Search results for NADH

1225 hits were found for NADH

#	Family	MCID	Name	MIFTS	Score
1		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	35	44.624

2		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	61	41.306

3	P	MTH007	Methemoglobinemia	46	10.669

4	P	MPL001	Maple Syrup Urine Disease	70	10.018

5		PYR031	Pyruvate Dehydrogenase E3-Binding Protein Deficiency	43	9.193

6		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	47	9.193

7		ANX004	Anoxia	40	9.107

8	c	CNG223	Congenital Methemoglobinemia	39	9.019

9	P	MYP004	Myopathy	67	7.725

10	P	LCT001	Lactic Acidosis	51	6.566

11		HYP266	Hypoxia	57	6.490

12		MTC005	Mitochondrial Metabolism Disease	45	6.409

13	P	OPT006	Optic Nerve Disease	58	6.115

14	P	MTC133	Mitochondrial Myopathy	50	6.080

15	P	HRD217	Hereditary Optic Neuropathy	36	6.041

16	P	NRP001	Neuropathy	60	5.193

17	P	MTC069	Mitochondrial Disorders	57	5.133

18		CYN002	Cyanosis, Transient Neonatal	43	5.128

19		FTT001	Fatty Liver Disease	62	5.036

20		LBR038	Leber Hereditary Optic Neuropathy, Modifier of	62	4.935

21	P	MYC084	Mycobacterium Tuberculosis 1	68	4.843

22		HLX001	Helix Syndrome	48	4.715

23	P	PRK039	Parkinsonism	55	4.638

24		HYP066	Hyperglycemia	61	4.603

25	P	NRB001	Neuroblastoma	66	4.383

26	c	ATS307	Autosomal Recessive Cerebellar Ataxia	39	4.211

27		LGH007	Leigh Syndrome	70	4.202

28	P	ENC018	Encephalopathy	62	3.978

29		MTC004	Mitochondrial Encephalomyopathy	42	3.966

30		CHR066	Chronic Fatigue Syndrome	60	3.873

31		GLL048	Glial Tumor	52	3.855

32		GLM045	Glioma	63	3.855

33		NNL005	Non-Alcoholic Fatty Liver Disease	63	3.843

34		CHG001	Chagas Disease	66	3.801

35	P	ALZ034	Alzheimer Disease	87	3.781

36	c	ATR087	Atrial Standstill 1	74	3.559

37		AGN016	Aging	54	3.540

38		HYP056	Hypoglycemia	65	3.461

39		ECH003	Echinococcosis	53	3.428

40		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	3.374

41		CHL014	Cholera	62	3.319

42		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	3.287

43		LPD008	Lipid Metabolism Disorder	62	3.287

44	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	3.227

45		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	44	3.189

46		BRN071	Brain Injury	50	3.088

47		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	3.079

48		PRT037	Pertussis	65	3.066

49		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	3.043

50	P	HYP265	Hypotonia	42	3.043

51	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	2.998

52	P	BRS047	Breast Cancer	98	2.959

53	c	MCR115	Microvascular Complications of Diabetes 5	65	2.922

54		CYS001	Cystic Fibrosis	78	2.899

55	P	CHR012	Chronic Granulomatous Disease	69	2.890

56		MTB004	Metabolic Acidosis	48	2.885

57	P	KLZ004	Kala-Azar 1	41	2.857

58		LSH001	Leishmaniasis	64	2.857

59		IRN002	Iron Metabolism Disease	57	2.857

60		48X005	48,xyyy	39	2.827

61	P	MSC005	Muscular Dystrophy	67	2.797

62		47X002	47,xyy	48	2.793

63	P	DYS154	Dystonia	64	2.786

64		HMP009	Haemophilus Influenzae	41	2.786

65		CTR172	Citrullinemia, Classic	65	2.736

66		CRT015	Carotid Artery Occlusion	45	2.705

67	P	PRK057	Parkinson Disease, Late-Onset	80	2.691

68		OST159	Osteogenic Sarcoma	66	2.691

69	P	HNT016	Huntington Disease	73	2.656

70		CRB004	Cerebral Artery Occlusion	45	2.642

71		ISC004	Ischemia	61	2.635

72		MTH072	Methemoglobin Reductase Deficiency	15	2.597

73	c	MJR022	Major Affective Disorder 8	38	2.595

74	c	MJR024	Major Affective Disorder 9	41	2.595

75	P	BPL003	Bipolar Disorder	56	2.595

76		TRM010	Traumatic Brain Injury	51	2.584

77	P	HYP061	Hypertrophic Cardiomyopathy	69	2.566

78		LBR036	Leber Plus Disease	66	2.546

79		GLB002	Glioblastoma	67	2.546

80		ALC007	Alcohol Dependence	66	2.509

81	c	DLT002	Dilated Cardiomyopathy	78	2.440

82	P	GST053	Gastric Cancer	83	2.425

83		CYS008	Cystic Echinococcosis	57	2.420

84	P	MSC003	Muscular Atrophy	52	2.404

85	P	SZR006	Seizure Disorder	70	2.389

86		MLR004	Malaria	80	2.389

87		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.389

88		HRW001	Hair Whorl	35	2.389

89		DYS015	Dysentery	50	2.381

90		NRM005	Neuromuscular Disease	63	2.367

91		PST092	Posttransplant Acute Limbic Encephalitis	28	2.347

92	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	55	2.334

93		ART140	Arteries, Anomalies of	53	2.334

94		LPP008	Lipoprotein Quantitative Trait Locus	65	2.334

95		SCC003	Succinic Acidemia	10	2.308

96		ATH013	Atherosclerosis Susceptibility	63	2.304

97		KRN002	Kearns-Sayre Syndrome	63	2.292

98		CRN030	Coronary Stenosis	50	2.285

99	c	BRN108	Branchiootic Syndrome 1	62	2.260

100		DNT012	Dental Caries	53	2.260

101	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	2.253

102	P	LTR001	Lateral Sclerosis	58	2.253

103		HYP060	Hyperinsulinism	54	2.253

104		CHL068	Cholestasis	61	2.244

105		ATS010	Autosomal Recessive Disease	42	2.235

106	P	SPP010	Suppressor of Tumorigenicity 3	51	2.215

107	P	CTR002	Cataract	60	2.215

108		STN013	Stenotrophomonas Maltophilia Infection	26	2.213

109	c	HPT001	Hepatitis C	62	2.213

110	P	MLN008	Melanoma	76	2.183

111	P	PHC003	Pheochromocytoma	69	2.172

112		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	2.172

113	c	HPT073	Hepatitis C Virus	71	2.131

114		SLP001	Sleeping Sickness	56	2.119

115	P	VSC007	Vascular Disease	63	2.119

116		ALL014	Allergic Encephalomyelitis	34	2.119

117	c	HYP836	Hypercholesterolemia, Familial, 1	73	2.088

118		ORL011	Oral Cancer	60	2.088

119	P	RSP003	Respiratory Failure	74	2.069

120	P	LVR013	Liver Disease	69	2.054

121		SQM006	Squamous Cell Carcinoma	60	2.044

122	P	BRS044	Breast Adenocarcinoma	58	2.017

123		GLC003	Glucose Intolerance	54	1.998

124		CRB090	Cerebral Hypoxia	42	1.998

125	c	DNT047	Dentinogenesis Imperfecta Type 2	35	1.998

126	P	ATS364	Autism	69	1.951

127	c	HYP595	Hypertension, Essential	85	1.951

128		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	17	1.951

129		PRM329	Premature Aging	36	1.905

130	P	INF032	Infertility	57	1.905

131	P	LPR021	Leprosy 3	71	1.903

132		URT049	Urate Oxidase, Pseudogene	24	1.903

133	P	MCR010	Microcephaly	60	1.903

134		HNS001	Hansen's Disease	32	1.903

135		CND006	Candida Glabrata	30	1.903

136	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	1.853

137		RPD005	Rapidly Involuting Congenital Hemangioma	46	1.853

138		HYP014	Hyperuricemia	51	1.853

139		CNT047	Contact Dermatitis	57	1.846

140	c	MCR130	Microvascular Complications of Diabetes 6	41	1.845

141	c	MCR120	Microvascular Complications of Diabetes 7	47	1.845

142	c	MCR113	Microvascular Complications of Diabetes 3	52	1.845

143	c	MCR133	Microvascular Complications of Diabetes 4	41	1.845

144	P	SCK005	Sickle Cell Disease	56	1.845

145		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	1.800

146		HMC014	Homocysteinemia	52	1.800

147	P	SCH015	Schizophrenia	74	1.800

148	P	PRS040	Prostate Cancer	95	1.800

149	c	CHR095	Chronic Progressive External Ophthalmoplegia	49	1.800

150	P	LPS004	Lupus Erythematosus	61	1.800

151	P	MYC033	Myoclonus	47	1.800

152	c	THY056	Thyroid Dyshormonogenesis 3	31	1.782

153		CHL065	Cholangiocarcinoma	58	1.782

154		TRN015	Transient Cerebral Ischemia	63	1.782

155		INT079	Intrahepatic Cholangiocarcinoma	51	1.782

156	P	PLM037	Pulmonary Hypertension	72	1.770

157		DBT010	Diabetic Neuropathy	54	1.770

158	P	THL005	Thalassemia	56	1.746

159		CRV035	Cervical Cancer	73	1.746

160	c	SYS001	Systemic Lupus Erythematosus	87	1.746

161	P	MLT020	Multiple Sclerosis	79	1.746

162	P	FBR017	Fibrosarcoma	56	1.746

163		HDN002	Head Injury	44	1.746

164		CRV040	Cervix Carcinoma	50	1.715

165		PPL052	Papillomatosis, Confluent and Reticulated	34	1.691

166		ART002	Arts Syndrome	66	1.689

167	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	54	1.689

168	P	ANP001	Anaplastic Large Cell Lymphoma	61	1.689

169	c	LKM061	Leukemia, Acute Myeloid	83	1.689

170	c	ACT068	Acute Cystitis	61	1.689

171		TTN003	Tetanus	65	1.689

172	P	PTS002	Ptosis	52	1.689

173	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	1.650

174	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	1.650

175	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	1.650

176	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	1.650

177	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	1.650

178	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	1.650

179	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	1.650

180	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	1.650

181	c	TYP009	Type 2 Diabetes Mellitus	92	1.650

182	P	PRD008	Periodontitis	64	1.650

183	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	1.650

184		TXC005	Toxic Shock Syndrome	62	1.650

185		STT001	Status Epilepticus	59	1.650

186		SPS057	Spasticity	42	1.629

187		VLV047	Volvulus of Midgut	52	1.629

188	P	EXN002	Exanthem	58	1.629

189		SCK003	Sickle Cell Anemia	74	1.629

190	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	49	1.629

191		OCL069	Ocular Motor Apraxia	57	1.629

192	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	53	1.629

193	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	52	1.629

194		ORL015	Oral Squamous Cell Carcinoma	43	1.629

195	P	CRD119	Cardiac Arrest	67	1.629

196	P	MYC008	Myocarditis	59	1.629

197	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	41	1.608

198	P	LNG032	Lung Cancer	98	1.566

199	P	BLD134	Bladder Cancer	79	1.566

200		ACT098	Acute Erythroid Leukemia	55	1.566

201	P	FRD001	Friedreich Ataxia	61	1.566

202		DBT084	Diabetes Mellitus, Ketosis-Prone	60	1.566

203	P	MLG056	Malignant Hyperthermia	66	1.566

204	P	CRV031	Cervical Adenocarcinoma	48	1.566

205		INS001	Insulinoma	59	1.566

206	P	GST044	Gastritis	55	1.566

207		INT071	Intestinal Perforation	49	1.566

208		ALV002	Alveolar Echinococcosis	57	1.566

209	P	HPT021	Hepatitis	69	1.566

210		FLR002	Filariasis	55	1.566

211	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	1.566

212		PHN003	Phenylketonuria	76	1.566

213		PLM129	Pulmonary Disease, Chronic Obstructive	74	1.564

214	P	PSR002	Psoriasis	63	1.564

215		PST011	Pustulosis of Palm and Sole	52	1.564

216		GRD001	Giardiasis	46	1.564

217		CRB037	Cerebral Palsy	67	1.564

218		ADR040	Adrenal Gland Pheochromocytoma	46	1.521

219	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	1.521

220	P	BCL017	B-Cell Lymphoma	59	1.521

221	P	SKN015	Skin Carcinoma	71	1.521

222	c	ACT071	Acute Kidney Failure	60	1.521

223	c	MGR028	Migraine with or Without Aura 1	64	1.499

224		OTT002	Otitis Media	71	1.499

225	P	MYL006	Myeloid Leukemia	61	1.499

226	c	PRC016	Pre-Eclampsia	65	1.499

227		HGH043	High Grade Glioma	45	1.499

228		LTH004	Lathyrism	15	1.499

229		SVR001	Severe Acute Respiratory Syndrome	67	1.477

230	P	GLC113	Galactosemia I	66	1.476

231		HPT022	Hepatoblastoma	54	1.476

232		CNG034	Congestive Heart Failure	69	1.476

233	P	TRM003	Tremor	48	1.429

234	P	LNG064	Lung Cancer Susceptibility 3	70	1.429

235		INS024	Insulin-Like Growth Factor I	78	1.426

236		VSC003	Visceral Leishmaniasis	55	1.426

237		RSC001	Rosacea	55	1.426

238		PRM236	Primary Biliary Cholangitis	60	1.426

239		ONC002	Onchocerciasis	51	1.426

240		PTH003	Pathologic Nystagmus	52	1.426

241		DYS073	Dysphagia	53	1.426

242	c	RNG015	Ring Chromosome 2	22	1.426

243	P	MYP087	Myopathy, Tubular Aggregate, 1	49	1.416

244	c	TYP008	Type 1 Diabetes Mellitus	70	1.381

245		BRN004	Brain Edema	54	1.381

246		RBF001	Riboflavin Deficiency	49	1.378

247		LCT008	Lactate Dehydrogenase Deficiency	14	1.377

248		CYN003	Cyanide Poisoning	22	1.347

249		MSC007	Muscle Hypertrophy	64	1.347

250		INF034	Infective Endocarditis	54	1.347

251	c	THY071	Thyroid Dyshormonogenesis 1	31	1.347

252		RTN212	Retinal Dystrophy with or Without Macular Staphyloma	31	1.347

253	P	MTH008	Methylmalonic Acidemia	52	1.347

254		PRT036	Peritonitis	65	1.347

255		CLR030	Clear Cell Renal Cell Carcinoma	54	1.347

256	P	CCK001	Cockayne Syndrome	68	1.347

257	P	ECL001	Eclampsia	52	1.347

258		GLC009	Glucosephosphate Dehydrogenase Deficiency	53	1.347

259		CHL123	Chlamydia	58	1.347

260	P	END033	Endocarditis	58	1.347

261	P	BNG032	Benign Mesothelioma	53	1.347

262	P	PRP029	Porphyria	60	1.347

263		ISL099	Isolated Methylmalonic Acidemia	36	1.347

264	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	1.330

265		DFC004	Deficiency Anemia	74	1.330

266		BCT022	Bacterial Infectious Disease	56	1.330

267		MTH071	Methane Production	25	1.278

268	P	BRG001	Brugada Syndrome	69	1.278

269		ARG004	Argyria	26	1.278

270		CYS005	Cysticercosis	60	1.278

271		PRP027	Peripheral Vascular Disease	71	1.260

272		ANG054	Angina Pectoris	66	1.260

273		EXT007	Extracutaneous Mastocytoma	38	1.260

274		MST004	Mast Cell Neoplasm	42	1.260

275	P	HRD018	Hair Disease	44	1.260

276		HLL004	Hellp Syndrome	53	1.260

277		KRT002	Keratomalacia	55	1.240

278	c	SPR086	Spermatogenic Failure 3	46	1.224

279		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	1.224

280	P	PNC035	Pancreatic Cancer	86	1.224

281	P	HML002	Hemolytic Anemia	62	1.224

282	P	RRH023	Rare Hereditary Hemochromatosis	54	1.224

283		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	1.224

284		HMS001	Hemosiderosis	48	1.224

285		SCH014	Schistosomiasis	56	1.224

286	P	HYP076	Hyperthyroidism	53	1.224

287		HRT015	Heritable Pulmonary Arterial Hypertension	46	1.224

288		BRN056	Bronchopulmonary Dysplasia	56	1.224

289		CRT020	Cortisone Reductase Deficiency	34	1.209

290	c	PLM164	Pulmonary Hypertension, Primary, 1	76	1.167

291	P	ALC033	Alcohol Use Disorder	61	1.167

292		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	1.167

293	P	LKM002	Leukemia	67	1.167

294	c	ACT027	Acute Pancreatitis	60	1.167

295		MNK001	Menkes Disease	64	1.161

296		BRK010	Burkitt Lymphoma	66	1.161

297		LBR031	Leber Optic Atrophy and Dystonia	39	1.161

298		DWN001	Down Syndrome	70	1.161

299		ESP021	Esophageal Cancer	83	1.161

300		ORG002	Organic Acidemia	44	1.161

301		PRX097	Paroxysmal Dystonia	32	1.161

302		LYD001	Leydig Cell Tumor	45	1.161

303	P	HYD006	Hydrocephalus	61	1.161

304		CRB039	Cerebrovascular Disease	66	1.161

305	P	LRY044	Larynx Cancer	54	1.161

306	c	SPR009	Sporadic Breast Cancer	42	1.108

307	c	THY107	Thymoma, Familial	42	1.107

308		ONC007	Oncocytoma	50	1.107

309	P	OVR042	Ovarian Cancer	88	1.107

310	P	CLR023	Colorectal Cancer	100	1.107

311	c	DVL036	Developmental and Epileptic Encephalopathy 39	39	1.107

312	P	HPT023	Hepatocellular Carcinoma	96	1.107

313		DSS032	Disease by Infectious Agent	55	1.107

314		HPT004	Hepatic Coma	43	1.107

315	c	CHR684	Chronic Kidney Disease	69	1.107

316	P	MLN007	Male Infertility	56	1.107

317		HPT019	Hepatic Encephalopathy	59	1.107

318		DPH001	Diphtheria	59	1.107

319	P	HRT032	Heart Disease	81	1.107

320	P	MYG005	Myoglobinuria	40	1.107

321	P	PRP019	Peripheral Nervous System Disease	58	1.107

322	P	THY023	Thymoma	64	1.107

323		LKS001	Leukostasis	41	1.107

324	P	RRT020	Rare Tumor	39	1.044

325	P	DFN349	Deafness, Nonsyndromic Sensorineural, Mitochondrial	34	1.044

326		KRT058	Keratoderma, Palmoplantar, with Deafness	43	1.044

327		HMM004	Hamamy Syndrome	39	1.044

328		SNG007	Sengers Syndrome	45	1.044

329		MYL069	Myeloma, Multiple	77	1.044

330		PLT031	Platelet Membrane Fluidity	28	1.044

331		SCR011	Scrapie	39	1.044

332		PRS034	Parasitic Helminthiasis Infectious Disease	51	1.044

333		ALL010	Allergic Contact Dermatitis	56	1.044

334	P	BRN006	Branchiootorenal Syndrome	50	1.044

335		CNR001	Coenurosis	26	1.044

336		TNS005	Tonsillitis	57	1.044

337	P	GRV001	Graves' Disease	55	1.044

338		ANS011	Anus Cancer	57	1.044

339		NNS010	Nonsyndromic Hearing Loss and Deafness, Mitochondrial	13	1.044

340		PRS119	Persistent Genital Arousal Disorder	18	1.044

341	P	LKM062	Leukemia, Acute Lymphoblastic	69	1.044

342		BRT005	Barth Syndrome	56	1.044

343		RCH002	Richards-Rundle Syndrome	31	1.044

344	P	SCL018	Scoliosis	57	1.044

345		THY029	Thyroid Carcinoma	51	1.044

346	P	DBT009	Diabetes Mellitus	67	1.044

347		YLL002	Yellow Fever	61	1.044

348		PLC005	Placental Insufficiency	56	1.044

349		MLT006	Multidrug-Resistant Tuberculosis	47	1.044

350		ADN018	Adenoma	59	1.044

351		END086	End Stage Renal Disease	52	1.044

352	P	BRB001	Beriberi	44	1.044

353	P	ADN016	Adenocarcinoma	63	1.044

354	P	INS002	in Situ Carcinoma	53	1.044

355		SPN186	Spinal Cord Injury	61	0.976

356	c	ACT134	Acute Liver Failure	59	0.976

357		ACR009	Acromesomelic Dysplasia, Hunter-Thompson Type	41	0.976

358	P	RTN008	Retinitis Pigmentosa	80	0.976

359	c	OPT053	Optic Atrophy 1	62	0.976

360	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.976

361	P	APL001	Aplastic Anemia	73	0.976

362	c	2HY001	2-Hydroxyglutaric Aciduria	38	0.976

363	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.976

364		BTT016	Batten-Turner Congenital Myopathy	53	0.976

365	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	52	0.976

366		NRR001	Neuroretinitis	42	0.976

367		MDD018	Middle East Respiratory Syndrome	44	0.976

368		RTN023	Retinitis	46	0.976

369	P	MVM001	Movement Disease	61	0.976

370	P	RNV001	Renovascular Hypertension	49	0.976

371		SKN016	Skin Disease	63	0.976

372	P	CNT004	Centronuclear Myopathy	57	0.976

373		SPN035	Spindle Cell Sarcoma	54	0.976

374	P	RTN016	Retinal Degeneration	52	0.976

375	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.976

376	P	SNS001	Sensorineural Hearing Loss	59	0.976

377		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.976

378	P	BRS053	Breast Fibroadenoma	49	0.976

379	P	GLY013	Glycogen Storage Disease	60	0.976

380		SRC014	Sarcoma	65	0.976

381		LVR012	Liver Cirrhosis	63	0.976

382	P	ADL010	Adult Respiratory Distress Syndrome	71	0.976

383		CYT002	Cytokine Deficiency	43	0.976

384		MSC157	Muscular Dystrophy, Duchenne Type	79	0.904

385		STR067	Stroke, Ischemic	80	0.904

386	P	MYS005	Myositis	56	0.904

387	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.904

388	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.904

389		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.904

390	c	PCH010	Pachyonychia Congenita 3	43	0.904

391	P	ASP006	Aspergillosis	72	0.904

392	P	GLM040	Glioma Susceptibility 1	71	0.904

393		RNL077	Renal Fibrosis	46	0.904

394	P	PLY041	Polymyositis	59	0.904

395		INT075	Intracranial Hypertension	53	0.904

396	P	RBL001	Rubella	58	0.904

397		VCC001	Vaccinia	47	0.904

398		TRY001	Trypanosomiasis	50	0.904

399	P	DRM010	Dermatomyositis	61	0.904

400		RCK004	Rickets	68	0.904

401		TLN003	Telangiectasis	51	0.904

402		ALC006	Alcoholic Hepatitis	61	0.904

403		PSY004	Psychotic Disorder	66	0.904

404		CCC002	Coccidiosis	50	0.904

405		MLG169	Malignant Astrocytoma	57	0.904

406		ERL001	Early Myoclonic Encephalopathy	62	0.904

407	P	KDN017	Kidney Cancer	61	0.904

408		GST045	Gastroenteritis	58	0.904

409		DBT007	Diabetic Cataract	36	0.904

410		IDP022	Idiopathic Spinal Cord Herniation	17	0.904

411	P	DBT005	Diabetes Insipidus	54	0.891

412	P	MCH002	Machado-Joseph Disease	62	0.891

413		ALZ029	Alzheimer Disease Mitochondrial	24	0.891

414		ARG002	Argininosuccinic Aciduria	61	0.891

415		ASP002	Aspartylglucosaminuria	58	0.891

416		SPS007	Spastic Cerebral Palsy	46	0.891

417		APR001	Apraxia	52	0.891

418		PNB004	Panbronchiolitis, Diffuse	34	0.891

419		HYP690	Hyper-Beta-Alaninemia	24	0.891

420		EST002	Estrogen-Receptor Negative Breast Cancer	45	0.891

421	P	BLD062	Bile Duct Cancer	67	0.891

422		PTN001	Patent Foramen Ovale	62	0.891

423	P	DRR001	Diarrhea	55	0.891

424		MYP161	Myopathy, Congenital Proximal, with Minicore Lesions	17	0.855

425		PRS129	Prostatic Hyperplasia, Benign	49	0.825

426		FRN006	Frontotemporal Dementia	68	0.825

427		PLY150	Polykaryocytosis Inducer	29	0.825

428	P	ATX030	Ataxia-Telangiectasia	80	0.825

429		HMN044	Human Immunodeficiency Virus Type 1	78	0.825

430	c	ATS007	Autism Spectrum Disorder	72	0.825

431		CLT003	Colitis	63	0.825

432	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.825

433	P	MYC007	Myocardial Infarction	70	0.825

434	P	HYP098	Hypereosinophilic Syndrome	66	0.825

435	P	CND004	Candidiasis	58	0.825

436	P	RNL017	Renal Oncocytoma	54	0.825

437		PRP016	Paraplegia	52	0.825

438		CHL045	Choline Deficiency Disease	39	0.825

439		STR103	Streptococcus Pneumonia	47	0.825

440		CRN019	Coronary Artery Vasospasm	47	0.825

441		CNS004	Constipation	56	0.825

442		PRS021	Prostatic Adenoma	43	0.825

443	c	BSL007	Basal Cell Carcinoma	68	0.825

444		FCL014	Focal Epilepsy	53	0.825

445	P	RNL015	Renal Hypertension	45	0.825

446		LYM017	Lyme Disease	62	0.825

447		PRS045	Prostatic Hypertrophy	53	0.825

448		SVR004	Severe Combined Immunodeficiency	72	0.825

449	P	ART021	Arteriosclerosis	54	0.825

450	P	OVR049	Ovarian Disease	52	0.825

451	P	LMB006	Limb-Girdle Muscular Dystrophy	52	0.825

452		STM007	Stomatitis	54	0.825

453		MYC005	Myocardial Stunning	46	0.825

454		WLL004	Wallerian Degeneration	38	0.825

455	P	MRC003	Mercury Poisoning	49	0.825

456	P	MYC026	Myoclonus Epilepsy	35	0.825

457		MYC015	Mycobacterium Fortuitum	28	0.825

458		ADR022	Adrenomyeloneuropathy	39	0.738

459		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	0.738

460	P	CRN300	Coronary Heart Disease 1	73	0.738

461		ADR007	Adrenoleukodystrophy	73	0.738

462		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	0.738

463	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.738

464	c	ATM006	Autoimmune Lymphoproliferative Syndrome	75	0.738

465		ATM095	Autoimmune Disease	61	0.738

466		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	0.738

467	P	SLP006	Sleep Apnea	69	0.738

468		FML037	Female Breast Cancer	51	0.738

469		CHK001	Chikungunya	60	0.738

470	P	URN019	Urinary Tract Infection	49	0.738

471		NNL006	Non-Alcoholic Steatohepatitis	54	0.738

472		HLC007	Helicobacter Pylori Infection	67	0.738

473		VRC005	Varicose Veins	60	0.738

474	c	HYP368	Hyperphenylalaninemia, Bh4-Deficient, C	37	0.738

475		MNN043	Meningioma, Familial	79	0.738

476		FSC002	Fascioliasis	44	0.738

477	c	ACT075	Acute Myocardial Infarction	56	0.738

478	P	KDN018	Kidney Disease	72	0.738

479	P	RHB003	Rhabdomyosarcoma	66	0.738

480		GSG001	Gas Gangrene	52	0.738

481		ULC004	Ulcerative Colitis	74	0.738

482		CHR074	Choriocarcinoma	46	0.738

483	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	0.738

484	P	PTT006	Pituitary Adenoma	55	0.738

485		TRC003	Trichomoniasis	53	0.738

486		ART016	Aortic Aneurysm	68	0.738

487		GLC008	Glucose Metabolism Disease	40	0.738

488		SCR001	Secretory Meningioma	40	0.738

489		LYM002	Lymphoplasmacyte-Rich Meningioma	35	0.738

490		LNG099	Lung Disease	62	0.738

491	P	KRT007	Keratoconus	50	0.738

492	P	CHR071	Charcot-Marie-Tooth Disease	64	0.738

493	P	SPN046	Spinal Muscular Atrophy	63	0.738

494		KRT009	Keratosis	53	0.738

495		CLN015	Colon Adenocarcinoma	65	0.738

496		HMG005	Hemoglobinopathy	56	0.738

497	P	MYS079	Miyoshi Muscular Dystrophy	54	0.738

498	P	BND020	Bone Disease	59	0.738

499		TTH006	Tooth Disease	51	0.738

500	P	PLY011	Polycystic Ovary Syndrome	57	0.738

501	P	PRN023	Prion Disease	60	0.738

502	P	PNC044	Pancreatitis	61	0.738

503	P	EYD002	Eye Disease	57	0.738

504	P	PRM002	Primary Hyperoxaluria	65	0.738

505	P	OBS001	Obstructive Jaundice	48	0.738

506		IDP070	Idiopathic Scoliosis	42	0.738

507		FML035	Familial Hyperlipidemia	55	0.738

508		SPN021	Spinal Meningioma	50	0.738

509	P	CRD246	Cardiovascular System Disease	56	0.738

510		HYP141	Hyperphenylalaninemia	42	0.738

511	P	MYT002	Myotonic Dystrophy	51	0.738

512		NCL011	Nuclear Gene-Encoded Leigh Syndrome Spectrum	21	0.738

513	P	TXP001	Toxoplasmosis	60	0.738

514		AGR019	Age-Related Hearing Loss	41	0.738

515		ANR040	Aneurysm	61	0.738

516		FST010	Fasting Hypoglycemia	33	0.738

517		HYP781	Hypoascorbemia	52	0.719

518		RHB024	Rhabdomyosarcoma 2	67	0.719

519		ANT039	Antisynthetase Syndrome	55	0.719

520		FST001	Foster-Kennedy Syndrome	39	0.719

521		FRC013	Fructose Utilization	15	0.639

522		PLY100	Polyploidy	36	0.639

523		ETH012	Ethylene Glycol Poisoning	29	0.639

524	c	ACQ047	Acquired Methemoglobinemia	30	0.639

525	P	RTT002	Rett Syndrome	79	0.639

526	c	GLL024	Gallbladder Disease 1	52	0.639

527		MHR001	Mohr-Tranebjaerg Syndrome	49	0.639

528	P	MTR004	Maturity-Onset Diabetes of the Young	68	0.639

529		DGL002	D-Glyceric Aciduria	41	0.639

530		MTC205	Mitochondrial Complex Iv Deficiency, Nuclear Type 1	57	0.639

531		HYP814	Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency	34	0.639

532	c	MSC106	Mosaic Variegated Aneuploidy Syndrome 2	41	0.639

533	P	INF037	Inflammatory Bowel Disease	53	0.639

534		DFF005	Diffuse Large B-Cell Lymphoma	54	0.639

535		LMB062	Limb Ischemia	55	0.639

536		INV001	Invasive Aspergillosis	49	0.639

537	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.639

538		MLD018	Mild Cognitive Impairment	48	0.639

539		DBT090	Diabetes and Deafness, Maternally Inherited	45	0.639

540		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.639

541		TRD006	Tardive Dyskinesia	53	0.639

542		WRN002	Wernicke-Korsakoff Syndrome	50	0.639

543	c	HYP602	Hyperoxaluria, Primary, Type Ii	49	0.639

544	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.639

545	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.639

546	P	SCL057	Scoliosis, Isolated 1	40	0.639

547	c	MTR019	Maturity-Onset Diabetes of the Young, Type 2	53	0.639

548		INC002	Inclusion Body Myositis	57	0.639

549		CMR002	Coumarin Resistance	59	0.639

550		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	0.639

551		ACH004	Achondroplasia	66	0.639

552		RHM034	Rahman Syndrome	37	0.639

553	c	ACT073	Acute Leukemia	58	0.639

554	P	ZLL001	Zellweger Syndrome	65	0.639

555		BRR002	Barrett's Adenocarcinoma	37	0.639

556		URM002	Uremia	47	0.639

557		CRC021	Carcinosarcoma	64	0.639

558		SKN019	Skin Melanoma	71	0.639

559		MSC193	Muscular Lipidosis	22	0.639

560	c	PRG106	Progressive Muscular Dystrophy	32	0.639

561		PNC129	Pancreatic Adenocarcinoma	65	0.639

562	P	EPL164	Epilepsy	68	0.639

563	P	PLM036	Pulmonary Fibrosis	66	0.639

564		GST040	Gastric Adenocarcinoma	67	0.639

565		ANV001	Anovulation	47	0.639

566		OVR063	Overnutrition	42	0.639

567	P	BNG002	Benign Meningioma	36	0.639

568		PPT005	Peptic Ulcer Disease	58	0.639

569	P	PLL002	Pellagra	46	0.639

570	P	ART022	Arthritis	71	0.639

571		OST012	Osteoarthritis	77	0.639

572	P	INT070	Intestinal Obstruction	57	0.639

573	P	DNG005	Dengue Virus	56	0.639

574		SPR006	Sparganosis	35	0.639

575	P	DMN002	Dementia	66	0.639

576		ALL029	Allergic Disease	59	0.639

577		VRC001	Varicocele	48	0.639

578		PCD001	Pica Disease	38	0.639

579		SKN005	Skin Atrophy	41	0.639

580		NRT004	Neuritis	53	0.639

581	P	HYP086	Hypothyroidism	69	0.639

582		GLN002	Glanders	38	0.639

583		GST033	Gestational Diabetes	61	0.639

584		MST005	Mastitis	53	0.639

585	P	FNC004	Fanconi Syndrome	60	0.639

586		BRN024	Bronchitis	67	0.639

587	P	CWD010	Cowden Syndrome	70	0.639

588		NRT001	Neurotic Disorder	56	0.639

589	P	RTN018	Retinal Disease	53	0.639

590		ACT058	Active Peptic Ulcer Disease	56	0.639

591		MDD011	Mood Disorder	62	0.639

592	P	GLM007	Glomerulonephritis	60	0.639

593		DMY004	Demyelinating Disease	50	0.639

594	P	PLY019	Polyneuropathy	52	0.639

595		GST023	Gastric Ulcer	52	0.639

596		QDR001	Quadriplegia	50	0.639

597	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	0.639

598	c	HPT016	Hepatitis B	62	0.639

599		GRN017	Granulocytopenia	42	0.639

600		SYS003	Systolic Heart Failure	49	0.639

601	P	DRM053	Dermatitis, Atopic	65	0.522

602	c	ALP101	Alpha-Thalassemia	62	0.522

603	c	LCT020	Lactic Acidosis, Chronic Adult Form	8	0.522

604		PLG003	Polg-Related Disorders	20	0.522

605		MTH047	Methanol Poisoning	37	0.522

606		CNG506	Congenital Amyoplasia	27	0.522

607		GRN033	Granulomatous Mastitis	32	0.522

608		GLM044	Glomerular Disease	35	0.522

609	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	0.522

610	P	NSP012	Nasopharyngeal Carcinoma	61	0.522

611		CHR696	Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia	32	0.522

612		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.522

613		3HY007	3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency	51	0.522

614	P	MYS003	Myasthenia Gravis	68	0.522

615		SCC001	Succinic Semialdehyde Dehydrogenase Deficiency	59	0.522

616	c	SPS222	Spastic Paraplegia 20, Autosomal Recessive	56	0.522

617		SQM013	Squamous Cell Carcinoma, Head and Neck	73	0.522

618	P	ALB003	Albinism-Deafness Syndrome	34	0.522

619		CMB017	Combined Oxidative Phosphorylation Deficiency 6	41	0.522

620		CRD223	Cardiac Arrhythmia	63	0.522

621		ANR007	Anorexia Nervosa	60	0.522

622		ALL003	Allergic Rhinitis	67	0.522

623	c	CTR132	Cataract 3, Multiple Types	42	0.522

624		PRK088	Parkinson Disease, Mitochondrial	19	0.522

625		MTC029	Mitochondrial Complex V Deficiency, Nuclear Type 1	40	0.522

626		END057	Endometrial Cancer	72	0.522

627	P	TRC072	Treacher Collins Syndrome 1	62	0.522

628		HMF006	Hemifacial Microsomia	55	0.522

629		PHS025	Phosphatase, Acid, of Tissues	28	0.522

630		CRT072	Creutzfeldt-Jakob Disease	68	0.522

631		CRZ001	Crouzon Syndrome	65	0.522

632		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.522

633	c	LKM063	Leukemia, Chronic Myeloid	71	0.522

634		CHR100	Chronic Ulcer of Skin	57	0.522

635		EPD015	Epidemic Typhus	44	0.522

636		ALC001	Alcohol-Related Birth Defect	36	0.522

637	P	FML011	Familial Adenomatous Polyposis	71	0.522

638		VTM002	Vitamin B12 Deficiency	48	0.522

639	P	PRG013	Paraganglioma	57	0.522

640		CRB150	Cerebral Creatine Deficiency Syndrome 2	54	0.522

641		PYR012	Pyruvate Dehydrogenase E1-Beta Deficiency	41	0.522

642		PRT251	Proteinuria, Chronic Benign	57	0.522

643		NRN005	Neuronal Ceroid-Lipofuscinoses	61	0.522

644		BCT021	Bacterial Sepsis	43	0.522

645	P	HYP111	Hyperprolinemia	45	0.522

646	P	PLY014	Polycystic Kidney Disease	69	0.522

647	P	ATR011	Atrial Fibrillation	66	0.522

648	P	FTL001	Fetal Alcohol Syndrome	55	0.522

649		CRD231	Cardiomyopathy, Infantile Histiocytoid	45	0.522

650		SLF014	Sulfite Oxidase Deficiency, Isolated	53	0.522

651		CNT105	Central Core Disease of Muscle	59	0.522

652	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	0.522

653	P	MCR129	Microvascular Complications of Diabetes 1	68	0.522

654	c	MTH083	Methemoglobinemia, Beta Type	22	0.522

655	c	MTH084	Methemoglobinemia, Alpha Type	11	0.522

656		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.522

657		EWN003	Ewing Sarcoma	70	0.522

658	P	MJR001	Major Depressive Disorder	68	0.522

659		ACT119	Acute Promyelocytic Leukemia	62	0.522

660	c	BRS111	Breast-Ovarian Cancer, Familial 2	53	0.522

661	c	SCH079	Schizophrenia 1	44	0.522

662		TBL029	Tubulin, Beta	28	0.522

663	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.522

664	c	HYP597	Hyperprolinemia, Type Ii	43	0.522

665	P	TRT019	Torticollis	47	0.522

666	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	70	0.522

667		KRT071	Keratosis, Seborrheic	56	0.522

668		PTR032	Peters-Plus Syndrome	63	0.522

669		RFS006	Refsum Disease, Classic	63	0.522

670	c	TBR025	Tuberous Sclerosis 1	84	0.522

671	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	69	0.522

672	c	SML038	Small Cell Cancer of the Lung	69	0.522

673	P	HYP726	Hypercalcemia, Infantile, 1	58	0.522

674	P	HYP750	Hypertriglyceridemia, Familial	62	0.522

675		MLT157	Multiple System Atrophy 1	69	0.522

676	P	MDL005	Medulloblastoma	75	0.522

677		NPH091	Nephrolithiasis, Calcium Oxalate	61	0.522

678	P	MYP105	Myopathy, Myosin Storage, Autosomal Dominant	40	0.522

679	c	CHR489	Charcot-Marie-Tooth Disease, Axonal, Type 2q	32	0.522

680		MLD001	Melioidosis	67	0.522

681		MTC155	Mitochondrial Complex I Deficiency, Nuclear Type 7	22	0.522

682		CHR431	Chronic Venous Insufficiency	48	0.522

683		CRD137	Cardiogenic Shock	56	0.522

684	P	NRD007	Neurodegeneration with Brain Iron Accumulation	52	0.522

685	c	CHR697	Charcot-Marie-Tooth Disease X-Linked Recessive 4	31	0.522

686	P	HRD144	Hereditary Mixed Polyposis Syndrome	54	0.522

687		RGD003	Rigid Spine Muscular Dystrophy 1	56	0.522

688		LMY002	Leiomyoma	51	0.522

689	P	FML068	Familial Hypocalciuric Hypercalcemia	55	0.522

690		FBR009	Fibrous Dysplasia	48	0.522

691	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	0.522

692	P	SDR003	Sideroblastic Anemia	51	0.522

693		SCT002	Scotoma	42	0.522

694	P	HLP001	Holoprosencephaly	69	0.522

695		NTR005	Nutritional Deficiency Disease	61	0.522

696		URT010	Ureteral Obstruction	45	0.522

697	P	EMB005	Embryonal Rhabdomyosarcoma	53	0.522

698		INT007	Intermediate Coronary Syndrome	54	0.522

699		DRM011	Dermatophytosis	52	0.522

700		BLT006	Bilateral Breast Cancer	48	0.522

701		GLY085	Glycogen Storage Disease Due to Lactate Dehydrogenase Deficiency	16	0.522

702		EMR021	Emery-Dreifuss Syndrome	11	0.522

703	c	VRL010	Viral Hepatitis	53	0.522

704		MNT002	Mental Depression	57	0.522

705		PSD009	Pseudohermaphroditism	46	0.522

706		PYD002	Pyoderma	50	0.522

707		MLG077	Malignant Peripheral Nerve Sheath Tumor	54	0.522

708		ACQ007	Acquired Immunodeficiency Syndrome	59	0.522

709		ILS001	Ileus	50	0.522

710		NPH009	Nephrolithiasis	54	0.522

711		TNC002	Tinea Capitis	42	0.522

712		CMB007	Combined Immunodeficiency	57	0.522

713	P	VNS003	Venous Insufficiency	55	0.522

714	c	MCR112	Microvascular Complications of Diabetes 2	42	0.522

715	c	DVL110	Developmental and Epileptic Encephalopathy 88	20	0.522

716	P	MGR003	Migraine with Aura	52	0.522

717		OST003	Osteonecrosis	61	0.522

718		ANT018	Anthracosis	51	0.522

719		OST011	Osteomalacia	52	0.522

720	P	MGR001	Migraine Without Aura	49	0.522

721		ALC010	Alcoholic Cardiomyopathy	42	0.522

722		GT001	Gout	64	0.522

723		DNG003	Dengue Disease	65	0.522

724		CRY005	Cryptococcosis	60	0.522

725		GTR002	Goiter	53	0.522

726		FLR001	Filarial Elephantiasis	59	0.522

727		PNC001	Pancytopenia	53	0.522

728		CRT012	Cortical Blindness	42	0.522

729		NRX001	Neuroaxonal Dystrophy	38	0.522

730	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	0.522

731		RYS001	Reye Syndrome	49	0.522

732	c	ATM011	Autoimmune Hepatitis	63	0.522

733	P	CRN037	Craniosynostosis	68	0.522

734	P	TBR001	Tuberous Sclerosis	69	0.522

735	P	LNG028	Long Qt Syndrome	64	0.522

736	P	END044	Endometriosis	62	0.522

737		ING001	Inguinal Hernia	59	0.522

738	P	MTC010	Mitochondrial Dna Depletion Syndrome	47	0.522

739		LPR001	Lepromatous Leprosy	49	0.522

740		HMP005	Hemiplegia	54	0.522

741		VTM033	Vitamin K Deficiency Bleeding	48	0.522

742		MCR013	Microphthalmia	60	0.522

743	c	INH020	Inherited Metabolic Disorder	48	0.522

744	P	PSD003	Pseudohypoaldosteronism	44	0.522

745	P	SLP005	Sleep Disorder	61	0.522

746	P	AXN001	Axonal Neuropathy	35	0.522

747		CCN002	Cocaine Abuse	49	0.522

748	P	TRT010	Teratoma	51	0.522

749		INT066	Interstitial Lung Disease	60	0.522

750		MLG067	Malignant Giant Cell Tumor	28	0.522

751	P	MTR014	Motor Neuron Disease	65	0.522

752	P	TMP001	Temporal Lobe Epilepsy	49	0.522

753		BRS051	Breast Disease	58	0.522

754		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.522

755		LYS002	Lysosomal Storage Disease	51	0.522

756		AMN001	Amenorrhea	54	0.522

757		KLB003	Klebsiella Pneumonia	50	0.522

758		OPS001	Opisthorchiasis	41	0.522

759		DBT002	Diabetic Autonomic Neuropathy	41	0.522

760		LCH001	Leech Infestation	38	0.522

761		MYS004	Myiasis	39	0.522

762		HYP080	Hypogonadism	50	0.522

763		PST028	Post-Traumatic Stress Disorder	59	0.522

764		BBS001	Babesiosis	49	0.522

765		INV005	Inverted Follicular Keratosis	32	0.522

766	P	NRF002	Neurofibromatosis	57	0.522

767		DST006	Diastolic Heart Failure	45	0.522

768		HYD005	Hydrocele	46	0.522

769		TTR005	Tetrahydrobiopterin Deficiency	48	0.522

770	P	RDC010	Reducing Body Myopathy	33	0.522

771		DPR016	Depression	65	0.522

772	P	CRB088	Cerebral Atrophy	33	0.522

773		MYT011	Myotonia	39	0.522

774		OVR094	Ovarian Epithelial Cancer	39	0.522

775		GST039	Gastroduodenitis	37	0.522

776		LYM133	Lymphoma, Hodgkin, Classic	74	0.369

777		SPN050	Spinocerebellar Degeneration	39	0.369

778		CLF004	Cleft Lip/palate	57	0.369

779	P	OTT001	Otitis Externa	42	0.369

780	c	BCT007	Bacterial Meningitis	55	0.369

781		SCL025	Scleromyxedema	32	0.369

782		VNZ002	Venezuelan Equine Encephalitis	46	0.369

783		SLN002	Selenium Poisoning	10	0.369

784		CNN002	Cannabis Abuse	45	0.369

785	c	INF185	Infantile Epilepsy Syndrome	29	0.369

786		RFR010	Refractory Anemia	49	0.369

787		ACT181	Acute Motor Axonal Neuropathy	22	0.369

788		MTB016	Metabolic Myopathy	30	0.369

789		IDP079	Idiopathic Dropped Head Syndrome	10	0.369

790		BNG077	Benign Idiopathic Neonatal Seizures	23	0.369

791		NRM022	Neurometabolic Disease	24	0.369

792		CCN009	Cocaine Intoxication	30	0.369

793		PRC051	Paracetamol Poisoning	29	0.369

794	c	ADL084	Adult-Onset Myasthenia Gravis	21	0.369

795		SPS019	Spastic Paraparesis	38	0.369

796		SDD008	Sudden Sensorineural Hearing Loss	41	0.369

797		GNT167	Genetic Obesity	30	0.369

798		THY128	Thyroid Tumor	35	0.369

799	c	AMY088	Amyotrophic Lateral Sclerosis 3	31	0.369

800	c	ART068	Aortic Aneurysm, Familial Thoracic 2	33	0.369

801		EPL050	Epilepsy, Partial, with Pericentral Spikes	26	0.369

802	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	58	0.369

803		SPP011	Suppression of Tumorigenicity 12	61	0.369

804		PLM061	Pulmonary Edema of Mountaineers	26	0.369

805	c	SCL052	Scleroderma, Familial Progressive	61	0.369

806	P	DNT020	Dent Disease 1	63	0.369

807		DNN001	Danon Disease	59	0.369

808		MSC152	Muscular Dystrophy, Becker Type	69	0.369

809		MTC147	Mitochondrial Complex I Deficiency, Nuclear Type 12	21	0.369

810		CRD132	Cardiac Conduction Defect	60	0.369

811	c	MCL013	Mucolipidosis Iv	65	0.369

812		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	64	0.369

813		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.369

814		ALK013	Alkaptonuria	59	0.369

815		FBR012	Fabry Disease	70	0.369

816		KFR001	Kufor-Rakeb Syndrome	59	0.369

817		SNS008	Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis	60	0.369

818		MTC149	Mitochondrial Complex I Deficiency, Mitochondrial Type 1	14	0.369

819	c	NPH049	Nephrotic Syndrome, Type 2	51	0.369

820	P	SPR120	Supranuclear Palsy, Progressive, 1	69	0.369

821		ENC055	Encephalopathy, Ethylmalonic	51	0.369

822		PRS127	Pearson Marrow-Pancreas Syndrome	52	0.369

823	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	0.369

824	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	52	0.369

825		ASC010	Ascaris Lumbricoides Infection	49	0.369

826	P	RHM011	Rheumatoid Arthritis	82	0.369

827		HRD029	Hereditary Leiomyomatosis and Renal Cell Cancer	56	0.369

828	P	FCS012	Facioscapulohumeral Muscular Dystrophy 1	68	0.369

829	P	OST002	Osteoporosis	76	0.369

830	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.369

831		CLF027	Cleft Palate, Isolated	64	0.369

832	c	SPN225	Spondyloarthropathy 1	70	0.369

833	c	SYN084	Synpolydactyly 1	36	0.369

834		SYR010	Syringomyelia, Noncommunicating Isolated	36	0.369

835	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.369

836		ARG007	Argininemia	58	0.369

837		CYS019	Cystathioninuria	46	0.369

838	c	NRD017	Neurodegeneration with Brain Iron Accumulation 1	63	0.369

839		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.369

840		SRB001	Sorbitol Dehydrogenase Deficiency with Peripheral Neuropathy	21	0.369

841	c	FNC066	Fanconi Renotubular Syndrome 5	27	0.369

842		ADR016	Adrenal Cortical Carcinoma	62	0.369

843	P	LSS002	Lissencephaly	50	0.369

844		END014	Endemic Typhus	32	0.369

845		HYP017	Hypophosphatemia	49	0.369

846		CRR001	Carrion's Disease	31	0.369

847	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	0.369

848		DSR012	Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency	39	0.369

849	c	LBR006	Leber Congenital Amaurosis 11	35	0.369

850	P	MGL010	Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a	40	0.369

851	c	BTT014	Beta-Thalassemia	72	0.369

852		MYL009	Myelodysplastic Syndrome	67	0.369

853	P	HRD021	Hereditary Sensory Neuropathy	48	0.369

854	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.369

855	c	RTN143	Retinitis Pigmentosa 47	41	0.369

856		HRS016	Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction	26	0.369

857	P	HMG032	Hemoglobin H Disease	51	0.369

858		MLT150	Multiple Mitochondrial Dysfunctions Syndrome 2 with Hyperglycinemia	36	0.369

859		HMN002	Human Granulocytic Anaplasmosis	31	0.369

860		RCK002	Rocky Mountain Spotted Fever	34	0.369

861	P	MCL001	Mucolipidosis	49	0.369

862		THY121	Thyroid Gland Anaplastic Carcinoma	67	0.369

863		ADT001	Auditory Agnosia	26	0.369

864		CRT007	Cortical Deafness	26	0.369

865		HMN047	Human Cytomegalovirus Infection	57	0.369

866	c	HRD201	Hereditary Sensory and Autonomic Neuropathy Type 1	43	0.369

867		OLG022	Oligoasthenoteratozoospermia	36	0.369

868	c	3MT007	3-Methylglutaconic Aciduria	37	0.369

869		PLL012	Pollen Allergy	45	0.369

870		PHY002	Physical Disorder	41	0.369

871		CHL152	Childhood Acute Lymphocytic Leukemia	50	0.369

872	P	LYM118	Lymphoma	67	0.369

873		HYP025	Hyperphosphatemia	48	0.369

874	c	PRM032	Primary Congenital Glaucoma	41	0.369

875		TNS007	Taeniasis	46	0.369

876		INT017	Intestinal Schistosomiasis	51	0.369

877	P	MYF003	Myofibrillar Myopathy	49	0.369

878		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	64	0.369

879	c	DFN251	Deafness, Autosomal Dominant 11	44	0.369

880	c	HYP839	Hyperlipidemia, Familial Combined, 1	30	0.369

881	c	PRX059	Peroxisome Biogenesis Disorder 1a	56	0.369

882		CYS044	Cystic Disease of Lung	20	0.369

883	c	GLC112	Galactosemia Iii	51	0.369

884	P	HYP768	Hyperlipoproteinemia, Type I	67	0.369

885	c	GRV008	Graves Disease 1	54	0.369

886		MYC079	Myoclonic Epilepsy of Lafora	64	0.369

887		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.369

888		SPN354	Spinal Arachnoiditis	36	0.369

889		CTY001	Cat Eye Syndrome	44	0.369

890		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.369

891	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.369

892	P	PLV020	Pelvic Organ Prolapse	58	0.369

893		KRT019	Keratitis, Hereditary	66	0.369

894		KPS004	Kaposi Sarcoma	77	0.369

895		GRG001	Greig Cephalopolysyndactyly Syndrome	64	0.369

896		EXF001	Exfoliation Syndrome	56	0.369

897		CHD004	Chudley-Mccullough Syndrome	48	0.369

898	c	TTH012	Tooth Agenesis, Selective, 3	25	0.369

899	P	ORT004	Orthostatic Intolerance	63	0.369

900		LTN004	Late-Onset Retinal Degeneration	60	0.369

901	c	TTH011	Tooth Agenesis, Selective, 2	13	0.369

902	c	LNG048	Long Qt Syndrome 3	53	0.369

903	c	MLT068	Multiple Mitochondrial Dysfunctions Syndrome 1	45	0.369

904		LYM143	Lymphoma, Non-Hodgkin, Familial	75	0.369

905		PHL006	Phelan-Mcdermid Syndrome	60	0.369

906	c	LNG047	Long Qt Syndrome 2	59	0.369

907	c	ART101	Aortic Valve Disease 2	66	0.369

908		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	0.369

909		MYP099	Myopathy, Isolated Mitochondrial, Autosomal Dominant	27	0.369

910		AKL001	Au-Kline Syndrome	39	0.369

911		HRT037	Heart and Brain Malformation Syndrome	31	0.369

912		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	0.369

913		MLC004	Mulchandani-Bhoj-Conlin Syndrome	51	0.369

914		INT258	Interstitial Nephritis, Karyomegalic	45	0.369

915	c	RTN140	Retinitis Pigmentosa 67	32	0.369

916	c	DFN360	Deafness, Autosomal Dominant 69	34	0.369

917	c	MCR312	Microphthalmia, Syndromic 10	40	0.369

918		HRN029	Hearing Loss, Noise-Induced	37	0.369

919	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	65	0.369

920		WST005	West Nile Virus	57	0.369

921		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	0.369

922		2MN001	2-Aminoadipic 2-Oxoadipic Aciduria	34	0.369

923		PRP083	Porphyria, Acute Intermittent	65	0.369

924	c	NTR047	Neutropenia, Severe Congenital, 1, Autosomal Dominant	37	0.369

925		MLL018	Miller-Dieker Lissencephaly Syndrome	52	0.369

926		MTC207	Mitochondrial Complex Ii Deficiency, Nuclear Type 1	55	0.369

927		ADR054	Adrenocortical Carcinoma, Hereditary	47	0.369

928	c	MTC056	Mitochondrial Dna Depletion Syndrome 4a	62	0.369

929		LWC002	Lowe Oculocerebrorenal Syndrome	68	0.369

930		LGN006	Legionnaire Disease	52	0.369

931	c	MYC058	Myocardial Infarction 2	24	0.369

932		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.369

933		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	0.369

934		ENT011	Enterocolitis	55	0.369

935	c	GLY008	Glycogen Storage Disease Ii	72	0.369

936		HLT002	Halothane Hepatitis	31	0.369

937	P	HYP058	Hypervitaminosis a	47	0.369

938		HYP784	Hypogonadism, Male	43	0.369

939		TRG002	Trigeminal Neuralgia	61	0.369

940		CRN295	Carnitine Palmitoyltransferase I Deficiency	55	0.369

941		MYP091	Myopathy, Congenital, with Fiber-Type Disproportion	43	0.369

942		MYL013	Myeloperoxidase Deficiency	44	0.369

943	c	PRD040	Periodontitis, Chronic	52	0.369

944		PLY001	Polycythemia Vera	69	0.369

945		MYC080	Myoclonic Epilepsy of Unverricht and Lundborg	53	0.369

946		MYP097	Myopathy with Lactic Acidosis, Hereditary	31	0.369

947	c	NPH055	Nephrotic Syndrome, Type 1	52	0.369

948	P	TTR001	Tetralogy of Fallot	69	0.369

949		WLF001	Wolff-Parkinson-White Syndrome	65