Search results for Nicotinamide

1552 hits were found for Nicotinamide

#	Family	MCID	Name	MIFTS	Score
1		HYP066	Hyperglycemia	61	9.554

2		AGN016	Aging	54	8.995

3	P	SKN015	Skin Carcinoma	71	8.282

4		NNL005	Non-Alcoholic Fatty Liver Disease	63	8.111

5	P	ACN011	Acne	57	7.973

6		FTT001	Fatty Liver Disease	62	7.905

7	P	CHR012	Chronic Granulomatous Disease	69	6.970

8		CRB004	Cerebral Artery Occlusion	45	6.943

9	c	TYP008	Type 1 Diabetes Mellitus	70	6.650

10		HYP266	Hypoxia	57	6.629

11	c	MCR130	Microvascular Complications of Diabetes 6	41	6.492

12	c	MCR120	Microvascular Complications of Diabetes 7	47	6.492

13	c	MCR113	Microvascular Complications of Diabetes 3	52	6.492

14	c	MCR133	Microvascular Complications of Diabetes 4	41	6.492

15	P	PLL002	Pellagra	46	6.488

16		LPD008	Lipid Metabolism Disorder	62	6.282

17	P	NRP001	Neuropathy	60	6.228

18	P	ALZ034	Alzheimer Disease	87	6.164

19	c	CHR684	Chronic Kidney Disease	69	6.133

20		HYP025	Hyperphosphatemia	48	5.986

21	c	TYP009	Type 2 Diabetes Mellitus	92	5.974

22	P	MLN008	Melanoma	76	5.913

23		TRM010	Traumatic Brain Injury	51	5.862

24		ISC004	Ischemia	61	5.849

25		DPH001	Diphtheria	59	5.735

26	P	KDN018	Kidney Disease	72	5.656

27		BRN071	Brain Injury	50	5.633

28		GLC003	Glucose Intolerance	54	5.544

29	P	VSC007	Vascular Disease	63	5.542

30		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	5.353

31	c	PRC016	Pre-Eclampsia	65	5.300

32	P	PRP019	Peripheral Nervous System Disease	58	5.206

33	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	5.200

34	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	5.113

35	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	5.113

36	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	5.113

37	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	5.113

38	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	5.113

39	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	5.113

40	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	5.113

41	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	5.113

42	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	5.113

43	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	5.084

44		GLB002	Glioblastoma	67	5.060

45		PMP014	Pemphigoid	51	5.053

46	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	4.973

47		ATH013	Atherosclerosis Susceptibility	63	4.973

48	P	MYP004	Myopathy	67	4.907

49	P	DBT009	Diabetes Mellitus	67	4.894

50		WLL004	Wallerian Degeneration	38	4.892

51	P	BLD134	Bladder Cancer	79	4.868

52		CHL014	Cholera	62	4.822

53	P	NRB001	Neuroblastoma	66	4.761

54	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	4.757

55	P	LVR013	Liver Disease	69	4.746

56	P	PSR002	Psoriasis	63	4.690

57		PST011	Pustulosis of Palm and Sole	52	4.655

58		DBT010	Diabetic Neuropathy	54	4.581

59		BLL006	Bullous Pemphigoid	61	4.529

60		SQM006	Squamous Cell Carcinoma	60	4.512

61	P	DRM053	Dermatitis, Atopic	65	4.409

62	P	PRK039	Parkinsonism	55	4.409

63	c	ATR087	Atrial Standstill 1	74	4.284

64		CNG034	Congestive Heart Failure	69	4.256

65	P	LTR001	Lateral Sclerosis	58	4.247

66		RNL114	Renal Cell Carcinoma, Nonpapillary	80	4.237

67		NNL006	Non-Alcoholic Steatohepatitis	54	4.212

68		HMP009	Haemophilus Influenzae	41	4.212

69	c	HYP595	Hypertension, Essential	85	4.210

70	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	4.198

71	P	HNT016	Huntington Disease	73	4.179

72		PRT037	Pertussis	65	4.161

73		END086	End Stage Renal Disease	52	4.159

74		HYP056	Hypoglycemia	65	4.139

75		PRT251	Proteinuria, Chronic Benign	57	4.129

76		48X005	48,xyyy	39	4.110

77		STR067	Stroke, Ischemic	80	4.094

78		RPD005	Rapidly Involuting Congenital Hemangioma	46	3.968

79		ART016	Aortic Aneurysm	68	3.937

80	P	FRD001	Friedreich Ataxia	61	3.919

81		ANX004	Anoxia	40	3.896

82		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	3.882

83		SKN016	Skin Disease	63	3.871

84	P	CLR023	Colorectal Cancer	100	3.802

85	P	INF032	Infertility	57	3.800

86	c	HYP836	Hypercholesterolemia, Familial, 1	73	3.769

87		HYP060	Hyperinsulinism	54	3.767

88		ART140	Arteries, Anomalies of	53	3.744

89	P	BCL017	B-Cell Lymphoma	59	3.732

90		INT323	Intraocular Pressure Quantitative Trait Locus	64	3.719

91	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	3.717

92	P	MYC084	Mycobacterium Tuberculosis 1	68	3.678

93	c	SML038	Small Cell Cancer of the Lung	69	3.678

94	c	BSL007	Basal Cell Carcinoma	68	3.678

95	P	DMN002	Dementia	66	3.656

96		ANR040	Aneurysm	61	3.650

97		MLD018	Mild Cognitive Impairment	48	3.624

98	P	LNG032	Lung Cancer	98	3.612

99	P	ADL010	Adult Respiratory Distress Syndrome	71	3.542

100		INS001	Insulinoma	59	3.516

101		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	3.515

102		FML063	Familial Glucocorticoid Deficiency	58	3.476

103	P	OVR042	Ovarian Cancer	88	3.476

104		RSC001	Rosacea	55	3.468

105	P	SCK005	Sickle Cell Disease	56	3.463

106	P	THR014	Thrombocytopenia	66	3.451

107	c	LKM061	Leukemia, Acute Myeloid	83	3.450

108	P	PLM037	Pulmonary Hypertension	72	3.435

109	P	PRK057	Parkinson Disease, Late-Onset	80	3.420

110	P	HPT023	Hepatocellular Carcinoma	96	3.399

111	P	HRT032	Heart Disease	81	3.338

112	P	LCT001	Lactic Acidosis	51	3.337

113		SKN019	Skin Melanoma	71	3.329

114		CYT002	Cytokine Deficiency	43	3.310

115	P	LKM002	Leukemia	67	3.276

116		DBT002	Diabetic Autonomic Neuropathy	41	3.272

117		GLM045	Glioma	63	3.252

118		GLL048	Glial Tumor	52	3.227

119	P	MYL006	Myeloid Leukemia	61	3.211

120		IMP005	Impotence	52	3.203

121	c	MCR115	Microvascular Complications of Diabetes 5	65	3.192

122		HMC014	Homocysteinemia	52	3.154

123	P	MTC133	Mitochondrial Myopathy	50	3.123

124		TXC005	Toxic Shock Syndrome	62	3.109

125	P	PLY019	Polyneuropathy	52	3.084

126	c	MCL042	Macular Degeneration, Age-Related, 1	85	3.057

127	P	PNC035	Pancreatic Cancer	86	3.043

128	P	PMP001	Pemphigus	55	3.037

129		LPP008	Lipoprotein Quantitative Trait Locus	65	3.022

130	c	SYS001	Systemic Lupus Erythematosus	87	3.006

131		MTC005	Mitochondrial Metabolism Disease	45	2.976

132		DRM006	Dermatitis	62	2.972

133		HLX001	Helix Syndrome	48	2.945

134	P	GST053	Gastric Cancer	83	2.912

135		RNL077	Renal Fibrosis	46	2.907

136	c	DLT002	Dilated Cardiomyopathy	78	2.867

137		HRT031	Hartnup Disorder	52	2.854

138	P	PRS040	Prostate Cancer	95	2.851

139		BRN004	Brain Edema	54	2.846

140	P	MTC069	Mitochondrial Disorders	57	2.836

141	P	ART022	Arthritis	71	2.830

142	P	LPS004	Lupus Erythematosus	61	2.818

143	P	EXN002	Exanthem	58	2.814

144		DFC004	Deficiency Anemia	74	2.808

145		ALL014	Allergic Encephalomyelitis	34	2.807

146	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	16	2.793

147	P	ECL001	Eclampsia	52	2.785

148	P	PRD008	Periodontitis	64	2.782

149		PLM129	Pulmonary Disease, Chronic Obstructive	74	2.768

150	P	RTN016	Retinal Degeneration	52	2.735

151	P	ENC018	Encephalopathy	62	2.734

152		CNS004	Constipation	56	2.729

153		ORL015	Oral Squamous Cell Carcinoma	43	2.721

154	P	OPT006	Optic Nerve Disease	58	2.717

155		SPN186	Spinal Cord Injury	61	2.700

156	P	LKM071	Leukemia, Chronic Lymphocytic	75	2.696

157	P	ALC033	Alcohol Use Disorder	61	2.690

158	P	PLY011	Polycystic Ovary Syndrome	57	2.690

159		ATM095	Autoimmune Disease	61	2.670

160		ART002	Arts Syndrome	66	2.663

161	P	PLM036	Pulmonary Fibrosis	66	2.663

162	P	PNC044	Pancreatitis	61	2.663

163		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	2.663

164		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	44	2.663

165		ALL029	Allergic Disease	59	2.657

166		KRT009	Keratosis	53	2.657

167	P	BRS047	Breast Cancer	98	2.649

168	P	ATR011	Atrial Fibrillation	66	2.649

169	P	MYC007	Myocardial Infarction	70	2.647

170		KRT002	Keratomalacia	55	2.644

171	P	MTH007	Methemoglobinemia	46	2.627

172	P	ACT008	Actinic Keratosis	54	2.618

173		SVR004	Severe Combined Immunodeficiency	72	2.614

174	c	PLM164	Pulmonary Hypertension, Primary, 1	76	2.577

175	P	FBR017	Fibrosarcoma	56	2.577

176	P	MLT020	Multiple Sclerosis	79	2.545

177		BCT022	Bacterial Infectious Disease	56	2.545

178		ALC007	Alcohol Dependence	66	2.522

179	P	HYP069	Hyperparathyroidism	62	2.505

180		OST012	Osteoarthritis	77	2.476

181	P	INF037	Inflammatory Bowel Disease	53	2.467

182	P	ADN016	Adenocarcinoma	63	2.467

183	P	SLP006	Sleep Apnea	69	2.467

184		CRV035	Cervical Cancer	73	2.428

185	P	MLN007	Male Infertility	56	2.416

186		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	2.398

187	P	KDN017	Kidney Cancer	61	2.390

188	P	LNG064	Lung Cancer Susceptibility 3	70	2.389

189		MCS002	Mucositis	56	2.389

190	P	CTN003	Cutaneous Lupus Erythematosus	52	2.363

191		THY029	Thyroid Carcinoma	51	2.356

192	P	MSC005	Muscular Dystrophy	67	2.351

193	P	KLZ004	Kala-Azar 1	41	2.341

194		LSH001	Leishmaniasis	64	2.341

195		GST033	Gestational Diabetes	61	2.341

196	c	MJR022	Major Affective Disorder 8	38	2.323

197		CLT003	Colitis	63	2.323

198	c	MJR024	Major Affective Disorder 9	41	2.323

199	P	BPL003	Bipolar Disorder	56	2.323

200	P	LRY044	Larynx Cancer	54	2.322

201		CVD001	Covid-19	57	2.311

202	c	ACT071	Acute Kidney Failure	60	2.303

203	P	NRV007	Nervous System Disease	67	2.303

204	c	ACT134	Acute Liver Failure	59	2.264

205	P	BRS044	Breast Adenocarcinoma	58	2.264

206	c	LKM063	Leukemia, Chronic Myeloid	71	2.259

207	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	2.237

208	P	ATS364	Autism	69	2.228

209	P	LPR021	Leprosy 3	71	2.224

210	P	HYP750	Hypertriglyceridemia, Familial	62	2.224

211		ULC004	Ulcerative Colitis	74	2.224

212		HNS001	Hansen's Disease	32	2.224

213		CLR030	Clear Cell Renal Cell Carcinoma	54	2.220

214	P	HML002	Hemolytic Anemia	62	2.210

215		DWN001	Down Syndrome	70	2.207

216	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	2.204

217		47X002	47,xyy	48	2.204

218		MTC004	Mitochondrial Encephalomyopathy	42	2.204

219	P	GRV001	Graves' Disease	55	2.203

220	P	LYM118	Lymphoma	67	2.201

221		GLC009	Glucosephosphate Dehydrogenase Deficiency	53	2.182

222		PMP006	Pemphigus Vulgaris, Familial	58	2.174

223	P	CYS018	Cystitis	59	2.163

224		PNC041	Pancreatic Ductal Adenocarcinoma	51	2.163

225		ORL011	Oral Cancer	60	2.149

226	c	ATS007	Autism Spectrum Disorder	72	2.135

227		NPH009	Nephrolithiasis	54	2.120

228		CHG001	Chagas Disease	66	2.120

229		RTN003	Retinal Ischemia	49	2.120

230	P	OPN001	Open-Angle Glaucoma	55	2.115

231		CHR066	Chronic Fatigue Syndrome	60	2.096

232	P	MYC008	Myocarditis	59	2.096

233		SCK003	Sickle Cell Anemia	74	2.091

234	P	MCR129	Microvascular Complications of Diabetes 1	68	2.091

235	c	PCH010	Pachyonychia Congenita 3	43	2.078

236		OST159	Osteogenic Sarcoma	66	2.078

237		SPN035	Spindle Cell Sarcoma	54	2.078

238		SRC014	Sarcoma	65	2.078

239	P	BND020	Bone Disease	59	2.076

240		IMM167	Immune Deficiency Disease	78	2.057

241	P	DRR001	Diarrhea	55	2.057

242	P	SZR006	Seizure Disorder	70	2.041

243	c	DNT047	Dentinogenesis Imperfecta Type 2	35	2.041

244		MYL069	Myeloma, Multiple	77	2.036

245		LNG099	Lung Disease	62	2.036

246	c	HPT016	Hepatitis B	62	2.036

247	P	RHB003	Rhabdomyosarcoma	66	2.030

248		CND006	Candida Glabrata	30	2.030

249		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	2.028

250	P	LKM062	Leukemia, Acute Lymphoblastic	69	2.022

251		CRB039	Cerebrovascular Disease	66	1.992

252	P	RHM011	Rheumatoid Arthritis	82	1.983

253		PRP016	Paraplegia	52	1.983

254		NRR001	Neuroretinitis	42	1.983

255		RTN023	Retinitis	46	1.983

256		CCT002	Cicatricial Pemphigoid	53	1.983

257		PRM329	Premature Aging	36	1.975

258	P	MSC003	Muscular Atrophy	52	1.975

259		ATS010	Autosomal Recessive Disease	42	1.975

260		KRN002	Kearns-Sayre Syndrome	63	1.942

261	c	ACT068	Acute Cystitis	61	1.934

262		GST023	Gastric Ulcer	52	1.934

263	P	CTR002	Cataract	60	1.932

264		HYP014	Hyperuricemia	51	1.932

265	c	DWL002	Dowling-Degos Disease 1	58	1.930

266		CRH001	Crohn's Disease	80	1.930

267	P	ART021	Arteriosclerosis	54	1.930

268		ANX010	Anxiety	70	1.928

269		PRP027	Peripheral Vascular Disease	71	1.910

270		PRP080	Peripheral Artery Disease	54	1.910

271		LSC001	Lesch-Nyhan Syndrome	62	1.884

272	c	CNG223	Congenital Methemoglobinemia	39	1.884

273		URT010	Ureteral Obstruction	45	1.884

274	P	HYP265	Hypotonia	42	1.884

275	P	ATX030	Ataxia-Telangiectasia	80	1.878

276		TLN003	Telangiectasis	51	1.878

277	P	MTR014	Motor Neuron Disease	65	1.877

278	P	HYP086	Hypothyroidism	69	1.869

279		ATN004	Autonomic Neuropathy	42	1.869

280	P	PLY006	Polydactyly	59	1.842

281		HDN002	Head Injury	44	1.841

282		SYS003	Systolic Heart Failure	49	1.839

283	P	PRC031	Preeclampsia/eclampsia 1	43	1.836

284	P	OVR082	Overgrowth Syndrome	49	1.831

285		LRY018	Laryngeal Squamous Cell Carcinoma	44	1.831

286		PLL014	Pellagra-Like Syndrome	17	1.812

287	P	SCH015	Schizophrenia	74	1.808

288		HMN044	Human Immunodeficiency Virus Type 1	78	1.808

289	P	HYP076	Hyperthyroidism	53	1.800

290		OST017	Osteomyelitis	63	1.795

291		PLR008	Pleurisy	50	1.795

292		ACT088	Acute Insulin Response	39	1.775

293	c	GLC092	Glaucoma, Primary Open Angle	62	1.775

294		CRC021	Carcinosarcoma	64	1.775

295		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.775

296	P	CRD246	Cardiovascular System Disease	56	1.751

297		MTB004	Metabolic Acidosis	48	1.747

298		ACT098	Acute Erythroid Leukemia	55	1.747

299	P	ASP006	Aspergillosis	72	1.747

300		CHL045	Choline Deficiency Disease	39	1.747

301		RTN020	Retinal Vascular Disease	46	1.747

302		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	1.742

303	P	RHN004	Rhinitis	57	1.742

304	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	1.734

305	P	NSP012	Nasopharyngeal Carcinoma	61	1.717

306		NPH091	Nephrolithiasis, Calcium Oxalate	61	1.717

307		DGN001	Degenerative Disc Disease	49	1.717

308	c	SCN007	Secondary Hyperparathyroidism	51	1.717

309		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	17	1.717

310		GLC105	Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency	33	1.709

311		ALC001	Alcohol-Related Birth Defect	36	1.696

312	P	FTL001	Fetal Alcohol Syndrome	55	1.696

313	P	GRF003	Graft-Versus-Host Disease	71	1.696

314	P	RTN018	Retinal Disease	53	1.696

315		KHL003	Kohlschutter-Tonz Syndrome	59	1.681

316	c	PSR028	Psoriasis 7	43	1.681

317	c	PSR017	Psoriasis 2	53	1.681

318		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	38	1.681

319	c	PSR018	Psoriasis 13	52	1.681

320	c	PSR023	Psoriasis 1	52	1.681

321	c	PSR032	Psoriasis 11	47	1.681

322	P	CRN300	Coronary Heart Disease 1	73	1.681

323		SBC016	Subacute Delirium	43	1.681

324	c	MGR028	Migraine with or Without Aura 1	64	1.672

325		NRL016	Neural Tube Defects	81	1.672

326	c	DRM040	Dermatitis Herpetiformis, Familial	35	1.656

327	P	DRM007	Dermatitis Herpetiformis	54	1.656

328		GRD001	Giardiasis	46	1.656

329		PLR005	Pleuropneumonia	33	1.656

330		PLM010	Pulmonary Edema	55	1.656

331		NTR005	Nutritional Deficiency Disease	61	1.647

332		LNG031	Lung Benign Neoplasm	51	1.647

333	P	HRD217	Hereditary Optic Neuropathy	36	1.643

334		PHS004	Phosphoribosylpyrophosphate Synthetase Superactivity	49	1.643

335	P	RTN008	Retinitis Pigmentosa	80	1.643

336		URM002	Uremia	47	1.643

337	P	EPL164	Epilepsy	68	1.643

338	P	GST044	Gastritis	55	1.643

339	P	MCR010	Microcephaly	60	1.643

340	P	PLY014	Polycystic Kidney Disease	69	1.642

341		MSC157	Muscular Dystrophy, Duchenne Type	79	1.642

342		RCK004	Rickets	68	1.633

343	c	ACT027	Acute Pancreatitis	60	1.633

344		PLM001	Pulmonary Tuberculosis	69	1.595

345		ACQ007	Acquired Immunodeficiency Syndrome	59	1.595

346		PRM013	Premature Menopause	58	1.595

347		EWN003	Ewing Sarcoma	70	1.590

348		ART004	Aortic Atherosclerosis	47	1.590

349		SPL018	Splenomegaly	49	1.590

350		ANG054	Angina Pectoris	66	1.588

351		HRW001	Hair Whorl	35	1.588

352		SVR001	Severe Acute Respiratory Syndrome	67	1.588

353		PYR009	Pyridoxine Deficiency Anemia	35	1.588

354	P	MNC007	Monocytic Leukemia	47	1.588

355		TRY001	Trypanosomiasis	50	1.588

356	P	GLM007	Glomerulonephritis	60	1.588

357		RCT020	Rectum Adenocarcinoma	48	1.588

358	P	MNN013	Meningitis	65	1.588

359		GTR002	Goiter	53	1.587

360	c	JVN010	Juvenile Rheumatoid Arthritis	66	1.587

361		MLR004	Malaria	80	1.583

362		DPR016	Depression	65	1.544

363	P	HPT021	Hepatitis	69	1.530

364		ASP026	Asplenia, Isolated Congenital	43	1.529

365		ONC007	Oncocytoma	50	1.529

366		PPL052	Papillomatosis, Confluent and Reticulated	34	1.529

367		HYP017	Hypophosphatemia	49	1.529

368	P	URN019	Urinary Tract Infection	49	1.529

369	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	1.529

370		CHR177	Chromophobe Renal Cell Carcinoma	54	1.529

371		SLP001	Sleeping Sickness	56	1.529

372	P	NTR004	Neutropenia	63	1.529

373		HYP043	Hyperandrogenism	48	1.529

374		CLC006	Calcinosis	47	1.529

375		STT001	Status Epilepticus	59	1.529

376		FML091	Familial Tumoral Calcinosis	43	1.529

377		URM005	Uremic Pruritus	45	1.520

378	P	VSC011	Vasculitis	61	1.520

379		BRN056	Bronchopulmonary Dysplasia	56	1.520

380		BLD131	Bladder Urothelial Carcinoma	60	1.511

381		TRG019	Trigonocephaly with Short Stature and Developmental Delay	38	1.490

382		RHB024	Rhabdomyosarcoma 2	67	1.490

383	P	ANR048	Aniridia 1	64	1.490

384		ACR006	Aceruloplasminemia	63	1.480

385	P	ATX024	Ataxia-Oculomotor Apraxia 3	45	1.480

386		LBR036	Leber Plus Disease	66	1.479

387		HPT022	Hepatoblastoma	54	1.479

388	P	CRD119	Cardiac Arrest	67	1.479

389		PRT036	Peritonitis	65	1.474

390	P	AST005	Asthma	76	1.468

391	P	PHC003	Pheochromocytoma	69	1.468

392		CYN002	Cyanosis, Transient Neonatal	43	1.468

393		LGH007	Leigh Syndrome	70	1.468

394	P	RRH023	Rare Hereditary Hemochromatosis	54	1.468

395		ADN018	Adenoma	59	1.468

396		OST003	Osteonecrosis	61	1.468

397		HMS001	Hemosiderosis	48	1.468

398	c	RNG019	Ring Chromosome 3	19	1.468

399		MNT002	Mental Depression	57	1.448

400		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	61	1.443

401		HRN029	Hearing Loss, Noise-Induced	37	1.443

402	P	CTN015	Cutaneous T Cell Lymphoma	48	1.415

403	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	1.415

404	P	LCH002	Lichen Planus	54	1.406

405	c	GRN062	Granulomatous Disease, Chronic, Autosomal Recessive, 1	46	1.402

406		PHN003	Phenylketonuria	76	1.402

407	P	HYP733	Hypercalciuria, Absorptive, 2	45	1.402

408	P	CHR071	Charcot-Marie-Tooth Disease	64	1.402

409		TTH006	Tooth Disease	51	1.402

410		VSC002	Vascular Dementia	60	1.402

411	c	ACT135	Acute Graft Versus Host Disease	51	1.402

412		IRR002	Irritable Bowel Syndrome	65	1.402

413		FST010	Fasting Hypoglycemia	33	1.402

414		STN013	Stenotrophomonas Maltophilia Infection	26	1.358

415		PMP008	Pemphigus Vegetans	27	1.358

416		CHR074	Choriocarcinoma	46	1.358

417	P	CCK001	Cockayne Syndrome	68	1.358

418		AMN003	Amnestic Disorder	54	1.358

419		ENT004	Enthesopathy	51	1.358

420	P	INS002	in Situ Carcinoma	53	1.358

421		CYS001	Cystic Fibrosis	78	1.355

422	c	HPT001	Hepatitis C	62	1.355

423		NRM005	Neuromuscular Disease	63	1.342

424		VGN023	Vaginitis	56	1.334

425		RCR030	Recurrent Idiopathic Neuroretinitis	11	1.332

426	P	MLN069	Melanoma, Uveal	61	1.332

427	c	SVR003	Severe Congenital Neutropenia	59	1.332

428		DFF005	Diffuse Large B-Cell Lymphoma	54	1.332

429	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	56	1.332

430		LBR038	Leber Hereditary Optic Neuropathy, Modifier of	62	1.332

431		GRN051	Granulomatous Disease, Chronic, X-Linked	57	1.332

432		MST005	Mastitis	53	1.332

433		CHL123	Chlamydia	58	1.332

434		DSS009	Disseminated Intravascular Coagulation	57	1.332

435	P	NRF002	Neurofibromatosis	57	1.332

436	c	RNG015	Ring Chromosome 2	22	1.332

437		FML035	Familial Hyperlipidemia	55	1.309

438		LYM133	Lymphoma, Hodgkin, Classic	74	1.301

439		LMY002	Leiomyoma	51	1.301

440		PRT038	Protein-Energy Malnutrition	53	1.301

441		BRN024	Bronchitis	67	1.301

442		PLC008	Placenta Disease	49	1.301

443	P	GLM040	Glioma Susceptibility 1	71	1.289

444		PSY004	Psychotic Disorder	66	1.289

445		IRN002	Iron Metabolism Disease	57	1.289

446		LYM019	Lymphosarcoma	46	1.289

447		ANT066	Anterior Cutaneous Nerve Entrapment Syndrome	35	1.288

448	c	SYS043	Systemic Lupus Erythematosus 1	38	1.288

449	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	1.288

450	c	BSL024	Basal Cell Carcinoma 1	55	1.288

451		TMR016	Tumor Suppressor Gene on Chromosome 11	28	1.288

452		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	34	1.288

453	c	CHL140	Chilblain Lupus 1	58	1.288

454		ERY029	Erythermalgia, Primary	58	1.288

455		SPR126	Superior Semicircular Canal Dehiscence	41	1.288

456	P	PTT014	Pitt-Hopkins Syndrome	64	1.288

457		SKN013	Skin Benign Neoplasm	50	1.288

458		DBT004	Diabetic Polyneuropathy	50	1.288

459		AND005	Androgen Insensitivity Syndrome, Mild	21	1.288

460	c	HMG029	Hemoglobin Se Disease	40	1.288

461		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	1.288

462	c	VRT015	Vertebral, Cardiac, Renal, and Limb Defects Syndrome 2	19	1.281

463		PLY100	Polyploidy	36	1.255

464		ALL003	Allergic Rhinitis	67	1.255

465		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	35	1.255

466	P	CLD001	Cleidocranial Dysplasia	64	1.255

467		CRV002	Cervix Uteri Carcinoma in Situ	47	1.255

468		PNC129	Pancreatic Adenocarcinoma	65	1.255

469		TRN015	Transient Cerebral Ischemia	63	1.255

470	P	RNL015	Renal Hypertension	45	1.255

471	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	1.255

472	c	CLD019	Cleidocranial Dysplasia Spectrum Disorder	20	1.255

473		CRV045	Cervical Intraepithelial Neoplasia	39	1.255

474	c	BDY007	Body Mass Index Quantitative Trait Locus 1	40	1.242

475		PST092	Posttransplant Acute Limbic Encephalitis	28	1.242

476		CHL068	Cholestasis	61	1.242

477		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	1.219

478	P	EYD002	Eye Disease	57	1.219

479	c	SCL052	Scleroderma, Familial Progressive	61	1.190

480		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	1.190

481		SXL003	Sexual Disorder	49	1.185

482	P	OBS001	Obstructive Jaundice	48	1.185

483		ALC006	Alcoholic Hepatitis	61	1.178

484		SPC026	Specific Granule Deficiency 1	31	1.171

485	c	OPT053	Optic Atrophy 1	62	1.171

486	P	FTL069	Fetal Akinesia Deformation Sequence 1	63	1.171

487		HYD038	Hydrops Fetalis, Nonimmune	59	1.171

488		FTL006	Fetal Alcohol Spectrum Disorder	43	1.171

489		XRD010	Xeroderma Pigmentosum, Variant Type	73	1.171

490		HYP114	Hypertensive Nephropathy	36	1.171

491	c	HYD046	Hydatidiform Mole, Recurrent, 1	59	1.171

492		GST010	Gestational Trophoblastic Neoplasm	52	1.171

493	P	CND004	Candidiasis	58	1.171

494		OVR063	Overnutrition	42	1.171

495		LYM027	Lymphopenia	56	1.171

496	P	SNS001	Sensorineural Hearing Loss	59	1.171

497	P	SLP005	Sleep Disorder	61	1.171

498		LST001	Listeriosis	59	1.171

499		NNT021	Neonatal Meningitis	22	1.171

500		NTR011	Neutrophil-Specific Granule Deficiency	36	1.171

501		INT002	Intermittent Claudication	61	1.161

502		GLC008	Glucose Metabolism Disease	40	1.161

503		LRY017	Laryngeal Disease	45	1.161

504	P	LRY019	Laryngitis	53	1.161

505		MYL005	Myelofibrosis	71	1.152

506		MYF001	Myofibroma	42	1.152

507		FBR047	Fibromyalgia	58	1.152

508		MCL006	Macular Retinal Edema	57	1.152

509		PMP004	Pemphigus Foliaceus	43	1.148

510		BLD044	Bladder Disease	48	1.148

511		NRT004	Neuritis	53	1.148

512	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	1.142

513	c	VRL010	Viral Hepatitis	53	1.142

514	c	MCR112	Microvascular Complications of Diabetes 2	42	1.142

515	c	HPT073	Hepatitis C Virus	71	1.134

516	c	LBR019	Leber Congenital Amaurosis 9	44	1.134

517		DSS032	Disease by Infectious Agent	55	1.134

518		HGH043	High Grade Glioma	45	1.134

519		PRS045	Prostatic Hypertrophy	53	1.134

520		THR024	Thrombosis	56	1.076

521	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	1.076

522		PRS021	Prostatic Adenoma	43	1.076

523		GLM044	Glomerular Disease	35	1.075

524	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	1.075

525		END057	Endometrial Cancer	72	1.075

526		BRK010	Burkitt Lymphoma	66	1.075

527	P	ANP001	Anaplastic Large Cell Lymphoma	61	1.075

528		APP015	Apparent Mineralocorticoid Excess	57	1.075

529		HYD030	Hydroxykynureninuria	27	1.075

530	c	TBR025	Tuberous Sclerosis 1	84	1.075

531		ADN011	Adenoid Cystic Carcinoma	68	1.075

532		OBS082	Obstructive Nephropathy	41	1.075

533		CLF001	Cleft Lip	53	1.075

534		VCC001	Vaccinia	47	1.075

535		ANT024	Anthrax Disease	58	1.075

536		AML001	Amelanotic Melanoma	37	1.075

537		SLD003	Sialadenitis	48	1.075

538		NNT012	Neonatal Jaundice	53	1.075

539	P	TBR001	Tuberous Sclerosis	69	1.075

540	P	PYL005	Pyelonephritis	57	1.075

541		TRC008	Trachoma	53	1.075

542		URN010	Urinary Tract Obstruction	55	1.075

543		MNN017	Mononeuropathy	41	1.075

544		DBT007	Diabetic Cataract	36	1.075

545		HYP080	Hypogonadism	50	1.075

546		KDN013	Kidney Hypertrophy	34	1.075

547	P	PRC019	Precocious Puberty	47	1.075

548		MNT001	Mantle Cell Lymphoma	67	1.057

549	P	CNJ013	Conjunctivitis	66	1.057

550		CNT047	Contact Dermatitis	57	1.057

551		PST028	Post-Traumatic Stress Disorder	59	1.057

552		PRS129	Prostatic Hyperplasia, Benign	49	1.014

553		INS024	Insulin-Like Growth Factor I	78	1.014

554	c	SPR086	Spermatogenic Failure 3	46	1.014

555	c	LKM070	Leukemia, Acute Monocytic	56	1.014

556		BNR002	Bone Resorption Disease	47	1.014

557	c	BRN108	Branchiootic Syndrome 1	62	1.014

558	P	RTN024	Retinoblastoma	73	1.014

559		TST044	Testicular Torsion	45	1.014

560		ESP021	Esophageal Cancer	83	1.014

561		ADR040	Adrenal Gland Pheochromocytoma	46	1.014

562		ALL006	Allergic Asthma	56	1.014

563	P	HRP006	Herpes Simplex	65	1.014

564		ADN001	Adenosine Deaminase Deficiency	59	1.014

565	P	RSP003	Respiratory Failure	74	1.014

566		LVR012	Liver Cirrhosis	63	1.014

567		ACT200	Acute Monoblastic Leukemia	41	1.014

568		DST006	Diastolic Heart Failure	45	1.014

569		PTT037	Pituitary Tumors	44	1.014

570		ATN005	Autonomic Dysfunction	46	1.014

571		PMP013	Pemphigus Gestationis	19	1.000

572		DYS015	Dysentery	50	1.000

573		PMP002	Pemphigoid Gestationis	38	1.000

574	c	BDY021	Body Mass Index Quantitative Trait Locus 20	49	0.993

575		HYP781	Hypoascorbemia	52	0.981

576		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	0.961

577	P	MJR001	Major Depressive Disorder	68	0.961

578	c	HPT003	Hepatitis a	63	0.961

579	P	THY032	Thyroiditis	57	0.961

580		ACT084	Acute Stress Disorder	54	0.961

581		HMT002	Hematologic Cancer	61	0.961

582		LYM040	Lymphoblastic Lymphoma	53	0.961

583		BCK006	Back Pain	47	0.961

584		PST021	Postpartum Depression	50	0.961

585		BLL012	Bullous Impetigo	38	0.961

586	P	VTR007	Vitreoretinopathy	46	0.961

587	c	ACT150	Acute Adrenal Insufficiency	48	0.961

588		MTH071	Methane Production	25	0.961

589		RTN017	Retinal Detachment	60	0.961

590	c	GRN063	Granulomatous Disease, Chronic, Autosomal Recessive, 2	39	0.961

591		ATR057	Atrioventricular Block	54	0.961

592		DFN191	Deafness, Congenital Heart Defects, and Posterior Embryotoxon	22	0.961

593		BLD065	Blue Diaper Syndrome	20	0.961

594		OCL069	Ocular Motor Apraxia	57	0.961

595	P	TTR001	Tetralogy of Fallot	69	0.961

596		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.961

597	c	SPN291	Spinocerebellar Ataxia 7	53	0.961

598	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	65	0.961

599		DBT081	Diabetic Encephalopathy	36	0.961

600	P	DYS154	Dystonia	64	0.961

601	P	PLY017	Polyarteritis Nodosa	60	0.961

602		TRT001	Teratocarcinoma	42	0.961

603		CRV038	Cervical Squamous Cell Carcinoma	58	0.961

604	P	PLY018	Polycythemia	56	0.961

605		IMP004	Impetigo	48	0.961

606	P	DRM010	Dermatomyositis	61	0.961

607		ALC010	Alcoholic Cardiomyopathy	42	0.961

608		ADR001	Adrenal Rest Tumor	30	0.961

609		PLP001	Pulpitis	48	0.961

610		ORL004	Oral Submucous Fibrosis	56	0.961

611	P	LMY004	Leiomyosarcoma	62	0.961

612	P	BNG095	Benign Giant Cell Tumor	43	0.961

613		MYT011	Myotonia	39	0.961

614		CRD132	Cardiac Conduction Defect	60	0.949

615		LMB062	Limb Ischemia	55	0.949

616		INV001	Invasive Aspergillosis	49	0.949

617		ENT011	Enterocolitis	55	0.949

618		CHL065	Cholangiocarcinoma	58	0.949

619	P	SYS005	Systemic Scleroderma	74	0.949

620		GT001	Gout	64	0.949

621		MLG169	Malignant Astrocytoma	57	0.949

622		INT079	Intrahepatic Cholangiocarcinoma	51	0.949

623	P	PLY180	Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy 1	56	0.879

624	c	THY107	Thymoma, Familial	42	0.879

625	P	OST002	Osteoporosis	76	0.879

626	c	EXD008	Exudative Vitreoretinopathy 1	71	0.879

627	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	0.879

628	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.879

629		HLC007	Helicobacter Pylori Infection	67	0.879

630	c	PRD040	Periodontitis, Chronic	52	0.879

631		EPL131	Epilepsy, Pyridoxine-Dependent	45	0.879

632		URT049	Urate Oxidase, Pseudogene	24	0.879

633		MDD018	Middle East Respiratory Syndrome	44	0.879

634	c	ACT075	Acute Myocardial Infarction	56	0.879

635	P	RNV001	Renovascular Hypertension	49	0.879

636		MLT006	Multidrug-Resistant Tuberculosis	47	0.879

637		BLR008	Bilirubin Metabolic Disorder	57	0.879

638	P	BRB001	Beriberi	44	0.879

639		ECH003	Echinococcosis	53	0.879

640		PRT013	Portal Hypertension	59	0.879

641	P	CRN026	Corneal Edema	42	0.879

642	P	PRN023	Prion Disease	60	0.879

643		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.879

644		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	0.879

645	P	PNM007	Pneumonia	67	0.879

646		CRT015	Carotid Artery Occlusion	45	0.879

647	P	THY023	Thymoma	64	0.879

648		MDD011	Mood Disorder	62	0.879

649		LYM021	Lymphadenitis	56	0.879

650	c	LKM005	Leukemia, T-Cell, Chronic	34	0.879

651		DYS073	Dysphagia	53	0.879

652		PRN019	Perinatal Necrotizing Enterocolitis	60	0.879

653		SQM013	Squamous Cell Carcinoma, Head and Neck	73	0.847

654	c	PRM196	Premature Ovarian Failure 1	59	0.847

655	P	SRC025	Sarcoidosis 1	71	0.847

656		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.847

657		KHN001	Kuhnt-Junius Degeneration	48	0.847

658		HMN014	Human Immunodeficiency Virus Infectious Disease	54	0.847

659		DWR001	Dwarfism	44	0.847

660	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.826

661		GLS018	Glass Syndrome	61	0.826

662		END040	Endogenous Depression	55	0.826

663		NRT001	Neurotic Disorder	56	0.826

664		DMN026	Dementia Pugilistica	27	0.812

665		TTR011	Tetraploidy	43	0.812

666		DRV001	Dravet Syndrome	69	0.812

667		ADR016	Adrenal Cortical Carcinoma	62	0.812

668		PRP036	Peripheral T-Cell Lymphoma	53	0.812

669	c	PRM093	Premature Ovarian Failure 7	48	0.812

670		GLC086	Glucocorticoid-Induced Osteoporosis	43	0.812

671		PRT082	Preterm Premature Rupture of the Membranes	57	0.812

672		ADR054	Adrenocortical Carcinoma, Hereditary	47	0.812

673		PLY001	Polycythemia Vera	69	0.812

674	P	FLL037	Follicular Lymphoma	74	0.812

675		ARG004	Argyria	26	0.812

676		OCC016	Occupational Asthma	33	0.812

677		CMB039	Combined Pulmonary Fibrosis-Emphysema Syndrome	18	0.812

678		CTN007	Cutaneous Leishmaniasis	62	0.812

679		LNG030	Lung Adenoma	37	0.812

680		DRM011	Dermatophytosis	52	0.812

681	P	SBR004	Seborrheic Dermatitis	44	0.812

682		PRX097	Paroxysmal Dystonia	32	0.812

683	P	HYP098	Hypereosinophilic Syndrome	66	0.812

684		ADR004	Adrenal Cortical Adenocarcinoma	38	0.812

685		RTR001	Retrograde Amnesia	41	0.812

686		CMB007	Combined Immunodeficiency	57	0.812

687		ACR007	Acromegaly	70	0.812

688		SNS003	Sensory Peripheral Neuropathy	52	0.812

689	P	ESS003	Essential Thrombocythemia	69	0.812

690		MYL031	Myeloproliferative Neoplasm	66	0.812

691		CRB025	Carbohydrate Metabolic Disorder	40	0.812

692		NRD001	Neurodermatitis	39	0.812

693		NCR002	Necrobiosis Lipoidica	38	0.812

694		KLB003	Klebsiella Pneumonia	50	0.812

695		HML018	Homologous Wasting Disease	21	0.812

696		ANC002	Anca-Associated Vasculitis	44	0.812

697		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.802

698	P	LFR001	Li-Fraumeni Syndrome	73	0.802

699		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	57	0.802

700		SBJ001	Subjective Cognitive Decline	30	0.802

701		VCT005	Vacterl Association, X-Linked, with or Without Hydrocephalus	41	0.802

702	c	HYP272	Hypercholesterolemia, Familial, 3	45	0.802

703		ACR041	Acromelic Frontonasal Dysostosis	53	0.802

704		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	55	0.802

705	c	PRM092	Primary Lateral Sclerosis, Adult, 1	38	0.802

706		PLY105	Polycystic Ovary Syndrome 1	39	0.802

707	c	LFR007	Li-Fraumeni Syndrome 2	46	0.802

708		VTR016	Vater/vacterl Association	49	0.802

709		ADL002	Adult Syndrome	70	0.802

710	c	HYP724	Hyperlipoproteinemia, Type Iii	67	0.802

711	c	CHR095	Chronic Progressive External Ophthalmoplegia	49	0.802

712		VCT001	Vacterl Association	47	0.802

713	c	INH030	Inherited Retinal Disorder	28	0.802

714	P	THL005	Thalassemia	56	0.802

715		LPD012	Lipoid Congenital Adrenal Hyperplasia	70	0.802

716		PLY150	Polykaryocytosis Inducer	29	0.802

717	c	CNG006	Congenital Hypothyroidism	63	0.802

718	P	CRP001	Carpal Tunnel Syndrome	66	0.802

719	P	HRS035	Hirschsprung Disease 1	66	0.802

720	P	SCL018	Scoliosis	57	0.802

721	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	0.802

722		CRT020	Cortisone Reductase Deficiency	34	0.802

723		FND002	Fundus Dystrophy	55	0.802

724		SLC006	Silicosis	56	0.802

725	P	HYP061	Hypertrophic Cardiomyopathy	69	0.802

726		VRC001	Varicocele	48	0.802

727	P	NPH012	Nephrotic Syndrome	60	0.802

728	c	ATM011	Autoimmune Hepatitis	63	0.802

729	c	INH020	Inherited Metabolic Disorder	48	0.802

730		CYS008	Cystic Echinococcosis	57	0.802

731		CYT014	Cytochrome P450 Oxidoreductase Deficiency	34	0.802

732		HYP572	Hypoganglionosis	27	0.802

733		CRB090	Cerebral Hypoxia	42	0.802

734		AGR019	Age-Related Hearing Loss	41	0.802

735	P	MYC033	Myoclonus	47	0.802

736		PRT058	Pure Autonomic Failure	58	0.802

737	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.793

738	c	BCT007	Bacterial Meningitis	55	0.717

739		PNM013	Pneumococcal Meningitis	43	0.717

740		SPS057	Spasticity	42	0.717

741	P	RTT002	Rett Syndrome	79	0.717

742		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.717

743		TND004	Tendinopathy	45	0.717

744	P	ADL017	Adult T-Cell Leukemia	56	0.717

745		DSR012	Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency	39	0.717

746		MSC007	Muscle Hypertrophy	64	0.717

747		TND005	Tendinitis	54	0.717

748		ART074	Aortic Dissection	53	0.717

749		ANT003	Antley-Bixler Syndrome	49	0.717

750		LKC009	Leukocyte Adhesion Deficiency, Type I	70	0.717

751		CNT105	Central Core Disease of Muscle	59	0.717

752		KPS004	Kaposi Sarcoma	77	0.717

753		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	44	0.717

754		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.717

755		ACT119	Acute Promyelocytic Leukemia	62	0.717

756	P	SPP010	Suppressor of Tumorigenicity 3	51	0.717

757	c	SPN294	Spinocerebellar Ataxia 1	53	0.717

758		CLR109	Colorectal Adenocarcinoma	50	0.717

759		BLP004	Blepharophimosis	36	0.717

760	c	PRM340	Primary Adrenal Insufficiency	38	0.717

761	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	0.717

762	P	TRM003	Tremor	48	0.717

763	P	HMP002	Hemophagocytic Lymphohistiocytosis	61	0.717

764		CRT013	Carotid Stenosis	51	0.717

765		CLN015	Colon Adenocarcinoma	65	0.717

766		SCH014	Schistosomiasis	56	0.717

767		TRN018	Transitional Cell Carcinoma	56	0.717

768		LYM017	Lyme Disease	62	0.717

769		TTN003	Tetanus	65	0.717

770	P	TMP001	Temporal Lobe Epilepsy	49	0.717

771		IRT001	Iritis	45	0.717

772	P	AGG001	Aggressive Periodontitis	55	0.717

773	P	ICH004	Ichthyosis	56	0.717

774		ADS004	Aids Dementia Complex	40	0.717

775		CRB086	Cerebral Aneurysms	40	0.717

776		RYN005	Raynaud Phenomenon	45	0.717

777	c	RNG024	Ring Chromosome 8	28	0.717

778		CRC006	Carcinoid Syndrome	55	0.717

779	c	ART115	Aortic Valve Disease 1	74	0.699

780		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.699

781		SMT004	Smith-Lemli-Opitz Syndrome	70	0.699

782		OBS002	Obsessive-Compulsive Disorder	68	0.699

783	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	59	0.699

784		NRL018	Neural Tube Defects, Folate-Sensitive	45	0.699

785		LYM143	Lymphoma, Non-Hodgkin, Familial	75	0.699

786	P	HYP838	Hyperlipidemia, Familial Combined, 3	61	0.699

787		PRD013	Periodic Fever, Familial, Autosomal Dominant	68	0.699

788		APN008	Apnea, Obstructive Sleep	67	0.699

789		MCR004	Macroglobulinemia	49	0.699

790		HYP005	Hypokalemia	55	0.699

791		HMG005	Hemoglobinopathy	56	0.699

792		PRD004	Prediabetes Syndrome	52	0.699

793		THY030	Thyroid Gland Disease	50	0.699

794	c	FML021	Familial Hypercholesterolemia	72	0.699

795		CRB037	Cerebral Palsy	67	0.699

796	P	HYP121	Hypoalphalipoproteinemia	43	0.699

797		RNL065	Renal Cell Carcinoma, Papillary, 1	79	0.658

798	P	SCK002	Sick Sinus Syndrome	55	0.641

799	P	URT039	Urticaria	58	0.641

800		ART035	Arterial Calcification of Infancy	58	0.624

801		CLC017	Calcification of Joints and Arteries	44	0.624

802		CLD014	Cole Disease	38	0.624

803		24D001	2,4-Dienoyl-Coa Reductase Deficiency	34	0.624

804		PRQ002	Paraquat Poisoning	28	0.621

805	c	ACQ047	Acquired Methemoglobinemia	30	0.621

806		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	0.621

807	P	MYS003	Myasthenia Gravis	68	0.621

808		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	0.621

809		SJG002	Sjogren-Larsson Syndrome	54	0.621

810		PSR001	Psoriatic Arthritis	62	0.621

811	P	CLC063	Celiac Disease 1	66	0.621

812		BCT021	Bacterial Sepsis	43	0.621

813	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.621

814		IGR001	Ige Responsiveness, Atopic	59	0.621

815	c	DMN005	Diamond-Blackfan Anemia 2	28	0.621

816	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	55	0.621

817	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	41	0.621

818		LPT014	Leptin Deficiency or Dysfunction	78	0.621

819		ADR042	Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency	50	0.621

820		GLC042	Glucocorticoid Deficiency 1	50	0.621

821		CTR172	Citrullinemia, Classic	65	0.621

822		BTT016	Batten-Turner Congenital Myopathy	53	0.621

823	P	MYP087	Myopathy, Tubular Aggregate, 1	49	0.621

824		RBF001	Riboflavin Deficiency	49	0.621

825		PNG002	Pain Agnosia	51	0.621

826	c	HYP807	Hyperinsulinemic Hypoglycemia, Familial, 6	52	0.621

827		CNG184	Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects	56	0.621

828		ACT003	Acute Kidney Tubular Necrosis	46	0.621

829	P	AMY004	Amyloidosis	70	0.621

830		ACH005	Achalasia	55	0.621

831	P	MLG056	Malignant Hyperthermia	66	0.621

832		CHC001	Chickenpox	57	0.621

833		IGG001	Iga Glomerulonephritis	50	0.621

834	P	CNT004	Centronuclear Myopathy	57	0.621

835	P	MMB011	Membranous Nephropathy	50	0.621

836	P	UVT001	Uveitis	57	0.621

837		BRN028	Brain Cancer	74	0.621

838		CRN019	Coronary Artery Vasospasm	47	0.621

839		FLR001	Filarial Elephantiasis	59	0.621

840		CRV040	Cervix Carcinoma	50	0.621

841	P	GLY013	Glycogen Storage Disease	60	0.621

842		FLR002	Filariasis	55	0.621

843	P	END047	Endophthalmitis	53	0.621

844		ALC005	Alcoholic Pancreatitis	38	0.621

845	P	INT068	Intestinal Disease	53	0.621

846		GST050	Gastrointestinal System Disease	55	0.621

847	P	TRT010	Teratoma	51	0.621

848		ERL001	Early Myoclonic Encephalopathy	62	0.621

849	P	TCD001	Tic Disorder	49	0.621

850	P	NML001	Nemaline Myopathy	48	0.621

851		OLG001	Oligospermia	45	0.621

852	P	PTS002	Ptosis	52	0.621

853		IDP070	Idiopathic Scoliosis	42	0.621

854	P	OVR049	Ovarian Disease	52	0.621

855		AZS001	Azoospermia	45	0.621

856	c	SVR005	Severe Pre-Eclampsia	50	0.621

857		NCL011	Nuclear Gene-Encoded Leigh Syndrome Spectrum	21	0.621

858		STM007	Stomatitis	54	0.621

859	P	CHR345	Chronic Pain	50	0.621

860		MYC017	Mycobacterium Kansasii	36	0.621

861		ETN001	Eating Disorder	59	0.621

862		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	42	0.507

863		VRS002	Virus-Associated Trichodysplasia Spinulosa	30	0.507

864		CLP005	Ciliopathy	41	0.507

865		MTB016	Metabolic Myopathy	30	0.507

866		STR077	Streptococcal Toxic-Shock Syndrome	35	0.507

867		BNG077	Benign Idiopathic Neonatal Seizures	23	0.507

868		CCN009	Cocaine Intoxication	30	0.507

869		ACT228	Acute Radiation Syndrome	30	0.507

870		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	0.507

871		BLP046	Blepharophimosis, Ptosis, and Epicanthus Inversus	56	0.507

872		EPL050	Epilepsy, Partial, with Pericentral Spikes	26	0.507

873		FRN006	Frontotemporal Dementia	68	0.507

874		CRD223	Cardiac Arrhythmia	63	0.507

875		ANR007	Anorexia Nervosa	60	0.507

876	P	MTR004	Maturity-Onset Diabetes of the Young	68	0.507

877	P	MYS005	Myositis	56	0.507

878		LNT004	Lentigines	46	0.507

879		CLF027	Cleft Palate, Isolated	64	0.507

880		EPC005	Epicanthus	36	0.507

881		ARY002	Aryl Hydrocarbon Hydroxylase Inducibility	24	0.507

882		GST092	Gastroesophageal Reflux	61	0.507

883		VLV047	Volvulus of Midgut	52	0.507

884	c	MST023	Mesothelioma, Malignant	56	0.507

885	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.507

886		HYP457	Hypertrophic Scars	42	0.507

887	P	BRG001	Brugada Syndrome	69	0.507

888	P	PRG013	Paraganglioma	57	0.507

889		HMR023	Hemorrhagic Cystitis	43	0.507

890		MYL009	Myelodysplastic Syndrome	67	0.507

891		CHL152	Childhood Acute Lymphocytic Leukemia	50	0.507

892		CLR108	Colorectal Adenoma	64	0.507

893	c	ATM022	Autoimmune Myocarditis	36	0.507

894	P	CHN012	Chondrosarcoma	57	0.507

895		WRN002	Wernicke-Korsakoff Syndrome	50	0.507

896	c	HYP602	Hyperoxaluria, Primary, Type Ii	49	0.507

897		BSM002	Bosma Arhinia Microphthalmia Syndrome	44	0.507

898		CHD004	Chudley-Mccullough Syndrome	48	0.507

899	P	ORT004	Orthostatic Intolerance	63	0.507

900		IMP012	Impdh2 Enzyme Activity, Variation in	8	0.507

901		IMM224	Immunodeficiency 68	36	0.507

902	c	LNG109	Lung Cancer Susceptibility 1	26	0.507

903	P	TMR018	Tumoral Calcinosis, Hyperphosphatemic, Familial, 1	60	0.507

904	c	WLM013	Wilms Tumor 1	66	0.507

905	P	SCL057	Scoliosis, Isolated 1	40	0.507

906		GLB001	Gilbert Syndrome	53	0.507

907		MLT157	Multiple System Atrophy 1	69	0.507

908		INC002	Inclusion Body Myositis	57	0.507

909	P	MDL005	Medulloblastoma	75	0.507

910		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	0.507

911		TNG009	Tongue Squamous Cell Carcinoma	43	0.507

912		MTC111	Mitochondrial Neurogastrointestinal Encephalomyopathy	47	0.507

913	P	HRD144	Hereditary Mixed Polyposis Syndrome	54	0.507

914		HPT004	Hepatic Coma	43	0.507

915		PRN049	Paraneoplastic Pemphigus	44	0.507

916		FSC002	Fascioliasis	44	0.507

917		CRN030	Coronary Stenosis	50	0.507

918		CHR078	Chorioretinitis	51	0.507

919		GSG001	Gas Gangrene	52	0.507

920	P	ATR005	Atrophic Gastritis	50	0.507

921	P	PLM034	Pulmonary Emphysema	58	0.507

922	P	ALP008	Alopecia	54	0.507

923		ACT168	Acute Annular Outer Retinopathy	10	0.507

924	P	ANT006	Antiphospholipid Syndrome	55	0.507

925		PHG002	Phagocyte Bactericidal Dysfunction	34	0.507

926		PNM008	Pneumothorax	54	0.507

927		PLC005	Placental Insufficiency	56	0.507

928		GRN007	Granuloma Annulare	43	0.507

929		FLL031	Follicular Adenoma	40	0.507

930		ILS001	Ileus	50	0.507

931	P	INF038	Influenza	68	0.507

932		EPD006	Epidermolysis Bullosa Acquisita	48	0.507

933		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	0.507

934	P	VNS003	Venous Insufficiency	55	0.507

935		CRT017	Cartilage Disease	53	0.507

936		PLC002	Plica Syndrome	35	0.507

937		CRN017	Coronary Thrombosis	46	0.507

938		CRY005	Cryptococcosis	60	0.507

939	P	ESP024	Esophagitis	60	0.507

940	P	OPT009	Optic Neuritis	57	0.507

941		SHG001	Shigellosis	63	0.507

942		LWC001	Low Compliance Bladder	45	0.507

943		HPT019	Hepatic Encephalopathy	59	0.507

944		ALC009	Alcoholic Liver Cirrhosis	54	0.507

945		TST015	Testicular Disease	42	0.507

946		CHR063	Chronic Mucocutaneous Candidiasis	68	0.507

947	P	KRN004	Kernicterus	46	0.507

948