Search results for Calcium

5473 hits were found for Calcium

#	Family	MCID	Name	MIFTS	Score
1		NPH091	Nephrolithiasis, Calcium Oxalate	61	56.308

2	P	HYP069	Hyperparathyroidism	62	50.644

3	c	CHN022	Chondrocalcinosis 2	39	41.429

4		RCK004	Rickets	68	39.588

5	P	OST002	Osteoporosis	76	39.200

6	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	37.636

7	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	37.636

8		BNR002	Bone Resorption Disease	47	35.469

9		NPH009	Nephrolithiasis	54	33.373

10	c	SCN007	Secondary Hyperparathyroidism	51	32.910

11		FML307	Familial Calcium Pyrophosphate Deposition	38	32.843

12	c	PRM005	Primary Hyperparathyroidism	59	31.623

13	c	CHR684	Chronic Kidney Disease	69	27.548

14		URL001	Urolithiasis	46	27.008

15	P	BND020	Bone Disease	59	26.705

16	c	HYP595	Hypertension, Essential	85	26.052

17	P	HYP024	Hypoparathyroidism	55	25.807

18		PRT037	Pertussis	65	25.472

19	P	CHN059	Chondrocalcinosis	52	25.282

20		IMM066	Immunodeficiency 9	39	24.747

21	P	KDN018	Kidney Disease	72	24.264

22		HYP025	Hyperphosphatemia	48	24.201

23		IMM065	Immunodeficiency 10	47	22.898

24	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	21.007

25		LPP008	Lipoprotein Quantitative Trait Locus	65	19.205

26		END086	End Stage Renal Disease	52	19.117

27		ATH013	Atherosclerosis Susceptibility	63	18.991

28		ADN018	Adenoma	59	18.692

29		OST011	Osteomalacia	52	18.364

30		ART140	Arteries, Anomalies of	53	18.068

31		ANG054	Angina Pectoris	66	17.740

32	c	PRC016	Pre-Eclampsia	65	17.365

33	P	CRN300	Coronary Heart Disease 1	73	17.190

34	P	NRB001	Neuroblastoma	66	16.831

35		NPH003	Nephrocalcinosis	49	16.439

36		IDP073	Idiopathic Hypercalciuria	40	16.252

37	P	FML068	Familial Hypocalciuric Hypercalcemia	55	15.479

38		CLC006	Calcinosis	47	15.052

39		RPD005	Rapidly Involuting Congenital Hemangioma	46	14.959

40	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	14.957

41		HYP017	Hypophosphatemia	49	14.346

42	c	ACT027	Acute Pancreatitis	60	14.178

43		ISC004	Ischemia	61	14.083

44		MTB004	Metabolic Acidosis	48	13.864

45		HLX001	Helix Syndrome	48	13.830

46		RNL011	Renal Osteodystrophy	49	13.778

47	P	MSC005	Muscular Dystrophy	67	13.776

48	P	PNC044	Pancreatitis	61	13.714

49	P	CLR023	Colorectal Cancer	100	13.666

50		PRT029	Parathyroid Adenoma	51	13.640

51		PRT251	Proteinuria, Chronic Benign	57	13.626

52		48X005	48,xyyy	39	13.489

53		LPD008	Lipid Metabolism Disorder	62	13.477

54		DNT012	Dental Caries	53	13.469

55		AGN016	Aging	54	13.408

56	P	VSC007	Vascular Disease	63	13.248

57	P	HRT032	Heart Disease	81	13.193

58	P	PRD008	Periodontitis	64	13.077

59	c	HYP836	Hypercholesterolemia, Familial, 1	73	13.072

60	c	CHN021	Chondrocalcinosis 1	17	12.955

61		OST159	Osteogenic Sarcoma	66	12.826

62	P	HYP726	Hypercalcemia, Infantile, 1	58	12.718

63	P	ECL001	Eclampsia	52	12.620

64	c	ATR087	Atrial Standstill 1	74	12.565

65	c	GLL024	Gallbladder Disease 1	52	12.551

66	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	12.407

67		URM002	Uremia	47	12.362

68	c	TYP009	Type 2 Diabetes Mellitus	92	12.305

69		HYP266	Hypoxia	57	12.284

70	c	BLD126	Bleeding Disorder, Platelet-Type, 18	39	12.228

71		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	12.178

72		CHL014	Cholera	62	12.070

73	P	LTR001	Lateral Sclerosis	58	11.947

74		ALL029	Allergic Disease	59	11.936

75	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	11.915

76	c	ACT071	Acute Kidney Failure	60	11.818

77	P	ALZ034	Alzheimer Disease	87	11.679

78		ANX004	Anoxia	40	11.642

79		HYP005	Hypokalemia	55	11.618

80	P	SRC025	Sarcoidosis 1	71	11.609

81		INS001	Insulinoma	59	11.495

82	P	DBT009	Diabetes Mellitus	67	11.426

83	P	MLG056	Malignant Hyperthermia	66	11.411

84		GT001	Gout	64	11.382

85		CNG034	Congestive Heart Failure	69	11.362

86		THY029	Thyroid Carcinoma	51	11.321

87	P	MYP004	Myopathy	67	11.297

88	c	MCR120	Microvascular Complications of Diabetes 7	47	11.130

89		GLM045	Glioma	63	11.121

90	P	CRD119	Cardiac Arrest	67	11.107

91		TTN003	Tetanus	65	11.013

92	c	MCR113	Microvascular Complications of Diabetes 3	52	11.008

93		GLL048	Glial Tumor	52	11.001

94	P	PLM037	Pulmonary Hypertension	72	10.918

95	c	DLT002	Dilated Cardiomyopathy	78	10.826

96	P	PHC003	Pheochromocytoma	69	10.816

97		ADR040	Adrenal Gland Pheochromocytoma	46	10.800

98	c	MCR130	Microvascular Complications of Diabetes 6	41	10.795

99	c	MCR133	Microvascular Complications of Diabetes 4	41	10.795

100		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	10.781

101		CYS001	Cystic Fibrosis	78	10.765

102	c	MGR028	Migraine with or Without Aura 1	64	10.727

103		MYL069	Myeloma, Multiple	77	10.707

104	P	HYP076	Hyperthyroidism	53	10.666

105		MSC157	Muscular Dystrophy, Duchenne Type	79	10.652

106		KRT002	Keratomalacia	55	10.543

107		47X002	47,xyy	48	10.514

108		CNS004	Constipation	56	10.439

109	P	ART021	Arteriosclerosis	54	10.426

110	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	10.408

111		CLR108	Colorectal Adenoma	64	10.298

112		INT007	Intermediate Coronary Syndrome	54	10.232

113	P	ATR011	Atrial Fibrillation	66	10.195

114		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	10.127

115	P	HYP086	Hypothyroidism	69	10.112

116	P	ART023	Arthropathy	61	10.073

117		IRN002	Iron Metabolism Disease	57	9.962

118	P	PSD015	Pseudohypoparathyroidism	55	9.942

119		CRN030	Coronary Stenosis	50	9.897

120	P	PRM002	Primary Hyperoxaluria	65	9.895

121		HYP056	Hypoglycemia	65	9.887

122	P	HYP733	Hypercalciuria, Absorptive, 2	45	9.865

123	P	SZR006	Seizure Disorder	70	9.856

124		LMB002	Lambert-Eaton Myasthenic Syndrome	52	9.813

125		PRT010	Parathyroid Carcinoma	68	9.726

126		AML006	Amelogenesis Imperfecta Hypoplastic Type, Ig	21	9.688

127		OST012	Osteoarthritis	77	9.663

128		CRD132	Cardiac Conduction Defect	60	9.638

129	P	MYC007	Myocardial Infarction	70	9.601

130	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	9.581

131		CMB055	Combined Immunodeficiency Due to Crac Channel Dysfunction	32	9.540

132	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	9.488

133		HRW001	Hair Whorl	35	9.482

134		CLC001	Calciphylaxis	51	9.466

135	P	HYP061	Hypertrophic Cardiomyopathy	69	9.454

136		SPN186	Spinal Cord Injury	61	9.407

137		HYP066	Hyperglycemia	61	9.398

138	P	PLY014	Polycystic Kidney Disease	69	9.377

139	c	NRL030	Neurological Muscular Channelopathy Due to a Genetic Calcium Channel Defect	3	9.357

140	c	NRL036	Neurological Channelopathy of the Central Nervous System Due to a Genetic Calcium Channel Defect	2	9.357

141	P	EPL164	Epilepsy	68	9.341

142	P	BPL003	Bipolar Disorder	56	9.298

143	c	MJR022	Major Affective Disorder 8	38	9.265

144	c	MJR024	Major Affective Disorder 9	41	9.265

145		OST017	Osteomyelitis	63	9.196

146	P	PRS040	Prostate Cancer	95	9.189

147	c	ACT075	Acute Myocardial Infarction	56	9.111

148		MMM001	Mammary Paget's Disease	53	9.086

149	P	ADN016	Adenocarcinoma	63	9.066

150	P	ART022	Arthritis	71	9.003

151	P	BRS047	Breast Cancer	98	8.970

152		HYP060	Hyperinsulinism	54	8.953

153		TRM010	Traumatic Brain Injury	51	8.872

154	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	8.865

155	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	8.865

156	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	8.865

157	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	8.865

158	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	8.865

159	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	8.865

160	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	8.865

161	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	8.865

162	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	8.865

163	P	URN019	Urinary Tract Infection	49	8.857

164	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	8.852

165	P	RNL007	Renal Tubular Acidosis	50	8.801

166		CYT002	Cytokine Deficiency	43	8.797

167	c	MCR115	Microvascular Complications of Diabetes 5	65	8.770

168		INS024	Insulin-Like Growth Factor I	78	8.746

169	P	CHR345	Chronic Pain	50	8.729

170	P	RHM011	Rheumatoid Arthritis	82	8.722

171		PLY150	Polykaryocytosis Inducer	29	8.683

172	P	LKM002	Leukemia	67	8.619

173	P	PSR002	Psoriasis	63	8.619

174	P	NRP001	Neuropathy	60	8.558

175		BRN071	Brain Injury	50	8.540

176		CRB039	Cerebrovascular Disease	66	8.459

177		HMN044	Human Immunodeficiency Virus Type 1	78	8.407

178	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	8.405

179	P	DRR001	Diarrhea	55	8.378

180		BNN003	Bone Inflammation Disease	48	8.350

181		GTR002	Goiter	53	8.340

182		CRB004	Cerebral Artery Occlusion	45	8.314

183		PRP027	Peripheral Vascular Disease	71	8.293

184	P	LCT002	Lactose Intolerance	52	8.226

185	P	PRP019	Peripheral Nervous System Disease	58	8.176

186		PST011	Pustulosis of Palm and Sole	52	8.134

187	P	MLT074	Multiple Endocrine Neoplasia	59	8.101

188		PPL052	Papillomatosis, Confluent and Reticulated	34	8.072

189		CRD223	Cardiac Arrhythmia	63	8.061

190	P	INF037	Inflammatory Bowel Disease	53	8.034

191	P	LKM062	Leukemia, Acute Lymphoblastic	69	8.010

192		LVR012	Liver Cirrhosis	63	7.973

193	P	OVR082	Overgrowth Syndrome	49	7.963

194	P	OVR042	Ovarian Cancer	88	7.950

195		STR067	Stroke, Ischemic	80	7.916

196		CRH001	Crohn's Disease	80	7.912

197	P	LYM118	Lymphoma	67	7.902

198		PNG002	Pain Agnosia	51	7.900

199		ATR057	Atrioventricular Block	54	7.885

200	P	GLM007	Glomerulonephritis	60	7.855

201		GLC086	Glucocorticoid-Induced Osteoporosis	43	7.844

202	P	HNT016	Huntington Disease	73	7.842

203	P	INF032	Infertility	57	7.803

204		TXC005	Toxic Shock Syndrome	62	7.799

205	P	PNC035	Pancreatic Cancer	86	7.791

206		RYN005	Raynaud Phenomenon	45	7.773

207		RTR008	Root Resorption	44	7.724

208	c	PLM164	Pulmonary Hypertension, Primary, 1	76	7.707

209		ALC007	Alcohol Dependence	66	7.701

210	P	RCT021	Rectum Cancer	54	7.698

211		OST004	Osteitis Fibrosa	38	7.681

212		CLN015	Colon Adenocarcinoma	65	7.674

213	c	ATS007	Autism Spectrum Disorder	72	7.653

214		FTT001	Fatty Liver Disease	62	7.645

215		PTT037	Pituitary Tumors	44	7.627

216		GLB002	Glioblastoma	67	7.604

217		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	7.600

218		STT001	Status Epilepticus	59	7.592

219	P	HYP776	Hyperparathyroidism, Neonatal Severe	46	7.579

220	P	TRM003	Tremor	48	7.560

221		GLC003	Glucose Intolerance	54	7.514

222	P	GLM040	Glioma Susceptibility 1	71	7.510

223		IMM167	Immune Deficiency Disease	78	7.476

224	P	CTR002	Cataract	60	7.465

225	c	HYP794	Hyperoxaluria, Primary, Type I	63	7.460

226		PRT036	Peritonitis	65	7.408

227	P	THL005	Thalassemia	56	7.336

228	P	PRK039	Parkinsonism	55	7.307

229		OST003	Osteonecrosis	61	7.305

230	c	TYP008	Type 1 Diabetes Mellitus	70	7.276

231		DWN001	Down Syndrome	70	7.255

232	P	LNG032	Lung Cancer	98	7.239

233		MLG169	Malignant Astrocytoma	57	7.227

234		SCN001	Secondary Hyperparathyroidism of Renal Origin	24	7.217

235		NNL005	Non-Alcoholic Fatty Liver Disease	63	7.189

236		ATM095	Autoimmune Disease	61	7.182

237	P	BCL017	B-Cell Lymphoma	59	7.163

238	c	SYS001	Systemic Lupus Erythematosus	87	7.150

239		SKN016	Skin Disease	63	7.128

240	c	SCL052	Scleroderma, Familial Progressive	61	7.126

241		ZLL002	Zollinger-Ellison Syndrome	55	7.119

242		THY111	Thyroid Carcinoma, Familial Medullary	67	7.113

243		MNT002	Mental Depression	57	7.094

244		LPT014	Leptin Deficiency or Dysfunction	78	7.082

245		HYP014	Hyperuricemia	51	7.072

246		IRR002	Irritable Bowel Syndrome	65	7.053

247		MYC005	Myocardial Stunning	46	6.977

248		HMS001	Hemosiderosis	48	6.973

249	P	NPH012	Nephrotic Syndrome	60	6.967

250	c	HYP752	Hypocalciuric Hypercalcemia, Familial, Type I	46	6.924

251	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	6.891

252		RNL114	Renal Cell Carcinoma, Nonpapillary	80	6.872

253	P	SYS005	Systemic Scleroderma	74	6.867

254	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	6.863

255	P	ENC018	Encephalopathy	62	6.862

256		DPR016	Depression	65	6.860

257	P	LPS004	Lupus Erythematosus	61	6.831

258	P	RRH023	Rare Hereditary Hemochromatosis	54	6.809

259		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	6.779

260	P	LNG028	Long Qt Syndrome	64	6.749

261		IMP005	Impotence	52	6.746

262		THY125	Thyroid Gland Medullary Carcinoma	48	6.723

263	P	GST053	Gastric Cancer	83	6.720

264	P	PGT001	Paget's Disease of Bone	61	6.702

265		CNN003	Conn's Syndrome	79	6.697

266		HYP080	Hypogonadism	50	6.655

267		PRM020	Premenstrual Tension	39	6.650

268	P	MLT020	Multiple Sclerosis	79	6.639

269	c	ART101	Aortic Valve Disease 2	66	6.637

270	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	63	6.626

271	P	BRT004	Bartter Disease	58	6.611

272		DFC004	Deficiency Anemia	74	6.610

273		TND005	Tendinitis	54	6.603

274		DNT006	Dental Pulp Necrosis	43	6.596

275		LYM019	Lymphosarcoma	46	6.577

276	P	PLY011	Polycystic Ovary Syndrome	57	6.569

277	P	GRV001	Graves' Disease	55	6.557

278		PPT005	Peptic Ulcer Disease	58	6.555

279	P	ATS364	Autism	69	6.541

280	P	HRD086	Hereditary Hypophosphatemic Rickets	40	6.538

281	P	LVR013	Liver Disease	69	6.508

282		SYN036	Syncope	45	6.448

283	P	FML187	Familial Hypertension	34	6.429

284	P	RSP003	Respiratory Failure	74	6.425

285	P	DST107	Distal Renal Tubular Acidosis	48	6.419

286		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	6.399

287		ESP021	Esophageal Cancer	83	6.357

288		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	6.348

289		GNG012	Gingival Overgrowth	49	6.347

290		ACR007	Acromegaly	70	6.339

291	P	CLC063	Celiac Disease 1	66	6.337

292	P	MSC003	Muscular Atrophy	52	6.331

293	P	DRM053	Dermatitis, Atopic	65	6.319

294	c	BRN108	Branchiootic Syndrome 1	62	6.314

295	P	CRD246	Cardiovascular System Disease	56	6.298

296	P	ALC033	Alcohol Use Disorder	61	6.286

297	P	SCL018	Scoliosis	57	6.277

298	P	PSD087	Pseudoxanthoma Elasticum	67	6.267

299	P	MLN007	Male Infertility	56	6.220

300		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	6.197

301		ACQ007	Acquired Immunodeficiency Syndrome	59	6.196

302		BRT054	Brittle Bone Disorder	74	6.153

303	P	HPT023	Hepatocellular Carcinoma	96	6.132

304		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	6.129

305		HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	6.118

306		PLM129	Pulmonary Disease, Chronic Obstructive	74	6.117

307	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	6.107

308		CHL068	Cholestasis	61	6.097

309	P	FML023	Familial Hemiplegic Migraine	53	6.061

310		BCT022	Bacterial Infectious Disease	56	6.038

311	P	HDC001	Headache	57	5.984

312	P	PRD021	Periodic Paralysis	41	5.980

313	c	GRV008	Graves Disease 1	54	5.958

314		MDD011	Mood Disorder	62	5.948

315		SQM006	Squamous Cell Carcinoma	60	5.911

316	P	MLN008	Melanoma	76	5.884

317	P	SCH015	Schizophrenia	74	5.883

318		LNG099	Lung Disease	62	5.874

319		GST092	Gastroesophageal Reflux	61	5.872

320		ART016	Aortic Aneurysm	68	5.872

321	c	HYP243	Hyperparathyroidism 1	47	5.867

322		TRN015	Transient Cerebral Ischemia	63	5.856

323	P	AMY004	Amyloidosis	70	5.844

324	P	DDN001	Duodenal Ulcer	53	5.838

325	P	RHN004	Rhinitis	57	5.826

326		PLM010	Pulmonary Edema	55	5.824

327	P	PRK057	Parkinson Disease, Late-Onset	80	5.819

328	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	5.806

329	P	EPS003	Episodic Ataxia	59	5.801

330	P	THY032	Thyroiditis	57	5.790

331	P	TXP001	Toxoplasmosis	60	5.754

332	c	LKM005	Leukemia, T-Cell, Chronic	34	5.738

333	P	OST001	Osteopetrosis	71	5.715

334		INT323	Intraocular Pressure Quantitative Trait Locus	64	5.708

335	c	ART115	Aortic Valve Disease 1	74	5.699

336	c	ACT068	Acute Cystitis	61	5.686

337	P	DMN002	Dementia	66	5.649

338		OCL069	Ocular Motor Apraxia	57	5.633

339		ULC004	Ulcerative Colitis	74	5.617

340	P	BLD134	Bladder Cancer	79	5.585

341	c	SVR005	Severe Pre-Eclampsia	50	5.570

342		CHL004	Cholelithiasis	49	5.568

343		GST030	Gastrinoma	45	5.523

344		PLP001	Pulpitis	48	5.517

345		CRY024	Crystal Arthropathies	18	5.486

346		WTH001	Withdrawal Disorder	48	5.460

347		ANR007	Anorexia Nervosa	60	5.444

348		CRN019	Coronary Artery Vasospasm	47	5.427

349	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	5.409

350	P	HYP750	Hypertriglyceridemia, Familial	62	5.403

351	P	ALP008	Alopecia	54	5.401

352	P	BRG001	Brugada Syndrome	69	5.385

353		CLT003	Colitis	63	5.379

354	c	FML021	Familial Hypercholesterolemia	72	5.360

355	P	HYP265	Hypotonia	42	5.356

356	P	TMP001	Temporal Lobe Epilepsy	49	5.345

357		CYS013	Cystinuria	66	5.334

358		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	5.333

359	c	LKM061	Leukemia, Acute Myeloid	83	5.331

360		MCS002	Mucositis	56	5.318

361		DSS032	Disease by Infectious Agent	55	5.306

362	P	HPT021	Hepatitis	69	5.306

363		AMN001	Amenorrhea	54	5.300

364		CNT105	Central Core Disease of Muscle	59	5.297

365	P	LCT001	Lactic Acidosis	51	5.278

366	P	RNV001	Renovascular Hypertension	49	5.277

367		ANR040	Aneurysm	61	5.269

368	P	MJR001	Major Depressive Disorder	68	5.257

369		WLL001	Williams-Beuren Syndrome	61	5.257

370		STM007	Stomatitis	54	5.257

371	P	DYS154	Dystonia	64	5.248

372	P	MYS003	Myasthenia Gravis	68	5.242

373	P	END044	Endometriosis	62	5.240

374	P	MYC008	Myocarditis	59	5.230

375		DYS073	Dysphagia	53	5.226

376	P	DRM010	Dermatomyositis	61	5.220

377		IDP085	Idiopathic Infantile Hypercalcemia	32	5.220

378		DBT010	Diabetic Neuropathy	54	5.214

379		CRD137	Cardiogenic Shock	56	5.210

380	c	EPS035	Episodic Ataxia, Type 2	63	5.204

381	P	ESP024	Esophagitis	60	5.182

382	P	SKN015	Skin Carcinoma	71	5.174

383	P	RTN016	Retinal Degeneration	52	5.146

384	c	PRD040	Periodontitis, Chronic	52	5.135

385	P	MYT002	Myotonic Dystrophy	51	5.117

386	P	LNG064	Lung Cancer Susceptibility 3	70	5.107

387		ANK001	Ankylosis	51	5.107

388		MRF001	Marfan Syndrome	76	5.104

389		BLR008	Bilirubin Metabolic Disorder	57	5.096

390	c	MCL042	Macular Degeneration, Age-Related, 1	85	5.091

391	c	THR092	Thrombophilia Due to Thrombin Defect	74	5.081

392		THR024	Thrombosis	56	5.076

393		SPN035	Spindle Cell Sarcoma	54	5.069

394		SRC014	Sarcoma	65	5.069

395	P	ADL017	Adult T-Cell Leukemia	56	5.068

396	P	AST005	Asthma	76	5.049

397		ALL003	Allergic Rhinitis	67	5.033

398	P	MYL006	Myeloid Leukemia	61	5.030

399		THY030	Thyroid Gland Disease	50	5.017

400		HYP057	Hypervitaminosis D	37	5.017

401		ALL014	Allergic Encephalomyelitis	34	5.014

402		DRM006	Dermatitis	62	5.008

403	P	THR014	Thrombocytopenia	66	4.991

404		PRP016	Paraplegia	52	4.980

405	P	PNM007	Pneumonia	67	4.965

406		SPN051	Spondylitis	51	4.962

407	P	HRP006	Herpes Simplex	65	4.960

408		VSC002	Vascular Dementia	60	4.958

409	P	ENC004	Encephalitis	61	4.927

410	P	EXN002	Exanthem	58	4.904

411	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	4.902

412	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	4.892

413		GTL001	Gitelman Syndrome	65	4.879

414		PLM001	Pulmonary Tuberculosis	69	4.875

415		RST023	Resting Heart Rate, Variation in	40	4.873

416	P	CYS039	Cystic Kidney Disease	53	4.870

417	P	TRC031	Trichorhinophalangeal Syndrome	38	4.862

418		PLC002	Plica Syndrome	35	4.845

419		SYN007	Synovitis	55	4.845

420		LYM133	Lymphoma, Hodgkin, Classic	74	4.831

421	P	TRN020	Turner Syndrome	67	4.830

422		HYP020	Hyperprolactinemia	63	4.829

423	c	SPN309	Spinocerebellar Ataxia 6	58	4.827

424		PRP080	Peripheral Artery Disease	54	4.815

425		CNN005	Connective Tissue Disease	67	4.806

426	P	SCK005	Sickle Cell Disease	56	4.803

427	P	GST044	Gastritis	55	4.801

428	P	PYL005	Pyelonephritis	57	4.800

429	P	MTR014	Motor Neuron Disease	65	4.795

430		CHL065	Cholangiocarcinoma	58	4.789

431		INT079	Intrahepatic Cholangiocarcinoma	51	4.789

432		NTR005	Nutritional Deficiency Disease	61	4.758

433	c	SPN225	Spondyloarthropathy 1	70	4.756

434	P	HYP035	Hypophosphatasia	62	4.749

435		END057	Endometrial Cancer	72	4.736

436		BRN004	Brain Edema	54	4.736

437		BCK006	Back Pain	47	4.735

438		HDN002	Head Injury	44	4.734

439		PRS021	Prostatic Adenoma	43	4.731

440	c	JVN010	Juvenile Rheumatoid Arthritis	66	4.730

441		NRR001	Neuroretinitis	42	4.717

442		RTN023	Retinitis	46	4.708

443	P	RTN018	Retinal Disease	53	4.704

444		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	4.703

445		SVR004	Severe Combined Immunodeficiency	72	4.696

446		URN010	Urinary Tract Obstruction	55	4.686

447		MLR004	Malaria	80	4.684

448		NRM005	Neuromuscular Disease	63	4.682

449		MYT011	Myotonia	39	4.669

450		BSL009	Basal Ganglia Calcification	45	4.668

451		CLC004	Calcific Tendinitis	33	4.666

452	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	4.664

453		PNC129	Pancreatic Adenocarcinoma	65	4.655

454		HYD002	Hydronephrosis	58	4.654

455	P	ACN011	Acne	57	4.646

456		RHB024	Rhabdomyosarcoma 2	67	4.638

457		MSC007	Muscle Hypertrophy	64	4.638

458	P	RTN024	Retinoblastoma	73	4.637

459		PST092	Posttransplant Acute Limbic Encephalitis	28	4.625

460	P	SLP006	Sleep Apnea	69	4.622

461		ENM002	Enamel Erosion	25	4.620

462		PRS129	Prostatic Hyperplasia, Benign	49	4.616

463	P	RNL015	Renal Hypertension	45	4.612

464		CMM004	Common Variable Immunodeficiency	72	4.612

465	c	SML038	Small Cell Cancer of the Lung	69	4.608

466	P	LKM071	Leukemia, Chronic Lymphocytic	75	4.585

467	P	DNT020	Dent Disease 1	63	4.580

468	P	ANR048	Aniridia 1	64	4.577

469	P	CNG010	Congenital Stationary Night Blindness	56	4.570

470		CRB037	Cerebral Palsy	67	4.570

471	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	4.564

472		HRT012	Heart Valve Disease	53	4.556

473		ANX010	Anxiety	70	4.550

474		CRT013	Carotid Stenosis	51	4.548

475		INT067	Interstitial Nephritis	46	4.547

476		NRL016	Neural Tube Defects	81	4.547

477	c	HYP608	Hypocalciuric Hypercalcemia, Familial, Type Iii	42	4.539

478	P	KDN017	Kidney Cancer	61	4.538

479		GST033	Gestational Diabetes	61	4.517

480		INF009	Inflammatory Spondylopathy	30	4.502

481		HMN014	Human Immunodeficiency Virus Infectious Disease	54	4.491

482	c	PSD108	Pseudohypoparathyroidism, Type Ia	65	4.478

483		PRT030	Parathyroid Gland Disease	45	4.470

484		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	4.460

485	P	OPN001	Open-Angle Glaucoma	55	4.458

486	P	MYC084	Mycobacterium Tuberculosis 1	68	4.456

487	c	HPT003	Hepatitis a	63	4.453

488		SCK003	Sickle Cell Anemia	74	4.443

489		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	4.442

490	P	SHR001	Short Bowel Syndrome	53	4.441

491	c	PRG042	Progressive Familial Heart Block, Type Ia	66	4.434

492		CRT015	Carotid Artery Occlusion	45	4.432

493	P	VTM027	Vitamin D-Dependent Rickets, Type 2a	53	4.427

494		PRS045	Prostatic Hypertrophy	53	4.427

495		ATS010	Autosomal Recessive Disease	42	4.396

496		GNG013	Gingivitis	59	4.373

497	P	MYS005	Myositis	56	4.368

498	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	4.363

499	c	PCH010	Pachyonychia Congenita 3	43	4.349

500		ALL006	Allergic Asthma	56	4.348

501		MST005	Mastitis	53	4.348

502	P	NGH001	Night Blindness	52	4.348

503	P	VSC011	Vasculitis	61	4.344

504		IDP070	Idiopathic Scoliosis	42	4.326

505		BRN024	Bronchitis	67	4.323

506	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	60	4.323

507		HMC014	Homocysteinemia	52	4.321

508	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	4.320

509	c	HMC039	Hemochromatosis, Type 1	73	4.302

510	c	HYP603	Hyperoxaluria, Primary, Type Iii	50	4.297

511		LYM143	Lymphoma, Non-Hodgkin, Familial	75	4.290

512	c	HPT016	Hepatitis B	62	4.281

513	c	HYP602	Hyperoxaluria, Primary, Type Ii	49	4.279

514	c	LKM063	Leukemia, Chronic Myeloid	71	4.278

515		PLM033	Pulmonary Embolism	58	4.259

516		PRP030	Purpura	54	4.258

517		PRS047	Prostatitis	58	4.245

518		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	4.238

519	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	4.238

520		HYP789	Hypophosphatemic Rickets with Hypercalciuria, Hereditary	49	4.230

521		DGR001	Digeorge Syndrome	62	4.221

522		PTH003	Pathologic Nystagmus	52	4.218

523	P	TMT001	Timothy Syndrome	55	4.215

524		MLG086	Malignant Hyperthermia Susceptibility	39	4.205

525	c	BTT014	Beta-Thalassemia	72	4.204

526		PRT058	Pure Autonomic Failure	58	4.181

527	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	4.156

528		ETN001	Eating Disorder	59	4.154

529	c	PNC108	Pancreatitis, Hereditary	69	4.143

530	P	SNS001	Sensorineural Hearing Loss	59	4.130

531		ACT098	Acute Erythroid Leukemia	55	4.126

532		BNG018	Benign Paroxysmal Positional Nystagmus	41	4.121

533	P	NTR004	Neutropenia	63	4.118

534		SPS057	Spasticity	42	4.117

535		ACT003	Acute Kidney Tubular Necrosis	46	4.117

536	P	ADL010	Adult Respiratory Distress Syndrome	71	4.112

537	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	4.105

538		PRM236	Primary Biliary Cholangitis	60	4.091

539		CHL067	Cholecystitis	60	4.089

540		PLM017	Pulmonary Alveolar Microlithiasis	47	4.083

541		ENT004	Enthesopathy	51	4.080

542	P	PLY019	Polyneuropathy	52	4.069

543	P	PMP001	Pemphigus	55	4.065

544	P	HYP098	Hypereosinophilic Syndrome	66	4.049

545	P	DBT005	Diabetes Insipidus	54	4.048

546	c	ACT073	Acute Leukemia	58	4.039

547	P	PTT014	Pitt-Hopkins Syndrome	64	4.035

548		PRT013	Portal Hypertension	59	4.007

549		BRK010	Burkitt Lymphoma	66	4.004

550		SBC016	Subacute Delirium	43	4.001

551		ADL002	Adult Syndrome	70	3.992

552	P	MCR129	Microvascular Complications of Diabetes 1	68	3.991

553	P	BSL038	Basal Ganglia Calcification, Idiopathic, 1	53	3.990

554	P	HMP007	Hemophilia	52	3.989

555	c	CRN243	Carney Complex, Type 1	53	3.981

556	P	CRB059	Cerebellar Degeneration	36	3.979

557		MTR002	Mitral Valve Insufficiency	52	3.978

558	c	DNT047	Dentinogenesis Imperfecta Type 2	35	3.961

559	P	ANP001	Anaplastic Large Cell Lymphoma	61	3.960

560		ART002	Arts Syndrome	66	3.952

561	P	FCL005	Focal Segmental Glomerulosclerosis	57	3.950

562	P	GRF003	Graft-Versus-Host Disease	71	3.949

563		DNT001	Dental Fluorosis	43	3.945

564		PRS063	Paresthesia	39	3.945

565		NPH010	Nephrosclerosis	50	3.944

566	P	FBR017	Fibrosarcoma	56	3.944

567		ENM001	Enamel Caries	27	3.940

568	P	CNR004	Cone-Rod Dystrophy 2	74	3.938

569		LWC001	Low Compliance Bladder	45	3.921

570	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	3.901

571	c	THY107	Thymoma, Familial	42	3.899

572	P	THY023	Thymoma	64	3.899

573		URT010	Ureteral Obstruction	45	3.896

574		MLK006	Milk Allergy	47	3.888

575	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	65	3.872

576		MDL009	Medullary Sponge Kidney	39	3.868

577	P	MTR003	Mitral Valve Stenosis	53	3.856

578	P	VNS003	Venous Insufficiency	55	3.852

579		DST006	Diastolic Heart Failure	45	3.851

580		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	3.850

581		SCH014	Schistosomiasis	56	3.850

582	c	HYP753	Hypocalciuric Hypercalcemia, Familial, Type Ii	41	3.848

583		IRN001	Iron Deficiency Anemia	58	3.847

584		ENT011	Enterocolitis	55	3.846

585		PRN039	Paraneoplastic Syndromes	37	3.838

586		VTM033	Vitamin K Deficiency Bleeding	48	3.830

587		AMN006	Aminoaciduria	37	3.824

588		OVR029	Ovarian Hyperstimulation Syndrome	63	3.818

589		SYS003	Systolic Heart Failure	49	3.817

590	P	PLM036	Pulmonary Fibrosis	66	3.804

591	P	ART018	Aortic Valve Insufficiency	52	3.792

592		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	3.791

593		THR035	Thrombasthenia	48	3.787

594	P	SCL057	Scoliosis, Isolated 1	40	3.786

595		ETH012	Ethylene Glycol Poisoning	29	3.781

596		CLR109	Colorectal Adenocarcinoma	50	3.778

597		AMN003	Amnestic Disorder	54	3.777

598	P	RTN008	Retinitis Pigmentosa	80	3.769

599	c	MCR112	Microvascular Complications of Diabetes 2	42	3.766

600	c	HYP724	Hyperlipoproteinemia, Type Iii	67	3.765

601	P	FRG001	Fragile X Syndrome	70	3.763

602	P	FNC004	Fanconi Syndrome	60	3.758

603	P	CND004	Candidiasis	58	3.757

604		BRD001	Brody Myopathy	55	3.726

605		PRR001	Periarthritis	34	3.722

606	P	INT068	Intestinal Disease	53	3.720

607		CVD001	Covid-19	57	3.719

608		WLL004	Wallerian Degeneration	38	3.718

609		CHG001	Chagas Disease	66	3.709

610		ATN005	Autonomic Dysfunction	46	3.699

611		CHL152	Childhood Acute Lymphocytic Leukemia	50	3.695

612	P	NRF002	Neurofibromatosis	57	3.692

613	P	SML001	Small Cell Carcinoma	52	3.690

614		SNS003	Sensory Peripheral Neuropathy	52	3.690

615		LMB062	Limb Ischemia	55	3.689

616		IGG001	Iga Glomerulonephritis	50	3.677

617	P	KLZ004	Kala-Azar 1	41	3.667

618		LSH001	Leishmaniasis	64	3.667

619		CHR074	Choriocarcinoma	46	3.666

620		GLM044	Glomerular Disease	35	3.665

621	P	MLT008	Multinodular Goiter	42	3.660

622		SXL003	Sexual Disorder	49	3.652

623		OST115	Osteonecrosis of the Jaw	41	3.649

624		TRD006	Tardive Dyskinesia	53	3.642

625	P	BNC003	Bone Cancer	58	3.637

626		CHR431	Chronic Venous Insufficiency	48	3.636

627		FBR047	Fibromyalgia	58	3.629

628		HLL004	Hellp Syndrome	53	3.628

629		GRW007	Growth Hormone Deficiency	46	3.627

630	P	MGR003	Migraine with Aura	52	3.627

631	P	EYD002	Eye Disease	57	3.626

632	P	CHL002	Childhood Absence Epilepsy	63	3.620

633	P	HML002	Hemolytic Anemia	62	3.607

634		CRB090	Cerebral Hypoxia	42	3.598

635	P	CNJ013	Conjunctivitis	66	3.591

636	P	MVM001	Movement Disease	61	3.590

637		GST040	Gastric Adenocarcinoma	67	3.590

638	P	PRN023	Prion Disease	60	3.586

639		HYP006	Hypertensive Heart Disease	49	3.585

640	P	PTT006	Pituitary Adenoma	55	3.580

641		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	61	3.579

642	P	ASP006	Aspergillosis	72	3.575

643		INT075	Intracranial Hypertension	53	3.573

644	P	CYS018	Cystitis	59	3.566

645		SPT004	Septic Arthritis	58	3.559

646		GST050	Gastrointestinal System Disease	55	3.555

647		HPT004	Hepatic Coma	43	3.552

648		HGH043	High Grade Glioma	45	3.547

649	P	LMB006	Limb-Girdle Muscular Dystrophy	52	3.545

650		KRT008	Keratopathy	46	3.542

651		BRR014	Barrett Esophagus	66	3.538

652	P	CHL066	Cholangitis	52	3.537

653	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	3.536

654		EXR010	Exercise-Induced Bronchoconstriction	34	3.535

655	P	NRV007	Nervous System Disease	67	3.533

656		RYN001	Raynaud Disease	50	3.525

657		DSS009	Disseminated Intravascular Coagulation	57	3.505

658		TND004	Tendinopathy	45	3.502

659		MNN043	Meningioma, Familial	79	3.500

660		GST045	Gastroenteritis	58	3.498

661		FDL002	Food Allergy	47	3.493

662		SVR001	Severe Acute Respiratory Syndrome	67	3.485

663	P	SCK002	Sick Sinus Syndrome	55	3.481

664		ANT024	Anthrax Disease	58	3.476

665		SCR001	Secretory Meningioma	40	3.475

666		LYM002	Lymphoplasmacyte-Rich Meningioma	35	3.475

667		SPN021	Spinal Meningioma	50	3.475

668		PLG002	Plague	58	3.475

669		HYP068	Hyperostosis	47	3.474

670		ARG004	Argyria	26	3.472

671	c	HPT073	Hepatitis C Virus	71	3.468

672	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	69	3.461

673		ACH005	Achalasia	55	3.459

674		LYM040	Lymphoblastic Lymphoma	53	3.458

675		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	3.457

676		HPT019	Hepatic Encephalopathy	59	3.457

677	P	OPT006	Optic Nerve Disease	58	3.454

678		ILS001	Ileus	50	3.447

679	P	HYP050	Hyperinsulinemic Hypoglycemia	57	3.441

680	c	BLD140	Blood Group, I System	46	3.439

681		PNC041	Pancreatic Ductal Adenocarcinoma	51	3.432

682		EMB004	Embryonal Carcinoma	56	3.425

683		KLD004	Keloid Disorder	39	3.425

684		RTC003	Root Caries	32	3.424

685		BNG091	Benign Chronic Pemphigus	57	3.418

686		GST023	Gastric Ulcer	52	3.413

687		DRR014	Darier-White Disease	59	3.407

688		INT066	Interstitial Lung Disease	60	3.405

689	P	RTT002	Rett Syndrome	79	3.405

690	P	URT039	Urticaria	58	3.405

691	c	ATM068	Autoimmune Hypoparathyroidism	30	3.402

692	c	MLG069	Malignant Hypertension	46	3.393

693		DGN001	Degenerative Disc Disease	49	3.392

694		ISL001	Islet Cell Tumor	56	3.390

695	P	SPR041	Spermatogenic Failure 6	47	3.388

696		OVR094	Ovarian Epithelial Cancer	39	3.387

697		VRC005	Varicose Veins	60	3.383

698	P	MYP087	Myopathy, Tubular Aggregate, 1	49	3.374

699	P	GCH001	Gaucher's Disease	70	3.367

700		CNT047	Contact Dermatitis	57	3.361

701		NRN004	Neuroendocrine Tumor	59	3.359

702	P	INF038	Influenza	68	3.356

703	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	3.351

704		PSR001	Psoriatic Arthritis	62	3.345

705		CHR100	Chronic Ulcer of Skin	57	3.344

706		TRN018	Transitional Cell Carcinoma	56	3.339

707		DPH001	Diphtheria	59	3.338

708		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	3.338

709	P	FML362	Familial Isolated Hypoparathyroidism	48	3.336

710		MST004	Mast Cell Neoplasm	42	3.331

711		MLD018	Mild Cognitive Impairment	48	3.326

712		PPL022	Papilloma	53	3.322

713		GSG001	Gas Gangrene	52	3.320

714		ORL015	Oral Squamous Cell Carcinoma	43	3.320

715	P	TRT010	Teratoma	51	3.318

716		TBC004	Tobacco Addiction	63	3.318

717		END040	Endogenous Depression	55	3.316

718	P	INS002	in Situ Carcinoma	53	3.316

719	c	INH020	Inherited Metabolic Disorder	48	3.312

720		FRZ001	Frozen Shoulder	55	3.306

721	P	INT143	Interstitial Cystitis	60	3.304

722		BRS051	Breast Disease	58	3.292

723		DMY004	Demyelinating Disease	50	3.292

724	P	MYP006	Myopia	56	3.274

725		PMP014	Pemphigoid	51	3.274

726	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	60	3.273

727		VLK001	Volkmann Contracture	23	3.267

728	P	END033	Endocarditis	58	3.266

729	P	FML011	Familial Adenomatous Polyposis	71	3.264

730	P	RHB003	Rhabdomyosarcoma	66	3.262

731		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	3.261

732	c	DWL002	Dowling-Degos Disease 1	58	3.259

733		EXT007	Extracutaneous Mastocytoma	38	3.253

734		FCL014	Focal Epilepsy	53	3.247

735		RNL077	Renal Fibrosis	46	3.246

736		OTT002	Otitis Media	71	3.239

737	P	BRS044	Breast Adenocarcinoma	58	3.230

738	c	PRG043	Progressive Familial Heart Block, Type Ib	54	3.229

739		ORL011	Oral Cancer	60	3.226

740		SQM002	Squamous Cell Papilloma	46	3.225

741		SPL018	Splenomegaly	49	3.225

742		HYP540	Hypertension, Diastolic	37	3.222

743		QDR001	Quadriplegia	50	3.214

744		SCT005	Scott Syndrome	50	3.200

745		BRS064	Bursitis	51	3.195

746	P	GLY013	Glycogen Storage Disease	60	3.194

747		VCC001	Vaccinia	47	3.190

748	c	VSC019	Vesicoureteral Reflux 1	57	3.174

749	P	UVT001	Uveitis	57	3.170

750	c	HPT001	Hepatitis C	62	3.169

751		CRV035	Cervical Cancer	73	3.168

752	c	PNS012	Paine Syndrome	60	3.168

753		CMB007	Combined Immunodeficiency	57	3.166

754	P	TTR001	Tetralogy of Fallot	69	3.165

755		CTS005	Catastrophic Antiphospholipid Syndrome	43	3.153

756		CRY008	Cryopyrin-Associated Periodic Syndrome	48	3.153

757		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	3.137

758	P	MJR007	Major Affective Disorder 1	42	3.133

759	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	3.128

760	P	SLP005	Sleep Disorder	61	3.127

761	P	AVS003	Avascular Necrosis	41	3.126

762	P	HYD006	Hydrocephalus	61	3.123

763		OST016	Osteochondrosis	52	3.113

764	P	MDL005	Medulloblastoma	75	3.112

765		HLC007	Helicobacter Pylori Infection	67	3.109

766		PMP006	Pemphigus Vulgaris, Familial	58	3.094

767		HYP741	Hyperparathyroidism 2 with Jaw Tumors	51	3.092

768		DFF005	Diffuse Large B-Cell Lymphoma	54	3.090

769	P	MTR012	Mitral Valve Disease	57	3.089

770	P	LPR021	Leprosy 3	71	3.088

771		HNS001	Hansen's Disease	32	3.088

772	c	MGR032	Migraine, Familial Hemiplegic, 1	54	3.085

773		RTN020	Retinal Vascular Disease	46	3.084

774		BTT017	Beta-Thalassemia Major	51	3.076

775	P	CRC039	Coarctation of Aorta	46	3.074

776		ART074	Aortic Dissection	53	3.070

777		BRN056	Bronchopulmonary Dysplasia	56	3.068

778	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	3.064

779		CHL028	Childhood Type Dermatomyositis	59	3.050

780		PRP017	Periapical Periodontitis	46	3.049

781		NDL007	Nodular Goiter	48	3.041

782	c	ESS001	Essential Tremor	57	3.032

783	P	GLL018	Gallbladder Cancer	53	3.028

784	c	CHL119	Cholangitis, Primary Sclerosing	58	3.026

785		CLN045	Colonic Benign Neoplasm	48	3.022

786		TLN003	Telangiectasis	51	3.018

787		ALD013	Aldosterone-Producing Adenoma	36	3.017

788		PHN003	Phenylketonuria	76	3.013

789		CRB086	Cerebral Aneurysms	40	3.012

790		GNG003	Gingival Recession	49	3.010

791	P	MNC007	Monocytic Leukemia	47	3.007

792		KRT009	Keratosis	53	3.005

793		CHL123	Chlamydia	58	3.004

794	c	GLC092	Glaucoma, Primary Open Angle	62	2.999

795		PRN019	Perinatal Necrotizing Enterocolitis	60	2.993

796		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	2.991

797	P	SBS003	Substance Abuse	54	2.988

798		RLP002	Relapsing-Remitting Multiple Sclerosis	56	2.980

799	P	CHR012	Chronic Granulomatous Disease	69	2.979

800		MYL009	Myelodysplastic Syndrome	67	2.977

801	P	HMR005	Hemorrhoid	49	2.975

802	P	PLY018	Polycythemia	56	2.972

803		CCN002	Cocaine Abuse	49	2.968

804		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	36	2.964

805		DYS015	Dysentery	50	2.964

806		MTH071	Methane Production	25	2.958

807		STR081	Stormorken Syndrome	55	2.956

808		PRM013	Premature Menopause	58	2.950

809		OCL006	Ocular Hypertension	53	2.945

810	c	HMP004	Hemophilia B	68	2.944

811		SPN027	Spinal Stenosis	59	2.943

812	P	SJG008	Sjogren Syndrome	61	2.939

813		PSD014	Pseudopseudohypoparathyroidism	54	2.939

814	c	BSL007	Basal Cell Carcinoma	68	2.936

815	P	PRS038	Personality Disorder	65	2.934

816		FBR009	Fibrous Dysplasia	48	2.933

817		BCK003	Background Diabetic Retinopathy	47	2.925

818	P	MYC033	Myoclonus	47	2.924

819		ATN004	Autonomic Neuropathy	42	2.923

820		DRG003	Drug Dependence	46	2.921

821		PRN032	Paraneoplastic Cerebellar Degeneration	25	2.905

822	P	BNG032	Benign Mesothelioma	53	2.902

823		PRT038	Protein-Energy Malnutrition	53	2.899

824		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	2.895

825	c	JVN025	Juvenile Primary Osteoporosis	21	2.894

826		CRN288	Corneal Dystrophy, Band-Shaped	36	2.894

827	c	CHR098	Chronic Pyelonephritis	34	2.893

828	P	ANG015	Angioedema	56	2.893

829		INT030	Intracranial Aneurysm	55	2.890

830		HVY002	Heavy Metal Poisoning	22	2.881

831		MSC152	Muscular Dystrophy, Becker Type	69	2.880

832	P	NSP012	Nasopharyngeal Carcinoma	61	2.880

833	P	EPL140	Epilepsy, Idiopathic Generalized	62	2.879

834	P	LTH003	Lethal Congenital Contracture Syndrome	41	2.878

835		SNT005	Sinoatrial Node Disease	47	2.874

836		NPH078	Nephrolithiasis, Uric Acid	39	2.869

837		ASP004	Asphyxia Neonatorum	50	2.869

838		PLC007	Placental Abruption	47	2.868

839		LMY002	Leiomyoma	51	2.868

840	P	CHN012	Chondrosarcoma	57	2.866

841		ANT039	Antisynthetase Syndrome	55	2.862

842		CRC021	Carcinosarcoma	64	2.861

843		PST053	Postherpetic Neuralgia	40	2.860

844		SFT003	Soft Tissue Sarcoma	57	2.856

845		BRN028	Brain Cancer	74	2.852

846		RGH001	Right Bundle Branch Block	47	2.847

847	P	GLL022	Guillain-Barre Syndrome	60	2.837

848		PNM001	Pneumocystosis	61	2.829

849		NNL006	Non-Alcoholic Steatohepatitis	54	2.828

850		PRM329	Premature Aging	36	2.827

851		URM005	Uremic Pruritus	45	2.826

852	P	TMP003	Temporal Arteritis	69	2.823

853		ERL001	Early Myoclonic Encephalopathy	62	2.822

854		ASP026	Asplenia, Isolated Congenital	43	2.814

855		RTN003	Retinal Ischemia	49	2.810

856		GLC036	Glucagonoma	46	2.806

857		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	2.805

858		PST028	Post-Traumatic Stress Disorder	59	2.803

859		LFT001	Left Bundle Branch Hemiblock	47	2.801

860	c	VRL010	Viral Hepatitis	53	2.798

861		INT002	Intermittent Claudication	61	2.797

862		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	2.797

863		CHR178	Chromosomal Triplication	34	2.796

864	P	PTS002	Ptosis	52	2.785

865		FRN006	Frontotemporal Dementia	68	2.782

866		TRT001	Teratocarcinoma	42	2.782

867		SQM013	Squamous Cell Carcinoma, Head and Neck	73	2.781

868	P	SPP010	Suppressor of Tumorigenicity 3	51	2.779

869		HRN029	Hearing Loss, Noise-Induced	37	2.778

870		ANR004	Anuria	44	2.777

871		MST020	Mast Cell Activation Syndrome	28	2.774

872		KRT019	Keratitis, Hereditary	66	2.772

873		GLN010	Glanzmann Thrombasthenia	66	2.768

874		EWN003	Ewing Sarcoma	70	2.765

875		URT014	Ureterolithiasis	43	2.763

876	c	OST164	Osteoporosis, Juvenile	54	2.762

877		PST021	Postpartum Depression	50	2.761

878		MMM006	Mammographic Density	39	2.754

879		ACT119	Acute Promyelocytic Leukemia	62	2.750

880	P	WLF004	Wolfram Syndrome	61	2.744

881	P	CNT004	Centronuclear Myopathy	57	2.740

882		DMP001	Dumping Syndrome	43	2.733

883		HMP005	Hemiplegia	54	2.726

884	P	ANT006	Antiphospholipid Syndrome	55	2.717

885		ONC003	Oncogenic Osteomalacia	42	2.716

886	P	PNC025	Panic Disorder	52	2.708

887		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	2.706

888	P	CLS010	Cluster Headache	42	2.705

889	P	SCL048	Sclerosteosis	58	2.704

890		HYP052	Hyperkalemic Periodic Paralysis	63	2.699

891		DFF036	Differentiated Thyroid Carcinoma	51	2.691

892		BLL006	Bullous Pemphigoid	61	2.689

893	P	SCL009	Sclerosing Cholangitis	48	2.686

894	c	HYP272	Hypercholesterolemia, Familial, 3	45	2.683

895		MYL005	Myelofibrosis	71	2.678

896		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	2.677

897		NRD100	Neurodevelopmental, Jaw, Eye, and Digital Syndrome	49	2.675

898		PLM031	Poliomyelitis	63	2.673

899		VSC003	Visceral Leishmaniasis	55	2.672

900	c	PSD066	Pseudohypoparathyroidism, Type Ib	52	2.663

901		PHS001	Phosphorus Metabolism Disease	38	2.662

902	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	2.660

903		SMT003	Somatostatinoma	52	2.658

904	P	TBR001	Tuberous Sclerosis	69	2.656

905		CRT016	Carotid Artery Disease	52	2.656

906	P	MNN013	Meningitis	65	2.654

907	P	LCH002	Lichen Planus	54	2.652

908		VTM002	Vitamin B12 Deficiency	48	2.649

909		AZS001	Azoospermia	45	2.649

910		PLR008	Pleurisy	50	2.649

911	P	MLT007	Multiple Epiphyseal Dysplasia	56	2.649

912		BCT004	Bacteriuria	47	2.647

913	c	ACT134	Acute Liver Failure	59	2.647

914	P	DNT007	Dentin Sensitivity	34	2.646

915	P	NMN002	Niemann-Pick Disease	60	2.628

916	c	ACT249	Acute Asthma	40	2.626

917		SCR011	Scrapie	39	2.621

918		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	64	2.615

919	P	BRB001	Beriberi	44	2.609

920		PCD001	Pica Disease	38	2.606

921	P	CMP008	Compartment Syndrome	50	2.602

922		NWC001	Newcastle Disease	47	2.600

923		DNT010	Dentin Caries	31	2.600

924	c	CTR132	Cataract 3, Multiple Types	42	2.598

925	c	BPL002	Bipolar I Disorder	47	2.598

926		LWC002	Lowe Oculocerebrorenal Syndrome	68	2.595

927		KWS002	Kawasaki Disease	65	2.595

928		MYL031	Myeloproliferative Neoplasm	66	2.595

929		THR004	Thrombocytosis	53	2.592

930		ODN023	Odontochondrodysplasia	67	2.591

931		MSL001	Measles	61	2.583

932	P	CRP001	Carpal Tunnel Syndrome	66	2.583

933	P	GLL020	Gallbladder Disease	56	2.583

934		XLN012	X-Linked Congenital Stationary Night Blindness	28	2.579

935	c	BCT007	Bacterial Meningitis	55	2.578

936	P	PLY041	Polymyositis	59	2.577

937		DCT002	Ductal Carcinoma in Situ	58	2.576

938		PLS009	Plasma Cell Neoplasm	64	2.571

939	P	ICH004	Ichthyosis	56	2.569

940		SLL001	Sialolithiasis	36	2.567

941		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	2.562

942		DBT084	Diabetes Mellitus, Ketosis-Prone	60	2.562

943		CHR073	Choreatic Disease	54	2.562

944	c	MCL013	Mucolipidosis Iv	65	2.558

945		CMP034	Complete Androgen Insensitivity Syndrome	55	2.556

946		ART004	Aortic Atherosclerosis	47	2.555

947		HSH003	Hashimoto Thyroiditis	60	2.552

948		CRT084	Creatinine Clearance Quantitative Trait Locus	25	2.547