Search results for Calcium citrate

1386 hits were found for Calcium citrate

#	Family	MCID	Name	MIFTS	Score
1		NPH009	Nephrolithiasis	55	0.412

2	P	HYP069	Hyperparathyroidism	63	0.379

3		URL001	Urolithiasis	45	0.354

4	P	KDN018	Kidney Disease	72	0.340

5	P	OST002	Osteoporosis	74	0.338

6		BNR002	Bone Resorption Disease	48	0.325

7	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.323

8	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.323

9		RCK004	Rickets	68	0.315

10	c	HYP595	Hypertension, Essential	84	0.313

11	P	PLY011	Polycystic Ovary Syndrome	56	0.299

12	P	INF032	Infertility	57	0.296

13		IMP005	Impotence	52	0.285

14		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.273

15	c	CHR684	Chronic Kidney Disease	70	0.269

16		HYP025	Hyperphosphatemia	48	0.239

17		PRT037	Pertussis	65	0.237

18	c	SCN007	Secondary Hyperparathyroidism	51	0.236

19		END086	End Stage Renal Disease	51	0.231

20	c	PRM005	Primary Hyperparathyroidism	58	0.222

21		48X005	48,xyyy	39	0.220

22	P	CLR023	Colorectal Cancer	99	0.219

23	P	BND020	Bone Disease	59	0.213

24	P	BRS047	Breast Cancer	97	0.208

25		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.205

26		MTB004	Metabolic Acidosis	50	0.204

27	c	ACT071	Acute Kidney Failure	60	0.202

28	c	PRC016	Pre-Eclampsia	63	0.196

29		CNG034	Congestive Heart Failure	69	0.195

30	c	RHB024	Rhabdomyosarcoma 2	67	0.194

31	P	NRB001	Neuroblastoma	72	0.193

32		LPP008	Lipoprotein Quantitative Trait Locus	62	0.190

33		HYP005	Hypokalemia	55	0.188

34		ANG054	Angina Pectoris	66	0.187

35		ISC004	Ischemia	58	0.186

36	P	HRT032	Heart Disease	75	0.183

37	P	HYP024	Hypoparathyroidism	56	0.183

38	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.182

39		ANV001	Anovulation	47	0.182

40	P	PLM037	Pulmonary Hypertension	67	0.182

41	P	ADN016	Adenocarcinoma	64	0.176

42		HYP266	Hypoxia	57	0.175

43		ART140	Arteries, Anomalies of	52	0.175

44		IRN002	Iron Metabolism Disease	57	0.174

45		ADN018	Adenoma	59	0.173

46		HLX001	Helix Syndrome	47	0.173

47	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.173

48	c	PLY105	Polycystic Ovary Syndrome 1	38	0.171

49		DWN001	Down Syndrome	70	0.165

50		ATH013	Atherosclerosis Susceptibility	65	0.162

51	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.162

52		NPH003	Nephrocalcinosis	51	0.158

53		ALL026	Allergic Hypersensitivity Disease	62	0.157

54	P	VSC007	Vascular Disease	63	0.156

55	P	GLM045	Glioma	63	0.155

56		GLL048	Glial Tumor	45	0.154

57	P	CRN300	Coronary Heart Disease 1	63	0.152

58	P	PRS040	Prostate Cancer	97	0.152

59	P	LYM118	Lymphoma	68	0.151

60	P	CRD119	Cardiac Arrest	67	0.150

61	P	DRR001	Diarrhea	55	0.150

62		OST017	Osteomyelitis	64	0.147

63		CHL014	Cholera	59	0.147

64		IDP073	Idiopathic Hypercalciuria	43	0.146

65		DNT012	Dental Caries	53	0.145

66		CNS004	Constipation	58	0.144

67	P	MYC007	Myocardial Infarction	70	0.143

68	P	SRC025	Sarcoidosis 1	70	0.143

69	c	MGR028	Migraine with or Without Aura 1	67	0.141

70		LPD008	Lipid Metabolism Disorder	62	0.140

71	P	LVR013	Liver Disease	68	0.140

72	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.140

73	P	MSC005	Muscular Dystrophy	66	0.140

74		HYP056	Hypoglycemia	66	0.139

75		HYP080	Hypogonadism	50	0.139

76	P	ECL001	Eclampsia	50	0.139

77		PNG002	Pain Agnosia	51	0.138

78		OST159	Osteogenic Sarcoma	66	0.138

79	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.138

80		DFC004	Deficiency Anemia	70	0.137

81	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.137

82		47X002	47,xyy	49	0.136

83	P	RNL007	Renal Tubular Acidosis	51	0.136

84	P	DDN001	Duodenal Ulcer	52	0.136

85	P	ALZ034	Alzheimer Disease	88	0.136

86		HYP060	Hyperinsulinism	54	0.135

87	P	MLN007	Male Infertility	55	0.133

88	P	LKM002	Leukemia	68	0.133

89		ADL002	Adult Syndrome	70	0.133

90	P	TRN020	Turner Syndrome	67	0.132

91		MYL069	Myeloma, Multiple	85	0.132

92		HYP017	Hypophosphatemia	50	0.131

93		ATX019	Ataxia with Vitamin E Deficiency	42	0.131

94		LYM019	Lymphosarcoma	46	0.130

95		OVR029	Ovarian Hyperstimulation Syndrome	64	0.130

96		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.130

97	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.129

98		ANX004	Anoxia	40	0.129

99	P	HYP086	Hypothyroidism	69	0.128

100		INS001	Insulinoma	60	0.128

101	P	RCT021	Rectum Cancer	52	0.128

102		AGN016	Aging	56	0.127

103	P	NRP001	Neuropathy	56	0.126

104		OST011	Osteomalacia	52	0.125

105		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.125

106	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.124

107	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.123

108	P	CRD246	Cardiovascular System Disease	57	0.123

109		AMN001	Amenorrhea	54	0.123

110	P	LTR001	Lateral Sclerosis	54	0.123

111		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.122

112		CRB039	Cerebrovascular Disease	67	0.122

113	c	ATR087	Atrial Standstill 1	75	0.121

114	P	SZR006	Seizure Disorder	56	0.121

115		URM002	Uremia	49	0.121

116		HRW001	Hair Whorl	36	0.120

117	P	MLG056	Malignant Hyperthermia	67	0.120

118		LVR012	Liver Cirrhosis	62	0.120

119		STR067	Stroke, Ischemic	81	0.120

120	P	ART023	Arthropathy	62	0.120

121		HMS001	Hemosiderosis	54	0.120

122	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.120

123		TTN003	Tetanus	65	0.120

124		GT001	Gout	64	0.120

125	P	PHC003	Pheochromocytoma	71	0.119

126	P	HYP076	Hyperthyroidism	55	0.119

127		ADR040	Adrenal Gland Pheochromocytoma	46	0.119

128	P	PRD008	Periodontitis	64	0.118

129	P	DBT009	Diabetes Mellitus	64	0.118

130	P	ENC018	Encephalopathy	61	0.117

131		CYS001	Cystic Fibrosis	81	0.117

132	P	RRH023	Rare Hereditary Hemochromatosis	41	0.117

133		DPR016	Depression	63	0.116

134		OST012	Osteoarthritis	78	0.116

135		HYP066	Hyperglycemia	61	0.116

136		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.116

137	c	ACT075	Acute Myocardial Infarction	57	0.115

138		PPT005	Peptic Ulcer Disease	59	0.115

139		GLB015	Glioblastoma Multiforme	75	0.115

140		INT007	Intermediate Coronary Syndrome	55	0.114

141	c	ACT027	Acute Pancreatitis	60	0.114

142		CLC006	Calcinosis	48	0.114

143	P	HYP726	Hypercalcemia, Infantile, 1	58	0.113

144		NTR005	Nutritional Deficiency Disease	62	0.113

145	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.113

146		LNG099	Lung Disease	60	0.113

147	c	MCR120	Microvascular Complications of Diabetes 7	47	0.112

148		VSL002	Visual Epilepsy	59	0.112

149	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.112

150	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.112

151	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.112

152	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.112

153	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.112

154	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.112

155	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.112

156	c	MCR113	Microvascular Complications of Diabetes 3	52	0.112

157	P	BPL003	Bipolar Disorder	56	0.112

158	c	MCR130	Microvascular Complications of Diabetes 6	41	0.111

159	c	MCR133	Microvascular Complications of Diabetes 4	41	0.111

160	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.111

161	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.111

162	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.111

163	c	MJR024	Major Affective Disorder 9	41	0.111

164	c	MJR022	Major Affective Disorder 8	38	0.111

165		MSC157	Muscular Dystrophy, Duchenne Type	72	0.111

166		BRN071	Brain Injury	49	0.111

167		TXC005	Toxic Shock Syndrome	62	0.111

168	c	GLL024	Gallbladder Disease 1	53	0.110

169		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.110

170	c	DLT002	Dilated Cardiomyopathy	79	0.110

171	P	OVR042	Ovarian Cancer	88	0.109

172		SPN186	Spinal Cord Injury	60	0.109

173	c	ACT068	Acute Cystitis	63	0.109

174		FTT001	Fatty Liver Disease	61	0.108

175		CYT002	Cytokine Deficiency	42	0.107

176		HLC007	Helicobacter Pylori Infection	59	0.107

177		THY029	Thyroid Carcinoma	59	0.107

178		INS024	Insulin-Like Growth Factor I	79	0.107

179	c	PNS012	Paine Syndrome	61	0.106

180		HYP043	Hyperandrogenism	48	0.106

181	P	MYP004	Myopathy	70	0.106

182		TRM010	Traumatic Brain Injury	51	0.106

183		HMN044	Human Immunodeficiency Virus Type 1	71	0.106

184	P	PNC044	Pancreatitis	61	0.106

185		ATM095	Autoimmune Disease	62	0.105

186	P	CHR345	Chronic Pain	44	0.105

187		MNT002	Mental Depression	58	0.105

188	P	END044	Endometriosis	63	0.104

189		ALC007	Alcohol Dependence	66	0.104

190	P	THR014	Thrombocytopenia	67	0.104

191	P	HDC001	Headache	57	0.104

192	P	ATR011	Atrial Fibrillation	66	0.104

193	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.104

194	P	PLY014	Polycystic Kidney Disease	62	0.103

195		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.103

196	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.103

197	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.103

198	P	CTR002	Cataract	60	0.102

199	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.102

200	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.102

201		CRN030	Coronary Stenosis	50	0.102

202	P	PNC035	Pancreatic Cancer	84	0.101

203		PPL052	Papillomatosis, Confluent and Reticulated	33	0.100

204		IRR002	Irritable Bowel Syndrome	65	0.100

205	P	LNG032	Lung Cancer	98	0.099

206		HYP020	Hyperprolactinemia	64	0.098

207		CRD223	Cardiac Arrhythmia	60	0.098

208		GLS018	Glass Syndrome	57	0.098

209		GLC003	Glucose Intolerance	54	0.098

210	P	NTR004	Neutropenia	63	0.098

211	P	OVR082	Overgrowth Syndrome	50	0.097

212	P	GST044	Gastritis	56	0.097

213		PLS009	Plasma Cell Neoplasm	51	0.096

214	P	MCR115	Microvascular Complications of Diabetes 5	66	0.096

215		ANX010	Anxiety	73	0.096

216	P	HPT023	Hepatocellular Carcinoma	100	0.096

217	P	DST107	Distal Renal Tubular Acidosis	42	0.096

218		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	0.096

219	P	PRP019	Peripheral Nervous System Disease	58	0.096

220	P	GST053	Gastric Cancer	83	0.095

221		IRN001	Iron Deficiency Anemia	59	0.095

222		IMM167	Immune Deficiency Disease	78	0.095

223		ACQ007	Acquired Immunodeficiency Syndrome	60	0.095

224	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.094

225		RNL011	Renal Osteodystrophy	50	0.094

226	P	RHM011	Rheumatoid Arthritis	80	0.094

227	P	ART022	Arthritis	69	0.093

228	P	RHN004	Rhinitis	57	0.093

229	P	AST007	Astrocytoma	51	0.093

230	P	HYP061	Hypertrophic Cardiomyopathy	70	0.093

231		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.092

232		RYN005	Raynaud Phenomenon	47	0.092

233		CHL079	Children's Interstitial Lung Disease	26	0.092

234		LYM040	Lymphoblastic Lymphoma	54	0.091

235		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.091

236	P	ART021	Arteriosclerosis	54	0.091

237		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.090

238	P	BCL017	B-Cell Lymphoma	58	0.090

239	c	PRM038	Primary Agammaglobulinemia	44	0.090

240		ESP021	Esophageal Cancer	90	0.089

241		THR024	Thrombosis	57	0.089

242		AST005	Asthma	76	0.088

243	P	TRM003	Tremor	54	0.088

244	P	LCT001	Lactic Acidosis	51	0.088

245	P	INF037	Inflammatory Bowel Disease	54	0.088

246		PRS021	Prostatic Adenoma	51	0.088

247		CRD132	Cardiac Conduction Defect	58	0.087

248		PRT029	Parathyroid Adenoma	50	0.087

249	P	PSR002	Psoriasis	62	0.087

250		PRS045	Prostatic Hypertrophy	53	0.087

251	c	NRF023	Neurofibromatosis, Type Ii	80	0.086

252		PRS129	Prostatic Hyperplasia, Benign	49	0.086

253	P	PNM007	Pneumonia	68	0.086

254		ATR057	Atrioventricular Block	55	0.085

255		PRP027	Peripheral Vascular Disease	71	0.085

256	P	PRM002	Primary Hyperoxaluria	62	0.085

257		SXL003	Sexual Disorder	47	0.085

258	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.085

259		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.084

260	P	EXN002	Exanthem	57	0.084

261	P	INS002	in Situ Carcinoma	53	0.084

262		DRM006	Dermatitis	61	0.084

263	c	XNT010	Xanthinuria, Type I	53	0.083

264	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.083

265	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.083

266		GST092	Gastroesophageal Reflux	67	0.083

267	c	SYS001	Systemic Lupus Erythematosus	86	0.083

268		MMM001	Mammary Paget's Disease	53	0.083

269		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.082

270		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.082

271		SKN016	Skin Disease	63	0.082

272		PST011	Pustulosis of Palm and Sole	52	0.082

273		SYN007	Synovitis	54	0.082

274		PLC002	Plica Syndrome	36	0.082

275	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.082

276	c	SML038	Small Cell Cancer of the Lung	65	0.082

277	P	CNR004	Cone-Rod Dystrophy 2	73	0.082

278	c	SCL052	Scleroderma, Familial Progressive	61	0.081

279	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.081

280		LYM133	Lymphoma, Hodgkin, Classic	69	0.081

281	P	MYL006	Myeloid Leukemia	60	0.081

282	P	MLN008	Melanoma	69	0.081

283		CRB004	Cerebral Artery Occlusion	45	0.080

284		ACR007	Acromegaly	71	0.080

285	P	ALP008	Alopecia	54	0.080

286	c	LKM061	Leukemia, Acute Myeloid	84	0.080

287		GST023	Gastric Ulcer	53	0.079

288		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.079

289		END057	Endometrial Cancer	74	0.079

290		BRN056	Bronchopulmonary Dysplasia	57	0.079

291		MLR004	Malaria	81	0.078

292		PLM010	Pulmonary Edema	54	0.078

293	c	ATS007	Autism Spectrum Disorder	67	0.078

294	P	RSP003	Respiratory Failure	74	0.078

295	c	DRR009	Diarrhea 6	46	0.078

296	P	BLD134	Bladder Cancer	79	0.077

297		ALL003	Allergic Rhinitis	67	0.077

298	P	THL005	Thalassemia	60	0.077

299		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.077

300	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.077

301		OCL069	Ocular Motor Apraxia	51	0.076

302	P	EPL164	Epilepsy	71	0.076

303		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.076

304		SRC014	Sarcoma	65	0.076

305		SPN035	Spindle Cell Sarcoma	53	0.076

306		MSC007	Muscle Hypertrophy	64	0.076

307	P	DMN002	Dementia	66	0.076

308	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.075

309		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.075

310		BRN024	Bronchitis	68	0.075

311		PPL001	Papillary Adenoma	44	0.075

312	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	46	0.075

313		LPT014	Leptin Deficiency or Dysfunction	74	0.075

314		MDD011	Mood Disorder	62	0.075

315		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.075

316		AZS001	Azoospermia	50	0.075

317	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.075

318		CRH001	Crohn's Disease	74	0.075

319		HYP014	Hyperuricemia	52	0.075

320	P	TXP001	Toxoplasmosis	60	0.075

321		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.074

322		GTR002	Goiter	53	0.074

323	P	SCK005	Sickle Cell Disease	50	0.074

324	P	MJR001	Major Depressive Disorder	68	0.074

325		ANR040	Aneurysm	59	0.074

326		CNN005	Connective Tissue Disease	68	0.074

327		THY111	Thyroid Carcinoma, Familial Medullary	67	0.074

328		BCT022	Bacterial Infectious Disease	56	0.073

329		CLT003	Colitis	62	0.073

330		ECT026	Ectopic Pregnancy	50	0.073

331		APN006	Apnea of Prematurity	24	0.073

332	P	RNL015	Renal Hypertension	47	0.073

333	P	LPS004	Lupus Erythematosus	61	0.073

334	P	GLM040	Glioma Susceptibility 1	81	0.073

335		49X006	49, Xxxxy Syndrome	41	0.072

336		MYC005	Myocardial Stunning	46	0.072

337		PLM001	Pulmonary Tuberculosis	69	0.072

338		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.072

339		PLM033	Pulmonary Embolism	59	0.072

340	c	BRN108	Branchiootic Syndrome 1	62	0.072

341		THY125	Thyroid Gland Medullary Carcinoma	50	0.072

342		MCS002	Mucositis	56	0.072

343	c	LKM005	Leukemia, T-Cell, Chronic	34	0.072

344		BRS099	Breast Ductal Carcinoma	62	0.071

345	P	OCY003	Oocyte Maturation Defect 1	45	0.071

346		ENT011	Enterocolitis	51	0.071

347		CLN045	Colonic Benign Neoplasm	46	0.071

348	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.071

349	c	MLG068	Malignant Glioma	46	0.071

350	P	ATS364	Autism	70	0.071

351	P	SYS005	Systemic Scleroderma	68	0.071

352	P	SCL018	Scoliosis	60	0.071

353	P	OVR049	Ovarian Disease	52	0.070

354		PNC129	Pancreatic Adenocarcinoma	68	0.070

355		TRN015	Transient Cerebral Ischemia	63	0.070

356	P	PYL005	Pyelonephritis	56	0.070

357		SCK003	Sickle Cell Anemia	74	0.070

358	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.070

359	P	CYS039	Cystic Kidney Disease	54	0.070

360		DBT010	Diabetic Neuropathy	54	0.070

361	P	GLM007	Glomerulonephritis	57	0.070

362	P	AMY004	Amyloidosis	70	0.070

363		FCT007	Factor Vii Deficiency	67	0.070

364		ILS001	Ileus	51	0.070

365	P	PRK057	Parkinson Disease, Late-Onset	78	0.069

366		CNT033	Central Nervous System Cancer	47	0.069

367		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.069

368	P	NPH012	Nephrotic Syndrome	60	0.069

369	P	LCT002	Lactose Intolerance	53	0.069

370		GST050	Gastrointestinal System Disease	56	0.069

371	P	PRC031	Preeclampsia/eclampsia 1	38	0.068

372	P	HYP750	Hypertriglyceridemia, Familial	62	0.068

373	P	PLM036	Pulmonary Fibrosis	65	0.068

374		OVR094	Ovarian Epithelial Cancer	38	0.068

375	P	MLT020	Multiple Sclerosis	72	0.068

376	c	ACT073	Acute Leukemia	58	0.068

377	c	PCH010	Pachyonychia Congenita 3	44	0.068

378		BRN028	Brain Cancer	74	0.068

379		HYD002	Hydronephrosis	60	0.068

380		MST005	Mastitis	53	0.067

381	P	HYP265	Hypotonia	43	0.067

382		DNT006	Dental Pulp Necrosis	41	0.067

383	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.067

384	c	ACT134	Acute Liver Failure	56	0.067

385		PLC008	Placenta Disease	50	0.067

386	P	HYP730	Hypogonadotropic Hypogonadism	52	0.067

387		HPR003	Heparin-Induced Thrombocytopenia	48	0.067

388		SFT003	Soft Tissue Sarcoma	56	0.067

389		PHS001	Phosphorus Metabolism Disease	40	0.067

390		GST033	Gestational Diabetes	61	0.067

391	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.067

392	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.066

393		NRL016	Neural Tube Defects	82	0.066

394		GNG013	Gingivitis	59	0.066

395		HRT015	Heritable Pulmonary Arterial Hypertension	44	0.066

396		CRB037	Cerebral Palsy	69	0.066

397	P	MSC003	Muscular Atrophy	52	0.066

398	P	OPT006	Optic Nerve Disease	60	0.066

399	c	SVR005	Severe Pre-Eclampsia	50	0.066

400	c	HMC039	Hemochromatosis, Type 1	74	0.066

401	P	DRM053	Dermatitis, Atopic	66	0.066

402		DCT002	Ductal Carcinoma in Situ	59	0.066

403		CHL068	Cholestasis	61	0.066

404		OST003	Osteonecrosis	61	0.066

405	c	HYP864	Hypoparathyroidism, Familial Isolated, 1	48	0.065

406		SQM006	Squamous Cell Carcinoma	60	0.065

407		URN010	Urinary Tract Obstruction	55	0.065

408		BCK006	Back Pain	42	0.065

409		ART016	Aortic Aneurysm	69	0.065

410		PRT010	Parathyroid Carcinoma	67	0.065

411	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.065

412	P	MYC008	Myocarditis	59	0.065

413		STM007	Stomatitis	50	0.064

414		ULC004	Ulcerative Colitis	73	0.064

415		SBC016	Subacute Delirium	44	0.064

416		PRT013	Portal Hypertension	59	0.064

417	P	ALC033	Alcohol Use Disorder	58	0.064

418	c	INF145	Infantile Liver Failure Syndrome 1	50	0.064

419	P	LNG028	Long Qt Syndrome	66	0.064

420	P	ESP024	Esophagitis	62	0.064

421	P	CYS018	Cystitis	59	0.064

422	P	MLG074	Malignant Mesenchymoma	40	0.064

423	c	MCR129	Microvascular Complications of Diabetes 1	66	0.064

424	c	LKM063	Leukemia, Chronic Myeloid	72	0.064

425		PRT036	Peritonitis	64	0.063

426		BRK010	Burkitt Lymphoma	67	0.063

427		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.063

428		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.063

429	P	SCH015	Schizophrenia	74	0.063

430		GST045	Gastroenteritis	59	0.063

431		RDN001	Reading Disorder	40	0.063

432	c	FML021	Familial Hypercholesterolemia	66	0.062

433		SCN001	Secondary Hyperparathyroidism of Renal Origin	27	0.062

434		LWC001	Low Compliance Bladder	43	0.062

435	P	GRF003	Graft-Versus-Host Disease	72	0.062

436		SYN036	Syncope	45	0.062

437		WTH001	Withdrawal Disorder	48	0.062

438		PRN019	Perinatal Necrotizing Enterocolitis	59	0.062

439	P	URT039	Urticaria	58	0.062

440		TRP009	Triple X Syndrome	42	0.062

441		TND005	Tendinitis	54	0.061

442		CMR002	Coumarin Resistance	56	0.061

443	P	TMP001	Temporal Lobe Epilepsy	50	0.061

444	P	SLP006	Sleep Apnea	69	0.061

445	P	MYS005	Myositis	56	0.061

446		OLG001	Oligospermia	45	0.061

447	P	BCT020	Bacteremia 2	44	0.061

448		HYP784	Hypogonadism, Male	40	0.061

449		MYL009	Myelodysplastic Syndrome	70	0.061

450		ENT004	Enthesopathy	49	0.061

451		MNT001	Mantle Cell Lymphoma	69	0.061

452	P	KDN017	Kidney Cancer	60	0.061

453		HPT004	Hepatic Coma	45	0.061

454		GST020	Gastric Antral Vascular Ectasia	41	0.061

455		ACR041	Acromelic Frontonasal Dysostosis	52	0.061

456	P	ADL017	Adult T-Cell Leukemia	56	0.060

457		ANR007	Anorexia Nervosa	63	0.060

458		TXC002	Toxic Encephalopathy	53	0.060

459		GST040	Gastric Adenocarcinoma	70	0.060

460	P	BRS044	Breast Adenocarcinoma	59	0.060

461		SPS057	Spasticity	45	0.060

462	P	DRM010	Dermatomyositis	61	0.060

463		SCH014	Schistosomiasis	57	0.060

464		ERY051	Erythroleukemia, Familial	56	0.060

465		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.060

466	P	SYP003	Syphilis	58	0.060

467	c	GRV008	Graves Disease 1	56	0.059

468	c	DBT099	Diabetes Mellitus, Type I	65	0.059

469	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.059

470		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.059

471	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	0.059

472		END040	Endogenous Depression	55	0.059

473		LNG031	Lung Benign Neoplasm	51	0.059

474		MDL009	Medullary Sponge Kidney	40	0.059

475		RTN023	Retinitis	46	0.059

476		NRR001	Neuroretinitis	42	0.059

477		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.059

478		BRR014	Barrett Esophagus	65	0.059

479		BRT054	Brittle Bone Disorder	72	0.059

480	P	MYS003	Myasthenia Gravis	68	0.059

481	P	RTN016	Retinal Degeneration	53	0.059

482		MXD026	Mixed Glioma	45	0.059

483		HPT019	Hepatic Encephalopathy	60	0.058

484	P	PLY019	Polyneuropathy	56	0.058

485		PPL049	Papillon-Lefevre Syndrome	65	0.058

486		PRS047	Prostatitis	56	0.058

487		CYT018	Cytochrome P450 2d6 Variant	27	0.058

488	c	HPT016	Hepatitis B	59	0.058

489	P	FBR017	Fibrosarcoma	56	0.058

490	P	HRP006	Herpes Simplex	65	0.058

491		CLC001	Calciphylaxis	51	0.058

492	c	BRS049	Breast Carcinoma in Situ	51	0.058

493	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.058

494		SPT004	Septic Arthritis	58	0.058

495	c	ART101	Aortic Valve Disease 2	65	0.057

496		CHL004	Cholelithiasis	49	0.057

497		OLG003	Oligohydramnios	51	0.057

498		PRT058	Pure Autonomic Failure	59	0.057

499	P	THY032	Thyroiditis	52	0.057

500	c	FML001	Familial Atrial Fibrillation	65	0.057

501	P	DYS154	Dystonia	65	0.057

502	P	ADL010	Adult Respiratory Distress Syndrome	65	0.057

503		PLC007	Placental Abruption	48	0.057

504		INT067	Interstitial Nephritis	48	0.057

505	P	PTN014	Patent Ductus Arteriosus 1	60	0.057

506		EYD002	Eye Disease	58	0.057

507		DSS009	Disseminated Intravascular Coagulation	57	0.057

508		HRT012	Heart Valve Disease	53	0.057

509	P	PNC025	Panic Disorder	53	0.057

510	P	LNG064	Lung Cancer Susceptibility 3	78	0.057

511	c	FML035	Familial Hyperlipidemia	55	0.056

512		PLS025	Plasmablastic Lymphoma	47	0.056

513	c	MCR112	Microvascular Complications of Diabetes 2	41	0.056

514		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.056

515		ASC001	Ascaridiasis	35	0.056

516	P	MYT002	Myotonic Dystrophy	49	0.056

517		NNL006	Non-Alcoholic Steatohepatitis	54	0.056

518	P	MTR014	Motor Neuron Disease	65	0.056

519		PST092	Posttransplant Acute Limbic Encephalitis	29	0.056

520		APP009	Appendix Adenocarcinoma	44	0.056

521		FBR047	Fibromyalgia	58	0.056

522		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.056

523		ADR056	Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete	56	0.055

524		SPS003	Spastic Diplegia	51	0.055

525		URN009	Urinary System Disease	48	0.055

526		LWR018	Lower Urinary Tract Obstruction, Congenital	40	0.055

527		DGR001	Digeorge Syndrome	64	0.055

528		DYS015	Dysentery	52	0.055

529		CYS013	Cystinuria	63	0.055

530		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.055

531		BLR008	Bilirubin Metabolic Disorder	57	0.055

532		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.055

533	P	RTN018	Retinal Disease	53	0.055

534		ACT003	Acute Kidney Tubular Necrosis	45	0.055

535		ASC010	Ascaris Lumbricoides Infection	50	0.055

536	P	OVR046	Ovarian Cyst	47	0.055

537	c	PNC108	Pancreatitis, Hereditary	70	0.055

538	P	THY023	Thymoma	65	0.055

539		CHL067	Cholecystitis	57	0.055

540	c	THY107	Thymoma, Familial	52	0.055

541		VTM033	Vitamin K Deficiency Bleeding	48	0.055

542	c	BTT014	Beta-Thalassemia	74	0.055

543	P	MNC007	Monocytic Leukemia	53	0.055

544		HMT002	Hematologic Cancer	62	0.055

545		NRM005	Neuromuscular Disease	64	0.054

546	c	HYP794	Hyperoxaluria, Primary, Type I	63	0.054

547		GNG003	Gingival Recession	44	0.054

548		ETH012	Ethylene Glycol Poisoning	26	0.054

549	c	SVR001	Severe Acute Respiratory Syndrome	62	0.054

550		SYS003	Systolic Heart Failure	49	0.054

551		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.054

552	P	MTC069	Mitochondrial Disorders	56	0.054

553		OPT003	Opiate Dependence	50	0.054

554		CVD001	Covid-19	44	0.054

555		HYP815	Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome	53	0.054

556	P	RTN008	Retinitis Pigmentosa	79	0.054

557		RYN001	Raynaud Disease	48	0.054

558		KRT002	Keratomalacia	47	0.054

559		KPS004	Kaposi Sarcoma	75	0.054

560	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.054

561	P	END033	Endocarditis	57	0.054

562		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.054

563	P	MYC033	Myoclonus	46	0.054

564		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.054

565		RST023	Resting Heart Rate, Variation in	41	0.054

566		GYN001	Gynecomastia	49	0.054

567		INF021	Infant Gynecomastia	31	0.054

568	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.054

569		PTH003	Pathologic Nystagmus	52	0.054

570	c	EXD008	Exudative Vitreoretinopathy 1	71	0.054

571	P	URF003	Urofacial Syndrome 1	57	0.054

572		MCR004	Macroglobulinemia	49	0.054

573	P	CND004	Candidiasis	58	0.053

574	c	OVR114	Ovarian Cancer 1	38	0.053

575	P	NRV007	Nervous System Disease	66	0.053

576	P	HMP007	Hemophilia	51	0.053

577		CNN003	Conn's Syndrome	79	0.053

578		THY122	Thyroid Gland Cancer	57	0.053

579	P	MJR007	Major Affective Disorder 1	43	0.053

580		PRS063	Paresthesia	41	0.052

581	P	DNT007	Dentin Sensitivity	36	0.052

582		PSY004	Psychotic Disorder	67	0.052

583		KRT019	Keratitis, Hereditary	65	0.052

584		MRG003	Marginal Zone B-Cell Lymphoma	52	0.052

585	P	PGT001	Paget's Disease of Bone	58	0.052

586	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.052

587		HRT011	Heart Septal Defect	50	0.052

588		BWN001	Bowen-Conradi Syndrome	52	0.052

589		KHL003	Kohlschutter-Tonz Syndrome	65	0.052

590		RTN020	Retinal Vascular Disease	46	0.052

591		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.051

592	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.051

593		PST028	Post-Traumatic Stress Disorder	58	0.051

594		NRT001	Neurotic Disorder	53	0.051

595	c	INH020	Inherited Metabolic Disorder	47	0.051

596	c	MCL013	Mucolipidosis Iv	66	0.051

597		HLL004	Hellp Syndrome	54	0.051

598	P	BNG032	Benign Mesothelioma	46	0.051

599		FLL027	Fallopian Tube Carcinoma	67	0.051

600		GLS001	Gliosarcoma	54	0.051

601		BCT004	Bacteriuria	49	0.051

602		BRN004	Brain Edema	56	0.051

603		MLG086	Malignant Hyperthermia Susceptibility	39	0.051

604		CRV035	Cervical Cancer	76	0.051

605	P	SLP005	Sleep Disorder	59	0.051

606		PRP030	Purpura	54	0.051

607		RNL077	Renal Fibrosis	47	0.051

608		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.050

609	c	MNN043	Meningioma, Familial	74	0.050

610		MNN042	Meningioma, Radiation-Induced	62	0.050

611		VRC005	Varicose Veins	60	0.050

612	P	MGR003	Migraine with Aura	52	0.050

613		SPN021	Spinal Meningioma	50	0.050

614		DST006	Diastolic Heart Failure	45	0.050

615		SCR001	Secretory Meningioma	41	0.050

616		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.050

617	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	0.050

618		SKN019	Skin Melanoma	68	0.050

619	P	HPT021	Hepatitis	67	0.050

620	P	HYD006	Hydrocephalus	66	0.050

621	P	SJG008	Sjogren Syndrome	61	0.050

622		HMR039	Hemorrhage, Intracerebral	57	0.050

623		PRT038	Protein-Energy Malnutrition	54	0.050

624	P	MNN013	Meningitis	66	0.050

625	P	INT143	Interstitial Cystitis	61	0.050

626	P	ACT105	Acute Mountain Sickness	52	0.050

627		HYP781	Hypoascorbemia	51	0.050

628		WLD007	Waldenstroem's Macroglobulinemia	61	0.050

629	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.050

630	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.050

631		TYP007	Typhoid Fever	63	0.050

632	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	0.050

633		MCN017	Meconium Ileus	52	0.050

634	P	BRN035	Brain Stem Glioma	52	0.050

635		ASP004	Asphyxia Neonatorum	46	0.049

636	P	ASP006	Aspergillosis	69	0.049

637	P	LMB006	Limb-Girdle Muscular Dystrophy	53	0.049

638		CYS014	Cystadenocarcinoma	51	0.049

639	P	FNC004	Fanconi Syndrome	50	0.049

640		KRT008	Keratopathy	47	0.049

641	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.049

642		FRZ001	Frozen Shoulder	53	0.049

643		PRP007	Priapism	47	0.049

644	P	VNT002	Ventricular Septal Defect	60	0.049

645		GRD007	Grade Iii Astrocytoma	59	0.049

646		NWB001	Newborn Respiratory Distress Syndrome	58	0.049

647		PLC005	Placental Insufficiency	57	0.049

648	P	ACT010	Acth-Secreting Pituitary Adenoma	55	0.049

649		ENT001	Enterocele	39	0.049

650		MLT157	Multiple System Atrophy 1	70	0.049

651		THY030	Thyroid Gland Disease	52	0.048

652		DYS073	Dysphagia	50	0.048

653	c	HPT073	Hepatitis C Virus	72	0.048

654	c	INF071	Inflammatory Bowel Disease 1	67	0.048

655	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.048

656		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.048

657	P	HML002	Hemolytic Anemia	63	0.048

658	P	MVM001	Movement Disease	63	0.048

659		DPH001	Diphtheria	60	0.048

660	P	INT068	Intestinal Disease	53	0.048

661		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.048

662	P	MDL005	Medulloblastoma	77	0.048

663	P	PTT006	Pituitary Adenoma	55	0.048

664		ONC002	Onchocerciasis	52	0.048

665		LYM012	Lymphoplasmacytic Lymphoma	47	0.048

666		PLM031	Poliomyelitis	64	0.048

667		CHR074	Choriocarcinoma	47	0.048

668	P	ALP009	Alopecia Areata	60	0.047

669		VRC001	Varicocele	49	0.047

670		PRM003	Premature Ejaculation	44	0.047

671		CNT060	Central Serous Chorioretinopathy	38	0.047

672	P	FLL037	Follicular Lymphoma	67	0.047

673	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.047

674		VRL011	Viral Infectious Disease	61	0.047

675		CHR100	Chronic Ulcer of Skin	55	0.047

676	c	FLL041	Follicular Lymphoma 1	49	0.047

677		PRC013	Pericarditis	54	0.047

678		ASP008	Aspiration Pneumonitis	45	0.047

679		PPT001	Peptic Esophagitis	52	0.047

680		PRV004	Periventricular Leukomalacia	52	0.047

681		ACR008	Acrocallosal Syndrome	69	0.047

682		MYL031	Myeloproliferative Neoplasm	66	0.047

683		CHL123	Chlamydia	59	0.047

684	P	GLL022	Guillain-Barre Syndrome	59	0.047

685	P	UVT001	Uveitis	57	0.047

686		LRN003	Learning Disability	49	0.047

687		RTC005	Reticulosarcoma	47	0.047

688		ATN004	Autonomic Neuropathy	45	0.047

689		BNM001	Bone Marrow Cancer	43	0.047

690	c	CHR064	Chronic Monocytic Leukemia	33	0.047

691	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.047

692	c	BNG091	Benign Chronic Pemphigus	58	0.047

693	P	VNS003	Venous Insufficiency	55	0.047

694		GST037	Gastroparesis	54	0.047

695		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.047

696		GNT002	Giant Cell Glioblastoma	50	0.047

697	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.047

698		INT053	Intracranial Vasospasm	24	0.047

699		SLC024	Slc4a1-Associated Distal Renal Tubular Acidosis	19	0.047

700		NRN004	Neuroendocrine Tumor	55	0.047

701		HMC014	Homocysteinemia	53	0.047

702		BRS064	Bursitis	48	0.047

703		CHR178	Chromosomal Triplication	35	0.047

704		MYL005	Myelofibrosis	70	0.046

705	P	HYP098	Hypereosinophilic Syndrome	67	0.046

706		PPL022	Papilloma	54	0.046

707		GST049	Gastrointestinal System Cancer	49	0.046

708		GST071	Gastrointestinal Carcinoma	47	0.046

709		SQM002	Squamous Cell Papilloma	46	0.046

710	c	AGR019	Age-Related Hearing Loss	42	0.046

711	P	RTN024	Retinoblastoma	73	0.046

712	P	PMP001	Pemphigus	54	0.046

713		ADR007	Adrenoleukodystrophy	75	0.046

714		APN008	Apnea, Obstructive Sleep	64	0.046

715	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.046

716		ATN011	Autoinflammation with Infantile Enterocolitis	44	0.046

717		PRT035	Peritoneum Cancer	44	0.046

718	c	SPR086	Spermatogenic Failure 3	44	0.046

719	P	OCL013	Oculodentodigital Dysplasia	69	0.046

720	P	PLY018	Polycythemia	56	0.046

721		INT030	Intracranial Aneurysm	56	0.046

722	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.046

723		ANT024	Anthrax Disease	58	0.046

724	P	BNC003	Bone Cancer	58	0.046

725		LMB062	Limb Ischemia	55	0.046

726	P	SML001	Small Cell Carcinoma	52	0.046

727		CCN002	Cocaine Abuse	49	0.046

728		THR035	Thrombasthenia	40	0.046

729		MGC001	Megacolon	46	0.045

730		OPD001	Opioid Abuse	46	0.045

731		GST010	Gestational Trophoblastic Neoplasm	46	0.045

732		TRD006	Tardive Dyskinesia	54	0.045

733	c	FML008	Familial Retinoblastoma	53	0.045

734	c	HPT001	Hepatitis C	62	0.045

735	P	MTR012	Mitral Valve Disease	58	0.045

736		ATS010	Autosomal Recessive Disease	48	0.045

737		HRN029	Hearing Loss, Noise-Induced	37	0.045

738		PRP001	Propionic Acidemia	65	0.045

739		HMG005	Hemoglobinopathy	56	0.045

740	c	PYR010	Peyronie's Disease	50	0.045

741		ASP007	Aspiration Pneumonia	48	0.045

742		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.045

743		CRP001	Carpal Tunnel Syndrome	67	0.045

744	P	PRM006	Primary Biliary Cirrhosis	62	0.045

745	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.045

746	P	MYP006	Myopia	55	0.045

747		GRW007	Growth Hormone Deficiency	46	0.045

748		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.045

749	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.045

750		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.044

751	P	INT070	Intestinal Obstruction	58	0.044

752		HMT008	Hematuria, Benign Familial	56	0.044

753	P	DBT005	Diabetes Insipidus	55	0.044

754		HMP005	Hemiplegia	55	0.044

755		LPT006	Leptin Receptor Deficiency	48	0.044

756		OPD006	Opioid Addiction	48	0.044

757	P	VSC011	Vasculitis	62	0.044

758		CRT013	Carotid Stenosis	50	0.044

759		GST019	Gastrointestinal Stromal Tumor	78	0.044

760		PNM008	Pneumothorax	56	0.044

761		PLS011	Plasmacytoma	56	0.044

762		CYN002	Cyanosis, Transient Neonatal	45	0.044

763	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.044

764		DFF003	Diffuse Scleroderma	41	0.044

765		MSC152	Muscular Dystrophy, Becker Type	63	0.044

766	c	ALP101	Alpha-Thalassemia	62	0.044

767		ING001	Inguinal Hernia	60	0.044

768		ETN001	Eating Disorder	60	0.044

769		INC002	Inclusion Body Myositis	58	0.044

770	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.044

771		PRD004	Prediabetes Syndrome	47	0.044

772		URT014	Ureterolithiasis	44	0.044

773	c	SRC023	Sarcoidosis 2	43	0.044

774		HML018	Homologous Wasting Disease	22	0.044

775		PSR001	Psoriatic Arthritis	61	0.043

776	c	JVN061	Juvenile Arthritis	60	0.043

777		RDC002	Radiculopathy	50	0.043

778		CRB086	Cerebral Aneurysms	40	0.043

779		MTH071	Methane Production	26	0.043

780		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.043

781		MCN001	Mucinous Adenocarcinoma	49	0.043

782	c	HYP057	Hypervitaminosis D	42	0.043

783	c	RNL046	Renal Tubular Acidosis, Distal, Autosomal Dominant	37	0.043

784	c	MJR008	Major Affective Disorder 2	35	0.043

785	c	MJR023	Major Affective Disorder 7	33	0.043

786	c	MJR003	Major Affective Disorder 6	33	0.043

787	c	MJR006	Major Affective Disorder 5	33	0.043

788	c	MJR004	Major Affective Disorder 4	28	0.043

789		ORG002	Organic Acidemia	44	0.043

790		TXC001	Toxic Megacolon	38	0.043

791		MLG164	Malignant Epithelial Tumor of Ovary	26	0.043

792		ACT119	Acute Promyelocytic Leukemia	63	0.043

793	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.043

794	c	MST023	Mesothelioma, Malignant	57	0.043

795		CMM005	Common Cold	57	0.043

796	P	PLM034	Pulmonary Emphysema	55	0.043

797		FNG017	Fungal Infectious Disease	53	0.043

798		NPH018	Nephrogenic Systemic Fibrosis	50	0.043

799		DRY001	Dry Eye Syndrome	47	0.043

800		GRM010	Germ Cells Tumors	34	0.043

801	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.043

802		SNG003	Single Ventricular Heart	30	0.043

803		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.043

804		OTT002	Otitis Media	72	0.043

805	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.043

806	c	ACT135	Acute Graft Versus Host Disease	52	0.043

807	P	SPP010	Suppressor of Tumorigenicity 3	51	0.043

808		CNT017	Central Nervous System Origin Vertigo	45	0.043

809	P	DNT020	Dent Disease 1	62	0.042

810	P	OLG002	Oligodendroglioma	67	0.042

811	P	BNG030	Benign Ependymoma	60	0.042

812		AYM001	Ayme-Gripp Syndrome	57	0.042

813		CLL010	Cellular Ependymoma	54	0.042

814	c	TRC022	Tricuspid Valve Insufficiency	45	0.042

815	c	HMP004	Hemophilia B	68	0.042

816		MSL001	Measles	62	0.042

817	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	60	0.042

818		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.042

819	P	CLS010	Cluster Headache	42	0.042

820		CRN288	Corneal Dystrophy, Band-Shaped	38	0.042

821		PLG002	Plague	63	0.041

822		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.041

823		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.041

824	c	MTR002	Mitral Valve Insufficiency	48	0.041

825	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.041

826		MYC006	Mycosis Fungoides	66	0.041

827	c	DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.041

828		ART002	Arts Syndrome	64	0.041

829		SZR001	Sezary's Disease	60	0.041

830		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.041

831		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.041

832	P	THR015	Thrombophilia	51	0.041

833		RFR010	Refractory Anemia	48	0.041

834		VTM002	Vitamin B12 Deficiency	48	0.041

835		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	0.041

836		GLN010	Glanzmann Thrombasthenia	66	0.041

837		INT066	Interstitial Lung Disease	60	0.041

838		DFF005	Diffuse Large B-Cell Lymphoma	55	0.041

839		INT075	Intracranial Hypertension	53	0.041

840		BHR001	Behr Syndrome	51	0.041

841		PRP017	Periapical Periodontitis	46	0.041

842	P	CNJ013	Conjunctivitis	65	0.041

843		PTT048	Pituitary Adenoma, Prolactin-Secreting	65	0.041

844		MNR012	Meniere Disease	57	0.041

845		GNR004	Generalized Anxiety Disorder	56	0.041

846		HRY003	Hairy Cell Leukemia	55	0.041

847	c	CNT035	Central Nervous System Disease	52	0.041

848		LMY002	Leiomyoma	52	0.041

849		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.041

850		SPL004	Splenic Marginal Zone Lymphoma	51	0.041

851	P	MGR001	Migraine Without Aura	49	0.041

852		HST010	Histiocytosis	48	0.041

853		SPL018	Splenomegaly	48	0.041

854		ANT018	Anthracosis	48	0.041

855		KRT013	Keratolytic Winter Erythema	46	0.041

856		MYF001	Myofibroma	45	0.041

857		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.041

858	P	VNW001	Von Willebrand's Disease	65	0.041

859	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.041

860	P	END084	Endocrine System Disease	45	0.041

861	P	PRG002	Progesterone-Receptor Positive Breast Cancer	35	0.041

862		BRS051	Breast Disease	58	0.040

863		EMB004	Embryonal Carcinoma	56	0.040

864		SPN051	Spondylitis	51	0.040

865		URT010	Ureteral Obstruction	45	0.040

866		GRN017	Granulocytopenia	44	0.040

867	c	LCL006	Localized Scleroderma	62	0.040

868		BRN002	Bronchiolitis	59	0.040

869		JVN009	Juvenile Pilocytic Astrocytoma	55	0.040

870		DFF035	Diffuse Cutaneous Systemic Sclerosis	49	0.040

871		LMT001	Limited Scleroderma	47	0.040

872		SMN007	Seminoma	43	0.040

873	P	INF038	Influenza	68	0.040

874	P	RHB003	Rhabdomyosarcoma	63	0.040

875	P	GLY013	Glycogen Storage Disease	60	0.040

876	P	SBS003	Substance Abuse	55	0.040

877	P	SLM003	Salmonellosis	55	0.040

878		CRT017	Cartilage Disease	54	0.040

879		LYS002	Lysosomal Storage Disease	52	0.040

880		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.040

881	P	HYP040	Hypospadias	51	0.040

882	P	TTR001	Tetralogy of Fallot	70	0.040

883	P	ESS003	Essential Thrombocythemia	68	0.040

884		CNT061	Conotruncal Heart Malformations	63	0.040

885	P	MLN069	Melanoma, Uveal	59	0.040

886		CMP010	Complex Regional Pain Syndrome	58	0.040

887		NTR018	Neutrophilia, Hereditary	52	0.040

888		LNG015	Lingual-Facial-Buccal Dyskinesia	50	0.040

889		BLD053	Blood Platelet Disease	49	0.040

890		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.040

891		SRT004	Serotonin Syndrome	47	0.040

892		IDP033	Idiopathic Edema	44	0.040

893		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.040

894		NPH078	Nephrolithiasis, Uric Acid	41	0.040

895		PST053	Postherpetic Neuralgia	40	0.040

896		VRS002	Virus-Associated Trichodysplasia Spinulosa	32	0.040

897		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.040

898		PNM010	Pneumothorax, Primary Spontaneous	60	0.040

899	c	LKM070	Leukemia, Acute Monocytic	57	0.040

900		VLC001	Velocardiofacial Syndrome	54	0.040

901	P	HMR003	Hemorrhagic Disease	53	0.040

902		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	0.040

903		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.040

904		PRL017	Prolymphocytic Leukemia	47	0.040

905	c	OPT050	Opitz Gbbb Syndrome, Type Ii	47	0.040

906		ANP006	Anaplastic Ependymoma	46	0.040

907	c	MLG064	Malignant Ependymoma	41	0.040

908		DBT002	Diabetic Autonomic Neuropathy	41	0.040

909		RSP007	Respiratory Distress Syndrome, Infant	30	0.040

910		INF009	Inflammatory Spondylopathy	31	0.039

911		APL002	Aplasia of Lacrimal and Salivary Glands	57	0.039

912		MTH009	Mouth Disease	56	0.039

913		THR004	Thrombocytosis	51	0.039

914		PST021	Postpartum Depression	50	0.039

915		DMP001	Dumping Syndrome	44	0.039

916		URM005	Uremic Pruritus	42	0.039

917	P	MYC084	Mycobacterium Tuberculosis 1	68	0.038

918		DRG003	Drug Dependence	47	0.038

919		DNT001	Dental Fluorosis	43	0.038

920		ARG004	Argyria	27	0.038

921		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.038

922		PLY001	Polycythemia Vera	69	0.038

923		MST024	Mastocytosis, Cutaneous	69	0.038

924	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.038

925	c	HMP029	Hemophilia a	67	0.038

926		MGK001	Megakaryocytic Leukemia	64	0.038

927	P	DST002	Distal Arthrogryposis	63	0.038

928	P	PTT014	Pitt-Hopkins Syndrome	63	0.038

929	c	ART144	Arthrogryposis, Distal, Type 1a	61	0.038

930		PTN001	Patent Foramen Ovale	60	0.038

931		MXD005	Mixed Connective Tissue Disease	58	0.038

932	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.038

933		LBL001	Lobular Neoplasia	56	0.038

934		RFL001	Reflex Sympathetic Dystrophy	54	0.038

935		PLM012	Pulmonary Sarcoidosis	53	0.038

936		ALK024	Alkuraya-Kucinskas Syndrome	51	0.038

937	P	CHL066	Cholangitis	51	0.038

938		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.038

939		MNC019	Monocarboxylate Transporter 1 Deficiency	47	0.038

940		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.038

941		MCC013	Mucocutaneous Ulceration, Chronic	39	0.038

942	c	SYS043	Systemic Lupus Erythematosus 1	38	0.038

943	P	HYP120	Hypoaldosteronism	36	0.038

944		MSC012	Muscular Dystrophy, Duchenne and Becker Type	34	0.038

945		CNG506	Congenital Amyoplasia	27	0.038

946	P	APL001	Aplastic Anemia	74	0.038

947		PRM126	Primary Peritoneal Carcinoma	62	0.038

948		HYD038	Hydrops Fetalis, Nonimmune	62	0.038

949		ORL005	Oral Candidiasis	56	0.038

950		SLC006	Silicosis	56	0.038

951		KRT006	Keratoconjunctivitis	53	0.038

952		IRD001	Iridocyclitis	53	0.038

953		FBR008	Fibrillary Astrocytoma	51	0.038

954		KRT001	Keratoconjunctivitis Sicca	49	0.038

955		SBP004	Subependymoma	46	0.038

956		MYX001	Myxopapillary Ependymoma	46	0.038

957	c	EST002	Estrogen-Receptor Negative Breast Cancer	45	0.038

958		ANP009	Anaplastic Oligodendroglioma	43	0.038

959		HYP344	Hyperthyroidism, Familial Gestational	39	0.038

960	c	PLM022	Pulmonary Valve Insufficiency	39	0.038

961		PSD088	Pseudobulbar Affect	36	0.038

962	c	ADL008	Adult Oligodendroglioma	34	0.038

963		CHL057	Childhood Brain Stem Glioma	32	0.038

964	c	ADL054	Adult Brain Stem Glioma	30	0.038

965	c	MLG023	Malignant Adult Ependymoma	15	0.038

966		SPS150	Spastic Ataxia, Charlevoix-Saguenay Type	58	0.037

967		EWN003	Ewing Sarcoma	69	0.037

968		ORL011	Oral Cancer	60	0.037

969	P	TRT010	Teratoma	52	0.037

970		VCC001	Vaccinia	49	0.037

971		MNG007	Manganese Poisoning	29	0.037

972	P	PNM006	Pneumoconiosis	56	0.037

973	P	ANT006	Antiphospholipid Syndrome	55	0.037

974	c	PSR017	Psoriasis 2	53	0.037

975	c	PSR023	Psoriasis 1	52	0.037

976		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.037

977	c	PSR032	Psoriasis 11	47	0.037

978		PRT019	Protein-Losing Enteropathy	45	0.037

979		TND004	Tendinopathy	43	0.037

980	c	PSR028	Psoriasis 7	42	0.037

981	c	PSR018	Psoriasis 13	41	0.037

982	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.037

983		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.037

984		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.036

985		PLM070	Pulmonic Stenosis	57	0.036

986	c	PLY172	Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease	57	0.036

987		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.036

988	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.036

989	P	CRB194	Cerebroretinal Microangiopathy with Calcifications and Cysts 1	53	0.036

990		PRS030	Persistent Fetal Circulation Syndrome	52	0.036

991		FCT001	Factor Viii Deficiency	51	0.036

992	c	PRM012	Primary Polycythemia	50	0.036

993	c	THR090	Thrombocythemia 1	49	0.036

994		END021	Endomyocardial Fibrosis	49	0.036

995	P	MST002	Mast-Cell Leukemia	49	0.036

996		PLM041	Pulmonary Valve Stenosis	49	0.036

997		ADR016	Adrenal Cortical Carcinoma	48	0.036

998	P	CPL014	Capillary Malformation-Arteriovenous Malformation 1	48	0.036

999		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.036

1000		ACT084	Acute Stress Disorder	47	0.036

1001	c	PRM093	Premature Ovarian Failure 7	47	0.036

1002		HMP009	Haemophilus Influenzae	43	0.036

1003		CLP006	Clopidogrel Resistance	40	0.036

1004		ADR004	Adrenal Cortical Adenocarcinoma	39	0.036

1005		MYL074	Myelodysplastic Syndrome with Excess Blasts	38	0.036

1006	P	VSC018	Visceral Steatosis	33	0.036

1007	P	OVR096	Overlap Myositis	27	0.036

1008		RFR007	Refractory Anemia with Excess Blasts in Transformation	27	0.036

1009		SCR003	Secretory Diarrhea	37	0.036

1010		HVY002	Heavy Metal Poisoning	22	0.036

1011	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	64	0.036

1012		WST001	West Syndrome	61	0.036

1013	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.036

1014		INT051	Intussusception	53	0.036

1015	P	RTN022	Retinal Vein Occlusion	53	0.036

1016	P	PRC012	Pericardial Effusion	51	0.036

1017		HMP001	Hemopericardium	48	0.036

1018		TST014	Testicular Cancer	46	0.036

1019	c	CHR417	Chronic Graft Versus Host Disease	57	0.035

1020	c	CRD184	Ceroid Lipofuscinosis, Neuronal, 5	55	0.035

1021		ACT200	Acute Monoblastic Leukemia	52	0.035

1022	c	ALM001	Al Amyloidosis	50	0.035

1023		SLD003	Sialadenitis	49	0.035

1024		MCR018	Microcytic Anemia	47	0.035

1025		IRN004	Iron-Refractory Iron Deficiency Anemia	47	0.035

1026		SPR126	Superior Semicircular Canal Dehiscence	40	0.035

1027		DFF039	Diffuse Midline Glioma, H3 K27m-Mutant	36	0.035

1028	P	GLL020	Gallbladder Disease	57	0.035

1029		CLL003	Cellulitis	54	0.035

1030	P	PTS002	Ptosis	53	0.035

1031	c	VRL010	Viral Hepatitis	52	0.035

1032		FBR009	Fibrous Dysplasia	48	0.035

1033	P	AVS003	Avascular Necrosis	42	0.035

1034		AMN006	Aminoaciduria	38	0.035

1035	P	NJM001	Nijmegen Breakage Syndrome	74	0.035

1036		NDL024	Nodal Marginal Zone Lymphoma	38	0.035

1037	P	LPS002	Liposarcoma	65	0.034

1038		ATX029	Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia	65	0.034

1039		KND001	Kindler Syndrome	64	0.034

1040	P	LYM033	Lymphoproliferative Syndrome	59	0.034

1041		ADR005	Adrenal Carcinoma	58	0.034

1042	P	PRV006	Pervasive Developmental Disorder	57	0.034

1043		FND002	Fundus Dystrophy	55	0.034

1044	P	DYS193	Dystonia 11, Myoclonic	55	0.034

1045		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.034

1046	P	SPN429	Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2	52	0.034

1047		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.034

1048	P	NRC002	Narcolepsy	52	0.034

1049		ACT017	Acute Chest Syndrome	51	0.034

1050		PLR007	Pleural Empyema	50	0.034

1051		OCL022	Ocular Melanoma	50	0.034

1052		CHL018	Childhood Medulloblastoma	49	0.034

1053		INT017	Intestinal Schistosomiasis	48	0.034

1054		ALV007	Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins	48	0.034

1055	P	BLR006	Biliary Tract Disease	47	0.034

1056	c	ADL023	Adult Medulloblastoma	44	0.034

1057		MND023	Mend Syndrome	43	0.034

1058	P	VTL001	Vitelliform Macular Dystrophy	42	0.034

1059		FBR019	Fibromatosis	41	0.034

1060	c	MYT029	Myotonia Congenita, Autosomal Recessive	41	0.034

1061	c	ADL096	Adult Hepatocellular Carcinoma	40	0.034

1062		CGN005	Cognitive Impairment with or Without Cerebellar Ataxia	39	0.034

1063		CRB026	Cerebellar Astrocytoma	37	0.034

1064		HND015	Hand Skill, Relative	33	0.034

1065		PDT014	Pediatric Ependymoma	32	0.034

1066		UNV002	Univentricular Heart	28	0.034

1067		CRT064	Corticosterone Methyloxidase Deficiency	20	0.034

1068		PNL001	Pineal Gland Astrocytoma	14	0.034

1069		CHL009	Childhood Cerebral Astrocytoma	14	0.034

1070	P	3MT016