Search results for Adenosine monophosphate

1776 hits were found for Adenosine monophosphate

#	Family	MCID	Name	MIFTS	Score
1		ADN001	Adenosine Deaminase Deficiency	59	58.325

2		MYP071	Myopathy Due to Myoadenylate Deaminase Deficiency	44	51.058

3		URD002	Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to	26	34.112

4		ORT008	Orotic Aciduria	56	22.584

5		ERY039	Erythrocyte Amp Deaminase Deficiency	21	20.123

6		PRT037	Pertussis	49	17.346

7		CHL014	Cholera	62	16.524

8		SVR004	Severe Combined Immunodeficiency	70	13.734

9		ISC004	Ischemia	61	13.012

10		LPP008	Lipoprotein Quantitative Trait Locus	65	11.952

11		CMB007	Combined Immunodeficiency	56	11.340

12		ART140	Arteries, Anomalies of	52	10.982

13	P	NRB001	Neuroblastoma	66	10.877

14		HYP266	Hypoxia	56	9.812

15	P	AST005	Asthma	75	9.084

16		IMM167	Immune Deficiency Disease	76	8.930

17		ATR057	Atrioventricular Block	54	8.538

18	P	LKM071	Leukemia, Chronic Lymphocytic	74	8.505

19		CRN030	Coronary Stenosis	50	8.472

20	P	CRN300	Coronary Heart Disease 1	73	8.160

21	P	ATR011	Atrial Fibrillation	66	8.104

22	P	LKM002	Leukemia	65	8.085

23		48X005	48,xyyy	39	7.863

24	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	79	7.519

25		GLL048	Glial Tumor	51	7.465

26		GLM045	Glioma	62	7.415

27	P	MYC007	Myocardial Infarction	69	7.262

28		ANX004	Anoxia	40	7.230

29		ANG054	Angina Pectoris	65	7.228

30	c	ACT075	Acute Myocardial Infarction	55	7.139

31	P	SZR006	Seizure Disorder	69	7.012

32		CYT002	Cytokine Deficiency	43	7.012

33	P	PLM037	Pulmonary Hypertension	69	6.978

34		PLM129	Pulmonary Disease, Chronic Obstructive	74	6.890

35		HYP066	Hyperglycemia	60	6.869

36	P	RHN004	Rhinitis	56	6.833

37	P	PHC003	Pheochromocytoma	70	6.716

38		ADR040	Adrenal Gland Pheochromocytoma	45	6.714

39	c	PRC016	Pre-Eclampsia	64	6.687

40		CYS001	Cystic Fibrosis	77	6.678

41	P	HML002	Hemolytic Anemia	62	6.611

42		ALL003	Allergic Rhinitis	66	6.567

43		IMP005	Impotence	52	6.510

44		ALL029	Allergic Disease	61	6.508

45		DFC004	Deficiency Anemia	74	6.507

46		CNG034	Congestive Heart Failure	69	6.487

47		ALL006	Allergic Asthma	55	6.417

48	P	HYP069	Hyperparathyroidism	62	6.412

49	P	HRT032	Heart Disease	84	6.294

50	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	6.273

51	c	HYP595	Hypertension, Essential	84	6.261

52	P	LYM118	Lymphoma	66	6.257

53		BNR002	Bone Resorption Disease	47	6.045

54		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	6.029

55	P	GLM040	Glioma Susceptibility 1	70	6.029

56		MLG169	Malignant Astrocytoma	57	5.991

57	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	5.939

58		HLX001	Helix Syndrome	47	5.930

59	P	VSC007	Vascular Disease	62	5.916

60	P	SCK005	Sickle Cell Disease	56	5.858

61		NNL005	Non-Alcoholic Fatty Liver Disease	63	5.829

62	P	HRP006	Herpes Simplex	65	5.825

63		LNG099	Lung Disease	62	5.788

64	P	MYL006	Myeloid Leukemia	60	5.784

65	P	CRD119	Cardiac Arrest	68	5.768

66		OST159	Osteogenic Sarcoma	66	5.744

67	c	ATR087	Atrial Standstill 1	74	5.743

68		FTT001	Fatty Liver Disease	61	5.738

69		SYN036	Syncope	44	5.680

70	P	DBT009	Diabetes Mellitus	67	5.655

71		ATH013	Atherosclerosis Susceptibility	63	5.632

72	P	HYP086	Hypothyroidism	68	5.597

73		CRB004	Cerebral Artery Occlusion	45	5.590

74		MYL069	Myeloma, Multiple	76	5.522

75		PLR008	Pleurisy	49	5.516

76	P	LKM062	Leukemia, Acute Lymphoblastic	69	5.502

77		HMN044	Human Immunodeficiency Virus Type 1	76	5.468

78	P	OVR042	Ovarian Cancer	88	5.457

79	P	PRK057	Parkinson Disease, Late-Onset	79	5.424

80	P	MNN013	Meningitis	65	5.420

81		SPN186	Spinal Cord Injury	60	5.414

82	P	HYP076	Hyperthyroidism	53	5.406

83	c	MCR113	Microvascular Complications of Diabetes 3	52	5.290

84	c	MCR133	Microvascular Complications of Diabetes 4	41	5.285

85	c	MCR130	Microvascular Complications of Diabetes 6	41	5.285

86	c	MCR120	Microvascular Complications of Diabetes 7	47	5.285

87	P	HNT016	Huntington Disease	73	5.254

88		PNG002	Pain Agnosia	51	5.253

89	P	BDY004	Body Mass Index Quantitative Trait Locus 11	82	5.242

90	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	5.224

91	c	BDY006	Body Mass Index Quantitative Trait Locus 8	43	5.221

92	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	5.221

93	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	5.221

94	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	5.221

95	c	BDY012	Body Mass Index Quantitative Trait Locus 7	43	5.221

96	c	BDY019	Body Mass Index Quantitative Trait Locus 18	46	5.221

97	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	5.221

98	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	5.221

99		INS024	Insulin-Like Growth Factor I	77	5.195

100		GLB002	Glioblastoma	67	5.189

101	P	TRM003	Tremor	50	5.177

102	c	TYP009	Type 2 Diabetes Mellitus	91	5.104

103	P	ADL010	Adult Respiratory Distress Syndrome	70	5.077

104		LYM027	Lymphopenia	56	5.075

105		HYP056	Hypoglycemia	65	5.068

106	P	CHR345	Chronic Pain	50	5.043

107	P	MYC084	Mycobacterium Tuberculosis 1	68	4.986

108	c	PRM005	Primary Hyperparathyroidism	59	4.951

109	P	LVR013	Liver Disease	68	4.950

110		PRT036	Peritonitis	65	4.922

111		BRN071	Brain Injury	50	4.873

112		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	4.870

113	P	DRM053	Dermatitis, Atopic	65	4.870

114	c	LKM061	Leukemia, Acute Myeloid	83	4.842

115		CHR074	Choriocarcinoma	46	4.830

116		TXC005	Toxic Shock Syndrome	61	4.829

117		WLF001	Wolff-Parkinson-White Syndrome	63	4.823

118		LYM019	Lymphosarcoma	46	4.818

119	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	4.805

120	P	ART022	Arthritis	70	4.780

121		AGN016	Aging	53	4.771

122	P	GRF003	Graft-Versus-Host Disease	71	4.723

123		RPD005	Rapidly Involuting Congenital Hemangioma	48	4.721

124		MYC005	Myocardial Stunning	45	4.697

125	P	ALZ034	Alzheimer Disease	87	4.692

126	c	PLM164	Pulmonary Hypertension, Primary, 1	75	4.691

127		CLT003	Colitis	63	4.689

128	c	DLT002	Dilated Cardiomyopathy	79	4.622

129	P	PRK039	Parkinsonism	55	4.591

130	P	RHM011	Rheumatoid Arthritis	81	4.589

131		HYP060	Hyperinsulinism	53	4.567

132	P	GRV001	Graves' Disease	54	4.549

133		TRM010	Traumatic Brain Injury	50	4.525

134	P	HYP098	Hypereosinophilic Syndrome	66	4.514

135		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	4.499

136	c	ACT071	Acute Kidney Failure	60	4.496

137	P	BCL017	B-Cell Lymphoma	57	4.466

138	P	KDN018	Kidney Disease	71	4.465

139	c	HYP836	Hypercholesterolemia, Familial, 1	73	4.459

140	P	CLR023	Colorectal Cancer	100	4.439

141	P	HPT023	Hepatocellular Carcinoma	95	4.406

142	c	SYS001	Systemic Lupus Erythematosus	85	4.346

143	c	MGR028	Migraine with or Without Aura 1	63	4.319

144		VCC001	Vaccinia	49	4.309

145	c	ACT073	Acute Leukemia	59	4.298

146		PLM010	Pulmonary Edema	54	4.297

147		PTT037	Pituitary Tumors	44	4.273

148	P	MLN008	Melanoma	75	4.257

149	P	PSR002	Psoriasis	63	4.241

150		PLM001	Pulmonary Tuberculosis	69	4.235

151		PST011	Pustulosis of Palm and Sole	52	4.215

152	c	LKM063	Leukemia, Chronic Myeloid	70	4.157

153		MNT002	Mental Depression	56	4.152

154		LPD008	Lipid Metabolism Disorder	61	4.123

155	P	LPS004	Lupus Erythematosus	61	4.057

156	P	PSD015	Pseudohypoparathyroidism	54	4.055

157		OCL069	Ocular Motor Apraxia	57	4.047

158	P	HYP024	Hypoparathyroidism	55	4.038

159	c	HPT073	Hepatitis C Virus	70	4.023

160	P	DRR001	Diarrhea	55	4.021

161	P	ECL001	Eclampsia	52	4.020

162		DPR016	Depression	64	4.009

163		ADN018	Adenoma	58	4.009

164	P	THR014	Thrombocytopenia	66	4.006

165	P	DBT005	Diabetes Insipidus	54	3.997

166		DRM006	Dermatitis	61	3.988

167	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	3.983

168	P	LTR001	Lateral Sclerosis	57	3.983

169	P	MJR001	Major Depressive Disorder	68	3.969

170	P	HPT021	Hepatitis	68	3.919

171		RNL077	Renal Fibrosis	46	3.913

172	P	VSC011	Vasculitis	61	3.903

173	P	EPL164	Epilepsy	70	3.881

174	c	MCR115	Microvascular Complications of Diabetes 5	65	3.868

175		DBT010	Diabetic Neuropathy	54	3.866

176		END086	End Stage Renal Disease	54	3.839

177		ACQ007	Acquired Immunodeficiency Syndrome	58	3.822

178		MST004	Mast Cell Neoplasm	41	3.819

179		EXT007	Extracutaneous Mastocytoma	38	3.819

180	P	MSC005	Muscular Dystrophy	66	3.804

181	P	BRS047	Breast Cancer	97	3.797

182	P	GST053	Gastric Cancer	82	3.790

183		HYP005	Hypokalemia	55	3.789

184		GST033	Gestational Diabetes	60	3.761

185		TBR011	Tuberculous Meningitis	48	3.758

186		THY029	Thyroid Carcinoma	55	3.732

187		IGR001	Ige Responsiveness, Atopic	58	3.728

188		INT007	Intermediate Coronary Syndrome	53	3.727

189		PRT251	Proteinuria, Chronic Benign	58	3.719

190		CHC001	Chickenpox	56	3.709

191	P	PLM036	Pulmonary Fibrosis	65	3.702

192		STT001	Status Epilepticus	58	3.674

193		TTN003	Tetanus	64	3.671

194	P	PNC035	Pancreatic Cancer	87	3.656

195		PST028	Post-Traumatic Stress Disorder	58	3.649

196		MTB004	Metabolic Acidosis	48	3.645

197		MYL009	Myelodysplastic Syndrome	67	3.630

198	P	ENC018	Encephalopathy	62	3.628

199	c	CHR684	Chronic Kidney Disease	73	3.614

200		PPL052	Papillomatosis, Confluent and Reticulated	34	3.596

201		NRR001	Neuroretinitis	42	3.590

202		RTN023	Retinitis	45	3.590

203		THR024	Thrombosis	56	3.583

204		PPT005	Peptic Ulcer Disease	58	3.568

205	c	TYP008	Type 1 Diabetes Mellitus	77	3.544

206	P	ADN016	Adenocarcinoma	63	3.536

207		47X002	47,xyy	47	3.518

208		ACT084	Acute Stress Disorder	53	3.468

209		LVR012	Liver Cirrhosis	62	3.439

210	c	MJR022	Major Affective Disorder 8	37	3.425

211	c	MJR024	Major Affective Disorder 9	40	3.425

212	P	BPL003	Bipolar Disorder	56	3.425

213	P	NTR004	Neutropenia	62	3.424

214	P	DMN001	Diamond-Blackfan Anemia	73	3.422

215		SCK003	Sickle Cell Anemia	74	3.421

216		STM007	Stomatitis	52	3.399

217		SLP001	Sleeping Sickness	56	3.387

218	P	ENC004	Encephalitis	61	3.360

219	P	HYP061	Hypertrophic Cardiomyopathy	68	3.337

220	P	HDC001	Headache	56	3.324

221	P	PLY014	Polycystic Kidney Disease	71	3.297

222	P	TMP001	Temporal Lobe Epilepsy	49	3.279

223		ACT098	Acute Erythroid Leukemia	55	3.246

224		ATS010	Autosomal Recessive Disease	42	3.246

225	P	NRP001	Neuropathy	59	3.245

226	P	MYP004	Myopathy	67	3.233

227		HRY003	Hairy Cell Leukemia	53	3.232

228		EXR010	Exercise-Induced Bronchoconstriction	34	3.229

229	P	PRP019	Peripheral Nervous System Disease	57	3.222

230		CHL068	Cholestasis	61	3.221

231		ULC004	Ulcerative Colitis	74	3.219

232		LWC001	Low Compliance Bladder	44	3.210

233		ESP021	Esophageal Cancer	84	3.192

234		ATM095	Autoimmune Disease	61	3.192

235		ADR016	Adrenal Cortical Carcinoma	61	3.192

236	P	PRD008	Periodontitis	63	3.168

237		TRN015	Transient Cerebral Ischemia	62	3.167

238		BCT022	Bacterial Infectious Disease	55	3.153

239		MDD011	Mood Disorder	61	3.152

240	P	INF037	Inflammatory Bowel Disease	53	3.139

241	P	ALC033	Alcohol Use Disorder	67	3.138

242		WTH001	Withdrawal Disorder	47	3.126

243		PRS045	Prostatic Hypertrophy	53	3.121

244	c	PCH010	Pachyonychia Congenita 3	43	3.088

245	P	THY032	Thyroiditis	56	3.083

246		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	3.079

247		INS001	Insulinoma	59	3.074

248		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	3.072

249	P	TRN020	Turner Syndrome	67	3.062

250	P	OST001	Osteopetrosis	70	3.051

251	P	SLP006	Sleep Apnea	69	3.051

252		HYP014	Hyperuricemia	51	3.046

253	P	SRC025	Sarcoidosis 1	70	3.043

254	P	GLM007	Glomerulonephritis	59	3.042

255		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	3.021

256	c	BCT007	Bacterial Meningitis	55	3.017

257	P	CHR012	Chronic Granulomatous Disease	69	3.004

258	P	PRP029	Porphyria	60	2.992

259		ALL014	Allergic Encephalomyelitis	34	2.984

260	c	HPT001	Hepatitis C	61	2.972

261	c	DMN023	Diamond-Blackfan Anemia 1	68	2.968

262	P	INF032	Infertility	60	2.961

263	c	HPT016	Hepatitis B	62	2.960

264		CRV035	Cervical Cancer	72	2.960

265		CLN015	Colon Adenocarcinoma	64	2.945

266		ANT039	Antisynthetase Syndrome	55	2.942

267		NNL006	Non-Alcoholic Steatohepatitis	54	2.941

268	c	INH020	Inherited Metabolic Disorder	47	2.935

269		STR067	Stroke, Ischemic	79	2.931

270	P	LNG032	Lung Cancer	98	2.930

271		DPH001	Diphtheria	59	2.927

272		ALC007	Alcohol Dependence	65	2.922

273	P	LNG064	Lung Cancer Susceptibility 3	69	2.919

274	c	LKM005	Leukemia, T-Cell, Chronic	33	2.919

275		ADR054	Adrenocortical Carcinoma, Hereditary	47	2.913

276		ADR004	Adrenal Cortical Adenocarcinoma	38	2.913

277		SKN016	Skin Disease	63	2.906

278		GTR002	Goiter	52	2.896

279		RCK004	Rickets	64	2.884

280		RHB024	Rhabdomyosarcoma 2	65	2.880

281	P	RTN008	Retinitis Pigmentosa	79	2.875

282	P	PLY011	Polycystic Ovary Syndrome	57	2.874

283		DWN001	Down Syndrome	70	2.871

284		PRS021	Prostatic Adenoma	43	2.868

285	P	RSP003	Respiratory Failure	73	2.864

286		LYM040	Lymphoblastic Lymphoma	53	2.861

287		SRC014	Sarcoma	64	2.855

288	P	PRS040	Prostate Cancer	95	2.855

289		BRN004	Brain Edema	54	2.854

290	P	SLP005	Sleep Disorder	61	2.852

291	P	PNC025	Panic Disorder	52	2.836

292	c	FML001	Familial Atrial Fibrillation	65	2.832

293		OST012	Osteoarthritis	77	2.828

294		MLR004	Malaria	77	2.820

295	P	CNR004	Cone-Rod Dystrophy 2	74	2.806

296		CRH001	Crohn's Disease	80	2.802

297		SPN035	Spindle Cell Sarcoma	51	2.798

298	c	ACT027	Acute Pancreatitis	60	2.797

299		PRP027	Peripheral Vascular Disease	71	2.794

300	c	VRL010	Viral Hepatitis	52	2.793

301		URT010	Ureteral Obstruction	44	2.792

302		PRS129	Prostatic Hyperplasia, Benign	48	2.789

303	P	UVT001	Uveitis	57	2.775

304	c	GRV008	Graves Disease 1	54	2.755

305		PLY150	Polykaryocytosis Inducer	29	2.749

306		ANR040	Aneurysm	60	2.749

307		PNC001	Pancytopenia	52	2.748

308	P	PNM007	Pneumonia	64	2.747

309	P	GST044	Gastritis	55	2.742

310		HMP009	Haemophilus Influenzae	41	2.740

311		HYP017	Hypophosphatemia	49	2.728

312		MSL001	Measles	61	2.723

313		CRT015	Carotid Artery Occlusion	45	2.722

314		BRN002	Bronchiolitis	57	2.712

315	P	DYS154	Dystonia	64	2.702

316		LSC001	Lesch-Nyhan Syndrome	62	2.700

317		PRN001	Purine Nucleoside Phosphorylase Deficiency	53	2.693

318		TRY001	Trypanosomiasis	50	2.686

319		BRN024	Bronchitis	67	2.686

320	P	MYC008	Myocarditis	59	2.680

321	P	BNG032	Benign Mesothelioma	53	2.678

322	P	BLD134	Bladder Cancer	79	2.678

323		AMN003	Amnestic Disorder	53	2.670

324		SDD001	Sudden Infant Death Syndrome	60	2.670

325	P	RTN024	Retinoblastoma	72	2.647

326		GLC003	Glucose Intolerance	53	2.634

327	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	64	2.632

328		END057	Endometrial Cancer	76	2.629

329	P	BND020	Bone Disease	60	2.624

330		HMC014	Homocysteinemia	52	2.616

331		LYM143	Lymphoma, Non-Hodgkin, Familial	74	2.596

332	P	SCH015	Schizophrenia	74	2.596

333		OCL006	Ocular Hypertension	53	2.592

334		LYM133	Lymphoma, Hodgkin, Classic	69	2.590

335		HPT004	Hepatic Coma	43	2.587

336	P	ANR048	Aniridia 1	66	2.581

337	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	2.577

338	P	OST002	Osteoporosis	76	2.577

339	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	2.577

340		HRP004	Herpes Zoster	60	2.572

341		RTN020	Retinal Vascular Disease	45	2.567

342		GT001	Gout	63	2.562

343		IRN002	Iron Metabolism Disease	56	2.550

344	P	KLZ004	Kala-Azar 1	41	2.547

345		LSH001	Leishmaniasis	63	2.547

346	c	THY107	Thymoma, Familial	42	2.541

347	P	THY023	Thymoma	64	2.541

348	P	SCK002	Sick Sinus Syndrome	55	2.536

349	c	SCN007	Secondary Hyperparathyroidism	50	2.533

350	P	BRS044	Breast Adenocarcinoma	58	2.526

351	c	ATS007	Autism Spectrum Disorder	71	2.525

352	P	FBR017	Fibrosarcoma	55	2.525

353	P	MVM001	Movement Disease	61	2.525

354		MSC157	Muscular Dystrophy, Duchenne Type	78	2.524

355	P	SYS005	Systemic Scleroderma	73	2.520

356		VLK001	Volkmann Contracture	23	2.518

357	P	MLN007	Male Infertility	56	2.511

358		TRT001	Teratocarcinoma	41	2.501

359		URM002	Uremia	47	2.485

360		OVR094	Ovarian Epithelial Cancer	39	2.479

361	c	SML038	Small Cell Cancer of the Lung	68	2.460

362	P	PNC044	Pancreatitis	61	2.460

363	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	2.449

364	c	SCL052	Scleroderma, Familial Progressive	60	2.446

365		PRT013	Portal Hypertension	59	2.436

366	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	62	2.434

367		HMN014	Human Immunodeficiency Virus Infectious Disease	54	2.426

368	P	ATS364	Autism	72	2.426

369	P	NPH012	Nephrotic Syndrome	61	2.425

370		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	51	2.424

371	P	MYP006	Myopia	55	2.419

372		HGH043	High Grade Glioma	46	2.412

373	c	TBR025	Tuberous Sclerosis 1	84	2.409

374		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	2.403

375	P	DNG005	Dengue Virus	55	2.400

376	P	TXP001	Toxoplasmosis	59	2.395

377		ADN022	Adenylosuccinase Deficiency	44	2.387

378	P	RNV001	Renovascular Hypertension	48	2.382

379	c	CHR064	Chronic Monocytic Leukemia	35	2.381

380		RNL114	Renal Cell Carcinoma, Nonpapillary	79	2.381

381		CRB039	Cerebrovascular Disease	65	2.380

382	P	END044	Endometriosis	62	2.372

383	c	ACT135	Acute Graft Versus Host Disease	51	2.367

384		ASP003	Aseptic Meningitis	50	2.359

385		CMP010	Complex Regional Pain Syndrome	59	2.334

386		CVD001	Covid-19	59	2.334

387		MRP001	Morphine Dependence	41	2.333

388	c	MCL042	Macular Degeneration, Age-Related, 1	84	2.323

389		ARG004	Argyria	26	2.319

390	P	EXN002	Exanthem	58	2.313

391		GST023	Gastric Ulcer	52	2.312

392	P	RTN016	Retinal Degeneration	52	2.304

393		PLR007	Pleural Empyema	50	2.283

394		ANX010	Anxiety	70	2.277

395	P	THL005	Thalassemia	56	2.275

396		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	2.273

397		MYL005	Myelofibrosis	70	2.269

398	P	EYD002	Eye Disease	57	2.265

399		LYD001	Leydig Cell Tumor	45	2.264

400		PRP007	Priapism	46	2.260

401		BRN056	Bronchopulmonary Dysplasia	57	2.254

402		APN006	Apnea of Prematurity	24	2.243

403		BRK012	Broken Heart Syndrome	42	2.242

404		CRB086	Cerebral Aneurysms	40	2.240

405	P	HYP750	Hypertriglyceridemia, Familial	61	2.240

406		LGH007	Leigh Syndrome	70	2.239

407		CHG001	Chagas Disease	65	2.238

408		MLY001	Molybdenum Cofactor Deficiency	40	2.230

409	c	ACT134	Acute Liver Failure	57	2.229

410		IRR002	Irritable Bowel Syndrome	64	2.224

411	c	BRN108	Branchiootic Syndrome 1	63	2.215

412	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	2.209

413		PNC129	Pancreatic Adenocarcinoma	64	2.197

414		ACT119	Acute Promyelocytic Leukemia	62	2.194

415	P	ART021	Arteriosclerosis	53	2.194

416	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	2.192

417		NRM005	Neuromuscular Disease	62	2.188

418	c	ATM011	Autoimmune Hepatitis	62	2.184

419	P	ACT105	Acute Mountain Sickness	52	2.178

420	P	CRD246	Cardiovascular System Disease	55	2.175

421	P	TBR001	Tuberous Sclerosis	69	2.164

422	P	OPT006	Optic Nerve Disease	57	2.157

423		INT002	Intermittent Claudication	61	2.156

424	P	HYP265	Hypotonia	42	2.149

425		PRT029	Parathyroid Adenoma	51	2.137

426		CNS004	Constipation	56	2.134

427		CRD132	Cardiac Conduction Defect	59	2.131

428		RTN003	Retinal Ischemia	48	2.122

429	c	CNG027	Congenital Hemolytic Anemia	49	2.116

430		PSR001	Psoriatic Arthritis	61	2.114

431	P	MCR129	Microvascular Complications of Diabetes 1	67	2.110

432		CRN019	Coronary Artery Vasospasm	47	2.108

433		BRK010	Burkitt Lymphoma	65	2.102

434		INT040	Intrinsic Asthma	36	2.093

435	P	INF038	Influenza	68	2.083

436		PRP016	Paraplegia	52	2.080

437		HPT019	Hepatic Encephalopathy	59	2.077

438		INT030	Intracranial Aneurysm	55	2.074

439		END040	Endogenous Depression	54	2.073

440		SPL018	Splenomegaly	47	2.065

441		SPR126	Superior Semicircular Canal Dehiscence	41	2.061

442	c	HMG029	Hemoglobin Se Disease	41	2.061

443		ADG002	Audiogenic Seizures	25	2.057

444		NWC001	Newcastle Disease	47	2.049

445		BRN012	Bronchiolitis Obliterans	56	2.041

446		PLS011	Plasmacytoma	56	2.038

447	c	DNT047	Dentinogenesis Imperfecta Type 2	35	2.036

448	P	LCT001	Lactic Acidosis	50	2.031

449		LMB062	Limb Ischemia	55	2.029

450		THR004	Thrombocytosis	52	2.029

451		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	2.021

452		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	44	2.019

453		CRD223	Cardiac Arrhythmia	63	2.013

454		SQM006	Squamous Cell Carcinoma	59	2.012

455		PYR041	Pyruvate Kinase Deficiency of Red Cells	56	2.011

456	c	CHR711	Chronic Asthma	41	2.009

457	P	OPN001	Open-Angle Glaucoma	55	2.007

458		KRT019	Keratitis, Hereditary	66	2.000

459		INT066	Interstitial Lung Disease	60	1.989

460		SVR001	Severe Acute Respiratory Syndrome	68	1.987

461		DSS009	Disseminated Intravascular Coagulation	56	1.979

462	P	RHB003	Rhabdomyosarcoma	66	1.976

463		THY030	Thyroid Gland Disease	50	1.975

464		PLS009	Plasma Cell Neoplasm	64	1.973

465		RSP007	Respiratory Distress Syndrome, Infant	41	1.964

466		TLN003	Telangiectasis	51	1.953

467		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	1.948

468	P	RTN018	Retinal Disease	53	1.942

469		NPH009	Nephrolithiasis	54	1.941

470		MYX004	Myxedema	43	1.938

471		ILT001	Ileitis	49	1.936

472		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	1.935

473		INT323	Intraocular Pressure Quantitative Trait Locus	63	1.932

474	P	SBS003	Substance Abuse	54	1.931

475		CRB090	Cerebral Hypoxia	42	1.926

476	P	CYS018	Cystitis	58	1.920

477		RST023	Resting Heart Rate, Variation in	40	1.919

478	P	OVR082	Overgrowth Syndrome	41	1.916

479	P	PTT006	Pituitary Adenoma	55	1.911

480		HRW001	Hair Whorl	35	1.908

481		HSH003	Hashimoto Thyroiditis	60	1.908

482		GST040	Gastric Adenocarcinoma	66	1.900

483	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	60	1.891

484		NRF007	Neurofibroma	63	1.891

485	P	CHN012	Chondrosarcoma	56	1.890

486		MLT157	Multiple System Atrophy 1	69	1.884

487		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	1.884

488		SCH014	Schistosomiasis	56	1.884

489	P	INT068	Intestinal Disease	53	1.880

490	P	MNC007	Monocytic Leukemia	48	1.877

491		DFF005	Diffuse Large B-Cell Lymphoma	55	1.876

492		CHL065	Cholangiocarcinoma	57	1.872

493		INT079	Intrahepatic Cholangiocarcinoma	51	1.872

494	P	MLT020	Multiple Sclerosis	79	1.864

495		ATX019	Ataxia with Vitamin E Deficiency	44	1.859

496		PLG002	Plague	58	1.857

497		WST005	West Nile Virus	55	1.856

498		PST092	Posttransplant Acute Limbic Encephalitis	29	1.855

499		CHL123	Chlamydia	58	1.855

500	P	SNS001	Sensorineural Hearing Loss	60	1.850

501	P	ESP024	Esophagitis	60	1.847

502	c	SPN225	Spondyloarthropathy 1	70	1.847

503	P	LNG028	Long Qt Syndrome	63	1.846

504	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	59	1.845

505		VSC003	Visceral Leishmaniasis	54	1.843

506	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	1.837

507	P	CRN038	Carney Complex Variant	63	1.837

508		CLR109	Colorectal Adenocarcinoma	50	1.837

509		MCR013	Microphthalmia	59	1.836

510		ANT024	Anthrax Disease	57	1.829

511		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	1.827

512	P	VTR007	Vitreoretinopathy	45	1.827

513	P	KDN017	Kidney Cancer	60	1.824

514		MCR004	Macroglobulinemia	48	1.816

515	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	1.811

516	P	MYS003	Myasthenia Gravis	67	1.810

517		DMY004	Demyelinating Disease	50	1.808

518		MYL031	Myeloproliferative Neoplasm	66	1.803

519		HYP003	Hypermethioninemia	51	1.803

520		ASP030	Aspirin Resistance	41	1.799

521	c	MCR112	Microvascular Complications of Diabetes 2	42	1.794

522	P	OBS001	Obstructive Jaundice	49	1.790

523		GST050	Gastrointestinal System Disease	55	1.783

524		SXL003	Sexual Disorder	49	1.781

525		SCR003	Secretory Diarrhea	35	1.778

526		GST045	Gastroenteritis	58	1.777

527		NRT004	Neuritis	53	1.771

528	P	CYS039	Cystic Kidney Disease	52	1.767

529		TYP007	Typhoid Fever	63	1.765

530		MSC007	Muscle Hypertrophy	64	1.763

531		KRT002	Keratomalacia	54	1.761

532		ACR007	Acromegaly	70	1.758

533		DWR001	Dwarfism	44	1.755

534	c	ATM099	Autoimmune Uveitis	44	1.743

535		RTN017	Retinal Detachment	60	1.734

536		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	1.734

537		HYP020	Hyperprolactinemia	63	1.734

538	P	HRD011	Hereditary Spherocytosis	63	1.733

539		PPL002	Papillary Carcinoma	46	1.732

540	P	BRB001	Beriberi	44	1.726

541		HND015	Hand Skill, Relative	29	1.720

542		ART016	Aortic Aneurysm	68	1.720

543	P	LPR021	Leprosy 3	71	1.720

544		HNS001	Hansen's Disease	32	1.720

545	P	SKN015	Skin Carcinoma	71	1.717

546	P	ALP008	Alopecia	53	1.716

547		CMM004	Common Variable Immunodeficiency	71	1.713

548	P	MLG056	Malignant Hyperthermia	65	1.712

549	c	BCT013	Bacterial Pneumonia	47	1.710

550	c	PRG020	Paragangliomas 3	39	1.706

551	P	INT143	Interstitial Cystitis	59	1.703

552	P	FRG001	Fragile X Syndrome	70	1.698

553		TND005	Tendinitis	53	1.697

554	P	URT039	Urticaria	57	1.696

555		BLD053	Blood Platelet Disease	51	1.690

556		PLY023	Polycystic Liver Disease	62	1.688

557		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	1.687

558		AND005	Androgen Insensitivity Syndrome, Mild	21	1.686

559	c	PSD108	Pseudohypoparathyroidism, Type Ia	64	1.685

560	c	DWL002	Dowling-Degos Disease 1	58	1.674

561		OST011	Osteomalacia	52	1.674

562		CRY035	Cryptorchidism, Unilateral or Bilateral	57	1.671

563		URL001	Urolithiasis	45	1.671

564	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	1.671

565		PRN011	Pernicious Anemia	52	1.664

566		THY111	Thyroid Carcinoma, Familial Medullary	67	1.655

567		THY125	Thyroid Gland Medullary Carcinoma	48	1.655

568	P	PLY019	Polyneuropathy	52	1.655

569		MTB008	Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration	42	1.654

570	c	PRM038	Primary Agammaglobulinemia	47	1.648

571		SNG003	Single Ventricular Heart	30	1.644

572		ATY005	Atypical Teratoid Rhabdoid Tumor	69	1.641

573	c	GLC092	Glaucoma, Primary Open Angle	60	1.632

574	c	EXD008	Exudative Vitreoretinopathy 1	71	1.632

575		PLS037	Plasma Cell Tumor	20	1.630

576		MMM001	Mammary Paget's Disease	53	1.627

577		ORL015	Oral Squamous Cell Carcinoma	43	1.616

578	c	RTN047	Retinitis Pigmentosa 18	45	1.610

579	P	ACN011	Acne	55	1.609

580	P	NRC002	Narcolepsy	55	1.601

581		MCL006	Macular Retinal Edema	56	1.600

582	P	CTR002	Cataract	59	1.597

583		MLD018	Mild Cognitive Impairment	48	1.590

584		MLY008	Molybdenum Cofactor Deficiency, Complementation Group a	47	1.585

585		BLR008	Bilirubin Metabolic Disorder	57	1.584

586		END072	Endotheliitis	36	1.579

587	c	GLL024	Gallbladder Disease 1	53	1.577

588		INT394	Intermittent Asthma	21	1.574

589	P	ADL017	Adult T-Cell Leukemia	53	1.571

590		IDP073	Idiopathic Hypercalciuria	41	1.566

591		ACT003	Acute Kidney Tubular Necrosis	46	1.566

592		CRD137	Cardiogenic Shock	56	1.566

593		OPT003	Opiate Dependence	49	1.566

594		MTB016	Metabolic Myopathy	30	1.565

595	P	BRN022	Bronchiectasis	59	1.565

596		NNT012	Neonatal Jaundice	53	1.563

597	P	RRH023	Rare Hereditary Hemochromatosis	52	1.560

598		PLM134	Pulmonary Fibrosis, Idiopathic	76	1.557

599	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	1.556

600		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	1.556

601		PSD014	Pseudopseudohypoparathyroidism	54	1.555

602		SYS003	Systolic Heart Failure	49	1.553

603		MYT011	Myotonia	37	1.552

604		PPL022	Papilloma	53	1.549

605		SQM002	Squamous Cell Papilloma	45	1.549

606	c	ESS001	Essential Tremor	56	1.549

607		DSS032	Disease by Infectious Agent	55	1.545

608		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	42	1.541

609		MYC006	Mycosis Fungoides	64	1.540

610		PLT016	Platelet Adenylate Cyclase Activity	16	1.538

611		TRD006	Tardive Dyskinesia	53	1.538

612		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	1.537

613		CHD001	Chediak-Higashi Syndrome	66	1.536

614		CNN003	Conn's Syndrome	77	1.536

615	P	FML068	Familial Hypocalciuric Hypercalcemia	55	1.535

616		HRT012	Heart Valve Disease	53	1.534

617		MDD018	Middle East Respiratory Syndrome	44	1.531

618	c	ART101	Aortic Valve Disease 2	65	1.527

619	P	PRM051	Primary Pigmented Nodular Adrenocortical Disease	55	1.517

620		CLF027	Cleft Palate, Isolated	64	1.516

621		ALC001	Alcohol-Related Birth Defect	36	1.515

622		BRC012	Brucellosis	66	1.515

623	P	GLL022	Guillain-Barre Syndrome	59	1.512

624	P	MCR010	Microcephaly	59	1.510

625		CRY003	Cryptosporidiosis	55	1.508

626		HPT022	Hepatoblastoma	54	1.506

627	P	DDN001	Duodenal Ulcer	52	1.505

628	P	HYP263	Hypersomnia	40	1.505

629		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	1.499

630	P	SLM003	Salmonellosis	54	1.498

631		HMN047	Human Cytomegalovirus Infection	59	1.498

632	P	NRF002	Neurofibromatosis	60	1.495

633	P	FTL001	Fetal Alcohol Syndrome	55	1.493

634	c	OST131	Osteopetrosis, Autosomal Dominant 2	52	1.492

635	c	HPT015	Hepatitis D	49	1.490

636	c	WLM013	Wilms Tumor 1	65	1.488

637		CHL004	Cholelithiasis	48	1.481

638		HYP458	Hyper Ige Syndrome	60	1.481

639		HDN002	Head Injury	44	1.481

640		OPD006	Opioid Addiction	48	1.479

641		ENT004	Enthesopathy	51	1.479

642		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	1.477

643		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	65	1.472

644	c	LKM056	Leukemia, Chronic Lymphocytic 2	47	1.472

645		LNT004	Lentigines	45	1.472

646		THY122	Thyroid Gland Cancer	59	1.471

647	P	BNC003	Bone Cancer	58	1.467

648	c	VRL007	Viral Encephalitis	50	1.466

649		APN008	Apnea, Obstructive Sleep	66	1.464

650		ATY042	Atypical Chronic Myeloid Leukemia	50	1.463

651		OCL010	Ocular Hypotension	37	1.462

652	c	ACT249	Acute Asthma	40	1.461

653	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	1.444

654		RSP019	Respiratory Distress Syndrome in Premature Infants	52	1.444

655		NWB001	Newborn Respiratory Distress Syndrome	56	1.444

656	c	ART115	Aortic Valve Disease 1	72	1.440

657		FBR009	Fibrous Dysplasia	48	1.437

658	c	BTT014	Beta-Thalassemia	72	1.436

659	c	CNT035	Central Nervous System Disease	53	1.435

660	c	SVR005	Severe Pre-Eclampsia	49	1.434

661	P	PLY018	Polycythemia	56	1.434

662	c	HPT003	Hepatitis a	63	1.434

663		PRP083	Porphyria, Acute Intermittent	64	1.430

664		LKC009	Leukocyte Adhesion Deficiency, Type I	69	1.430

665	P	FBR031	Febrile Seizures	52	1.429

666		FCL014	Focal Epilepsy	53	1.428

667	c	DRR009	Diarrhea 6	46	1.424

668		CLP006	Clopidogrel Resistance	44	1.421

669		PRP030	Purpura	54	1.411

670	c	BLD120	Bleeding Disorder, Platelet-Type, 8	35	1.406

671		MCC012	Mccune-Albright Syndrome	69	1.402

672		PLL012	Pollen Allergy	44	1.399

673		DSR074	Disorder of Purine Metabolism	24	1.398

674		WLL004	Wallerian Degeneration	38	1.394

675		BRN028	Brain Cancer	73	1.394

676		ETN001	Eating Disorder	59	1.387

677		CRN017	Coronary Thrombosis	46	1.385

678	P	PRC031	Preeclampsia/eclampsia 1	43	1.383

679		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	58	1.382

680		OCL052	Ocular Dominance	40	1.380

681	P	CTN015	Cutaneous T Cell Lymphoma	48	1.378

682		VSC002	Vascular Dementia	59	1.378

683	P	PRR002	Pure Red-Cell Aplasia	46	1.376

684	c	PST005	Posterior Uveitis	54	1.374

685	P	PTS002	Ptosis	52	1.372

686		PRP080	Peripheral Artery Disease	54	1.367

687		MCL003	Macular Holes	44	1.360

688		RYN005	Raynaud Phenomenon	45	1.360

689	P	SPP010	Suppressor of Tumorigenicity 3	50	1.358

690		RSP021	Respiratory Allergy	41	1.357

691		CWP001	Cowpox	44	1.357

692		SML019	Smallpox	55	1.356

693	c	PRG106	Progressive Muscular Dystrophy	31	1.354

694	c	MST023	Mesothelioma, Malignant	56	1.348

695		YLL002	Yellow Fever	61	1.346

696		DRG003	Drug Dependence	46	1.345

697		ADR007	Adrenoleukodystrophy	73	1.344

698		ADR022	Adrenomyeloneuropathy	38	1.344

699		MTH009	Mouth Disease	57	1.340

700		PLY001	Polycythemia Vera	69	1.340

701		NRL005	Neurilemmoma	60	1.339

702		PLY100	Polyploidy	36	1.339

703	c	OVR114	Ovarian Cancer 1	60	1.336

704		ACT113	Acute Myeloblastic Leukemia with Maturation	46	1.334

705	P	INS002	in Situ Carcinoma	52	1.333

706	P	TTR001	Tetralogy of Fallot	69	1.333

707		VRC005	Varicose Veins	59	1.329

708		OBS082	Obstructive Nephropathy	41	1.325

709		TRC003	Trichomoniasis	53	1.325

710		ATN004	Autonomic Neuropathy	42	1.322

711		HRN029	Hearing Loss, Noise-Induced	37	1.321

712		ORL011	Oral Cancer	60	1.320

713	P	GLY013	Glycogen Storage Disease	59	1.319

714	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	1.317

715	P	PRD021	Periodic Paralysis	42	1.316

716		ADR041	Adrenal Cortical Adenoma	48	1.316

717		PTT046	Pituitary Hormone Deficiency, Combined, 2	62	1.316

718	c	HMP023	Hemophagocytic Lymphohistiocytosis, Familial, 5	42	1.316

719	c	JVN010	Juvenile Rheumatoid Arthritis	52	1.315

720		LNG030	Lung Adenoma	37	1.313

721	P	HMC002	Homocystinuria	52	1.312

722		PLM033	Pulmonary Embolism	58	1.312

723		END041	Endometrial Adenocarcinoma	63	1.309

724		SYN007	Synovitis	54	1.306

725		PLC002	Plica Syndrome	35	1.306

726		CHR178	Chromosomal Triplication	33	1.306

727	P	FLL037	Follicular Lymphoma	66	1.305

728	c	ANM038	Anemia, Autoimmune Hemolytic	63	1.304

729		TCL003	T Cell Deficiency	44	1.296

730		FDL002	Food Allergy	47	1.296

731		GRN017	Granulocytopenia	42	1.293

732	P	PMP001	Pemphigus	54	1.293

733		SBC016	Subacute Delirium	42	1.289

734		RTH007	Rothmund-Thomson Syndrome, Type 1	37	1.287

735	P	HYP083	Hypopituitarism	51	1.278

736		PFF001	Pfeiffer Syndrome	77	1.272

737	P	HYD006	Hydrocephalus	62	1.270

738		ACT200	Acute Monoblastic Leukemia	40	1.261

739	P	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	66	1.260

740	c	VRL012	Viral Meningitis	46	1.259

741		MYM001	Myoma	54	1.253

742	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	1.252

743	c	LKM070	Leukemia, Acute Monocytic	56	1.249

744		DYS192	Dystonia, Dopa-Responsive	56	1.248

745		LKS001	Leukostasis	40	1.246

746	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	1.245

747	P	ANT080	Antigen Defined by Monoclonal Antibody Aj9	18	1.244

748	P	ACR001	Aicardi-Goutieres Syndrome	63	1.244

749		IFP003	Ifap Syndrome 2	41	1.242

750		PRS063	Paresthesia	39	1.239

751		URT049	Urate Oxidase, Pseudogene	24	1.239

752		PRQ002	Paraquat Poisoning	28	1.238

753		ILS001	Ileus	49	1.231

754	P	DMN002	Dementia	65	1.223

755		HRT011	Heart Septal Defect	49	1.218

756	c	HYP331	Hyperphenylalaninemia, Bh4-Deficient, a	59	1.214

757		OST003	Osteonecrosis	60	1.212

758	P	LCH002	Lichen Planus	54	1.209

759		TCK001	Tick-Borne Encephalitis	58	1.206

760		GNG005	Gangliocytoma	54	1.206

761		GNG002	Ganglioneuroma	52	1.206

762		PRT058	Pure Autonomic Failure	58	1.204

763		PYR010	Peyronie's Disease	50	1.202

764		THR100	Thrombocytopenic Purpura, Autoimmune	60	1.198

765		OST015	Osteochondrodysplasia	60	1.197

766		ART002	Arts Syndrome	66	1.192

767	P	PRC019	Precocious Puberty	48	1.192

768		HLC007	Helicobacter Pylori Infection	67	1.190

769	P	RNL015	Renal Hypertension	45	1.190

770	P	MTR014	Motor Neuron Disease	65	1.188

771		NDL007	Nodular Goiter	48	1.184

772	c	PLY172	Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease	53	1.180

773		LYM017	Lyme Disease	63	1.178

774	P	CND004	Candidiasis	57	1.176

775		FBR047	Fibromyalgia	57	1.175

776		TCL027	T-Cell Acute Lymphoblastic Leukemia	52	1.168

777	P	MGR001	Migraine Without Aura	48	1.168

778		GRW007	Growth Hormone Deficiency	47	1.165

779	P	MLT074	Multiple Endocrine Neoplasia	58	1.163

780		ECT026	Ectopic Pregnancy	47	1.162

781		CGH001	Cough Variant Asthma	35	1.162

782		PRL017	Prolymphocytic Leukemia	47	1.161

783	P	ART023	Arthropathy	59	1.159

784		HPT014	Hepatorenal Syndrome	49	1.156

785		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	40	1.155

786		CHR073	Choreatic Disease	53	1.155

787		VTM002	Vitamin B12 Deficiency	48	1.154

788		VLV047	Volvulus of Midgut	55	1.147

789		PST053	Postherpetic Neuralgia	39	1.146

790		ARR042	Arrhythmogenic Right Ventricular Cardiomyopathy	61	1.140

791		DBT084	Diabetes Mellitus, Ketosis-Prone	59	1.138

792		HMS001	Hemosiderosis	48	1.135

793		GLM044	Glomerular Disease	34	1.135

794	P	ERY036	Erythema Nodosum	49	1.132

795		CRY014	Cryptococcal Meningitis	48	1.132

796		XRD010	Xeroderma Pigmentosum, Variant Type	72	1.131

797	P	PSD087	Pseudoxanthoma Elasticum	66	1.129

798		RCT020	Rectum Adenocarcinoma	48	1.126

799		OVR059	Ovary Adenocarcinoma	49	1.126

800	P	VNS003	Venous Insufficiency	54	1.122

801		SNS003	Sensory Peripheral Neuropathy	51	1.121

802		DST006	Diastolic Heart Failure	45	1.120

803		CHK001	Chikungunya	60	1.117

804	P	ATR005	Atrophic Gastritis	50	1.117

805	c	OTP006	Otopalatodigital Syndrome, Type I	59	1.117

806	c	HYP374	Hypothyroidism, Congenital, Nongoitrous, 1	51	1.117

807		CHR593	Chromosome 16p13.3 Deletion Syndrome, Proximal	68	1.117

808		ERY004	Erysipelas	47	1.117

809		DRM011	Dermatophytosis	52	1.117

810		GRV012	Grover's Disease	30	1.117

811	P	URN019	Urinary Tract Infection	48	1.113

812		PTH003	Pathologic Nystagmus	52	1.113

813		INS015	Inosine Triphosphatase Deficiency	22	1.112

814		INF013	Inferior Myocardial Infarction	33	1.110

815		SQM013	Squamous Cell Carcinoma, Head and Neck	75	1.110

816		ISL001	Islet Cell Tumor	55	1.101

817		RNL011	Renal Osteodystrophy	48	1.101

818	P	FML011	Familial Adenomatous Polyposis	70	1.098

819		CNN005	Connective Tissue Disease	66	1.097

820	P	ESN008	Eosinophilic Pneumonia	50	1.089

821		ISL151	Isolated Elevated Serum Creatine Phosphokinase Levels	39	1.081

822	P	HRD221	Hereditary Nephrogenic Diabetes Insipidus	18	1.081

823		OTT002	Otitis Media	70	1.081

824		ANC002	Anca-Associated Vasculitis	44	1.080

825		MLG079	Malignant Pleural Mesothelioma	42	1.080

826		PMP006	Pemphigus Vulgaris, Familial	57	1.077

827	P	BRT004	Bartter Disease	58	1.076

828	P	MYT002	Myotonic Dystrophy	51	1.072

829	P	FML187	Familial Hypertension	34	1.069

830	P	MDL005	Medulloblastoma	75	1.067

831		CRC006	Carcinoid Syndrome	55	1.063

832		CLR030	Clear Cell Renal Cell Carcinoma	53	1.061

833	P	PRP003	Porphyria Cutanea Tarda	66	1.060

834		BYS001	Byssinosis	27	1.060

835		HYP026	Hypoglycemic Coma	37	1.060

836		SPN051	Spondylitis	51	1.058

837		INF009	Inflammatory Spondylopathy	30	1.058

838		EPD015	Epidemic Typhus	44	1.056

839		CCN002	Cocaine Abuse	49	1.049

840	P	HMG032	Hemoglobin H Disease	51	1.049

841		CTN007	Cutaneous Leishmaniasis	61	1.049

842		CRB037	Cerebral Palsy	66	1.048

843	P	ANP001	Anaplastic Large Cell Lymphoma	59	1.045

844	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	1.043

845		ANV001	Anovulation	46	1.041

846		DSR013	Disorders of Gnas Inactivation	15	1.041

847	P	HRD217	Hereditary Optic Neuropathy	36	1.034

848		THY128	Thyroid Tumor	33	1.034

849	P	PNV001	Panuveitis	48	1.034

850		SCT005	Scott Syndrome	51	1.034

851		PRS047	Prostatitis	57	1.033

852		DBT006	Diabetic Macular Edema	48	1.031

853		CLF001	Cleft Lip	54	1.031

854	P	OLG002	Oligodendroglioma	66	1.031

855	P	AGM001	Agammaglobulinemia	67	1.030

856		HYP025	Hyperphosphatemia	47	1.027

857	P	ESS003	Essential Thrombocythemia	68	1.025

858		PNF002	Painful Legs and Moving Toes Syndrome	14	1.024

859	P	PLM034	Pulmonary Emphysema	58	1.023

860	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	65	1.022

861		RFR010	Refractory Anemia	49	1.022

862		BRN032	Brain Glioma	45	1.019

863		HRP009	Herpes Simplex Encephalitis	58	1.019

864		IDP033	Idiopathic Edema	41	1.019

865	P	END047	Endophthalmitis	53	1.016

866		DSM004	Desmoid Tumor	65	1.015

867		NRT001	Neurotic Disorder	56	1.011

868		SPS057	Spasticity	43	1.010

869		PLM031	Poliomyelitis	62	1.004

870		KPS004	Kaposi Sarcoma	76	1.003

871		ESP002	Esophageal Varix	51	1.000

872		HND002	Hand, Foot and Mouth Disease	50	1.000

873		CYN003	Cyanide Poisoning	22	0.997

874		PNM008	Pneumothorax	54	0.997

875	P	ART018	Aortic Valve Insufficiency	52	0.997

876		JVN004	Juvenile Myelomonocytic Leukemia	66	0.996

877		AST002	Astroblastoma	34	0.996

878		SNL007	Senile Cataract	40	0.996

879	c	CRN243	Carney Complex, Type 1	53	0.993

880		MTP034	Metaphyseal Chondrodysplasia, Jansen Type	50	0.993

881		FML063	Familial Glucocorticoid Deficiency	58	0.993

882		RTR001	Retrograde Amnesia	41	0.993

883	c	SBC007	Subacute Thyroiditis	43	0.993

884	c	NMN014	Niemann-Pick Disease, Type C2	49	0.981

885		LWC002	Lowe Oculocerebrorenal Syndrome	68	0.980

886	P	AMY004	Amyloidosis	69	0.977

887		HMG005	Hemoglobinopathy	55	0.974

888		MST020	Mast Cell Activation Syndrome	27	0.972

889		AGR019	Age-Related Hearing Loss	41	0.969

890		FRC011	Fructose Intolerance, Hereditary	55	0.969

891	P	GCH001	Gaucher's Disease	69	0.967

892		NCL008	Nuclear Ribonucleic Acid	15	0.963

893		CRT072	Creutzfeldt-Jakob Disease	67	0.962

894		SGW002	Segawa Syndrome, Autosomal Recessive	44	0.959

895		SLW005	Slowed Nerve Conduction Velocity, Autosomal Dominant	35	0.959

896		THY121	Thyroid Gland Anaplastic Carcinoma	66	0.959

897		THY123	Thyroid Gland Follicular Carcinoma	53	0.959

898		WHP002	Whiplash	35	0.959

899	c	RTN150	Retinitis Pigmentosa 10	44	0.954

900		HYP114	Hypertensive Nephropathy	35	0.950

901		TRN030	Transient Erythroblastopenia of Childhood	34	0.950

902		HML018	Homologous Wasting Disease	21	0.947

903		CNT047	Contact Dermatitis	56	0.944

904		MST005	Mastitis	52	0.942

905	P	CMP008	Compartment Syndrome	49	0.942

906	P	MGR003	Migraine with Aura	51	0.940

907	P	PRN023	Prion Disease	60	0.940

908	c	CHR418	Chronic Leukemia	48	0.937

909		STT041	Stuttering	52	0.933

910		PSY004	Psychotic Disorder	66	0.932

911		BLM002	Bulimia Nervosa	56	0.931

912	P	GLL020	Gallbladder Disease	57	0.931

913	c	PSD104	Pseudohypoparathyroidism, Type Ii	31	0.931

914		DBT092	Diabetes Insipidus, Nephrogenic, X-Linked	39	0.931

915		GRG001	Greig Cephalopolysyndactyly Syndrome	64	0.931

916	c	46X049	46,xy Sex Reversal 2	51	0.931

917		GLC043	Glucocorticoid Deficiency 2	27	0.931

918		MYB001	Myoblastoma	28	0.931

919		MGL001	Megaloblastic Anemia	59	0.929

920		CTN011	Cutaneous Porphyria	45	0.926

921		MNN009	Meningoencephalitis	47	0.926

922		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.916

923		RBF001	Riboflavin Deficiency	49	0.909

924		PLM035	Pulmonary Eosinophilia	49	0.902

925		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	0.902

926	P	MJR007	Major Affective Disorder 1	42	0.902

927		GNT167	Genetic Obesity	33	0.901

928	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.900

929		INT075	Intracranial Hypertension	52	0.900

930		APH001	Aphthous Stomatitis	57	0.898

931		PRM236	Primary Biliary Cholangitis	62	0.894

932		VSC004	Vasculogenic Impotence	29	0.892

933	P	ANT006	Antiphospholipid Syndrome	55	0.892

934	P	HRM001	Hermansky-Pudlak Syndrome	65	0.884

935		ACR013	Acrodysostosis	53	0.883

936		NPH091	Nephrolithiasis, Calcium Oxalate	61	0.882

937	P	MTR003	Mitral Valve Stenosis	53	0.882

938		HDG004	Hodgkin's Granuloma	22	0.879

939