Search results for Chloride ion

2519 hits were found for Chloride ion

#	Family	MCID	Name	MIFTS	Score
1		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	63.001

2		CYS001	Cystic Fibrosis	78	45.060

3		DRR008	Diarrhea 1, Secretory Chloride, Congenital	51	41.923

4		CNG064	Congenital Chloride Diarrhea	34	37.735

5		HRW001	Hair Whorl	35	32.428

6	P	BRN076	Bronchiectasis with or Without Elevated Sweat Chloride 1	33	31.931

7	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	27.546

8		MTB004	Metabolic Acidosis	48	26.552

9		RPD005	Rapidly Involuting Congenital Hemangioma	46	26.350

10		HLX001	Helix Syndrome	48	25.827

11		HYP005	Hypokalemia	55	22.286

12		48X005	48,xyyy	39	20.557

13		HYP266	Hypoxia	57	19.652

14	c	DNT047	Dentinogenesis Imperfecta Type 2	35	19.506

15	P	DRR001	Diarrhea	55	18.900

16	c	HYP595	Hypertension, Essential	85	17.918

17		ALL029	Allergic Disease	59	17.840

18	P	NRB001	Neuroblastoma	66	17.698

19	P	ANP001	Anaplastic Large Cell Lymphoma	61	17.484

20		MYT011	Myotonia	39	17.169

21		CHL014	Cholera	62	17.146

22		PRT037	Pertussis	65	16.676

23	c	ACT071	Acute Kidney Failure	60	16.547

24	P	KDN018	Kidney Disease	72	16.296

25	c	PSD092	Pseudohypoaldosteronism, Type Iie	48	15.937

26		LNG099	Lung Disease	62	15.931

27		GLL048	Glial Tumor	52	15.683

28		GLM045	Glioma	63	15.639

29		ISC004	Ischemia	61	15.284

30		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	15.262

31	P	LNG028	Long Qt Syndrome	64	15.104

32		ANX004	Anoxia	40	14.956

33		NPH009	Nephrolithiasis	54	14.588

34		GLB002	Glioblastoma	67	14.322

35	c	CHR684	Chronic Kidney Disease	69	14.078

36	P	EPL164	Epilepsy	68	13.953

37	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	13.888

38		CRB004	Cerebral Artery Occlusion	45	13.771

39		CNT047	Contact Dermatitis	57	13.750

40		BNR002	Bone Resorption Disease	47	13.707

41	P	SZR006	Seizure Disorder	70	13.374

42		PPL052	Papillomatosis, Confluent and Reticulated	34	13.328

43		LWC001	Low Compliance Bladder	45	13.274

44	P	RNL007	Renal Tubular Acidosis	50	13.199

45	P	ALZ034	Alzheimer Disease	87	12.924

46		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	12.875

47	P	BRT004	Bartter Disease	58	12.773

48		ISL119	Isolated Optic Neuritis	26	12.738

49		OST159	Osteogenic Sarcoma	66	12.422

50		CNG034	Congestive Heart Failure	69	12.388

51	P	PRS040	Prostate Cancer	95	12.291

52		CRD132	Cardiac Conduction Defect	60	12.267

53		ATS010	Autosomal Recessive Disease	42	12.228

54	P	BPL003	Bipolar Disorder	56	12.224

55	P	CHR345	Chronic Pain	50	12.142

56	c	MJR022	Major Affective Disorder 8	38	12.113

57	c	MJR024	Major Affective Disorder 9	41	12.113

58	P	MYT023	Myotonia Congenita	55	12.091

59	P	PNC035	Pancreatic Cancer	86	11.791

60	c	BRN108	Branchiootic Syndrome 1	62	11.768

61		AGN016	Aging	54	11.760

62	c	MGR028	Migraine with or Without Aura 1	64	11.723

63		ANG020	Angiosarcoma	64	11.701

64		47X002	47,xyy	48	11.642

65		CNS004	Constipation	56	11.612

66	P	HYP069	Hyperparathyroidism	62	11.591

67	P	PLY014	Polycystic Kidney Disease	69	11.541

68	P	CRD119	Cardiac Arrest	67	11.441

69		SCR003	Secretory Diarrhea	35	11.416

70		CYT002	Cytokine Deficiency	43	11.371

71	P	LTR001	Lateral Sclerosis	58	11.338

72	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	11.272

73		SPN186	Spinal Cord Injury	61	11.122

74		BRN004	Brain Edema	54	11.112

75		DNT012	Dental Caries	53	11.103

76		PNG002	Pain Agnosia	51	11.085

77	P	PRD021	Periodic Paralysis	41	10.926

78		TXC005	Toxic Shock Syndrome	62	10.915

79		DRM006	Dermatitis	62	10.893

80		PRT251	Proteinuria, Chronic Benign	57	10.883

81		CRD223	Cardiac Arrhythmia	63	10.792

82	P	PHC003	Pheochromocytoma	69	10.761

83		ADR040	Adrenal Gland Pheochromocytoma	46	10.761

84		IRN002	Iron Metabolism Disease	57	10.705

85		PST092	Posttransplant Acute Limbic Encephalitis	28	10.649

86		BRN071	Brain Injury	50	10.638

87		URL001	Urolithiasis	46	10.607

88		BCT022	Bacterial Infectious Disease	56	10.522

89		GTL001	Gitelman Syndrome	65	10.520

90	P	HPT023	Hepatocellular Carcinoma	96	10.513

91		ALL010	Allergic Contact Dermatitis	56	10.496

92	P	MYC007	Myocardial Infarction	70	10.486

93	P	ENC018	Encephalopathy	62	10.483

94	P	NSP012	Nasopharyngeal Carcinoma	61	10.442

95		HYP066	Hyperglycemia	61	10.427

96	P	MLN008	Melanoma	76	10.330

97	P	INF032	Infertility	57	10.324

98		GNG013	Gingivitis	59	10.316

99		PLM010	Pulmonary Edema	55	10.239

100		BRN024	Bronchitis	67	10.234

101		INT323	Intraocular Pressure Quantitative Trait Locus	64	10.220

102	P	PRD008	Periodontitis	64	10.198

103	P	NRP001	Neuropathy	60	10.177

104	P	RSP003	Respiratory Failure	74	10.152

105		TRM010	Traumatic Brain Injury	51	10.144

106		OST012	Osteoarthritis	77	10.097

107		OCL069	Ocular Motor Apraxia	57	10.080

108	P	LNG032	Lung Cancer	98	9.982

109		CNN003	Conn's Syndrome	79	9.962

110		NPH091	Nephrolithiasis, Calcium Oxalate	61	9.926

111	P	HRT032	Heart Disease	81	9.871

112		PLM129	Pulmonary Disease, Chronic Obstructive	74	9.871

113		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	9.850

114	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	9.846

115	P	BND020	Bone Disease	59	9.839

116		SVR001	Severe Acute Respiratory Syndrome	67	9.743

117		NPH003	Nephrocalcinosis	49	9.566

118		HMN044	Human Immunodeficiency Virus Type 1	78	9.476

119		ADN018	Adenoma	59	9.466

120	P	ADN016	Adenocarcinoma	63	9.459

121	P	MSC005	Muscular Dystrophy	67	9.369

122	P	INF038	Influenza	68	9.363

123		END086	End Stage Renal Disease	52	9.318

124		PLY150	Polykaryocytosis Inducer	29	9.298

125	c	PLM127	Pulmonary Hypertension, Primary, 3	34	9.276

126	c	ACT027	Acute Pancreatitis	60	9.270

127	P	MRC003	Mercury Poisoning	49	9.234

128		TTN003	Tetanus	65	9.184

129		DFC004	Deficiency Anemia	74	9.173

130		RCK004	Rickets	68	9.170

131	P	DST107	Distal Renal Tubular Acidosis	48	9.158

132	P	RHN004	Rhinitis	57	9.126

133	P	ATR011	Atrial Fibrillation	66	9.099

134	P	GLM040	Glioma Susceptibility 1	71	9.080

135		ATM095	Autoimmune Disease	61	9.078

136	P	DRM053	Dermatitis, Atopic	65	9.059

137	P	PNC044	Pancreatitis	61	9.054

138	P	GST044	Gastritis	55	9.038

139	P	CTR002	Cataract	60	9.011

140	P	BRS047	Breast Cancer	98	8.996

141	c	PRC016	Pre-Eclampsia	65	8.951

142		HMS001	Hemosiderosis	48	8.938

143		DPH001	Diphtheria	59	8.932

144		SQM006	Squamous Cell Carcinoma	60	8.876

145	P	MYC084	Mycobacterium Tuberculosis 1	68	8.849

146		CLT003	Colitis	63	8.836

147	P	TRM003	Tremor	48	8.825

148		LVR012	Liver Cirrhosis	63	8.806

149	c	HYP836	Hypercholesterolemia, Familial, 1	73	8.803

150		ALC007	Alcohol Dependence	66	8.780

151	P	BRN022	Bronchiectasis	60	8.748

152	P	AST005	Asthma	76	8.744

153	P	PSD003	Pseudohypoaldosteronism	44	8.678

154		SKN016	Skin Disease	63	8.635

155		STT001	Status Epilepticus	59	8.594

156		IRR002	Irritable Bowel Syndrome	65	8.581

157		DWN001	Down Syndrome	70	8.577

158		BRN028	Brain Cancer	74	8.541

159	P	PLM037	Pulmonary Hypertension	72	8.519

160	P	TMP001	Temporal Lobe Epilepsy	49	8.494

161	P	LNG064	Lung Cancer Susceptibility 3	70	8.494

162		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	8.468

163		ARG004	Argyria	26	8.447

164	c	ACT075	Acute Myocardial Infarction	56	8.425

165	P	LVR013	Liver Disease	69	8.408

166	c	ATR087	Atrial Standstill 1	74	8.355

167	P	MYP004	Myopathy	67	8.314

168		CHR072	Chordoma	57	8.299

169		MDD018	Middle East Respiratory Syndrome	44	8.295

170	P	MYS003	Myasthenia Gravis	68	8.276

171	P	URN019	Urinary Tract Infection	49	8.266

172	P	MLN007	Male Infertility	56	8.254

173	P	RRH023	Rare Hereditary Hemochromatosis	54	8.188

174		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	8.166

175	c	ACT068	Acute Cystitis	61	8.161

176	P	HRP006	Herpes Simplex	65	8.156

177		HYP056	Hypoglycemia	65	8.082

178	P	PRK039	Parkinsonism	55	8.081

179	P	HNT016	Huntington Disease	73	8.050

180	P	HPT021	Hepatitis	69	8.030

181	P	MYT002	Myotonic Dystrophy	51	8.013

182		ATH013	Atherosclerosis Susceptibility	63	7.983

183	P	BRG001	Brugada Syndrome	69	7.983

184		CRT084	Creatinine Clearance Quantitative Trait Locus	25	7.966

185	P	ADL010	Adult Respiratory Distress Syndrome	71	7.956

186		MCS002	Mucositis	56	7.947

187	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	7.930

188	P	INF037	Inflammatory Bowel Disease	53	7.904

189		HPT004	Hepatic Coma	43	7.850

190		SRC014	Sarcoma	65	7.845

191		MLG169	Malignant Astrocytoma	57	7.841

192		SPN035	Spindle Cell Sarcoma	54	7.821

193		CRV035	Cervical Cancer	73	7.814

194	P	BCL017	B-Cell Lymphoma	59	7.800

195		MDD011	Mood Disorder	62	7.795

196	P	GLM007	Glomerulonephritis	60	7.794

197	P	OPN001	Open-Angle Glaucoma	55	7.771

198		SYN036	Syncope	45	7.768

199	P	CHN012	Chondrosarcoma	57	7.767

200	P	VSC007	Vascular Disease	63	7.759

201	c	MCR130	Microvascular Complications of Diabetes 6	41	7.759

202	c	MCR120	Microvascular Complications of Diabetes 7	47	7.759

203	c	MCR113	Microvascular Complications of Diabetes 3	52	7.759

204	c	MCR133	Microvascular Complications of Diabetes 4	41	7.759

205		NNL005	Non-Alcoholic Fatty Liver Disease	63	7.737

206		FTT001	Fatty Liver Disease	62	7.735

207	c	HPT073	Hepatitis C Virus	71	7.727

208	c	MCL042	Macular Degeneration, Age-Related, 1	85	7.722

209	P	OST002	Osteoporosis	76	7.701

210	P	HYP086	Hypothyroidism	69	7.698

211	c	SML038	Small Cell Cancer of the Lung	69	7.693

212		THR024	Thrombosis	56	7.686

213	P	INT070	Intestinal Obstruction	57	7.665

214	P	OVR042	Ovarian Cancer	88	7.631

215	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	7.613

216	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	7.613

217	P	OVR082	Overgrowth Syndrome	49	7.579

218	P	PLM036	Pulmonary Fibrosis	66	7.561

219	P	PRP019	Peripheral Nervous System Disease	58	7.533

220		GST045	Gastroenteritis	58	7.518

221		PRT036	Peritonitis	65	7.496

222		HPT019	Hepatic Encephalopathy	59	7.492

223		ANT024	Anthrax Disease	58	7.481

224	P	LCT001	Lactic Acidosis	51	7.472

225	P	PRK057	Parkinson Disease, Late-Onset	80	7.464

226		STR067	Stroke, Ischemic	80	7.454

227		SVR004	Severe Combined Immunodeficiency	72	7.411

228	P	FBR017	Fibrosarcoma	56	7.406

229	P	KLZ004	Kala-Azar 1	41	7.405

230		LSH001	Leishmaniasis	64	7.405

231		VCC001	Vaccinia	47	7.379

232		ALL003	Allergic Rhinitis	67	7.356

233	P	SCH015	Schizophrenia	74	7.344

234	P	OST001	Osteopetrosis	71	7.332

235		HYP025	Hyperphosphatemia	48	7.317

236	P	OPT006	Optic Nerve Disease	58	7.300

237	P	DNT020	Dent Disease 1	63	7.294

238	c	HPT001	Hepatitis C	62	7.273

239		URM002	Uremia	47	7.253

240	P	AMY004	Amyloidosis	70	7.244

241		PRS047	Prostatitis	58	7.217

242	c	TYP009	Type 2 Diabetes Mellitus	92	7.216

243		PPT005	Peptic Ulcer Disease	58	7.215

244	P	GST053	Gastric Cancer	83	7.198

245		GTR002	Goiter	53	7.195

246	P	EYD002	Eye Disease	57	7.170

247		ULC004	Ulcerative Colitis	74	7.163

248	P	EPS003	Episodic Ataxia	59	7.085

249	P	DBT005	Diabetes Insipidus	54	7.068

250	P	SKN015	Skin Carcinoma	71	7.062

251	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	7.029

252	c	LKM061	Leukemia, Acute Myeloid	83	7.019

253		KRT019	Keratitis, Hereditary	66	7.013

254		STM007	Stomatitis	54	7.003

255		ILS001	Ileus	50	6.986

256		HVY002	Heavy Metal Poisoning	22	6.960

257		LPP008	Lipoprotein Quantitative Trait Locus	65	6.959

258	P	SNS001	Sensorineural Hearing Loss	59	6.946

259		HGH043	High Grade Glioma	45	6.901

260		IMP005	Impotence	52	6.867

261		INS024	Insulin-Like Growth Factor I	78	6.856

262	P	CRN300	Coronary Heart Disease 1	73	6.841

263	P	THL005	Thalassemia	56	6.828

264		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	6.819

265	P	VSC011	Vasculitis	61	6.812

266		OCL006	Ocular Hypertension	53	6.795

267		PLY012	Polyhydramnios	46	6.790

268	P	CLR023	Colorectal Cancer	100	6.765

269		THY029	Thyroid Carcinoma	51	6.748

270	P	ALC033	Alcohol Use Disorder	61	6.742

271		LYS002	Lysosomal Storage Disease	51	6.730

272	c	PCH010	Pachyonychia Congenita 3	43	6.727

273	P	BRS044	Breast Adenocarcinoma	58	6.703

274	P	HYP076	Hyperthyroidism	53	6.693

275	P	DBT009	Diabetes Mellitus	67	6.676

276	c	SCN007	Secondary Hyperparathyroidism	51	6.661

277		HYP014	Hyperuricemia	51	6.656

278	P	PLY019	Polyneuropathy	52	6.629

279		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	6.605

280		ADN011	Adenoid Cystic Carcinoma	68	6.599

281	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	6.590

282	c	PRM005	Primary Hyperparathyroidism	59	6.584

283		HMP009	Haemophilus Influenzae	41	6.573

284		ART140	Arteries, Anomalies of	53	6.571

285	P	DDN001	Duodenal Ulcer	53	6.541

286	c	MCR115	Microvascular Complications of Diabetes 5	65	6.524

287	c	ATS007	Autism Spectrum Disorder	72	6.495

288	P	ECL001	Eclampsia	52	6.492

289	P	MLG056	Malignant Hyperthermia	66	6.481

290	P	ART022	Arthritis	71	6.473

291		HYP060	Hyperinsulinism	54	6.461

292	P	RTN016	Retinal Degeneration	52	6.434

293		PLG002	Plague	58	6.384

294		OST011	Osteomalacia	52	6.365

295	P	CYS018	Cystitis	59	6.322

296		CHL068	Cholestasis	61	6.321

297	P	SYS005	Systemic Scleroderma	74	6.317

298		MLR004	Malaria	80	6.307

299	c	DLT002	Dilated Cardiomyopathy	78	6.269

300	P	INT068	Intestinal Disease	53	6.263

301		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	6.262

302		DYS073	Dysphagia	53	6.251

303		ALL014	Allergic Encephalomyelitis	34	6.245

304		ESP021	Esophageal Cancer	83	6.244

305	c	BRT024	Bartter Syndrome Type 4	25	6.207

306		DBT084	Diabetes Mellitus, Ketosis-Prone	60	6.202

307		MNN043	Meningioma, Familial	79	6.193

308		SCR001	Secretory Meningioma	40	6.193

309		LYM002	Lymphoplasmacyte-Rich Meningioma	35	6.193

310		SPN021	Spinal Meningioma	50	6.193

311		CRH001	Crohn's Disease	80	6.185

312	c	HPT003	Hepatitis a	63	6.153

313		DSS012	Disseminated Infection with Mycobacterium Avium Complex	19	6.128

314		ACT098	Acute Erythroid Leukemia	55	6.118

315	P	TRC031	Trichorhinophalangeal Syndrome	38	6.110

316		MNT002	Mental Depression	57	6.099

317		PNC129	Pancreatic Adenocarcinoma	65	6.099

318		HYP017	Hypophosphatemia	49	6.083

319	P	BRT053	Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness	45	6.083

320	P	SCK005	Sickle Cell Disease	56	6.077

321		MSC157	Muscular Dystrophy, Duchenne Type	79	6.062

322	P	FBR031	Febrile Seizures	52	6.060

323		SFT003	Soft Tissue Sarcoma	57	6.047

324	c	BRT042	Bartter Syndrome, Type 3	46	6.029

325	P	PRN023	Prion Disease	60	6.026

326		ALL006	Allergic Asthma	56	6.024

327		GST023	Gastric Ulcer	52	6.001

328	c	SHR030	Short Qt Syndrome	44	5.974

329		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	5.973

330		DSS032	Disease by Infectious Agent	55	5.971

331		MST005	Mastitis	53	5.968

332		NRG002	Neurogenic Bladder	55	5.966

333	P	RCT021	Rectum Cancer	54	5.959

334	P	PNM007	Pneumonia	67	5.955

335		SPS057	Spasticity	42	5.950

336	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	5.939

337	P	NPH012	Nephrotic Syndrome	60	5.921

338		ORL011	Oral Cancer	60	5.918

339		ORL015	Oral Squamous Cell Carcinoma	43	5.913

340	P	BLD134	Bladder Cancer	79	5.911

341		MTH071	Methane Production	25	5.890

342		PTT037	Pituitary Tumors	44	5.888

343	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	5.882

344	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	5.882

345	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	5.882

346	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	5.882

347	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	5.882

348	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	5.882

349	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	5.882

350	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	5.882

351	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	5.882

352	P	CND004	Candidiasis	58	5.877

353	c	GLL024	Gallbladder Disease 1	52	5.871

354		IMM167	Immune Deficiency Disease	78	5.868

355		GST092	Gastroesophageal Reflux	61	5.858

356	P	HDC001	Headache	57	5.853

357		TRY001	Trypanosomiasis	50	5.824

358		DPR016	Depression	65	5.776

359		DMP001	Dumping Syndrome	43	5.749

360	P	HYP097	Hyperekplexia	62	5.744

361		CLN015	Colon Adenocarcinoma	65	5.742

362		ATR057	Atrioventricular Block	54	5.742

363		STN013	Stenotrophomonas Maltophilia Infection	26	5.723

364		NRT004	Neuritis	53	5.706

365	c	FML191	Familial Long Qt Syndrome	55	5.697

366	P	MYC008	Myocarditis	59	5.683

367		ANG054	Angina Pectoris	66	5.675

368	c	HPT015	Hepatitis D	49	5.674

369		TLN003	Telangiectasis	51	5.670

370		VGN023	Vaginitis	56	5.666

371		PHN003	Phenylketonuria	76	5.661

372		MYL069	Myeloma, Multiple	77	5.660

373		GT001	Gout	64	5.655

374		PND002	Pendred Syndrome	57	5.643

375		RNL114	Renal Cell Carcinoma, Nonpapillary	80	5.639

376		CHD004	Chudley-Mccullough Syndrome	48	5.635

377		PST011	Pustulosis of Palm and Sole	52	5.629

378	P	MYL006	Myeloid Leukemia	61	5.609

379	P	ENC004	Encephalitis	61	5.602

380		CHL123	Chlamydia	58	5.601

381		DYS015	Dysentery	50	5.581

382		HYP052	Hyperkalemic Periodic Paralysis	63	5.547

383		OST003	Osteonecrosis	61	5.524

384	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	5.502

385		IRN001	Iron Deficiency Anemia	58	5.493

386		CRB039	Cerebrovascular Disease	66	5.483

387		INS001	Insulinoma	59	5.482

388	P	ALP008	Alopecia	54	5.480

389		BCT002	Bacterial Vaginosis	53	5.472

390	P	MLT020	Multiple Sclerosis	79	5.469

391	P	HYP750	Hypertriglyceridemia, Familial	62	5.461

392		DBT010	Diabetic Neuropathy	54	5.460

393		HND015	Hand Skill, Relative	30	5.456

394		GST050	Gastrointestinal System Disease	55	5.443

395	P	MJR001	Major Depressive Disorder	68	5.435

396	P	PSR002	Psoriasis	63	5.434

397		SBC016	Subacute Delirium	43	5.414

398	c	PLM164	Pulmonary Hypertension, Primary, 1	76	5.410

399	P	HML002	Hemolytic Anemia	62	5.403

400	P	LKD001	Leukodystrophy	59	5.394

401	P	MNN013	Meningitis	65	5.394

402		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	5.393

403		ART016	Aortic Aneurysm	68	5.385

404		MSC007	Muscle Hypertrophy	64	5.384

405		CRT015	Carotid Artery Occlusion	45	5.380

406	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	63	5.370

407	P	SCL018	Scoliosis	57	5.337

408		ACQ007	Acquired Immunodeficiency Syndrome	59	5.324

409	P	ATS364	Autism	69	5.304

410		PLM001	Pulmonary Tuberculosis	69	5.296

411	c	TYP008	Type 1 Diabetes Mellitus	70	5.253

412		ACT003	Acute Kidney Tubular Necrosis	46	5.242

413		OST017	Osteomyelitis	63	5.234

414		LPD008	Lipid Metabolism Disorder	62	5.229

415	P	DMN002	Dementia	66	5.220

416	P	RTN018	Retinal Disease	53	5.219

417	P	PRP029	Porphyria	60	5.195

418		NWC001	Newcastle Disease	47	5.193

419		MTH009	Mouth Disease	57	5.184

420	P	EXN002	Exanthem	58	5.166

421	P	ART023	Arthropathy	61	5.163

422		MST021	Meester-Loeys Syndrome	42	5.163

423	P	LKM002	Leukemia	67	5.160

424		PRT013	Portal Hypertension	59	5.155

425		AMN003	Amnestic Disorder	54	5.151

426		OTT002	Otitis Media	71	5.144

427		SCK003	Sickle Cell Anemia	74	5.143

428		PNC041	Pancreatic Ductal Adenocarcinoma	51	5.132

429	c	ACT134	Acute Liver Failure	59	5.128

430	c	HPT016	Hepatitis B	62	5.123

431	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	5.114

432	P	KDN017	Kidney Cancer	61	5.084

433		SCR011	Scrapie	39	5.050

434	c	GLC092	Glaucoma, Primary Open Angle	62	5.042

435		FBR047	Fibromyalgia	58	5.034

436		ANX010	Anxiety	70	5.027

437		MCN017	Meconium Ileus	53	5.010

438	P	SPP010	Suppressor of Tumorigenicity 3	51	4.997

439		DMY004	Demyelinating Disease	50	4.991

440	P	MSC003	Muscular Atrophy	52	4.989

441	P	EPL140	Epilepsy, Idiopathic Generalized	62	4.988

442		PPL022	Papilloma	53	4.983

443		PTH003	Pathologic Nystagmus	52	4.970

444		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	4.970

445		SDD001	Sudden Infant Death Syndrome	60	4.951

446	P	ACN011	Acne	57	4.945

447	P	INT143	Interstitial Cystitis	60	4.940

448	P	PYL005	Pyelonephritis	57	4.938

449	P	MVM001	Movement Disease	61	4.938

450	P	BNG032	Benign Mesothelioma	53	4.937

451		CTN007	Cutaneous Leishmaniasis	62	4.933

452		MNK001	Menkes Disease	64	4.929

453		SQM002	Squamous Cell Papilloma	46	4.929

454		YLL002	Yellow Fever	61	4.918

455	P	ART021	Arteriosclerosis	54	4.917

456		CHR100	Chronic Ulcer of Skin	57	4.914

457	P	FML023	Familial Hemiplegic Migraine	53	4.900

458		HDN002	Head Injury	44	4.893

459		RYN005	Raynaud Phenomenon	45	4.882

460		PRS045	Prostatic Hypertrophy	53	4.879

461		HYP267	Hyperchlorhidrosis, Isolated	24	4.878

462	P	FML187	Familial Hypertension	34	4.874

463	P	HYD006	Hydrocephalus	61	4.868

464		PRM057	Paramyotonia Congenita of Von Eulenburg	59	4.863

465		KRT006	Keratoconjunctivitis	53	4.862

466		ANR040	Aneurysm	61	4.834

467	P	ESP024	Esophagitis	60	4.831

468	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	4.828

469		INT075	Intracranial Hypertension	53	4.801

470	P	THR014	Thrombocytopenia	66	4.792

471		CVD001	Covid-19	57	4.790

472		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	4.781

473		SCH014	Schistosomiasis	56	4.781

474		END057	Endometrial Cancer	72	4.775

475	P	HYP265	Hypotonia	42	4.774

476	P	RHB003	Rhabdomyosarcoma	66	4.762

477		CHG001	Chagas Disease	66	4.761

478		AVN001	Avian Influenza	61	4.756

479		MTL005	Metal Allergy	40	4.744

480		SPL018	Splenomegaly	49	4.733

481	P	CNJ013	Conjunctivitis	66	4.731

482	c	PNS012	Paine Syndrome	60	4.712

483		ERL001	Early Myoclonic Encephalopathy	62	4.706

484		DRY001	Dry Eye Syndrome	50	4.693

485		DNT001	Dental Fluorosis	43	4.691

486	P	MYP006	Myopia	56	4.687

487		NRL016	Neural Tube Defects	81	4.682

488		VLV047	Volvulus of Midgut	52	4.681

489	P	RHM011	Rheumatoid Arthritis	82	4.657

490		CHL065	Cholangiocarcinoma	58	4.638

491		INT079	Intrahepatic Cholangiocarcinoma	51	4.638

492	P	TRN020	Turner Syndrome	67	4.636

493		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	4.619

494	P	OPT009	Optic Neuritis	57	4.613

495	P	HYP061	Hypertrophic Cardiomyopathy	69	4.598

496	P	PRD017	Periodic Paralyses	24	4.598

497	P	URT039	Urticaria	58	4.597

498	c	RTN047	Retinitis Pigmentosa 18	46	4.580

499		BRN002	Bronchiolitis	57	4.564

500	P	INS002	in Situ Carcinoma	53	4.560

501		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	4.554

502		GLC003	Glucose Intolerance	54	4.545

503	P	CRN026	Corneal Edema	42	4.529

504		ENT011	Enterocolitis	55	4.523

505		BNG077	Benign Idiopathic Neonatal Seizures	23	4.522

506	c	INH020	Inherited Metabolic Disorder	48	4.520

507	c	LNG047	Long Qt Syndrome 2	59	4.510

508	P	DYS154	Dystonia	64	4.493

509	P	DNG005	Dengue Virus	56	4.492

510		TRG002	Trigeminal Neuralgia	61	4.488

511	c	MCL013	Mucolipidosis Iv	65	4.485

512	c	PRD040	Periodontitis, Chronic	52	4.474

513	P	RTN024	Retinoblastoma	73	4.466

514	P	LKM062	Leukemia, Acute Lymphoblastic	69	4.460

515		NRR001	Neuroretinitis	42	4.456

516		RTN023	Retinitis	46	4.456

517		CMM005	Common Cold	56	4.456

518	P	END044	Endometriosis	62	4.453

519		CHR178	Chromosomal Triplication	34	4.438

520		AZS001	Azoospermia	45	4.432

521	P	RTN008	Retinitis Pigmentosa	80	4.423

522		CND006	Candida Glabrata	30	4.422

523	P	CLC063	Celiac Disease 1	66	4.414

524		NRM005	Neuromuscular Disease	63	4.400

525		MSL001	Measles	61	4.399

526	P	HYP024	Hypoparathyroidism	55	4.392

527	P	SLP006	Sleep Apnea	69	4.373

528		OCC016	Occupational Asthma	33	4.355

529		URN010	Urinary Tract Obstruction	55	4.349

530		ADG002	Audiogenic Seizures	25	4.344

531	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	4.322

532	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	4.322

533	P	CRD246	Cardiovascular System Disease	56	4.322

534	P	ART005	Arteriovenous Malformation	65	4.318

535		MLC004	Mulchandani-Bhoj-Conlin Syndrome	51	4.312

536	P	ATX030	Ataxia-Telangiectasia	80	4.301

537		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	4.293

538		PLM031	Poliomyelitis	63	4.259

539		IRR003	Irritant Dermatitis	47	4.257

540		ADL002	Adult Syndrome	70	4.246

541		PRS063	Paresthesia	39	4.215

542		PRS021	Prostatic Adenoma	43	4.215

543	P	CYS039	Cystic Kidney Disease	53	4.215

544		PHR003	Pharyngitis	58	4.214

545		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	26	4.213

546	P	HYP733	Hypercalciuria, Absorptive, 2	45	4.206

547		KRT001	Keratoconjunctivitis Sicca	50	4.205

548		EXR010	Exercise-Induced Bronchoconstriction	34	4.199

549		INT066	Interstitial Lung Disease	60	4.195

550		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	4.194

551	P	MJR007	Major Affective Disorder 1	42	4.186

552		SLP001	Sleeping Sickness	56	4.185

553		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	36	4.175

554		WLS001	Wilson Disease	70	4.160

555	P	SCK002	Sick Sinus Syndrome	55	4.157

556	P	LCH002	Lichen Planus	54	4.157

557		GST040	Gastric Adenocarcinoma	67	4.149

558	c	SCL052	Scleroderma, Familial Progressive	61	4.149

559		KRT009	Keratosis	53	4.141

560		VRC005	Varicose Veins	60	4.140

561		OST062	Osteoarthritis with Mild Chondrodysplasia	47	4.140

562		BCK006	Back Pain	47	4.137

563		PRR019	Perioral Myoclonia with Absences	27	4.129

564	P	CHR012	Chronic Granulomatous Disease	69	4.116

565	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	60	4.112

566		CLC006	Calcinosis	47	4.105

567	P	FNC004	Fanconi Syndrome	60	4.099

568	c	VRL010	Viral Hepatitis	53	4.094

569		RBS001	Rabies	58	4.091

570		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	4.077

571	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	4.077

572	P	MCL001	Mucolipidosis	49	4.071

573	P	SLP005	Sleep Disorder	61	4.059

574		PRS129	Prostatic Hyperplasia, Benign	49	4.057

575	P	CNG001	Congenital Myasthenic Syndrome	68	4.056

576		PMP014	Pemphigoid	51	4.055

577		URT010	Ureteral Obstruction	45	4.040

578	P	RBL001	Rubella	58	4.031

579	c	BTT014	Beta-Thalassemia	72	4.022

580		HMG005	Hemoglobinopathy	56	4.017

581		CRB037	Cerebral Palsy	67	4.015

582	P	LPS004	Lupus Erythematosus	61	4.003

583	P	NTR004	Neutropenia	63	4.001

584		BCT004	Bacteriuria	47	4.000

585		SNS003	Sensory Peripheral Neuropathy	52	3.999

586	P	RRT020	Rare Tumor	39	3.987

587	P	MLN069	Melanoma, Uveal	61	3.981

588		SKN019	Skin Melanoma	71	3.979

589	P	EPL198	Epilepsy, Myoclonic Juvenile	61	3.976

590		END040	Endogenous Depression	55	3.976

591		RTN017	Retinal Detachment	60	3.959

592	c	HMC039	Hemochromatosis, Type 1	73	3.949

593		LYM133	Lymphoma, Hodgkin, Classic	74	3.945

594		LST001	Listeriosis	59	3.942

595		ATN005	Autonomic Dysfunction	46	3.937

596		AMN006	Aminoaciduria	37	3.936

597	P	FRG001	Fragile X Syndrome	70	3.930

598		PLM033	Pulmonary Embolism	58	3.928

599	c	THY107	Thymoma, Familial	42	3.924

600	P	THY023	Thymoma	64	3.924

601		GRN017	Granulocytopenia	42	3.915

602		HMC014	Homocysteinemia	52	3.914

603		PRP027	Peripheral Vascular Disease	71	3.905

604	P	THY032	Thyroiditis	57	3.897

605		LTH043	Lithium Transport	17	3.891

606	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	3.886

607		RHB024	Rhabdomyosarcoma 2	67	3.885

608	P	VTL001	Vitelliform Macular Dystrophy	46	3.882

609	c	GRV008	Graves Disease 1	54	3.882

610		CRB090	Cerebral Hypoxia	42	3.878

611		IGR001	Ige Responsiveness, Atopic	59	3.867

612		ECT026	Ectopic Pregnancy	48	3.866

613		PRP016	Paraplegia	52	3.864

614	P	MGR003	Migraine with Aura	52	3.847

615	P	CNR004	Cone-Rod Dystrophy 2	74	3.847

616		HLC007	Helicobacter Pylori Infection	67	3.847

617	c	PLM128	Pulmonary Hypertension, Primary, 2	28	3.839

618	P	CHR071	Charcot-Marie-Tooth Disease	64	3.838

619		BLL006	Bullous Pemphigoid	61	3.832

620	P	MTH007	Methemoglobinemia	46	3.822

621		SPN051	Spondylitis	51	3.822

622		INF009	Inflammatory Spondylopathy	30	3.822

623		PRP030	Purpura	54	3.814

624		DGN001	Degenerative Disc Disease	49	3.813

625		PCD001	Pica Disease	38	3.812

626		MNR012	Meniere Disease	56	3.808

627		NND001	Nondystrophic Myotonia	20	3.806

628		NPH018	Nephrogenic Systemic Fibrosis	49	3.804

629		PYL006	Pyloric Stenosis	48	3.785

630		SQM013	Squamous Cell Carcinoma, Head and Neck	73	3.781

631		DST005	Diastrophic Dysplasia	57	3.776

632	P	SBS003	Substance Abuse	54	3.774

633		CHR074	Choriocarcinoma	46	3.770

634	c	SPN225	Spondyloarthropathy 1	70	3.756

635		PLC002	Plica Syndrome	35	3.749

636		SYN007	Synovitis	55	3.749

637		VSC002	Vascular Dementia	60	3.748

638		RTN003	Retinal Ischemia	49	3.745

639	P	ASP006	Aspergillosis	72	3.743

640	c	SYS001	Systemic Lupus Erythematosus	87	3.728

641	P	MNC007	Monocytic Leukemia	47	3.725

642	c	PNC108	Pancreatitis, Hereditary	69	3.716

643	c	MYT029	Myotonia Congenita, Autosomal Recessive	40	3.715

644	P	GRV001	Graves' Disease	55	3.712

645		IDP073	Idiopathic Hypercalciuria	40	3.711

646		ANR004	Anuria	44	3.711

647		MNG007	Manganese Poisoning	28	3.710

648	P	BNC003	Bone Cancer	58	3.703

649		NNL006	Non-Alcoholic Steatohepatitis	54	3.697

650	P	SRC025	Sarcoidosis 1	71	3.695

651	P	PNC025	Panic Disorder	52	3.679

652		GNT046	Genetic Epilepsy with Febrile Seizures Plus	29	3.672

653		BST008	Bestrophinopathy, Autosomal Recessive	46	3.656

654		CLF027	Cleft Palate, Isolated	64	3.653

655		GSG001	Gas Gangrene	52	3.652

656	P	UVT001	Uveitis	57	3.651

657	P	HYP098	Hypereosinophilic Syndrome	66	3.649

658		SPP011	Suppression of Tumorigenicity 12	61	3.637

659		FCL014	Focal Epilepsy	53	3.637

660		CLR109	Colorectal Adenocarcinoma	50	3.634

661		HRD218	Hereditary Stomatocytosis	30	3.633

662	P	HMP007	Hemophilia	52	3.616

663		VSD002	Vas Deferens, Congenital Bilateral Aplasia of	49	3.604

664		NRT001	Neurotic Disorder	56	3.596

665	P	MDL005	Medulloblastoma	75	3.585

666		NTR005	Nutritional Deficiency Disease	61	3.580

667		BRN056	Bronchopulmonary Dysplasia	56	3.580

668	P	NGH001	Night Blindness	52	3.577

669	c	PSD093	Pseudohypoaldosteronism, Type Iid	32	3.577

670	P	CHL066	Cholangitis	52	3.576

671	c	HNT011	Huntington Disease-Like 3	34	3.575

672	P	SYP003	Syphilis	59	3.570

673	c	ACT249	Acute Asthma	40	3.562

674		ONC002	Onchocerciasis	51	3.562

675	P	SHR001	Short Bowel Syndrome	53	3.559

676	c	DWL002	Dowling-Degos Disease 1	58	3.556

677		CMB007	Combined Immunodeficiency	57	3.548

678		URT049	Urate Oxidase, Pseudogene	24	3.544

679	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	3.543

680		DSS009	Disseminated Intravascular Coagulation	57	3.541

681		MYC005	Myocardial Stunning	46	3.541

682		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	3.532

683	c	LKM005	Leukemia, T-Cell, Chronic	34	3.532

684		ART002	Arts Syndrome	66	3.522

685		THY128	Thyroid Tumor	35	3.514

686	c	PLM121	Pulmonary Hypertension, Primary, 4	28	3.513

687		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	61	3.506

688		PRT058	Pure Autonomic Failure	58	3.506

689		EMB004	Embryonal Carcinoma	56	3.501

690	P	THY054	Thyrotoxic Periodic Paralysis	50	3.489

691	P	MTR014	Motor Neuron Disease	65	3.488

692		BLD044	Bladder Disease	48	3.481

693		INS023	Insensitivity to Pain, Congenital, with Anhidrosis	57	3.481

694		FLR002	Filariasis	55	3.477

695		CRD137	Cardiogenic Shock	56	3.465

696	P	FML011	Familial Adenomatous Polyposis	71	3.461

697		FML036	Familial Periodic Paralysis	43	3.450

698		HNS001	Hansen's Disease	32	3.444

699		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	3.444

700	c	HNT004	Huntington Disease-Like 2	52	3.441

701		ANR007	Anorexia Nervosa	60	3.438

702		CHL004	Cholelithiasis	49	3.438

703		MGL009	Megalencephalic Leukoencephalopathy with Subcortical Cysts 1	48	3.436

704		ACT119	Acute Promyelocytic Leukemia	62	3.434

705		BLR008	Bilirubin Metabolic Disorder	57	3.430

706	P	MCR010	Microcephaly	60	3.430

707	c	MYT027	Myotonia Congenita, Autosomal Dominant	34	3.417

708	P	SLM003	Salmonellosis	54	3.413

709	c	ACT004	Acute Diarrhea	40	3.408

710		HYD002	Hydronephrosis	58	3.407

711	P	HMR005	Hemorrhoid	49	3.400

712		KRT002	Keratomalacia	55	3.397

713	P	GCH001	Gaucher's Disease	70	3.394

714		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	3.394

715		CHR073	Choreatic Disease	54	3.394

716		TBR011	Tuberculous Meningitis	48	3.389

717		EPT021	Epithelial Recurrent Erosion Dystrophy	46	3.382

718		CHR066	Chronic Fatigue Syndrome	60	3.378

719		JMP002	Jumping Frenchmen of Maine	21	3.378

720	c	BRT052	Bartter Syndrome, Type 1, Antenatal	43	3.369

721		ENT004	Enthesopathy	51	3.368

722		DRV001	Dravet Syndrome	69	3.366

723		WTH001	Withdrawal Disorder	48	3.360

724		GLM044	Glomerular Disease	35	3.352

725		BRC012	Brucellosis	66	3.351

726	P	LKM071	Leukemia, Chronic Lymphocytic	75	3.350

727	P	OBS001	Obstructive Jaundice	48	3.340

728		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	3.331

729		CRC006	Carcinoid Syndrome	55	3.330

730	P	RNL015	Renal Hypertension	45	3.330

731		TRN015	Transient Cerebral Ischemia	63	3.327

732		KRT008	Keratopathy	46	3.323

733		NRM001	Neuromyelitis Optica	61	3.322

734		MST020	Mast Cell Activation Syndrome	28	3.321

735	c	PRS136	Prostate Cancer, Hereditary, 6	33	3.307

736	c	PRS130	Prostate Cancer, Hereditary, 8	32	3.307

737		CCC002	Coccidiosis	50	3.300

738	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	3.299

739	P	PNM006	Pneumoconiosis	55	3.295

740		ANT018	Anthracosis	51	3.295

741		ALB002	Albinism	47	3.290

742		LCH001	Leech Infestation	38	3.286

743	P	ANT061	Antenatal Bartter Syndrome	36	3.280

744	P	ANR048	Aniridia 1	64	3.268

745		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	25	3.263

746		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	3.257

747	P	NRV007	Nervous System Disease	67	3.253

748	P	MTH008	Methylmalonic Acidemia	52	3.253

749		PLY100	Polyploidy	36	3.244

750	P	TCD001	Tic Disorder	49	3.223

751	P	LPS002	Liposarcoma	64	3.222

752	P	CRV039	Cervicitis	52	3.221

753		CNT105	Central Core Disease of Muscle	59	3.208

754	P	ACT105	Acute Mountain Sickness	52	3.203

755	P	HYP120	Hypoaldosteronism	35	3.202

756		KLB003	Klebsiella Pneumonia	50	3.199

757	P	AVS003	Avascular Necrosis	41	3.197

758		CHK001	Chikungunya	60	3.193

759	P	LMB006	Limb-Girdle Muscular Dystrophy	52	3.191

760	P	SJG008	Sjogren Syndrome	61	3.191

761		PRM236	Primary Biliary Cholangitis	60	3.190

762		LYM143	Lymphoma, Non-Hodgkin, Familial	75	3.168

763	P	GRF003	Graft-Versus-Host Disease	71	3.166

764		HRY003	Hairy Cell Leukemia	61	3.157

765		RTR008	Root Resorption	44	3.147

766	c	EPS042	Episodic Ataxia, Type 1	58	3.147

767		WST005	West Nile Virus	57	3.136

768		ENM002	Enamel Erosion	25	3.135

769		PNM008	Pneumothorax	54	3.133

770		MCL006	Macular Retinal Edema	57	3.133

771	P	PTT006	Pituitary Adenoma	55	3.132

772		TRN018	Transitional Cell Carcinoma	56	3.129

773		MYL020	Myelomeningocele	51	3.119

774		DDN004	Duodenogastric Reflux	31	3.119

775		MCP006	Mucoepidermoid Carcinoma	48	3.110

776	P	LPR021	Leprosy 3	71	3.099

777	P	RTT002	Rett Syndrome	79	3.092

778		LBR035	Liberfarb Syndrome	27	3.088

779		FDB001	Foodborne Botulism	55	3.088

780		AND005	Androgen Insensitivity Syndrome, Mild	21	3.084

781		DWR001	Dwarfism	44	3.075

782	c	BSL007	Basal Cell Carcinoma	68	3.074

783		CRN019	Coronary Artery Vasospasm	47	3.070

784		CRT004	Carotid Artery Thrombosis	39	3.069

785	P	SML001	Small Cell Carcinoma	52	3.068

786		SYS071	Systemic Autoimmune Disease	35	3.066

787	P	MPL001	Maple Syrup Urine Disease	70	3.066

788		FCS002	Fucosidosis	62	3.064

789	P	TBR001	Tuberous Sclerosis	69	3.060

790		MMM001	Mammary Paget's Disease	53	3.060

791		MCR013	Microphthalmia	60	3.058

792		EXT007	Extracutaneous Mastocytoma	38	3.057

793		MST004	Mast Cell Neoplasm	42	3.057

794	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	3.055

795		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	3.052

796		SNT005	Sinoatrial Node Disease	47	3.040

797		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	43	3.036

798		SCT005	Scott Syndrome	50	3.031

799		HMP005	Hemiplegia	54	3.031

800		CYN003	Cyanide Poisoning	22	3.023

801	P	RNV001	Renovascular Hypertension	49	3.022

802		VSC003	Visceral Leishmaniasis	55	3.019

803	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	3.013

804	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	3.008

805	c	HMP029	Hemophilia a	68	3.000

806		BRN014	Bronchopneumonia	53	2.998

807	P	MCR129	Microvascular Complications of Diabetes 1	68	2.997

808		IDP070	Idiopathic Scoliosis	42	2.996

809		EXC002	Exocrine Pancreatic Insufficiency	42	2.995

810		CRB086	Cerebral Aneurysms	40	2.994

811	c	FML001	Familial Atrial Fibrillation	65	2.992

812		ORL005	Oral Candidiasis	56	2.985

813	P	MYC033	Myoclonus	47	2.984

814	P	FCL005	Focal Segmental Glomerulosclerosis	57	2.980

815		HYP080	Hypogonadism	50	2.977

816		FCT001	Factor Viii Deficiency	60	2.976

817		AGR019	Age-Related Hearing Loss	41	2.976

818	c	SCN036	Secondary Progressive Multiple Sclerosis	55	2.974

819	P	ATS011	Autosomal Dominant Nocturnal Frontal Lobe Epilepsy	48	2.971

820		PRP080	Peripheral Artery Disease	54	2.970

821	P	HRD011	Hereditary Spherocytosis	64	2.969

822	c	MYT020	Myotonic Dystrophy 2	57	2.967

823	P	PTN014	Patent Ductus Arteriosus 1	59	2.958

824	P	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	65	2.957

825		LMB002	Lambert-Eaton Myasthenic Syndrome	52	2.952

826	P	HYP009	Hypertrophic Pyloric Stenosis	41	2.949

827	P	JVN007	Juvenile Absence Epilepsy	47	2.948

828		HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	2.947

829		ANT039	Antisynthetase Syndrome	55	2.946

830		HRN029	Hearing Loss, Noise-Induced	37	2.946

831		CHL067	Cholecystitis	60	2.942

832		CYN002	Cyanosis, Transient Neonatal	43	2.940

833		BNG006	Benign Familial Neonatal Epilepsy	55	2.939

834	c	TBR025	Tuberous Sclerosis 1	84	2.939

835	c	MST023	Mesothelioma, Malignant	56	2.937

836	P	TXP001	Toxoplasmosis	60	2.937

837		CLC058	Clcn2-Related Leukoencephalopathy	21	2.937

838		CMP034	Complete Androgen Insensitivity Syndrome	55	2.935

839		CRT072	Creutzfeldt-Jakob Disease	68	2.932

840		FLR001	Filarial Elephantiasis	59	2.931

841	c	ACT073	Acute Leukemia	58	2.931

842		LNG031	Lung Benign Neoplasm	51	2.922

843		EXN003	Exencephaly	30	2.920

844		PSY004	Psychotic Disorder	66	2.907

845		ACR007	Acromegaly	70	2.904

846		ANH002	Anhidrosis	46	2.903

847	P	KRT007	Keratoconus	50	2.902

848	c	MLG084	Malignant Fibrous Histiocytoma	62	2.902

849	P	LYM118	Lymphoma	67	2.900

850	P	JRV004	Jervell and Lange-Nielsen Syndrome 1	56	2.893

851	P	LRY044	Larynx Cancer	54	2.891

852		CNN005	Connective Tissue Disease	67	2.886

853	c	BCT007	Bacterial Meningitis	55	2.878

854		PLM134	Pulmonary Fibrosis, Idiopathic	76	2.876

855		MNN009	Meningoencephalitis	48	2.866

856	P	EPD016	Epidermolysis Bullosa	53	2.866

857		MYT030	Myotonia, Potassium-Aggravated	46	2.862

858		ESP023	Esophageal Disease	52	2.862

859	c	HPT007	Hepatitis E	51	2.860

860		PRT029	Parathyroid Adenoma	51	2.860

861	P	LTH003	Lethal Congenital Contracture Syndrome	41	2.856

862	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	2.855

863		RNL077	Renal Fibrosis	46	2.854

864		ANP005	Anaplastic Astrocytoma	57	2.851

865	P	CRN025	Corneal Dystrophy	49	2.850

866	P	PRS038	Personality Disorder	65	2.847

867		FML159	Familial Periodic Paralyses	16	2.844

868	P	LDD007	Liddle Syndrome 1	57	2.843

869	P	HMN010	Hemangioma	62	2.841

870		CYS013	Cystinuria	66	2.836

871		OPD006	Opioid Addiction	48	2.817

872	P	FBR003	Fibrous Histiocytoma	43	2.809

873	P	APL001	Aplastic Anemia	73	2.808

874	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	2.808

875		NVS001	Neovascular Glaucoma	52	2.807

876		VGN019	Vaginal Discharge	47	2.806

877		THY030	Thyroid Gland Disease	50	2.800

878		CHP002	Chops Syndrome	47	2.800

879		PRM020	Premenstrual Tension	39	2.798

880	P	PTS002	Ptosis	52	2.783

881		BRR014	Barrett Esophagus	66	2.779

882		FDL002	Food Allergy	47	2.778

883		RTC003	Root Caries	32	2.776

884		CCN002	Cocaine Abuse	49	2.769

885		RTN020	Retinal Vascular Disease	46	2.769

886		MYL009	Myelodysplastic Syndrome	67	2.767

887	P	SLV026	Salivary Gland Carcinoma	58	2.758

888		CHR576	Chronic Beryllium Disease	42	2.757

889	P	BRY005	Beryllium Disease	39	2.757

890	c	SVR005	Severe Pre-Eclampsia	50	2.757

891	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	70	2.754

892		HRP004	Herpes Zoster	61	2.747

893		INT067	Interstitial Nephritis	46	2.745

894	P	NJM001	Nijmegen Breakage Syndrome	76	2.740

895		GNG003	Gingival Recession	49	2.740

896		ZLL002	Zollinger-Ellison Syndrome	55	2.737

897		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	61	2.729

898	P	SDR002	Siderosis	43	2.728

899	P	VTR007	Vitreoretinopathy	46	2.725

900	P	GLL018	Gallbladder Cancer	53	2.720

901		TYP007	Typhoid Fever	64	2.719

902	P	RNL115	Renal Tubular Acidosis, Proximal	32	2.718

903		HYP264	Hypertonia	36	2.709

904		CRY003	Cryptosporidiosis	56	2.708

905		FNG016	Fungal Keratitis	39	2.704

906	P	NRF002	Neurofibromatosis	57	2.703

907		PRN019	Perinatal Necrotizing Enterocolitis	60	2.700

908		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	2.696

909	P	MYG005	Myoglobinuria	40	2.696

910		HMN016	Hemangioendothelioma	34	2.692

911	c	CHR711	Chronic Asthma	41	2.692

912	c	FML116	Familial Cold Autoinflammatory Syndrome 1	55	2.690

913	P	PLY018	Polycythemia	56	2.687

914		XRD010	Xeroderma Pigmentosum, Variant Type	73	2.685

915		MTN003	Motion Sickness	51	2.681

916		GST019	Gastrointestinal Stromal Tumor	78	2.675

917		PLC008	Placenta Disease	49	2.667

918	P	GLY013	Glycogen Storage Disease	60	2.660

919	P	PRM002	Primary Hyperoxaluria	65	2.659

920	P	CHN059	Chondrocalcinosis	52	2.656

921	P	VNS003	Venous Insufficiency	55	2.646

922	c	HRD219	Hereditary Distal Renal Tubular Acidosis	25	2.645

923	P	HRD012	Hereditary Elliptocytosis	55	2.643

924		ANP008	Anaplastic Oligoastrocytoma	29	2.642

925	c	EXD008	Exudative Vitreoretinopathy 1	71	2.639

926	c	OPT053	Optic Atrophy 1	62	2.636

927		BRK010	Burkitt Lymphoma	66	2.636

928		JPN002	Japanese Encephalitis	61	2.636

929	c	LKM063	Leukemia, Chronic Myeloid	71	2.630

930		MCL027	Macular Dystrophy, Dominant Cystoid	51	2.628

931		DSS010	Dissociative Disorder	39	2.626

932	c	EPS035	Episodic Ataxia, Type 2	63	2.624

933		NRM009	Normokalemic Periodic Paralysis	28	2.622

934	c	THR092	Thrombophilia Due to Thrombin Defect	74	2.616

935		APP008	Appendicitis	62	2.614

936		PRX035	Paroxysmal Dyskinesia	30	2.613

937	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	2.608

938		CRV038	Cervical Squamous Cell Carcinoma	58	2.606

939	c	MYT021	Myotonic Dystrophy 1	68	2.597

940	c	ATM045	Autoimmune Glomerulonephritis	35	2.597

941		KLD004	Keloid Disorder	39	2.594

942		OSM001	Osmotic Diarrhea	28	2.592

943	c	ELL005	Elliptocytosis 2	37	2.590

944	c	ELL006	Elliptocytosis 3	34	2.590

945	c	ATM011	Autoimmune Hepatitis	63	2.590

946		WLL004	Wallerian Degeneration