Search results for NADH

1236 hits were found for NADH

#	Family	MCID	Name	MIFTS	Score
1		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	36	42.250

2		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	59	38.963

3	P	MPL001	Maple Syrup Urine Disease	69	9.403

4		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	48	9.289

5		PYR031	Pyruvate Dehydrogenase E3-Binding Protein Deficiency	43	9.197

6	P	MTH007	Methemoglobinemia	46	6.746

7	c	CNG223	Congenital Methemoglobinemia	39	5.883

8		ANX004	Anoxia	40	4.193

9	P	MYP004	Myopathy	67	3.636

10	P	OPT006	Optic Nerve Disease	57	3.310

11	P	LCT001	Lactic Acidosis	50	3.301

12	P	HRD217	Hereditary Optic Neuropathy	36	3.292

13		MTC005	Mitochondrial Metabolism Disease	44	3.215

14	P	MTC133	Mitochondrial Myopathy	51	3.085

15	P	NRP001	Neuropathy	59	2.804

16		LBR038	Leber Hereditary Optic Neuropathy, Modifier of	62	2.800

17		CYN002	Cyanosis, Transient Neonatal	43	2.751

18		HYP266	Hypoxia	56	2.593

19	P	MTC069	Mitochondrial Disorders	57	2.525

20	P	PRK039	Parkinsonism	55	2.485

21		LGH007	Leigh Syndrome	70	2.415

22		CHR066	Chronic Fatigue Syndrome	59	2.375

23		HLX001	Helix Syndrome	47	2.285

24	P	NRB001	Neuroblastoma	66	2.107

25		FTT001	Fatty Liver Disease	61	2.010

26		CHG001	Chagas Disease	65	1.985

27		MTC004	Mitochondrial Encephalomyopathy	42	1.956

28	P	MYC084	Mycobacterium Tuberculosis 1	68	1.938

29	c	ATS307	Autosomal Recessive Cerebellar Ataxia	38	1.927

30		SCC003	Succinic Acidemia	10	1.918

31		LBR036	Leber Plus Disease	67	1.901

32	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	1.891

33	c	ATR087	Atrial Standstill 1	74	1.883

34	P	ENC018	Encephalopathy	62	1.875

35		GLL048	Glial Tumor	51	1.875

36		HYP066	Hyperglycemia	60	1.778

37		GLM045	Glioma	62	1.746

38	P	ALZ034	Alzheimer Disease	87	1.715

39		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	1.704

40		CHL014	Cholera	62	1.704

41		LPD008	Lipid Metabolism Disorder	61	1.697

42		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	44	1.680

43		AGN016	Aging	53	1.648

44		CYS001	Cystic Fibrosis	77	1.599

45		PRT037	Pertussis	49	1.549

46		HYP056	Hypoglycemia	65	1.536

47		MTH072	Methemoglobin Reductase Deficiency	15	1.524

48		BRN071	Brain Injury	50	1.449

49	P	HYP061	Hypertrophic Cardiomyopathy	68	1.424

50	P	KLZ004	Kala-Azar 1	41	1.392

51		IRN002	Iron Metabolism Disease	56	1.392

52		LSH001	Leishmaniasis	63	1.392

53		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	1.390

54	P	GST053	Gastric Cancer	82	1.389

55	P	DYS154	Dystonia	64	1.383

56		TRM010	Traumatic Brain Injury	50	1.383

57		HMP009	Haemophilus Influenzae	41	1.374

58		NNL005	Non-Alcoholic Fatty Liver Disease	63	1.356

59	c	MJR022	Major Affective Disorder 8	37	1.326

60	c	MJR024	Major Affective Disorder 9	40	1.326

61	P	BPL003	Bipolar Disorder	56	1.326

62	P	HYP265	Hypotonia	42	1.321

63		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	1.306

64	c	MCR115	Microvascular Complications of Diabetes 5	65	1.283

65	P	CHR012	Chronic Granulomatous Disease	69	1.275

66		DYS015	Dysentery	49	1.273

67		ART140	Arteries, Anomalies of	52	1.261

68		LPP008	Lipoprotein Quantitative Trait Locus	65	1.261

69	P	BRS047	Breast Cancer	97	1.251

70	P	VSC007	Vascular Disease	62	1.249

71		CRN030	Coronary Stenosis	50	1.249

72		ECH003	Echinococcosis	52	1.247

73		ATS010	Autosomal Recessive Disease	42	1.236

74		OST159	Osteogenic Sarcoma	66	1.226

75	P	PRK057	Parkinson Disease, Late-Onset	79	1.226

76	P	HNT016	Huntington Disease	73	1.217

77		CRT020	Cortisone Reductase Deficiency	36	1.211

78		GLB002	Glioblastoma	67	1.199

79		HRW001	Hair Whorl	35	1.160

80		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	1.160

81		RNL114	Renal Cell Carcinoma, Nonpapillary	79	1.150

82	P	SZR006	Seizure Disorder	69	1.150

83	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	1.140

84		PST092	Posttransplant Acute Limbic Encephalitis	29	1.140

85	c	BRN108	Branchiootic Syndrome 1	63	1.118

86		DNT012	Dental Caries	53	1.118

87		MTB004	Metabolic Acidosis	48	1.112

88	P	SPP010	Suppressor of Tumorigenicity 3	50	1.107

89	P	CTR002	Cataract	59	1.107

90		48X005	48,xyyy	39	1.097

91		SLP001	Sleeping Sickness	56	1.095

92	P	MSC005	Muscular Dystrophy	66	1.090

93		MLR004	Malaria	77	1.083

94	P	RSP003	Respiratory Failure	73	1.083

95		ALL014	Allergic Encephalomyelitis	34	1.083

96		CTR172	Citrullinemia, Classic	64	1.075

97		CRT015	Carotid Artery Occlusion	45	1.067

98	P	BRS044	Breast Adenocarcinoma	58	1.057

99		CRB004	Cerebral Artery Occlusion	45	1.051

100	P	INF032	Infertility	60	1.030

101		PRM329	Premature Aging	36	1.030

102	P	MYP087	Myopathy, Tubular Aggregate, 1	49	1.025

103		CNT047	Contact Dermatitis	56	1.015

104		ALC007	Alcohol Dependence	65	1.010

105	c	DLT002	Dilated Cardiomyopathy	79	1.001

106	c	THY056	Thyroid Dyshormonogenesis 3	32	0.999

107		CHL065	Cholangiocarcinoma	57	0.999

108		TRN015	Transient Cerebral Ischemia	62	0.999

109		INT079	Intrahepatic Cholangiocarcinoma	51	0.999

110	P	MSC003	Muscular Atrophy	52	0.992

111		LCT008	Lactate Dehydrogenase Deficiency	14	0.986

112		NRM005	Neuromuscular Disease	62	0.983

113		DRM006	Dermatitis	61	0.982

114		CRV040	Cervix Carcinoma	50	0.982

115		KRN002	Kearns-Sayre Syndrome	62	0.973

116	c	AMY091	Amyotrophic Lateral Sclerosis 1	87	0.964

117	P	LTR001	Lateral Sclerosis	57	0.964

118		HYP060	Hyperinsulinism	53	0.954

119		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.944

120		CRB037	Cerebral Palsy	66	0.944

121		PST011	Pustulosis of Palm and Sole	52	0.944

122		GRD001	Giardiasis	46	0.944

123	P	PSR002	Psoriasis	63	0.944

124	c	HPT001	Hepatitis C	61	0.944

125		STN013	Stenotrophomonas Maltophilia Infection	26	0.944

126	P	PHC003	Pheochromocytoma	70	0.934

127		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	0.934

128	P	ATS364	Autism	72	0.924

129	c	HPT073	Hepatitis C Virus	70	0.924

130	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.913

131		ORL011	Oral Cancer	60	0.913

132		SQM006	Squamous Cell Carcinoma	59	0.902

133		RBF001	Riboflavin Deficiency	49	0.898

134		GLC003	Glucose Intolerance	53	0.891

135	c	DNT047	Dentinogenesis Imperfecta Type 2	35	0.891

136		CRB090	Cerebral Hypoxia	42	0.891

137		ATH013	Atherosclerosis Susceptibility	63	0.879

138	c	HYP595	Hypertension, Essential	84	0.879

139	P	MCR010	Microcephaly	59	0.879

140		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	24	0.879

141		URT049	Urate Oxidase, Pseudogene	24	0.867

142	P	LPR021	Leprosy 3	71	0.867

143		HNS001	Hansen's Disease	32	0.867

144		CND006	Candida Glabrata	29	0.867

145		MYP161	Myopathy, Congenital Proximal, with Minicore Lesions	17	0.856

146	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	79	0.854

147		RPD005	Rapidly Involuting Congenital Hemangioma	48	0.854

148		HYP014	Hyperuricemia	51	0.854

149	c	CHR095	Chronic Progressive External Ophthalmoplegia	48	0.854

150		KRT002	Keratomalacia	54	0.841

151	P	CRD119	Cardiac Arrest	68	0.841

152	P	MLT020	Multiple Sclerosis	79	0.841

153		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.841

154		HMC014	Homocysteinemia	52	0.841

155	P	LPS004	Lupus Erythematosus	61	0.841

156	P	MYC033	Myoclonus	46	0.841

157	c	SPR009	Sporadic Breast Cancer	42	0.830

158		ORL015	Oral Squamous Cell Carcinoma	43	0.828

159	c	SYS001	Systemic Lupus Erythematosus	85	0.828

160	P	PRS040	Prostate Cancer	95	0.828

161	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	54	0.828

162		CRV035	Cervical Cancer	72	0.828

163	P	FBR017	Fibrosarcoma	55	0.828

164	P	THL005	Thalassemia	56	0.828

165		HDN002	Head Injury	44	0.828

166	P	PTS002	Ptosis	52	0.813

167	P	SCH015	Schizophrenia	74	0.813

168	c	LKM061	Leukemia, Acute Myeloid	83	0.813

169		ART002	Arts Syndrome	66	0.813

170	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	49	0.813

171	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	52	0.813

172	P	ANP001	Anaplastic Large Cell Lymphoma	59	0.813

173	c	ACT068	Acute Cystitis	60	0.813

174		TTN003	Tetanus	64	0.813

175		SPS057	Spasticity	43	0.813

176	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	52	0.798

177		OCL069	Ocular Motor Apraxia	57	0.798

178		SCK003	Sickle Cell Anemia	74	0.798

179	P	EXN002	Exanthem	58	0.798

180		VLV047	Volvulus of Midgut	55	0.798

181	P	MYC008	Myocarditis	59	0.798

182		DBT084	Diabetes Mellitus, Ketosis-Prone	59	0.783

183	P	FRD001	Friedreich Ataxia	62	0.783

184		INT071	Intestinal Perforation	49	0.783

185	P	CRV031	Cervical Adenocarcinoma	48	0.783

186		ACT098	Acute Erythroid Leukemia	55	0.783

187		INS001	Insulinoma	59	0.783

188	P	GST044	Gastritis	55	0.783

189		FLR002	Filariasis	55	0.783

190		ALV002	Alveolar Echinococcosis	56	0.783

191	P	MLG056	Malignant Hyperthermia	65	0.783

192	c	MGR028	Migraine with or Without Aura 1	63	0.766

193		OTT002	Otitis Media	70	0.766

194	P	BLD134	Bladder Cancer	79	0.766

195		HGH043	High Grade Glioma	46	0.766

196	c	PRC016	Pre-Eclampsia	64	0.766

197	P	MYL006	Myeloid Leukemia	60	0.766

198		LTH004	Lathyrism	15	0.766

199		INS024	Insulin-Like Growth Factor I	77	0.748

200	P	LNG032	Lung Cancer	98	0.748

201		ONC002	Onchocerciasis	50	0.748

202		PRM236	Primary Biliary Cholangitis	62	0.748

203		RSC001	Rosacea	55	0.748

204		VSC003	Visceral Leishmaniasis	54	0.748

205		PTH003	Pathologic Nystagmus	52	0.748

206	c	RNG015	Ring Chromosome 2	22	0.748

207		DYS073	Dysphagia	53	0.748

208		INF034	Infective Endocarditis	53	0.728

209		PRT251	Proteinuria, Chronic Benign	58	0.728

210		RTN212	Retinal Dystrophy with or Without Macular Staphyloma	31	0.728

211		MSC007	Muscle Hypertrophy	64	0.728

212	c	THY071	Thyroid Dyshormonogenesis 1	31	0.728

213		CHL123	Chlamydia	58	0.728

214	P	BNG032	Benign Mesothelioma	53	0.728

215	P	ECL001	Eclampsia	52	0.728

216		CLR030	Clear Cell Renal Cell Carcinoma	53	0.728

217	P	END033	Endocarditis	58	0.728

218	P	PRP029	Porphyria	60	0.728

219		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.728

220	P	CCK001	Cockayne Syndrome	67	0.728

221	P	MTH008	Methylmalonic Acidemia	52	0.728

222		ISL099	Isolated Methylmalonic Acidemia	35	0.728

223		PRT036	Peritonitis	65	0.728

224		CYN003	Cyanide Poisoning	22	0.728

225		RHB024	Rhabdomyosarcoma 2	65	0.711

226		HYP781	Hypoascorbemia	52	0.711

227		ANT039	Antisynthetase Syndrome	55	0.711

228		FST001	Foster-Kennedy Syndrome	39	0.711

229		ORG002	Organic Acidemia	43	0.706

230	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	0.706

231		PRP027	Peripheral Vascular Disease	71	0.706

232		ANG054	Angina Pectoris	65	0.706

233		MST004	Mast Cell Neoplasm	41	0.706

234		EXT007	Extracutaneous Mastocytoma	38	0.706

235	P	HRD018	Hair Disease	43	0.706

236		HLL004	Hellp Syndrome	53	0.706

237		ISC004	Ischemia	61	0.683

238		DWN001	Down Syndrome	70	0.682

239		MNK001	Menkes Disease	64	0.682

240		LBR031	Leber Optic Atrophy and Dystonia	39	0.682

241		BRK010	Burkitt Lymphoma	65	0.682

242		ESP021	Esophageal Cancer	84	0.682

243	P	LRY044	Larynx Cancer	53	0.682

244	P	HPT021	Hepatitis	68	0.682

245		LYD001	Leydig Cell Tumor	45	0.682

246	P	HYD006	Hydrocephalus	62	0.682

247		CRB039	Cerebrovascular Disease	65	0.682

248		PRX097	Paroxysmal Dystonia	32	0.682

249		HMM004	Hamamy Syndrome	39	0.652

250		SNG007	Sengers Syndrome	45	0.652

251		PLT031	Platelet Membrane Fluidity	28	0.652

252		KRT058	Keratoderma, Palmoplantar, with Deafness	42	0.652

253		MYL069	Myeloma, Multiple	76	0.652

254	P	DFN349	Deafness, Nonsyndromic Sensorineural, Mitochondrial	35	0.652

255		CNR001	Coenurosis	26	0.652

256		PRS119	Persistent Genital Arousal Disorder	18	0.652

257		ANS011	Anus Cancer	55	0.652

258		SVR001	Severe Acute Respiratory Syndrome	68	0.652

259		ALL010	Allergic Contact Dermatitis	55	0.652

260	P	GRV001	Graves' Disease	54	0.652

261		TNS005	Tonsillitis	57	0.652

262	P	BRN006	Branchiootorenal Syndrome	51	0.652

263		SCR011	Scrapie	39	0.652

264		NNS010	Nonsyndromic Hearing Loss and Deafness, Mitochondrial	13	0.652

265		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.652

266	P	RRT020	Rare Tumor	39	0.652

267		EST002	Estrogen-Receptor Negative Breast Cancer	45	0.614

268		APR001	Apraxia	51	0.614

269		ARG002	Argininosuccinic Aciduria	61	0.614

270	P	MCH002	Machado-Joseph Disease	62	0.614

271		ALZ029	Alzheimer Disease Mitochondrial	24	0.614

272		SPS007	Spastic Cerebral Palsy	45	0.614

273		ASP002	Aspartylglucosaminuria	57	0.614

274		HYP690	Hyper-Beta-Alaninemia	24	0.614

275		PNB004	Panbronchiolitis, Diffuse	34	0.614

276		PTN001	Patent Foramen Ovale	61	0.614

277	P	DRR001	Diarrhea	55	0.614

278	P	BLD062	Bile Duct Cancer	69	0.614

279	P	DBT005	Diabetes Insipidus	54	0.614

280		CYS008	Cystic Echinococcosis	57	0.604

281	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	56	0.583

282		CHL068	Cholestasis	61	0.560

283	P	MLN008	Melanoma	75	0.553

284	c	ALP101	Alpha-Thalassemia	62	0.522

285	P	DRM053	Dermatitis, Atopic	65	0.522

286	c	LCT020	Lactic Acidosis, Chronic Adult Form	8	0.522

287		PLG003	Polg-Related Disorders	21	0.522

288	P	LVR013	Liver Disease	68	0.521

289	P	SCK005	Sickle Cell Disease	56	0.470

290	c	MCR133	Microvascular Complications of Diabetes 4	41	0.461

291	c	MCR113	Microvascular Complications of Diabetes 3	52	0.461

292	c	MCR130	Microvascular Complications of Diabetes 6	41	0.461

293	c	MCR120	Microvascular Complications of Diabetes 7	47	0.461

294	P	PLM037	Pulmonary Hypertension	69	0.442

295		DBT010	Diabetic Neuropathy	54	0.442

296		47X002	47,xyy	47	0.432

297		PPL052	Papillomatosis, Confluent and Reticulated	34	0.422

298		STT001	Status Epilepticus	58	0.412

299		TXC005	Toxic Shock Syndrome	61	0.412

300	P	PRD008	Periodontitis	63	0.412

301	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	41	0.402

302	c	TYP009	Type 2 Diabetes Mellitus	91	0.402

303	c	ACT071	Acute Kidney Failure	60	0.402

304		PHN003	Phenylketonuria	76	0.391

305	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	0.380

306	c	BDY006	Body Mass Index Quantitative Trait Locus 8	43	0.380

307	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.380

308	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.380

309	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.380

310	c	BDY012	Body Mass Index Quantitative Trait Locus 7	43	0.380

311	c	BDY019	Body Mass Index Quantitative Trait Locus 18	46	0.380

312	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.380

313	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.380

314		ADR040	Adrenal Gland Pheochromocytoma	45	0.380

315	P	SKN015	Skin Carcinoma	71	0.380

316	P	BCL017	B-Cell Lymphoma	57	0.380

317	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	0.380

318	P	GLC113	Galactosemia I	65	0.369

319		HPT022	Hepatoblastoma	54	0.369

320	P	BDY004	Body Mass Index Quantitative Trait Locus 11	82	0.357

321	P	LNG064	Lung Cancer Susceptibility 3	69	0.357

322		CNG034	Congestive Heart Failure	69	0.357

323		HRT015	Heritable Pulmonary Arterial Hypertension	46	0.357

324	P	TRM003	Tremor	50	0.357

325	c	TYP008	Type 1 Diabetes Mellitus	77	0.345

326		BRN004	Brain Edema	54	0.345

327		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	51	0.332

328	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	58	0.332

329		MTB008	Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration	42	0.332

330		BCT022	Bacterial Infectious Disease	55	0.332

331	P	BRG001	Brugada Syndrome	69	0.319

332		MTH071	Methane Production	24	0.319

333		CYS005	Cysticercosis	60	0.319

334		ARG004	Argyria	26	0.319

335		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.306

336	c	SPR086	Spermatogenic Failure 3	47	0.306

337	P	LKM002	Leukemia	65	0.306

338		HMS001	Hemosiderosis	48	0.306

339	c	ACT027	Acute Pancreatitis	60	0.306

340		SCH014	Schistosomiasis	56	0.306

341	P	HML002	Hemolytic Anemia	62	0.306

342		BRN056	Bronchopulmonary Dysplasia	57	0.306

343	c	CHR684	Chronic Kidney Disease	73	0.306

344	P	HYP076	Hyperthyroidism	53	0.306

345	P	RRH023	Rare Hereditary Hemochromatosis	52	0.306

346		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.291

347	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.291

348		DSS032	Disease by Infectious Agent	55	0.291

349	P	PNC035	Pancreatic Cancer	87	0.291

350	P	ALC033	Alcohol Use Disorder	67	0.291

351	P	DBT009	Diabetes Mellitus	67	0.291

352	P	OVR042	Ovarian Cancer	88	0.276

353	P	CLR023	Colorectal Cancer	100	0.276

354	c	THY107	Thymoma, Familial	42	0.276

355	c	DVL036	Developmental and Epileptic Encephalopathy 39	39	0.276

356	P	HPT023	Hepatocellular Carcinoma	95	0.276

357		ONC007	Oncocytoma	49	0.276

358	P	MYG005	Myoglobinuria	40	0.276

359		DPH001	Diphtheria	59	0.276

360		HPT019	Hepatic Encephalopathy	59	0.276

361	P	THY023	Thymoma	64	0.276

362	P	MLN007	Male Infertility	56	0.276

363	P	PRP019	Peripheral Nervous System Disease	57	0.276

364	P	HRT032	Heart Disease	84	0.276

365		LKS001	Leukostasis	40	0.276

366		HPT004	Hepatic Coma	43	0.276

367	P	SCL018	Scoliosis	57	0.261

368	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	0.261

369		BRT005	Barth Syndrome	55	0.261

370		ACR009	Acromesomelic Dysplasia, Hunter-Thompson Type	41	0.261

371		RCH002	Richards-Rundle Syndrome	31	0.261

372	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.261

373	P	GLY013	Glycogen Storage Disease	59	0.261

374	P	BRB001	Beriberi	44	0.261

375		ADN018	Adenoma	58	0.261

376	P	ADN016	Adenocarcinoma	63	0.261

377		SPN035	Spindle Cell Sarcoma	51	0.261

378		PLC005	Placental Insufficiency	55	0.261

379		MLT006	Multidrug-Resistant Tuberculosis	47	0.261

380		SRC014	Sarcoma	64	0.261

381		YLL002	Yellow Fever	61	0.261

382		END086	End Stage Renal Disease	54	0.261

383	P	INS002	in Situ Carcinoma	52	0.261

384		THY029	Thyroid Carcinoma	55	0.261

385	P	APL001	Aplastic Anemia	72	0.244

386	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.244

387		BTT016	Batten-Turner Congenital Myopathy	54	0.244

388	c	MCL042	Macular Degeneration, Age-Related, 1	84	0.244

389	c	2HY001	2-Hydroxyglutaric Aciduria	38	0.244

390	P	RTN008	Retinitis Pigmentosa	79	0.244

391	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	50	0.244

392	c	OPT053	Optic Atrophy 1	62	0.244

393	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	52	0.244

394	P	SNS001	Sensorineural Hearing Loss	60	0.244

395		TRY001	Trypanosomiasis	50	0.244

396	P	RNV001	Renovascular Hypertension	48	0.244

397		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.244

398	P	BRS053	Breast Fibroadenoma	48	0.244

399	P	MVM001	Movement Disease	61	0.244

400		MDD018	Middle East Respiratory Syndrome	44	0.244

401		NRR001	Neuroretinitis	42	0.244

402	P	ADL010	Adult Respiratory Distress Syndrome	70	0.244

403	P	CNT004	Centronuclear Myopathy	56	0.244

404		RTN023	Retinitis	45	0.244

405		SKN016	Skin Disease	63	0.244

406	P	RTN016	Retinal Degeneration	52	0.244

407	c	ACT134	Acute Liver Failure	57	0.244

408		DFC004	Deficiency Anemia	74	0.226

409	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.226

410	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.226

411		RNL077	Renal Fibrosis	46	0.226

412		MSC157	Muscular Dystrophy, Duchenne Type	78	0.226

413		STR067	Stroke, Ischemic	79	0.226

414		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.226

415	c	PCH010	Pachyonychia Congenita 3	43	0.226

416	P	ASP006	Aspergillosis	71	0.226

417	P	MYS005	Myositis	55	0.226

418	P	GLM040	Glioma Susceptibility 1	70	0.226

419	P	PLY041	Polymyositis	58	0.226

420		MLG169	Malignant Astrocytoma	57	0.226

421		VCC001	Vaccinia	49	0.226

422		CCC002	Coccidiosis	50	0.226

423		DBT007	Diabetic Cataract	36	0.226

424		LVR012	Liver Cirrhosis	62	0.226

425		GST045	Gastroenteritis	58	0.226

426	P	HYP086	Hypothyroidism	68	0.226

427	P	CND004	Candidiasis	57	0.226

428	P	KDN017	Kidney Cancer	60	0.226

429		CNS004	Constipation	56	0.226

430		ERL001	Early Myoclonic Encephalopathy	62	0.226

431		PSY004	Psychotic Disorder	66	0.226

432		ALC006	Alcoholic Hepatitis	61	0.226

433		RCK004	Rickets	64	0.226

434	P	DRM010	Dermatomyositis	61	0.226

435		TLN003	Telangiectasis	51	0.226

436	P	RBL001	Rubella	58	0.226

437		STM007	Stomatitis	52	0.226

438		IDP022	Idiopathic Spinal Cord Herniation	17	0.226

439		INT075	Intracranial Hypertension	52	0.226

440	c	ATS007	Autism Spectrum Disorder	71	0.206

441		CLT003	Colitis	63	0.206

442	P	INF037	Inflammatory Bowel Disease	53	0.206

443		PLY150	Polykaryocytosis Inducer	29	0.206

444		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	58	0.206

445	P	ATX030	Ataxia-Telangiectasia	80	0.206

446		FRN006	Frontotemporal Dementia	68	0.206

447		HMN044	Human Immunodeficiency Virus Type 1	76	0.206

448		PRS129	Prostatic Hyperplasia, Benign	48	0.206

449		FCL014	Focal Epilepsy	53	0.206

450	P	ART021	Arteriosclerosis	53	0.206

451	c	BSL007	Basal Cell Carcinoma	67	0.206

452		STR103	Streptococcus Pneumonia	47	0.206

453		PRP016	Paraplegia	52	0.206

454		SVR004	Severe Combined Immunodeficiency	70	0.206

455		LYM017	Lyme Disease	63	0.206

456		CRN019	Coronary Artery Vasospasm	47	0.206

457	P	OVR049	Ovarian Disease	50	0.206

458		PRS021	Prostatic Adenoma	43	0.206

459	P	RNL015	Renal Hypertension	45	0.206

460		PRS045	Prostatic Hypertrophy	53	0.206

461	P	RNL017	Renal Oncocytoma	54	0.206

462	P	LMB006	Limb-Girdle Muscular Dystrophy	52	0.206

463		CHL045	Choline Deficiency Disease	39	0.206

464	P	TXP001	Toxoplasmosis	59	0.206

465	P	HYP098	Hypereosinophilic Syndrome	66	0.206

466		WLL004	Wallerian Degeneration	38	0.206

467		MYC005	Myocardial Stunning	45	0.206

468	P	MRC003	Mercury Poisoning	48	0.206

469		MYC015	Mycobacterium Fortuitum	28	0.206

470	P	MYC026	Myoclonus Epilepsy	35	0.206

471		IDP070	Idiopathic Scoliosis	41	0.184

472	P	CRN300	Coronary Heart Disease 1	73	0.184

473	P	SLP006	Sleep Apnea	69	0.184

474		VRC005	Varicose Veins	59	0.184

475		ADR007	Adrenoleukodystrophy	73	0.184

476	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	0.184

477	c	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.184

478		FML037	Female Breast Cancer	51	0.184

479	c	HYP368	Hyperphenylalaninemia, Bh4-Deficient, C	35	0.184

480		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	0.184

481		MNN043	Meningioma, Familial	79	0.184

482		ATM095	Autoimmune Disease	61	0.184

483		HLC007	Helicobacter Pylori Infection	67	0.184

484	P	BND020	Bone Disease	60	0.184

485		CHK001	Chikungunya	60	0.184

486	P	MYS079	Miyoshi Muscular Dystrophy	53	0.184

487		FML035	Familial Hyperlipidemia	54	0.184

488		NNL006	Non-Alcoholic Steatohepatitis	54	0.184

489		TTH006	Tooth Disease	51	0.184

490		CLN015	Colon Adenocarcinoma	64	0.184

491	P	PRM002	Primary Hyperoxaluria	65	0.184

492		TRC003	Trichomoniasis	53	0.184

493		KRT009	Keratosis	52	0.184

494	P	SPN046	Spinal Muscular Atrophy	62	0.184

495		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.184

496	P	EYD002	Eye Disease	57	0.184

497	P	KDN018	Kidney Disease	71	0.184

498	P	PLY011	Polycystic Ovary Syndrome	57	0.184

499	P	URN019	Urinary Tract Infection	48	0.184

500	P	OBS001	Obstructive Jaundice	49	0.184

501		HMG005	Hemoglobinopathy	55	0.184

502		SCR001	Secretory Meningioma	40	0.184

503	P	PLM036	Pulmonary Fibrosis	65	0.184

504	P	PTT006	Pituitary Adenoma	55	0.184

505	P	RHB003	Rhabdomyosarcoma	66	0.184

506		ART016	Aortic Aneurysm	68	0.184

507	P	PNC044	Pancreatitis	61	0.184

508		GLC008	Glucose Metabolism Disease	40	0.184

509	P	CHR071	Charcot-Marie-Tooth Disease	64	0.184

510		INT395	Intracranial Meningioma	47	0.184

511	P	CRD246	Cardiovascular System Disease	55	0.184

512	P	KRT007	Keratoconus	49	0.184

513	P	PRN023	Prion Disease	60	0.184

514		CHR074	Choriocarcinoma	46	0.184

515		FSC002	Fascioliasis	43	0.184

516		GSG001	Gas Gangrene	52	0.184

517		HYP141	Hyperphenylalaninemia	42	0.184

518	P	MYT002	Myotonic Dystrophy	51	0.184

519		ADR022	Adrenomyeloneuropathy	38	0.184

520		ULC004	Ulcerative Colitis	74	0.184

521	c	ACT075	Acute Myocardial Infarction	55	0.184

522		LNG099	Lung Disease	62	0.184

523		AGR019	Age-Related Hearing Loss	41	0.184

524		FST010	Fasting Hypoglycemia	33	0.184

525		NCL011	Nuclear Gene-Encoded Leigh Syndrome Spectrum	21	0.184

526	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	0.184

527		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	44	0.184

528		RHM034	Rahman Syndrome	37	0.160

529		MTC029	Mitochondrial Complex V Deficiency, Nuclear Type 1	40	0.160

530	P	MTR004	Maturity-Onset Diabetes of the Young	66	0.160

531		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.160

532		ACH004	Achondroplasia	65	0.160

533	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.160

534		CRY035	Cryptorchidism, Unilateral or Bilateral	57	0.160

535	c	MTR019	Maturity-Onset Diabetes of the Young, Type 2	53	0.160

536	P	SCL057	Scoliosis, Isolated 1	40	0.160

537		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	0.160

538	P	RTT002	Rett Syndrome	79	0.160

539		WRN002	Wernicke-Korsakoff Syndrome	49	0.160

540		MHR001	Mohr-Tranebjaerg Syndrome	49	0.160

541	c	HYP602	Hyperoxaluria, Primary, Type Ii	51	0.160

542		TRD006	Tardive Dyskinesia	53	0.160

543		DBT090	Diabetes and Deafness, Maternally Inherited	44	0.160

544		HYP814	Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency	34	0.160

545	c	MSC106	Mosaic Variegated Aneuploidy Syndrome 2	41	0.160

546		MTC205	Mitochondrial Complex Iv Deficiency, Nuclear Type 1	57	0.160

547		DGL002	D-Glyceric Aciduria	40	0.160

548	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.160

549	c	GLL024	Gallbladder Disease 1	53	0.160

550	P	DNG005	Dengue Virus	55	0.160

551		INC002	Inclusion Body Myositis	56	0.160

552		CMR002	Coumarin Resistance	59	0.160

553		FRC013	Fructose Utilization	15	0.160

554		DFF005	Diffuse Large B-Cell Lymphoma	55	0.160

555		INV001	Invasive Aspergillosis	48	0.160

556	c	PRG106	Progressive Muscular Dystrophy	31	0.160

557		MLD018	Mild Cognitive Impairment	48	0.160

558		LMB062	Limb Ischemia	55	0.160

559		GST023	Gastric Ulcer	52	0.160

560		SKN005	Skin Atrophy	41	0.160

561		NRT004	Neuritis	53	0.160

562		GLN002	Glanders	38	0.160

563		NRT001	Neurotic Disorder	56	0.160

564		OVR063	Overnutrition	42	0.160

565	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.160

566	P	PLY019	Polyneuropathy	52	0.160

567	P	GLM007	Glomerulonephritis	59	0.160

568	c	HPT016	Hepatitis B	62	0.160

569	P	BNG002	Benign Meningioma	36	0.160

570		CRC021	Carcinosarcoma	62	0.160

571		PNC129	Pancreatic Adenocarcinoma	64	0.160

572		ANV001	Anovulation	46	0.160

573		DMY004	Demyelinating Disease	50	0.160

574		MDD011	Mood Disorder	61	0.160

575		URM002	Uremia	47	0.160

576		ALL029	Allergic Disease	61	0.160

577		GST033	Gestational Diabetes	60	0.160

578	P	FNC004	Fanconi Syndrome	60	0.160

579	c	ACT073	Acute Leukemia	59	0.160

580		QDR001	Quadriplegia	49	0.160

581		MST005	Mastitis	52	0.160

582		PCD001	Pica Disease	38	0.160

583	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	0.160

584	P	DMN002	Dementia	65	0.160

585		SPR006	Sparganosis	35	0.160

586		VRC001	Varicocele	48	0.160

587	P	INT070	Intestinal Obstruction	57	0.160

588	P	RTN018	Retinal Disease	53	0.160

589	P	CWD010	Cowden Syndrome	70	0.160

590		GST040	Gastric Adenocarcinoma	66	0.160

591		BRN024	Bronchitis	67	0.160

592		BRR002	Barrett's Adenocarcinoma	37	0.160

593		SKN019	Skin Melanoma	70	0.160

594	P	ZLL001	Zellweger Syndrome	65	0.160

595		ACT058	Active Peptic Ulcer Disease	55	0.160

596		PPT005	Peptic Ulcer Disease	58	0.160

597	P	PLL002	Pellagra	46	0.160

598		OST012	Osteoarthritis	77	0.160

599		CYT002	Cytokine Deficiency	43	0.160

600		SYS003	Systolic Heart Failure	49	0.160

601		GRN017	Granulocytopenia	42	0.160

602		PLY100	Polyploidy	36	0.160

603		ETH012	Ethylene Glycol Poisoning	29	0.160

604		SPN186	Spinal Cord Injury	60	0.160

605		MSC193	Muscular Lipidosis	23	0.160

606	c	ACQ047	Acquired Methemoglobinemia	30	0.160

607		ACT119	Acute Promyelocytic Leukemia	62	0.130

608		ALL003	Allergic Rhinitis	66	0.130

609	P	ATR011	Atrial Fibrillation	66	0.130

610		CRB137	Cerebral Creatine Deficiency Syndrome	31	0.130

611	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	62	0.130

612	P	MYP105	Myopathy, Myosin Storage, Autosomal Dominant	39	0.130

613	P	PRG013	Paraganglioma	57	0.130

614	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.130

615		ING001	Inguinal Hernia	59	0.130

616	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	69	0.130

617		PHS025	Phosphatase, Acid, of Tissues	28	0.130

618	P	MDL005	Medulloblastoma	75	0.130

619	c	SCH079	Schizophrenia 1	44	0.130

620		KRT071	Keratosis, Seborrheic	56	0.130

621	c	SML038	Small Cell Cancer of the Lung	68	0.130

622		NPH091	Nephrolithiasis, Calcium Oxalate	61	0.130

623		CRZ001	Crouzon Syndrome	64	0.130

624		CRD223	Cardiac Arrhythmia	63	0.130

625		3HY007	3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency	51	0.130

626	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.130

627		CHR696	Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia	32	0.130

628		RFS006	Refsum Disease, Classic	63	0.130

629	P	MCR129	Microvascular Complications of Diabetes 1	67	0.130

630	c	CTR132	Cataract 3, Multiple Types	41	0.130

631		RGD003	Rigid Spine Muscular Dystrophy 1	56	0.130

632		PTR032	Peters-Plus Syndrome	63	0.130

633		SCC001	Succinic Semialdehyde Dehydrogenase Deficiency	59	0.130

634	P	NSP012	Nasopharyngeal Carcinoma	60	0.130

635		MTC155	Mitochondrial Complex I Deficiency, Nuclear Type 7	24	0.130

636		CHR100	Chronic Ulcer of Skin	57	0.130

637	P	FML011	Familial Adenomatous Polyposis	70	0.130

638		VTM002	Vitamin B12 Deficiency	48	0.130

639		INT323	Intraocular Pressure Quantitative Trait Locus	63	0.130

640		EWN003	Ewing Sarcoma	69	0.130

641	c	MTH083	Methemoglobinemia, Beta Type	21	0.130

642	c	MTH084	Methemoglobinemia, Alpha Type	10	0.130

643		NRN005	Neuronal Ceroid-Lipofuscinoses	61	0.130

644	c	MCR112	Microvascular Complications of Diabetes 2	42	0.130

645		PYR012	Pyruvate Dehydrogenase E1-Beta Deficiency	40	0.130

646		ANR007	Anorexia Nervosa	59	0.130

647	c	DVL110	Developmental and Epileptic Encephalopathy 88	21	0.130

648		ALC001	Alcohol-Related Birth Defect	36	0.130

649		SLF014	Sulfite Oxidase Deficiency, Isolated	53	0.130

650	c	SPS222	Spastic Paraplegia 20, Autosomal Recessive	56	0.130

651	P	ALB003	Albinism-Deafness Syndrome	33	0.130

652		CMB017	Combined Oxidative Phosphorylation Deficiency 6	41	0.130

653		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.130

654	c	TBR025	Tuberous Sclerosis 1	84	0.130

655	P	HYP750	Hypertriglyceridemia, Familial	61	0.130

656		CNT105	Central Core Disease of Muscle	59	0.130

657	P	TRT019	Torticollis	47	0.130

658	c	HYP597	Hyperprolinemia, Type Ii	43	0.130

659	P	MYS003	Myasthenia Gravis	67	0.130

660		SQM013	Squamous Cell Carcinoma, Head and Neck	75	0.130

661		TBL029	Tubulin, Beta	28	0.130

662		CRB150	Cerebral Creatine Deficiency Syndrome 2	54	0.130

663	P	MYC007	Myocardial Infarction	69	0.130

664	P	MJR001	Major Depressive Disorder	68	0.130

665	c	LKM063	Leukemia, Chronic Myeloid	70	0.130

666	c	CHR489	Charcot-Marie-Tooth Disease, Axonal, Type 2q	32	0.130

667		MLD001	Melioidosis	67	0.130

668	c	BTT014	Beta-Thalassemia	72	0.130

669		HMF006	Hemifacial Microsomia	55	0.130

670	P	HYP726	Hypercalcemia, Infantile, 1	58	0.130

671		CRT072	Creutzfeldt-Jakob Disease	67	0.130

672		MLT157	Multiple System Atrophy 1	69	0.130

673	P	TRC072	Treacher Collins Syndrome 1	62	0.130

674		END057	Endometrial Cancer	76	0.130

675		PRK088	Parkinson Disease, Mitochondrial	19	0.130

676		CRD231	Cardiomyopathy, Infantile Histiocytoid	47	0.130

677	c	BRS111	Breast-Ovarian Cancer, Familial 2	53	0.130

678		EPD015	Epidemic Typhus	44	0.130

679	P	FTL001	Fetal Alcohol Syndrome	55	0.130

680		FBR009	Fibrous Dysplasia	48	0.130

681	P	FML068	Familial Hypocalciuric Hypercalcemia	55	0.130

682		BCT021	Bacterial Sepsis	43	0.130

683	P	HRD144	Hereditary Mixed Polyposis Syndrome	54	0.130

684		CMB007	Combined Immunodeficiency	56	0.130

685	P	VNS003	Venous Insufficiency	54	0.130

686		OST003	Osteonecrosis	60	0.130

687	P	MTC010	Mitochondrial Dna Depletion Syndrome	46	0.130

688		VTM033	Vitamin K Deficiency Bleeding	49	0.130

689	P	PLY014	Polycystic Kidney Disease	71	0.130

690	P	HYP111	Hyperprolinemia	44	0.130

691		CHR431	Chronic Venous Insufficiency	48	0.130

692		ANT018	Anthracosis	50	0.130

693	P	MGR003	Migraine with Aura	51	0.130

694		PNC001	Pancytopenia	52	0.130

695		NRX001	Neuroaxonal Dystrophy	38	0.130

696		PST028	Post-Traumatic Stress Disorder	58	0.130

697	P	CRN037	Craniosynostosis	67	0.130

698	c	ATM011	Autoimmune Hepatitis	62	0.130

699		HYP080	Hypogonadism	49	0.130

700	P	TMP001	Temporal Lobe Epilepsy	49	0.130

701	P	LNG028	Long Qt Syndrome	63	0.130

702		MLG067	Malignant Giant Cell Tumor	28	0.130

703	P	TBR001	Tuberous Sclerosis	69	0.130

704		OPS001	Opisthorchiasis	41	0.130

705	c	CHR697	Charcot-Marie-Tooth Disease X-Linked Recessive 4	33	0.130

706	P	NRD007	Neurodegeneration with Brain Iron Accumulation	51	0.130

707		URT010	Ureteral Obstruction	44	0.130

708		PSD009	Pseudohermaphroditism	46	0.130

709		TNC002	Tinea Capitis	42	0.130

710		NTR005	Nutritional Deficiency Disease	60	0.130

711	P	EMB005	Embryonal Rhabdomyosarcoma	53	0.130

712		NPH009	Nephrolithiasis	54	0.130

713	P	MTR014	Motor Neuron Disease	65	0.130

714		AMN001	Amenorrhea	53	0.130

715		RYS001	Reye Syndrome	49	0.130

716	P	EPL164	Epilepsy	70	0.130

717	c	VRL010	Viral Hepatitis	52	0.130

718		HMP005	Hemiplegia	53	0.130

719		MYS004	Myiasis	38	0.130

720		CRT012	Cortical Blindness	42	0.130

721		LCH001	Leech Infestation	37	0.130

722		KLB003	Klebsiella Pneumonia	49	0.130

723	P	END044	Endometriosis	62	0.130

724		PYD002	Pyoderma	49	0.130

725		INT066	Interstitial Lung Disease	60	0.130

726		LYS002	Lysosomal Storage Disease	51	0.130

727	P	TRT010	Teratoma	50	0.130

728	P	PSD003	Pseudohypoaldosteronism	45	0.130

729	P	HLP001	Holoprosencephaly	68	0.130

730		GTR002	Goiter	52	0.130

731		DBT002	Diabetic Autonomic Neuropathy	40	0.130

732		OST011	Osteomalacia	52	0.130

733		MCR013	Microphthalmia	59	0.130

734		LPR001	Lepromatous Leprosy	49	0.130

735		LMY002	Leiomyoma	51	0.130

736	P	MGR001	Migraine Without Aura	48	0.130

737		MNT002	Mental Depression	56	0.130

738	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.130

739		DMP001	Dumping Syndrome	43	0.130

740		ALC010	Alcoholic Cardiomyopathy	42	0.130

741		CRY005	Cryptococcosis	61	0.130

742		DNG003	Dengue Disease	65	0.130

743		FLR001	Filarial Elephantiasis	59	0.130

744		GT001	Gout	63	0.130

745	P	ART022	Arthritis	70	0.130

746	P	SLP005	Sleep Disorder	61	0.130

747		MLG077	Malignant Peripheral Nerve Sheath Tumor	53	0.130

748	c	INH020	Inherited Metabolic Disorder	47	0.130

749		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.130

750		BRS051	Breast Disease	58	0.130

751		ACQ007	Acquired Immunodeficiency Syndrome	58	0.130

752		INV005	Inverted Follicular Keratosis	31	0.130

753	P	AXN001	Axonal Neuropathy	33	0.130

754		ILS001	Ileus	49	0.130

755	P	NRF002	Neurofibromatosis	60	0.130

756		BLT006	Bilateral Breast Cancer	48	0.130

757		CRT055	Creatine Deficiency Syndromes	38	0.130

758		SCT002	Scotoma	42	0.130

759		BBS001	Babesiosis	48	0.130

760		DRM011	Dermatophytosis	52	0.130

761	P	SDR003	Sideroblastic Anemia	49	0.130

762	P	INF038	Influenza	68	0.130

763		GST039	Gastroduodenitis	37	0.130

764		INT007	Intermediate Coronary Syndrome	53	0.130

765		EMR021	Emery-Dreifuss Syndrome	11	0.130

766		TTR005	Tetrahydrobiopterin Deficiency	49	0.130

767	P	THY032	Thyroiditis	56	0.130

768		CCN002	Cocaine Abuse	49	0.130

769	P	RDC010	Reducing Body Myopathy	33	0.130

770		HYD005	Hydrocele	46	0.130

771	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	0.130

772		OVR094	Ovarian Epithelial Cancer	39	0.130

773		DST006	Diastolic Heart Failure	45	0.130

774		CNG506	Congenital Amyoplasia	27	0.130

775		GLM044	Glomerular Disease	34	0.130

776		MYT011	Myotonia	37	0.130

777		DPR016	Depression	64	0.130

778	P	CRB088	Cerebral Atrophy	32	0.130

779		GLY085	Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency	16	0.130

780		MTH047	Methanol Poisoning	37	0.130

781		GRN033	Granulomatous Mastitis	31	0.130

782		CRD137	Cardiogenic Shock	56	0.130

783		ADT001	Auditory Agnosia	25	0.092

784	c	3MT007	3-Methylglutaconic Aciduria	37	0.092

785		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	0.092

786	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	0.092

787		MYP099	Myopathy, Isolated Mitochondrial, Autosomal Dominant	27	0.092

788	c	MYP118	Myopathy, Myofibrillar, 8	31	0.092

789		MTC158	Mitochondrial Complex I Deficiency, Nuclear Type 10	26	0.092

790		MTC164	Mitochondrial Complex I Deficiency, Nuclear Type 17	24	0.092

791		SRB001	Sorbitol Dehydrogenase Deficiency with Peripheral Neuropathy	21	0.092

792	c	FNC066	Fanconi Renotubular Syndrome 5	25	0.092

793	c	AMY088	Amyotrophic Lateral Sclerosis 3	33	0.092

794		KFR001	Kufor-Rakeb Syndrome	59	0.092

795		SNS008	Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis	59	0.092

796		CRT007	Cortical Deafness	26	0.092

797		MYL009	Myelodysplastic Syndrome	67	0.092

798		LYM143	Lymphoma, Non-Hodgkin, Familial	74	0.092

799	c	MLT068	Multiple Mitochondrial Dysfunctions Syndrome 1	45	0.092

800		LTN004	Late-Onset Retinal Degeneration	59	0.092

801		ASC010	Ascaris Lumbricoides Infection	49	0.092

802	P	LYM118	Lymphoma	66	0.092

803		ART110	Arteritic Anterior Ischemic Optic Neuropathy	34	0.092

804		TNG009	Tongue Squamous Cell Carcinoma	43	0.092

805	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	0.092

806		PNG002	Pain Agnosia	51	0.092

807	P	HRD021	Hereditary Sensory Neuropathy	48	0.092

808	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.092

809		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	63	0.092

810		LPD012	Lipoid Congenital Adrenal Hyperplasia	68	0.092

811		CYS019	Cystathioninuria	46	0.092

812	c	NTR047	Neutropenia, Severe Congenital, 1, Autosomal Dominant	37	0.092

813		ALK013	Alkaptonuria	58	0.092

814	c	MTC056	Mitochondrial Dna Depletion Syndrome 4a	62	0.092

815		CYS044	Cystic Disease of Lung	19	0.092

816	P	FCS012	Facioscapulohumeral Muscular Dystrophy 1	68	0.092

817	P	OST002	Osteoporosis	76	0.092

818		CRN048	Craniofacial-Deafness-Hand Syndrome	52	0.092

819	c	DNT027	Dentin Dysplasia, Type Ii	36	0.092

820	P	MJR007	Major Affective Disorder 1	42	0.092

821		EXF001	Exfoliation Syndrome	55	0.092

822	c	SCL052	Scleroderma, Familial Progressive	60	0.092

823	P	PLV020	Pelvic Organ Prolapse	57	0.092

824		PLM061	Pulmonary Edema of Mountaineers	25	0.092

825	c	RTN150	Retinitis Pigmentosa 10	44	0.092

826		LYM133	Lymphoma, Hodgkin, Classic	69	0.092

827		MTC207	Mitochondrial Complex Ii Deficiency, Nuclear Type 1	57	0.092

828	c	MCL013	Mucolipidosis Iv	64	0.092

829		CRN295	Carnitine Palmitoyltransferase I Deficiency	55	0.092

830		MYP097	Myopathy with Lactic Acidosis, Hereditary	33	0.092

831		MYP091	Myopathy, Congenital, with Fiber-Type Disproportion	44	0.092

832	c	NPH055	Nephrotic Syndrome, Type 1	52	0.092

833	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	0.092

834	c	GLC092	Glaucoma, Primary Open Angle	60	0.092

835		CRD132	Cardiac Conduction Defect	59	0.092

836	P	HYP768	Hyperlipoproteinemia, Type I	67	0.092

837		HYP784	Hypogonadism, Male	43	0.092

838		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	50	0.092

839		MYC079	Myoclonic Epilepsy of Lafora	63	0.092

840		MYC080	Myoclonic Epilepsy of Unverricht and Lundborg	52	0.092

841		SPN354	Spinal Arachnoiditis	35	0.092

842	c	SYN084	Synpolydactyly 1	36	0.092

843	c	GLC112	Galactosemia Iii	51	0.092

844	c	GLY008	Glycogen Storage Disease Ii	72	0.092

845		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	63	0.092

846	c	SPN225	Spondyloarthropathy 1	70	0.092

847	c	PRD040	Periodontitis, Chronic	52	0.092

848		GTL001	Gitelman Syndrome	65	0.092

849		ENC055	Encephalopathy, Ethylmalonic	51	0.092

850	c	TTH011	Tooth Agenesis, Selective, 2	13	0.092

851		SPP011	Suppression of Tumorigenicity 12	61	0.092

852	c	DFN251	Deafness, Autosomal Dominant 11	44	0.092

853	c	LNG048	Long Qt Syndrome 3	52	0.092

854		SCT005	Scott Syndrome	51	0.092

855		DNN001	Danon Disease	59	0.092

856		GRN051	Granulomatous Disease, Chronic, X-Linked	57	0.092

857		CNG184	Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects	56	0.092

858		MTC149	Mitochondrial Complex I Deficiency, Mitochondrial Type 1	14	0.092

859	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	53	0.092

860	c	ART068	Aortic Aneurysm, Familial Thoracic 2	34	0.092

861		EPL050	Epilepsy, Partial, with Pericentral Spikes	26	0.092

862	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	58	0.092

863		ART164	Arthrogryposis Multiplex Congenita 1, Neurogenic, with Myelin Defect	24	0.092

864		MTC156	Mitochondrial Complex I Deficiency, Nuclear Type 8	21	0.092

865		ART166	Arthrogryposis Multiplex Congenita 4, Neurogenic, with Agenesis of the Corpus Callosum	22	0.092

866		HYP017	Hypophosphatemia	49	0.092

867		CRR001	Carrion's Disease	31	0.092

868		HYP025	Hyperphosphatemia	47	0.092

869	c	PRM032	Primary Congenital Glaucoma	40	0.092

870		TNS007	Taeniasis	46	0.092

871		INT017	Intestinal Schistosomiasis	51	0.092

872		CNN008	Cinnamon Odor, Pleasantness of	13	0.092

873	c	MCR312	Microphthalmia, Syndromic 10	39	0.092

874	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.092

875	c	LNG047	Long Qt Syndrome 2	59	0.092

876		HRT037	Heart and Brain Malformation Syndrome	32	0.092

877		MLC004	Mulchandani-Bhoj-Conlin Syndrome	51	0.092

878		ART167	Arthrogryposis Multiplex Congenita 5	21	0.092

879	c	SPR162	Spermatogenic Failure 50	42	0.092

880		IMM065	Immunodeficiency 10	47	0.092

881		DSR012	Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency	39	0.092

882	P	HMG032	Hemoglobin H Disease	51	0.092

883		AKL001	Au-Kline Syndrome	38	0.092

884	c	DFN360	Deafness, Autosomal Dominant 69	34	0.092

885		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	40	0.092

886		ADR016	Adrenal Cortical Carcinoma	61	0.092

887	P	LSS002	Lissencephaly	52	0.092

888		PLY001	Polycythemia Vera	69	0.092

889	P	DNT020	Dent Disease 1	63	0.092

890		MSC152	Muscular Dystrophy, Becker Type	69	0.092

891		LWC002	Lowe Oculocerebrorenal Syndrome	68	0.092

892		WLF001	Wolff-Parkinson-White Syndrome	63	0.092

893		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	0.092

894		ARG007	Argininemia	58	0.092

895	c	PRX059	Peroxisome Biogenesis Disorder 1a	57	0.092

896		ENT011	Enterocolitis	55	0.092

897		ADR054	Adrenocortical Carcinoma, Hereditary	47	0.092

898		KRT019	Keratitis, Hereditary	66	0.092

899	P	KBK002	Kabuki Syndrome 1	66	0.092

900		CTY001	Cat Eye Syndrome	45	0.092

901		KPS004	Kaposi Sarcoma	76	0.092

902		SYR010	Syringomyelia, Noncommunicating Isolated	36	0.092

903	P	TTR001	Tetralogy of Fallot	69	0.092

904		TRG002	Trigeminal Neuralgia	61	0.092

905		PCK003	Pick Disease of Brain	70	0.092

906		GRG001	Greig Cephalopolysyndactyly Syndrome	64	0.092

907		PRP083	Porphyria, Acute Intermittent	64	0.092

908		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.092

909		HRD029	Hereditary Leiomyomatosis and Renal Cell Cancer	56	0.092

910	P	HYP058	Hypervitaminosis a	47	0.092

911	c	NRD017	Neurodegeneration with Brain Iron Accumulation 1	63	0.092

912		HLT002	Halothane Hepatitis	32	0.092

913		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.092

914		MLL018	Miller-Dieker Lissencephaly Syndrome	53	0.092

915		MYL013	Myeloperoxidase Deficiency	44	0.092

916	c	GRV008	Graves Disease 1	54	0.092

917		MTC147	Mitochondrial Complex I Deficiency, Nuclear Type 12	21	0.092

918		FBR012	Fabry Disease	71	0.092

919		STR081	Stormorken Syndrome	56	0.092

920	P	STR020	Strabismus	56	0.092

921	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.092

922	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	64	0.092

923	c	RTN143	Retinitis Pigmentosa 47	42	0.092

924	c	LBR006	Leber Congenital Amaurosis 11	35	0.092

925		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.092

926		CNZ006	Coenzyme Q10 Deficiency, Primary, 1	42	0.092

927	c	ART101	Aortic Valve Disease 2	65	0.092

928		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.092

929		LGN006	Legionnaire Disease	52	0.092

930	c	MYC058	Myocardial Infarction 2	23	0.092

931	c	ATS371	Autism 6	21	0.092

932		CTN028	Cutaneous Telangiectasia and Cancer Syndrome, Familial	70	0.092

933		INT258	Interstitial Nephritis, Karyomegalic	46	0.092

934	c	INC015	Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2	33	0.092

935	P	TMR010	Tumor Predisposition Syndrome	69	0.092

936	c	PRS114	Prostate Cancer, Hereditary, 2	33	0.092

937	c	HYP326	Hyperinsulinemic Hypoglycemia, Familial, 5	50	0.092

938	c	HYP271	Hyperinsulinemic Hypoglycemia, Familial, 4	52	0.092

939		HYP555	Hypertriglyceridemia, Transient Infantile	39	0.092

940	c	RTN140	Retinitis Pigmentosa 67	32	0.092

941		HRN029	Hearing Loss, Noise-Induced	37	0.092

942		HRS016	Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction	26	0.092

943	P	MGL010	Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a	39	0.092

944		APN008	Apnea, Obstructive Sleep	66	0.092

945	P	LKM071	Leukemia, Chronic Lymphocytic	74	0.092

946		THY111	Thyroid Carcinoma, Familial Medullary	67	0.092

947	c