Search results for Potassium

2140 hits were found for Potassium

#	Family	MCID	Name	MIFTS	Score
1		MYT030	Myotonia, Potassium-Aggravated	45	6.463

2		HYP005	Hypokalemia	55	5.923

3		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	4.364

4		OVR093	Overhydrated Hereditary Stomatocytosis	43	3.877

5		GTL001	Gitelman Syndrome	65	3.434

6		HYP052	Hyperkalemic Periodic Paralysis	61	2.086

7	P	BRT004	Bartter Disease	52	2.048

8		KND001	Kindler Syndrome	64	2.010

9		SDM004	Sodium-Potassium-Atpase Activity of Red Cell	7	1.959

10		PTS020	Potassium Dichromate Allergic Contact Dermatitis	3	1.959

11	c	NRL029	Neurological Muscular Channelopathy Due to a Genetic Potassium Channel Defect	3	1.951

12	c	NRL037	Neurological Channelopathy of the Central Nervous System Due to a Genetic Potassium Channel Defect	2	1.951

13		NRM009	Normokalemic Periodic Paralysis	28	1.943

14		ALP077	Alpha-Methylacetoacetic Aciduria	55	1.933

15	c	PRG143	Progressive Myoclonus Epilepsy 7	16	1.933

16	c	EPL134	Epilepsy, Progressive Myoclonic 7	27	1.920

17	c	HYP595	Hypertension, Essential	84	0.305

18	P	KDN018	Kidney Disease	72	0.246

19	P	LNG028	Long Qt Syndrome	66	0.232

20	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.208

21	P	CRD119	Cardiac Arrest	67	0.206

22		HRW001	Hair Whorl	36	0.201

23	c	ACT075	Acute Myocardial Infarction	57	0.198

24		CNG034	Congestive Heart Failure	69	0.197

25		ALL026	Allergic Hypersensitivity Disease	62	0.190

26		PRT037	Pertussis	65	0.184

27	c	CHR684	Chronic Kidney Disease	70	0.181

28		HLX001	Helix Syndrome	47	0.174

29		MTB004	Metabolic Acidosis	50	0.173

30	P	HRT032	Heart Disease	75	0.168

31		ANX004	Anoxia	40	0.167

32		ISC004	Ischemia	58	0.160

33	P	PRD021	Periodic Paralysis	45	0.159

34		HYP266	Hypoxia	57	0.158

35	P	ENC004	Encephalitis	61	0.157

36		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.157

37		NPH009	Nephrolithiasis	55	0.153

38	P	MYC007	Myocardial Infarction	70	0.150

39	P	DRR001	Diarrhea	55	0.147

40		HYP056	Hypoglycemia	66	0.146

41	P	NRB001	Neuroblastoma	72	0.145

42		CRD223	Cardiac Arrhythmia	60	0.144

43		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.144

44		48X005	48,xyyy	39	0.144

45		CRD132	Cardiac Conduction Defect	58	0.143

46	P	SZR006	Seizure Disorder	56	0.140

47		END086	End Stage Renal Disease	51	0.140

48		VSL002	Visual Epilepsy	59	0.139

49		LMB024	Limbic Encephalitis	41	0.138

50	P	HYP076	Hyperthyroidism	55	0.133

51		LVR012	Liver Cirrhosis	62	0.127

52	c	MGR028	Migraine with or Without Aura 1	67	0.126

53	P	GLM045	Glioma	63	0.123

54	P	ATR011	Atrial Fibrillation	66	0.122

55		GLL048	Glial Tumor	45	0.122

56		HYP066	Hyperglycemia	61	0.121

57	c	GRV008	Graves Disease 1	56	0.121

58	P	EPL164	Epilepsy	71	0.119

59	P	HYP086	Hypothyroidism	69	0.118

60	P	ENC018	Encephalopathy	61	0.118

61	P	EPS003	Episodic Ataxia	59	0.117

62		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.110

63		HYP060	Hyperinsulinism	54	0.110

64	P	LVR013	Liver Disease	68	0.109

65		ATM095	Autoimmune Disease	62	0.109

66		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.109

67		OCL069	Ocular Motor Apraxia	51	0.109

68		ANG054	Angina Pectoris	66	0.108

69	P	CYS018	Cystitis	59	0.108

70	P	DBT009	Diabetes Mellitus	64	0.107

71		PRS021	Prostatic Adenoma	51	0.105

72		PRS045	Prostatic Hypertrophy	53	0.104

73		PRS129	Prostatic Hyperplasia, Benign	49	0.104

74	c	BRN108	Branchiootic Syndrome 1	62	0.103

75		LPP008	Lipoprotein Quantitative Trait Locus	62	0.103

76		ADN018	Adenoma	59	0.103

77	P	INT143	Interstitial Cystitis	61	0.102

78	c	ACT071	Acute Kidney Failure	60	0.101

79	P	VSC007	Vascular Disease	63	0.100

80		DRM006	Dermatitis	61	0.100

81	c	FML191	Familial Long Qt Syndrome	53	0.100

82		CRB004	Cerebral Artery Occlusion	45	0.100

83		DWN001	Down Syndrome	70	0.098

84		GTR002	Goiter	53	0.098

85		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.097

86	P	RNL007	Renal Tubular Acidosis	51	0.097

87		URM002	Uremia	49	0.097

88	P	GST053	Gastric Cancer	83	0.096

89	P	PLM037	Pulmonary Hypertension	67	0.096

90		BNR002	Bone Resorption Disease	48	0.096

91		STR067	Stroke, Ischemic	81	0.095

92	P	TMP001	Temporal Lobe Epilepsy	50	0.095

93		URL001	Urolithiasis	45	0.095

94	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	0.093

95	P	DNT007	Dentin Sensitivity	36	0.093

96		CYS001	Cystic Fibrosis	81	0.091

97	P	TRN020	Turner Syndrome	67	0.091

98		TXC005	Toxic Shock Syndrome	62	0.089

99	P	CRD246	Cardiovascular System Disease	57	0.089

100		ATR057	Atrioventricular Block	55	0.089

101		HYP014	Hyperuricemia	52	0.089

102	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.088

103		ADL002	Adult Syndrome	70	0.088

104		TTN003	Tetanus	65	0.088

105		PPT005	Peptic Ulcer Disease	59	0.088

106	P	PYL005	Pyelonephritis	56	0.088

107		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.087

108		CHL014	Cholera	59	0.085

109	c	LNG047	Long Qt Syndrome 2	58	0.085

110	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.085

111	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.085

112	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.085

113	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.085

114	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.085

115	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.085

116		SPR010	Sporotrichosis	46	0.085

117	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.085

118	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.085

119	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.085

120	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.085

121	P	OST002	Osteoporosis	74	0.084

122	P	MYP004	Myopathy	70	0.084

123		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.084

124	P	ADN016	Adenocarcinoma	64	0.084

125	P	CRN300	Coronary Heart Disease 1	63	0.084

126		SPN186	Spinal Cord Injury	60	0.084

127		CNS004	Constipation	58	0.084

128	P	GRV001	Graves' Disease	55	0.084

129	P	THY054	Thyrotoxic Periodic Paralysis	46	0.084

130	c	PRC016	Pre-Eclampsia	63	0.082

131	c	PNS012	Paine Syndrome	61	0.082

132		STT001	Status Epilepticus	60	0.082

133	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.082

134	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.082

135	c	EPS042	Episodic Ataxia, Type 1	60	0.081

136		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.081

137		BRN004	Brain Edema	56	0.081

138	P	TRM003	Tremor	54	0.081

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

140		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.081

141	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.081

142		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.079

143	P	MSC005	Muscular Dystrophy	66	0.079

144	c	ACT068	Acute Cystitis	63	0.079

145		LWC001	Low Compliance Bladder	43	0.079

146	c	SZR022	Seizures, Benign Familial Neonatal, 1	42	0.079

147		MYT011	Myotonia	34	0.079

148		CYN003	Cyanide Poisoning	24	0.079

149	c	FML001	Familial Atrial Fibrillation	65	0.078

150		PRT036	Peritonitis	64	0.078

151	P	NRP001	Neuropathy	56	0.078

152	P	PHC003	Pheochromocytoma	71	0.076

153		ATH013	Atherosclerosis Susceptibility	65	0.076

154		CLT003	Colitis	62	0.076

155		MLL001	Molluscum Contagiosum	50	0.076

156		ADR040	Adrenal Gland Pheochromocytoma	46	0.076

157	P	CHR345	Chronic Pain	44	0.076

158	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.075

159	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.075

160	P	MYS003	Myasthenia Gravis	68	0.075

161		CRB039	Cerebrovascular Disease	67	0.075

162		HLC007	Helicobacter Pylori Infection	59	0.075

163	P	GLM007	Glomerulonephritis	57	0.075

164		GLC003	Glucose Intolerance	54	0.075

165	P	DST107	Distal Renal Tubular Acidosis	42	0.075

166		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.075

167	P	CLR023	Colorectal Cancer	99	0.073

168		ULC004	Ulcerative Colitis	73	0.073

169		ALC007	Alcohol Dependence	66	0.073

170	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.073

171	P	DBT005	Diabetes Insipidus	55	0.073

172	c	FML036	Familial Periodic Paralysis	44	0.073

173	P	BRS047	Breast Cancer	97	0.071

174	P	ALZ034	Alzheimer Disease	88	0.071

175		PLM010	Pulmonary Edema	54	0.071

176		NPH003	Nephrocalcinosis	51	0.071

177		ILS001	Ileus	51	0.071

178		PLP001	Pulpitis	49	0.071

179		BRN071	Brain Injury	49	0.071

180		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.071

181	P	RSP003	Respiratory Failure	74	0.070

182	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.070

183		ANX010	Anxiety	73	0.070

184	c	RHB024	Rhabdomyosarcoma 2	67	0.070

185	P	PRD008	Periodontitis	64	0.070

186	P	NPH012	Nephrotic Syndrome	60	0.070

187		CNT047	Contact Dermatitis	58	0.070

188		TRM010	Traumatic Brain Injury	51	0.070

189	P	PSD003	Pseudohypoaldosteronism	44	0.070

190	P	HYP120	Hypoaldosteronism	36	0.070

191		GLB015	Glioblastoma Multiforme	75	0.068

192		OTT002	Otitis Media	72	0.068

193		PLM001	Pulmonary Tuberculosis	69	0.068

194		NTR005	Nutritional Deficiency Disease	62	0.068

195	P	CTR002	Cataract	60	0.068

196		INS001	Insulinoma	60	0.068

197	P	HDC001	Headache	57	0.068

198		DNT012	Dental Caries	53	0.068

199		ART140	Arteries, Anomalies of	52	0.068

200	P	RNL015	Renal Hypertension	47	0.068

201	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.066

202	P	MLT020	Multiple Sclerosis	72	0.066

203	P	BRG001	Brugada Syndrome	71	0.066

204	P	PNM007	Pneumonia	68	0.066

205		RCK004	Rickets	68	0.066

206	P	PSR002	Psoriasis	62	0.066

207	P	ESP024	Esophagitis	62	0.066

208		PST011	Pustulosis of Palm and Sole	52	0.066

209		HYP017	Hypophosphatemia	50	0.066

210		ATX019	Ataxia with Vitamin E Deficiency	42	0.066

211		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	0.066

212		ALL014	Allergic Encephalomyelitis	38	0.066

213	c	ATM075	Autoimmune Encephalitis	38	0.066

214	c	FML159	Familial Periodic Paralyses	16	0.066

215	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.064

216		HMN044	Human Immunodeficiency Virus Type 1	71	0.064

217	P	LKM002	Leukemia	68	0.064

218		GST092	Gastroesophageal Reflux	67	0.064

219		DPR016	Depression	63	0.064

220	P	BND020	Bone Disease	59	0.064

221		GLS018	Glass Syndrome	57	0.064

222		IRN002	Iron Metabolism Disease	57	0.064

223	P	GST044	Gastritis	56	0.064

224		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.064

225		AMN003	Amnestic Disorder	54	0.064

226	P	LTR001	Lateral Sclerosis	54	0.064

227	P	DDN001	Duodenal Ulcer	52	0.064

228	P	BNG026	Benign Neonatal Seizures	49	0.064

229		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.064

230	P	AMY004	Amyloidosis	70	0.062

231	P	RHN004	Rhinitis	57	0.062

232	P	BPL003	Bipolar Disorder	56	0.062

233		IMP005	Impotence	52	0.062

234		PNG002	Pain Agnosia	51	0.062

235	c	SHR030	Short Qt Syndrome	46	0.062

236		MYC005	Myocardial Stunning	46	0.062

237	P	HMR005	Hemorrhoid	46	0.062

238	P	MYC033	Myoclonus	46	0.062

239		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.062

240	c	MJR024	Major Affective Disorder 9	41	0.062

241	c	MJR022	Major Affective Disorder 8	38	0.062

242	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.060

243		AST005	Asthma	76	0.060

244	c	ATR087	Atrial Standstill 1	75	0.060

245		GT001	Gout	64	0.060

246	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.060

247	P	EXN002	Exanthem	57	0.060

248		SCH014	Schistosomiasis	57	0.060

249		INT007	Intermediate Coronary Syndrome	55	0.060

250		PPL022	Papilloma	54	0.060

251	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	53	0.060

252	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	50	0.060

253	c	MCR120	Microvascular Complications of Diabetes 7	47	0.060

254	c	DRR009	Diarrhea 6	46	0.060

255		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.060

256		CHL079	Children's Interstitial Lung Disease	26	0.060

257	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.058

258	P	LYM118	Lymphoma	68	0.058

259		OST159	Osteogenic Sarcoma	66	0.058

260	P	MNN013	Meningitis	66	0.058

261	P	THY023	Thymoma	65	0.058

262	P	PLY014	Polycystic Kidney Disease	62	0.058

263	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.058

264		GST023	Gastric Ulcer	53	0.058

265	c	THY107	Thymoma, Familial	52	0.058

266	P	LCT001	Lactic Acidosis	51	0.058

267	P	ECL001	Eclampsia	50	0.058

268	P	RNV001	Renovascular Hypertension	48	0.058

269		HYP025	Hyperphosphatemia	48	0.058

270		DHY016	Dehydrated Hereditary Stomatocytosis 1 with or Without Pseudohyperkalemia and/or Perinatal Edema	46	0.058

271		HDN002	Head Injury	46	0.058

272		SYN036	Syncope	45	0.058

273		PPL052	Papillomatosis, Confluent and Reticulated	33	0.058

274	P	SCH015	Schizophrenia	74	0.056

275		DFC004	Deficiency Anemia	70	0.056

276	P	FRG001	Fragile X Syndrome	70	0.056

277		NRM005	Neuromuscular Disease	64	0.056

278	P	SNS001	Sensorineural Hearing Loss	60	0.056

279		PRM057	Paramyotonia Congenita of Von Eulenburg	58	0.056

280	P	ALC033	Alcohol Use Disorder	58	0.056

281		BCT022	Bacterial Infectious Disease	56	0.056

282		AGN016	Aging	56	0.056

283		HRT012	Heart Valve Disease	53	0.056

284	c	MCR113	Microvascular Complications of Diabetes 3	52	0.056

285		DMY004	Demyelinating Disease	52	0.056

286		DRM011	Dermatophytosis	52	0.056

287		47X002	47,xyy	49	0.056

288	P	BNG032	Benign Mesothelioma	46	0.056

289		ANR004	Anuria	46	0.056

290		IDP073	Idiopathic Hypercalciuria	43	0.056

291	c	MCR130	Microvascular Complications of Diabetes 6	41	0.056

292	c	MCR133	Microvascular Complications of Diabetes 4	41	0.056

293		ALD013	Aldosterone-Producing Adenoma	39	0.056

294		KCN010	Kcnq2-Related Disorders	27	0.056

295	P	LNG032	Lung Cancer	98	0.054

296	P	RHM011	Rheumatoid Arthritis	80	0.054

297		SCK003	Sickle Cell Anemia	74	0.054

298	P	ATS364	Autism	70	0.054

299		BRN024	Bronchitis	68	0.054

300		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.054

301	P	NTR004	Neutropenia	63	0.054

302	P	HYP069	Hyperparathyroidism	63	0.054

303		ANR007	Anorexia Nervosa	63	0.054

304	P	EPL140	Epilepsy, Idiopathic Generalized	62	0.054

305	P	VSC011	Vasculitis	62	0.054

306		ACQ007	Acquired Immunodeficiency Syndrome	60	0.054

307		LNG099	Lung Disease	60	0.054

308		SQM006	Squamous Cell Carcinoma	60	0.054

309		GST045	Gastroenteritis	59	0.054

310	P	PRP019	Peripheral Nervous System Disease	58	0.054

311		PRS047	Prostatitis	56	0.054

312	P	JRV004	Jervell and Lange-Nielsen Syndrome 1	56	0.054

313		FCL014	Focal Epilepsy	54	0.054

314	c	VRL010	Viral Hepatitis	52	0.054

315	P	MSC003	Muscular Atrophy	52	0.054

316		THR004	Thrombocytosis	51	0.054

317	P	SCK005	Sickle Cell Disease	50	0.054

318		LYM019	Lymphosarcoma	46	0.054

319	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.054

320		HPT004	Hepatic Coma	45	0.054

321	c	PRM038	Primary Agammaglobulinemia	44	0.054

322		HMP009	Haemophilus Influenzae	43	0.054

323	c	CHR098	Chronic Pyelonephritis	38	0.054

324	c	INT059	Internal Hemorrhoid	34	0.054

325		KCN014	Kcnq3-Related Disorders	9	0.054

326		CNN003	Conn's Syndrome	79	0.052

327	P	PRK057	Parkinson Disease, Late-Onset	78	0.052

328		CRH001	Crohn's Disease	74	0.052

329	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	65	0.052

330	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.052

331		PLM031	Poliomyelitis	64	0.052

332		TRN015	Transient Cerebral Ischemia	63	0.052

333		HPT019	Hepatic Encephalopathy	60	0.052

334		THY029	Thyroid Carcinoma	59	0.052

335	P	LDD007	Liddle Syndrome 1	59	0.052

336	P	INT070	Intestinal Obstruction	58	0.052

337		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.052

338		TNS005	Tonsillitis	57	0.052

339		PHR003	Pharyngitis	57	0.052

340	P	INF037	Inflammatory Bowel Disease	54	0.052

341	P	AST007	Astrocytoma	51	0.052

342		SQM002	Squamous Cell Papilloma	46	0.052

343		SPS057	Spasticity	45	0.052

344		PTT037	Pituitary Tumors	44	0.052

345		MST020	Mast Cell Activation Syndrome	26	0.052

346		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.049

347		IMM167	Immune Deficiency Disease	78	0.049

348		OST012	Osteoarthritis	78	0.049

349		CRV035	Cervical Cancer	76	0.049

350	P	GRF003	Graft-Versus-Host Disease	72	0.049

351		CRT072	Creutzfeldt-Jakob Disease	70	0.049

352	P	SYS005	Systemic Scleroderma	68	0.049

353	P	MCR115	Microvascular Complications of Diabetes 5	66	0.049

354	c	DBT099	Diabetes Mellitus, Type I	65	0.049

355	P	MVM001	Movement Disease	63	0.049

356		ERL001	Early Myoclonic Encephalopathy	62	0.049

357		LPD008	Lipid Metabolism Disorder	62	0.049

358	c	SVR001	Severe Acute Respiratory Syndrome	62	0.049

359		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.049

360		FTT001	Fatty Liver Disease	61	0.049

361	P	BCL017	B-Cell Lymphoma	58	0.049

362	P	URT039	Urticaria	58	0.049

363	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.049

364		GST050	Gastrointestinal System Disease	56	0.049

365	P	ART021	Arteriosclerosis	54	0.049

366		DBT010	Diabetic Neuropathy	54	0.049

367	c	XNT010	Xanthinuria, Type I	53	0.049

368		SZR026	Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance	51	0.049

369		STM007	Stomatitis	50	0.049

370		ECT026	Ectopic Pregnancy	50	0.049

371		INT067	Interstitial Nephritis	48	0.049

372		CRN019	Coronary Artery Vasospasm	46	0.049

373		GNG003	Gingival Recession	44	0.049

374	c	SYS001	Systemic Lupus Erythematosus	86	0.047

375		INS024	Insulin-Like Growth Factor I	79	0.047

376	P	HNT016	Huntington Disease	72	0.047

377	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.047

378	c	LNG044	Long Qt Syndrome 1	66	0.047

379	P	DYS154	Dystonia	65	0.047

380		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.047

381		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.047

382		MDD011	Mood Disorder	62	0.047

383		CHL068	Cholestasis	61	0.047

384	c	ACT027	Acute Pancreatitis	60	0.047

385	P	MYC008	Myocarditis	59	0.047

386	P	SYP003	Syphilis	58	0.047

387	P	END033	Endocarditis	57	0.047

388		ALL010	Allergic Contact Dermatitis	56	0.047

389		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.047

390		PRT038	Protein-Energy Malnutrition	54	0.047

391		PRP016	Paraplegia	52	0.047

392		DYS015	Dysentery	52	0.047

393		TLN003	Telangiectasis	52	0.047

394	P	MGR003	Migraine with Aura	52	0.047

395		ENT011	Enterocolitis	51	0.047

396		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.047

397		NTR046	Neutrophil Migration	50	0.047

398		QDR001	Quadriplegia	48	0.047

399		TBR011	Tuberculous Meningitis	48	0.047

400		RNL077	Renal Fibrosis	47	0.047

401		CRD137	Cardiogenic Shock	47	0.047

402		SBC016	Subacute Delirium	44	0.047

403		CRB090	Cerebral Hypoxia	44	0.047

404	P	HYP265	Hypotonia	43	0.047

405		CYT002	Cytokine Deficiency	42	0.047

406	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.047

407		HYP540	Hypertension, Diastolic	40	0.047

408	P	FML187	Familial Hypertension	37	0.047

409	P	PRD017	Periodic Paralyses	25	0.047

410	P	HPT023	Hepatocellular Carcinoma	100	0.044

411	P	PRS040	Prostate Cancer	97	0.044

412	c	LKM061	Leukemia, Acute Myeloid	84	0.044

413		PRP027	Peripheral Vascular Disease	71	0.044

414	P	SLP006	Sleep Apnea	69	0.044

415		LYM133	Lymphoma, Hodgkin, Classic	69	0.044

416	P	MYC084	Mycobacterium Tuberculosis 1	68	0.044

417	P	INF038	Influenza	68	0.044

418	c	ATS007	Autism Spectrum Disorder	67	0.044

419		MSC007	Muscle Hypertrophy	64	0.044

420		OST017	Osteomyelitis	64	0.044

421		SKN016	Skin Disease	63	0.044

422	P	END044	Endometriosis	63	0.044

423	P	HMN010	Hemangioma	61	0.044

424		DPH001	Diphtheria	60	0.044

425	c	HYP731	Hyperaldosteronism, Familial, Type I	60	0.044

426	c	ACT073	Acute Leukemia	58	0.044

427		MNT002	Mental Depression	58	0.044

428		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.044

429		CMM005	Common Cold	57	0.044

430		ALL006	Allergic Asthma	56	0.044

431	P	HYP050	Hyperinsulinemic Hypoglycemia	55	0.044

432	P	RNL017	Renal Oncocytoma	53	0.044

433		INF034	Infective Endocarditis	53	0.044

434		THY030	Thyroid Gland Disease	52	0.044

435		PTH003	Pathologic Nystagmus	52	0.044

436	c	PYR010	Peyronie's Disease	50	0.044

437	P	OVR082	Overgrowth Syndrome	50	0.044

438		PYD002	Pyoderma	50	0.044

439	P	NNT009	Neonatal Diabetes Mellitus	50	0.044

440	c	BNG006	Benign Familial Neonatal Epilepsy	50	0.044

441	P	MYT002	Myotonic Dystrophy	49	0.044

442		CLS016	Clostridium Difficile Colitis	48	0.044

443		PYL006	Pyloric Stenosis	48	0.044

444	c	BRT050	Bartter Syndrome, Type 2, Antenatal	46	0.044

445	c	DBT103	Diabetes Mellitus, Permanent Neonatal 4	46	0.044

446	c	MLG068	Malignant Glioma	46	0.044

447		KWS001	Kwashiorkor	44	0.044

448		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.044

449	c	KCN020	Kcnt1-Related Epilepsy	14	0.044

450		LPT014	Leptin Deficiency or Dysfunction	74	0.041

451	P	ART022	Arthritis	69	0.041

452		CRB037	Cerebral Palsy	69	0.041

453	P	OCL013	Oculodentodigital Dysplasia	69	0.041

454		CNN005	Connective Tissue Disease	68	0.041

455	P	MLG056	Malignant Hyperthermia	67	0.041

456		WLF001	Wolff-Parkinson-White Syndrome	66	0.041

457	P	DMN002	Dementia	66	0.041

458	P	CNJ013	Conjunctivitis	65	0.041

459	P	MTR014	Motor Neuron Disease	65	0.041

460		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.041

461	P	HML002	Hemolytic Anemia	63	0.041

462	P	HYP750	Hypertriglyceridemia, Familial	62	0.041

463	P	MYL006	Myeloid Leukemia	60	0.041

464	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.041

465	P	SLP005	Sleep Disorder	59	0.041

466	P	DBT100	Diabetes Mellitus, Permanent Neonatal 1	59	0.041

467		MNR012	Meniere Disease	57	0.041

468		CMR002	Coumarin Resistance	56	0.041

469	P	MYT023	Myotonia Congenita	56	0.041

470	P	SCK002	Sick Sinus Syndrome	55	0.041

471	P	PMP001	Pemphigus	54	0.041

472		NNL006	Non-Alcoholic Steatohepatitis	54	0.041

473	P	RTN016	Retinal Degeneration	53	0.041

474		MRG003	Marginal Zone B-Cell Lymphoma	52	0.041

475	P	RCT021	Rectum Cancer	52	0.041

476		PPT001	Peptic Esophagitis	52	0.041

477		KRT009	Keratosis	51	0.041

478		PNN001	Panniculitis	51	0.041

479		TRY001	Trypanosomiasis	50	0.041

480		DYS073	Dysphagia	50	0.041

481	c	SPN311	Spinocerebellar Ataxia 13	50	0.041

482	c	BRT042	Bartter Syndrome, Type 3	46	0.041

483		ACT003	Acute Kidney Tubular Necrosis	45	0.041

484		49X006	49, Xxxxy Syndrome	41	0.041

485	P	DYS021	Dysautonomia	39	0.041

486		VLK001	Volkmann Contracture	25	0.041

487		OBN001	Ouabain Resistance	18	0.041

488	P	OVR042	Ovarian Cancer	88	0.038

489		MYL069	Myeloma, Multiple	85	0.038

490	P	BLD134	Bladder Cancer	79	0.038

491		BRN028	Brain Cancer	74	0.038

492		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.038

493		MNT001	Mantle Cell Lymphoma	69	0.038

494	P	HPT021	Hepatitis	67	0.038

495	P	HYP098	Hypereosinophilic Syndrome	67	0.038

496	P	NSP012	Nasopharyngeal Carcinoma	66	0.038

497		CHG001	Chagas Disease	66	0.038

498	P	PLM036	Pulmonary Fibrosis	65	0.038

499	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.038

500		SRC014	Sarcoma	65	0.038

501		IRR002	Irritable Bowel Syndrome	65	0.038

502	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.038

503	P	PNC044	Pancreatitis	61	0.038

504		GST033	Gestational Diabetes	61	0.038

505		SDD001	Sudden Infant Death Syndrome	61	0.038

506	P	LPS004	Lupus Erythematosus	61	0.038

507		VRC005	Varicose Veins	60	0.038

508		ETN001	Eating Disorder	60	0.038

509	P	BNC003	Bone Cancer	58	0.038

510	c	DWL002	Dowling-Degos Disease 1	58	0.038

511	P	ESP035	Esophagitis, Eosinophilic, 1	57	0.038

512	P	ANG015	Angioedema	57	0.038

513	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.038

514		URN010	Urinary Tract Obstruction	55	0.038

515		AMN001	Amenorrhea	54	0.038

516		SNS003	Sensory Peripheral Neuropathy	54	0.038

517		FNG017	Fungal Infectious Disease	53	0.038

518		SPN035	Spindle Cell Sarcoma	53	0.038

519	P	THY032	Thyroiditis	52	0.038

520		CRN030	Coronary Stenosis	50	0.038

521	c	SVR005	Severe Pre-Eclampsia	50	0.038

522		ENT004	Enthesopathy	49	0.038

523		WTH001	Withdrawal Disorder	48	0.038

524		ASP007	Aspiration Pneumonia	48	0.038

525	c	MLG069	Malignant Hypertension	47	0.038

526		RTN023	Retinitis	46	0.038

527		ATN005	Autonomic Dysfunction	46	0.038

528		RTN020	Retinal Vascular Disease	46	0.038

529	P	BRT053	Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness	46	0.038

530		BRN032	Brain Glioma	45	0.038

531		ATN011	Autoinflammation with Infantile Enterocolitis	44	0.038

532	c	BRT052	Bartter Syndrome, Type 1, Antenatal	43	0.038

533		TRP009	Triple X Syndrome	42	0.038

534		NRR001	Neuroretinitis	42	0.038

535		MDL009	Medullary Sponge Kidney	40	0.038

536		PRM020	Premenstrual Tension	40	0.038

537	c	PSD092	Pseudohypoaldosteronism, Type Iie	39	0.038

538	c	HYP438	Hyperaldosteronism, Familial, Type Iii	35	0.038

539	c	THY084	Thyrotoxic Periodic Paralysis 1	35	0.038

540	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.038

541		MTH071	Methane Production	26	0.038

542		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.038

543		URT049	Urate Oxidase, Pseudogene	25	0.038

544		ADG002	Audiogenic Seizures	25	0.038

545		PRN068	Paraneoplastic Limbic Encephalitis	21	0.038

546		CNV009	Convulsions Benign Familial Neonatal Dominant Form	17	0.038

547		KCN019	Kcnk9 Imprinting Syndrome	13	0.038

548	P	PNC035	Pancreatic Cancer	84	0.035

549	c	DLT002	Dilated Cardiomyopathy	79	0.035

550	P	RTN008	Retinitis Pigmentosa	79	0.035

551	P	LNG064	Lung Cancer Susceptibility 3	78	0.035

552	P	MDL005	Medulloblastoma	77	0.035

553		MSC157	Muscular Dystrophy, Duchenne Type	72	0.035

554	c	LKM063	Leukemia, Chronic Myeloid	72	0.035

555		WLS001	Wilson Disease	71	0.035

556	P	SRC025	Sarcoidosis 1	70	0.035

557		GST040	Gastric Adenocarcinoma	70	0.035

558	P	MLN008	Melanoma	69	0.035

559	P	LPR021	Leprosy 3	69	0.035

560		BRK010	Burkitt Lymphoma	67	0.035

561	P	FLL037	Follicular Lymphoma	67	0.035

562		ALL003	Allergic Rhinitis	67	0.035

563		PSY004	Psychotic Disorder	67	0.035

564	c	MCR129	Microvascular Complications of Diabetes 1	66	0.035

565		KRT019	Keratitis, Hereditary	65	0.035

566		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.035

567	c	ART101	Aortic Valve Disease 2	65	0.035

568	P	ADL010	Adult Respiratory Distress Syndrome	65	0.035

569	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.035

570	c	EPS035	Episodic Ataxia, Type 2	63	0.035

571		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	63	0.035

572		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.035

573	c	HPT001	Hepatitis C	62	0.035

574	c	HPT003	Hepatitis a	62	0.035

575		APP008	Appendicitis	61	0.035

576		ACN002	Acanthosis Nigricans	60	0.035

577		HYD002	Hydronephrosis	60	0.035

578		PLM033	Pulmonary Embolism	59	0.035

579		GNG013	Gingivitis	59	0.035

580		BRN002	Bronchiolitis	59	0.035

581		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.035

582	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.035

583		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.035

584		BNG009	Benign Epilepsy with Centrotemporal Spikes	58	0.035

585	P	CND004	Candidiasis	58	0.035

586	P	INF032	Infertility	57	0.035

587		CHL067	Cholecystitis	57	0.035

588	c	VSC019	Vesicoureteral Reflux 1	57	0.035

589		THR024	Thrombosis	57	0.035

590		CHR177	Chromophobe Renal Cell Carcinoma	57	0.035

591		VSC002	Vascular Dementia	57	0.035

592	c	INT072	Intestinal Pseudo-Obstruction	56	0.035

593		MCR141	Mucormycosis	56	0.035

594	P	HYP024	Hypoparathyroidism	56	0.035

595	P	MYP006	Myopia	55	0.035

596		LYM040	Lymphoblastic Lymphoma	54	0.035

597	c	LNG048	Long Qt Syndrome 3	53	0.035

598		INT075	Intracranial Hypertension	53	0.035

599	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.035

600		MCN017	Meconium Ileus	52	0.035

601		SPL004	Splenic Marginal Zone Lymphoma	51	0.035

602		HYP781	Hypoascorbemia	51	0.035

603		INT071	Intestinal Perforation	51	0.035

604	c	ALM001	Al Amyloidosis	50	0.035

605		ALL009	Allergic Conjunctivitis	50	0.035

606	c	CNG027	Congenital Hemolytic Anemia	50	0.035

607		VLV047	Volvulus of Midgut	49	0.035

608	c	FLL041	Follicular Lymphoma 1	49	0.035

609		VCC001	Vaccinia	49	0.035

610		KRT002	Keratomalacia	47	0.035

611		PLS025	Plasmablastic Lymphoma	47	0.035

612	c	PRM093	Premature Ovarian Failure 7	47	0.035

613	P	MTH007	Methemoglobinemia	46	0.035

614		NWC001	Newcastle Disease	45	0.035

615		PRL008	Paralytic Ileus	45	0.035

616	c	PCH010	Pachyonychia Congenita 3	44	0.035

617		CVD001	Covid-19	44	0.035

618		IDP033	Idiopathic Edema	44	0.035

619		DVR002	Diverticulitis	43	0.035

620		ORL015	Oral Squamous Cell Carcinoma	43	0.035

621		SNL007	Senile Cataract	42	0.035

622	c	FML294	Familial Short Qt Syndrome	41	0.035

623		PRS063	Paresthesia	41	0.035

624	c	MCR112	Microvascular Complications of Diabetes 2	41	0.035

625		ENT001	Enterocele	39	0.035

626		HRN029	Hearing Loss, Noise-Induced	37	0.035

627		CHR178	Chromosomal Triplication	35	0.035

628		HNS001	Hansen's Disease	34	0.035

629		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.035

630	P	VSC018	Visceral Steatosis	33	0.035

631	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.035

632		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.035

633		CYT018	Cytochrome P450 2d6 Variant	27	0.035

634	c	BRT024	Bartter Syndrome Type 4	20	0.035

635		CRM010	Cramp-Fasciculation Syndrome	16	0.035

636		ESP021	Esophageal Cancer	90	0.031

637		NRL016	Neural Tube Defects	82	0.031

638	c	NRF023	Neurofibromatosis, Type Ii	80	0.031

639		GST019	Gastrointestinal Stromal Tumor	78	0.031

640		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.031

641		END057	Endometrial Cancer	74	0.031

642	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.031

643	c	HPT073	Hepatitis C Virus	72	0.031

644		ACR007	Acromegaly	71	0.031

645		MYL009	Myelodysplastic Syndrome	70	0.031

646	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.031

647	P	ESS003	Essential Thrombocythemia	68	0.031

648	P	MJR001	Major Depressive Disorder	68	0.031

649		MYC006	Mycosis Fungoides	66	0.031

650		LPT001	Leptospirosis	66	0.031

651	P	SKN015	Skin Carcinoma	66	0.031

652	c	DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.031

653	P	HYD006	Hydrocephalus	66	0.031

654	P	DRM053	Dermatitis, Atopic	66	0.031

655		MYL031	Myeloproliferative Neoplasm	66	0.031

656	P	NRV007	Nervous System Disease	66	0.031

657	c	SML038	Small Cell Cancer of the Lung	65	0.031

658		KHL003	Kohlschutter-Tonz Syndrome	65	0.031

659	P	MTR004	Maturity-Onset Diabetes of the Young	65	0.031

660	P	HRP006	Herpes Simplex	65	0.031

661		APN008	Apnea, Obstructive Sleep	64	0.031

662	P	ANR048	Aniridia 1	63	0.031

663	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.031

664		TYP007	Typhoid Fever	63	0.031

665	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.031

666	P	MCH002	Machado-Joseph Disease	62	0.031

667	P	EPL198	Epilepsy, Myoclonic Juvenile	62	0.031

668	P	ART023	Arthropathy	62	0.031

669	P	PRM006	Primary Biliary Cirrhosis	62	0.031

670		OST003	Osteonecrosis	61	0.031

671		WST001	West Syndrome	61	0.031

672		YLL002	Yellow Fever	61	0.031

673		VRL011	Viral Infectious Disease	61	0.031

674		RHM001	Rheumatic Fever	60	0.031

675		SPP011	Suppression of Tumorigenicity 12	59	0.031

676		PRT013	Portal Hypertension	59	0.031

677	c	DNG003	Dengue Disease	59	0.031

678		CHL123	Chlamydia	59	0.031

679	P	BRS044	Breast Adenocarcinoma	59	0.031

680	P	GLL022	Guillain-Barre Syndrome	59	0.031

681		ANR040	Aneurysm	59	0.031

682		BLR008	Bilirubin Metabolic Disorder	57	0.031

683		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.031

684	c	FML035	Familial Hyperlipidemia	55	0.031

685		ANG005	Anogenital Venereal Wart	55	0.031

686		ESN005	Eosinophilic Gastroenteritis	55	0.031

687	P	DRM007	Dermatitis Herpetiformis	55	0.031

688	P	SLM003	Salmonellosis	55	0.031

689		PRP030	Purpura	54	0.031

690		RSC001	Rosacea	54	0.031

691		PYD001	Pyoderma Gangrenosum	54	0.031

692		THR013	Thoracic Outlet Syndrome	54	0.031

693		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.031

694	P	FML023	Familial Hemiplegic Migraine	53	0.031

695		OCL006	Ocular Hypertension	53	0.031

696		MST005	Mastitis	53	0.031

697	c	PRD040	Periodontitis, Chronic	53	0.031

698		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.031

699	P	ACT008	Actinic Keratosis	53	0.031

700	P	RTN018	Retinal Disease	53	0.031

701		ACR041	Acromelic Frontonasal Dysostosis	52	0.031

702		ONC002	Onchocerciasis	52	0.031

703		PLS009	Plasma Cell Neoplasm	51	0.031

704		IFP001	Ifap Syndrome with or Without Bresheck Syndrome	51	0.031

705		NRM004	Neuroma	51	0.031

706	c	SCN007	Secondary Hyperparathyroidism	51	0.031

707		HPT014	Hepatorenal Syndrome	50	0.031

708	c	INF145	Infantile Liver Failure Syndrome 1	50	0.031

709		PLC008	Placenta Disease	50	0.031

710		SNT005	Sinoatrial Node Disease	49	0.031

711		CHL004	Cholelithiasis	49	0.031

712		LRN003	Learning Disability	49	0.031

713	c	BCT013	Bacterial Pneumonia	48	0.031

714	P	ATS011	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy	48	0.031

715		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.031

716		CHR031	Chromoblastomycosis	47	0.031

717		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.031

718		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.031

719		MNG006	Monogenic Diabetes	46	0.031

720		URT010	Ureteral Obstruction	45	0.031

721		CYN002	Cyanosis, Transient Neonatal	45	0.031

722		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.031

723		ATN004	Autonomic Neuropathy	45	0.031

724		PNC085	Penicillin Allergy	45	0.031

725		GRN017	Granulocytopenia	44	0.031

726	P	BCT020	Bacteremia 2	44	0.031

727		GRN007	Granuloma Annulare	44	0.031

728	P	MYG005	Myoglobinuria	44	0.031

729		BCK006	Back Pain	42	0.031

730		BRK002	Birk-Barel Syndrome	41	0.031

731		RDN001	Reading Disorder	40	0.031

732		FNG016	Fungal Keratitis	40	0.031

733		LKP003	Leukoplakia	39	0.031

734		WLL004	Wallerian Degeneration	39	0.031

735		HYP344	Hyperthyroidism, Familial Gestational	39	0.031

736		AMN006	Aminoaciduria	38	0.031

737		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.031

738	P	ANT061	Antenatal Bartter Syndrome	37	0.031

739	c	RNL046	Renal Tubular Acidosis, Distal, Autosomal Dominant	37	0.031

740		SCR003	Secretory Diarrhea	37	0.031

741	P	MXL015	Maxillary Sinusitis	36	0.031

742	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.031

743	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.031

744	c	PRG106	Progressive Muscular Dystrophy	33	0.031

745	c	THY083	Thyrotoxic Periodic Paralysis 2	31	0.031

746		PLY150	Polykaryocytosis Inducer	31	0.031

747		SLC024	Slc4a1-Associated Distal Renal Tubular Acidosis	19	0.031

748	P	ATX030	Ataxia-Telangiectasia	82	0.027

749	P	GLM040	Glioma Susceptibility 1	81	0.027

750		SVR004	Severe Combined Immunodeficiency	73	0.027

751	c	SPN225	Spondyloarthropathy 1	73	0.027

752		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.027

753		MYL005	Myelofibrosis	70	0.027

754	P	TTR001	Tetralogy of Fallot	70	0.027

755	P	TBR001	Tuberous Sclerosis	70	0.027

756		PLY001	Polycythemia Vera	69	0.027

757	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.027

758		ART016	Aortic Aneurysm	69	0.027

759	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.027

760	P	ANG001	Angelman Syndrome	69	0.027

761		PNC129	Pancreatic Adenocarcinoma	68	0.027

762	P	THR014	Thrombocytopenia	67	0.027

763		GLL008	Gilles De La Tourette Syndrome	66	0.027

764		PPL049	Papillon-Lefevre Syndrome	65	0.027

765	P	LPS002	Liposarcoma	65	0.027

766		BRR014	Barrett Esophagus	65	0.027

767		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	65	0.027

768		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.027

769		CLN015	Colon Adenocarcinoma	65	0.027

770	P	CHR071	Charcot-Marie-Tooth Disease	65	0.027

771	P	RHB003	Rhabdomyosarcoma	63	0.027

772	P	HRD008	Hereditary Hemorrhagic Telangiectasia	63	0.027

773		HMT002	Hematologic Cancer	62	0.027

774	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	62	0.027

775	c	DYS056	Dystonia 12	62	0.027

776	P	BCK002	Beckwith-Wiedemann Syndrome	62	0.027

777		MSL001	Measles	62	0.027

778		INT002	Intermittent Claudication	61	0.027

779		TMT001	Timothy Syndrome	61	0.027

780		CHR066	Chronic Fatigue Syndrome	61	0.027

781		WLD007	Waldenstroem's Macroglobulinemia	61	0.027

782		PNM010	Pneumothorax, Primary Spontaneous	60	0.027

783		SZR001	Sezary's Disease	60	0.027

784		TRG002	Trigeminal Neuralgia	60	0.027

785		INT066	Interstitial Lung Disease	60	0.027

786		ING001	Inguinal Hernia	60	0.027

787	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.027

788		IDP011	Idiopathic Interstitial Pneumonia	59	0.027

789	c	HPT016	Hepatitis B	59	0.027

790	P	BRN022	Bronchiectasis	59	0.027

791		CYS010	Cystinosis	59	0.027

792	c	SPN301	Spinocerebellar Ataxia 2	58	0.027

793		PST028	Post-Traumatic Stress Disorder	58	0.027

794		FBR047	Fibromyalgia	58	0.027

795		CHR072	Chordoma	58	0.027

796		NWB001	Newborn Respiratory Distress Syndrome	58	0.027

797	P	GLL020	Gallbladder Disease	57	0.027

798	P	PLV020	Pelvic Organ Prolapse	57	0.027

799		BLM002	Bulimia Nervosa	57	0.027

800		BRN056	Bronchopulmonary Dysplasia	57	0.027

801	P	PLY041	Polymyositis	57	0.027

802	c	MST023	Mesothelioma, Malignant	57	0.027

803	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.027

804		PNM008	Pneumothorax	56	0.027

805	P	PLY018	Polycythemia	56	0.027

806	P	ADL017	Adult T-Cell Leukemia	56	0.027

807		LST001	Listeriosis	56	0.027

808		PLS011	Plasmacytoma	56	0.027

809	c	ACT134	Acute Liver Failure	56	0.027

810		ADN027	Adenomyosis	56	0.027

811		INS023	Insensitivity to Pain, Congenital, with Anhidrosis	56	0.027

812		ADR056	Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete	56	0.027

813	P	NRF002	Neurofibromatosis	56	0.027

814	P	PNM006	Pneumoconiosis	56	0.027

815	P	PLY019	Polyneuropathy	56	0.027

816		NRN004	Neuroendocrine Tumor	55	0.027

817	P	MLN007	Male Infertility	55	0.027

818	c	BCT007	Bacterial Meningitis	55	0.027

819		HMP005	Hemiplegia	55	0.027

820	c	PRG043	Progressive Familial Heart Block, Type Ib	54	0.027

821		CRT017	Cartilage Disease	54	0.027

822	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.027

823		PRC013	Pericarditis	54	0.027

824		CLL003	Cellulitis	54	0.027

825	P	TCD001	Tic Disorder	53	0.027

826	P	HMR003	Hemorrhagic Disease	53	0.027

827		NRT001	Neurotic Disorder	53	0.027

828		TXC002	Toxic Encephalopathy	53	0.027

829		ALC009	Alcoholic Liver Cirrhosis	53	0.027

830		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.027

831		NRT004	Neuritis	52	0.027

832		MYC080	Myoclonic Epilepsy of Unverricht and Lundborg	52	0.027

833	P	HMP007	Hemophilia	51	0.027

834	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.027

835		THR016	Thrombophlebitis	51	0.027

836		ACH005	Achalasia	51	0.027

837		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.027

838		HYP081	Hypolipoproteinemia	51	0.027

839		RSP002	Respiratory Syncytial Virus Infectious Disease	51	0.027

840	P	HYP077	Hypertrichosis	50	0.027

841	c	PRM012	Primary Polycythemia	50	0.027

842		AZS001	Azoospermia	50	0.027

843		OPT003	Opiate Dependence	50	0.027

844	c	DYS119	Dystonia 9	50	0.027

845	P	OTS001	Otosclerosis	49	0.027

846		ATY042	Atypical Chronic Myeloid Leukemia	49	0.027

847		URT001	Urethritis	49	0.027

848	c	THR090	Thrombocythemia 1	49	0.027

849		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.027

850		GYN001	Gynecomastia	49	0.027

851		CCN002	Cocaine Abuse	49	0.027

852	P	OPN001	Open-Angle Glaucoma	49	0.027

853		MCR004	Macroglobulinemia	49	0.027

854	c	BPL002	Bipolar I Disorder	49	0.027

855		ACT029	Acute Interstitial Pneumonia	49	0.027

856	P	CMP008	Compartment Syndrome	49	0.027

857		BCT004	Bacteriuria	49	0.027

858	P	CTN015	Cutaneous T Cell Lymphoma	49	0.027

859	P	CNT056	Cantu Syndrome	48	0.027

860	c	ACT150	Acute Adrenal Insufficiency	48	0.027

861		INT054	Intraocular Lymphoma	48	0.027

862		ATS010	Autosomal Recessive Disease	48	0.027

863		CHR563	Chronic Eosinophilic Leukemia	48	0.027

864	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.027

865		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.027

866		BLD044	Bladder Disease	48	0.027

867	P	MRC003	Mercury Poisoning	48	0.027

868		ANT018	Anthracosis	48	0.027

869		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.027

870		THY128	Thyroid Tumor	47	0.027

871		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.027

872	P	CRC039	Coarctation of Aorta	47	0.027

873	P	OVR046	Ovarian Cyst	47	0.027

874		MNC019	Monocarboxylate Transporter 1 Deficiency	47	0.027

875	P	VTR007	Vitreoretinopathy	46	0.027

876	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.027

877		TNP001	Tinea Pedis	46	0.027

878		PRP017	Periapical Periodontitis	46	0.027

879		CLN045	Colonic Benign Neoplasm	46	0.027

880		EXT010	Extramedullary Plasmacytoma	45	0.027

881		LYM051	Lymphomatoid Granulomatosis	45	0.027

882		CRT015	Carotid Artery Occlusion	45	0.027

883		CNT017	Central Nervous System Origin Vertigo	45	0.027

884		ASP008	Aspiration Pneumonitis	45	0.027

885		HRT015	Heritable Pulmonary Arterial Hypertension	44	0.027

886	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.027

887		DMP001	Dumping Syndrome	44	0.027

888		MYX004	Myxedema	43	0.027

889		BNM001	Bone Marrow Cancer	43	0.027

890	P	CND005	Cone Dystrophy	43	0.027

891		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.027

892	P	MJR007	Major Affective Disorder 1	43	0.027

893	c	AGR019	Age-Related Hearing Loss	42	0.027

894		MRS001	Marasmus	42	0.027

895		CHR286	Chronic Neutrophilic Leukemia	42	0.027

896		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.027

897	c	LNG053	Long Qt Syndrome 9	41	0.027

898		GST020	Gastric Antral Vascular Ectasia	41	0.027

899		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.027

900		RST023	Resting Heart Rate, Variation in	41	0.027

901		CRN322	Coronavirus Infectious Disease	40	0.027

902		VLL006	Villous Adenoma	40	0.027

903		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.027

904		ANG049	Angioedema Induced by Ace Inhibitors	40	0.027

905	P	FML156	Familial Hyperaldosteronism	39	0.027

906		CRV045	Cervical Intraepithelial Neoplasia	39	0.027

907	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.027

908		SCR011	Scrapie	39	0.027

909		URT004	Urethral Syndrome	38	0.027

910		VLV042	Vulvar Vestibulitis Syndrome	38	0.027

911		TNC002	Tinea Capitis	38	0.027

912	P	PST059	Pustular Psoriasis	37	0.027

913		ATM052	Autoimmune Disease 1	37	0.027

914	P	CRB088	Cerebral Atrophy	37	0.027

915		MYL067	Myeloproliferative Disorder, Chronic, with Eosinophilia	37	0.027

916		TMP011	Temple-Baraitser Syndrome	36	0.027

917		DRM009	Dermatomycosis	36	0.027

918		ABD010	Abdominal Wall Defect	36	0.027

919		MYT003	Myotonic Disease	35	0.027

920		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	35	0.027

921		CRY019	Cryohydrocytosis	34	0.027

922	c	LKM005	Leukemia, T-Cell, Chronic	34	0.027

923		PST010	Pasteurellosis	34	0.027

924		BNN005	Bunion	33	0.027

925	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.027

926		HND015	Hand Skill, Relative	33	0.027

927		CND006	Candida Glabrata	32	0.027

928		CNG064	Congenital Chloride Diarrhea	32	0.027

929	c	PSD090	Pseudohypoaldosteronism, Type Iia	32	0.027

930		CLN006	Colonic Pseudo-Obstruction	32	0.027

931	c	PSD093	Pseudohypoaldosteronism, Type Iid	31	0.027

932	P	RNL115	Renal Tubular Acidosis, Proximal	31	0.027

933		INF021	Infant Gynecomastia	31	0.027

934		KPP002	Keppen-Lubinsky Syndrome	31	0.027

935	P	ATS382	Autosomal Dominant Tubulointerstitial Kidney Disease	30	0.027

936		FNT004	Fainting	30	0.027

937		PST092	Posttransplant Acute Limbic Encephalitis	29	0.027

938		EPL230	Epilepsy with Myoclonic-Atonic Seizures	28	0.027

939	c	LNG052	Long Qt Syndrome 8	27	0.027

940		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.027

941	c	HRD219	Hereditary Distal Renal Tubular Acidosis	27	0.027

942		MYP026	Myopathy - Thyrotoxic	17	0.027

943		DGT004	Digitalis Poisoning	14	0.027

944		HRD103	Hereditary Motor and Sensory Neuropathy with Agenesis of the Corpus Callosum	13	0.027

945		NNP018	Non-Paraneoplastic Limbic Encephalitis	12	0.027

946	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.022

947		MLR004	Malaria	81	0.022

948	P	RTT002	Rett Syndrome	80	0.022

949		MRF001	Marfan Syndrome	77	0.022

950	c	TBR025	Tuberous Sclerosis 1	77	0.022

951		ADR007	Adrenoleukodystrophy	75	0.022

952	P	APL001	Aplastic Anemia	74	0.022

953	P	FML018	Familial Mediterranean Fever	73	0.022

954		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.022

955		EWN003	Ewing Sarcoma	69	0.022

956	c	MYT021	Myotonic Dystrophy 1	69	0.022

957	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.022

958		SKN019	Skin Melanoma	68	0.022

959	P	ALP004	Alport Syndrome	68	0.022

960	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.022

961		FCT007	Factor Vii Deficiency	67	0.022

962	c	HMP029	Hemophilia a	67	0.022

963		GRG001	Greig Cephalopolysyndactyly Syndrome	66	0.022

964		LYS012	Lysosomal Acid Lipase Deficiency	65	0.022

965		ANG020	Angiosarcoma	64	0.022

966		CLR108	Colorectal Adenoma	64	0.022

967		BRC012	Brucellosis	64	0.022

968		ART002	Arts Syndrome	64	0.022

969		CYS013	Cystinuria	63	0.022

970		ACT119	Acute Promyelocytic Leukemia	63	0.022

971		HYP780	Hypoadrenocorticism, Familial	63	0.022

972		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.022

973	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.022

974		HYD038	Hydrops Fetalis, Nonimmune	62	0.022

975	P	DRM010	Dermatomyositis	61	0.022

976		NRM001	Neuromyelitis Optica	61	0.022

977	P	CHL002	Childhood Absence Epilepsy	61	0.022

978	c	SCL052	Scleroderma, Familial Progressive	61	0.022

979		ALC006	Alcoholic Hepatitis	61	0.022

980		RTN017	Retinal Detachment	61	0.022

981	P	KDN017	Kidney Cancer	60	0.022

982		HRP004	Herpes Zoster	60	0.022

983		WLL001	Williams-Beuren Syndrome	60	0.022

984	P	VNT002	Ventricular Septal Defect	60	0.022

985	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.022

986		ORL011	Oral Cancer	60	0.022

987		STF001	Stiff-Person Syndrome	60	0.022

988	P	THL005	Thalassemia	60	0.022

989	P	OPT006	Optic Nerve Disease	60	0.022

990	P	LKD001	Leukodystrophy	59	0.022

991	P	SPN309	Spinocerebellar Ataxia 6	59	0.022

992		PRT058	Pure Autonomic Failure	59	0.022

993		PRN019	Perinatal Necrotizing Enterocolitis	59	0.022

994	P	PRD006	Prader-Willi Syndrome	59	0.022

995		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	59	0.022

996		GRD007	Grade Iii Astrocytoma	59	0.022

997		AVN001	Avian Influenza	59	0.022

998		IRN001	Iron Deficiency Anemia	59	0.022

999	P	NPH005	Nephronophthisis	59	0.022

1000		RNL024	Renal Glucosuria	58	0.022

1001		CRY005	Cryptococcosis	58	0.022

1002		ERY029	Erythermalgia, Primary	58	0.022

1003		FML063	Familial Glucocorticoid Deficiency	58	0.022

1004	c	PRM005	Primary Hyperparathyroidism	58	0.022

1005		ERY003	Erythema Multiforme	58	0.022

1006		EYD002	Eye Disease	58	0.022

1007		DSS008	Disease of Mental Health	58	0.022

1008	P	MMP001	Mumps	58	0.022

1009		APP015	Apparent Mineralocorticoid Excess	58	0.022

1010		EXT034	Extrinsic Allergic Alveolitis	58	0.022

1011	P	OPT009	Optic Neuritis	57	0.022

1012		LYM021	Lymphadenitis	57	0.022

1013	P	PRN023	Prion Disease	57	0.022

1014		APH001	Aphthous Stomatitis	57	0.022

1015	P	URF003	Urofacial Syndrome 1	57	0.022

1016	P	FBR017	Fibrosarcoma	56	0.022

1017		LMY014	Leiomyoma, Uterine	56	0.022

1018		ERY051	Erythroleukemia, Familial	56	0.022

1019		SFT003	Soft Tissue Sarcoma	56	0.022

1020		MTH009	Mouth Disease	56	0.022

1021		HMG005	Hemoglobinopathy	56	0.022

1022		INT030	Intracranial Aneurysm	56	0.022

1023	c	PRG126	Progressive Familial Heart Block	55	0.022

1024		ADR008	Adrenal Adenoma	55	0.022

1025		NRG002	Neurogenic Bladder	55	0.022

1026		FDB001	Foodborne Botulism	55	0.022

1027		PLV003	Pelvic Inflammatory Disease	55	0.022

1028	P	PTT006	Pituitary Adenoma	55	0.022

1029	P	STR020	Strabismus	55	0.022

1030	P	SBS003	Substance Abuse	55	0.022

1031		HDR002	Hidradenitis Suppurativa	55	0.022

1032	P	ALP106	Alport Syndrome 1, X-Linked	55	0.022

1033		END040	Endogenous Depression	55	0.022

1034		HRY003	Hairy Cell Leukemia	55	0.022

1035		SYN007	Synovitis	54	0.022

1036		VGN023	Vaginitis	54	0.022

1037	P	RST001	Restless Legs Syndrome	54	0.022

1038	P	NLD001	Nail Disease	54	0.022

1039	P	CYS039	Cystic Kidney Disease	54	0.022

1040		GST037	Gastroparesis	54	0.022

1041		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.022

1042		ANL018	Analbuminemia	54	0.022

1043	c	SPN294	Spinocerebellar Ataxia 1	53	0.022

1044		RHM028	Rheumatic Heart Disease	53	0.022

1045	P	INS002	in Situ Carcinoma	53	0.022

1046		KRT006	Keratoconjunctivitis	53	0.022

1047	P	MNC007	Monocytic Leukemia	53	0.022

1048		CRH005	Crohn's Colitis	53	0.022

1049		BRN038	Bronchial Disease	53	0.022

1050		HYP815	Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome	53	0.022

1051	c	PRM092	Primary Lateral Sclerosis, Adult, 1	53	0.022

1052		CLF001	Cleft Lip	53	0.022

1053		GSG001	Gas Gangrene	53	0.022

1054		PRN011	Pernicious Anemia	53	0.022

1055	P	RTN022	Retinal Vein Occlusion	53	0.022

1056		PRP080	Peripheral Artery Disease	53	0.022

1057	c	GLL024	Gallbladder Disease 1	53	0.022

1058	P	INT068	Intestinal Disease	53	0.022

1059	c	CNT035	Central Nervous System Disease	52	0.022

1060		CHR073	Choreatic Disease	52	0.022

1061	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	52	0.022

1062	P	ACT105	Acute Mountain Sickness	52	0.022

1063		AGN003	Agenesis of the Corpus Callosum with Peripheral Neuropathy	52	0.022

1064		ART074	Aortic Dissection	52	0.022

1065		LMY002	Leiomyoma	52	0.022

1066		SPS003	Spastic Diplegia	51	0.022

1067	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.022

1068		FCT001	Factor Viii Deficiency	51	0.022

1069	c	ART120	Arthrogryposis, Distal, Type 3	51	0.022

1070	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.022

1071	P	PRC012	Pericardial Effusion	51	0.022

1072		TNG007	Tongue Carcinoma	51	0.022

1073	P	CHL066	Cholangitis	51	0.022

1074		PLR007	Pleural Empyema	50	0.022

1075