Search results for Calcium Phosphate

2117 hits were found for Calcium Phosphate

#	Family	MCID	Name	MIFTS	Score
1	P	HYP069	Hyperparathyroidism	63	0.507

2		RCK004	Rickets	68	0.431

3	P	KDN018	Kidney Disease	72	0.411

4		HYP025	Hyperphosphatemia	48	0.383

5		BNR002	Bone Resorption Disease	48	0.372

6	c	CHR684	Chronic Kidney Disease	70	0.362

7		NPH009	Nephrolithiasis	55	0.360

8	P	OST002	Osteoporosis	74	0.350

9		PRT037	Pertussis	65	0.349

10	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.336

11	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.336

12	c	SCN007	Secondary Hyperparathyroidism	51	0.334

13		URL001	Urolithiasis	45	0.304

14		HYP017	Hypophosphatemia	50	0.285

15		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.278

16	P	BND020	Bone Disease	59	0.277

17	c	HYP595	Hypertension, Essential	84	0.270

18	c	PRM005	Primary Hyperparathyroidism	58	0.261

19		END086	End Stage Renal Disease	51	0.258

20		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.243

21	P	NRB001	Neuroblastoma	72	0.240

22	P	LKM002	Leukemia	68	0.238

23		OST011	Osteomalacia	52	0.232

24	P	CLR023	Colorectal Cancer	99	0.226

25	P	LYM118	Lymphoma	68	0.220

26		LYM019	Lymphosarcoma	46	0.215

27		DNT012	Dental Caries	53	0.213

28		HLX001	Helix Syndrome	47	0.210

29	P	HYP024	Hypoparathyroidism	56	0.209

30		48X005	48,xyyy	39	0.205

31		CNG034	Congestive Heart Failure	69	0.200

32		LPP008	Lipoprotein Quantitative Trait Locus	62	0.199

33	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.196

34		ISC004	Ischemia	58	0.195

35		OST159	Osteogenic Sarcoma	66	0.191

36	P	ADN016	Adenocarcinoma	64	0.190

37		ANG054	Angina Pectoris	66	0.189

38		ART140	Arteries, Anomalies of	52	0.188

39	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.185

40		NPH003	Nephrocalcinosis	51	0.184

41		ATH013	Atherosclerosis Susceptibility	65	0.183

42		ADN018	Adenoma	59	0.180

43		HYP266	Hypoxia	57	0.179

44		ANX004	Anoxia	40	0.179

45		MTB004	Metabolic Acidosis	50	0.177

46	P	MYL006	Myeloid Leukemia	60	0.176

47		ALL026	Allergic Hypersensitivity Disease	62	0.175

48	P	HRT032	Heart Disease	75	0.175

49		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.174

50	P	CRN300	Coronary Heart Disease 1	63	0.174

51		CHL014	Cholera	59	0.174

52	P	GLM045	Glioma	63	0.172

53		GLL048	Glial Tumor	45	0.171

54		OST017	Osteomyelitis	64	0.170

55	c	LKM061	Leukemia, Acute Myeloid	84	0.169

56		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.169

57	P	PRS040	Prostate Cancer	97	0.169

58		LYM040	Lymphoblastic Lymphoma	54	0.168

59	P	PRD008	Periodontitis	64	0.167

60	P	VSC007	Vascular Disease	63	0.167

61	P	GRF003	Graft-Versus-Host Disease	72	0.166

62		URM002	Uremia	49	0.165

63	c	RHB024	Rhabdomyosarcoma 2	67	0.165

64	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.164

65		CLC006	Calcinosis	48	0.163

66	P	MSC005	Muscular Dystrophy	66	0.163

67		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.162

68		TTN003	Tetanus	65	0.159

69	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.158

70		HRW001	Hair Whorl	36	0.158

71	c	PRC016	Pre-Eclampsia	63	0.158

72		IDP073	Idiopathic Hypercalciuria	43	0.155

73		MYL069	Myeloma, Multiple	85	0.155

74	P	DBT009	Diabetes Mellitus	64	0.155

75		ADL002	Adult Syndrome	70	0.153

76		RNL011	Renal Osteodystrophy	50	0.153

77	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.153

78	P	NRP001	Neuropathy	56	0.153

79	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.152

80	c	ACT071	Acute Kidney Failure	60	0.151

81		LYM133	Lymphoma, Hodgkin, Classic	69	0.150

82		HYP005	Hypokalemia	55	0.150

83	P	BCL017	B-Cell Lymphoma	58	0.149

84		47X002	47,xyy	49	0.149

85		HYP056	Hypoglycemia	66	0.148

86	P	CHN059	Chondrocalcinosis	52	0.147

87	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.147

88	P	CRD119	Cardiac Arrest	67	0.146

89		DWN001	Down Syndrome	70	0.146

90		DFC004	Deficiency Anemia	70	0.145

91	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.145

92	P	SRC025	Sarcoidosis 1	70	0.143

93	c	LKM063	Leukemia, Chronic Myeloid	72	0.143

94	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.142

95		OST012	Osteoarthritis	78	0.141

96		CNS004	Constipation	58	0.140

97		INS001	Insulinoma	60	0.140

98	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.140

99		MYL009	Myelodysplastic Syndrome	70	0.140

100	P	DRR001	Diarrhea	55	0.139

101	c	NRF023	Neurofibromatosis, Type Ii	80	0.139

102		GT001	Gout	64	0.137

103		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.137

104	P	TRN020	Turner Syndrome	67	0.137

105	P	LTR001	Lateral Sclerosis	54	0.137

106		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.136

107	P	MYC007	Myocardial Infarction	70	0.136

108		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.135

109	P	SZR006	Seizure Disorder	56	0.135

110		AGN016	Aging	56	0.134

111	P	HYP076	Hyperthyroidism	55	0.133

112	P	MYP004	Myopathy	70	0.133

113		LPD008	Lipid Metabolism Disorder	62	0.133

114		VSL002	Visual Epilepsy	59	0.133

115	P	BRS047	Breast Cancer	97	0.133

116	P	ALZ034	Alzheimer Disease	88	0.132

117	P	ART023	Arthropathy	62	0.132

118	c	ATR087	Atrial Standstill 1	75	0.132

119	P	PHC003	Pheochromocytoma	71	0.131

120	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.131

121		ADR040	Adrenal Gland Pheochromocytoma	46	0.131

122	c	MGR028	Migraine with or Without Aura 1	67	0.130

123		HYP066	Hyperglycemia	61	0.130

124	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.128

125		CYS001	Cystic Fibrosis	81	0.128

126	P	HYP086	Hypothyroidism	69	0.128

127		HMN044	Human Immunodeficiency Virus Type 1	71	0.126

128		IRN002	Iron Metabolism Disease	57	0.126

129	P	RCT021	Rectum Cancer	52	0.126

130	P	MLG056	Malignant Hyperthermia	67	0.125

131	P	OVR042	Ovarian Cancer	88	0.124

132	P	CTR002	Cataract	60	0.124

133	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.124

134	P	HYP726	Hypercalcemia, Infantile, 1	58	0.123

135	P	CRD246	Cardiovascular System Disease	57	0.122

136		LMB002	Lambert-Eaton Myasthenic Syndrome	53	0.122

137	P	ENC018	Encephalopathy	61	0.120

138	c	ACT027	Acute Pancreatitis	60	0.120

139	P	FLL037	Follicular Lymphoma	67	0.120

140	P	LVR013	Liver Disease	68	0.119

141		MNT001	Mantle Cell Lymphoma	69	0.119

142	c	DLT002	Dilated Cardiomyopathy	79	0.119

143		PPL052	Papillomatosis, Confluent and Reticulated	33	0.119

144	P	ART021	Arteriosclerosis	54	0.118

145	c	GLL024	Gallbladder Disease 1	53	0.118

146		PLS009	Plasma Cell Neoplasm	51	0.118

147	c	MCR113	Microvascular Complications of Diabetes 3	52	0.117

148	c	FLL041	Follicular Lymphoma 1	49	0.117

149		BRK010	Burkitt Lymphoma	67	0.117

150	c	MCR120	Microvascular Complications of Diabetes 7	47	0.117

151		CYT002	Cytokine Deficiency	42	0.117

152	P	NTR004	Neutropenia	63	0.116

153	c	MCR130	Microvascular Complications of Diabetes 6	41	0.116

154	c	MCR133	Microvascular Complications of Diabetes 4	41	0.116

155	c	PRM038	Primary Agammaglobulinemia	44	0.116

156		THY029	Thyroid Carcinoma	59	0.115

157		PNG002	Pain Agnosia	51	0.115

158		INS024	Insulin-Like Growth Factor I	79	0.115

159		IMM167	Immune Deficiency Disease	78	0.115

160	c	CHR064	Chronic Monocytic Leukemia	33	0.115

161	P	PLM037	Pulmonary Hypertension	67	0.114

162		LVR012	Liver Cirrhosis	62	0.114

163	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.114

164		MSC157	Muscular Dystrophy, Duchenne Type	72	0.114

165		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.114

166		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.114

167	P	PRP019	Peripheral Nervous System Disease	58	0.113

168	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.112

169	P	FML068	Familial Hypocalciuric Hypercalcemia	54	0.112

170	c	LKM005	Leukemia, T-Cell, Chronic	34	0.111

171		INT007	Intermediate Coronary Syndrome	55	0.111

172	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	64	0.111

173		PLS025	Plasmablastic Lymphoma	47	0.110

174		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.110

175	P	CNR004	Cone-Rod Dystrophy 2	73	0.110

176		ATM095	Autoimmune Disease	62	0.110

177	P	BPL003	Bipolar Disorder	56	0.110

178		CLN015	Colon Adenocarcinoma	65	0.110

179	P	ATR011	Atrial Fibrillation	66	0.109

180	c	MJR024	Major Affective Disorder 9	41	0.109

181	c	MJR022	Major Affective Disorder 8	38	0.109

182		HMT002	Hematologic Cancer	62	0.109

183	P	PSR002	Psoriasis	62	0.109

184		CRB039	Cerebrovascular Disease	67	0.109

185	P	CHR345	Chronic Pain	44	0.108

186	c	ACT075	Acute Myocardial Infarction	57	0.107

187		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.106

188	P	ECL001	Eclampsia	50	0.106

189		ACQ007	Acquired Immunodeficiency Syndrome	60	0.106

190	P	HYP061	Hypertrophic Cardiomyopathy	70	0.106

191		GLB015	Glioblastoma Multiforme	75	0.106

192	P	PNC035	Pancreatic Cancer	84	0.105

193	c	ACT073	Acute Leukemia	58	0.105

194		STR067	Stroke, Ischemic	81	0.105

195		ATX019	Ataxia with Vitamin E Deficiency	42	0.105

196		NTR005	Nutritional Deficiency Disease	62	0.105

197		HYP060	Hyperinsulinism	54	0.105

198		OST003	Osteonecrosis	61	0.105

199		TRM010	Traumatic Brain Injury	51	0.105

200		BRN071	Brain Injury	49	0.105

201		HML018	Homologous Wasting Disease	22	0.105

202		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.105

203		CRN030	Coronary Stenosis	50	0.105

204	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.105

205		MYL031	Myeloproliferative Neoplasm	66	0.104

206	P	AST007	Astrocytoma	51	0.104

207		FML307	Familial Calcium Pyrophosphate Deposition	40	0.104

208		SKN016	Skin Disease	63	0.104

209		PST011	Pustulosis of Palm and Sole	52	0.104

210	P	OVR082	Overgrowth Syndrome	50	0.104

211	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.103

212		BNM001	Bone Marrow Cancer	43	0.103

213		DPR016	Depression	63	0.103

214	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.102

215	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.102

216	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.102

217	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.102

218	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.102

219	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.102

220	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.102

221		RTR008	Root Resorption	45	0.102

222	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.102

223	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.102

224	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.102

225		SPN186	Spinal Cord Injury	60	0.102

226	P	PNC044	Pancreatitis	61	0.102

227		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.102

228	P	MCR115	Microvascular Complications of Diabetes 5	66	0.102

229	P	MLN008	Melanoma	69	0.101

230		PLY150	Polykaryocytosis Inducer	31	0.101

231	P	LNG032	Lung Cancer	98	0.101

232		MLR004	Malaria	81	0.101

233	P	HML002	Hemolytic Anemia	63	0.100

234	P	ADL017	Adult T-Cell Leukemia	56	0.100

235	c	CHR417	Chronic Graft Versus Host Disease	57	0.099

236		LNG099	Lung Disease	60	0.099

237	P	PSD015	Pseudohypoparathyroidism	56	0.099

238		OCL069	Ocular Motor Apraxia	51	0.099

239	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	60	0.099

240	P	PLY014	Polycystic Kidney Disease	62	0.099

241	P	RNL007	Renal Tubular Acidosis	51	0.098

242		MRG003	Marginal Zone B-Cell Lymphoma	52	0.098

243		ALC007	Alcohol Dependence	66	0.098

244	c	ACT135	Acute Graft Versus Host Disease	52	0.098

245		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.098

246	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.098

247	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.097

248		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.097

249		DRM006	Dermatitis	61	0.097

250		TXC005	Toxic Shock Syndrome	62	0.097

251		FTT001	Fatty Liver Disease	61	0.097

252		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.096

253		PRT029	Parathyroid Adenoma	50	0.096

254		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.096

255	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.095

256		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.095

257		CRB004	Cerebral Artery Occlusion	45	0.095

258	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.094

259	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.094

260	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.094

261	c	SML038	Small Cell Cancer of the Lung	65	0.094

262	P	NPH012	Nephrotic Syndrome	60	0.094

263	P	HPT023	Hepatocellular Carcinoma	100	0.093

264	P	GST053	Gastric Cancer	83	0.093

265	c	ACT068	Acute Cystitis	63	0.093

266		MCS002	Mucositis	56	0.093

267		MYL005	Myelofibrosis	70	0.093

268		STT001	Status Epilepticus	60	0.092

269	P	ART022	Arthritis	69	0.092

270		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.092

271		MMM001	Mammary Paget's Disease	53	0.091

272	P	EPL164	Epilepsy	71	0.091

273		CLR108	Colorectal Adenoma	64	0.091

274		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.091

275		ATR057	Atrioventricular Block	55	0.091

276		PRP027	Peripheral Vascular Disease	71	0.091

277		MCR004	Macroglobulinemia	49	0.091

278		STM007	Stomatitis	50	0.091

279		PRS021	Prostatic Adenoma	51	0.090

280		PRS045	Prostatic Hypertrophy	53	0.089

281	P	PNM007	Pneumonia	68	0.089

282	P	THR014	Thrombocytopenia	67	0.089

283		PRS129	Prostatic Hyperplasia, Benign	49	0.089

284		MNT002	Mental Depression	58	0.089

285	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.089

286	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.088

287		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.088

288		RFR010	Refractory Anemia	48	0.088

289		SVR004	Severe Combined Immunodeficiency	73	0.087

290		DPH001	Diphtheria	60	0.087

291		CRD132	Cardiac Conduction Defect	58	0.087

292	P	RHM011	Rheumatoid Arthritis	80	0.087

293	P	TRM003	Tremor	54	0.087

294		BCT022	Bacterial Infectious Disease	56	0.086

295		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.086

296		ERY051	Erythroleukemia, Familial	56	0.086

297		ONC003	Oncogenic Osteomalacia	42	0.086

298		SPL004	Splenic Marginal Zone Lymphoma	51	0.085

299	c	SYS001	Systemic Lupus Erythematosus	86	0.085

300		GNG003	Gingival Recession	44	0.085

301	P	HNT016	Huntington Disease	72	0.085

302		HYP014	Hyperuricemia	52	0.085

303		SQM006	Squamous Cell Carcinoma	60	0.085

304	P	INF037	Inflammatory Bowel Disease	54	0.085

305		PPT005	Peptic Ulcer Disease	59	0.084

306		CRD223	Cardiac Arrhythmia	60	0.084

307		WLD007	Waldenstroem's Macroglobulinemia	61	0.084

308		SCK003	Sickle Cell Anemia	74	0.084

309		HMS001	Hemosiderosis	54	0.084

310		FCT007	Factor Vii Deficiency	67	0.083

311		ESP021	Esophageal Cancer	90	0.083

312		PTT037	Pituitary Tumors	44	0.083

313	P	HRP006	Herpes Simplex	65	0.083

314	P	RSP003	Respiratory Failure	74	0.083

315		GLS018	Glass Syndrome	57	0.082

316	P	HDC001	Headache	57	0.082

317		SYN007	Synovitis	54	0.082

318		PLC002	Plica Syndrome	36	0.082

319		CHL149	Childhood Acute Myeloid Leukemia	44	0.082

320		PRT036	Peritonitis	64	0.082

321	P	THL005	Thalassemia	60	0.081

322		LYM012	Lymphoplasmacytic Lymphoma	47	0.081

323	P	INF032	Infertility	57	0.081

324		AST005	Asthma	76	0.081

325		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.081

326	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	46	0.081

327	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.081

328	c	PRD040	Periodontitis, Chronic	53	0.080

329		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.080

330		ANK001	Ankylosis	51	0.080

331	P	RRH023	Rare Hereditary Hemochromatosis	41	0.080

332	P	FNC004	Fanconi Syndrome	50	0.080

333		GLC003	Glucose Intolerance	54	0.080

334		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.080

335	P	TXP001	Toxoplasmosis	60	0.079

336	P	DMN002	Dementia	66	0.079

337		MYC006	Mycosis Fungoides	66	0.078

338	P	GLM007	Glomerulonephritis	57	0.078

339	P	BLD134	Bladder Cancer	79	0.078

340	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.078

341	P	MSC003	Muscular Atrophy	52	0.078

342		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.078

343		GTR002	Goiter	53	0.077

344	P	DDN001	Duodenal Ulcer	52	0.077

345	P	LPS004	Lupus Erythematosus	61	0.077

346		ENM002	Enamel Erosion	26	0.077

347	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.077

348	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.076

349		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.076

350		BNN003	Bone Inflammation Disease	48	0.076

351		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.076

352	P	SCK005	Sickle Cell Disease	50	0.076

353		WTH001	Withdrawal Disorder	48	0.075

354	P	PRM002	Primary Hyperoxaluria	62	0.075

355		FNG017	Fungal Infectious Disease	53	0.075

356		ACR007	Acromegaly	71	0.075

357	P	KDN017	Kidney Cancer	60	0.075

358		RTC005	Reticulosarcoma	47	0.075

359	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.075

360		PLM033	Pulmonary Embolism	59	0.075

361	P	SCL018	Scoliosis	60	0.075

362	P	LCT001	Lactic Acidosis	51	0.075

363	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.075

364	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.074

365		CLN045	Colonic Benign Neoplasm	46	0.074

366	P	MLN007	Male Infertility	55	0.074

367	P	SKN015	Skin Carcinoma	66	0.074

368	P	ALP008	Alopecia	54	0.074

369	P	HYP776	Hyperparathyroidism, Neonatal Severe	47	0.074

370	P	PLY018	Polycythemia	56	0.074

371	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.074

372		SCN001	Secondary Hyperparathyroidism of Renal Origin	27	0.074

373		SKN019	Skin Melanoma	68	0.074

374		SYN036	Syncope	45	0.074

375		DFF005	Diffuse Large B-Cell Lymphoma	55	0.073

376	c	BRN108	Branchiootic Syndrome 1	62	0.073

377		TND005	Tendinitis	54	0.073

378		SZR001	Sezary's Disease	60	0.073

379		SRC014	Sarcoma	65	0.073

380	P	INF038	Influenza	68	0.073

381		HYP789	Hypophosphatemic Rickets with Hypercalciuria, Hereditary	51	0.073

382		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	0.073

383	P	PLY019	Polyneuropathy	56	0.073

384	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	61	0.072

385		ALL014	Allergic Encephalomyelitis	38	0.072

386	c	DRR009	Diarrhea 6	46	0.072

387		PST092	Posttransplant Acute Limbic Encephalitis	29	0.072

388		IRR002	Irritable Bowel Syndrome	65	0.072

389	P	LCT002	Lactose Intolerance	53	0.072

390		SPN035	Spindle Cell Sarcoma	53	0.072

391	P	MYS003	Myasthenia Gravis	68	0.072

392	P	DRM053	Dermatitis, Atopic	66	0.072

393	P	RHN004	Rhinitis	57	0.072

394		CHL079	Children's Interstitial Lung Disease	26	0.072

395	P	EXN002	Exanthem	57	0.071

396	c	SVR001	Severe Acute Respiratory Syndrome	62	0.071

397	c	JVN004	Juvenile Myelomonocytic Leukemia	67	0.071

398	P	PLY011	Polycystic Ovary Syndrome	56	0.071

399	c	GRV008	Graves Disease 1	56	0.071

400	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.071

401		PLP001	Pulpitis	49	0.071

402		PRM020	Premenstrual Tension	40	0.071

403	c	HPT016	Hepatitis B	59	0.071

404		PRL017	Prolymphocytic Leukemia	47	0.071

405		HMP009	Haemophilus Influenzae	43	0.071

406		MYL074	Myelodysplastic Syndrome with Excess Blasts	38	0.071

407		CLC001	Calciphylaxis	51	0.071

408		NRM005	Neuromuscular Disease	64	0.071

409		IMP005	Impotence	52	0.071

410		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.071

411	P	PLM036	Pulmonary Fibrosis	65	0.071

412		TLN003	Telangiectasis	52	0.071

413		ATY042	Atypical Chronic Myeloid Leukemia	49	0.071

414		CHL068	Cholestasis	61	0.071

415	P	HYP035	Hypophosphatasia	61	0.070

416	c	SCL052	Scleroderma, Familial Progressive	61	0.070

417		DNT006	Dental Pulp Necrosis	41	0.070

418	P	HYP265	Hypotonia	43	0.070

419		MYC005	Myocardial Stunning	46	0.070

420		ANX010	Anxiety	73	0.070

421		BRN004	Brain Edema	56	0.070

422		PLM001	Pulmonary Tuberculosis	69	0.070

423		ATS010	Autosomal Recessive Disease	48	0.070

424	P	SYS005	Systemic Scleroderma	68	0.069

425	P	UVT001	Uveitis	57	0.069

426		MRF001	Marfan Syndrome	77	0.069

427		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.069

428		HDG004	Hodgkin's Granuloma	23	0.069

429		HDG006	Hodgkin's Paragranuloma	22	0.069

430		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.069

431	P	FBR017	Fibrosarcoma	56	0.069

432		BRN024	Bronchitis	68	0.069

433	P	SCH015	Schizophrenia	74	0.069

434	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	19	0.069

435		RYN005	Raynaud Phenomenon	47	0.069

436	c	MLG068	Malignant Glioma	46	0.068

437		END057	Endometrial Cancer	74	0.068

438		CLT003	Colitis	62	0.068

439	P	ALC033	Alcohol Use Disorder	58	0.068

440	c	ATS007	Autism Spectrum Disorder	67	0.068

441	P	HYP750	Hypertriglyceridemia, Familial	62	0.068

442		CHG001	Chagas Disease	66	0.068

443		HRY003	Hairy Cell Leukemia	55	0.067

444		ENM001	Enamel Caries	28	0.067

445		ART016	Aortic Aneurysm	69	0.067

446	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.067

447	P	MLT020	Multiple Sclerosis	72	0.067

448		CRH001	Crohn's Disease	74	0.067

449		49X006	49, Xxxxy Syndrome	41	0.066

450		GST050	Gastrointestinal System Disease	56	0.066

451		PLY001	Polycythemia Vera	69	0.066

452	P	PRK057	Parkinson Disease, Late-Onset	78	0.066

453	P	ENC004	Encephalitis	61	0.066

454	P	DST107	Distal Renal Tubular Acidosis	42	0.066

455	P	PGT001	Paget's Disease of Bone	58	0.065

456	c	PCH010	Pachyonychia Congenita 3	44	0.065

457	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.065

458		VCC001	Vaccinia	49	0.065

459	P	MJR001	Major Depressive Disorder	68	0.065

460		MSC007	Muscle Hypertrophy	64	0.065

461		ANR040	Aneurysm	59	0.065

462		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.065

463		PYR009	Pyridoxine Deficiency Anemia	34	0.065

464	P	LNG064	Lung Cancer Susceptibility 3	78	0.065

465		MDD011	Mood Disorder	62	0.065

466	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.064

467	P	MYC008	Myocarditis	59	0.064

468	P	ATS364	Autism	70	0.064

469	P	MNC007	Monocytic Leukemia	53	0.064

470	P	FML187	Familial Hypertension	37	0.064

471	P	ESS003	Essential Thrombocythemia	68	0.064

472	P	AMY004	Amyloidosis	70	0.064

473		LSH001	Leishmaniasis	63	0.064

474	P	KLZ004	Kala-Azar 1	41	0.064

475	P	CHR012	Chronic Granulomatous Disease	67	0.064

476		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.064

477		OST004	Osteitis Fibrosa	41	0.064

478		SFT003	Soft Tissue Sarcoma	56	0.064

479		TRN015	Transient Cerebral Ischemia	63	0.064

480	P	TMP001	Temporal Lobe Epilepsy	50	0.064

481	P	BRB001	Beriberi	46	0.064

482		THY111	Thyroid Carcinoma, Familial Medullary	67	0.064

483	c	PNS012	Paine Syndrome	61	0.064

484		PNC129	Pancreatic Adenocarcinoma	68	0.064

485		BRT054	Brittle Bone Disorder	72	0.063

486		CRY024	Crystal Arthropathies	20	0.063

487		ENT004	Enthesopathy	49	0.063

488		VRL011	Viral Infectious Disease	61	0.063

489	P	PYL005	Pyelonephritis	56	0.063

490	P	BSL038	Basal Ganglia Calcification, Idiopathic, 1	52	0.063

491	P	LNG028	Long Qt Syndrome	66	0.063

492	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.063

493		FBR047	Fibromyalgia	58	0.063

494		CNT047	Contact Dermatitis	58	0.063

495	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.063

496		KRT002	Keratomalacia	47	0.063

497		ALL003	Allergic Rhinitis	67	0.063

498		PLM031	Poliomyelitis	64	0.063

499		CHR074	Choriocarcinoma	47	0.063

500		BCK006	Back Pain	42	0.063

501		LPT014	Leptin Deficiency or Dysfunction	74	0.063

502	c	PRM012	Primary Polycythemia	50	0.062

503		RFR007	Refractory Anemia with Excess Blasts in Transformation	27	0.062

504		SCH014	Schistosomiasis	57	0.062

505		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.062

506		PLM017	Pulmonary Alveolar Microlithiasis	50	0.062

507		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.062

508		THY125	Thyroid Gland Medullary Carcinoma	50	0.062

509	P	PRD021	Periodic Paralysis	45	0.062

510	P	GLM040	Glioma Susceptibility 1	81	0.062

511	P	GRV001	Graves' Disease	55	0.062

512		LYM051	Lymphomatoid Granulomatosis	45	0.062

513		LNG031	Lung Benign Neoplasm	51	0.062

514		OVR094	Ovarian Epithelial Cancer	38	0.062

515		THY030	Thyroid Gland Disease	52	0.062

516	P	MTR014	Motor Neuron Disease	65	0.061

517		BRR014	Barrett Esophagus	65	0.061

518		PRM329	Premature Aging	35	0.061

519		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.061

520		CVD001	Covid-19	44	0.061

521		WLL004	Wallerian Degeneration	39	0.061

522		ZLL002	Zollinger-Ellison Syndrome	55	0.061

523		BLR008	Bilirubin Metabolic Disorder	57	0.061

524		MGK001	Megakaryocytic Leukemia	64	0.061

525	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.061

526		ULC004	Ulcerative Colitis	73	0.060

527	P	END044	Endometriosis	63	0.060

528		GST023	Gastric Ulcer	53	0.060

529		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.060

530	P	CYS018	Cystitis	59	0.060

531	P	MLG074	Malignant Mesenchymoma	40	0.060

532		THR024	Thrombosis	57	0.060

533		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.060

534		DBT010	Diabetic Neuropathy	54	0.060

535	P	GST044	Gastritis	56	0.060

536		PRP080	Peripheral Artery Disease	53	0.060

537		ANR007	Anorexia Nervosa	63	0.060

538		IDP070	Idiopathic Scoliosis	42	0.060

539	c	THR090	Thrombocythemia 1	49	0.060

540		FBR009	Fibrous Dysplasia	48	0.059

541	c	EPS035	Episodic Ataxia, Type 2	63	0.059

542		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.059

543		KRT008	Keratopathy	47	0.059

544	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.059

545	P	RTN024	Retinoblastoma	73	0.059

546	P	SLP006	Sleep Apnea	69	0.059

547		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.059

548		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.059

549		CLR109	Colorectal Adenocarcinoma	51	0.059

550		CNN005	Connective Tissue Disease	68	0.059

551		PRT013	Portal Hypertension	59	0.059

552	P	MYT002	Myotonic Dystrophy	49	0.059

553	P	DNT020	Dent Disease 1	62	0.058

554		MTH071	Methane Production	26	0.058

555	c	HPT073	Hepatitis C Virus	72	0.058

556		CMM004	Common Variable Immunodeficiency	68	0.058

557		PRP016	Paraplegia	52	0.058

558	c	INH020	Inherited Metabolic Disorder	47	0.058

559	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.058

560		ENT011	Enterocolitis	51	0.058

561	c	FML001	Familial Atrial Fibrillation	65	0.058

562		TXC002	Toxic Encephalopathy	53	0.058

563	c	FML008	Familial Retinoblastoma	53	0.058

564		PRR001	Periarthritis	32	0.058

565		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.058

566	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.058

567		HPT004	Hepatic Coma	45	0.058

568	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.058

569	P	LYM033	Lymphoproliferative Syndrome	59	0.058

570		HYD002	Hydronephrosis	60	0.057

571		GST092	Gastroesophageal Reflux	67	0.057

572	P	DYS154	Dystonia	65	0.057

573		VSC002	Vascular Dementia	57	0.057

574	P	MYS005	Myositis	56	0.057

575		EWN003	Ewing Sarcoma	69	0.057

576	P	HPT021	Hepatitis	67	0.057

577	P	GLY013	Glycogen Storage Disease	60	0.057

578		LYM027	Lymphopenia	58	0.057

579	c	DBT099	Diabetes Mellitus, Type I	65	0.057

580		FRZ001	Frozen Shoulder	53	0.057

581	c	CHR418	Chronic Leukemia	49	0.057

582	P	BRS044	Breast Adenocarcinoma	59	0.057

583		GST045	Gastroenteritis	59	0.057

584	c	PSR017	Psoriasis 2	53	0.057

585	c	PSR023	Psoriasis 1	52	0.057

586	c	PSR032	Psoriasis 11	47	0.057

587	c	PSR028	Psoriasis 7	42	0.057

588	c	PSR018	Psoriasis 13	41	0.057

589		CHL065	Cholangiocarcinoma	68	0.057

590	c	HYP794	Hyperoxaluria, Primary, Type I	63	0.057

591		PLM010	Pulmonary Edema	54	0.057

592	P	NRV007	Nervous System Disease	66	0.056

593	P	BNC003	Bone Cancer	58	0.056

594		GRN017	Granulocytopenia	44	0.056

595	P	CYS039	Cystic Kidney Disease	54	0.056

596	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.056

597		SPN027	Spinal Stenosis	59	0.056

598		EYD002	Eye Disease	58	0.056

599		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.056

600		TRP009	Triple X Syndrome	42	0.056

601	c	HMC039	Hemochromatosis, Type 1	74	0.056

602	P	RTN016	Retinal Degeneration	53	0.056

603		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.056

604		PPL022	Papilloma	54	0.056

605	c	ART101	Aortic Valve Disease 2	65	0.056

606		PTH003	Pathologic Nystagmus	52	0.056

607		CRD137	Cardiogenic Shock	47	0.056

608	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.056

609		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.056

610	c	FML035	Familial Hyperlipidemia	55	0.055

611		SBC016	Subacute Delirium	44	0.055

612		BRN028	Brain Cancer	74	0.055

613		CRP001	Carpal Tunnel Syndrome	67	0.055

614		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.055

615		DGN001	Degenerative Disc Disease	48	0.055

616	c	MCR129	Microvascular Complications of Diabetes 1	66	0.055

617	P	PMP001	Pemphigus	54	0.055

618	c	SPN225	Spondyloarthropathy 1	73	0.055

619	P	THY023	Thymoma	65	0.055

620		SPT004	Septic Arthritis	58	0.055

621	c	THY107	Thymoma, Familial	52	0.055

622		MYL067	Myeloproliferative Disorder, Chronic, with Eosinophilia	37	0.055

623	P	DRM010	Dermatomyositis	61	0.055

624		GST020	Gastric Antral Vascular Ectasia	41	0.055

625	P	RHB003	Rhabdomyosarcoma	63	0.055

626	P	ATX030	Ataxia-Telangiectasia	82	0.055

627		CNT033	Central Nervous System Cancer	47	0.054

628	P	SCK002	Sick Sinus Syndrome	55	0.054

629		HYP081	Hypolipoproteinemia	51	0.054

630		HYP080	Hypogonadism	50	0.054

631		SYS003	Systolic Heart Failure	49	0.054

632		PRT010	Parathyroid Carcinoma	67	0.054

633	P	SNS001	Sensorineural Hearing Loss	60	0.054

634		HRT012	Heart Valve Disease	53	0.054

635	P	PNC025	Panic Disorder	53	0.054

636		BRS064	Bursitis	48	0.054

637		HPT019	Hepatic Encephalopathy	60	0.054

638		PRP030	Purpura	54	0.054

639		RTN023	Retinitis	46	0.054

640		PPL001	Papillary Adenoma	44	0.054

641		NRR001	Neuroretinitis	42	0.054

642	P	OPT006	Optic Nerve Disease	60	0.054

643	P	RNL015	Renal Hypertension	47	0.054

644		AMN003	Amnestic Disorder	54	0.054

645	P	SCL057	Scoliosis, Isolated 1	41	0.054

646	c	VRL010	Viral Hepatitis	52	0.053

647		CHL004	Cholelithiasis	49	0.053

648		LMB062	Limb Ischemia	55	0.053

649		URT010	Ureteral Obstruction	45	0.053

650		GNG013	Gingivitis	59	0.053

651		SYS070	Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood	36	0.053

652	P	HYP098	Hypereosinophilic Syndrome	67	0.053

653	P	TRT010	Teratoma	52	0.053

654	P	MLT074	Multiple Endocrine Neoplasia	56	0.053

655		GRM010	Germ Cells Tumors	34	0.053

656	c	LKM070	Leukemia, Acute Monocytic	57	0.053

657		DYS073	Dysphagia	50	0.053

658	c	HYP057	Hypervitaminosis D	42	0.053

659		INT079	Intrahepatic Cholangiocarcinoma	51	0.053

660	P	CHN012	Chondrosarcoma	56	0.053

661		END040	Endogenous Depression	55	0.053

662		HMC014	Homocysteinemia	53	0.053

663		MDL009	Medullary Sponge Kidney	40	0.053

664	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.052

665	P	CLC063	Celiac Disease 1	66	0.052

666		PNM001	Pneumocystosis	59	0.052

667		TRD006	Tardive Dyskinesia	54	0.052

668		CHR286	Chronic Neutrophilic Leukemia	42	0.052

669	P	BRT004	Bartter Disease	52	0.052

670		RST023	Resting Heart Rate, Variation in	41	0.052

671		KHL003	Kohlschutter-Tonz Syndrome	65	0.052

672	P	GCH001	Gaucher's Disease	63	0.052

673	c	HYP864	Hypoparathyroidism, Familial Isolated, 1	48	0.052

674	P	NSP012	Nasopharyngeal Carcinoma	66	0.052

675	c	DWL002	Dowling-Degos Disease 1	58	0.052

676		SLP001	Sleeping Sickness	54	0.052

677	P	AVS003	Avascular Necrosis	42	0.052

678		KRT019	Keratitis, Hereditary	65	0.052

679	P	MDL005	Medulloblastoma	77	0.052

680	c	HPT001	Hepatitis C	62	0.052

681		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.052

682	c	XNT010	Xanthinuria, Type I	53	0.052

683		AYM001	Ayme-Gripp Syndrome	57	0.052

684		NNT012	Neonatal Jaundice	53	0.052

685		PRS063	Paresthesia	41	0.052

686		ANT024	Anthrax Disease	58	0.051

687	P	RNV001	Renovascular Hypertension	48	0.051

688	P	NGH001	Night Blindness	48	0.051

689		INT054	Intraocular Lymphoma	48	0.051

690		PLS011	Plasmacytoma	56	0.051

691	P	SLP005	Sleep Disorder	59	0.051

692	P	CND004	Candidiasis	58	0.051

693		RDC002	Radiculopathy	50	0.051

694		ARG004	Argyria	27	0.051

695		NRL016	Neural Tube Defects	82	0.051

696		HYP020	Hyperprolactinemia	64	0.051

697	P	RTN018	Retinal Disease	53	0.051

698		OTT002	Otitis Media	72	0.051

699		INT002	Intermittent Claudication	61	0.051

700	P	SPP010	Suppressor of Tumorigenicity 3	51	0.051

701	P	APL001	Aplastic Anemia	74	0.051

702		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.051

703	c	MNN043	Meningioma, Familial	74	0.051

704		MNN042	Meningioma, Radiation-Induced	62	0.051

705		SPN021	Spinal Meningioma	50	0.051

706		SCR001	Secretory Meningioma	41	0.051

707		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.051

708		CHL123	Chlamydia	59	0.051

709		ALL006	Allergic Asthma	56	0.051

710		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.050

711		VLK001	Volkmann Contracture	25	0.050

712	P	SYP003	Syphilis	58	0.050

713		ILS001	Ileus	51	0.050

714		INT067	Interstitial Nephritis	48	0.050

715		HMG002	Hemoglobinuria	50	0.050

716		RTC003	Root Caries	33	0.050

717	P	OST001	Osteopetrosis	70	0.050

718		SNS003	Sensory Peripheral Neuropathy	54	0.050

719		MST005	Mastitis	53	0.050

720		CRB090	Cerebral Hypoxia	44	0.050

721		IRN001	Iron Deficiency Anemia	59	0.050

722	P	ANG015	Angioedema	57	0.050

723	c	PRM226	Primary Central Nervous System Lymphoma	48	0.050

724		SQM002	Squamous Cell Papilloma	46	0.050

725	P	BRG001	Brugada Syndrome	71	0.050

726	P	ASP006	Aspergillosis	69	0.050

727	P	PSD087	Pseudoxanthoma Elasticum	65	0.050

728	P	SML001	Small Cell Carcinoma	52	0.050

729		GST040	Gastric Adenocarcinoma	70	0.049

730	P	LPR021	Leprosy 3	69	0.049

731		VTM033	Vitamin K Deficiency Bleeding	48	0.049

732		HNS001	Hansen's Disease	34	0.049

733		CLC004	Calcific Tendinitis	30	0.049

734		CRV035	Cervical Cancer	76	0.049

735		NNL006	Non-Alcoholic Steatohepatitis	54	0.049

736	P	CNJ013	Conjunctivitis	65	0.049

737	P	INT070	Intestinal Obstruction	58	0.049

738		KRT013	Keratolytic Winter Erythema	46	0.049

739	c	SVR005	Severe Pre-Eclampsia	50	0.049

740	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.049

741		THR004	Thrombocytosis	51	0.049

742		PLS007	Plasmodium Falciparum Malaria	52	0.049

743		ACT119	Acute Promyelocytic Leukemia	63	0.049

744	P	SJG008	Sjogren Syndrome	61	0.049

745		CMR002	Coumarin Resistance	56	0.049

746		CLL003	Cellulitis	54	0.049

747		CHN010	Chondroma	43	0.049

748		GST033	Gestational Diabetes	61	0.049

749	c	HYP243	Hyperparathyroidism 1	51	0.049

750		CNG486	Congenital Disorders of N-Linked Glycosylation and Multiple Pathway	30	0.049

751	c	PSD108	Pseudohypoparathyroidism, Type Ia	66	0.049

752		PRS047	Prostatitis	56	0.049

753		RDN001	Reading Disorder	40	0.049

754		PRN019	Perinatal Necrotizing Enterocolitis	59	0.048

755	P	MYP006	Myopia	55	0.048

756		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.048

757		OST115	Osteonecrosis of the Jaw	40	0.048

758		OST016	Osteochondrosis	53	0.048

759		CHR178	Chromosomal Triplication	35	0.048

760		MYT011	Myotonia	34	0.048

761	P	CNT005	Central Nervous System Lymphoma	53	0.048

762		NWC001	Newcastle Disease	45	0.048

763		LTH001	Lethal Midline Granuloma	44	0.048

764		MXD050	Mixed Phenotype Acute Leukemia	43	0.048

765		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.048

766		APP009	Appendix Adenocarcinoma	44	0.048

767		PRP036	Peripheral T-Cell Lymphoma	53	0.048

768		HST010	Histiocytosis	48	0.048

769		SPL018	Splenomegaly	48	0.048

770		MXD026	Mixed Glioma	45	0.048

771		KPS004	Kaposi Sarcoma	75	0.048

772	P	HMN010	Hemangioma	61	0.048

773	c	ACT134	Acute Liver Failure	56	0.048

774		MTH009	Mouth Disease	56	0.048

775		RYS001	Reye Syndrome	51	0.048

776		EMB004	Embryonal Carcinoma	56	0.047

777	P	SHR001	Short Bowel Syndrome	53	0.047

778	P	HMP007	Hemophilia	51	0.047

779		CYS014	Cystadenocarcinoma	51	0.047

780		IDP085	Idiopathic Infantile Hypercalcemia	28	0.047

781	P	ADL010	Adult Respiratory Distress Syndrome	65	0.047

782		RNL077	Renal Fibrosis	47	0.047

783		IRD001	Iridocyclitis	53	0.047

784	c	PNC108	Pancreatitis, Hereditary	70	0.047

785		ACH005	Achalasia	51	0.047

786		SPS057	Spasticity	45	0.047

787	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	0.047

788		OVR029	Ovarian Hyperstimulation Syndrome	64	0.047

789		TCL002	T-Cell Large Granular Lymphocyte Leukemia	49	0.047

790		LRG008	Large Granular Lymphocyte Leukemia	41	0.047

791		INT066	Interstitial Lung Disease	60	0.047

792		TRY001	Trypanosomiasis	50	0.047

793	P	BNG032	Benign Mesothelioma	46	0.047

794	P	TST021	Testicular Germ Cell Tumor	60	0.047

795		GST030	Gastrinoma	45	0.047

796		CRT015	Carotid Artery Occlusion	45	0.047

797	c	BTT014	Beta-Thalassemia	74	0.046

798	P	ESP024	Esophagitis	62	0.046

799	P	URT039	Urticaria	58	0.046

800		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.046

801		ENC014	Enchondroma	29	0.046

802		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.046

803	P	INS002	in Situ Carcinoma	53	0.046

804		ADR007	Adrenoleukodystrophy	75	0.046

805		PYR016	Pyridoxine Deficiency	30	0.046

806		TBC004	Tobacco Addiction	64	0.046

807	P	VSC011	Vasculitis	62	0.046

808	c	MCR112	Microvascular Complications of Diabetes 2	41	0.046

809	P	RTN008	Retinitis Pigmentosa	79	0.046

810		CRB037	Cerebral Palsy	69	0.046

811		PLG002	Plague	63	0.046

812		BRN056	Bronchopulmonary Dysplasia	57	0.046

813		GRM005	Germ Cell Cancer	47	0.046

814	P	HYD006	Hydrocephalus	66	0.046

815	c	ALP101	Alpha-Thalassemia	62	0.046

816		THY122	Thyroid Gland Cancer	57	0.046

817	P	SBS003	Substance Abuse	55	0.046

818		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.046

819		MCC012	Mccune-Albright Syndrome	70	0.045

820	P	MYC084	Mycobacterium Tuberculosis 1	68	0.045

821	c	PLY105	Polycystic Ovary Syndrome 1	38	0.045

822		HYP006	Hypertensive Heart Disease	49	0.045

823		HDN002	Head Injury	46	0.045

824	P	VNS003	Venous Insufficiency	55	0.045

825	P	OPN001	Open-Angle Glaucoma	49	0.045

826	c	MCL013	Mucolipidosis Iv	66	0.045

827		CYT018	Cytochrome P450 2d6 Variant	27	0.045

828		WST001	West Syndrome	61	0.045

829		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.045

830	c	HPT003	Hepatitis a	62	0.045

831		CRC021	Carcinosarcoma	62	0.045

832	P	PRP029	Porphyria	62	0.045

833	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.045

834	P	LCH002	Lichen Planus	53	0.045

835		CLF001	Cleft Lip	53	0.045

836	P	OCL013	Oculodentodigital Dysplasia	69	0.044

837		VSC003	Visceral Leishmaniasis	55	0.044

838	P	MYC033	Myoclonus	46	0.044

839		ACT003	Acute Kidney Tubular Necrosis	45	0.044

840	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.044

841		CHL067	Cholecystitis	57	0.044

842		SKN013	Skin Benign Neoplasm	51	0.044

843		MSL001	Measles	62	0.044

844		OCL006	Ocular Hypertension	53	0.044

845		TST015	Testicular Disease	43	0.044

846		GLM044	Glomerular Disease	37	0.044

847	c	INF071	Inflammatory Bowel Disease 1	67	0.044

848	P	MVM001	Movement Disease	63	0.044

849	P	PRM006	Primary Biliary Cirrhosis	62	0.044

850	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.044

851	P	INT068	Intestinal Disease	53	0.044

852		GRW007	Growth Hormone Deficiency	46	0.044

853	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.044

854		CHR563	Chronic Eosinophilic Leukemia	48	0.044

855		CNN003	Conn's Syndrome	79	0.044

856		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.044

857	P	NMN002	Niemann-Pick Disease	59	0.044

858		INC002	Inclusion Body Myositis	58	0.044

859		SPN019	Spondylolisthesis	51	0.044

860		PRD004	Prediabetes Syndrome	47	0.044

861		BCT002	Bacterial Vaginosis	53	0.043

862	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.043

863		VRC005	Varicose Veins	60	0.043

864		DSS009	Disseminated Intravascular Coagulation	57	0.043

865		NRN004	Neuroendocrine Tumor	55	0.043

866	P	HYP050	Hyperinsulinemic Hypoglycemia	55	0.043

867		GSG001	Gas Gangrene	53	0.043

868	P	MGR003	Migraine with Aura	52	0.043

869	c	MTR002	Mitral Valve Insufficiency	48	0.043

870		ATN005	Autonomic Dysfunction	46	0.043

871	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.043

872	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.043

873		CLR030	Clear Cell Renal Cell Carcinoma	53	0.043

874		KRT009	Keratosis	51	0.043

875	P	MTC069	Mitochondrial Disorders	56	0.043

876	P	PTT006	Pituitary Adenoma	55	0.043

877		ACR041	Acromelic Frontonasal Dysostosis	52	0.043

878		HVY002	Heavy Metal Poisoning	22	0.043

879	c	GCH015	Gaucher Disease, Type I	70	0.043

880	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.043

881		PSR001	Psoriatic Arthritis	61	0.043

882		PMP006	Pemphigus Vulgaris, Familial	57	0.043

883	P	ANG001	Angelman Syndrome	69	0.043

884		PSY004	Psychotic Disorder	67	0.043

885	P	PNM006	Pneumoconiosis	56	0.043

886	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.043

887		BNG036	Bone Giant Cell Tumor	49	0.043

888		ANT018	Anthracosis	48	0.043

889	P	EPN001	Ependymoblastoma	44	0.043

890	P	ALP009	Alopecia Areata	60	0.043

891		AMN001	Amenorrhea	54	0.042

892		LWC001	Low Compliance Bladder	43	0.042

893	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.042

894	P	DNG005	Dengue Virus	59	0.042

895		PLC008	Placenta Disease	50	0.042

896		SPN020	Spondylosis	46	0.042

897		URN010	Urinary Tract Obstruction	55	0.042

898		SPN051	Spondylitis	51	0.042

899		CCN002	Cocaine Abuse	49	0.042

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

901		HPT046	Hepatic Veno-Occlusive Disease	56	0.042

902		ACT200	Acute Monoblastic Leukemia	52	0.042

903	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	60	0.042

904	P	ATS406	Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2	45	0.042

905		FML091	Familial Tumoral Calcinosis	44	0.042

906		PRT058	Pure Autonomic Failure	59	0.042

907		CRN288	Corneal Dystrophy, Band-Shaped	38	0.042

908	P	MCR010	Microcephaly	59	0.042

909		PRT038	Protein-Energy Malnutrition	54	0.042

910		CRH005	Crohn's Colitis	53	0.042

911		LYS002	Lysosomal Storage Disease	52	0.042

912		DYS015	Dysentery	52	0.042

913		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.042

914		URC002	Urea Cycle Disorder	51	0.041

915		CLF004	Cleft Lip/palate	54	0.041

916		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.041

917	c	BCT013	Bacterial Pneumonia	48	0.041

918	P	BCT020	Bacteremia 2	44	0.041

919		ATM052	Autoimmune Disease 1	37	0.041

920		WLF001	Wolff-Parkinson-White Syndrome	66	0.041

921		MCL006	Macular Retinal Edema	55	0.041

922		RSC001	Rosacea	54	0.041

923	c	INF145	Infantile Liver Failure Syndrome 1	50	0.041

924		DRY001	Dry Eye Syndrome	47	0.041

925		SPR008	Supratentorial Primitive Neuroectodermal Tumor	43	0.041

926		BSL009	Basal Ganglia Calcification	41	0.041

927	c	OVR114	Ovarian Cancer 1	38	0.041

928		BLL006	Bullous Pemphigoid	62	0.041

929		INF009	Inflammatory Spondylopathy	31	0.041

930	P	OLG002	Oligodendroglioma	67	0.041

931		ALL010	Allergic Contact Dermatitis	56	0.041

932		MDD018	Middle East Respiratory Syndrome	43	0.041

933		ANG049	Angioedema Induced by Ace Inhibitors	40	0.041

934		RFR009	Refractory Cytopenia with Multilineage Dysplasia	31	0.041

935	P	MNN013	Meningitis	66	0.041

936		INT146	Intervertebral Disc Disease	63	0.041

937		ERY003	Erythema Multiforme	58	0.041

938		NRT004	Neuritis	52	0.041

939		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.041

940		INT253	Intestinal Benign Neoplasm	45	0.041

941		TND004	Tendinopathy	43	0.041

942		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.041

943	P	ZLL001	Zellweger Syndrome	57	0.041

944		CLS052	Classic Hairy Cell Leukemia	27	0.041

945	c	CNG027	Congenital Hemolytic Anemia	50	0.041

946		NPH010	Nephrosclerosis	50	0.041

947	c	MLG069	Malignant Hypertension	47	0.041

948		PRT030	Parathyroid Gland Disease	45	0.041

949		PHS001	Phosphorus Metabolism Disease	40	0.041

950		INT075	Intracranial Hypertension	53	0.040

951		SCH012	Schizoaffective Disorder	50	0.040

952		NRT001	Neurotic Disorder	53	0.040

953	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.040

954	P	BCL013	B-Cell Adult Acute Lymphocytic Leukemia	32	0.040

955		CHC001	Chickenpox	60	0.040

956		RBS001	Rabies	58	0.040

957		NWB001	Newborn Respiratory Distress Syndrome	58	0.040

958		DFF003	Diffuse Scleroderma	41	0.040

959	c	SYS043	Systemic Lupus Erythematosus 1	38	0.040

960		RYN001	Raynaud Disease	48	0.040

961		DST006	Diastolic Heart Failure	45	0.040

962	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.039

963	c	ALM001	Al Amyloidosis	50	0.039

964		RFR002	Refractory Hairy Cell Leukemia	33	0.039

965		CRN036	Craniopharyngioma	65	0.039

966		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	65	0.039

967		LNG108	Langerhans Cell Histiocytosis	58	0.039

968		THR013	Thoracic Outlet Syndrome	54	0.039

969	P	MST002	Mast-Cell Leukemia	49	0.039

970		CND006	Candida Glabrata	32	0.039

971		HRP008	Herpes Simiae	25	0.039

972		FLL027	Fallopian Tube Carcinoma	67	0.039

973		AVN001	Avian Influenza	59	0.039

974		CMM005	Common Cold	57	0.039

975	c	HYP292	Hypophosphatasia, Infantile	57	0.039

976	P	PRC012	Pericardial Effusion	51	0.039

977		NPH018	Nephrogenic Systemic Fibrosis	50	0.039

978		HMP001	Hemopericardium	48	0.039

979		TST014	Testicular Cancer	46	0.039

980		ERY066	Erythema Multiforme Major	30	0.039

981		TRN018	Transitional Cell Carcinoma	56	0.039

982		CRT017	Cartilage Disease	54	0.039

983	P	MJR007	Major Affective Disorder 1	43	0.039

984		AMN006	Aminoaciduria	38	0.039

985		DNT010	Dentin Caries	32	0.039

986		CLF027	Cleft Palate, Isolated	64	0.039

987		ALL009	Allergic Conjunctivitis	50	0.039

988		GYN001	Gynecomastia	49	0.039

989	P	END039	Endodermal Sinus Tumor	44	0.039

990		TST018	Testicular Yolk Sac Tumor	39	0.039

991		INF021	Infant Gynecomastia	31	0.039

992	P	BLD062	Bile Duct Cancer	67	0.039

993		RHM001	Rheumatic Fever	60	0.039

994	P	PRN023	Prion Disease	57	0.039

995	P	THY032	Thyroiditis	52	0.039

996	c	BPL002	Bipolar I Disorder	49	0.039

997		BCK003	Background Diabetic Retinopathy	46	0.039

998	P	HMR005	Hemorrhoid	46	0.039

999		MST004	Mast Cell Neoplasm	42	0.039

1000	P	CLS010	Cluster Headache	42	0.039

1001		EXT007	Extracutaneous Mastocytoma	38	0.039

1002		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.039

1003	P	DNT007	Dentin Sensitivity	36	0.039

1004	P	INT143	Interstitial Cystitis	61	0.039

1005		ALC006	Alcoholic Hepatitis	61	0.039

1006		ACT058	Active Peptic Ulcer Disease	55	0.039

1007	c	CNT035	Central Nervous System Disease	52	0.039

1008		HYP781	Hypoascorbemia	51	0.039

1009		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.039

1010		SML008	Small Intestine Lymphoma	33	0.039

1011		TTH007	Tooth Erosion	31	0.039

1012		BRS051	Breast Disease	58	0.038

1013		BRD001	Brody Myopathy	57	0.038

1014	P	LMB006	Limb-Girdle Muscular Dystrophy	53	0.038

1015		FDL002	Food Allergy	51	0.038

1016	P	ART018	Aortic Valve Insufficiency	49	0.038

1017		THR035	Thrombasthenia	40	0.038

1018		MCN008	Mucinous Cystadenocarcinoma	40	0.038

1019		CYS010	Cystinosis	59	0.038

1020		PHN003	Phenylketonuria	75	0.038

1021		APL002	Aplasia of Lacrimal and Salivary Glands	57	0.038

1022	P	END033	Endocarditis	57	0.038

1023		CHR073	Choreatic Disease	52	0.038

1024		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	47	0.038

1025		CNT017	Central Nervous System Origin Vertigo	45	0.038

1026		URM005	Uremic Pruritus	42	0.038

1027		SCR011	Scrapie	39	0.038

1028		ADG002	Audiogenic Seizures	25	0.038

1029	P	SPN046	Spinal Muscular Atrophy	62	0.038

1030	P	BNG030	Benign Ependymoma	60	0.038

1031		CLL010	Cellular Ependymoma	54	0.038

1032		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.038

1033		DWR001	Dwarfism	44	0.038

1034		GRM004	Germinoma	40	0.038

1035		ACT011	Acute Contagious Conjunctivitis	40	0.038

1036	c	PRG106	Progressive Muscular Dystrophy	33	0.038

1037		ACN002	Acanthosis Nigricans	60	0.038

1038		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.038

1039		CLS016	Clostridium Difficile Colitis	48	0.038

1040		C1N001	C1 Inhibitor Deficiency	39	0.038

1041		PPL049	Papillon-Lefevre Syndrome	65	0.038

1042		END081	Endosteal Hyperostosis, Autosomal Dominant	60	0.038

1043		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	59	0.038

1044		ISL001	Islet Cell Tumor	56	0.038

1045		ART074	Aortic Dissection	52	0.038

1046		BHR001	Behr Syndrome	51	0.038

1047		OPT003	Opiate Dependence	50	0.038

1048		SNT005	Sinoatrial Node Disease	49	0.038

1049	P	CHL156	Childhood T-Cell Acute Lymphoblastic Leukemia	38	0.038

1050	c	HNT011	Huntington Disease-Like 3	38	0.038

1051		HRN029	Hearing Loss, Noise-Induced	37	0.038

1052		ENP001	Enophthalmos	35	0.038

1053	P	GLL018	Gallbladder Cancer	57	0.037

1054	c	VSC019	Vesicoureteral Reflux 1	57	0.037

1055		RTN020	Retinal Vascular Disease	46	0.037

1056		KLD004	Keloid Disorder	40	0.037

1057	P	WSK001	Wiskott-Aldrich Syndrome	72	0.037

1058		KRT006	Keratoconjunctivitis	53	0.037

1059		CHL018	Childhood Medulloblastoma	49	0.037

1060	c	DBT093	Diabetes Mellitus, Noninsulin-Dependent, 1	26	0.037

1061		SVR097	Severe Cutaneous Adverse Reaction	69	0.037

1062	c	PRM196	Premature Ovarian Failure 1	67	0.037

1063	P	HRD011	Hereditary Spherocytosis	60	0.037

1064		CRY005	Cryptococcosis	58	0.037

1065		LNG015	Lingual-Facial-Buccal Dyskinesia	50	0.037

1066	c	TCL001	T-Cell Adult Acute Lymphocytic Leukemia	43	0.037

1067		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.037

1068		CHN016	Cohen Syndrome	63	0.036

1069	P	HMC002	Homocystinuria	53	0.036

1070