Search results for Calcium

5588 hits were found for Calcium

#	Family	MCID	Name	MIFTS	Score
1		NPH091	Nephrolithiasis, Calcium Oxalate	61	54.585

2	c	CHN022	Chondrocalcinosis 2	40	40.554

3		FML307	Familial Calcium Pyrophosphate Deposition	38	38.932

4	P	HYP069	Hyperparathyroidism	62	25.161

5		IMM066	Immunodeficiency 9	39	24.376

6		IMM065	Immunodeficiency 10	47	22.906

7		RCK004	Rickets	64	22.508

8	P	OST002	Osteoporosis	76	22.294

9	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	20.711

10	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	20.711

11	P	CHN059	Chondrocalcinosis	51	20.216

12		NPH009	Nephrolithiasis	54	18.088

13	c	NRL036	Neurological Channelopathy of the Central Nervous System Due to a Genetic Calcium Channel Defect	2	17.804

14	c	NRL030	Neurological Muscular Channelopathy Due to a Genetic Calcium Channel Defect	3	17.804

15		BNR002	Bone Resorption Disease	47	17.651

16	c	SCN007	Secondary Hyperparathyroidism	50	16.572

17	c	PRM005	Primary Hyperparathyroidism	59	15.620

18	c	HYP595	Hypertension, Essential	84	15.524

19		URL001	Urolithiasis	45	14.641

20	P	BND020	Bone Disease	60	14.455

21	P	HYP024	Hypoparathyroidism	55	13.986

22	P	KDN018	Kidney Disease	71	13.617

23		PRT037	Pertussis	49	13.239

24		HYP025	Hyperphosphatemia	47	13.187

25	c	CHR684	Chronic Kidney Disease	73	12.995

26	c	CHN021	Chondrocalcinosis 1	17	12.720

27		LPP008	Lipoprotein Quantitative Trait Locus	65	12.085

28	c	BLD126	Bleeding Disorder, Platelet-Type, 18	39	11.993

29		ATH013	Atherosclerosis Susceptibility	63	11.243

30	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	11.232

31		ART140	Arteries, Anomalies of	52	11.113

32	P	FML068	Familial Hypocalciuric Hypercalcemia	55	11.029

33	P	CRN300	Coronary Heart Disease 1	73	10.808

34	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	10.264

35		END086	End Stage Renal Disease	54	10.253

36	P	CLR023	Colorectal Cancer	100	10.251

37		ANG054	Angina Pectoris	65	10.182

38	c	PRC016	Pre-Eclampsia	64	9.625

39		OST011	Osteomalacia	52	9.377

40		AML006	Amelogenesis Imperfecta Hypoplastic Type, Ig	25	9.350

41		ADN018	Adenoma	58	9.311

42		IDP073	Idiopathic Hypercalciuria	41	9.288

43		CMB055	Combined Immunodeficiency Due to Crac Channel Dysfunction	33	9.255

44	P	NRB001	Neuroblastoma	66	9.211

45		KRT002	Keratomalacia	54	9.041

46		AGN016	Aging	53	8.688

47		NPH003	Nephrocalcinosis	49	8.677

48		DNT012	Dental Caries	53	8.664

49		CLC006	Calcinosis	47	8.603

50		RPD005	Rapidly Involuting Congenital Hemangioma	48	8.552

51	P	PNC044	Pancreatitis	61	8.526

52	c	ACT027	Acute Pancreatitis	60	8.484

53		ISC004	Ischemia	61	8.274

54	P	HRT032	Heart Disease	84	8.257

55		LPD008	Lipid Metabolism Disorder	61	8.161

56	P	HYP726	Hypercalcemia, Infantile, 1	58	7.898

57	P	PRD008	Periodontitis	63	7.807

58	c	HYP836	Hypercholesterolemia, Familial, 1	73	7.686

59	c	TYP009	Type 2 Diabetes Mellitus	91	7.625

60	P	MSC005	Muscular Dystrophy	66	7.603

61		48X005	48,xyyy	39	7.544

62	P	VSC007	Vascular Disease	62	7.497

63		ALL029	Allergic Disease	61	7.396

64		PRT251	Proteinuria, Chronic Benign	58	7.376

65		OST159	Osteogenic Sarcoma	66	7.363

66		HLX001	Helix Syndrome	47	7.361

67		RNL011	Renal Osteodystrophy	48	7.262

68		HYP017	Hypophosphatemia	49	7.109

69	P	DBT009	Diabetes Mellitus	67	7.026

70	P	ECL001	Eclampsia	52	6.859

71	P	HYP733	Hypercalciuria, Absorptive, 2	45	6.788

72		MTB004	Metabolic Acidosis	48	6.773

73		HYP005	Hypokalemia	55	6.758

74		INS001	Insulinoma	59	6.756

75		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	6.730

76		GT001	Gout	63	6.719

77	c	ATR087	Atrial Standstill 1	74	6.663

78	P	ALZ034	Alzheimer Disease	87	6.658

79	P	SRC025	Sarcoidosis 1	70	6.609

80	P	ADN016	Adenocarcinoma	63	6.505

81		CNG034	Congestive Heart Failure	69	6.496

82		HYP266	Hypoxia	56	6.429

83		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	6.393

84	c	HYP752	Hypocalciuric Hypercalcemia, Familial, Type I	49	6.360

85		GLM045	Glioma	62	6.349

86	c	GLL024	Gallbladder Disease 1	53	6.331

87	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	6.294

88	P	LTR001	Lateral Sclerosis	57	6.290

89		GLL048	Glial Tumor	51	6.290

90	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	6.274

91	P	PRM002	Primary Hyperoxaluria	65	6.268

92	c	ACT071	Acute Kidney Failure	60	6.268

93	P	CRD119	Cardiac Arrest	68	6.230

94	P	ART023	Arthropathy	59	6.229

95	P	LKM002	Leukemia	65	6.193

96		THY029	Thyroid Carcinoma	55	6.183

97		CHL014	Cholera	62	6.176

98	P	ART021	Arteriosclerosis	53	6.167

99	c	MCR120	Microvascular Complications of Diabetes 7	47	6.116

100	P	PRS040	Prostate Cancer	95	6.105

101		ANX004	Anoxia	40	6.084

102		LMB002	Lambert-Eaton Myasthenic Syndrome	51	6.079

103		MYL069	Myeloma, Multiple	76	6.064

104	P	ATR011	Atrial Fibrillation	66	6.047

105	P	LYM118	Lymphoma	66	6.036

106		CYS001	Cystic Fibrosis	77	6.035

107	c	MCR113	Microvascular Complications of Diabetes 3	52	5.994

108	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	5.959

109	c	BDY006	Body Mass Index Quantitative Trait Locus 8	43	5.959

110	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	5.959

111	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	5.959

112	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	5.959

113	c	BDY012	Body Mass Index Quantitative Trait Locus 7	43	5.959

114	c	BDY019	Body Mass Index Quantitative Trait Locus 18	46	5.959

115	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	5.959

116	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	5.959

117		CLR108	Colorectal Adenoma	63	5.958

118		URM002	Uremia	47	5.955

119		IRN002	Iron Metabolism Disease	56	5.929

120	P	ART022	Arthritis	70	5.919

121	P	BDY004	Body Mass Index Quantitative Trait Locus 11	82	5.911

122		PRT029	Parathyroid Adenoma	51	5.904

123	P	BRS047	Breast Cancer	97	5.904

124		TTN003	Tetanus	64	5.901

125	P	MLG056	Malignant Hyperthermia	65	5.884

126		CLN015	Colon Adenocarcinoma	64	5.866

127	P	MYP004	Myopathy	67	5.850

128	P	PLM037	Pulmonary Hypertension	69	5.793

129	c	MGR028	Migraine with or Without Aura 1	63	5.786

130	c	MCR133	Microvascular Complications of Diabetes 4	41	5.782

131	c	MCR130	Microvascular Complications of Diabetes 6	41	5.782

132		MSC157	Muscular Dystrophy, Duchenne Type	78	5.773

133		OST012	Osteoarthritis	77	5.769

134	P	PHC003	Pheochromocytoma	70	5.758

135		ADR040	Adrenal Gland Pheochromocytoma	45	5.745

136	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	79	5.743

137		47X002	47,xyy	47	5.691

138		HMN044	Human Immunodeficiency Virus Type 1	76	5.601

139	P	MYC007	Myocardial Infarction	69	5.595

140	c	DLT002	Dilated Cardiomyopathy	79	5.582

141		OST017	Osteomyelitis	63	5.525

142	P	PSD015	Pseudohypoparathyroidism	54	5.495

143		INT007	Intermediate Coronary Syndrome	53	5.431

144	P	SZR006	Seizure Disorder	69	5.431

145	P	LKM062	Leukemia, Acute Lymphoblastic	69	5.405

146		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	5.363

147		LYM019	Lymphosarcoma	46	5.348

148	P	RHM011	Rheumatoid Arthritis	81	5.331

149		CNS004	Constipation	56	5.327

150	c	MCR115	Microvascular Complications of Diabetes 5	65	5.325

151	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	5.322

152	P	EPL164	Epilepsy	70	5.309

153	P	RCT021	Rectum Cancer	54	5.304

154		SPN186	Spinal Cord Injury	60	5.284

155	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	5.225

156	P	PNC035	Pancreatic Cancer	87	5.220

157	P	HYP086	Hypothyroidism	68	5.211

158	P	HYP776	Hyperparathyroidism, Neonatal Severe	46	5.202

159		HRW001	Hair Whorl	35	5.185

160	c	HYP794	Hyperoxaluria, Primary, Type I	63	5.181

161	P	PLY014	Polycystic Kidney Disease	71	5.156

162		PRT010	Parathyroid Carcinoma	68	5.154

163	P	HYP076	Hyperthyroidism	53	5.147

164		LVR012	Liver Cirrhosis	62	5.130

165		CRN030	Coronary Stenosis	50	5.092

166		MMM001	Mammary Paget's Disease	53	5.063

167		HYP056	Hypoglycemia	65	5.040

168		CLC001	Calciphylaxis	50	5.014

169	c	ACT075	Acute Myocardial Infarction	55	4.979

170	P	NRP001	Neuropathy	59	4.960

171		CRH001	Crohn's Disease	80	4.953

172		CRB039	Cerebrovascular Disease	65	4.927

173		PNG002	Pain Agnosia	51	4.918

174	P	PSR002	Psoriasis	63	4.912

175		DWN001	Down Syndrome	70	4.910

176	P	DRR001	Diarrhea	55	4.908

177	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	4.888

178	P	INF032	Infertility	60	4.882

179	P	HYP061	Hypertrophic Cardiomyopathy	68	4.832

180	P	LNG032	Lung Cancer	98	4.822

181	P	CRD246	Cardiovascular System Disease	55	4.791

182		CYT002	Cytokine Deficiency	43	4.783

183	P	CHR345	Chronic Pain	50	4.768

184	P	GST053	Gastric Cancer	82	4.736

185	P	BPL003	Bipolar Disorder	56	4.727

186		HYP066	Hyperglycemia	60	4.719

187	P	OVR042	Ovarian Cancer	88	4.713

188	c	MJR022	Major Affective Disorder 8	37	4.707

189	c	MJR024	Major Affective Disorder 9	40	4.707

190		IMM167	Immune Deficiency Disease	76	4.699

191	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	4.676

192		CRD132	Cardiac Conduction Defect	59	4.667

193		TRM010	Traumatic Brain Injury	50	4.656

194	P	PRP019	Peripheral Nervous System Disease	57	4.583

195		PRP027	Peripheral Vascular Disease	71	4.554

196		HYP060	Hyperinsulinism	53	4.553

197		PLY150	Polykaryocytosis Inducer	29	4.529

198		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	4.521

199	P	LCT002	Lactose Intolerance	51	4.519

200		ALC007	Alcohol Dependence	65	4.504

201		STR067	Stroke, Ischemic	79	4.496

202	P	RNL007	Renal Tubular Acidosis	52	4.493

203		PST011	Pustulosis of Palm and Sole	52	4.463

204		PRT036	Peritonitis	65	4.447

205		SCN001	Secondary Hyperparathyroidism of Renal Origin	24	4.444

206	c	ATS007	Autism Spectrum Disorder	71	4.429

207	P	URN019	Urinary Tract Infection	48	4.426

208		MNT002	Mental Depression	56	4.413

209		PPL052	Papillomatosis, Confluent and Reticulated	34	4.399

210		GLC003	Glucose Intolerance	53	4.377

211		GLB002	Glioblastoma	67	4.376

212	P	GLM040	Glioma Susceptibility 1	70	4.369

213		BRN071	Brain Injury	50	4.363

214		RYN005	Raynaud Phenomenon	45	4.328

215		PRM020	Premenstrual Tension	39	4.326

216		CRD223	Cardiac Arrhythmia	63	4.316

217		ZLL002	Zollinger-Ellison Syndrome	55	4.303

218		ATR057	Atrioventricular Block	54	4.300

219	P	INF037	Inflammatory Bowel Disease	53	4.283

220		PTT037	Pituitary Tumors	44	4.278

221		ACQ007	Acquired Immunodeficiency Syndrome	58	4.277

222		RNL114	Renal Cell Carcinoma, Nonpapillary	79	4.273

223		FTT001	Fatty Liver Disease	61	4.272

224		DNT006	Dental Pulp Necrosis	43	4.240

225	P	BRT004	Bartter Disease	58	4.235

226		BNN003	Bone Inflammation Disease	47	4.231

227	P	THL005	Thalassemia	56	4.223

228		DPR016	Depression	64	4.222

229	P	GLM007	Glomerulonephritis	59	4.220

230	P	BCL017	B-Cell Lymphoma	57	4.204

231		ESP021	Esophageal Cancer	84	4.195

232	c	PLM164	Pulmonary Hypertension, Primary, 1	75	4.194

233		TXC005	Toxic Shock Syndrome	61	4.190

234	P	MLT020	Multiple Sclerosis	79	4.171

235	P	PRK039	Parkinsonism	55	4.159

236	P	HPT023	Hepatocellular Carcinoma	95	4.156

237	P	MLT074	Multiple Endocrine Neoplasia	58	4.147

238	c	SCL052	Scleroderma, Familial Progressive	60	4.146

239		OST003	Osteonecrosis	60	4.146

240		INS024	Insulin-Like Growth Factor I	77	4.144

241		RHB024	Rhabdomyosarcoma 2	65	4.133

242		IRR002	Irritable Bowel Syndrome	64	4.132

243	c	ART101	Aortic Valve Disease 2	65	4.132

244		GLC086	Glucocorticoid-Induced Osteoporosis	43	4.130

245	c	TYP008	Type 1 Diabetes Mellitus	77	4.125

246		MLG169	Malignant Astrocytoma	57	4.115

247	P	ANR048	Aniridia 1	66	4.114

248		IDP085	Idiopathic Infantile Hypercalcemia	32	4.112

249		CRB004	Cerebral Artery Occlusion	45	4.109

250	P	TXP001	Toxoplasmosis	59	4.103

251	P	PGT001	Paget's Disease of Bone	60	4.100

252		STT001	Status Epilepticus	58	4.098

253	c	HYP243	Hyperparathyroidism 1	48	4.090

254	P	SYS005	Systemic Scleroderma	73	4.075

255	P	PSD087	Pseudoxanthoma Elasticum	66	4.071

256		GTR002	Goiter	52	4.036

257	c	CRN243	Carney Complex, Type 1	53	4.033

258		NNL005	Non-Alcoholic Fatty Liver Disease	63	4.032

259	P	OVR082	Overgrowth Syndrome	41	4.026

260	P	PLY011	Polycystic Ovary Syndrome	57	4.023

261	P	HRD086	Hereditary Hypophosphatemic Rickets	40	3.978

262		NTR005	Nutritional Deficiency Disease	60	3.966

263		LPT014	Leptin Deficiency or Dysfunction	77	3.957

264	c	SYS001	Systemic Lupus Erythematosus	85	3.934

265	P	NPH012	Nephrotic Syndrome	61	3.918

266	P	HNT016	Huntington Disease	73	3.897

267	P	TRN020	Turner Syndrome	67	3.891

268	P	LNG028	Long Qt Syndrome	63	3.874

269		MYC005	Myocardial Stunning	45	3.867

270		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	3.867

271	P	CTR002	Cataract	59	3.858

272		CRY024	Crystal Arthropathies	18	3.853

273	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	3.836

274	c	HYP608	Hypocalciuric Hypercalcemia, Familial, Type Iii	42	3.835

275	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	64	3.834

276	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	64	3.833

277	P	ATS364	Autism	72	3.833

278	P	LVR013	Liver Disease	68	3.820

279		HMS001	Hemosiderosis	48	3.807

280	P	TRM003	Tremor	50	3.802

281	c	HYP724	Hyperlipoproteinemia, Type Iii	66	3.799

282		RTR008	Root Resorption	44	3.778

283		ADL002	Adult Syndrome	69	3.777

284		HYP014	Hyperuricemia	51	3.766

285	P	SCL018	Scoliosis	57	3.741

286		ACR007	Acromegaly	70	3.721

287		SKN016	Skin Disease	63	3.720

288	P	PNM007	Pneumonia	64	3.710

289	P	RRH023	Rare Hereditary Hemochromatosis	52	3.707

290		OST004	Osteitis Fibrosa	38	3.699

291		MCS002	Mucositis	55	3.677

292		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	3.662

293		SYN036	Syncope	44	3.611

294		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	3.602

295	P	LPS004	Lupus Erythematosus	61	3.597

296	P	HPT021	Hepatitis	68	3.580

297		THR024	Thrombosis	56	3.569

298	P	MLN008	Melanoma	75	3.569

299		THY111	Thyroid Carcinoma, Familial Medullary	67	3.549

300		IMP005	Impotence	52	3.548

301		DFC004	Deficiency Anemia	74	3.543

302		BRT054	Brittle Bone Disorder	74	3.538

303	P	DST107	Distal Renal Tubular Acidosis	48	3.533

304	P	ENC018	Encephalopathy	62	3.510

305	c	LKM061	Leukemia, Acute Myeloid	83	3.491

306		ATM095	Autoimmune Disease	61	3.488

307	P	RSP003	Respiratory Failure	73	3.470

308		TND005	Tendinitis	53	3.466

309	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	62	3.458

310	P	ALC033	Alcohol Use Disorder	67	3.456

311		PLM129	Pulmonary Disease, Chronic Obstructive	74	3.442

312	P	MLN007	Male Infertility	56	3.442

313		HMN014	Human Immunodeficiency Virus Infectious Disease	54	3.430

314	c	BLD140	Blood Group, I System	47	3.430

315		WLL001	Williams-Beuren Syndrome	60	3.407

316		SQM006	Squamous Cell Carcinoma	59	3.406

317	P	OST001	Osteopetrosis	70	3.389

318	c	THR092	Thrombophilia Due to Thrombin Defect	74	3.387

319		GNG012	Gingival Overgrowth	49	3.370

320	P	MSC003	Muscular Atrophy	52	3.367

321		PLP001	Pulpitis	48	3.366

322	P	ESP024	Esophagitis	60	3.359

323	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	3.356

324	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	60	3.355

325	P	PRD021	Periodic Paralysis	42	3.343

326		GST092	Gastroesophageal Reflux	59	3.340

327	c	HYP753	Hypocalciuric Hypercalcemia, Familial, Type Ii	43	3.337

328	P	DDN001	Duodenal Ulcer	52	3.334

329		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	42	3.330

330	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	3.321

331		LYM133	Lymphoma, Hodgkin, Classic	69	3.320

332	c	HYP603	Hyperoxaluria, Primary, Type Iii	50	3.314

333	c	FML021	Familial Hypercholesterolemia	71	3.311

334	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	3.302

335	P	EPS003	Episodic Ataxia	59	3.300

336		PPT005	Peptic Ulcer Disease	58	3.298

337	P	PRK057	Parkinson Disease, Late-Onset	79	3.291

338		STM007	Stomatitis	52	3.284

339	c	LKM005	Leukemia, T-Cell, Chronic	33	3.278

340		BCT022	Bacterial Infectious Disease	55	3.267

341		PNC129	Pancreatic Adenocarcinoma	64	3.267

342	P	DMN002	Dementia	65	3.261

343		SPN035	Spindle Cell Sarcoma	51	3.252

344		SRC014	Sarcoma	64	3.252

345	P	FML023	Familial Hemiplegic Migraine	53	3.250

346		CLT003	Colitis	63	3.242

347		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	3.224

348	P	RHN004	Rhinitis	56	3.217

349	c	HPT003	Hepatitis a	63	3.214

350		CHL068	Cholestasis	61	3.211

351		HYP789	Hypophosphatemic Rickets with Hypercalciuria, Hereditary	49	3.205

352	P	THY032	Thyroiditis	56	3.202

353		ULC004	Ulcerative Colitis	74	3.200

354	P	BRG001	Brugada Syndrome	69	3.180

355	P	CNR004	Cone-Rod Dystrophy 2	74	3.177

356		THY125	Thyroid Gland Medullary Carcinoma	48	3.176

357	P	PTT014	Pitt-Hopkins Syndrome	63	3.173

358	P	HDC001	Headache	56	3.172

359	P	DNT020	Dent Disease 1	63	3.170

360	P	FML187	Familial Hypertension	34	3.168

361		GST030	Gastrinoma	45	3.148

362	c	HYP602	Hyperoxaluria, Primary, Type Ii	51	3.145

363		CTS005	Catastrophic Antiphospholipid Syndrome	43	3.143

364		CRY008	Cryopyrin-Associated Periodic Syndrome	48	3.143

365		CHL065	Cholangiocarcinoma	57	3.139

366		INT079	Intrahepatic Cholangiocarcinoma	51	3.139

367		CNT105	Central Core Disease of Muscle	59	3.135

368		DSS032	Disease by Infectious Agent	55	3.130

369		TRN015	Transient Cerebral Ischemia	62	3.127

370	c	PRD040	Periodontitis, Chronic	52	3.123

371		PLM010	Pulmonary Edema	54	3.121

372	P	END044	Endometriosis	62	3.109

373		PRS047	Prostatitis	57	3.105

374		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	3.101

375	P	HYP750	Hypertriglyceridemia, Familial	61	3.091

376	P	MYL006	Myeloid Leukemia	60	3.089

377		LNG099	Lung Disease	62	3.086

378	c	SPN309	Spinocerebellar Ataxia 6	58	3.078

379	P	DRM010	Dermatomyositis	61	3.076

380		PLM001	Pulmonary Tuberculosis	69	3.071

381	c	ART115	Aortic Valve Disease 1	72	3.061

382	P	DRM053	Dermatitis, Atopic	65	3.058

383		INT323	Intraocular Pressure Quantitative Trait Locus	63	3.053

384	P	ADL017	Adult T-Cell Leukemia	53	3.044

385		HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	3.042

386		HYP080	Hypogonadism	49	3.042

387	c	EPS035	Episodic Ataxia, Type 2	63	3.041

388		WTH001	Withdrawal Disorder	47	3.036

389		GTL001	Gitelman Syndrome	65	3.031

390	P	BLD134	Bladder Cancer	79	3.029

391		CLN045	Colonic Benign Neoplasm	48	3.014

392		ART016	Aortic Aneurysm	68	3.008

393	P	GRV001	Graves' Disease	54	3.004

394	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	3.004

395	c	BRN108	Branchiootic Syndrome 1	63	3.002

396	P	AST005	Asthma	75	2.998

397	c	SML038	Small Cell Cancer of the Lung	68	2.987

398	P	RNV001	Renovascular Hypertension	48	2.986

399		MDD011	Mood Disorder	61	2.982

400		BRD001	Brody Myopathy	55	2.978

401		LYM040	Lymphoblastic Lymphoma	53	2.978

402	P	SCH015	Schizophrenia	74	2.968

403	c	PNC108	Pancreatitis, Hereditary	68	2.959

404	P	AMY004	Amyloidosis	69	2.943

405		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	51	2.942

406		MTB008	Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration	42	2.942

407		PRT030	Parathyroid Gland Disease	44	2.939

408		THY030	Thyroid Gland Disease	50	2.932

409	c	MLT156	Multiple Endocrine Neoplasia, Type I	71	2.923

410		LYM143	Lymphoma, Non-Hodgkin, Familial	74	2.922

411	c	PSD108	Pseudohypoparathyroidism, Type Ia	64	2.920

412	P	RTN018	Retinal Disease	53	2.914

413		ART002	Arts Syndrome	66	2.898

414		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	2.889

415	c	GRV008	Graves Disease 1	54	2.886

416	P	ENC004	Encephalitis	61	2.885

417	P	VTM036	Vitamin D-Dependent Rickets	40	2.881

418		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	33	2.878

419		ANT039	Antisynthetase Syndrome	55	2.876

420	P	LNG064	Lung Cancer Susceptibility 3	69	2.870

421	P	CNG010	Congenital Stationary Night Blindness	56	2.866

422		ANK001	Ankylosis	50	2.864

423	c	SVR005	Severe Pre-Eclampsia	49	2.862

424	P	MYC084	Mycobacterium Tuberculosis 1	68	2.857

425	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	2.847

426		OVR029	Ovarian Hyperstimulation Syndrome	63	2.845

427	P	CYS039	Cystic Kidney Disease	52	2.845

428	P	HYP265	Hypotonia	42	2.841

429	P	BSL038	Basal Ganglia Calcification, Idiopathic, 1	51	2.832

430	P	CLC063	Celiac Disease 1	65	2.830

431	c	JVN010	Juvenile Rheumatoid Arthritis	52	2.827

432	P	ANP001	Anaplastic Large Cell Lymphoma	59	2.825

433		CHL004	Cholelithiasis	48	2.821

434		ANR007	Anorexia Nervosa	59	2.813

435		MYT011	Myotonia	37	2.810

436		DBT010	Diabetic Neuropathy	54	2.809

437	P	MCR129	Microvascular Complications of Diabetes 1	67	2.801

438	P	KDN017	Kidney Cancer	60	2.801

439	P	MYT002	Myotonic Dystrophy	51	2.801

440		MRF001	Marfan Syndrome	76	2.796

441	P	MJR001	Major Depressive Disorder	68	2.794

442		URN010	Urinary Tract Obstruction	55	2.791

443		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	2.789

444		CRN019	Coronary Artery Vasospasm	47	2.786

445	c	ACT068	Acute Cystitis	60	2.784

446		CYS013	Cystinuria	66	2.781

447		NRL016	Neural Tube Defects	80	2.773

448		PRP080	Peripheral Artery Disease	54	2.758

449	P	LCT001	Lactic Acidosis	50	2.753

450		BRR014	Barrett Esophagus	66	2.749

451	P	TMP001	Temporal Lobe Epilepsy	49	2.731

452		DRM006	Dermatitis	61	2.728

453	P	DYS154	Dystonia	64	2.728

454		ALL003	Allergic Rhinitis	66	2.715

455		DYS073	Dysphagia	53	2.712

456	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	2.711

457		PRP016	Paraplegia	52	2.705

458	P	MYS003	Myasthenia Gravis	67	2.702

459		CNN003	Conn's Syndrome	77	2.696

460		OCL069	Ocular Motor Apraxia	57	2.689

461	P	HRP006	Herpes Simplex	65	2.689

462		BLR008	Bilirubin Metabolic Disorder	57	2.687

463		PRS021	Prostatic Adenoma	43	2.681

464		MLR004	Malaria	77	2.677

465	c	HYP272	Hypercholesterolemia, Familial, 3	46	2.676

466	P	ALP008	Alopecia	53	2.669

467		IDP070	Idiopathic Scoliosis	41	2.665

468		CHL152	Childhood Acute Lymphocytic Leukemia	50	2.665

469	c	VTM027	Vitamin D-Dependent Rickets, Type 2a	54	2.660

470		CMM004	Common Variable Immunodeficiency	71	2.654

471		PRS129	Prostatic Hyperplasia, Benign	48	2.653

472	P	ACN011	Acne	55	2.650

473	c	LKM063	Leukemia, Chronic Myeloid	70	2.645

474		VSC002	Vascular Dementia	59	2.641

475		SPN051	Spondylitis	51	2.631

476		ANX010	Anxiety	70	2.628

477		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	2.626

478		RST023	Resting Heart Rate, Variation in	40	2.623

479	P	LKM071	Leukemia, Chronic Lymphocytic	74	2.621

480		HYP831	Hyperparathyroidism, Transient Neonatal	25	2.615

481	P	RNL015	Renal Hypertension	45	2.609

482		HYP020	Hyperprolactinemia	63	2.606

483		HYD002	Hydronephrosis	58	2.601

484	c	PNS012	Paine Syndrome	60	2.599

485	P	PYL005	Pyelonephritis	56	2.590

486	P	SLP006	Sleep Apnea	69	2.590

487	c	ACT073	Acute Leukemia	59	2.586

488		CLC004	Calcific Tendinitis	33	2.584

489		CRD137	Cardiogenic Shock	56	2.583

490	c	SPN225	Spondyloarthropathy 1	70	2.580

491	c	MCR112	Microvascular Complications of Diabetes 2	42	2.577

492		SYN007	Synovitis	54	2.577

493		PLC002	Plica Syndrome	35	2.577

494		HRT012	Heart Valve Disease	53	2.574

495		GNG013	Gingivitis	59	2.570

496	P	MYS005	Myositis	55	2.568

497		CVD001	Covid-19	59	2.564

498		PLM017	Pulmonary Alveolar Microlithiasis	48	2.556

499	P	THR014	Thrombocytopenia	66	2.555

500	P	OPN001	Open-Angle Glaucoma	55	2.554

501	P	SCK005	Sickle Cell Disease	56	2.554

502	P	RTN016	Retinal Degeneration	52	2.553

503		PNC041	Pancreatic Ductal Adenocarcinoma	51	2.551

504	c	MCL042	Macular Degeneration, Age-Related, 1	84	2.549

505		SCK003	Sickle Cell Anemia	74	2.544

506	P	TRC031	Trichorhinophalangeal Syndrome	37	2.542

507		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	58	2.540

508		AMN001	Amenorrhea	53	2.536

509	P	HYP035	Hypophosphatasia	61	2.535

510	P	FML362	Familial Isolated Hypoparathyroidism	49	2.533

511		BNG018	Benign Paroxysmal Positional Nystagmus	40	2.533

512	P	MYC008	Myocarditis	59	2.529

513	P	CNJ013	Conjunctivitis	66	2.527

514	P	EXN002	Exanthem	58	2.522

515	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	2.518

516		ANR040	Aneurysm	60	2.514

517		KLD004	Keloid Disorder	38	2.504

518		ETN001	Eating Disorder	59	2.494

519	P	SKN015	Skin Carcinoma	71	2.488

520	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	2.486

521		END057	Endometrial Cancer	76	2.481

522		MSC007	Muscle Hypertrophy	64	2.479

523	P	MTR014	Motor Neuron Disease	65	2.479

524	c	HMC039	Hemochromatosis, Type 1	73	2.472

525		HYP057	Hypervitaminosis D	37	2.472

526		PRP030	Purpura	54	2.464

527	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	2.451

528		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	2.451

529	P	NRV007	Nervous System Disease	65	2.448

530		CRB037	Cerebral Palsy	66	2.447

531		ENM002	Enamel Erosion	25	2.443

532		NRR001	Neuroretinitis	42	2.442

533		RTN023	Retinitis	45	2.440

534		CLR109	Colorectal Adenocarcinoma	50	2.439

535	c	PRG042	Progressive Familial Heart Block, Type Ia	65	2.439

536		PST092	Posttransplant Acute Limbic Encephalitis	29	2.435

537		ALL014	Allergic Encephalomyelitis	34	2.435

538		BCK006	Back Pain	43	2.434

539		SVR004	Severe Combined Immunodeficiency	70	2.431

540		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	35	2.427

541	P	SHR001	Short Bowel Syndrome	53	2.423

542	P	NTR004	Neutropenia	62	2.417

543	P	MYP087	Myopathy, Tubular Aggregate, 1	49	2.416

544	c	HPT016	Hepatitis B	62	2.410

545	P	NGH001	Night Blindness	52	2.405

546	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	2.404

547		BRN024	Bronchitis	67	2.402

548	P	GST044	Gastritis	55	2.398

549		CNN005	Connective Tissue Disease	66	2.397

550		STR081	Stormorken Syndrome	56	2.389

551		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	2.382

552	P	GRF003	Graft-Versus-Host Disease	71	2.374

553		HDN002	Head Injury	44	2.374

554		PNM001	Pneumocystosis	60	2.371

555		NRM005	Neuromuscular Disease	62	2.363

556		RYN001	Raynaud Disease	49	2.362

557	P	SCL057	Scoliosis, Isolated 1	40	2.352

558		BRN004	Brain Edema	54	2.350

559	c	BTT014	Beta-Thalassemia	72	2.349

560	c	PRS130	Prostate Cancer, Hereditary, 8	32	2.346

561	c	PRS136	Prostate Cancer, Hereditary, 6	33	2.346

562	P	RTN024	Retinoblastoma	72	2.339

563		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	2.337

564		CRT013	Carotid Stenosis	51	2.336

565		INT067	Interstitial Nephritis	46	2.334

566		PRT013	Portal Hypertension	59	2.330

567	P	HMP007	Hemophilia	52	2.322

568		END040	Endogenous Depression	54	2.315

569	P	PRS038	Personality Disorder	65	2.313

570		GST040	Gastric Adenocarcinoma	66	2.308

571		PRP017	Periapical Periodontitis	47	2.299

572		ENT004	Enthesopathy	51	2.296

573	P	BLD124	Bleeding Disorder, Platelet-Type, 11	68	2.291

574		PPL001	Papillary Adenoma	44	2.291

575		MLG086	Malignant Hyperthermia Susceptibility	40	2.290

576		ENM001	Enamel Caries	28	2.280

577		DNT001	Dental Fluorosis	43	2.269

578	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	2.268

579	P	BNC003	Bone Cancer	58	2.267

580	c	ATM068	Autoimmune Hypoparathyroidism	31	2.267

581		SFT003	Soft Tissue Sarcoma	43	2.265

582		PRS045	Prostatic Hypertrophy	53	2.260

583		ATX019	Ataxia with Vitamin E Deficiency	44	2.244

584		CHR074	Choriocarcinoma	46	2.243

585		LNG031	Lung Benign Neoplasm	51	2.238

586	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	65	2.234

587		BRK010	Burkitt Lymphoma	65	2.224

588		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	2.224

589	P	DNT007	Dentin Sensitivity	35	2.221

590		PRT058	Pure Autonomic Failure	58	2.219

591	P	SNS001	Sensorineural Hearing Loss	60	2.216

592	P	INT068	Intestinal Disease	53	2.213

593	P	ADL010	Adult Respiratory Distress Syndrome	70	2.209

594		DGN001	Degenerative Disc Disease	48	2.204

595	P	TMT001	Timothy Syndrome	55	2.203

596		SCT005	Scott Syndrome	51	2.184

597		GLS018	Glass Syndrome	60	2.183

598	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	2.183

599	c	PCH010	Pachyonychia Congenita 3	43	2.182

600	P	CRB059	Cerebellar Degeneration	36	2.179

601		CRT015	Carotid Artery Occlusion	45	2.177

602	c	INF071	Inflammatory Bowel Disease 1	65	2.173

603		MST005	Mastitis	52	2.173

604		BSL009	Basal Ganglia Calcification	45	2.171

605		INF009	Inflammatory Spondylopathy	30	2.171

606	c	OST164	Osteoporosis, Juvenile	55	2.169

607		SBC016	Subacute Delirium	42	2.167

608		ISL001	Islet Cell Tumor	55	2.166

609		SYS003	Systolic Heart Failure	49	2.160

610	P	VNS003	Venous Insufficiency	54	2.158

611	c	DNT047	Dentinogenesis Imperfecta Type 2	35	2.158

612		HGH043	High Grade Glioma	46	2.147

613	P	HYP098	Hypereosinophilic Syndrome	66	2.142

614		SPS057	Spasticity	43	2.138

615	P	GLL018	Gallbladder Cancer	59	2.136

616		RNL065	Renal Cell Carcinoma, Papillary, 1	79	2.136

617		PRM013	Premature Menopause	57	2.136

618		ALL006	Allergic Asthma	55	2.133

619	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	2.131

620	P	CHL002	Childhood Absence Epilepsy	62	2.127

621		HLL004	Hellp Syndrome	53	2.126

622		HYP741	Hyperparathyroidism 2 with Jaw Tumors	51	2.125

623		ACT098	Acute Erythroid Leukemia	55	2.124

624		PRN039	Paraneoplastic Syndromes	37	2.122

625		LWC001	Low Compliance Bladder	44	2.122

626		IGG001	Iga Glomerulonephritis	50	2.119

627		DRR014	Darier-White Disease	58	2.117

628		AMN006	Aminoaciduria	37	2.114

629		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	61	2.109

630		DGR001	Digeorge Syndrome	62	2.109

631		MYL031	Myeloproliferative Neoplasm	66	2.107

632	c	SRC023	Sarcoidosis 2	44	2.103

633		MLK006	Milk Allergy	47	2.103

634		BCK003	Background Diabetic Retinopathy	46	2.101

635		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	2.099

636		SCH014	Schistosomiasis	56	2.099

637		PLM033	Pulmonary Embolism	58	2.099

638	P	SPR041	Spermatogenic Failure 6	47	2.095

639		PSR001	Psoriatic Arthritis	61	2.095

640		HMC014	Homocysteinemia	52	2.093

641	c	CHL119	Cholangitis, Primary Sclerosing	57	2.088

642	P	FML364	Familial Thoracic Aortic Aneurysm and Aortic Dissection	70	2.084

643	P	DBT005	Diabetes Insipidus	54	2.083

644	P	TTR001	Tetralogy of Fallot	69	2.082

645	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	2.082

646	c	INH020	Inherited Metabolic Disorder	47	2.077

647		CHR431	Chronic Venous Insufficiency	48	2.077

648		PTH003	Pathologic Nystagmus	52	2.076

649	P	VSC011	Vasculitis	61	2.073

650	P	PLY019	Polyneuropathy	52	2.070

651		ETH012	Ethylene Glycol Poisoning	29	2.067

652		URT010	Ureteral Obstruction	44	2.065

653		AND005	Androgen Insensitivity Syndrome, Mild	21	2.065

654		DST006	Diastolic Heart Failure	45	2.060

655	P	VTM026	Vitamin D Hydroxylation-Deficient Rickets, Type 1a	46	2.056

656	P	FCL005	Focal Segmental Glomerulosclerosis	57	2.056

657		TRD006	Tardive Dyskinesia	53	2.055

658		INT075	Intracranial Hypertension	52	2.054

659		ACT003	Acute Kidney Tubular Necrosis	46	2.051

660	P	PMP001	Pemphigus	54	2.051

661		MDL009	Medullary Sponge Kidney	40	2.050

662	P	RTT002	Rett Syndrome	79	2.050

663		GST033	Gestational Diabetes	60	2.047

664		PHS001	Phosphorus Metabolism Disease	40	2.042

665	P	INF038	Influenza	68	2.042

666		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	36	2.041

667		SPT004	Septic Arthritis	58	2.039

668	P	INT143	Interstitial Cystitis	59	2.038

669		EWN003	Ewing Sarcoma	69	2.036

670		FRZ001	Frozen Shoulder	54	2.036

671		NPH010	Nephrosclerosis	50	2.033

672	P	MGR003	Migraine with Aura	51	2.030

673		BNM001	Bone Marrow Cancer	45	2.028

674	P	FNC004	Fanconi Syndrome	60	2.023

675		EXR010	Exercise-Induced Bronchoconstriction	34	2.022

676		ENT011	Enterocolitis	55	2.020

677	P	GCH001	Gaucher's Disease	69	2.019

678	P	SJG008	Sjogren Syndrome	60	2.016

679	P	MYP006	Myopia	55	2.016

680		BRS064	Bursitis	51	2.009

681	P	FBR017	Fibrosarcoma	55	2.006

682	c	THY107	Thymoma, Familial	42	2.003

683	P	THY023	Thymoma	64	2.003

684		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	2.002

685		SVR001	Severe Acute Respiratory Syndrome	68	1.999

686		MYL009	Myelodysplastic Syndrome	67	1.992

687		AMN003	Amnestic Disorder	53	1.991

688		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	44	1.991

689		VTM033	Vitamin K Deficiency Bleeding	49	1.991

690	c	PRM108	Primary Progressive Multiple Sclerosis	51	1.988

691		GST050	Gastrointestinal System Disease	55	1.984

692	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	69	1.983

693		PRR001	Periarthritis	33	1.983

694		LMB062	Limb Ischemia	55	1.979

695		FCL014	Focal Epilepsy	53	1.978

696		TXC002	Toxic Encephalopathy	51	1.978

697		SXL003	Sexual Disorder	49	1.977

698	P	PTT006	Pituitary Adenoma	55	1.975

699		ATN005	Autonomic Dysfunction	45	1.972

700		TBC004	Tobacco Addiction	63	1.969

701		GNG003	Gingival Recession	50	1.964

702		DFF005	Diffuse Large B-Cell Lymphoma	55	1.959

703	c	FML001	Familial Atrial Fibrillation	65	1.956

704	P	CNT004	Centronuclear Myopathy	56	1.955

705		LWC002	Lowe Oculocerebrorenal Syndrome	68	1.954

706	P	OPT006	Optic Nerve Disease	57	1.954

707		HYP827	Hypomagnesemia 5, Renal, with or Without Ocular Involvement	44	1.947

708	P	FRG001	Fragile X Syndrome	70	1.945

709		PLS009	Plasma Cell Neoplasm	64	1.942

710		VRC005	Varicose Veins	59	1.941

711		CHL067	Cholecystitis	59	1.941

712	P	ART018	Aortic Valve Insufficiency	52	1.933

713		MNN043	Meningioma, Familial	79	1.932

714		PRT018	Portal Vein Thrombosis	50	1.927

715		LYM002	Lymphoplasmacyte-Rich Meningioma	35	1.926

716		SCR001	Secretory Meningioma	40	1.926

717		INT395	Intracranial Meningioma	47	1.926

718	P	HMR005	Hemorrhoid	49	1.919

719	P	KLZ004	Kala-Azar 1	41	1.914

720		LSH001	Leishmaniasis	63	1.914

721		HPT004	Hepatic Coma	43	1.905

722		CHG001	Chagas Disease	65	1.905

723		INT066	Interstitial Lung Disease	60	1.905

724	P	RHB003	Rhabdomyosarcoma	66	1.903

725		PLG002	Plague	58	1.901

726		NRN004	Neuroendocrine Tumor	55	1.897

727		DNT010	Dentin Caries	32	1.896

728		OST015	Osteochondrodysplasia	60	1.896

729		TND004	Tendinopathy	45	1.895

730	P	ASP006	Aspergillosis	71	1.893

731		SPN027	Spinal Stenosis	58	1.893

732	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	1.893

733	c	XNT010	Xanthinuria, Type I	52	1.892

734	P	MDL005	Medulloblastoma	75	1.882

735		CRB090	Cerebral Hypoxia	42	1.881

736		BNG091	Benign Chronic Pemphigus	56	1.877

737	P	TRT010	Teratoma	50	1.876

738		SMT003	Somatostatinoma	52	1.871

739		CNT047	Contact Dermatitis	56	1.869

740		CRT017	Cartilage Disease	52	1.868

741	P	NJM001	Nijmegen Breakage Syndrome	75	1.865

742		IRN001	Iron Deficiency Anemia	58	1.863

743	c	MLG069	Malignant Hypertension	46	1.863

744		MTR002	Mitral Valve Insufficiency	51	1.861

745		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	1.861

746		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	1.859

747	P	MTR003	Mitral Valve Stenosis	53	1.858

748		DSS009	Disseminated Intravascular Coagulation	56	1.856

749		FDL002	Food Allergy	47	1.856

750		ATS010	Autosomal Recessive Disease	42	1.855

751	c	FML347	Familial Adenomatous Polyposis 2	56	1.853

752	P	EYD002	Eye Disease	57	1.852

753	c	HYP210	Hypomagnesemia 2, Renal	42	1.852

754		GRW007	Growth Hormone Deficiency	47	1.851

755		HYP068	Hyperostosis	47	1.846

756		MSC152	Muscular Dystrophy, Becker Type	69	1.844

757		THR035	Thrombasthenia	48	1.843

758		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	65	1.840

759		BRN028	Brain Cancer	73	1.837

760		CHR100	Chronic Ulcer of Skin	57	1.837

761		GLC036	Glucagonoma	45	1.837

762		5XP001	5-Oxoprolinase Deficiency	30	1.835

763	P	PRC031	Preeclampsia/eclampsia 1	43	1.834

764	P	HML002	Hemolytic Anemia	62	1.831

765	P	CHL066	Cholangitis	51	1.828

766	P	NRF002	Neurofibromatosis	60	1.828

767		PRM236	Primary Biliary Cholangitis	62	1.825

768	c	DWL002	Dowling-Degos Disease 1	58	1.824

769		PST021	Postpartum Depression	50	1.822

770		BRS051	Breast Disease	58	1.820

771		TRN018	Transitional Cell Carcinoma	56	1.813

772	c	JVN025	Juvenile Primary Osteoporosis	21	1.813

773		HPT019	Hepatic Encephalopathy	59	1.811

774	P	RTN008	Retinitis Pigmentosa	79	1.810

775		URT014	Ureterolithiasis	42	1.810

776		OVR094	Ovarian Epithelial Cancer	39	1.810

777	c	HPT073	Hepatitis C Virus	70	1.808

778		DPH001	Diphtheria	59	1.799

779	P	PLM036	Pulmonary Fibrosis	65	1.797

780		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.794

781	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	59	1.793

782	c	PRG043	Progressive Familial Heart Block, Type Ib	54	1.791

783	c	JVN061	Juvenile Arthritis	56	1.788

784		CHR682	Chronic Bilirubin Encephalopathy	37	1.786

785		PMP014	Pemphigoid	48	1.783

786	P	URT039	Urticaria	57	1.782

787		OST016	Osteochondrosis	52	1.776

788	P	GLY013	Glycogen Storage Disease	59	1.774

789	c	MCL013	Mucolipidosis Iv	64	1.771

790		NPH078	Nephrolithiasis, Uric Acid	39	1.771

791		CRV035	Cervical Cancer	72	1.769

792	P	EPL140	Epilepsy, Idiopathic Generalized	60	1.769

793		HYP006	Hypertensive Heart Disease	48	1.762

794		BSL043	Basal Ganglia Calcification, Idiopathic, Childhood-Onset	19	1.761

795		FBR047	Fibromyalgia	57	1.758

796		CCN002	Cocaine Abuse	49	1.758

797	P	SML001	Small Cell Carcinoma	52	1.756

798		SNS003	Sensory Peripheral Neuropathy	51	1.756

799		DMY004	Demyelinating Disease	50	1.756

800		ILS001	Ileus	49	1.755

801	P	PLY018	Polycythemia	56	1.750

802		HYP052	Hyperkalemic Periodic Paralysis	62	1.750

803		PLM031	Poliomyelitis	62	1.749

804		RTC003	Root Caries	33	1.749

805		KRT008	Keratopathy	46	1.749

806		ACR041	Acromelic Frontonasal Dysostosis	53	1.749

807	P	LMB006	Limb-Girdle Muscular Dystrophy	52	1.748

808	P	CND004	Candidiasis	57	1.742

809		GST045	Gastroenteritis	58	1.741

810	P	HYP050	Hyperinsulinemic Hypoglycemia	56	1.738

811		PSD014	Pseudopseudohypoparathyroidism	54	1.738

812		VLK001	Volkmann Contracture	23	1.737

813		HYP550	Hypomagnesemia 1, Intestinal	45	1.736

814		ANT024	Anthrax Disease	57	1.732

815		WLL004	Wallerian Degeneration	38	1.732

816	P	AVS003	Avascular Necrosis	41	1.730

817	P	INS002	in Situ Carcinoma	52	1.730

818	P	PRN023	Prion Disease	60	1.728

819		ACT011	Acute Contagious Conjunctivitis	41	1.727

820	c	PRM038	Primary Agammaglobulinemia	47	1.724

821		SQM013	Squamous Cell Carcinoma, Head and Neck	75	1.723

822	c	DRR009	Diarrhea 6	46	1.717

823		OST115	Osteonecrosis of the Jaw	40	1.715

824		RTN020	Retinal Vascular Disease	45	1.715

825		HVY002	Heavy Metal Poisoning	22	1.712

826		ART074	Aortic Dissection	53	1.712

827		PPL022	Papilloma	53	1.710

828		NDL007	Nodular Goiter	48	1.708

829	P	SCK002	Sick Sinus Syndrome	55	1.707

830		GST049	Gastrointestinal System Cancer	49	1.706

831		DYS015	Dysentery	49	1.706

832		MLD018	Mild Cognitive Impairment	48	1.705

833		DDN006	Duodenitis	49	1.702

834	c	HPT001	Hepatitis C	61	1.702

835	P	BRS044	Breast Adenocarcinoma	58	1.700

836		SPL018	Splenomegaly	47	1.699

837		ACH005	Achalasia	54	1.699

838	c	FNC043	Fanconi Anemia, Complementation Group E	62	1.698

839		CRB086	Cerebral Aneurysms	40	1.698

840	P	HYP534	Hypomagnesemia 3, Renal	46	1.697

841		CHL028	Childhood Type Dermatomyositis	58	1.694

842		ENP001	Enophthalmos	40	1.693

843		EMB004	Embryonal Carcinoma	55	1.690

844		CMB007	Combined Immunodeficiency	56	1.690

845		SQM002	Squamous Cell Papilloma	45	1.686

846		DRG003	Drug Dependence	46	1.675

847	P	CRC039	Coarctation of Aorta	46	1.674

848	P	LTH003	Lethal Congenital Contracture Syndrome	40	1.671

849		MNT001	Mantle Cell Lymphoma	65	1.671

850	c	ESS001	Essential Tremor	56	1.671

851	P	LCH002	Lichen Planus	54	1.669

852	P	END033	Endocarditis	58	1.669

853		VTM029	Vitamin D Hydroxylation-Deficient Rickets, Type 1b	28	1.668

854	P	CYS018	Cystitis	58	1.665

855	P	MNN013	Meningitis	65	1.665

856	c	MGR032	Migraine, Familial Hemiplegic, 1	54	1.664

857	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	58	1.661

858		GLM044	Glomerular Disease	34	1.659

859		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	37	1.658

860	P	BLD062	Bile Duct Cancer	69	1.657

861		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	1.657

862		HYP540	Hypertension, Diastolic	38	1.656

863		PRN032	Paraneoplastic Cerebellar Degeneration	25	1.647

864	P	PRV006	Pervasive Developmental Disorder	52	1.644

865		MMM006	Mammographic Density	39	1.644

866		MST020	Mast Cell Activation Syndrome	27	1.643

867		OCL006	Ocular Hypertension	53	1.642

868		ARG004	Argyria	26	1.640

869		FML035	Familial Hyperlipidemia	54	1.638

870		PRS063	Paresthesia	39	1.638

871	P	BNG032	Benign Mesothelioma	53	1.637

872	P	SLP005	Sleep Disorder	61	1.637

873		MTH071	Methane Production	24	1.633

874	c	HMP004	Hemophilia B	68	1.630

875	P	MVM001	Movement Disease	61	1.629

876	P	ANG015	Angioedema	56	1.628

877		NRT001	Neurotic Disorder	56	1.627

878		ASP004	Asphyxia Neonatorum	50	1.623

879	P	UVT001	Uveitis	57	1.619

880		RNL077	Renal Fibrosis	46	1.618

881	P	SCL009	Sclerosing Cholangitis	46	1.617

882	c	CHR098	Chronic Pyelonephritis	34	1.614

883		ERL001	Early Myoclonic Encephalopathy	62	1.612

884		TCL027	T-Cell Acute Lymphoblastic Leukemia	52	1.611

885		LFT001	Left Bundle Branch Hemiblock	47	1.611

886	P	CHN012	Chondrosarcoma	56	1.609

887	P	LPR021	Leprosy 3	71	1.607

888		HNS001	Hansen's Disease	32	1.607

889		CRH005	Crohn's Colitis	53	1.605

890		MST004	Mast Cell Neoplasm	41	1.605

891		LMY002	Leiomyoma	51	1.604

892	P	MJR007	Major Affective Disorder 1	42	1.604

893		CRB009	Cerebritis	43	1.602

894	P	CHR012	Chronic Granulomatous Disease	69	1.600

895	c	ACT004	Acute Diarrhea	40	1.598

896	c	VSC019	Vesicoureteral Reflux 1	56	1.597

897		ORL011	Oral Cancer	60	1.595

898		CHP002	Chops Syndrome	47	1.595

899		NNL006	Non-Alcoholic Steatohepatitis	54	1.594

900		AZS001	Azoospermia	45	1.593

901		INT030	Intracranial Aneurysm	55	1.591

902		CMP010	Complex Regional Pain Syndrome	59	1.590

903		HLC007	Helicobacter Pylori Infection	67	1.590

904		CRT016	Carotid Artery Disease	52	1.589

905		PRD004	Prediabetes Syndrome	52	1.588

906		VCC001	Vaccinia	49	1.586

907	P	MLT008	Multinodular Goiter	41	1.583

908	P	CLS010	Cluster Headache	42	1.583

909		OTT002	Otitis Media	70	1.582

910	P	SBS003	Substance Abuse	54	1.581

911		PRM237	Primary Hypomagnesemia	44	1.581

912		PST053	Postherpetic Neuralgia	39	1.580

913		GSG001	Gas Gangrene	52	1.577

914		SKN019	Skin Melanoma	70	1.576

915		PLY105	Polycystic Ovary Syndrome 1	39	1.575

916		EPT021	Epithelial Recurrent Erosion Dystrophy	45	1.572

917		ASP026	Asplenia, Isolated Congenital	43	1.569

918		PRN019	Perinatal Necrotizing Enterocolitis	60	1.562

919	P	LYN001	Lynch Syndrome	76	1.560

920		SPN369	Spinal Disease	43	1.558

921		RDC002	Radiculopathy	51	1.557

922		FBR009	Fibrous Dysplasia	48	1.557

923		GST023	Gastric Ulcer	52	1.557

924	P	MNC007	Monocytic Leukemia	48	1.556

925	c	BPL002	Bipolar I Disorder	47	1.556

926	c	BSL049	Basal Ganglia Calcification, Idiopathic, 8, Autosomal Recessive	23	1.555

927	P	FML011	Familial Adenomatous Polyposis	70	1.555

928		PLR008	Pleurisy	49	1.553

929	P	MLT007	Multiple Epiphyseal Dysplasia	56	1.553

930		EXT007	Extracutaneous Mastocytoma	38	1.552

931		OST062	Osteoarthritis with Mild Chondrodysplasia	46	1.551

932		PMP006	Pemphigus Vulgaris, Familial	57	1.546

933		BRN056	Bronchopulmonary Dysplasia	57	1.543

934	c	ACT135	Acute Graft Versus Host Disease	51	1.539

935		HST010	Histiocytosis	49	1.539

936		GST071	Gastrointestinal Carcinoma	46	1.535

937		CYS014	Cystadenocarcinoma	51	1.535

938	c	AML044	Amelogenesis Imperfecta, Type Ig	54	1.531

939		TLN003	Telangiectasis	51	1.530

940		BLL006	Bullous Pemphigoid	61	1.528

941	P	GLL022	Guillain-Barre Syndrome	59	1.527

942		RTC005	Reticulosarcoma	47	1.525

943		GST019	Gastrointestinal Stromal Tumor	78	1.525

944		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	1.524

945		MYL005	Myelofibrosis	70	1.518

946		OBS082