphoma	47	0.036

612		URT010	Ureteral Obstruction	46	0.036

613	P	MTH007	Methemoglobinemia	46	0.036

614		INT071	Intestinal Perforation	45	0.036

615		PRL008	Paralytic Ileus	44	0.036

616		DVR002	Diverticulitis	44	0.036

617	c	PCH010	Pachyonychia Congenita 3	43	0.036

618		ORL015	Oral Squamous Cell Carcinoma	43	0.036

619	c	FML294	Familial Short Qt Syndrome	43	0.036

620		IDP033	Idiopathic Edema	43	0.036

621		PRS063	Paresthesia	43	0.036

622	c	MCR112	Microvascular Complications of Diabetes 2	41	0.036

623	c	CNG027	Congenital Hemolytic Anemia	40	0.036

624		ENT001	Enterocele	39	0.036

625		ATM052	Autoimmune Disease 1	37	0.036

626		CHR178	Chromosomal Triplication	35	0.036

627		HNS001	Hansen's Disease	34	0.036

628		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.036

629	c	DNT047	Dentinogenesis Imperfecta Type 2	33	0.036

630		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.036

631		CYT018	Cytochrome P450 2d6 Variant	27	0.036

632		MTH071	Methane Production	26	0.036

633	c	BRT024	Bartter Syndrome Type 4	25	0.036

634		CRM010	Cramp-Fasciculation Syndrome	15	0.036

635		KCN019	Kcnk9 Imprinting Syndrome	14	0.036

636		ESP021	Esophageal Cancer	90	0.032

637		NRL016	Neural Tube Defects	82	0.032

638	P	NRF023	Neurofibromatosis, Type Ii	76	0.032

639		GST019	Gastrointestinal Stromal Tumor	76	0.032

640	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.032

641		ACR007	Acromegaly	71	0.032

642	c	HPT073	Hepatitis C Virus	70	0.032

643		MYL009	Myelodysplastic Syndrome	70	0.032

644	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.032

645	P	MJR001	Major Depressive Disorder	68	0.032

646	P	ESS003	Essential Thrombocythemia	67	0.032

647	P	SKN015	Skin Carcinoma	67	0.032

648	P	DRM053	Dermatitis, Atopic	66	0.032

649	P	MTR004	Maturity-Onset Diabetes of the Young	66	0.032

650		LPT001	Leptospirosis	66	0.032

651		MYC006	Mycosis Fungoides	66	0.032

652	P	NRV007	Nervous System Disease	66	0.032

653	P	HRP006	Herpes Simplex	65	0.032

654		MYL031	Myeloproliferative Neoplasm	65	0.032

655		APN008	Apnea, Obstructive Sleep	65	0.032

656		CLN015	Colon Adenocarcinoma	63	0.032

657		TYP007	Typhoid Fever	63	0.032

658		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	62	0.032

659	P	ART023	Arthropathy	62	0.032

660	P	EPL198	Epilepsy, Myoclonic Juvenile	62	0.032

661	P	PRM006	Primary Biliary Cirrhosis	61	0.032

662		OST003	Osteonecrosis	61	0.032

663		VRL011	Viral Infectious Disease	61	0.032

664		RHM001	Rheumatic Fever	61	0.032

665		PRT013	Portal Hypertension	60	0.032

666		YLL002	Yellow Fever	60	0.032

667		WST001	West Syndrome	60	0.032

668	P	GLL022	Guillain-Barre Syndrome	59	0.032

669		SPP011	Suppression of Tumorigenicity 12	59	0.032

670	c	DNG003	Dengue Disease	59	0.032

671		PLM033	Pulmonary Embolism	59	0.032

672		FBR047	Fibromyalgia	59	0.032

673	P	BRS044	Breast Adenocarcinoma	59	0.032

674		ANR040	Aneurysm	58	0.032

675		URN010	Urinary Tract Obstruction	57	0.032

676		BLR008	Bilirubin Metabolic Disorder	57	0.032

677		GST033	Gestational Diabetes	57	0.032

678	P	HYP024	Hypoparathyroidism	55	0.032

679		PRP030	Purpura	55	0.032

680	c	FML035	Familial Hyperlipidemia	55	0.032

681		RLP002	Relapsing-Remitting Multiple Sclerosis	55	0.032

682		RSC001	Rosacea	55	0.032

683	P	MYP006	Myopia	55	0.032

684		PYD001	Pyoderma Gangrenosum	54	0.032

685	P	DRM007	Dermatitis Herpetiformis	54	0.032

686	P	SLM003	Salmonellosis	54	0.032

687	c	PRD040	Periodontitis, Chronic	54	0.032

688	c	FML023	Familial Hemiplegic Migraine	54	0.032

689		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	53	0.032

690		OCL006	Ocular Hypertension	53	0.032

691		MST005	Mastitis	53	0.032

692	P	RTN018	Retinal Disease	52	0.032

693		ACR041	Acromelic Frontonasal Dysostosis	52	0.032

694		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	52	0.032

695	P	ACT008	Actinic Keratosis	52	0.032

696		PLS009	Plasma Cell Neoplasm	51	0.032

697		ONC002	Onchocerciasis	51	0.032

698		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.032

699		NRM004	Neuroma	51	0.032

700	c	SCN007	Secondary Hyperparathyroidism	50	0.032

701		HPT014	Hepatorenal Syndrome	50	0.032

702	c	INF145	Infantile Liver Failure Syndrome 1	50	0.032

703		CHL004	Cholelithiasis	49	0.032

704		PLC008	Placenta Disease	49	0.032

705		LRN003	Learning Disability	49	0.032

706	P	OPN001	Open-Angle Glaucoma	49	0.032

707		SNT005	Sinoatrial Node Disease	49	0.032

708	P	ATS011	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy	48	0.032

709	c	BCT013	Bacterial Pneumonia	47	0.032

710		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.032

711		LCK001	Locked-in Syndrome	46	0.032

712		CYN002	Cyanosis, Transient Neonatal	45	0.032

713		GRN007	Granuloma Annulare	45	0.032

714	P	HMP006	Hemiplegic Migraine	44	0.032

715		NWC001	Newcastle Disease	44	0.032

716		CHR031	Chromoblastomycosis	44	0.032

717		GRN017	Granulocytopenia	44	0.032

718		PNC085	Penicillin Allergy	44	0.032

719		ATN004	Autonomic Neuropathy	44	0.032

720	P	BCT020	Bacteremia 2	44	0.032

721		ESN004	Eosinophilic Gastritis	44	0.032

722	P	MYG005	Myoglobinuria	43	0.032

723		BCK006	Back Pain	42	0.032

724		RDN001	Reading Disorder	40	0.032

725		FNG016	Fungal Keratitis	40	0.032

726	P	ANT061	Antenatal Bartter Syndrome	40	0.032

727		LKP003	Leukoplakia	39	0.032

728		WLL004	Wallerian Degeneration	39	0.032

729		AMN006	Aminoaciduria	38	0.032

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

731		HRN029	Hearing Loss, Noise-Induced	37	0.032

732	P	MXL015	Maxillary Sinusitis	37	0.032

733		SCR003	Secretory Diarrhea	36	0.032

734	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.032

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

736	c	RNL046	Renal Tubular Acidosis, Distal, Autosomal Dominant	34	0.032

737	c	PRG106	Progressive Muscular Dystrophy	33	0.032

738	c	THY083	Thyrotoxic Periodic Paralysis 2	33	0.032

739	P	VSC018	Visceral Steatosis	33	0.032

740		PLY150	Polykaryocytosis Inducer	31	0.032

741		SLC024	Slc4a1-Associated Distal Renal Tubular Acidosis	19	0.032

742	P	ATX030	Ataxia-Telangiectasia	83	0.028

743	P	GLM040	Glioma Susceptibility 1	81	0.028

744	P	MDL005	Medulloblastoma	77	0.028

745		PLM134	Pulmonary Fibrosis, Idiopathic	75	0.028

746		SVR004	Severe Combined Immunodeficiency	73	0.028

747	c	SPN225	Spondyloarthropathy 1	73	0.028

748	c	LKM063	Leukemia, Chronic Myeloid	71	0.028

749		LPD012	Lipoid Congenital Adrenal Hyperplasia	71	0.028

750	P	TBR001	Tuberous Sclerosis	70	0.028

751	P	TTR001	Tetralogy of Fallot	69	0.028

752		PLY001	Polycythemia Vera	69	0.028

753		ART016	Aortic Aneurysm	68	0.028

754	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	0.028

755	P	THR014	Thrombocytopenia	68	0.028

756		PNC129	Pancreatic Adenocarcinoma	67	0.028

757		MYL005	Myelofibrosis	67	0.028

758	c	PRG042	Progressive Familial Heart Block, Type Ia	67	0.028

759	P	ANG001	Angelman Syndrome	67	0.028

760		GLL008	Gilles De La Tourette Syndrome	66	0.028

761		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.028

762	P	HYD006	Hydrocephalus	65	0.028

763	c	SML038	Small Cell Cancer of the Lung	65	0.028

764	P	LPS002	Liposarcoma	65	0.028

765		BRR014	Barrett Esophagus	64	0.028

766	P	CHR071	Charcot-Marie-Tooth Disease	64	0.028

767	c	DYS056	Dystonia 12	64	0.028

768		KHL003	Kohlschutter-Tonz Syndrome	64	0.028

769	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	63	0.028

770		NRF026	Neurofibromatosis, Type Iv, of Riccardi	63	0.028

771	P	MCH002	Machado-Joseph Disease	63	0.028

772		PPL049	Papillon-Lefevre Syndrome	63	0.028

773	P	HRD008	Hereditary Hemorrhagic Telangiectasia	62	0.028

774	P	RHB003	Rhabdomyosarcoma	62	0.028

775	P	BCK002	Beckwith-Wiedemann Syndrome	62	0.028

776		TMT001	Timothy Syndrome	62	0.028

777		HMT002	Hematologic Cancer	62	0.028

778	P	BLD124	Bleeding Disorder, Platelet-Type, 11	61	0.028

779		CHR066	Chronic Fatigue Syndrome	61	0.028

780		INT002	Intermittent Claudication	61	0.028

781	P	ANP001	Anaplastic Large Cell Lymphoma	61	0.028

782		LYM012	Lymphoplasmacytic Lymphoma	61	0.028

783		MSL001	Measles	61	0.028

784		SZR001	Sezary's Disease	60	0.028

785		ING001	Inguinal Hernia	60	0.028

786	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	60	0.028

787		TRG002	Trigeminal Neuralgia	60	0.028

788		CYS010	Cystinosis	60	0.028

789		PNM010	Pneumothorax, Primary Spontaneous	60	0.028

790	P	CNT110	Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a	60	0.028

791		CHR072	Chordoma	59	0.028

792		INT066	Interstitial Lung Disease	59	0.028

793	P	BRN022	Bronchiectasis	59	0.028

794	c	HPT016	Hepatitis B	59	0.028

795	P	CHR285	Chronic Myelomonocytic Leukemia	59	0.028

796	P	PLV020	Pelvic Organ Prolapse	59	0.028

797	c	SPN301	Spinocerebellar Ataxia 2	59	0.028

798	c	PRG043	Progressive Familial Heart Block, Type Ib	58	0.028

799		PST028	Post-Traumatic Stress Disorder	58	0.028

800	P	GLL020	Gallbladder Disease	58	0.028

801		NWB001	Newborn Respiratory Distress Syndrome	58	0.028

802		BLM002	Bulimia Nervosa	57	0.028

803	P	PLY041	Polymyositis	57	0.028

804	c	MST023	Mesothelioma, Malignant	57	0.028

805	c	ADL017	Adult T-Cell Leukemia	57	0.028

806		ADN027	Adenomyosis	57	0.028

807	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	56	0.028

808		PLS011	Plasmacytoma	56	0.028

809		ADR056	Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete	56	0.028

810	P	MLN007	Male Infertility	56	0.028

811		PNM008	Pneumothorax	56	0.028

812	P	PLY019	Polyneuropathy	56	0.028

813	P	PNM006	Pneumoconiosis	55	0.028

814	P	PLY018	Polycythemia	55	0.028

815	c	BCT007	Bacterial Meningitis	55	0.028

816	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.028

817		NRN004	Neuroendocrine Tumor	55	0.028

818		CLL003	Cellulitis	54	0.028

819		HMP005	Hemiplegia	54	0.028

820		CRT017	Cartilage Disease	54	0.028

821	P	TCD001	Tic Disorder	54	0.028

822	P	CYS039	Cystic Kidney Disease	54	0.028

823		LST001	Listeriosis	54	0.028

824		PRC013	Pericarditis	54	0.028

825		NRT004	Neuritis	53	0.028

826		RHM028	Rheumatic Heart Disease	53	0.028

827		ALC009	Alcoholic Liver Cirrhosis	53	0.028

828		NRT001	Neurotic Disorder	52	0.028

829	P	HMR003	Hemorrhagic Disease	52	0.028

830		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.028

831		TXC002	Toxic Encephalopathy	52	0.028

832	c	PRM012	Primary Polycythemia	52	0.028

833		MYC080	Myoclonic Epilepsy of Unverricht and Lundborg	52	0.028

834	P	HMP007	Hemophilia	51	0.028

835		THR016	Thrombophlebitis	51	0.028

836	c	ACT134	Acute Liver Failure	51	0.028

837		RSP002	Respiratory Syncytial Virus Infectious Disease	51	0.028

838	P	CNT056	Cantu Syndrome	51	0.028

839		AZS001	Azoospermia	50	0.028

840		HYP081	Hypolipoproteinemia	50	0.028

841	P	HYP077	Hypertrichosis	50	0.028

842		ACH005	Achalasia	50	0.028

843		MCR004	Macroglobulinemia	50	0.028

844		OPT003	Opiate Dependence	50	0.028

845	P	OTS001	Otosclerosis	50	0.028

846	P	CTN015	Cutaneous T Cell Lymphoma	49	0.028

847		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.028

848		LFT001	Left Bundle Branch Hemiblock	49	0.028

849	c	BPL002	Bipolar I Disorder	49	0.028

850		IFP001	Ifap Syndrome with or Without Bresheck Syndrome	49	0.028

851	c	DYS119	Dystonia 9	49	0.028

852		GYN001	Gynecomastia	49	0.028

853		ATY042	Atypical Chronic Myeloid Leukemia	49	0.028

854	c	THR090	Thrombocythemia 1	49	0.028

855		CLN045	Colonic Benign Neoplasm	49	0.028

856		URT001	Urethritis	48	0.028

857		BLD044	Bladder Disease	48	0.028

858		BCT004	Bacteriuria	48	0.028

859	P	CMP008	Compartment Syndrome	48	0.028

860	c	ACT150	Acute Adrenal Insufficiency	48	0.028

861	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.028

862		ATS010	Autosomal Recessive Disease	48	0.028

863		CHR563	Chronic Eosinophilic Leukemia	48	0.028

864		CCN002	Cocaine Abuse	48	0.028

865	P	MRC003	Mercury Poisoning	48	0.028

866		INT054	Intraocular Lymphoma	48	0.028

867		ANT018	Anthracosis	48	0.028

868		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.028

869		THY128	Thyroid Tumor	47	0.028

870	P	TCL004	T-Cell Leukemia	47	0.028

871	P	CRC039	Coarctation of Aorta	47	0.028

872		TNP001	Tinea Pedis	47	0.028

873		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.028

874	P	VTR007	Vitreoretinopathy	46	0.028

875		PRP017	Periapical Periodontitis	46	0.028

876		EXT010	Extramedullary Plasmacytoma	45	0.028

877	P	OVR046	Ovarian Cyst	45	0.028

878		LYM051	Lymphomatoid Granulomatosis	45	0.028

879		MYX004	Myxedema	44	0.028

880		ACT029	Acute Interstitial Pneumonia	44	0.028

881		HRT015	Heritable Pulmonary Arterial Hypertension	44	0.028

882		MNG006	Monogenic Diabetes	44	0.028

883		CRT015	Carotid Artery Occlusion	44	0.028

884	c	CRV002	Cervix Uteri Carcinoma in Situ	44	0.028

885		CNT017	Central Nervous System Origin Vertigo	44	0.028

886		DMP001	Dumping Syndrome	44	0.028

887	P	MJR007	Major Affective Disorder 1	43	0.028

888		BNM001	Bone Marrow Cancer	43	0.028

889	c	HYP272	Hypercholesterolemia, Familial, 3	43	0.028

890		MRS001	Marasmus	43	0.028

891		ASP008	Aspiration Pneumonitis	42	0.028

892		MYF002	Myofascial Pain Syndrome	42	0.028

893		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	42	0.028

894		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.028

895		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.028

896		CHR286	Chronic Neutrophilic Leukemia	41	0.028

897	P	CND005	Cone Dystrophy	41	0.028

898		GST020	Gastric Antral Vascular Ectasia	41	0.028

899		RST023	Resting Heart Rate, Variation in	41	0.028

900	P	FML156	Familial Hyperaldosteronism	41	0.028

901	c	LNG053	Long Qt Syndrome 9	41	0.028

902		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.028

903		VLV042	Vulvar Vestibulitis Syndrome	40	0.028

904		CRY019	Cryohydrocytosis	40	0.028

905		ANG049	Angioedema Induced by Ace Inhibitors	40	0.028

906		BRK002	Birk-Barel Syndrome	39	0.028

907		AGR019	Age-Related Hearing Loss	39	0.028

908		CRV045	Cervical Intraepithelial Neoplasia	39	0.028

909	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.028

910		VLL006	Villous Adenoma	38	0.028

911		SCR011	Scrapie	38	0.028

912	P	PST059	Pustular Psoriasis	38	0.028

913	P	CRB088	Cerebral Atrophy	38	0.028

914		TNC002	Tinea Capitis	38	0.028

915		URT004	Urethral Syndrome	38	0.028

916		ATX010	Ataxia Neuropathy Spectrum	38	0.028

917		MYT003	Myotonic Disease	37	0.028

918		DRM009	Dermatomycosis	36	0.028

919		ABD010	Abdominal Wall Defect	35	0.028

920		MYL067	Myeloproliferative Disorder, Chronic, with Eosinophilia	35	0.028

921		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	33	0.028

922		PST010	Pasteurellosis	33	0.028

923		BNN005	Bunion	33	0.028

924	c	PSD090	Pseudohypoaldosteronism, Type Iia	33	0.028

925		CLN006	Colonic Pseudo-Obstruction	33	0.028

926	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.028

927		HND015	Hand Skill, Relative	33	0.028

928		CND006	Candida Glabrata	32	0.028

929		ACT216	Acute Leukemia of Ambiguous Lineage	32	0.028

930		ACT064	Acute Necrotizing Encephalitis	32	0.028

931	P	ATS382	Autosomal Dominant Tubulointerstitial Kidney Disease	31	0.028

932		INF021	Infant Gynecomastia	31	0.028

933		FNT004	Fainting	31	0.028

934	c	PSD093	Pseudohypoaldosteronism, Type Iid	30	0.028

935		PST092	Posttransplant Acute Limbic Encephalitis	29	0.028

936		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.028

937	c	LNG052	Long Qt Syndrome 8	26	0.028

938	c	HRD219	Hereditary Distal Renal Tubular Acidosis	26	0.028

939		OBS168	Obsolete: Atypical Teratoid/rhabdoid Tumor	22	0.028

940		BLD137	Blood Group--Ahonen	19	0.028

941		MYP026	Myopathy - Thyrotoxic	17	0.028

942		DGT004	Digitalis Poisoning	14	0.028

943		HRD103	Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum	14	0.028

944		NNP018	Non-Paraneoplastic Limbic Encephalitis	12	0.028

945	P	OBS151	Obsolete: Channelopathy	8	0.028

946	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.023

947	P	RTT002	Rett Syndrome	80	0.023

948		MLR004	Malaria	80	0.023

949	c	TBR025	Tuberous Sclerosis 1	76	0.023

950		MRF001	Marfan Syndrome	75	0.023

951	P	APL001	Aplastic Anemia	74	0.023

952		ADR007	Adrenoleukodystrophy	74	0.023

953	P	FML018	Familial Mediterranean Fever	72	0.023

954		CNT097	Central Hypoventilation Syndrome, Congenital	70	0.023

955	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.023

956		EWN003	Ewing Sarcoma	68	0.023

957	P	ALP004	Alport Syndrome	68	0.023

958	c	INF071	Inflammatory Bowel Disease 1	68	0.023

959		SKN019	Skin Melanoma	67	0.023

960		GRG001	Greig Cephalopolysyndactyly Syndrome	67	0.023

961	c	MCL062	Mucolipidosis Ii Alpha/beta	66	0.023

962		FCT007	Factor Vii Deficiency	66	0.023

963	c	MYT021	Myotonic Dystrophy 1	66	0.023

964	c	HMP029	Hemophilia a	65	0.023

965		LYS012	Lysosomal Acid Lipase Deficiency	64	0.023

966		CLR108	Colorectal Adenoma	64	0.023

967		ART002	Arts Syndrome	63	0.023

968		ACT119	Acute Promyelocytic Leukemia	63	0.023

969	c	SCL052	Scleroderma, Familial Progressive	62	0.023

970		CYS013	Cystinuria	62	0.023

971		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.023

972		WLL001	Williams-Beuren Syndrome	62	0.023

973	c	GLC092	Glaucoma, Primary Open Angle	62	0.023

974		HYP780	Hypoadrenocorticism, Familial	62	0.023

975		ALC006	Alcoholic Hepatitis	61	0.023

976		HYD038	Hydrops Fetalis, Nonimmune	61	0.023

977		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	61	0.023

978	P	DRM010	Dermatomyositis	61	0.023

979	P	KDN017	Kidney Cancer	61	0.023

980	P	CHL002	Childhood Absence Epilepsy	60	0.023

981	P	NRM001	Neuromyelitis Optica	60	0.023

982	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.023

983	P	VNT002	Ventricular Septal Defect	60	0.023

984		RTN017	Retinal Detachment	60	0.023

985		STF001	Stiff-Person Syndrome	60	0.023

986		ORL011	Oral Cancer	60	0.023

987		HRP004	Herpes Zoster	60	0.023

988	P	THL005	Thalassemia	60	0.023

989	P	SPN309	Spinocerebellar Ataxia 6	59	0.023

990		PRT058	Pure Autonomic Failure	59	0.023

991	P	LKD001	Leukodystrophy	59	0.023

992	P	TRC086	Trichohepatoenteric Syndrome 1	59	0.023

993		GRD007	Grade Iii Astrocytoma	59	0.023

994		IRN001	Iron Deficiency Anemia	58	0.023

995		CRY005	Cryptococcosis	58	0.023

996		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	58	0.023

997	P	NPH005	Nephronophthisis	58	0.023

998		EYD002	Eye Disease	58	0.023

999		ERY029	Erythermalgia, Primary	58	0.023

1000		ANG020	Angiosarcoma	58	0.023

1001	c	PRG126	Progressive Familial Heart Block	58	0.023

1002		EXT034	Extrinsic Allergic Alveolitis	58	0.023

1003	c	PRM005	Primary Hyperparathyroidism	58	0.023

1004		LYM021	Lymphadenitis	58	0.023

1005	P	OPT006	Optic Nerve Disease	57	0.023

1006		ERY003	Erythema Multiforme	57	0.023

1007	P	MMP001	Mumps	57	0.023

1008		RNL024	Renal Glucosuria	57	0.023

1009		BRN056	Bronchopulmonary Dysplasia	57	0.023

1010		DSS008	Disease of Mental Health	57	0.023

1011	P	PRN023	Prion Disease	57	0.023

1012	c	MYT020	Myotonic Dystrophy 2	57	0.023

1013		APH001	Aphthous Stomatitis	57	0.023

1014	P	STR020	Strabismus	56	0.023

1015		ERY051	Erythroleukemia, Familial	56	0.023

1016	P	FBR017	Fibrosarcoma	56	0.023

1017	P	OPT009	Optic Neuritis	56	0.023

1018		SFT003	Soft Tissue Sarcoma	56	0.023

1019		LMY014	Leiomyoma, Uterine	56	0.023

1020		AVN001	Avian Influenza	56	0.023

1021		FDB001	Foodborne Botulism	56	0.023

1022		MTH009	Mouth Disease	56	0.023

1023		ADR008	Adrenal Adenoma	56	0.023

1024		INT030	Intracranial Aneurysm	56	0.023

1025		HMG005	Hemoglobinopathy	55	0.023

1026		SYN007	Synovitis	55	0.023

1027		HRY003	Hairy Cell Leukemia	55	0.023

1028		FCT001	Factor Viii Deficiency	55	0.023

1029		TNG003	Tongue Cancer	55	0.023

1030		VGN023	Vaginitis	55	0.023

1031	P	SBS003	Substance Abuse	54	0.023

1032		NRG002	Neurogenic Bladder	54	0.023

1033	P	PTT006	Pituitary Adenoma	54	0.023

1034		END040	Endogenous Depression	54	0.023

1035		INS023	Insensitivity to Pain, Congenital, with Anhidrosis	54	0.023

1036	c	CNT035	Central Nervous System Disease	54	0.023

1037		GST037	Gastroparesis	53	0.023

1038		HDR002	Hidradenitis Suppurativa	53	0.023

1039		BRN038	Bronchial Disease	53	0.023

1040		HYP815	Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome	53	0.023

1041	P	LYM025	Lymphedema	53	0.023

1042	P	ART018	Aortic Valve Insufficiency	53	0.023

1043		KRT006	Keratoconjunctivitis	53	0.023

1044	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	53	0.023

1045		CLF001	Cleft Lip	53	0.023

1046		PRP080	Peripheral Artery Disease	53	0.023

1047		CRH005	Crohn's Colitis	52	0.023

1048	c	PRM092	Primary Lateral Sclerosis, Adult, 1	52	0.023

1049	c	SPN294	Spinocerebellar Ataxia 1	52	0.023

1050		PRN011	Pernicious Anemia	52	0.023

1051	P	ACT105	Acute Mountain Sickness	52	0.023

1052	c	GLL024	Gallbladder Disease 1	52	0.023

1053		CHR073	Choreatic Disease	52	0.023

1054	P	RTN022	Retinal Vein Occlusion	52	0.023

1055		AGN003	Agenesis of the Corpus Callosum with Peripheral Neuropathy	52	0.023

1056	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.023

1057		FML063	Familial Glucocorticoid Deficiency	51	0.023

1058	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.023

1059	P	PRC012	Pericardial Effusion	51	0.023

1060		GSG001	Gas Gangrene	50	0.023

1061	c	BRG005	Brugada Syndrome 1	50	0.023

1062		HRT011	Heart Septal Defect	50	0.023

1063		RTN003	Retinal Ischemia	50	0.023

1064		ADT003	Auditory System Disease	50	0.023

1065		APL002	Aplasia of Lacrimal and Salivary Glands	50	0.023

1066		BRX001	Bruxism	50	0.023

1067	P	FNC004	Fanconi Syndrome	50	0.023

1068		SPS003	Spastic Diplegia	50	0.023

1069		SLD003	Sialadenitis	50	0.023

1070		LMY002	Leiomyoma	50	0.023

1071	P	CHL066	Cholangitis	50	0.023

1072		VPM001	Vipoma	50	0.023

1073		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.023

1074	c	MLG054	Malignant Histiocytosis	50	0.023