Search results for Calcium

3524 hits were found for Calcium

#	Family	MCID	Name	MIFTS	Score
1	c	CHN022	Chondrocalcinosis 2	41	8.286

2		NPH091	Nephrolithiasis, Calcium Oxalate	60	7.842

3		FML307	Familial Calcium Pyrophosphate Deposition	40	6.024

4		IMM066	Immunodeficiency 9	30	5.049

5		IMM065	Immunodeficiency 10	33	4.606

6	P	CHN059	Chondrocalcinosis	52	3.222

7	c	BLD126	Bleeding Disorder, Platelet-Type, 18	39	2.910

8	c	AML006	Amelogenesis Imperfecta Hypoplastic Type, Ig	18	2.080

9		CMB055	Combined Immunodeficiency Due to Crac Channel Dysfunction	17	2.080

10	c	NRL030	Neurological Muscular Channelopathy Due to a Genetic Calcium Channel Defect	3	2.080

11	c	NRL036	Neurological Channelopathy of the Central Nervous System Due to a Genetic Calcium Channel Defect	2	2.080

12	P	HYP069	Hyperparathyroidism	63	0.462

13	P	OST002	Osteoporosis	74	0.387

14		NPH009	Nephrolithiasis	55	0.371

15	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.370

16	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.370

17		BNR002	Bone Resorption Disease	48	0.362

18		RCK004	Rickets	68	0.354

19		PRT037	Pertussis	65	0.330

20		URL001	Urolithiasis	45	0.322

21	c	HYP595	Hypertension, Essential	84	0.307

22	P	KDN018	Kidney Disease	72	0.297

23	c	SCN007	Secondary Hyperparathyroidism	51	0.290

24	c	PRM005	Primary Hyperparathyroidism	58	0.264

25	P	CLR023	Colorectal Cancer	99	0.242

26	P	NRB001	Neuroblastoma	72	0.240

27	P	BND020	Bone Disease	59	0.238

28	c	CHR684	Chronic Kidney Disease	70	0.230

29	P	HYP024	Hypoparathyroidism	56	0.215

30		LPP008	Lipoprotein Quantitative Trait Locus	62	0.212

31		ANG054	Angina Pectoris	66	0.212

32	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.210

33		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.209

34		HYP025	Hyperphosphatemia	48	0.205

35		CNG034	Congestive Heart Failure	69	0.201

36		ART140	Arteries, Anomalies of	52	0.195

37		HLX001	Helix Syndrome	47	0.195

38		ISC004	Ischemia	58	0.188

39	P	CRN300	Coronary Heart Disease 1	63	0.187

40	c	PRC016	Pre-Eclampsia	63	0.186

41		ATH013	Atherosclerosis Susceptibility	65	0.185

42		END086	End Stage Renal Disease	51	0.183

43	P	HRT032	Heart Disease	75	0.181

44		ADN018	Adenoma	59	0.181

45		48X005	48,xyyy	39	0.178

46	P	ADN016	Adenocarcinoma	64	0.172

47		HYP266	Hypoxia	57	0.170

48	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.162

49	P	MSC005	Muscular Dystrophy	66	0.161

50		IDP073	Idiopathic Hypercalciuria	43	0.161

51	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.159

52		OST011	Osteomalacia	52	0.159

53		ANX004	Anoxia	40	0.158

54	P	GLM045	Glioma	63	0.156

55		CHL014	Cholera	59	0.156

56	P	ALZ034	Alzheimer Disease	88	0.155

57		GLL048	Glial Tumor	45	0.155

58	P	VSC007	Vascular Disease	63	0.153

59		INS001	Insulinoma	60	0.152

60	P	RCT021	Rectum Cancer	52	0.151

61		DNT012	Dental Caries	53	0.151

62	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.149

63		OST159	Osteogenic Sarcoma	66	0.149

64	P	LTR001	Lateral Sclerosis	54	0.149

65		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.149

66	P	MLG056	Malignant Hyperthermia	67	0.146

67		ALL026	Allergic Hypersensitivity Disease	62	0.145

68	c	MGR028	Migraine with or Without Aura 1	67	0.143

69		NPH003	Nephrocalcinosis	51	0.143

70	P	PRD008	Periodontitis	64	0.143

71	P	FML068	Familial Hypocalciuric Hypercalcemia	54	0.140

72	P	PHC003	Pheochromocytoma	71	0.140

73		ADR040	Adrenal Gland Pheochromocytoma	46	0.139

74	c	ATR087	Atrial Standstill 1	75	0.138

75		MTB004	Metabolic Acidosis	50	0.138

76		LPD008	Lipid Metabolism Disorder	62	0.137

77	P	MYC007	Myocardial Infarction	70	0.136

78		CLC006	Calcinosis	48	0.136

79		TTN003	Tetanus	65	0.135

80		GT001	Gout	64	0.135

81		47X002	47,xyy	49	0.135

82	P	HYP726	Hypercalcemia, Infantile, 1	58	0.135

83		HYP056	Hypoglycemia	66	0.133

84		AGN016	Aging	56	0.133

85		HYP017	Hypophosphatemia	50	0.133

86	P	CRD119	Cardiac Arrest	67	0.131

87	c	GLL024	Gallbladder Disease 1	53	0.130

88		OST017	Osteomyelitis	64	0.130

89	P	ART023	Arthropathy	62	0.128

90		CYS001	Cystic Fibrosis	81	0.128

91	P	ECL001	Eclampsia	50	0.128

92	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.127

93		MSC157	Muscular Dystrophy, Duchenne Type	72	0.127

94	c	ACT027	Acute Pancreatitis	60	0.127

95		URM002	Uremia	49	0.127

96		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.126

97	c	DLT002	Dilated Cardiomyopathy	79	0.125

98	P	HYP076	Hyperthyroidism	55	0.125

99	P	PLM037	Pulmonary Hypertension	67	0.123

100	c	RHB024	Rhabdomyosarcoma 2	67	0.123

101		LMB002	Lambert-Eaton Myasthenic Syndrome	53	0.123

102	P	LYM118	Lymphoma	68	0.122

103	c	ACT071	Acute Kidney Failure	60	0.121

104	P	SRC025	Sarcoidosis 1	70	0.121

105		INT007	Intermediate Coronary Syndrome	55	0.121

106		RNL011	Renal Osteodystrophy	50	0.120

107		HRW001	Hair Whorl	36	0.120

108	P	PRS040	Prostate Cancer	97	0.120

109	P	MYP004	Myopathy	70	0.120

110		CLN015	Colon Adenocarcinoma	65	0.119

111	P	HYP061	Hypertrophic Cardiomyopathy	70	0.118

112	P	NRP001	Neuropathy	56	0.118

113	c	MCR120	Microvascular Complications of Diabetes 7	47	0.117

114		LYM019	Lymphosarcoma	46	0.117

115	P	LKM002	Leukemia	68	0.117

116	P	HYP086	Hypothyroidism	69	0.116

117	P	DRR001	Diarrhea	55	0.116

118	c	MCR113	Microvascular Complications of Diabetes 3	52	0.116

119		PPL052	Papillomatosis, Confluent and Reticulated	33	0.116

120	P	SZR006	Seizure Disorder	56	0.116

121	P	ART021	Arteriosclerosis	54	0.116

122	c	MCR130	Microvascular Complications of Diabetes 6	41	0.116

123	c	MCR133	Microvascular Complications of Diabetes 4	41	0.116

124	P	BRS047	Breast Cancer	97	0.115

125		OST012	Osteoarthritis	78	0.114

126		VSL002	Visual Epilepsy	59	0.114

127		CRN030	Coronary Stenosis	50	0.114

128		DWN001	Down Syndrome	70	0.112

129	P	ATR011	Atrial Fibrillation	66	0.112

130		HYP066	Hyperglycemia	61	0.111

131		CLR108	Colorectal Adenoma	64	0.110

132		CRD132	Cardiac Conduction Defect	58	0.110

133		HYP060	Hyperinsulinism	54	0.110

134	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.109

135		CNS004	Constipation	58	0.108

136		HMN044	Human Immunodeficiency Virus Type 1	71	0.108

137	P	PNC044	Pancreatitis	61	0.108

138		HYP005	Hypokalemia	55	0.108

139	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.107

140		ATM095	Autoimmune Disease	62	0.107

141	P	BPL003	Bipolar Disorder	56	0.107

142	P	CHR345	Chronic Pain	44	0.107

143	c	MJR024	Major Affective Disorder 9	41	0.106

144	c	MJR022	Major Affective Disorder 8	38	0.106

145	P	DBT009	Diabetes Mellitus	64	0.106

146		THY029	Thyroid Carcinoma	59	0.106

147	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.105

148	P	MCR115	Microvascular Complications of Diabetes 5	66	0.105

149	P	CRD246	Cardiovascular System Disease	57	0.104

150		PLY150	Polykaryocytosis Inducer	31	0.104

151	P	CTR002	Cataract	60	0.103

152	c	ACT075	Acute Myocardial Infarction	57	0.102

153		RTR008	Root Resorption	45	0.102

154	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.101

155	P	PLY014	Polycystic Kidney Disease	62	0.101

156		INS024	Insulin-Like Growth Factor I	79	0.100

157		ATR057	Atrioventricular Block	55	0.100

158		CRB004	Cerebral Artery Occlusion	45	0.100

159		TRM010	Traumatic Brain Injury	51	0.099

160		IRN002	Iron Metabolism Disease	57	0.098

161		GLB015	Glioblastoma Multiforme	75	0.097

162		CRD223	Cardiac Arrhythmia	60	0.097

163		PRT029	Parathyroid Adenoma	50	0.097

164	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.096

165	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.095

166		CRB039	Cerebrovascular Disease	67	0.095

167		PNG002	Pain Agnosia	51	0.095

168	P	OVR082	Overgrowth Syndrome	50	0.095

169		BRN071	Brain Injury	49	0.095

170		CYT002	Cytokine Deficiency	42	0.095

171	P	PNC035	Pancreatic Cancer	84	0.095

172		PTT037	Pituitary Tumors	44	0.095

173	P	HNT016	Huntington Disease	72	0.094

174	P	LVR013	Liver Disease	68	0.094

175		LVR012	Liver Cirrhosis	62	0.094

176		STT001	Status Epilepticus	60	0.094

177		LYM040	Lymphoblastic Lymphoma	54	0.094

178	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.094

179		DPR016	Depression	63	0.093

180		SPN186	Spinal Cord Injury	60	0.093

181	P	PRP019	Peripheral Nervous System Disease	58	0.093

182		IMM167	Immune Deficiency Disease	78	0.092

183	P	ENC018	Encephalopathy	61	0.092

184	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.092

185	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.092

186	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.092

187	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.092

188	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.092

189	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.092

190	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.092

191	P	PSR002	Psoriasis	62	0.092

192	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.092

193	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.092

194	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.092

195	P	OVR042	Ovarian Cancer	88	0.091

196		ALC007	Alcohol Dependence	66	0.091

197		STR067	Stroke, Ischemic	81	0.090

198	P	GST053	Gastric Cancer	83	0.089

199		ACQ007	Acquired Immunodeficiency Syndrome	60	0.089

200	P	AST007	Astrocytoma	51	0.089

201	P	CTC001	Catecholaminergic Polymorphic Ventricular Tachycardia	63	0.088

202	P	RNL007	Renal Tubular Acidosis	51	0.088

203		NTR005	Nutritional Deficiency Disease	62	0.087

204	P	EPL164	Epilepsy	71	0.087

205	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.087

206	P	FML023	Familial Hemiplegic Migraine	53	0.087

207	P	PSD015	Pseudohypoparathyroidism	56	0.086

208	P	HYP776	Hyperparathyroidism, Neonatal Severe	47	0.086

209	P	LNG032	Lung Cancer	98	0.085

210		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.085

211		MYL069	Myeloma, Multiple	85	0.085

212		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.085

213		SKN016	Skin Disease	63	0.085

214		PST011	Pustulosis of Palm and Sole	52	0.085

215	P	TRN020	Turner Syndrome	67	0.084

216		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.084

217	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.084

218		GTR002	Goiter	53	0.084

219	P	DDN001	Duodenal Ulcer	52	0.084

220		RYN005	Raynaud Phenomenon	47	0.084

221	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.084

222		ADL002	Adult Syndrome	70	0.083

223	c	ATS007	Autism Spectrum Disorder	67	0.083

224	P	NPH012	Nephrotic Syndrome	60	0.083

225		PPT005	Peptic Ulcer Disease	59	0.083

226	P	LCT002	Lactose Intolerance	53	0.083

227		TXC005	Toxic Shock Syndrome	62	0.082

228		FTT001	Fatty Liver Disease	61	0.082

229	P	TRM003	Tremor	54	0.082

230		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.082

231		MMM001	Mammary Paget's Disease	53	0.082

232		PRP027	Peripheral Vascular Disease	71	0.081

233	P	PRM002	Primary Hyperoxaluria	62	0.081

234		MYC005	Myocardial Stunning	46	0.081

235		ATX019	Ataxia with Vitamin E Deficiency	42	0.080

236		LNG099	Lung Disease	60	0.079

237		CLN045	Colonic Benign Neoplasm	46	0.079

238		OST003	Osteonecrosis	61	0.078

239	P	BCL017	B-Cell Lymphoma	58	0.078

240	P	ART022	Arthritis	69	0.078

241	c	ACT068	Acute Cystitis	63	0.078

242		MNT002	Mental Depression	58	0.078

243		HMS001	Hemosiderosis	54	0.078

244	P	FML187	Familial Hypertension	37	0.078

245		ESP021	Esophageal Cancer	90	0.077

246		THY111	Thyroid Carcinoma, Familial Medullary	67	0.077

247	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.077

248	P	GLM007	Glomerulonephritis	57	0.077

249		AST005	Asthma	76	0.076

250	P	LNG028	Long Qt Syndrome	66	0.076

251	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.076

252	P	RHM011	Rheumatoid Arthritis	80	0.075

253	P	DMN002	Dementia	66	0.075

254	P	INF037	Inflammatory Bowel Disease	54	0.075

255		GNG012	Gingival Overgrowth	51	0.075

256	P	RRH023	Rare Hereditary Hemochromatosis	41	0.075

257	c	BRN108	Branchiootic Syndrome 1	62	0.074

258	P	EPS003	Episodic Ataxia	59	0.074

259	P	INF032	Infertility	57	0.074

260		GLC003	Glucose Intolerance	54	0.074

261		THY125	Thyroid Gland Medullary Carcinoma	50	0.074

262	P	PRD021	Periodic Paralysis	45	0.074

263	P	HPT023	Hepatocellular Carcinoma	100	0.074

264		HYP014	Hyperuricemia	52	0.074

265		DNT006	Dental Pulp Necrosis	41	0.074

266	P	ATS364	Autism	70	0.073

267	c	SML038	Small Cell Cancer of the Lung	65	0.073

268		IRR002	Irritable Bowel Syndrome	65	0.073

269	P	THL005	Thalassemia	60	0.073

270		ZLL002	Zollinger-Ellison Syndrome	55	0.073

271		WTH001	Withdrawal Disorder	48	0.073

272	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.072

273	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.072

274		DFC004	Deficiency Anemia	70	0.072

275	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.072

276		LYM133	Lymphoma, Hodgkin, Classic	69	0.072

277		TRN015	Transient Cerebral Ischemia	63	0.072

278		DRM006	Dermatitis	61	0.072

279	P	TMP001	Temporal Lobe Epilepsy	50	0.072

280		PLP001	Pulpitis	49	0.072

281		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.072

282		PRM020	Premenstrual Tension	40	0.072

283		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.072

284	c	SYS001	Systemic Lupus Erythematosus	86	0.071

285	c	EPS035	Episodic Ataxia, Type 2	63	0.071

286		CHL068	Cholestasis	61	0.071

287	P	MYL006	Myeloid Leukemia	60	0.071

288	P	MLN007	Male Infertility	55	0.071

289		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.070

290		ACR007	Acromegaly	71	0.070

291		PLM001	Pulmonary Tuberculosis	69	0.070

292		SQM006	Squamous Cell Carcinoma	60	0.070

293		GLS018	Glass Syndrome	57	0.070

294		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.070

295		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.070

296	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	46	0.070

297	c	LKM061	Leukemia, Acute Myeloid	84	0.069

298	P	PNM007	Pneumonia	68	0.069

299		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.069

300	P	TXP001	Toxoplasmosis	60	0.069

301	P	PLY011	Polycystic Ovary Syndrome	56	0.069

302	c	GRV008	Graves Disease 1	56	0.069

303		MCS002	Mucositis	56	0.069

304		BNN003	Bone Inflammation Disease	48	0.069

305	c	PRM038	Primary Agammaglobulinemia	44	0.069

306	c	LKM005	Leukemia, T-Cell, Chronic	34	0.069

307	P	HDC001	Headache	57	0.068

308	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.068

309		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.068

310	P	MLN008	Melanoma	69	0.068

311		PNC129	Pancreatic Adenocarcinoma	68	0.068

312		PRT036	Peritonitis	64	0.068

313	P	SPN309	Spinocerebellar Ataxia 6	59	0.068

314	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.068

315	P	LPS004	Lupus Erythematosus	61	0.067

316		SYN007	Synovitis	54	0.067

317	P	CYS039	Cystic Kidney Disease	54	0.067

318		DBT010	Diabetic Neuropathy	54	0.067

319	c	HYP752	Hypocalciuric Hypercalcemia, Familial, Type I	45	0.067

320		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.067

321		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	0.067

322		PLC002	Plica Syndrome	36	0.067

323		CRH001	Crohn's Disease	74	0.066

324		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.066

325	c	SCL052	Scleroderma, Familial Progressive	61	0.066

326		PLM033	Pulmonary Embolism	59	0.066

327	P	MSC003	Muscular Atrophy	52	0.066

328		SCN001	Secondary Hyperparathyroidism of Renal Origin	27	0.066

329		TND005	Tendinitis	54	0.065

330		OCL069	Ocular Motor Apraxia	51	0.065

331	P	MYT002	Myotonic Dystrophy	49	0.065

332		SVR004	Severe Combined Immunodeficiency	73	0.064

333		ART016	Aortic Aneurysm	69	0.064

334		PRT010	Parathyroid Carcinoma	67	0.064

335		BCT022	Bacterial Infectious Disease	56	0.064

336		IMP005	Impotence	52	0.064

337		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.064

338	P	BLD134	Bladder Cancer	79	0.063

339		SCK003	Sickle Cell Anemia	74	0.063

340		LPT014	Leptin Deficiency or Dysfunction	74	0.063

341		GST092	Gastroesophageal Reflux	67	0.063

342		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.063

343		MDD011	Mood Disorder	62	0.063

344		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.063

345		ANK001	Ankylosis	51	0.063

346	P	RNL015	Renal Hypertension	47	0.063

347		CHL079	Children's Interstitial Lung Disease	26	0.063

348	P	PRK057	Parkinson Disease, Late-Onset	78	0.062

349		MRF001	Marfan Syndrome	77	0.062

350		NRM005	Neuromuscular Disease	64	0.062

351	P	HYP370	Hypokalemic Periodic Paralysis, Type 1	64	0.062

352		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.062

353		TMT001	Timothy Syndrome	61	0.062

354	P	MLT074	Multiple Endocrine Neoplasia	56	0.062

355		CRN019	Coronary Artery Vasospasm	46	0.062

356		OST004	Osteitis Fibrosa	41	0.062

357		MLR004	Malaria	81	0.061

358	P	SCH015	Schizophrenia	74	0.061

359	c	HMC039	Hemochromatosis, Type 1	74	0.061

360		BRT054	Brittle Bone Disorder	72	0.061

361	P	MYS003	Myasthenia Gravis	68	0.061

362	P	MJR001	Major Depressive Disorder	68	0.061

363	P	DRM053	Dermatitis, Atopic	66	0.061

364		MSC007	Muscle Hypertrophy	64	0.061

365		ANR040	Aneurysm	59	0.061

366	P	RHN004	Rhinitis	57	0.061

367	P	RTN016	Retinal Degeneration	53	0.061

368	P	BRT004	Bartter Disease	52	0.061

369		CLR109	Colorectal Adenocarcinoma	51	0.061

370		NTR046	Neutrophil Migration	50	0.061

371		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.061

372		RST023	Resting Heart Rate, Variation in	41	0.061

373		ENM002	Enamel Erosion	26	0.061

374		CRY024	Crystal Arthropathies	20	0.061

375	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	19	0.061

376		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.060

377	P	SYS005	Systemic Scleroderma	68	0.060

378	P	HRP006	Herpes Simplex	65	0.060

379	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.060

380	P	HYP750	Hypertriglyceridemia, Familial	62	0.060

381	P	SCL018	Scoliosis	60	0.060

382	c	PRD040	Periodontitis, Chronic	53	0.060

383	P	LCT001	Lactic Acidosis	51	0.060

384		CLC001	Calciphylaxis	51	0.060

385	P	RNV001	Renovascular Hypertension	48	0.060

386		SYN036	Syncope	45	0.060

387		ALL014	Allergic Encephalomyelitis	38	0.060

388		ANX010	Anxiety	73	0.059

389	P	DYS154	Dystonia	65	0.059

390	P	PGT001	Paget's Disease of Bone	58	0.059

391	P	EXN002	Exanthem	57	0.059

392		VSC002	Vascular Dementia	57	0.059

393	P	GRV001	Graves' Disease	55	0.059

394		STM007	Stomatitis	50	0.059

395	P	CRB059	Cerebellar Degeneration	37	0.059

396	P	LNG064	Lung Cancer Susceptibility 3	78	0.058

397	P	OST001	Osteopetrosis	70	0.058

398	P	THR014	Thrombocytopenia	67	0.058

399	P	NTR004	Neutropenia	63	0.058

400	P	ADL017	Adult T-Cell Leukemia	56	0.058

401		PLM010	Pulmonary Edema	54	0.058

402	P	SCK005	Sickle Cell Disease	50	0.058

403	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.058

404	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.057

405	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.057

406		CMM004	Common Variable Immunodeficiency	68	0.057

407		BRN024	Bronchitis	68	0.057

408		BRK010	Burkitt Lymphoma	67	0.057

409	P	ENC004	Encephalitis	61	0.057

410		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.057

411		THR024	Thrombosis	57	0.057

412		SCH014	Schistosomiasis	57	0.057

413		ERY051	Erythroleukemia, Familial	56	0.057

414		BRN004	Brain Edema	56	0.057

415		PRP016	Paraplegia	52	0.057

416	c	SVR005	Severe Pre-Eclampsia	50	0.057

417	P	DST107	Distal Renal Tubular Acidosis	42	0.057

418		MLG086	Malignant Hyperthermia Susceptibility	39	0.057

419		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.057

420	P	CNR004	Cone-Rod Dystrophy 2	73	0.055

421	c	FML021	Familial Hypercholesterolemia	66	0.055

422	P	SKN015	Skin Carcinoma	66	0.055

423		BRR014	Barrett Esophagus	65	0.055

424		HYD002	Hydronephrosis	60	0.055

425	P	PYL005	Pyelonephritis	56	0.055

426	P	ALP008	Alopecia	54	0.055

427	c	HYP864	Hypoparathyroidism, Familial Isolated, 1	48	0.055

428		49X006	49, Xxxxy Syndrome	41	0.055

429		MYT011	Myotonia	34	0.055

430	P	RSP003	Respiratory Failure	74	0.054

431		CHL065	Cholangiocarcinoma	68	0.054

432		CNN005	Connective Tissue Disease	68	0.054

433	c	HYP794	Hyperoxaluria, Primary, Type I	63	0.054

434		PRT013	Portal Hypertension	59	0.054

435	P	ALC033	Alcohol Use Disorder	58	0.054

436	P	NGH001	Night Blindness	48	0.054

437	c	DRR009	Diarrhea 6	46	0.054

438		GNG003	Gingival Recession	44	0.054

439	P	LTH003	Lethal Congenital Contracture Syndrome	40	0.054

440	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.054

441		ETH012	Ethylene Glycol Poisoning	26	0.054

442	c	LKM063	Leukemia, Chronic Myeloid	72	0.053

443	c	ART101	Aortic Valve Disease 2	65	0.053

444	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.053

445	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.053

446	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.053

447		ALL006	Allergic Asthma	56	0.053

448		GST050	Gastrointestinal System Disease	56	0.053

449	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.053

450		THY030	Thyroid Gland Disease	52	0.053

451		PTH003	Pathologic Nystagmus	52	0.053

452		ENT004	Enthesopathy	49	0.053

453		CHL004	Cholelithiasis	49	0.053

454		CRD137	Cardiogenic Shock	47	0.053

455		GST030	Gastrinoma	45	0.053

456		CRT015	Carotid Artery Occlusion	45	0.053

457	P	MLT020	Multiple Sclerosis	72	0.052

458	P	BRG001	Brugada Syndrome	71	0.052

459		SRC014	Sarcoma	65	0.052

460	P	DRM010	Dermatomyositis	61	0.052

461	c	ACT073	Acute Leukemia	58	0.052

462	P	CNG010	Congenital Stationary Night Blindness	54	0.052

463		SPN035	Spindle Cell Sarcoma	53	0.052

464		INT079	Intrahepatic Cholangiocarcinoma	51	0.052

465	c	PCH010	Pachyonychia Congenita 3	44	0.052

466	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.052

467	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.051

468	c	NRF023	Neurofibromatosis, Type Ii	80	0.051

469		END057	Endometrial Cancer	74	0.051

470	P	GRF003	Graft-Versus-Host Disease	72	0.051

471	P	MTR014	Motor Neuron Disease	65	0.051

472	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.051

473		CLT003	Colitis	62	0.051

474	P	CHL002	Childhood Absence Epilepsy	61	0.051

475	P	MYC008	Myocarditis	59	0.051

476	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.051

477	c	BNG091	Benign Chronic Pemphigus	58	0.051

478	P	GST044	Gastritis	56	0.051

479	P	VNS003	Venous Insufficiency	55	0.051

480	c	XNT010	Xanthinuria, Type I	53	0.051

481		PRP080	Peripheral Artery Disease	53	0.051

482	c	HYP243	Hyperparathyroidism 1	51	0.051

483		ENT011	Enterocolitis	51	0.051

484	P	OPN001	Open-Angle Glaucoma	49	0.051

485		RTN023	Retinitis	46	0.051

486		PPL001	Papillary Adenoma	44	0.051

487	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.051

488		NRR001	Neuroretinitis	42	0.051

489		PST092	Posttransplant Acute Limbic Encephalitis	29	0.051

490		NRL016	Neural Tube Defects	82	0.050

491	P	RTN024	Retinoblastoma	73	0.050

492	P	SLP006	Sleep Apnea	69	0.050

493	c	MCR129	Microvascular Complications of Diabetes 1	66	0.050

494		CHG001	Chagas Disease	66	0.050

495		HYP020	Hyperprolactinemia	64	0.050

496		CNT105	Central Core Disease of Muscle	60	0.050

497	c	HPT016	Hepatitis B	59	0.050

498		GNG013	Gingivitis	59	0.050

499		BLR008	Bilirubin Metabolic Disorder	57	0.050

500	P	MYS005	Myositis	56	0.050

501	P	FBR017	Fibrosarcoma	56	0.050

502		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.050

503	P	PMP001	Pemphigus	54	0.050

504	P	RTN018	Retinal Disease	53	0.050

505		ACT003	Acute Kidney Tubular Necrosis	45	0.050

506	P	TRC031	Trichorhinophalangeal Syndrome	40	0.050

507	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	0.048

508	P	AMY004	Amyloidosis	70	0.048

509	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.048

510		FCT007	Factor Vii Deficiency	67	0.048

511		ALL003	Allergic Rhinitis	67	0.048

512	P	CLC063	Celiac Disease 1	66	0.048

513	c	FML001	Familial Atrial Fibrillation	65	0.048

514		OVR029	Ovarian Hyperstimulation Syndrome	64	0.048

515		LSH001	Leishmaniasis	63	0.048

516		ANR007	Anorexia Nervosa	63	0.048

517	c	SVR001	Severe Acute Respiratory Syndrome	62	0.048

518		PNM001	Pneumocystosis	59	0.048

519		TRD006	Tardive Dyskinesia	54	0.048

520		SNS003	Sensory Peripheral Neuropathy	54	0.048

521		MST005	Mastitis	53	0.048

522		TXC002	Toxic Encephalopathy	53	0.048

523	c	FML008	Familial Retinoblastoma	53	0.048

524		PRS021	Prostatic Adenoma	51	0.048

525		HYP081	Hypolipoproteinemia	51	0.048

526		HYP080	Hypogonadism	50	0.048

527		SYS003	Systolic Heart Failure	49	0.048

528	c	CHR431	Chronic Venous Insufficiency	49	0.048

529		PRS129	Prostatic Hyperplasia, Benign	49	0.048

530		CRB090	Cerebral Hypoxia	44	0.048

531	P	HYP265	Hypotonia	43	0.048

532		IDP070	Idiopathic Scoliosis	42	0.048

533	P	KLZ004	Kala-Azar 1	41	0.048

534	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.048

535	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.048

536		PRR001	Periarthritis	32	0.048

537	P	GLM040	Glioma Susceptibility 1	81	0.047

538		ULC004	Ulcerative Colitis	73	0.047

539	c	DBT099	Diabetes Mellitus, Type I	65	0.047

540		TBC004	Tobacco Addiction	64	0.047

541	P	END044	Endometriosis	63	0.047

542	P	VSC011	Vasculitis	62	0.047

543	P	HYP035	Hypophosphatasia	61	0.047

544		GST033	Gestational Diabetes	61	0.047

545	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.047

546	c	FML035	Familial Hyperlipidemia	55	0.047

547		AMN001	Amenorrhea	54	0.047

548		PRS045	Prostatic Hypertrophy	53	0.047

549		FRZ001	Frozen Shoulder	53	0.047

550		GST023	Gastric Ulcer	53	0.047

551		CRT013	Carotid Stenosis	50	0.047

552		PLS025	Plasmablastic Lymphoma	47	0.047

553		SBC016	Subacute Delirium	44	0.047

554		LWC001	Low Compliance Bladder	43	0.047

555	c	CTR132	Cataract 3, Multiple Types	41	0.047

556	c	MCR112	Microvascular Complications of Diabetes 2	41	0.047

557		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.047

558	c	PNS012	Paine Syndrome	61	0.046

559	P	PLY019	Polyneuropathy	56	0.046

560	P	SCK002	Sick Sinus Syndrome	55	0.046

561		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.046

562		DYS073	Dysphagia	50	0.046

563		MCN001	Mucinous Adenocarcinoma	49	0.046

564		HYP006	Hypertensive Heart Disease	49	0.046

565		HDN002	Head Injury	46	0.046

566		APP009	Appendix Adenocarcinoma	44	0.046

567	c	HYP057	Hypervitaminosis D	42	0.046

568		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.046

569		PRN032	Paraneoplastic Cerebellar Degeneration	28	0.046

570		VLK001	Volkmann Contracture	25	0.046

571	c	SPN225	Spondyloarthropathy 1	73	0.044

572		GST040	Gastric Adenocarcinoma	70	0.044

573	c	PNC108	Pancreatitis, Hereditary	70	0.044

574	P	LPR021	Leprosy 3	69	0.044

575	P	THY023	Thymoma	65	0.044

576	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.044

577		PLM031	Poliomyelitis	64	0.044

578	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.044

579	P	DNT020	Dent Disease 1	62	0.044

580	P	BRS044	Breast Adenocarcinoma	59	0.044

581		GST045	Gastroenteritis	59	0.044

582		SPT004	Septic Arthritis	58	0.044

583		CHL067	Cholecystitis	57	0.044

584		SFT003	Soft Tissue Sarcoma	56	0.044

585		AMN003	Amnestic Disorder	54	0.044

586	c	THY107	Thymoma, Familial	52	0.044

587		TLN003	Telangiectasis	52	0.044

588	c	MGR032	Migraine, Familial Hemiplegic, 1	51	0.044

589		ACH005	Achalasia	51	0.044

590	P	MTR003	Mitral Valve Stenosis	50	0.044

591		NPH010	Nephrosclerosis	50	0.044

592		VTM033	Vitamin K Deficiency Bleeding	48	0.044

593	c	MLG069	Malignant Hypertension	47	0.044

594		CHR074	Choriocarcinoma	47	0.044

595	c	MLG068	Malignant Glioma	46	0.044

596		PRT030	Parathyroid Gland Disease	45	0.044

597		SPS057	Spasticity	45	0.044

598	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.044

599		BCK006	Back Pain	42	0.044

600	P	SCL057	Scoliosis, Isolated 1	41	0.044

601		PHS001	Phosphorus Metabolism Disease	40	0.044

602		HNS001	Hansen's Disease	34	0.044

603		CLC004	Calcific Tendinitis	30	0.044

604		ENM001	Enamel Caries	28	0.044

605		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.043

606	P	RTN008	Retinitis Pigmentosa	79	0.043

607	c	MNN043	Meningioma, Familial	74	0.043

608		CRB037	Cerebral Palsy	69	0.043

609	P	PLM036	Pulmonary Fibrosis	65	0.043

610		PLG002	Plague	63	0.043

611	P	EPL140	Epilepsy, Idiopathic Generalized	62	0.043

612		MNN042	Meningioma, Radiation-Induced	62	0.043

613		WLL001	Williams-Beuren Syndrome	60	0.043

614	P	SNS001	Sensorineural Hearing Loss	60	0.043

615		VRC005	Varicose Veins	60	0.043

616		SPN027	Spinal Stenosis	59	0.043

617	P	CYS018	Cystitis	59	0.043

618		EYD002	Eye Disease	58	0.043

619		DSS009	Disseminated Intravascular Coagulation	57	0.043

620	P	CHN012	Chondrosarcoma	56	0.043

621		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.043

622		NRN004	Neuroendocrine Tumor	55	0.043

623	P	HYP050	Hyperinsulinemic Hypoglycemia	55	0.043

624		END040	Endogenous Depression	55	0.043

625		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.043

626		OST016	Osteochondrosis	53	0.043

627		HRT012	Heart Valve Disease	53	0.043

628		HMC014	Homocysteinemia	53	0.043

629		GSG001	Gas Gangrene	53	0.043

630	P	PNC025	Panic Disorder	53	0.043

631	P	MGR003	Migraine with Aura	52	0.043

632		LNG031	Lung Benign Neoplasm	51	0.043

633		SPN021	Spinal Meningioma	50	0.043

634		RYN001	Raynaud Disease	48	0.043

635		BRS064	Bursitis	48	0.043

636	c	MTR002	Mitral Valve Insufficiency	48	0.043

637		KRT002	Keratomalacia	47	0.043

638		ATN005	Autonomic Dysfunction	46	0.043

639		DST006	Diastolic Heart Failure	45	0.043

640	P	SPR041	Spermatogenic Failure 6	44	0.043

641		TRP009	Triple X Syndrome	42	0.043

642		SCR001	Secretory Meningioma	41	0.043

643	c	SPR043	Spermatogenic Failure 9	41	0.043

644	P	MLG074	Malignant Mesenchymoma	40	0.043

645		MDL009	Medullary Sponge Kidney	40	0.043

646		OVR094	Ovarian Epithelial Cancer	38	0.043

647		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.043

648		CHR178	Chromosomal Triplication	35	0.043

649	P	ASP006	Aspergillosis	69	0.042

650		MNT001	Mantle Cell Lymphoma	69	0.042

651	P	NRV007	Nervous System Disease	66	0.042

652	P	PSD087	Pseudoxanthoma Elasticum	65	0.042

653	P	KDN017	Kidney Cancer	60	0.042

654		ANT024	Anthrax Disease	58	0.042

655		FBR047	Fibromyalgia	58	0.042

656		CNT047	Contact Dermatitis	58	0.042

657		BRS051	Breast Disease	58	0.042

658	P	BNC003	Bone Cancer	58	0.042

659		BRD001	Brody Myopathy	57	0.042

660		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.042

661		EMB004	Embryonal Carcinoma	56	0.042

662		LMB062	Limb Ischemia	55	0.042

663		URN010	Urinary Tract Obstruction	55	0.042

664	P	SHR001	Short Bowel Syndrome	53	0.042

665	P	LMB006	Limb-Girdle Muscular Dystrophy	53	0.042

666	P	SML001	Small Cell Carcinoma	52	0.042

667		SPN051	Spondylitis	51	0.042

668	P	HMP007	Hemophilia	51	0.042

669		FDL002	Food Allergy	51	0.042

670		PLS009	Plasma Cell Neoplasm	51	0.042

671		CYS014	Cystadenocarcinoma	51	0.042

672	P	FNC004	Fanconi Syndrome	50	0.042

673	P	ART018	Aortic Valve Insufficiency	49	0.042

674		CCN002	Cocaine Abuse	49	0.042

675		KRT008	Keratopathy	47	0.042

676		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.042

677		URT010	Ureteral Obstruction	45	0.042

678		HPT004	Hepatic Coma	45	0.042

679		GRN017	Granulocytopenia	44	0.042

680	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.042

681		GST020	Gastric Antral Vascular Ectasia	41	0.042

682		THR035	Thrombasthenia	40	0.042

683		MCN008	Mucinous Cystadenocarcinoma	40	0.042

684	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.042

685		HYP540	Hypertension, Diastolic	40	0.042

686	c	CHL157	Childhood B-Cell Acute Lymphoblastic Leukemia	33	0.042

687		IDP085	Idiopathic Infantile Hypercalcemia	28	0.042

688		BRN028	Brain Cancer	74	0.040

689	c	BTT014	Beta-Thalassemia	74	0.040

690	c	HPT073	Hepatitis C Virus	72	0.040

691	c	INF071	Inflammatory Bowel Disease 1	67	0.040

692		CRP001	Carpal Tunnel Syndrome	67	0.040

693	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.040

694		KHL003	Kohlschutter-Tonz Syndrome	65	0.040

695		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.040

696	P	GCH001	Gaucher's Disease	63	0.040

697	P	HML002	Hemolytic Anemia	63	0.040

698	P	MVM001	Movement Disease	63	0.040

699	P	ESP024	Esophagitis	62	0.040

700		BLL006	Bullous Pemphigoid	62	0.040

701	P	PRM006	Primary Biliary Cirrhosis	62	0.040

702	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	61	0.040

703		DPH001	Diphtheria	60	0.040

704	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.040

705	P	OPT006	Optic Nerve Disease	60	0.040

706		PRN019	Perinatal Necrotizing Enterocolitis	59	0.040

707	P	SYP003	Syphilis	58	0.040

708	P	URT039	Urticaria	58	0.040

709	P	GLL018	Gallbladder Cancer	57	0.040

710	c	VSC019	Vesicoureteral Reflux 1	57	0.040

711	P	MYP006	Myopia	55	0.040

712	P	MNC007	Monocytic Leukemia	53	0.040

713	P	INT068	Intestinal Disease	53	0.040

714	P	BSL038	Basal Ganglia Calcification, Idiopathic, 1	52	0.040

715		ILS001	Ileus	51	0.040

716		RGH001	Right Bundle Branch Block	48	0.040

717		INT067	Interstitial Nephritis	48	0.040

718		DGN001	Degenerative Disc Disease	48	0.040

719		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.040

720		RTN020	Retinal Vascular Disease	46	0.040

721		GRW007	Growth Hormone Deficiency	46	0.040

722		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.040

723	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.040

724		OST115	Osteonecrosis of the Jaw	40	0.040

725		KLD004	Keloid Disorder	40	0.040

726		WLL004	Wallerian Degeneration	39	0.040

727		INF009	Inflammatory Spondylopathy	31	0.040

728		CRV035	Cervical Cancer	76	0.038

729		MYL009	Myelodysplastic Syndrome	70	0.038

730	c	GCH015	Gaucher Disease, Type I	70	0.038

731	P	FRG001	Fragile X Syndrome	70	0.038

732	P	MYC084	Mycobacterium Tuberculosis 1	68	0.038

733	P	FRN006	Frontotemporal Dementia	68	0.038

734	P	FLL037	Follicular Lymphoma	67	0.038

735		GTL001	Gitelman Syndrome	65	0.038

736	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.038

737		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.038

738		PSR001	Psoriatic Arthritis	61	0.038

739		VRL011	Viral Infectious Disease	61	0.038

740	c	JVN061	Juvenile Arthritis	60	0.038

741		HPT019	Hepatic Encephalopathy	60	0.038

742	P	SLP005	Sleep Disorder	59	0.038

743	P	CND004	Candidiasis	58	0.038

744		PMP006	Pemphigus Vulgaris, Familial	57	0.038

745		CHR100	Chronic Ulcer of Skin	55	0.038

746		PRP030	Purpura	54	0.038

747		NNL006	Non-Alcoholic Steatohepatitis	54	0.038

748		DMY004	Demyelinating Disease	52	0.038

749		RDC002	Radiculopathy	50	0.038

750		AZS001	Azoospermia	50	0.038

751	c	FLL041	Follicular Lymphoma 1	49	0.038

752		DRG003	Drug Dependence	47	0.038

753		RNL077	Renal Fibrosis	47	0.038

754		DNT001	Dental Fluorosis	43	0.038

755		CRB086	Cerebral Aneurysms	40	0.038

756	P	PRC031	Preeclampsia/eclampsia 1	38	0.038

757	c	PLY105	Polycystic Ovary Syndrome 1	38	0.038

758		PRN039	Paraneoplastic Syndromes	38	0.038

759		BNG018	Benign Paroxysmal Positional Nystagmus	37	0.038

760		ARG004	Argyria	27	0.038

761	c	LNG052	Long Qt Syndrome 8	27	0.038

762		MTH071	Methane Production	26	0.038

763		XLN012	X-Linked Congenital Stationary Night Blindness	26	0.038

764	P	FML011	Familial Adenomatous Polyposis	72	0.037

765		MYL005	Myelofibrosis	70	0.037

766		EWN003	Ewing Sarcoma	69	0.037

767	c	HMP004	Hemophilia B	68	0.037

768	P	HYP098	Hypereosinophilic Syndrome	67	0.037

769	P	BLD062	Bile Duct Cancer	67	0.037

770	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	63	0.037

771		CYS013	Cystinuria	63	0.037

772	c	GLC092	Glaucoma, Primary Open Angle	62	0.037

773		MSL001	Measles	62	0.037

774	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	60	0.037

775		RHM001	Rheumatic Fever	60	0.037

776		ORL011	Oral Cancer	60	0.037

777		PRT058	Pure Autonomic Failure	59	0.037

778		IRN001	Iron Deficiency Anemia	59	0.037

779	P	PRN023	Prion Disease	57	0.037

780	P	ANG015	Angioedema	57	0.037

781	c	ESS001	Essential Tremor	56	0.037

782		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.037

783	P	NRF002	Neurofibromatosis	56	0.037

784		PPL022	Papilloma	54	0.037

785	P	INS002	in Situ Carcinoma	53	0.037

786		OCL006	Ocular Hypertension	53	0.037

787	P	CNT005	Central Nervous System Lymphoma	53	0.037

788		NNT012	Neonatal Jaundice	53	0.037

789	P	THY032	Thyroiditis	52	0.037

790	P	TRT010	Teratoma	52	0.037

791		PLM017	Pulmonary Alveolar Microlithiasis	50	0.037

792		GST049	Gastrointestinal System Cancer	49	0.037

793	c	BPL002	Bipolar I Disorder	49	0.037

794		VCC001	Vaccinia	49	0.037

795		IGG001	Iga Glomerulonephritis	48	0.037

796	c	PRM226	Primary Central Nervous System Lymphoma	48	0.037

797		MLK006	Milk Allergy	48	0.037

798		GST071	Gastrointestinal Carcinoma	47	0.037

799		CNT033	Central Nervous System Cancer	47	0.037

800		ASP004	Asphyxia Neonatorum	46	0.037

801		BCK003	Background Diabetic Retinopathy	46	0.037

802	P	HMR005	Hemorrhoid	46	0.037

803		SQM002	Squamous Cell Papilloma	46	0.037

804		TRT001	Teratocarcinoma	45	0.037

805		NWC001	Newcastle Disease	45	0.037

806		LYM126	Lymphoma Aids Related	44	0.037

807		TST015	Testicular Disease	43	0.037

808		MST004	Mast Cell Neoplasm	42	0.037

809	c	AGR019	Age-Related Hearing Loss	42	0.037

810	c	HYP753	Hypocalciuric Hypercalcemia, Familial, Type Ii	42	0.037

811	P	CLS010	Cluster Headache	42	0.037

812	c	HYP608	Hypocalciuric Hypercalcemia, Familial, Type Iii	41	0.037

813		PRS063	Paresthesia	41	0.037

814		ALD013	Aldosterone-Producing Adenoma	39	0.037

815		MNR003	Mineral Metabolism Disease	39	0.037

816		EXT007	Extracutaneous Mastocytoma	38	0.037

817		CRN288	Corneal Dystrophy, Band-Shaped	38	0.037

818		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.037

819		GLM044	Glomerular Disease	37	0.037

820	P	DNT007	Dentin Sensitivity	36	0.037

821		MNG007	Manganese Poisoning	29	0.037

822	P	MDL005	Medulloblastoma	77	0.035

823	P	CHR012	Chronic Granulomatous Disease	67	0.035

824		GLN010	Glanzmann Thrombasthenia	66	0.035

825	c	PSD108	Pseudohypoparathyroidism, Type Ia	66	0.035

826	c	MCL013	Mucolipidosis Iv	66	0.035

827	P	ART005	Arteriovenous Malformation	65	0.035

828		PPL049	Papillon-Lefevre Syndrome	65	0.035

829		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	62	0.035

830		ERL001	Early Myoclonic Encephalopathy	62	0.035

831	c	HPT001	Hepatitis C	62	0.035

832		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.035

833		INT066	Interstitial Lung Disease	60	0.035

834		END081	Endosteal Hyperostosis, Autosomal Dominant	60	0.035

835		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	59	0.035

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

837	P	MTR012	Mitral Valve Disease	58	0.035

838	P	MTC069	Mitochondrial Disorders	56	0.035

839		PRS047	Prostatitis	56	0.035

840		ISL001	Islet Cell Tumor	56	0.035

841		DFF005	Diffuse Large B-Cell Lymphoma	55	0.035

842	P	PTT006	Pituitary Adenoma	55	0.035

843	c	PRG043	Progressive Familial Heart Block, Type Ib	54	0.035

844		FCL014	Focal Epilepsy	54	0.035

845		HLL004	Hellp Syndrome	54	0.035

846		HYP741	Hyperparathyroidism 2 with Jaw Tumors	53	0.035

847		INT075	Intracranial Hypertension	53	0.035

848		ACR041	Acromelic Frontonasal Dysostosis	52	0.035

849		ART074	Aortic Dissection	52	0.035

850		BHR001	Behr Syndrome	51	0.035

851		SCH012	Schizoaffective Disorder	50	0.035

852	c	HYP603	Hyperoxaluria, Primary, Type Iii	50	0.035

853		TRY001	Trypanosomiasis	50	0.035

854		OPT003	Opiate Dependence	50	0.035

855		LFT001	Left Bundle Branch Hemiblock	49	0.035

856		SNT005	Sinoatrial Node Disease	49	0.035

857		SCT005	Scott Syndrome	49	0.035

858		ATS010	Autosomal Recessive Disease	48	0.035

859		PRP017	Periapical Periodontitis	46	0.035

860	P	BNG032	Benign Mesothelioma	46	0.035

861		GST012	Gastroesophageal Junction Adenocarcinoma	46	0.035

862		ASP026	Asplenia, Isolated Congenital	44	0.035

863		CVD001	Covid-19	44	0.035

864		MMM006	Mammographic Density	41	0.035

865		RDN001	Reading Disorder	40	0.035

866	P	CHL156	Childhood T-Cell Acute Lymphoblastic Leukemia	38	0.035

867	c	HNT011	Huntington Disease-Like 3	38	0.035

868		HRN029	Hearing Loss, Noise-Induced	37	0.035

869		SCR003	Secretory Diarrhea	37	0.035

870		ENP001	Enophthalmos	35	0.035

871		RTC003	Root Caries	33	0.035

872		CYT018	Cytochrome P450 2d6 Variant	27	0.035

873		HVY002	Heavy Metal Poisoning	22	0.035

874	P	RTT002	Rett Syndrome	80	0.033

875		CNN003	Conn's Syndrome	79	0.033

876	P	TBR001	Tuberous Sclerosis	70	0.033

877		ACR008	Acrocallosal Syndrome	69	0.033

878		ODN023	Odontochondrodysplasia	68	0.033

879		OBS002	Obsessive-Compulsive Disorder	68	0.033

880		SKN019	Skin Melanoma	68	0.033

881	P	INF038	Influenza	68	0.033

882	P	HPT021	Hepatitis	67	0.033

883	P	HYD006	Hydrocephalus	66	0.033

884		MYL031	Myeloproliferative Neoplasm	66	0.033

885	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	65	0.033

886		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.033

887	P	ADL010	Adult Respiratory Distress Syndrome	65	0.033

888		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.033

889		DGR001	Digeorge Syndrome	64	0.033

890	P	RHB003	Rhabdomyosarcoma	63	0.033

891		MSC152	Muscular Dystrophy, Becker Type	63	0.033

892	c	ALP101	Alpha-Thalassemia	62	0.033

893	P	SJG008	Sjogren Syndrome	61	0.033

894		ING001	Inguinal Hernia	60	0.033

895		ETN001	Eating Disorder	60	0.033

896	P	GLY013	Glycogen Storage Disease	60	0.033

897	P	MCR010	Microcephaly	59	0.033

898		CHL123	Chlamydia	59	0.033

899	P	NMN002	Niemann-Pick Disease	59	0.033

900	P	GLL022	Guillain-Barre Syndrome	59	0.033

901		INC002	Inclusion Body Myositis	58	0.033

902		CHL028	Childhood Type Dermatomyositis	58	0.033

903	c	DWL002	Dowling-Degos Disease 1	58	0.033

904		LYM027	Lymphopenia	58	0.033

905	P	UVT001	Uveitis	57	0.033

906	P	GLL020	Gallbladder Disease	57	0.033

907		THY122	Thyroid Gland Cancer	57	0.033

908		TRP006	Tarp Syndrome	57	0.033

909	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.033

910		HMR039	Hemorrhage, Intracerebral	57	0.033

911		CMR002	Coumarin Resistance	56	0.033

912		TRN018	Transitional Cell Carcinoma	56	0.033

913	P	SBS003	Substance Abuse	55	0.033

914	P	SLM003	Salmonellosis	55	0.033

915		CRT017	Cartilage Disease	54	0.033

916		PRT038	Protein-Energy Malnutrition	54	0.033

917		SLP001	Sleeping Sickness	54	0.033

918		CLL003	Cellulitis	54	0.033

919		CRH005	Crohn's Colitis	53	0.033

920	P	PTS002	Ptosis	53	0.033

921		LYS002	Lysosomal Storage Disease	52	0.033

922	c	VRL010	Viral Hepatitis	52	0.033

923		DYS015	Dysentery	52	0.033

924	c	HYP602	Hyperoxaluria, Primary, Type Ii	51	0.033

925		SPN019	Spondylolisthesis	51	0.033

926		HYP789	Hypophosphatemic Rickets with Hypercalciuria, Hereditary	51	0.033

927		LRN003	Learning Disability	49	0.033

928		QDR001	Quadriplegia	48	0.033

929		HYP043	Hyperandrogenism	48	0.033

930		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.033

931		FBR009	Fibrous Dysplasia	48	0.033

932		PLC007	Placental Abruption	48	0.033

933		SXL003	Sexual Disorder	47	0.033

934		PRD004	Prediabetes Syndrome	47	0.033

935		NDL007	Nodular Goiter	47	0.033

936		RTC005	Reticulosarcoma	47	0.033

937	P	HRT035	Heart Block, Congenital	46	0.033

938	P	BRB001	Beriberi	46	0.033

939		ATN004	Autonomic Neuropathy	45	0.033

940		URT014	Ureterolithiasis	44	0.033

941		CHN010	Chondroma	43	0.033

942		BNM001	Bone Marrow Cancer	43	0.033

943	c	SRC023	Sarcoidosis 2	43	0.033

944	P	MJR007	Major Affective Disorder 1	43	0.033

945	P	AVS003	Avascular Necrosis	42	0.033

946		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.033

947		AMN006	Aminoaciduria	38	0.033

948	c	CHR098	Chronic Pyelonephritis	38	0.033

949		END028	Endemic Goiter	37	0.033

950		BCL014	B-Cell Growth Factor	35	0.033

951		PYR009	Pyridoxine Deficiency Anemia	34	0.033

952	c	CHR064	Chronic Monocytic Leukemia	33	0.033

953	c	ATM068	Autoimmune Hypoparathyroidism	32	0.033

954		DNT010	Dentin Caries	32	0.033

955		CLN002	Colon Mucinous Adenocarcinoma	28	0.033

956		MST020	Mast Cell Activation Syndrome	26	0.033

957		HML018	Homologous Wasting Disease	22	0.033

958	P	ATX030	Ataxia-Telangiectasia	82	0.031

959		KPS004	Kaposi Sarcoma	75	0.031

960		PHN003	Phenylketonuria	75	0.031

961	c	ART115	Aortic Valve Disease 1	75	0.031

962		OTT002	Otitis Media	72	0.031

963		MLT157	Multiple System Atrophy 1	70	0.031

964	P	OCL013	Oculodentodigital Dysplasia	69	0.031

965	c	NMN015	Niemann-Pick Disease, Type C1	68	0.031

966	P	NSP012	Nasopharyngeal Carcinoma	66	0.031

967		MSM014	Mismatch Repair Cancer Syndrome	65	0.031

968	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.031

969		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	63	0.031

970		INT002	Intermittent Claudication	61	0.031

971	P	HMN010	Hemangioma	61	0.031

972		TRG002	Trigeminal Neuralgia	60	0.031

973	P	WLF004	Wolfram Syndrome	60	0.031

974	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.031

975		DRR014	Darier-White Disease	60	0.031

976	P	CNT004	Centronuclear Myopathy	59	0.031

977	P	DNG005	Dengue Virus	59	0.031

978	c	SPN301	Spinocerebellar Ataxia 2	58	0.031

979		PST028	Post-Traumatic Stress Disorder	58	0.031

980		APL002	Aplasia of Lacrimal and Salivary Glands	57	0.031

981		BRN056	Bronchopulmonary Dysplasia	57	0.031

982	P	PLY041	Polymyositis	57	0.031

983	P	END033	Endocarditis	57	0.031

984	P	FTL001	Fetal Alcohol Syndrome	57	0.031

985	P	PLY018	Polycythemia	56	0.031

986	c	ACT134	Acute Liver Failure	56	0.031

987		MTH009	Mouth Disease	56	0.031

988		INT030	Intracranial Aneurysm	56	0.031

989	P	MYT023	Myotonia Congenita	56	0.031

990	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.031

991		VSC003	Visceral Leishmaniasis	55	0.031

992	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	55	0.031

993		MYM001	Myoma	54	0.031

994		NRT001	Neurotic Disorder	53	0.031

995	P	MYP087	Myopathy, Tubular Aggregate, 1	53	0.031

996		CHR073	Choreatic Disease	52	0.031

997		SMT003	Somatostatinoma	52	0.031

998	c	ACT135	Acute Graft Versus Host Disease	52	0.031

999		THR004	Thrombocytosis	51	0.031

1000	P	SPP010	Suppressor of Tumorigenicity 3	51	0.031

1001	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.031

1002		RYS001	Reye Syndrome	51	0.031

1003	c	HNT004	Huntington Disease-Like 2	50	0.031

1004		PST021	Postpartum Depression	50	0.031

1005		PLC008	Placenta Disease	50	0.031

1006		HYP068	Hyperostosis	48	0.031

1007	P	FML362	Familial Isolated Hypoparathyroidism	47	0.031

1008	P	CLL015	Collagen Disease	47	0.031

1009	c	INH020	Inherited Metabolic Disorder	47	0.031

1010		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.031

1011		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	47	0.031

1012	P	VTR007	Vitreoretinopathy	46	0.031

1013		SPN020	Spondylosis	46	0.031

1014		EXS001	Exostosis	46	0.031

1015	P	MYC033	Myoclonus	46	0.031

1016		CNT017	Central Nervous System Origin Vertigo	45	0.031

1017	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.031

1018		DMP001	Dumping Syndrome	44	0.031

1019		SPN369	Spinal Disease	43	0.031

1020		PMP004	Pemphigus Foliaceus	43	0.031

1021		URM005	Uremic Pruritus	42	0.031

1022		MRP001	Morphine Dependence	41	0.031

1023	c	ACT004	Acute Diarrhea	39	0.031

1024		SCR011	Scrapie	39	0.031

1025		HYP264	Hypertonia	38	0.031

1026		FRS012	First-Degree Atrioventricular Block	38	0.031

1027		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.031

1028		PRM329	Premature Aging	35	0.031

1029		CNC014	Cancer-Associated Retinopathy	34	0.031

1030	P	BCL013	B-Cell Adult Acute Lymphocytic Leukemia	32	0.031

1031	P	SPN202	Spinocerebellar Ataxia, X-Linked 1	32	0.031

1032	c	CHR013	Chronic Apical Periodontitis	31	0.031

1033		BRN055	Bronchogenic Cyst	27	0.031

1034		ADG002	Audiogenic Seizures	25	0.031

1035	c	HYP831	Hyperparathyroidism, Transient Neonatal	24	0.031

1036		CBP002	Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome	20	0.031

1037	P	LYN001	Lynch Syndrome	77	0.029

1038		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.029

1039	P	ANG001	Angelman Syndrome	69	0.029

1040	P	TMP003	Temporal Arteritis	68	0.029

1041		PSY004	Psychotic Disorder	67	0.029

1042	P	MNN013	Meningitis	66	0.029

1043		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.029

1044	P	CNJ013	Conjunctivitis	65	0.029

1045		KRT019	Keratitis, Hereditary	65	0.029

1046		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.029

1047		PTT048	Pituitary Adenoma, Prolactin-Secreting	65	0.029

1048	P	FRD001	Friedreich Ataxia	64	0.029

1049		INT146	Intervertebral Disc Disease	63	0.029

1050	c	OPT053	Optic Atrophy 1	63	0.029

1051		HMT002	Hematologic Cancer	62	0.029

1052	c	HPT003	Hepatitis a	62	0.029

1053		CRC021	Carcinosarcoma	62	0.029

1054	P	PRP029	Porphyria	62	0.029

1055	P	INT143	Interstitial Cystitis	61	0.029

1056		ALC006	Alcoholic Hepatitis	61	0.029

1057		HRP004	Herpes Zoster	60	0.029

1058	P	PTN014	Patent Ductus Arteriosus 1	60	0.029

1059		PSD012	Pseudoachondroplasia	58	0.029

1060	P	INT070	Intestinal Obstruction	58	0.029

1061	P	MLT007	Multiple Epiphyseal Dysplasia	58	0.029

1062		ERY003	Erythema Multiforme	58	0.029

1063		DSS008	Disease of Mental Health	58	0.029

1064		MNR012	Meniere Disease	57	0.029

1065		HMT008	Hematuria, Benign Familial	56	0.029

1066		GNR004	Generalized Anxiety Disorder	56	0.029

1067	P	PNM006	Pneumoconiosis	56	0.029

1068	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.029

1069	c	BCT007	Bacterial Meningitis	55	0.029

1070	P	ANT006	Antiphospholipid Syndrome	55	0.029

1071		ACT058	Active Peptic Ulcer Disease	55	0.029

1072	P	DBT005	Diabetes Insipidus	55	0.029

1073		HMP005	Hemiplegia	55	0.029

1074		HRY003	Hairy Cell Leukemia	55	0.029

1075	c	OST164	Osteoporosis, Juvenile	53	0.029

1076	c