Search results for Adenosine monophosphate

686 hits were found for Adenosine monophosphate

#	Family	MCID	Name	MIFTS	Score
1		MYP071	Myopathy Due to Myoadenylate Deaminase Deficiency	43	7.604

2		ERY039	Erythrocyte Amp Deaminase Deficiency	21	3.107

3		CHL014	Cholera	59	0.471

4		PRT037	Pertussis	65	0.426

5	P	NRB001	Neuroblastoma	72	0.301

6		ADN001	Adenosine Deaminase Deficiency	47	0.269

7		HYP266	Hypoxia	57	0.249

8		ISC004	Ischemia	58	0.249

9		IMM167	Immune Deficiency Disease	78	0.218

10		GLL048	Glial Tumor	45	0.208

11	P	GLM045	Glioma	63	0.206

12	P	HYP069	Hyperparathyroidism	63	0.190

13		CNG034	Congestive Heart Failure	69	0.185

14		48X005	48,xyyy	39	0.183

15	P	LKM002	Leukemia	68	0.179

16		ANX004	Anoxia	40	0.176

17	P	PHC003	Pheochromocytoma	71	0.175

18		ADR040	Adrenal Gland Pheochromocytoma	46	0.175

19		HLX001	Helix Syndrome	47	0.175

20	P	MYC084	Mycobacterium Tuberculosis 1	68	0.169

21	P	PLM037	Pulmonary Hypertension	67	0.168

22	P	HRP006	Herpes Simplex	65	0.168

23	P	HRT032	Heart Disease	75	0.166

24		HYP066	Hyperglycemia	61	0.166

25	P	SZR006	Seizure Disorder	56	0.165

26		VSL002	Visual Epilepsy	59	0.165

27	P	RHN004	Rhinitis	57	0.162

28	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.162

29		BNR002	Bone Resorption Disease	48	0.161

30		INS024	Insulin-Like Growth Factor I	79	0.159

31		AST005	Asthma	76	0.158

32		ALL003	Allergic Rhinitis	67	0.156

33	P	AST007	Astrocytoma	51	0.155

34		OST159	Osteogenic Sarcoma	66	0.155

35		HYP056	Hypoglycemia	66	0.154

36	c	PRM005	Primary Hyperparathyroidism	58	0.152

37		ALL006	Allergic Asthma	56	0.152

38	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.152

39	P	CRD119	Cardiac Arrest	67	0.151

40		PLR008	Pleurisy	50	0.150

41		ADN018	Adenoma	59	0.150

42	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.149

43		CHR074	Choriocarcinoma	47	0.148

44	P	HYP076	Hyperthyroidism	55	0.148

45	P	KDN018	Kidney Disease	72	0.148

46	P	ATR011	Atrial Fibrillation	66	0.146

47		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.145

48		CYS001	Cystic Fibrosis	81	0.144

49	c	ACT075	Acute Myocardial Infarction	57	0.144

50	P	MNN013	Meningitis	66	0.144

51		LNG099	Lung Disease	60	0.143

52	P	CLR023	Colorectal Cancer	99	0.143

53	P	LVR013	Liver Disease	68	0.143

54		IMP005	Impotence	52	0.141

55	P	TRM003	Tremor	54	0.141

56	P	HYP086	Hypothyroidism	69	0.140

57	c	PRC016	Pre-Eclampsia	63	0.138

58	c	HYP595	Hypertension, Essential	84	0.138

59	P	CRN300	Coronary Heart Disease 1	63	0.138

60		FTT001	Fatty Liver Disease	61	0.137

61		CRB004	Cerebral Artery Occlusion	45	0.136

62		ALL026	Allergic Hypersensitivity Disease	62	0.135

63	P	GRV001	Graves' Disease	55	0.135

64	c	MCR113	Microvascular Complications of Diabetes 3	52	0.134

65	c	MCR120	Microvascular Complications of Diabetes 7	47	0.134

66	c	MCR130	Microvascular Complications of Diabetes 6	41	0.134

67	c	MCR133	Microvascular Complications of Diabetes 4	41	0.134

68		LVR012	Liver Cirrhosis	62	0.132

69		PTT037	Pituitary Tumors	44	0.131

70	P	BRS047	Breast Cancer	97	0.130

71		GLB015	Glioblastoma Multiforme	75	0.129

72		CYT002	Cytokine Deficiency	42	0.128

73	P	LYM118	Lymphoma	68	0.128

74	P	HML002	Hemolytic Anemia	63	0.128

75	c	SYS001	Systemic Lupus Erythematosus	86	0.127

76	P	PRK057	Parkinson Disease, Late-Onset	78	0.126

77	P	VSC007	Vascular Disease	63	0.126

78		ANG054	Angina Pectoris	66	0.125

79		SPN186	Spinal Cord Injury	60	0.125

80		WLF001	Wolff-Parkinson-White Syndrome	66	0.124

81	P	HNT016	Huntington Disease	72	0.123

82		HMN044	Human Immunodeficiency Virus Type 1	71	0.121

83	P	ADN016	Adenocarcinoma	64	0.119

84	P	NRP001	Neuropathy	56	0.119

85	P	OVR042	Ovarian Cancer	88	0.119

86		LYM027	Lymphopenia	58	0.119

87		THY029	Thyroid Carcinoma	59	0.119

88		IGR001	Ige Responsiveness, Atopic	59	0.119

89	P	MYC007	Myocardial Infarction	70	0.118

90	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.117

91	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.117

92		HYP060	Hyperinsulinism	54	0.117

93		PRT036	Peritonitis	64	0.117

94	P	DBT005	Diabetes Insipidus	55	0.117

95	c	ACT073	Acute Leukemia	58	0.116

96	P	MYL006	Myeloid Leukemia	60	0.116

97		SYN036	Syncope	45	0.116

98		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.115

99	P	DRM053	Dermatitis, Atopic	66	0.115

100		OCL069	Ocular Motor Apraxia	51	0.114

101		BRN071	Brain Injury	49	0.113

102	P	PSD015	Pseudohypoparathyroidism	56	0.113

103		DPR016	Depression	63	0.113

104		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.113

105	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.112

106		MYL069	Myeloma, Multiple	85	0.112

107	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.111

108		ATM095	Autoimmune Disease	62	0.111

109	P	HYP024	Hypoparathyroidism	56	0.110

110		VCC001	Vaccinia	49	0.110

111	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.110

112		TXC005	Toxic Shock Syndrome	62	0.110

113		PNG002	Pain Agnosia	51	0.108

114	c	HPT016	Hepatitis B	59	0.108

115	P	PSR002	Psoriasis	62	0.108

116		PST011	Pustulosis of Palm and Sole	52	0.108

117		MST004	Mast Cell Neoplasm	42	0.107

118		EXT007	Extracutaneous Mastocytoma	38	0.107

119	P	RHM011	Rheumatoid Arthritis	80	0.107

120		DBT010	Diabetic Neuropathy	54	0.106

121		PLM001	Pulmonary Tuberculosis	69	0.104

122	P	LTR001	Lateral Sclerosis	54	0.104

123		DRM006	Dermatitis	61	0.103

124	P	ALZ034	Alzheimer Disease	88	0.103

125	P	SCK005	Sickle Cell Disease	50	0.103

126	c	ACT071	Acute Kidney Failure	60	0.103

127	P	GRF003	Graft-Versus-Host Disease	72	0.102

128		DFC004	Deficiency Anemia	70	0.101

129		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.101

130		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.099

131		ANX010	Anxiety	73	0.098

132		TTN003	Tetanus	65	0.098

133		GST033	Gestational Diabetes	61	0.098

134		PPT005	Peptic Ulcer Disease	59	0.098

135		PLM010	Pulmonary Edema	54	0.098

136	P	ENC004	Encephalitis	61	0.096

137	P	HYP098	Hypereosinophilic Syndrome	67	0.096

138	P	MCR115	Microvascular Complications of Diabetes 5	66	0.096

139	P	DBT009	Diabetes Mellitus	64	0.096

140	c	HPT073	Hepatitis C Virus	72	0.095

141		TRM010	Traumatic Brain Injury	51	0.095

142		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.094

143	P	BCL017	B-Cell Lymphoma	58	0.093

144	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.093

145	P	PLM036	Pulmonary Fibrosis	65	0.093

146		ATH013	Atherosclerosis Susceptibility	65	0.093

147	P	PRS040	Prostate Cancer	97	0.093

148	P	VSC011	Vasculitis	62	0.092

149		PPL052	Papillomatosis, Confluent and Reticulated	33	0.092

150	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.091

151		MTB004	Metabolic Acidosis	50	0.090

152	c	CHR684	Chronic Kidney Disease	70	0.090

153	P	PNC035	Pancreatic Cancer	84	0.090

154	c	SVR001	Severe Acute Respiratory Syndrome	62	0.089

155	P	GST053	Gastric Cancer	83	0.089

156	c	DLT002	Dilated Cardiomyopathy	79	0.089

157	P	LPS004	Lupus Erythematosus	61	0.089

158		ADR016	Adrenal Cortical Carcinoma	48	0.088

159		ADR004	Adrenal Cortical Adenocarcinoma	39	0.088

160	P	GLM007	Glomerulonephritis	57	0.087

161	c	LKM061	Leukemia, Acute Myeloid	84	0.087

162	c	DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.087

163		CHC001	Chickenpox	60	0.087

164		LPD008	Lipid Metabolism Disorder	62	0.086

165		ERY051	Erythroleukemia, Familial	56	0.086

166	P	LNG032	Lung Cancer	98	0.085

167	P	MLN008	Melanoma	69	0.085

168	c	BCT007	Bacterial Meningitis	55	0.085

169	P	INF037	Inflammatory Bowel Disease	54	0.085

170	P	NTR004	Neutropenia	63	0.085

171	P	BLD134	Bladder Cancer	79	0.084

172		MNT002	Mental Depression	58	0.084

173		RCK004	Rickets	68	0.084

174		INS001	Insulinoma	60	0.084

175	P	THR014	Thrombocytopenia	67	0.084

176		GTR002	Goiter	53	0.084

177	c	VRL010	Viral Hepatitis	52	0.084

178		LYM019	Lymphosarcoma	46	0.084

179		CLT003	Colitis	62	0.083

180		STR067	Stroke, Ischemic	81	0.083

181		RTN023	Retinitis	46	0.082

182		NRR001	Neuroretinitis	42	0.082

183		STT001	Status Epilepticus	60	0.082

184		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.082

185	P	PRP019	Peripheral Nervous System Disease	58	0.082

186	P	MJR001	Major Depressive Disorder	68	0.081

187		WTH001	Withdrawal Disorder	48	0.081

188		TRN015	Transient Cerebral Ischemia	63	0.081

189		END086	End Stage Renal Disease	51	0.081

190		RNL077	Renal Fibrosis	47	0.081

191	c	ATR087	Atrial Standstill 1	75	0.081

192		SLP001	Sleeping Sickness	54	0.081

193	P	BPL003	Bipolar Disorder	56	0.080

194	c	MJR024	Major Affective Disorder 9	41	0.080

195	c	MJR022	Major Affective Disorder 8	38	0.080

196	c	GRV008	Graves Disease 1	56	0.080

197	P	DRR001	Diarrhea	55	0.080

198		MSL001	Measles	62	0.079

199		DPH001	Diphtheria	60	0.079

200		MLR004	Malaria	81	0.078

201		INT007	Intermediate Coronary Syndrome	55	0.077

202		ACQ007	Acquired Immunodeficiency Syndrome	60	0.077

203		STM007	Stomatitis	50	0.077

204		47X002	47,xyy	49	0.077

205	P	MSC005	Muscular Dystrophy	66	0.076

206	P	CHR012	Chronic Granulomatous Disease	67	0.076

207	P	PLY014	Polycystic Kidney Disease	62	0.076

208	c	LKM063	Leukemia, Chronic Myeloid	72	0.076

209		CLN015	Colon Adenocarcinoma	65	0.076

210		SKN016	Skin Disease	63	0.076

211		TRT001	Teratocarcinoma	45	0.075

212		LYD001	Leydig Cell Tumor	45	0.075

213	P	HPT023	Hepatocellular Carcinoma	100	0.075

214	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.075

215	P	MLT020	Multiple Sclerosis	72	0.075

216	P	ART022	Arthritis	69	0.075

217		BCT022	Bacterial Infectious Disease	56	0.074

218	P	ECL001	Eclampsia	50	0.074

219		BRN004	Brain Edema	56	0.074

220		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.074

221		IRN002	Iron Metabolism Disease	57	0.074

222		URD002	Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to	25	0.073

223		ALC007	Alcohol Dependence	66	0.073

224	P	RTN008	Retinitis Pigmentosa	79	0.073

225	P	DYS154	Dystonia	65	0.073

226		MDD011	Mood Disorder	62	0.073

227		THR024	Thrombosis	57	0.073

228		URT010	Ureteral Obstruction	45	0.073

229	c	PCH010	Pachyonychia Congenita 3	44	0.073

230		ALL014	Allergic Encephalomyelitis	38	0.072

231	P	CNR004	Cone-Rod Dystrophy 2	73	0.072

232		PRS045	Prostatic Hypertrophy	53	0.072

233		PRT029	Parathyroid Adenoma	50	0.071

234		ESP021	Esophageal Cancer	90	0.071

235		CRB039	Cerebrovascular Disease	67	0.071

236	P	MYP006	Myopia	55	0.071

237		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.071

238		HMP009	Haemophilus Influenzae	43	0.071

239		OVR094	Ovarian Epithelial Cancer	38	0.071

240		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.071

241	P	SLP006	Sleep Apnea	69	0.070

242	P	ALC033	Alcohol Use Disorder	58	0.070

243		HYP005	Hypokalemia	55	0.070

244		LWC001	Low Compliance Bladder	43	0.070

245	P	RTN024	Retinoblastoma	73	0.069

246		DWN001	Down Syndrome	70	0.069

247		PST028	Post-Traumatic Stress Disorder	58	0.069

248	c	FML008	Familial Retinoblastoma	53	0.069

249		ACT084	Acute Stress Disorder	47	0.069

250	P	SRC025	Sarcoidosis 1	70	0.069

251	P	RSP003	Respiratory Failure	74	0.069

252		GT001	Gout	64	0.069

253	P	INF032	Infertility	57	0.069

254		PLY150	Polykaryocytosis Inducer	31	0.069

255	P	PNM007	Pneumonia	68	0.069

256		AMN003	Amnestic Disorder	54	0.069

257	c	ACT027	Acute Pancreatitis	60	0.068

258	c	LKM005	Leukemia, T-Cell, Chronic	34	0.068

259		BRN024	Bronchitis	68	0.067

260		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.067

261		LSC001	Lesch-Nyhan Syndrome	62	0.067

262		CHL068	Cholestasis	61	0.067

263	P	FBR017	Fibrosarcoma	56	0.067

264	P	THY032	Thyroiditis	52	0.067

265		ARG004	Argyria	27	0.067

266		MYL009	Myelodysplastic Syndrome	70	0.066

267	P	GST044	Gastritis	56	0.066

268	c	SCN007	Secondary Hyperparathyroidism	51	0.066

269	P	MYS003	Myasthenia Gravis	68	0.065

270		GST023	Gastric Ulcer	53	0.065

271		TRY001	Trypanosomiasis	50	0.065

272		HYP017	Hypophosphatemia	50	0.065

273	P	PLY011	Polycystic Ovary Syndrome	56	0.064

274	P	MLN007	Male Infertility	55	0.064

275		PRS021	Prostatic Adenoma	51	0.064

276		CRT015	Carotid Artery Occlusion	45	0.064

277	P	ADL010	Adult Respiratory Distress Syndrome	65	0.064

278		THY122	Thyroid Gland Cancer	57	0.064

279	P	MYP004	Myopathy	70	0.063

280	P	BND020	Bone Disease	59	0.063

281	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.063

282		HPT004	Hepatic Coma	45	0.063

283	P	SCH015	Schizophrenia	74	0.063

284	P	ENC018	Encephalopathy	61	0.063

285	P	UVT001	Uveitis	57	0.063

286		HRP004	Herpes Zoster	60	0.063

287		SCK003	Sickle Cell Anemia	74	0.062

288		PNC129	Pancreatic Adenocarcinoma	68	0.062

289	P	END044	Endometriosis	63	0.062

290		PRS129	Prostatic Hyperplasia, Benign	49	0.062

291		URM002	Uremia	49	0.062

292	c	ATM011	Autoimmune Hepatitis	63	0.061

293		MYX004	Myxedema	43	0.061

294		OST012	Osteoarthritis	78	0.061

295		CRV035	Cervical Cancer	76	0.061

296	P	SYS005	Systemic Scleroderma	68	0.061

297	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.061

298		AGN016	Aging	56	0.061

299		ASP003	Aseptic Meningitis	51	0.061

300		RTN020	Retinal Vascular Disease	46	0.061

301		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.061

302		BRN002	Bronchiolitis	59	0.061

303		HRY003	Hairy Cell Leukemia	55	0.061

304		ATS010	Autosomal Recessive Disease	48	0.061

305	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.059

306		NRM005	Neuromuscular Disease	64	0.059

307	c	WLM018	Wilms Tumor 5	61	0.059

308		PRT013	Portal Hypertension	59	0.059

309		BRN056	Bronchopulmonary Dysplasia	57	0.059

310	c	MLG068	Malignant Glioma	46	0.059

311	P	LNG064	Lung Cancer Susceptibility 3	78	0.059

312		ULC004	Ulcerative Colitis	73	0.059

313	P	HYP061	Hypertrophic Cardiomyopathy	70	0.059

314		HYP014	Hyperuricemia	52	0.059

315		NTR046	Neutrophil Migration	50	0.059

316	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.059

317	P	PRD008	Periodontitis	64	0.059

318	P	MYC008	Myocarditis	59	0.059

319	P	BRS044	Breast Adenocarcinoma	59	0.059

320		EYD002	Eye Disease	58	0.059

321		BRN012	Bronchiolitis Obliterans	55	0.059

322	P	ART021	Arteriosclerosis	54	0.059

323	P	RNV001	Renovascular Hypertension	48	0.059

324		MRP001	Morphine Dependence	41	0.059

325		KRT019	Keratitis, Hereditary	65	0.057

326		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.057

327	c	SCL052	Scleroderma, Familial Progressive	61	0.057

328	P	DNG005	Dengue Virus	59	0.057

329	P	OST001	Osteopetrosis	70	0.057

330		LYM133	Lymphoma, Hodgkin, Classic	69	0.057

331	P	HPT021	Hepatitis	67	0.057

332	c	HPT001	Hepatitis C	62	0.057

333	P	NPH012	Nephrotic Syndrome	60	0.057

334	P	CTR002	Cataract	60	0.057

335		NPH009	Nephrolithiasis	55	0.057

336		LYM040	Lymphoblastic Lymphoma	54	0.057

337	c	ACT135	Acute Graft Versus Host Disease	52	0.057

338	P	OST002	Osteoporosis	74	0.056

339	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.056

340		INT002	Intermittent Claudication	61	0.056

341		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.056

342		GLC003	Glucose Intolerance	54	0.056

343		THR013	Thoracic Outlet Syndrome	54	0.056

344	c	INH020	Inherited Metabolic Disorder	47	0.056

345	P	DMN001	Diamond-Blackfan Anemia	69	0.055

346	P	EXN002	Exanthem	57	0.055

347		HMC014	Homocysteinemia	53	0.055

348		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.054

349		SPL018	Splenomegaly	48	0.054

350	P	VTR007	Vitreoretinopathy	46	0.054

351	c	CHR064	Chronic Monocytic Leukemia	33	0.054

352		END057	Endometrial Cancer	74	0.054

353		CHG001	Chagas Disease	66	0.054

354		PLG002	Plague	63	0.054

355	P	THL005	Thalassemia	60	0.054

356		ILT001	Ileitis	50	0.054

357		NWC001	Newcastle Disease	45	0.054

358		HND015	Hand Skill, Relative	33	0.054

359		ACR007	Acromegaly	71	0.053

360		ACT119	Acute Promyelocytic Leukemia	63	0.053

361		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.053

362		PLY023	Polycystic Liver Disease	57	0.053

363	P	PTT006	Pituitary Adenoma	55	0.053

364	P	FML068	Familial Hypocalciuric Hypercalcemia	54	0.053

365		PPL002	Papillary Carcinoma	47	0.053

366		SPR126	Superior Semicircular Canal Dehiscence	40	0.053

367	c	HMG029	Hemoglobin Se Disease	39	0.053

368	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.053

369		PLS037	Plasma Cell Tumor	22	0.053

370	P	THY023	Thymoma	65	0.053

371	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.053

372		INT066	Interstitial Lung Disease	60	0.053

373	P	OPT006	Optic Nerve Disease	60	0.053

374		NNL006	Non-Alcoholic Steatohepatitis	54	0.053

375		PRP016	Paraplegia	52	0.053

376	c	THY107	Thymoma, Familial	52	0.053

377		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.053

378		ATX019	Ataxia with Vitamin E Deficiency	42	0.053

379	c	MCR129	Microvascular Complications of Diabetes 1	66	0.051

380	P	PRP029	Porphyria	62	0.051

381	c	ACT134	Acute Liver Failure	56	0.051

382		LMB062	Limb Ischemia	55	0.051

383		DFF005	Diffuse Large B-Cell Lymphoma	55	0.051

384	P	MNC007	Monocytic Leukemia	53	0.051

385		CLR109	Colorectal Adenocarcinoma	51	0.051

386		CRB090	Cerebral Hypoxia	44	0.051

387	P	HYP265	Hypotonia	43	0.051

388	c	MCR112	Microvascular Complications of Diabetes 2	41	0.051

389		ADG002	Audiogenic Seizures	25	0.051

390	c	TBR025	Tuberous Sclerosis 1	77	0.051

391		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.051

392		GST040	Gastric Adenocarcinoma	70	0.051

393	P	TBR001	Tuberous Sclerosis	70	0.051

394		IRR002	Irritable Bowel Syndrome	65	0.051

395	P	INT068	Intestinal Disease	53	0.051

396		THY030	Thyroid Gland Disease	52	0.051

397		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.051

398		GST045	Gastroenteritis	59	0.049

399		PLS009	Plasma Cell Neoplasm	51	0.049

400		DWR001	Dwarfism	44	0.049

401		SCH014	Schistosomiasis	57	0.049

402		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	45	0.049

403		IMM136	Immune System Disease	45	0.049

404		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.049

405	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.049

406		WST005	West Nile Virus	54	0.049

407		PRN011	Pernicious Anemia	53	0.049

408		NRT004	Neuritis	52	0.049

409	c	PRG020	Paragangliomas 3	39	0.049

410		THY111	Thyroid Carcinoma, Familial Medullary	67	0.047

411		CLF027	Cleft Palate, Isolated	64	0.047

412	P	CRN038	Carney Complex Variant	61	0.047

413	P	PLY019	Polyneuropathy	56	0.047

414	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	55	0.047

415	P	CYS039	Cystic Kidney Disease	54	0.047

416	P	RTN016	Retinal Degeneration	53	0.047

417	c	VRL007	Viral Encephalitis	51	0.047

418		THY125	Thyroid Gland Medullary Carcinoma	50	0.047

419	P	OPN001	Open-Angle Glaucoma	49	0.047

420	P	HYP263	Hypersomnia	41	0.047

421		MYT011	Myotonia	34	0.047

422		SRC014	Sarcoma	65	0.046

423	P	RHB003	Rhabdomyosarcoma	63	0.046

424	P	HYP750	Hypertriglyceridemia, Familial	62	0.046

425		HPT019	Hepatic Encephalopathy	60	0.046

426		CNS004	Constipation	58	0.046

427		DSS009	Disseminated Intravascular Coagulation	57	0.046

428	P	CHN012	Chondrosarcoma	56	0.046

429		PNC001	Pancytopenia	54	0.046

430	c	DMN023	Diamond-Blackfan Anemia 1	53	0.046

431		NNT012	Neonatal Jaundice	53	0.046

432	P	RTN018	Retinal Disease	53	0.046

433	P	OVR082	Overgrowth Syndrome	50	0.046

434	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.046

435	c	RTN047	Retinitis Pigmentosa 18	42	0.046

436	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.046

437	c	CHR417	Chronic Graft Versus Host Disease	57	0.044

438		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.044

439		SXL003	Sexual Disorder	47	0.044

440		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.044

441		MYL005	Myelofibrosis	70	0.043

442	P	TRN020	Turner Syndrome	67	0.043

443		PTT046	Pituitary Hormone Deficiency, Combined, 2	64	0.043

444	P	PRM006	Primary Biliary Cirrhosis	62	0.043

445		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.043

446	P	GLL022	Guillain-Barre Syndrome	59	0.043

447		HPT022	Hepatoblastoma	56	0.043

448		MYM001	Myoma	54	0.043

449	P	PRM051	Primary Pigmented Nodular Adrenocortical Disease	53	0.043

450		OST011	Osteomalacia	52	0.043

451	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.043

452		NDL007	Nodular Goiter	47	0.043

453		PLL012	Pollen Allergy	46	0.043

454	P	BRB001	Beriberi	46	0.043

455	c	CRN278	Craniosynostosis 1	45	0.043

456		URL001	Urolithiasis	45	0.043

457		ADR041	Adrenal Cortical Adenoma	43	0.043

458		IDP073	Idiopathic Hypercalciuria	43	0.043

459	c	HMP023	Hemophagocytic Lymphohistiocytosis, Familial, 5	41	0.043

460		LNG030	Lung Adenoma	39	0.043

461	c	RTH007	Rothmund-Thomson Syndrome, Type 1	37	0.043

462		SCR003	Secretory Diarrhea	37	0.043

463		PFF001	Pfeiffer Syndrome	79	0.043

464		MYC006	Mycosis Fungoides	66	0.043

465		HYP020	Hyperprolactinemia	64	0.043

466		HSH003	Hashimoto Thyroiditis	62	0.043

467		RTN017	Retinal Detachment	61	0.043

468		CHL123	Chlamydia	59	0.043

469		PRT058	Pure Autonomic Failure	59	0.043

470		ANT024	Anthrax Disease	58	0.043

471		PYR041	Pyruvate Kinase Deficiency of Red Cells	57	0.043

472		PLS011	Plasmacytoma	56	0.043

473		MCL006	Macular Retinal Edema	55	0.043

474		END040	Endogenous Depression	55	0.043

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

476		SPN035	Spindle Cell Sarcoma	53	0.043

477	c	CHR418	Chronic Leukemia	49	0.043

478		MCR004	Macroglobulinemia	49	0.043

479		KRT002	Keratomalacia	47	0.043

480		ORL015	Oral Squamous Cell Carcinoma	43	0.043

481		HRW001	Hair Whorl	36	0.043

482		DSR074	Disorder of Purine Metabolism	29	0.043

483		PST092	Posttransplant Acute Limbic Encephalitis	29	0.043

484		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.040

485	c	NRF023	Neurofibromatosis, Type Ii	80	0.040

486	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.040

487		APN008	Apnea, Obstructive Sleep	64	0.040

488		NRF007	Neurofibroma	64	0.040

489	P	ANR048	Aniridia 1	63	0.040

490		END041	Endometrial Adenocarcinoma	63	0.040

491		ANR007	Anorexia Nervosa	63	0.040

492	c	ANM038	Anemia, Autoimmune Hemolytic	62	0.040

493		ACN002	Acanthosis Nigricans	60	0.040

494	P	URT039	Urticaria	58	0.040

495	P	SLM003	Salmonellosis	55	0.040

496		DMY004	Demyelinating Disease	52	0.040

497	P	ACT105	Acute Mountain Sickness	52	0.040

498	P	LCT001	Lactic Acidosis	51	0.040

499	P	CHL066	Cholangitis	51	0.040

500		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.040

501	P	OBS001	Obstructive Jaundice	50	0.040

502	c	CNG027	Congenital Hemolytic Anemia	50	0.040

503		SBS004	Substance Dependence	48	0.040

504		OPD006	Opioid Addiction	48	0.040

505	P	PRD021	Periodic Paralysis	45	0.040

506		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.040

507		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.040

508		OCL052	Ocular Dominance	42	0.040

509		MCL003	Macular Holes	40	0.040

510		WLL004	Wallerian Degeneration	39	0.040

511		ATX010	Ataxia Neuropathy Spectrum	34	0.040

512	c	PRG106	Progressive Muscular Dystrophy	33	0.040

513		ACT064	Acute Necrotizing Encephalitis	33	0.040

514		PLT016	Platelet Adenylate Cyclase Activity	16	0.040

515		BLD137	Blood Group--Ahonen	16	0.040

516		LKC009	Leukocyte Adhesion Deficiency, Type I	69	0.038

517	P	FLL037	Follicular Lymphoma	67	0.038

518		CHD001	Chediak-Higashi Syndrome	66	0.038

519	c	PSD108	Pseudohypoparathyroidism, Type Ia	66	0.038

520		NRL005	Neurilemmoma	60	0.038

521	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.038

522		PSD014	Pseudopseudohypoparathyroidism	55	0.038

523		MMM001	Mammary Paget's Disease	53	0.038

524		MGL001	Megaloblastic Anemia	51	0.038

525		ATY042	Atypical Chronic Myeloid Leukemia	49	0.038

526		CHL004	Cholelithiasis	49	0.038

527		CWP001	Cowpox	46	0.038

528		RSP021	Respiratory Allergy	45	0.038

529		SBC016	Subacute Delirium	44	0.038

530		ADN022	Adenylosuccinase Deficiency	44	0.038

531	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.038

532		CNN003	Conn's Syndrome	79	0.036

533		ADR007	Adrenoleukodystrophy	75	0.036

534		LGH007	Leigh Syndrome	70	0.036

535	P	FRG001	Fragile X Syndrome	70	0.036

536	c	RHB024	Rhabdomyosarcoma 2	67	0.036

537	c	WLM013	Wilms Tumor 1	65	0.036

538		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.036

539		MSC007	Muscle Hypertrophy	64	0.036

540	c	GLC092	Glaucoma, Primary Open Angle	62	0.036

541	c	ALP101	Alpha-Thalassemia	62	0.036

542		VRC005	Varicose Veins	60	0.036

543		DSS008	Disease of Mental Health	58	0.036

544	P	BNC003	Bone Cancer	58	0.036

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

546	P	FTL001	Fetal Alcohol Syndrome	57	0.036

547	c	LKM070	Leukemia, Acute Monocytic	57	0.036

548		CYT008	Cytomegalovirus Infection	57	0.036

549		MTH009	Mouth Disease	56	0.036

550		HMG005	Hemoglobinopathy	56	0.036

551	P	NRF002	Neurofibromatosis	56	0.036

552		SML019	Smallpox	56	0.036

553	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.036

554		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.036

555		GNG005	Gangliocytoma	55	0.036

556	P	PMP001	Pemphigus	54	0.036

557	P	HYP083	Hypopituitarism	53	0.036

558	P	PTS002	Ptosis	53	0.036

559	c	OST131	Osteopetrosis, Autosomal Dominant 2	53	0.036

560		GNG002	Ganglioneuroma	52	0.036

561	P	RCT021	Rectum Cancer	52	0.036

562		ACT200	Acute Monoblastic Leukemia	52	0.036

563		THR004	Thrombocytosis	51	0.036

564	P	SPP010	Suppressor of Tumorigenicity 3	51	0.036

565	c	SVR005	Severe Pre-Eclampsia	50	0.036

566		ECT026	Ectopic Pregnancy	50	0.036

567		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	49	0.036

568		MDD018	Middle East Respiratory Syndrome	43	0.036

569		SNL007	Senile Cataract	42	0.036

570		PST053	Postherpetic Neuralgia	40	0.036

571		PLY100	Polyploidy	40	0.036

572	P	PRC031	Preeclampsia/eclampsia 1	38	0.036

573		ADR022	Adrenomyeloneuropathy	38	0.036

574		CGH001	Cough Variant Asthma	37	0.036

575		ALC001	Alcohol-Related Birth Defect	36	0.036

576		AST002	Astroblastoma	34	0.036

577	c	BLD140	Blood Group, I System	32	0.036

578	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.036

579		PNF002	Painful Legs and Moving Toes Syndrome	14	0.036

580		BRN028	Brain Cancer	74	0.031

581	P	FML011	Familial Adenomatous Polyposis	72	0.031

582		MCC012	Mccune-Albright Syndrome	70	0.031

583	P	TTR001	Tetralogy of Fallot	70	0.031

584		PLY001	Polycythemia Vera	69	0.031

585	P	INF038	Influenza	68	0.031

586	P	PRP003	Porphyria Cutanea Tarda	67	0.031

587		THY121	Thyroid Gland Anaplastic Carcinoma	66	0.031

588	P	SKN015	Skin Carcinoma	66	0.031

589		GRG001	Greig Cephalopolysyndactyly Syndrome	66	0.031

590		LBR036	Leber Plus Disease	66	0.031

591	P	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	64	0.031

592		CLR108	Colorectal Adenoma	64	0.031

593		DSM004	Desmoid Tumor	64	0.031

594		HMT002	Hematologic Cancer	62	0.031

595		OST003	Osteonecrosis	61	0.031

596		SDD001	Sudden Infant Death Syndrome	61	0.031

597	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.031

598		DNG002	Dengue Hemorrhagic Fever	60	0.031

599	P	MCR010	Microcephaly	59	0.031

600		FML063	Familial Glucocorticoid Deficiency	58	0.031

601		ADR005	Adrenal Carcinoma	58	0.031

602		CHL028	Childhood Type Dermatomyositis	58	0.031

603	c	DWL002	Dowling-Degos Disease 1	58	0.031

604	c	THY102	Thyroid Cancer, Nonmedullary, 2	58	0.031

605		PMP006	Pemphigus Vulgaris, Familial	57	0.031

606	P	GLL020	Gallbladder Disease	57	0.031

607		MCR013	Microphthalmia	57	0.031

608	P	PLY018	Polycythemia	56	0.031

609		HPT046	Hepatic Veno-Occlusive Disease	56	0.031

610	P	MLT074	Multiple Endocrine Neoplasia	56	0.031

611		ISL001	Islet Cell Tumor	56	0.031

612		SNS003	Sensory Peripheral Neuropathy	54	0.031

613	P	LCH002	Lichen Planus	53	0.031

614	P	END047	Endophthalmitis	53	0.031

615	P	INS002	in Situ Carcinoma	53	0.031

616	P	RNL017	Renal Oncocytoma	53	0.031

617		CLF001	Cleft Lip	53	0.031

618	c	HYP374	Hypothyroidism, Congenital, Nongoitrous, 1	53	0.031

619		OVR059	Ovary Adenocarcinoma	53	0.031

620		CHN054	Chondrodysplasia, Blomstrand Type	52	0.031

621		DRM011	Dermatophytosis	52	0.031

622		HRP009	Herpes Simplex Encephalitis	52	0.031

623	P	BRT004	Bartter Disease	52	0.031

624	c	HYP243	Hyperparathyroidism 1	51	0.031

625	c	NMN014	Niemann-Pick Disease, Type C2	51	0.031

626		MTP034	Metaphyseal Chondrodysplasia, Jansen Type	51	0.031

627		ESP002	Esophageal Varix	51	0.031

628		HND002	Hand, Foot and Mouth Disease	51	0.031

629		SGW002	Segawa Syndrome, Autosomal Recessive	51	0.031

630		ACT017	Acute Chest Syndrome	51	0.031

631		LNT004	Lentigines	50	0.031

632	c	PYR010	Peyronie's Disease	50	0.031

633		LPD016	Lipoid Proteinosis of Urbach and Wiethe	50	0.031

634	P	PNV001	Panuveitis	50	0.031

635		RNL011	Renal Osteodystrophy	50	0.031

636		ERY004	Erysipelas	49	0.031

637	P	CTN015	Cutaneous T Cell Lymphoma	49	0.031

638	c	46X049	46,xy Sex Reversal 2	48	0.031

639		DBT006	Diabetic Macular Edema	48	0.031

640		FBR009	Fibrous Dysplasia	48	0.031

641		RCT020	Rectum Adenocarcinoma	48	0.031

642		VTM002	Vitamin B12 Deficiency	48	0.031

643		PRL017	Prolymphocytic Leukemia	47	0.031

644		THY128	Thyroid Tumor	47	0.031

645		ANV001	Anovulation	47	0.031

646		RYN005	Raynaud Phenomenon	47	0.031

647	P	MTH007	Methemoglobinemia	46	0.031

648		GRW007	Growth Hormone Deficiency	46	0.031

649		LKS001	Leukostasis	46	0.031

650	c	SBC007	Subacute Thyroiditis	45	0.031

651		RTR001	Retrograde Amnesia	44	0.031

652	P	END039	Endodermal Sinus Tumor	44	0.031

653		IDP033	Idiopathic Edema	44	0.031

654	P	ATX039	Ataxia-Pancytopenia Syndrome	43	0.031

655		ANC002	Anca-Associated Vasculitis	41	0.031

656		DDN003	Duodenum Adenocarcinoma	41	0.031

657		PRS063	Paresthesia	41	0.031

658		ISL151	Isolated Elevated Serum Creatine Phosphokinase Levels	40	0.031

659		TST018	Testicular Yolk Sac Tumor	39	0.031

660		MYP001	Myoepithelioma	38	0.031

661		DBT092	Diabetes Insipidus, Nephrogenic, X-Linked	38	0.031

662		HRM003	Hormone Producing Pituitary Cancer	37	0.031

663	P	FML187	Familial Hypertension	37	0.031

664		HYP026	Hypoglycemic Coma	36	0.031

665	c	CRN277	Craniosynostosis 2	36	0.031

666		WHP002	Whiplash	36	0.031

667		INT040	Intrinsic Asthma	34	0.031

668		PTT001	Pituitary Hypoplasia	34	0.031

669		TQP001	Taqi Polymorphism	32	0.031

670		SLW005	Slowed Nerve Conduction Velocity, Autosomal Dominant	32	0.031

671	c	PSD104	Pseudohypoparathyroidism, Type Ii	31	0.031

672		SNG003	Single Ventricular Heart	30	0.031

673		GRV012	Grover's Disease	30	0.031

674		MNN024	Meningitis and Encephalitis	29	0.031

675		BYS001	Byssinosis	28	0.031

676		MYB001	Myoblastoma	28	0.031

677		GLC043	Glucocorticoid Deficiency 2	27	0.031

678		PRQ002	Paraquat Poisoning	26	0.031

679		INV018	Invasive Mole	25	0.031

680		HDG004	Hodgkin's Granuloma	23	0.031

681		HVY002	Heavy Metal Poisoning	22	0.031

682		HDG006	Hodgkin's Paragranuloma	22	0.031

683		HML018	Homologous Wasting Disease	22	0.031

684	P	HRD221	Hereditary Nephrogenic Diabetes Insipidus	17	0.031

685		NCL008	Nuclear Ribonucleic Acid	16	0.031

686		DSR013	Disorders of Gnas Inactivation	14	0.031