Search results for Succinic acid

1753 hits were found for Succinic acid

#	Family	MCID	Name	MIFTS	Score
1		SCC001	Succinic Semialdehyde Dehydrogenase Deficiency	59	58.789

2		LPD008	Lipid Metabolism Disorder	62	39.375

3		NNL005	Non-Alcoholic Fatty Liver Disease	63	37.868

4		FTT001	Fatty Liver Disease	62	36.287

5		MTC207	Mitochondrial Complex Ii Deficiency, Nuclear Type 1	55	35.729

6		GST092	Gastroesophageal Reflux	61	35.489

7		RPD005	Rapidly Involuting Congenital Hemangioma	46	35.164

8		CHL068	Cholestasis	61	34.700

9		ARM002	Aromatic L-Amino Acid Decarboxylase Deficiency	56	33.543

10	P	MPL001	Maple Syrup Urine Disease	70	32.770

11	P	NRB001	Neuroblastoma	66	29.653

12		HLX001	Helix Syndrome	48	29.608

13		MTB004	Metabolic Acidosis	48	28.928

14		RFS006	Refsum Disease, Classic	63	28.843

15		ARG002	Argininosuccinic Aciduria	61	28.355

16	P	LVR013	Liver Disease	69	28.231

17		NRL016	Neural Tube Defects	81	26.779

18		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	26.709

19		CLT003	Colitis	63	26.500

20	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	26.126

21		GT001	Gout	64	26.041

22	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	25.814

23	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	25.814

24	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	25.812

25	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	25.812

26	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	25.807

27	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	25.807

28	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	25.807

29	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	25.807

30	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	25.807

31	c	TYP009	Type 2 Diabetes Mellitus	92	25.444

32		48X005	48,xyyy	39	25.396

33	P	SZR006	Seizure Disorder	70	25.366

34	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	25.216

35		HYP066	Hyperglycemia	61	24.730

36		LVR012	Liver Cirrhosis	63	24.283

37	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	24.229

38		ISC004	Ischemia	61	24.154

39		ACT119	Acute Promyelocytic Leukemia	62	23.738

40		HYP266	Hypoxia	57	23.702

41	P	DDN001	Duodenal Ulcer	53	23.577

42		AMN002	Amino Acid Metabolic Disorder	39	23.379

43		AGN016	Aging	54	23.296

44		BNR002	Bone Resorption Disease	47	23.175

45		ALK013	Alkaptonuria	59	23.133

46	c	MTC059	Mitochondrial Dna Depletion Syndrome 5	48	23.118

47	P	HYP750	Hypertriglyceridemia, Familial	62	22.816

48	P	ENC018	Encephalopathy	62	22.806

49	P	CRN300	Coronary Heart Disease 1	73	22.780

50	P	MYP004	Myopathy	67	22.775

51	c	HYP836	Hypercholesterolemia, Familial, 1	73	22.605

52		GLL048	Glial Tumor	52	22.446

53		HYP781	Hypoascorbemia	52	22.394

54		GLM045	Glioma	63	22.352

55		ULC004	Ulcerative Colitis	74	22.215

56		ISV001	Isovaleric Acidemia	54	22.202

57	P	PHC003	Pheochromocytoma	69	22.182

58		NNL006	Non-Alcoholic Steatohepatitis	54	22.120

59		OST012	Osteoarthritis	77	21.577

60		ADR040	Adrenal Gland Pheochromocytoma	46	21.568

61	P	DBT009	Diabetes Mellitus	67	21.552

62	c	CHR684	Chronic Kidney Disease	69	21.552

63		IRN002	Iron Metabolism Disease	57	21.372

64	P	KDN018	Kidney Disease	72	21.350

65	P	BRS047	Breast Cancer	98	21.314

66	P	DRR001	Diarrhea	55	21.229

67		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	21.201

68		PPT005	Peptic Ulcer Disease	58	21.143

69		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	21.021

70		PRM236	Primary Biliary Cholangitis	60	20.748

71		GLB002	Glioblastoma	67	20.663

72	P	GST044	Gastritis	55	20.553

73		HYP056	Hypoglycemia	65	20.531

74		HMN044	Human Immunodeficiency Virus Type 1	78	20.518

75	P	LKM002	Leukemia	67	20.427

76		PRT037	Pertussis	65	20.403

77		ALL029	Allergic Disease	59	20.394

78	P	URN019	Urinary Tract Infection	49	20.389

79	P	ACN011	Acne	57	20.359

80		ORG002	Organic Acidemia	44	20.346

81	P	HNT016	Huntington Disease	73	20.196

82		ATH013	Atherosclerosis Susceptibility	63	20.111

83		MNT002	Mental Depression	57	20.103

84		GBM001	Gaba Aminotransferase Deficiency	29	20.094

85		DFC004	Deficiency Anemia	74	20.082

86	P	PRS040	Prostate Cancer	95	20.045

87		PHS025	Phosphatase, Acid, of Tissues	28	19.770

88		DPR016	Depression	65	19.626

89		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	19.572

90		CYS001	Cystic Fibrosis	78	19.559

91	P	CLR023	Colorectal Cancer	100	19.519

92	P	LCT001	Lactic Acidosis	51	19.452

93	P	HPT023	Hepatocellular Carcinoma	96	19.361

94	c	HYP595	Hypertension, Essential	85	19.291

95	P	HRT032	Heart Disease	81	19.155

96	P	EPL164	Epilepsy	68	19.110

97		47X002	47,xyy	48	18.984

98	P	OST002	Osteoporosis	76	18.930

99	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	18.899

100	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	18.899

101	P	INF038	Influenza	68	18.782

102		CRH001	Crohn's Disease	80	18.782

103	P	INF037	Inflammatory Bowel Disease	53	18.720

104	c	MGR028	Migraine with or Without Aura 1	64	18.623

105		HYP060	Hyperinsulinism	54	18.609

106	P	ART022	Arthritis	71	18.605

107	P	PRD008	Periodontitis	64	18.579

108		LPP008	Lipoprotein Quantitative Trait Locus	65	18.571

109	P	MJR001	Major Depressive Disorder	68	18.543

110	P	ALZ034	Alzheimer Disease	87	18.516

111		PHN003	Phenylketonuria	76	18.397

112		NPH009	Nephrolithiasis	54	18.277

113	P	PRG013	Paraganglioma	57	18.239

114	c	INH020	Inherited Metabolic Disorder	48	18.207

115		RNL114	Renal Cell Carcinoma, Nonpapillary	80	18.062

116	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	18.051

117		HRW001	Hair Whorl	35	17.991

118	P	MYC084	Mycobacterium Tuberculosis 1	68	17.958

119	P	HPT021	Hepatitis	69	17.932

120		HMC014	Homocysteinemia	52	17.916

121		STT001	Status Epilepticus	59	17.872

122	P	PNC035	Pancreatic Cancer	86	17.870

123	c	PRC016	Pre-Eclampsia	65	17.833

124	P	LNG032	Lung Cancer	98	17.746

125	c	ACT068	Acute Cystitis	61	17.586

126		GST023	Gastric Ulcer	52	17.544

127		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	17.473

128		IMM167	Immune Deficiency Disease	78	17.367

129		GBT001	Gaba-Transaminase Deficiency	37	17.357

130		ADN018	Adenoma	59	17.287

131		SPN186	Spinal Cord Injury	61	17.178

132		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	17.128

133	c	ACT071	Acute Kidney Failure	60	17.104

134	P	BPL003	Bipolar Disorder	56	17.097

135		CYT002	Cytokine Deficiency	43	17.026

136	c	MJR022	Major Affective Disorder 8	38	16.998

137	c	MJR024	Major Affective Disorder 9	41	16.998

138	P	VSC007	Vascular Disease	63	16.995

139		ART140	Arteries, Anomalies of	53	16.933

140	P	HYP265	Hypotonia	42	16.892

141		ADR007	Adrenoleukodystrophy	73	16.875

142	c	ACT027	Acute Pancreatitis	60	16.804

143	c	LKM061	Leukemia, Acute Myeloid	83	16.792

144	P	PSR002	Psoriasis	63	16.787

145		DRM006	Dermatitis	62	16.725

146	P	NRP001	Neuropathy	60	16.690

147		OCL069	Ocular Motor Apraxia	57	16.681

148		OST159	Osteogenic Sarcoma	66	16.644

149		CTR172	Citrullinemia, Classic	65	16.612

150	P	HRP006	Herpes Simplex	65	16.594

151		BRN071	Brain Injury	50	16.591

152		TRM010	Traumatic Brain Injury	51	16.578

153	P	CHL066	Cholangitis	52	16.574

154		ANX004	Anoxia	40	16.445

155	P	RHM011	Rheumatoid Arthritis	82	16.409

156		TRC120	Tricarboxylic Acid Cycle, Defect of	16	16.257

157		GMM004	Gamma-Amino Butyric Acid Metabolism Disorder	27	16.254

158		PPL052	Papillomatosis, Confluent and Reticulated	34	16.238

159	c	HPT073	Hepatitis C Virus	71	16.185

160	P	ATS364	Autism	69	16.177

161		CNG034	Congestive Heart Failure	69	16.165

162	c	TYP008	Type 1 Diabetes Mellitus	70	16.149

163		KRT002	Keratomalacia	55	16.141

164	P	PNC044	Pancreatitis	61	16.140

165	c	ATS007	Autism Spectrum Disorder	72	16.113

166		HPT004	Hepatic Coma	43	16.107

167		PST011	Pustulosis of Palm and Sole	52	16.058

168		ALC007	Alcohol Dependence	66	16.037

169	P	MYL006	Myeloid Leukemia	61	15.969

170		BCT022	Bacterial Infectious Disease	56	15.943

171	P	MYC007	Myocardial Infarction	70	15.904

172		CHL014	Cholera	62	15.889

173		PRT036	Peritonitis	65	15.885

174		HPT019	Hepatic Encephalopathy	59	15.877

175	P	ADN016	Adenocarcinoma	63	15.811

176		HMP009	Haemophilus Influenzae	41	15.808

177		SCC003	Succinic Acidemia	10	15.739

178		STR067	Stroke, Ischemic	80	15.725

179		MYL069	Myeloma, Multiple	77	15.711

180	P	OVR042	Ovarian Cancer	88	15.700

181	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	15.657

182	P	GST053	Gastric Cancer	83	15.625

183		SKN016	Skin Disease	63	15.583

184	c	PCH010	Pachyonychia Congenita 3	43	15.552

185	P	BND020	Bone Disease	59	15.549

186		MYP097	Myopathy with Lactic Acidosis, Hereditary	31	15.537

187	P	LTR001	Lateral Sclerosis	58	15.357

188		TXC005	Toxic Shock Syndrome	62	15.337

189	c	MCR120	Microvascular Complications of Diabetes 7	47	15.303

190		ATM095	Autoimmune Disease	61	15.232

191		END086	End Stage Renal Disease	52	15.221

192	c	DNT047	Dentinogenesis Imperfecta Type 2	35	15.209

193		ATS010	Autosomal Recessive Disease	42	15.177

194		PLM001	Pulmonary Tuberculosis	69	15.173

195	c	MCR113	Microvascular Complications of Diabetes 3	52	15.167

196		PRT251	Proteinuria, Chronic Benign	57	15.134

197	c	HPT001	Hepatitis C	62	15.127

198	c	MCR133	Microvascular Complications of Diabetes 4	41	14.990

199		INS024	Insulin-Like Growth Factor I	78	14.989

200	c	MCR130	Microvascular Complications of Diabetes 6	41	14.985

201	c	ATR087	Atrial Standstill 1	74	14.978

202	c	HPT016	Hepatitis B	62	14.929

203	P	HYP086	Hypothyroidism	69	14.893

204		GYR004	Gyrate Atrophy of Choroid and Retina	58	14.891

205	c	VSC019	Vesicoureteral Reflux 1	57	14.812

206		URL001	Urolithiasis	46	14.740

207		GLC003	Glucose Intolerance	54	14.724

208		CRV035	Cervical Cancer	73	14.712

209	P	MLN008	Melanoma	76	14.685

210	P	GLM040	Glioma Susceptibility 1	71	14.682

211		CNS004	Constipation	56	14.639

212		URT049	Urate Oxidase, Pseudogene	24	14.585

213	P	BLD134	Bladder Cancer	79	14.506

214		VTM002	Vitamin B12 Deficiency	48	14.354

215	c	MCR115	Microvascular Complications of Diabetes 5	65	14.338

216		CHL123	Chlamydia	58	14.306

217		SVR001	Severe Acute Respiratory Syndrome	67	14.284

218		ADR022	Adrenomyeloneuropathy	39	14.256

219	P	PRK039	Parkinsonism	55	14.245

220		DNT012	Dental Caries	53	14.174

221	P	OVR082	Overgrowth Syndrome	49	14.112

222	P	ADL010	Adult Respiratory Distress Syndrome	71	14.099

223	P	DRM053	Dermatitis, Atopic	65	14.014

224	P	MSC003	Muscular Atrophy	52	13.990

225		URM002	Uremia	47	13.981

226		ESP021	Esophageal Cancer	83	13.936

227	P	SCH015	Schizophrenia	74	13.845

228		AMN012	Aminoacidopathies	20	13.804

229		RCK004	Rickets	68	13.793

230		MTH071	Methane Production	25	13.732

231		STM007	Stomatitis	54	13.672

232		NPH091	Nephrolithiasis, Calcium Oxalate	61	13.583

233		CRB004	Cerebral Artery Occlusion	45	13.582

234	P	BCL017	B-Cell Lymphoma	59	13.579

235	P	INF032	Infertility	57	13.578

236		DBT010	Diabetic Neuropathy	54	13.570

237		PLM129	Pulmonary Disease, Chronic Obstructive	74	13.557

238	c	SML038	Small Cell Cancer of the Lung	69	13.527

239		HLC007	Helicobacter Pylori Infection	67	13.491

240	P	ENC004	Encephalitis	61	13.490

241	P	MLT020	Multiple Sclerosis	79	13.450

242	c	MCL042	Macular Degeneration, Age-Related, 1	85	13.420

243		VCC001	Vaccinia	47	13.394

244		THY029	Thyroid Carcinoma	51	13.386

245		BRN024	Bronchitis	67	13.354

246	P	PRP019	Peripheral Nervous System Disease	58	13.265

247	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	13.246

248		LWC001	Low Compliance Bladder	45	13.224

249	P	MSC005	Muscular Dystrophy	67	13.218

250	P	MTH008	Methylmalonic Acidemia	52	13.205

251	P	ALC033	Alcohol Use Disorder	61	13.132

252		SJG002	Sjogren-Larsson Syndrome	54	13.119

253		CRB039	Cerebrovascular Disease	66	13.104

254	c	HPT003	Hepatitis a	63	13.050

255		DWN001	Down Syndrome	70	12.945

256		SPN035	Spindle Cell Sarcoma	54	12.881

257		LNG099	Lung Disease	62	12.879

258		SRC014	Sarcoma	65	12.872

259	P	RHN004	Rhinitis	57	12.850

260	P	RSP003	Respiratory Failure	74	12.835

261	P	SKN015	Skin Carcinoma	71	12.798

262	P	GLM007	Glomerulonephritis	60	12.786

263		SQM006	Squamous Cell Carcinoma	60	12.719

264		TTN003	Tetanus	65	12.685

265		OST003	Osteonecrosis	61	12.606

266	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	12.556

267		EMB004	Embryonal Carcinoma	56	12.529

268		MLG169	Malignant Astrocytoma	57	12.526

269		GST045	Gastroenteritis	58	12.503

270	P	AST005	Asthma	76	12.462

271		HYP005	Hypokalemia	55	12.445

272		CLN015	Colon Adenocarcinoma	65	12.432

273	P	LKM062	Leukemia, Acute Lymphoblastic	69	12.422

274		KRT009	Keratosis	53	12.416

275		ZLL002	Zollinger-Ellison Syndrome	55	12.373

276		DSS032	Disease by Infectious Agent	55	12.292

277	P	ZLL001	Zellweger Syndrome	65	12.291

278		MLR004	Malaria	80	12.248

279	P	CTR002	Cataract	60	12.238

280		CRD132	Cardiac Conduction Defect	60	12.226

281	P	TRM003	Tremor	48	12.214

282	P	ATR011	Atrial Fibrillation	66	12.159

283	P	LPS004	Lupus Erythematosus	61	12.150

284	P	RTN024	Retinoblastoma	73	12.072

285	P	HDC001	Headache	57	12.069

286	c	ACT075	Acute Myocardial Infarction	56	12.064

287	P	PLY019	Polyneuropathy	52	12.052

288	P	EXN002	Exanthem	58	12.045

289	c	SYS001	Systemic Lupus Erythematosus	87	12.016

290		PRS045	Prostatic Hypertrophy	53	11.998

291	P	GLY013	Glycogen Storage Disease	60	11.996

292	P	THR014	Thrombocytopenia	66	11.970

293		ACQ007	Acquired Immunodeficiency Syndrome	59	11.882

294	P	BRS044	Breast Adenocarcinoma	58	11.875

295	P	PYL005	Pyelonephritis	57	11.861

296	P	INB001	Inborn Amino Acid Metabolism Disorder	11	11.825

297		GST033	Gestational Diabetes	61	11.824

298	P	DYS154	Dystonia	64	11.811

299	P	KDN017	Kidney Cancer	61	11.779

300	P	AMY004	Amyloidosis	70	11.760

301	c	DWL002	Dowling-Degos Disease 1	58	11.739

302	P	HYP076	Hyperthyroidism	53	11.733

303		GST019	Gastrointestinal Stromal Tumor	78	11.717

304		SVR004	Severe Combined Immunodeficiency	72	11.716

305		PLM010	Pulmonary Edema	55	11.699

306	P	FBR017	Fibrosarcoma	56	11.698

307		CYS013	Cystinuria	66	11.672

308		HGH043	High Grade Glioma	45	11.641

309		PRP001	Propionic Acidemia	65	11.639

310		AVN001	Avian Influenza	61	11.618

311	P	PNM007	Pneumonia	67	11.535

312		NRR001	Neuroretinitis	42	11.499

313		RTN023	Retinitis	46	11.497

314	P	LNG064	Lung Cancer Susceptibility 3	70	11.486

315		IRN001	Iron Deficiency Anemia	58	11.474

316		MDD011	Mood Disorder	62	11.466

317		HMS001	Hemosiderosis	48	11.465

318		MTH009	Mouth Disease	57	11.439

319	P	ECL001	Eclampsia	52	11.355

320	P	ART021	Arteriosclerosis	54	11.347

321	P	FRG001	Fragile X Syndrome	70	11.343

322		CHL004	Cholelithiasis	49	11.291

323		CLF027	Cleft Palate, Isolated	64	11.287

324		ALL014	Allergic Encephalomyelitis	34	11.240

325		IRR002	Irritable Bowel Syndrome	65	11.239

326		MYL009	Myelodysplastic Syndrome	67	11.198

327		PRS021	Prostatic Adenoma	43	11.157

328		PRS047	Prostatitis	58	11.154

329	P	PRP029	Porphyria	60	11.140

330	P	EYD002	Eye Disease	57	11.134

331		DPH001	Diphtheria	59	11.123

332		ANG054	Angina Pectoris	66	11.109

333	c	DLT002	Dilated Cardiomyopathy	78	11.065

334	P	TMP001	Temporal Lobe Epilepsy	49	11.050

335		PLM033	Pulmonary Embolism	58	11.045

336		PRX001	Peroxisomal Disease	46	11.012

337		MYP009	Myopathy with Deficiency of Iscu	12	11.006

338	P	NTR004	Neutropenia	63	10.948

339		PRP027	Peripheral Vascular Disease	71	10.947

340	P	NRF002	Neurofibromatosis	57	10.937

341	P	PLY011	Polycystic Ovary Syndrome	57	10.913

342	P	PLM037	Pulmonary Hypertension	72	10.903

343	P	NSP012	Nasopharyngeal Carcinoma	61	10.867

344	P	KLZ004	Kala-Azar 1	41	10.855

345		LSH001	Leishmaniasis	64	10.855

346		PRS129	Prostatic Hyperplasia, Benign	49	10.844

347	P	RRH023	Rare Hereditary Hemochromatosis	54	10.841

348	P	HYP098	Hypereosinophilic Syndrome	66	10.837

349		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	10.819

350	P	LYM118	Lymphoma	67	10.796

351	P	NPH012	Nephrotic Syndrome	60	10.744

352	P	PLM036	Pulmonary Fibrosis	66	10.728

353	c	ACT134	Acute Liver Failure	59	10.717

354		PST092	Posttransplant Acute Limbic Encephalitis	28	10.704

355		ACY011	Acyl-Coa Dehydrogenase Deficiency	30	10.692

356		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	10.689

357		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	10.680

358		LPT014	Leptin Deficiency or Dysfunction	78	10.664

359	P	MTC133	Mitochondrial Myopathy	50	10.654

360	P	PRK057	Parkinson Disease, Late-Onset	80	10.614

361	P	THL005	Thalassemia	56	10.565

362	P	CRD119	Cardiac Arrest	67	10.553

363	P	CYS018	Cystitis	59	10.515

364	P	CRD246	Cardiovascular System Disease	56	10.514

365	P	BNG032	Benign Mesothelioma	53	10.511

366	P	HYP069	Hyperparathyroidism	62	10.510

367		BRN004	Brain Edema	54	10.510

368	P	SPP010	Suppressor of Tumorigenicity 3	51	10.509

369	P	RTN008	Retinitis Pigmentosa	80	10.501

370		NTR005	Nutritional Deficiency Disease	61	10.494

371		CRB011	Cerebrotendinous Xanthomatosis	65	10.452

372	P	LKM071	Leukemia, Chronic Lymphocytic	75	10.400

373		GST050	Gastrointestinal System Disease	55	10.390

374		INS001	Insulinoma	59	10.380

375		PLY150	Polykaryocytosis Inducer	29	10.338

376		DYS073	Dysphagia	53	10.328

377		PPL022	Papilloma	53	10.320

378	c	VRL010	Viral Hepatitis	53	10.311

379	P	MLN007	Male Infertility	56	10.311

380		CNT047	Contact Dermatitis	57	10.285

381		CHG001	Chagas Disease	66	10.256

382	c	ACT073	Acute Leukemia	58	10.240

383	P	ALP008	Alopecia	54	10.217

384		ALL003	Allergic Rhinitis	67	10.172

385		ENT011	Enterocolitis	55	10.150

386		HNS001	Hansen's Disease	32	10.109

387	P	DMN002	Dementia	66	10.107

388	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	10.106

389		BRN028	Brain Cancer	74	10.100

390	P	URT039	Urticaria	58	10.081

391	P	LPR021	Leprosy 3	71	10.066

392		HDN002	Head Injury	44	10.063

393	P	CHR345	Chronic Pain	50	10.051

394		MST005	Mastitis	53	10.019

395		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	10.011

396	c	BRN108	Branchiootic Syndrome 1	62	10.005

397	P	PLY014	Polycystic Kidney Disease	69	9.977

398	P	MNN013	Meningitis	65	9.967

399		ACT098	Acute Erythroid Leukemia	55	9.940

400		THR024	Thrombosis	56	9.938

401		SCH014	Schistosomiasis	56	9.928

402		SQM002	Squamous Cell Papilloma	46	9.927

403		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	9.922

404		END057	Endometrial Cancer	72	9.922

405	P	MTC069	Mitochondrial Disorders	57	9.915

406		MSL001	Measles	61	9.905

407		PRP030	Purpura	54	9.843

408		INT323	Intraocular Pressure Quantitative Trait Locus	64	9.798

409	P	HMC002	Homocystinuria	53	9.773

410	P	MYC033	Myoclonus	47	9.773

411		NWC001	Newcastle Disease	47	9.770

412	c	LKM063	Leukemia, Chronic Myeloid	71	9.761

413	P	RTN016	Retinal Degeneration	52	9.731

414		GNG013	Gingivitis	59	9.712

415		TRT001	Teratocarcinoma	42	9.708

416		PNG002	Pain Agnosia	51	9.696

417	P	HYP061	Hypertrophic Cardiomyopathy	69	9.694

418	P	ATR005	Atrophic Gastritis	50	9.671

419	P	RCT021	Rectum Cancer	54	9.595

420		ARG004	Argyria	26	9.545

421	P	CND004	Candidiasis	58	9.542

422	P	ART023	Arthropathy	61	9.538

423		STF001	Stiff-Person Syndrome	58	9.532

424		ADL002	Adult Syndrome	70	9.527

425		XNT003	Xanthomatosis	49	9.500

426		ANX010	Anxiety	70	9.492

427	c	PRD040	Periodontitis, Chronic	52	9.482

428	P	OBS001	Obstructive Jaundice	48	9.478

429	P	INS002	in Situ Carcinoma	53	9.460

430	P	SHR001	Short Bowel Syndrome	53	9.424

431	P	TRN020	Turner Syndrome	67	9.409

432		BCT002	Bacterial Vaginosis	53	9.393

433		ACY009	Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of	59	9.349

434		BLR008	Bilirubin Metabolic Disorder	57	9.249

435		MLD018	Mild Cognitive Impairment	48	9.234

436	P	ANR048	Aniridia 1	64	9.220

437		CRV045	Cervical Intraepithelial Neoplasia	39	9.202

438		ORL015	Oral Squamous Cell Carcinoma	43	9.200

439		CRV002	Cervix Uteri Carcinoma in Situ	47	9.199

440		CVD001	Covid-19	57	9.194

441		RYS001	Reye Syndrome	49	9.177

442	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	9.141

443		ISL099	Isolated Methylmalonic Acidemia	36	9.140

444		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	9.124

445	c	LKM005	Leukemia, T-Cell, Chronic	34	9.096

446		RNL077	Renal Fibrosis	46	9.092

447	P	SCK005	Sickle Cell Disease	56	9.091

448		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	9.077

449	P	CNJ013	Conjunctivitis	66	9.029

450	P	MLT074	Multiple Endocrine Neoplasia	59	9.007

451		MDD018	Middle East Respiratory Syndrome	44	9.006

452		INT007	Intermediate Coronary Syndrome	54	8.941

453		VGN023	Vaginitis	56	8.924

454		CLR108	Colorectal Adenoma	64	8.854

455		LYS002	Lysosomal Storage Disease	51	8.820

456		CMM005	Common Cold	56	8.811

457	P	SYS005	Systemic Scleroderma	74	8.782

458		HYD002	Hydronephrosis	58	8.776

459		BLR001	Biliary Atresia	55	8.774

460	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	8.765

461		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	65	8.747

462		ORL011	Oral Cancer	60	8.743

463	P	INT068	Intestinal Disease	53	8.712

464	P	RNL007	Renal Tubular Acidosis	50	8.710

465	c	BSL007	Basal Cell Carcinoma	68	8.666

466		MSC007	Muscle Hypertrophy	64	8.663

467		SBC016	Subacute Delirium	43	8.660

468		MMM001	Mammary Paget's Disease	53	8.635

469	P	ACT008	Actinic Keratosis	54	8.630

470	P	HML002	Hemolytic Anemia	62	8.628

471		PSY004	Psychotic Disorder	66	8.623

472	P	SLP005	Sleep Disorder	61	8.602

473	P	MCR129	Microvascular Complications of Diabetes 1	68	8.583

474	P	TYR004	Tyrosinemia	50	8.582

475		END040	Endogenous Depression	55	8.578

476	c	PLM164	Pulmonary Hypertension, Primary, 1	76	8.574

477		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	8.545

478	P	CLC063	Celiac Disease 1	66	8.496

479		IGR001	Ige Responsiveness, Atopic	59	8.482

480	P	THY032	Thyroiditis	57	8.475

481		AMN006	Aminoaciduria	37	8.470

482		PLC002	Plica Syndrome	35	8.457

483		SYN007	Synovitis	55	8.457

484	P	GRF003	Graft-Versus-Host Disease	71	8.439

485		SCR011	Scrapie	39	8.398

486		TRN015	Transient Cerebral Ischemia	63	8.389

487	P	PTT006	Pituitary Adenoma	55	8.349

488		CHC001	Chickenpox	57	8.347

489		PTT037	Pituitary Tumors	44	8.346

490		NRT001	Neurotic Disorder	56	8.324

491	P	MYC008	Myocarditis	59	8.317

492		TYP007	Typhoid Fever	64	8.305

493		BRK010	Burkitt Lymphoma	66	8.274

494	P	FNC004	Fanconi Syndrome	60	8.266

495	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	8.223

496		TLN003	Telangiectasis	51	8.216

497		OTT002	Otitis Media	71	8.190

498		MSC157	Muscular Dystrophy, Duchenne Type	79	8.180

499		GST040	Gastric Adenocarcinoma	67	8.175

500		PRN011	Pernicious Anemia	53	8.164

501		CHR074	Choriocarcinoma	46	8.160

502	P	MCR010	Microcephaly	60	8.146

503		LYM133	Lymphoma, Hodgkin, Classic	74	8.140

504	c	SCL052	Scleroderma, Familial Progressive	61	8.132

505		PRN019	Perinatal Necrotizing Enterocolitis	60	8.119

506		DBT084	Diabetes Mellitus, Ketosis-Prone	60	8.094

507		FDL002	Food Allergy	47	8.074

508		PNC001	Pancytopenia	53	8.048

509	P	SRC025	Sarcoidosis 1	71	8.022

510		CHL067	Cholecystitis	60	8.015

511	P	FML011	Familial Adenomatous Polyposis	71	8.015

512	P	PRN023	Prion Disease	60	8.015

513		SPS057	Spasticity	42	7.981

514		DYS015	Dysentery	50	7.962

515		PNC041	Pancreatic Ductal Adenocarcinoma	51	7.961

516		MTC005	Mitochondrial Metabolism Disease	45	7.948

517		PNC129	Pancreatic Adenocarcinoma	65	7.944

518	P	END044	Endometriosis	62	7.936

519		RHB024	Rhabdomyosarcoma 2	67	7.928

520	c	ATS307	Autosomal Recessive Cerebellar Ataxia	39	7.923

521		MNN043	Meningioma, Familial	79	7.914

522		ASP036	Aspirin Allergy	27	7.911

523	P	UVT001	Uveitis	57	7.906

524		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	7.899

525	P	SCL018	Scoliosis	57	7.877

526	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	7.860

527		LYM019	Lymphosarcoma	46	7.850

528	P	LKD001	Leukodystrophy	59	7.835

529		HYP141	Hyperphenylalaninemia	42	7.829

530		GTR002	Goiter	53	7.823

531		CRB037	Cerebral Palsy	67	7.800

532	P	ANP001	Anaplastic Large Cell Lymphoma	61	7.782

533		PRT013	Portal Hypertension	59	7.781

534		GLT035	Glutaric Acidemia I	57	7.763

535	P	RHB003	Rhabdomyosarcoma	66	7.763

536	c	ACT042	Acute Pyelonephritis	45	7.752

537		SCR001	Secretory Meningioma	40	7.731

538		LYM002	Lymphoplasmacyte-Rich Meningioma	35	7.731

539		SPN021	Spinal Meningioma	50	7.731

540		ALL010	Allergic Contact Dermatitis	56	7.723

541	P	HYD006	Hydrocephalus	61	7.690

542	P	RTN018	Retinal Disease	53	7.682

543		KRN002	Kearns-Sayre Syndrome	63	7.664

544	P	MVM001	Movement Disease	61	7.657

545		SCK003	Sickle Cell Anemia	74	7.656

546		AMN003	Amnestic Disorder	54	7.639

547		RTN017	Retinal Detachment	60	7.608

548		SPL018	Splenomegaly	49	7.607

549		MGL001	Megaloblastic Anemia	58	7.597

550		ANT039	Antisynthetase Syndrome	55	7.584

551	P	SLP006	Sleep Apnea	69	7.557

552	P	MDL005	Medulloblastoma	75	7.552

553		PLC008	Placenta Disease	49	7.545

554	c	MST023	Mesothelioma, Malignant	56	7.538

555		ALL006	Allergic Asthma	56	7.527

556	P	VSC011	Vasculitis	61	7.522

557		CRH005	Crohn's Colitis	53	7.511

558		NRN004	Neuroendocrine Tumor	59	7.509

559		PRT038	Protein-Energy Malnutrition	53	7.490

560	c	SCN036	Secondary Progressive Multiple Sclerosis	55	7.479

561	P	SBR004	Seborrheic Dermatitis	44	7.439

562		IGG001	Iga Glomerulonephritis	50	7.433

563		MLK006	Milk Allergy	47	7.409

564		LGH007	Leigh Syndrome	70	7.387

565	P	END033	Endocarditis	58	7.383

566		ANT024	Anthrax Disease	58	7.377

567		DSS009	Disseminated Intravascular Coagulation	57	7.375

568		LYM143	Lymphoma, Non-Hodgkin, Familial	75	7.371

569		CLF001	Cleft Lip	53	7.339

570		CLR109	Colorectal Adenocarcinoma	50	7.333

571		VSC002	Vascular Dementia	60	7.307

572		RBS001	Rabies	58	7.303

573	P	OPN001	Open-Angle Glaucoma	55	7.257

574		SLP001	Sleeping Sickness	56	7.240

575	c	HNT011	Huntington Disease-Like 3	34	7.231

576	P	GRV001	Graves' Disease	55	7.208

577	c	BCT007	Bacterial Meningitis	55	7.194

578		RLP002	Relapsing-Remitting Multiple Sclerosis	56	7.157

579		PRP016	Paraplegia	52	7.148

580		VRC005	Varicose Veins	60	7.123

581		OST017	Osteomyelitis	63	7.120

582		URN010	Urinary Tract Obstruction	55	7.109

583		SQM013	Squamous Cell Carcinoma, Head and Neck	73	7.081

584		URT010	Ureteral Obstruction	45	7.078

585		PHR003	Pharyngitis	58	7.069

586		KRT006	Keratoconjunctivitis	53	7.051

587		PRP083	Porphyria, Acute Intermittent	65	7.041

588		PLM134	Pulmonary Fibrosis, Idiopathic	76	7.039

589		FBR047	Fibromyalgia	58	7.009

590	P	ANG015	Angioedema	56	7.003

591		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	6.993

592		CHR073	Choreatic Disease	54	6.993

593		VSC003	Visceral Leishmaniasis	55	6.992

594		ANR007	Anorexia Nervosa	60	6.965

595		ACR007	Acromegaly	70	6.944

596	P	SNS001	Sensorineural Hearing Loss	59	6.902

597		THY111	Thyroid Carcinoma, Familial Medullary	67	6.896

598		ANR040	Aneurysm	61	6.895

599		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	6.887

600		KRT019	Keratitis, Hereditary	66	6.869

601		TRN018	Transitional Cell Carcinoma	56	6.852

602	P	SPN046	Spinal Muscular Atrophy	63	6.847

603	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	6.839

604		LWC002	Lowe Oculocerebrorenal Syndrome	68	6.836

605	P	TBR001	Tuberous Sclerosis	69	6.827

606		GST030	Gastrinoma	45	6.805

607		TRY001	Trypanosomiasis	50	6.792

608		IMP005	Impotence	52	6.782

609		HPT022	Hepatoblastoma	54	6.775

610		LSC001	Lesch-Nyhan Syndrome	62	6.775

611		LNG031	Lung Benign Neoplasm	51	6.771

612		ACY005	Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of	55	6.768

613		SFT003	Soft Tissue Sarcoma	57	6.763

614	P	RTT002	Rett Syndrome	79	6.758

615	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	6.752

616		YLL002	Yellow Fever	61	6.742

617		WTH001	Withdrawal Disorder	48	6.720

618	c	MCR112	Microvascular Complications of Diabetes 2	42	6.716

619		ORT008	Orotic Aciduria	57	6.711

620		DWR001	Dwarfism	44	6.694

621		LYM027	Lymphopenia	56	6.681

622		PRP080	Peripheral Artery Disease	54	6.657

623		ART016	Aortic Aneurysm	68	6.656

624	P	CTN015	Cutaneous T Cell Lymphoma	48	6.641

625		LMY002	Leiomyoma	51	6.629

626		STN013	Stenotrophomonas Maltophilia Infection	26	6.624

627		CYS010	Cystinosis	62	6.617

628		JPN002	Japanese Encephalitis	61	6.609

629		DMY004	Demyelinating Disease	50	6.585

630		SPN051	Spondylitis	51	6.585

631		INF009	Inflammatory Spondylopathy	30	6.585

632		PRG017	Paraganglioma and Gastric Stromal Sarcoma	63	6.583

633	c	HMC039	Hemochromatosis, Type 1	73	6.577

634	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	6.575

635	P	LCH002	Lichen Planus	54	6.559

636		ARG007	Argininemia	58	6.559

637		MDM001	Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency	34	6.555

638		ILS001	Ileus	50	6.551

639		CND006	Candida Glabrata	30	6.550

640		CLR030	Clear Cell Renal Cell Carcinoma	54	6.548

641		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	6.530

642	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	6.530

643	P	MTR014	Motor Neuron Disease	65	6.514

644	P	BRB001	Beriberi	44	6.496

645	P	ICH004	Ichthyosis	56	6.492

646		DBT002	Diabetic Autonomic Neuropathy	41	6.466

647		PLM031	Poliomyelitis	63	6.456

648	c	BLD140	Blood Group, I System	46	6.455

649	c	2HY001	2-Hydroxyglutaric Aciduria	38	6.446

650	P	MYS005	Myositis	56	6.441

651		PLG002	Plague	58	6.433

652		HYP080	Hypogonadism	50	6.431

653	P	NRC002	Narcolepsy	56	6.419

654		OVR094	Ovarian Epithelial Cancer	39	6.409

655		DBT004	Diabetic Polyneuropathy	50	6.394

656		MST004	Mast Cell Neoplasm	42	6.375

657		PLS011	Plasmacytoma	56	6.374

658		CRT015	Carotid Artery Occlusion	45	6.365

659		EXT007	Extracutaneous Mastocytoma	38	6.361

660		VRL011	Viral Infectious Disease	61	6.359

661	P	PHC019	Pheochromocytoma-Paraganglioma	35	6.359

662		CHR066	Chronic Fatigue Syndrome	60	6.330

663		EXT006	Extrahepatic Cholestasis	40	6.325

664		MCR013	Microphthalmia	60	6.314

665		HND015	Hand Skill, Relative	30	6.305

666		THY125	Thyroid Gland Medullary Carcinoma	48	6.274

667	P	PLY018	Polycythemia	56	6.274

668	P	ASP006	Aspergillosis	72	6.273

669	P	CHN012	Chondrosarcoma	57	6.267

670		CNN005	Connective Tissue Disease	67	6.260

671	P	OPT006	Optic Nerve Disease	58	6.259

672		HYP025	Hyperphosphatemia	48	6.256

673		SKN019	Skin Melanoma	71	6.223

674	c	GRV008	Graves Disease 1	54	6.196

675		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	6.153

676		TNS005	Tonsillitis	57	6.151

677		RTN020	Retinal Vascular Disease	46	6.148

678		ERL001	Early Myoclonic Encephalopathy	62	6.107

679		PST021	Postpartum Depression	50	6.099

680	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	6.093

681	P	MYS003	Myasthenia Gravis	68	6.063

682		CHR100	Chronic Ulcer of Skin	57	6.060

683	c	SPN225	Spondyloarthropathy 1	70	6.056

684		HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	60	6.047

685		CRC021	Carcinosarcoma	64	6.023

686		BRT005	Barth Syndrome	56	6.009

687		KWS001	Kwashiorkor	45	6.002

688		BRN002	Bronchiolitis	57	5.995

689		ASP007	Aspiration Pneumonia	49	5.990

690	c	PRM005	Primary Hyperparathyroidism	59	5.989

691		EPT021	Epithelial Recurrent Erosion Dystrophy	46	5.985

692		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	5.983

693		CHK001	Chikungunya	60	5.974

694	P	VTR007	Vitreoretinopathy	46	5.967

695		HRY003	Hairy Cell Leukemia	61	5.960

696		CNV004	Canavan Disease	62	5.949

697		NRM005	Neuromuscular Disease	63	5.943

698	c	GLC092	Glaucoma, Primary Open Angle	62	5.939

699	c	EXD008	Exudative Vitreoretinopathy 1	71	5.936

700		FCL014	Focal Epilepsy	53	5.927

701		BTN004	Biotin Deficiency	45	5.922

702		LST001	Listeriosis	59	5.919

703	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	5.917

704	c	SCN007	Secondary Hyperparathyroidism	51	5.894

705		PRM329	Premature Aging	36	5.868

706		LKP003	Leukoplakia	39	5.852

707	P	FTL001	Fetal Alcohol Syndrome	55	5.850

708	P	PGT001	Paget's Disease of Bone	61	5.843

709		INT002	Intermittent Claudication	61	5.834

710	c	TBR025	Tuberous Sclerosis 1	84	5.832

711		SDD001	Sudden Infant Death Syndrome	60	5.829

712		VLV047	Volvulus of Midgut	52	5.826

713	P	CNR004	Cone-Rod Dystrophy 2	74	5.823

714		NRT004	Neuritis	53	5.821

715		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	5.811

716		RST023	Resting Heart Rate, Variation in	40	5.787

717		WST001	West Syndrome	59	5.781

718		CHR178	Chromosomal Triplication	34	5.777

719		MLT157	Multiple System Atrophy 1	69	5.775

720		PTH003	Pathologic Nystagmus	52	5.774

721		OBS002	Obsessive-Compulsive Disorder	68	5.771

722	P	OLG002	Oligodendroglioma	66	5.757

723	P	ADL017	Adult T-Cell Leukemia	56	5.737

724	P	CRV039	Cervicitis	52	5.731

725		FMR004	Fumarase Deficiency	50	5.727

726		BCT004	Bacteriuria	47	5.726

727		MTC004	Mitochondrial Encephalomyopathy	42	5.725

728	P	MRC003	Mercury Poisoning	49	5.701

729		LMY003	Leiomyomatosis	44	5.685

730		INT020	Intravenous Leiomyomatosis	36	5.685

731	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	5.682

732	P	INT070	Intestinal Obstruction	57	5.678

733		ALC006	Alcoholic Hepatitis	61	5.675

734	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	5.660

735		HRT011	Heart Septal Defect	49	5.659

736		PLR008	Pleurisy	50	5.649

737	P	ATX030	Ataxia-Telangiectasia	80	5.649

738		GSG001	Gas Gangrene	52	5.645

739		MNN009	Meningoencephalitis	48	5.639

740	P	DBT005	Diabetes Insipidus	54	5.637

741		CMB007	Combined Immunodeficiency	57	5.626

742		CYN002	Cyanosis, Transient Neonatal	43	5.621

743		SHG001	Shigellosis	63	5.603

744		ANP008	Anaplastic Oligoastrocytoma	29	5.600

745	P	MYG005	Myoglobinuria	40	5.599

746		HMG005	Hemoglobinopathy	56	5.591

747	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	5.590

748		CRD223	Cardiac Arrhythmia	63	5.579

749		TRD006	Tardive Dyskinesia	53	5.577

750	P	CHR071	Charcot-Marie-Tooth Disease	64	5.570

751	P	TRT010	Teratoma	51	5.565

752	c	TYR012	Tyrosinemia, Type I	61	5.559

753	P	HML001	Hemolytic-Uremic Syndrome	52	5.554

754		ILT001	Ileitis	48	5.546

755	P	SYP003	Syphilis	59	5.541

756		HPT014	Hepatorenal Syndrome	49	5.534

757	P	RBL001	Rubella	58	5.526

758		TBR011	Tuberculous Meningitis	48	5.516

759	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	5.513

760		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	5.512

761		KRT001	Keratoconjunctivitis Sicca	50	5.509

762		MCL006	Macular Retinal Edema	57	5.503

763		TCK001	Tick-Borne Encephalitis	59	5.502

764	c	3MT015	3-Methylglutaconic Aciduria, Type I	51	5.502

765	P	MNC007	Monocytic Leukemia	47	5.497

766		BRC012	Brucellosis	66	5.495

767	P	MMP001	Mumps	57	5.494

768	P	PTS002	Ptosis	52	5.492

769		INT066	Interstitial Lung Disease	60	5.476

770		MYL020	Myelomeningocele	51	5.475

771		ACT003	Acute Kidney Tubular Necrosis	46	5.474

772		SPT004	Septic Arthritis	58	5.469

773		CRB090	Cerebral Hypoxia	42	5.453

774		NRM022	Neurometabolic Disease	24	5.444

775		RTC012	Reticuloendotheliosis, X-Linked	35	5.431

776		PLC005	Placental Insufficiency	56	5.428

777		AMN001	Amenorrhea	54	5.420

778	P	THY023	Thymoma	64	5.419

779	c	THY107	Thymoma, Familial	42	5.415

780	P	LRY019	Laryngitis	53	5.406

781	P	TCD001	Tic Disorder	49	5.385

782	P	RNL015	Renal Hypertension	45	5.375

783	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	5.369

784		RHM035	Rheumatic Fever-Related Antigen	37	5.368

785		RHM001	Rheumatic Fever	59	5.368

786		BRN056	Bronchopulmonary Dysplasia	56	5.363

787	P	VNT002	Ventricular Septal Defect	58	5.359

788	P	PLM034	Pulmonary Emphysema	58	5.346

789		GLY010	Glycine Encephalopathy	57	5.336

790	P	HYP111	Hyperprolinemia	45	5.335

791	c	CNT035	Central Nervous System Disease	54	5.317

792		ALP077	Alpha-Methylacetoacetic Aciduria	52	5.308

793	P	ALP009	Alopecia Areata	59	5.299

794		LNT004	Lentigines	46	5.295

795		INT067	Interstitial Nephritis	46	5.294

796		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	5.266

797	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	5.262

798		SPP011	Suppression of Tumorigenicity 12	61	5.252

799		INT075	Intracranial Hypertension	53	5.248

800	P	RRT020	Rare Tumor	39	5.239

801		3HY007	3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency	51	5.234

802		ANP005	Anaplastic Astrocytoma	57	5.206

803	P	SPR120	Supranuclear Palsy, Progressive, 1	69	5.180

804		CLL003	Cellulitis	53	5.179

805	P	MTH007	Methemoglobinemia	46	5.171

806		HST006	Histidinemia	48	5.166

807	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	5.165

808		PSR001	Psoriatic Arthritis	62	5.139

809		MCR017	Macrocytic Anemia	44	5.136

810		DFF005	Diffuse Large B-Cell Lymphoma	54	5.134

811		HVY002	Heavy Metal Poisoning	22	5.133

812		CNN003	Conn's Syndrome	79	5.131

813		ATN005	Autonomic Dysfunction	46	5.119

814		PLR007	Pleural Empyema	51	5.106

815		VTM033	Vitamin K Deficiency Bleeding	48	5.101

816		PPL002	Papillary Carcinoma	46	5.094

817		OST011	Osteomalacia	52	5.088

818		URT001	Urethritis	53	5.084

819	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	5.084

820	c	PRS136	Prostate Cancer, Hereditary, 6	33	5.081

821	c	PRS130	Prostate Cancer, Hereditary, 8	32	5.081

822	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	52	5.078

823		CLL010	Cellular Ependymoma	57	5.071

824	P	APL001	Aplastic Anemia	73	5.052

825	c	RNG015	Ring Chromosome 2	22	5.049

826		LRN003	Learning Disability	49	5.047

827		HRD029	Hereditary Leiomyomatosis and Renal Cell Cancer	56	5.019

828	P	MLG056	Malignant Hyperthermia	66	5.009

829	P	MYP006	Myopia	56	4.998

830	P	FLL037	Follicular Lymphoma	74	4.993

831	P	BNG030	Benign Ependymoma	51	4.991

832		FNG017	Fungal Infectious Disease	54	4.983

833		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	4.972

834	c	PRX059	Peroxisome Biogenesis Disorder 1a	56	4.962

835		CTN007	Cutaneous Leishmaniasis	62	4.958

836		MLN011	Malonyl-Coa Decarboxylase Deficiency	37	4.951

837	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	4.950

838		CHL045	Choline Deficiency Disease	39	4.946

839	P	MYT002	Myotonic Dystrophy	51	4.942

840	P	MST009	Mastocytosis	64	4.938

841	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	4.931

842		OCL006	Ocular Hypertension	53	4.898

843		HYP043	Hyperandrogenism	48	4.892

844		INF034	Infective Endocarditis	54	4.890

845	c	MCL062	Mucolipidosis Ii Alpha/beta	68	4.876

846	c	NRF024	Neurofibromatosis, Type I	72	4.872

847		ALC001	Alcohol-Related Birth Defect	36	4.860

848		ENC005	Encephalomalacia	44	4.854

849		MLC004	Mulchandani-Bhoj-Conlin Syndrome	51	4.837

850		DMP001	Dumping Syndrome	43	4.828

851		SYS003	Systolic Heart Failure	49	4.811

852	P	CRB088	Cerebral Atrophy	33	4.809

853	c	PRG020	Paragangliomas 3	39	4.807

854		LPR001	Lepromatous Leprosy	49	4.800

855		EPL131	Epilepsy, Pyridoxine-Dependent	45	4.795

856		MSN004	Mesenchymal Cell Neoplasm	42	4.792

857		RTN003	Retinal Ischemia	49	4.775

858	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	67	4.774

859		TND005	Tendinitis	54	4.770

860	c	ATM075	Autoimmune Encephalitis	40	4.769

861		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	4.755

862		VNH007	Von Hippel-Lindau Syndrome	73	4.749

863	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	4.748

864		BNN003	Bone Inflammation Disease	48	4.737

865		GLC086	Glucocorticoid-Induced Osteoporosis	43	4.735

866		ERY003	Erythema Multiforme	56	4.734

867	P	PMP001	Pemphigus	55	4.733

868		MNT001	Mantle Cell Lymphoma	67	4.713

869	P	CHL002	Childhood Absence Epilepsy	63	4.709

870	P	PRP003	Porphyria Cutanea Tarda	66	4.709

871	c	HRD002	Hereditary Angioedema	62	4.707

872		SLC006	Silicosis	56	4.704

873		IDP070	Idiopathic Scoliosis	42	4.700

874		CHD004	Chudley-Mccullough Syndrome	48	4.695

875		VGN019	Vaginal Discharge	47	4.691

876		ASP008	Aspiration Pneumonitis	42	4.681

877		CRY003	Cryptosporidiosis	56	4.681

878	c	TYR013	Tyrosinemia, Type Ii	49	4.679

879	c	DFN360	Deafness, Autosomal Dominant 69	34	4.673

880		MYC006	Mycosis Fungoides	65	4.669

881	c	PRG018	Paragangliomas 1	59	4.667

882		NNT012	Neonatal Jaundice	53	4.654

883		RNL065	Renal Cell Carcinoma, Papillary, 1	79	4.653

884		HRP004	Herpes Zoster	61	4.647

885	c	PRG021	Paragangliomas 4	37	4.646

886		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	64	4.627

887	P	END047	Endophthalmitis	53	4.623

888		NRG002	Neurogenic Bladder	55	4.616

889		CHL147	Chlamydia Pneumonia	47	4.613

890		PLS007	Plasmodium Falciparum Malaria	52	4.596

891		LMB024	Limbic Encephalitis	43	4.593

892	P	DRM010	Dermatomyositis	61	4.589

893		CYS005	Cysticercosis	60	4.585

894		END072	Endotheliitis	36	4.583

895		LYM009	Lymphocytic Choriomeningitis	46	4.581

896		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	4.577

897		ORL005	Oral Candidiasis	56	4.570

898	P	HYP040	Hypospadias	51	4.561

899		CMB011	Combined Malonic and Methylmalonic Aciduria	42	4.561

900		ACT078	Acute Porphyria	49	4.553

901		CRD137	Cardiogenic Shock	56	4.548

902		AND005	Androgen Insensitivity Syndrome, Mild	21	4.541

903		NRN005	Neuronal Ceroid-Lipofuscinoses	61	4.537

904	c	SPR086	Spermatogenic Failure 3	46	4.521

905		CCC002	Coccidiosis	50	4.519

906	P	PLY041	Polymyositis	59	4.511

907		PNM008	Pneumothorax	54	4.505

908		SNS003	Sensory Peripheral Neuropathy	52	4.504

909		APH002	Aphasia	56	4.491

910		NRL005	Neurilemmoma	60	4.491

911		MLG079	Malignant Pleural Mesothelioma	42	4.490

912		PMP014	Pemphigoid	51	4.487

913	c	MTC060	Mitochondrial Dna Depletion Syndrome 9	50	4.482

914		NRF007	Neurofibroma	64	4.481

915		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	31	4.481

916	P	FCL005	Focal Segmental Glomerulosclerosis	57	4.481

917		ABT001	Abetalipoproteinemia	68	4.481

918		ATX019	Ataxia with Vitamin E Deficiency	44	4.469

919	c	ACT004	Acute Diarrhea	40	4.463

920	P	RNV001	Renovascular Hypertension	49	4.447

921		HST010	Histiocytosis	49	4.431

922		NWB001	Newborn Respiratory Distress Syndrome	56	4.422

923		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	4.422

924		APH001	Aphthous Stomatitis	58	4.416

925	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	60	4.405

926	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	55	4.387

927	P	ALG028	Alagille Syndrome 1	73	4.384

928		GST037	Gastroparesis	52	4.384

929	P	OPT009	Optic Neuritis	57	4.383

930		THR016	Thrombophlebitis	50	4.381

931	P	VSC018	Visceral Steatosis	32	4.381

932		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	47	4.377

933		BTN003	Biotinidase Deficiency	62	4.376

934	P	CLS010	Cluster Headache	42	4.374

935	P	HYP838	Hyperlipidemia, Familial Combined, 3	61	4.369

936	P	AGG001	Aggressive Periodontitis	55	4.369

937		ORL013	Oral Lichen Planus	46	4.365

938		KLB003	Klebsiella Pneumonia	50	4.361

939		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	4.353

940		PLY100	Polyploidy	36	4.350

941		HYP003	Hypermethioninemia	51	4.344

942		PYR037	Pyruvate Carboxylase Deficiency	45	4.328

943	c	PRT132	Protoporphyria, Erythropoietic, 1	61	4.328

944		MST020	Mast Cell Activation Syndrome	28	4.309

945		ADR016	Adrenal Cortical Carcinoma	62	4.306

946		PCK003	Pick Disease of Brain	69	4.305

947	P	GLL018	Gallbladder Cancer	53	4.305

948		RBF001	Riboflavin Deficiency	49	4.302

949	P	LMY004	Leiomyosarcoma	62	4.296

950