Search results for FAD

880 hits were found for FAD

#	Family	MCID	Name	MIFTS	Score
1	P	FTL069	Fetal Akinesia Deformation Sequence 1	63	34.333

2	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	59	19.896

3	P	ALZ034	Alzheimer Disease	87	15.045

4		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	65	14.550

5	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	11.689

6	c	FTL071	Fetal Akinesia Deformation Sequence 3	30	6.602

7		RBF001	Riboflavin Deficiency	49	5.732

8	P	CHR012	Chronic Granulomatous Disease	69	4.861

9		HLX001	Helix Syndrome	48	4.786

10		DRM006	Dermatitis	62	4.772

11		CNG506	Congenital Amyoplasia	27	4.604

12		DWN001	Down Syndrome	70	4.480

13	P	NRB001	Neuroblastoma	66	4.303

14		ETN001	Eating Disorder	59	4.063

15	P	MYP004	Myopathy	67	4.061

16		ACY011	Acyl-Coa Dehydrogenase Deficiency	30	4.010

17	P	DMN002	Dementia	66	3.886

18	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	65	3.683

19	P	AMY004	Amyloidosis	70	3.657

20	P	MYC033	Myoclonus	47	3.657

21	P	DST002	Distal Arthrogryposis	65	3.425

22	c	ALZ056	Alzheimer Disease 3	55	3.351

23		MLD018	Mild Cognitive Impairment	48	3.262

24		CHR178	Chromosomal Triplication	34	3.219

25	P	DRM053	Dermatitis, Atopic	65	3.205

26		CLF027	Cleft Palate, Isolated	64	3.196

27	P	MJR001	Major Depressive Disorder	68	3.042

28		MNT002	Mental Depression	57	3.009

29		AGN016	Aging	54	2.912

30	P	CNG001	Congenital Myasthenic Syndrome	68	2.906

31		IRN002	Iron Metabolism Disease	57	2.873

32		SPS019	Spastic Paraparesis	38	2.871

33		PRT037	Pertussis	65	2.871

34		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	2.834

35	P	MTH007	Methemoglobinemia	46	2.763

36		ATS010	Autosomal Recessive Disease	42	2.753

37		FRN006	Frontotemporal Dementia	68	2.751

38		SKN016	Skin Disease	63	2.726

39		ART140	Arteries, Anomalies of	53	2.705

40		LPP008	Lipoprotein Quantitative Trait Locus	65	2.705

41		DPR016	Depression	65	2.688

42	c	ALZ063	Alzheimer's Disease 1	31	2.628

43		APH002	Aphasia	56	2.610

44	c	MJR022	Major Affective Disorder 8	38	2.569

45	c	MJR024	Major Affective Disorder 9	41	2.569

46	P	PRK039	Parkinsonism	55	2.569

47	P	BPL003	Bipolar Disorder	56	2.569

48		PLY012	Polyhydramnios	46	2.560

49		NNL005	Non-Alcoholic Fatty Liver Disease	63	2.534

50		ISC004	Ischemia	61	2.444

51		NRL016	Neural Tube Defects	81	2.433

52		HYP266	Hypoxia	57	2.433

53	c	INH020	Inherited Metabolic Disorder	48	2.400

54		RPD005	Rapidly Involuting Congenital Hemangioma	46	2.388

55	c	DLT002	Dilated Cardiomyopathy	78	2.388

56		LPD008	Lipid Metabolism Disorder	62	2.337

57		CHL014	Cholera	62	2.309

58		CHG001	Chagas Disease	66	2.283

59	P	MYC008	Myocarditis	59	2.283

60	c	2HY001	2-Hydroxyglutaric Aciduria	38	2.262

61	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	2.262

62	P	CTR002	Cataract	60	2.228

63		HMC014	Homocysteinemia	52	2.214

64	P	HNT016	Huntington Disease	73	2.214

65		CRN048	Craniofacial-Deafness-Hand Syndrome	52	2.214

66		47X002	47,xyy	48	2.214

67	P	SYP003	Syphilis	59	2.214

68		HYP060	Hyperinsulinism	54	2.214

69		FTT001	Fatty Liver Disease	62	2.171

70	P	ENC018	Encephalopathy	62	2.171

71	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	2.164

72	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	2.164

73	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	2.164

74	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	2.164

75	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	2.164

76	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	2.164

77	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	2.164

78	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	2.164

79	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	2.164

80	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	2.164

81		PPL052	Papillomatosis, Confluent and Reticulated	34	2.112

82	c	CNG223	Congenital Methemoglobinemia	39	2.112

83	P	PSR002	Psoriasis	63	2.111

84		PST011	Pustulosis of Palm and Sole	52	2.111

85		IRR002	Irritable Bowel Syndrome	65	2.085

86		BCK006	Back Pain	47	2.076

87		MLT163	Multiple Pterygium Syndrome, Escobar Variant	64	2.068

88	c	ATS307	Autosomal Recessive Cerebellar Ataxia	39	2.059

89		ARG004	Argyria	26	2.059

90		GLB002	Glioblastoma	67	2.059

91		RST011	Restrictive Dermopathy, Lethal	51	2.059

92	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	2.004

93		LPD042	Lipid Storage Myopathy Due to Flavin Adenine Dinucleotide Synthetase Deficiency	22	2.004

94	P	MSC003	Muscular Atrophy	52	2.004

95		ALL014	Allergic Encephalomyelitis	34	2.004

96		ALL029	Allergic Disease	59	1.987

97	c	ATR087	Atrial Standstill 1	74	1.982

98		CNG065	Congenital Contractures	25	1.982

99		MTB004	Metabolic Acidosis	48	1.946

100	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	1.946

101		MLR009	Miliaria	33	1.946

102		GLC009	Glucosephosphate Dehydrogenase Deficiency	53	1.946

103		MLR001	Miliaria Rubra	32	1.946

104		NRN004	Neuroendocrine Tumor	59	1.946

105		CRC006	Carcinoid Syndrome	55	1.946

106	c	ALZ054	Alzheimer Disease 4	43	1.945

107		TRM010	Traumatic Brain Injury	51	1.945

108		PRN009	Paranoid Schizophrenia	49	1.945

109	P	AST005	Asthma	76	1.913

110		CND006	Candida Glabrata	30	1.913

111		MLT134	Multiple Pterygium Syndrome, Lethal Type	56	1.902

112		APR001	Apraxia	52	1.902

113	P	BRS053	Breast Fibroadenoma	49	1.902

114		KRT009	Keratosis	53	1.902

115		ANR007	Anorexia Nervosa	60	1.859

116	P	HYP069	Hyperparathyroidism	62	1.859

117		STN013	Stenotrophomonas Maltophilia Infection	26	1.824

118		CYN002	Cyanosis, Transient Neonatal	43	1.824

119		ANT003	Antley-Bixler Syndrome	49	1.824

120	P	HMC002	Homocystinuria	53	1.824

121	c	ALZ049	Alzheimer Disease 2	48	1.768

122	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	1.768

123		ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	36	1.768

124	P	LTR001	Lateral Sclerosis	58	1.768

125	P	PRS040	Prostate Cancer	95	1.759

126		PRT038	Protein-Energy Malnutrition	53	1.758

127		CYS002	Cystic Lymphangioma	45	1.758

128		HYP056	Hypoglycemia	65	1.758

129	c	FTL072	Fetal Akinesia Deformation Sequence 4	37	1.749

130		VRG001	Variegate Porphyria	56	1.721

131		TCK004	Tick Infestation	30	1.721

132		PSY004	Psychotic Disorder	66	1.721

133	P	PRP029	Porphyria	60	1.721

134	c	MCR115	Microvascular Complications of Diabetes 5	65	1.689

135	c	TYP009	Type 2 Diabetes Mellitus	92	1.689

136		BCT022	Bacterial Infectious Disease	56	1.689

137	c	ACT076	Acute Myocarditis	47	1.689

138		END086	End Stage Renal Disease	52	1.689

139	P	SPN046	Spinal Muscular Atrophy	63	1.689

140	P	SCL018	Scoliosis	57	1.673

141		ADN018	Adenoma	59	1.672

142		VSC002	Vascular Dementia	60	1.672

143		BRN071	Brain Injury	50	1.672

144		MSC193	Muscular Lipidosis	22	1.622

145		PST028	Post-Traumatic Stress Disorder	59	1.622

146		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	64	1.615

147	P	TRM004	Trimethylaminuria	45	1.615

148		CRY035	Cryptorchidism, Unilateral or Bilateral	58	1.615

149	P	DBT009	Diabetes Mellitus	67	1.615

150	P	EPL164	Epilepsy	68	1.615

151		DNT012	Dental Caries	53	1.615

152		INS024	Insulin-Like Growth Factor I	78	1.571

153	P	MYC084	Mycobacterium Tuberculosis 1	68	1.571

154	P	BRS047	Breast Cancer	98	1.571

155		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	1.571

156	P	AGN002	Agnosia	54	1.571

157	P	HYP265	Hypotonia	42	1.571

158	P	INF037	Inflammatory Bowel Disease	53	1.535

159		AMN003	Amnestic Disorder	54	1.535

160		STM007	Stomatitis	54	1.535

161	P	THL005	Thalassemia	56	1.518

162	P	BRW001	Brown-Vialetto-Van Laere Syndrome	50	1.518

163		MNC011	Minicore Myopathy with External Ophthalmoplegia	37	1.518

164		CRH001	Crohn's Disease	80	1.518

165		FLL031	Follicular Adenoma	40	1.518

166		NRM005	Neuromuscular Disease	63	1.518

167	P	LYM118	Lymphoma	67	1.499

168		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	1.499

169		LYM019	Lymphosarcoma	46	1.499

170	P	RCT021	Rectum Cancer	54	1.468

171	P	SCH015	Schizophrenia	74	1.462

172		HLT001	Holt-Oram Syndrome	66	1.462

173	c	VRL010	Viral Hepatitis	53	1.462

174		GTR002	Goiter	53	1.462

175	P	CRD246	Cardiovascular System Disease	56	1.462

176	P	ATS364	Autism	69	1.448

177		CVD001	Covid-19	57	1.448

178		CVT001	Cavitary Optic Disc Anomalies	37	1.448

179		THM002	Thiamine-Responsive Megaloblastic Anemia Syndrome	50	1.448

180		HMC041	Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity	48	1.448

181		HYP748	Hypertelorism	46	1.448

182	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	1.448

183		ALP089	Alopecia, Psychomotor Epilepsy, Pyorrhea, and Mental Subnormality	26	1.448

184		THY029	Thyroid Carcinoma	51	1.448

185		CRV002	Cervix Uteri Carcinoma in Situ	47	1.448

186		GRD001	Giardiasis	46	1.448

187		CRV045	Cervical Intraepithelial Neoplasia	39	1.448

188	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	1.405

189		EPD002	Epidermolytic Hyperkeratosis	56	1.405

190		HMR039	Hemorrhage, Intracerebral	57	1.405

191	P	ATS411	Autosomal Dominant Epidermolytic Ichthyosis	36	1.405

192		CYT014	Cytochrome P450 Oxidoreductase Deficiency	34	1.405

193		48X005	48,xyyy	39	1.405

194	P	CRB088	Cerebral Atrophy	33	1.405

195		PSD088	Pseudobulbar Affect	33	1.405

196	P	CRN300	Coronary Heart Disease 1	73	1.353

197	P	MYS003	Myasthenia Gravis	68	1.353

198		HYD038	Hydrops Fetalis, Nonimmune	59	1.353

199		PRT251	Proteinuria, Chronic Benign	57	1.353

200		RSP021	Respiratory Allergy	41	1.353

201		NPH009	Nephrolithiasis	54	1.353

202		PTH002	Pathological Gambling	48	1.353

203		PRM209	Primary Trimethylaminuria	19	1.353

204	P	SPR120	Supranuclear Palsy, Progressive, 1	69	1.345

205	P	KLZ004	Kala-Azar 1	41	1.345

206		AVN001	Avian Influenza	61	1.345

207		LSH001	Leishmaniasis	64	1.345

208		DSS008	Disease of Mental Health	74	1.345

209	P	HYP076	Hyperthyroidism	53	1.345

210		ORL011	Oral Cancer	60	1.345

211		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.339

212		BLM002	Bulimia Nervosa	57	1.283

213		DFC004	Deficiency Anemia	74	1.283

214		ORL015	Oral Squamous Cell Carcinoma	43	1.283

215	P	RTN016	Retinal Degeneration	52	1.283

216	P	THY032	Thyroiditis	57	1.283

217		MLT028	Multiminicore Disease	43	1.283

218		CRT033	Corticobasal Degeneration	47	1.283

219		DBT006	Diabetic Macular Edema	48	1.260

220		MCL006	Macular Retinal Edema	57	1.260

221		CNG538	Congenital Arthrogryposis with Anterior Horn Cell Disease	32	1.247

222	P	MTR004	Maturity-Onset Diabetes of the Young	68	1.244

223	P	CLR023	Colorectal Cancer	100	1.244

224		ANG054	Angina Pectoris	66	1.244

225	P	GST053	Gastric Cancer	83	1.244

226		PHN003	Phenylketonuria	76	1.244

227		NPH091	Nephrolithiasis, Calcium Oxalate	61	1.244

228	P	PRS038	Personality Disorder	65	1.244

229	P	LVR013	Liver Disease	69	1.244

230		FDL002	Food Allergy	47	1.244

231		MLT010	Multiple Personality Disorder	29	1.244

232		URN010	Urinary Tract Obstruction	55	1.244

233		KWS001	Kwashiorkor	45	1.244

234		LPT001	Leptospirosis	66	1.244

235		HYP014	Hyperuricemia	51	1.244

236		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	17	1.244

237		NCL011	Nuclear Gene-Encoded Leigh Syndrome Spectrum	21	1.244

238	c	HMC039	Hemochromatosis, Type 1	73	1.217

239		ATH013	Atherosclerosis Susceptibility	63	1.217

240		NND010	Nondisjunction	34	1.217

241	c	LKM061	Leukemia, Acute Myeloid	83	1.217

242	c	MCL042	Macular Degeneration, Age-Related, 1	85	1.217

243		SNL009	Senile Plaque Formation	29	1.217

244	c	HYP836	Hypercholesterolemia, Familial, 1	73	1.217

245		HML010	Hemolytic Anemia Due to Glutathione Reductase Deficiency	21	1.217

246	P	HYP086	Hypothyroidism	69	1.217

247		HMG005	Hemoglobinopathy	56	1.217

248		IRN001	Iron Deficiency Anemia	58	1.217

249	P	HYD006	Hydrocephalus	61	1.217

250	c	PRM005	Primary Hyperparathyroidism	59	1.217

251	P	NML001	Nemaline Myopathy	48	1.217

252	P	CLC063	Celiac Disease 1	66	1.171

253		CHR081	Choroideremia	58	1.171

254	c	TYP008	Type 1 Diabetes Mellitus	70	1.147

255		WRT005	Warty Dyskeratoma	16	1.147

256		MTH047	Methanol Poisoning	37	1.147

257	c	MYS052	Myasthenic Syndrome, Congenital, 10	43	1.147

258		ACY009	Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of	59	1.147

259		ANX010	Anxiety	70	1.147

260		PRN011	Pernicious Anemia	53	1.147

261		HSH003	Hashimoto Thyroiditis	60	1.147

262	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	1.147

263	c	CRB193	Cerebral Amyloid Angiopathy, App-Related	55	1.147

264		DYS004	Dyscalculia	35	1.147

265		PRT019	Protein-Losing Enteropathy	45	1.147

266	P	KDN018	Kidney Disease	72	1.147

267		ULC004	Ulcerative Colitis	74	1.147

268	P	ALP008	Alopecia	54	1.147

269	P	HRM001	Hermansky-Pudlak Syndrome	65	1.147

270		CNN003	Conn's Syndrome	79	1.147

271	P	VSC007	Vascular Disease	63	1.147

272		PPL002	Papillary Carcinoma	46	1.147

273		GST033	Gestational Diabetes	61	1.147

274		PLC008	Placenta Disease	49	1.147

275		MCR017	Macrocytic Anemia	44	1.147

276		MDM001	Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency	34	1.147

277		HDN002	Head Injury	44	1.147

278		CRB090	Cerebral Hypoxia	42	1.147

279		ART002	Arts Syndrome	66	1.115

280	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	1.115

281	c	ATS007	Autism Spectrum Disorder	72	1.115

282		LGH007	Leigh Syndrome	70	1.115

283		MYL069	Myeloma, Multiple	77	1.115

284	c	HYP595	Hypertension, Essential	85	1.115

285	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	63	1.115

286	c	MTR019	Maturity-Onset Diabetes of the Young, Type 2	53	1.115

287	P	PLY011	Polycystic Ovary Syndrome	57	1.115

288		CNT047	Contact Dermatitis	57	1.115

289		PYR012	Pyruvate Dehydrogenase E1-Beta Deficiency	41	1.073

290		CLT003	Colitis	63	1.073

291	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	1.073

292		NMN001	Nominal Aphasia	40	1.073

293		VSC003	Visceral Leishmaniasis	55	1.073

294	P	LCT001	Lactic Acidosis	51	1.073

295		DLS001	Delusional Disorder	45	1.073

296		CRB004	Cerebral Artery Occlusion	45	1.073

297	P	LNG064	Lung Cancer Susceptibility 3	70	1.073

298		TLN003	Telangiectasis	51	1.073

299		TRN015	Transient Cerebral Ischemia	63	1.073

300	P	EYD002	Eye Disease	57	1.073

301	P	SBS003	Substance Abuse	54	1.073

302		MDD011	Mood Disorder	62	1.073

303		NDL007	Nodular Goiter	48	1.073

304		GRV012	Grover's Disease	29	0.993

305	P	OVR042	Ovarian Cancer	88	0.993

306	c	MGR028	Migraine with or Without Aura 1	64	0.993

307	P	PTY003	Pityriasis Rubra Pilaris	57	0.993

308		KRN002	Kearns-Sayre Syndrome	63	0.993

309	c	ALZ050	Alzheimer Disease 5	33	0.993

310	P	CHN044	Chondrodysplasia Punctata Syndrome	43	0.993

311	P	MYC007	Myocardial Infarction	70	0.993

312		STR095	Structural Heart Defects and Renal Anomalies Syndrome	20	0.993

313		PRM329	Premature Aging	36	0.993

314		MTC004	Mitochondrial Encephalomyopathy	42	0.993

315		HYP066	Hyperglycemia	61	0.993

316		MTH009	Mouth Disease	57	0.993

317		ACT084	Acute Stress Disorder	54	0.993

318		LYM027	Lymphopenia	56	0.993

319	c	ACT004	Acute Diarrhea	40	0.993

320	c	PRC016	Pre-Eclampsia	65	0.993

321	P	RHZ001	Rhizomelic Chondrodysplasia Punctata	57	0.993

322	P	DRR001	Diarrhea	55	0.993

323		SQM006	Squamous Cell Carcinoma	60	0.993

324		GRN017	Granulocytopenia	42	0.993

325		DYS073	Dysphagia	53	0.993

326	c	DNT047	Dentinogenesis Imperfecta Type 2	35	0.993

327		HMP009	Haemophilus Influenzae	41	0.993

328		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.947

329		OTT002	Otitis Media	71	0.947

330	P	EXN002	Exanthem	58	0.947

331	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.947

332	P	SPP010	Suppressor of Tumorigenicity 3	51	0.947

333	P	FLL037	Follicular Lymphoma	74	0.947

334		OBS082	Obstructive Nephropathy	41	0.947

335	P	LPS004	Lupus Erythematosus	61	0.947

336		SKN019	Skin Melanoma	71	0.947

337		ALL010	Allergic Contact Dermatitis	56	0.947

338	P	ACN011	Acne	57	0.947

339		MLK006	Milk Allergy	47	0.947

340		MTC166	Mitochondrial Complex I Deficiency, Nuclear Type 19	23	0.947

341		STT001	Status Epilepticus	59	0.947

342	P	MYT002	Myotonic Dystrophy	51	0.947

343	P	CHR345	Chronic Pain	50	0.947

344		FML304	Familial Isolated Dilated Cardiomyopathy	49	0.907

345		ANX004	Anoxia	40	0.907

346		NRM022	Neurometabolic Disease	24	0.907

347		ACY005	Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of	55	0.907

348	c	HRM005	Hermansky-Pudlak Syndrome 1	55	0.907

349	P	RTN008	Retinitis Pigmentosa	80	0.907

350	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	52	0.907

351		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.907

352	P	MLT020	Multiple Sclerosis	79	0.907

353		FZL002	Fazio-Londe Disease	39	0.907

354		MND002	Mandibuloacral Dysplasia with Type B Lipodystrophy	37	0.907

355	c	CRD113	Cardiomyopathy, Dilated, 1v	24	0.907

356		LMB062	Limb Ischemia	55	0.907

357		PLY166	Polyunsaturated Fatty Acids Plasma Level Quantitative Trait Locus 1	8	0.907

358	P	FRD001	Friedreich Ataxia	61	0.907

359		GLT035	Glutaric Acidemia I	57	0.907

360		ORG002	Organic Acidemia	44	0.907

361		NRR001	Neuroretinitis	42	0.907

362		GLC003	Glucose Intolerance	54	0.907

363	c	PK3005	Pik3ca-Related Overgrowth Syndrome	33	0.907

364		RTN023	Retinitis	46	0.907

365		ART014	Articulation Disorder	34	0.907

366		ASP007	Aspiration Pneumonia	49	0.907

367		GT001	Gout	64	0.907

368		SCH014	Schistosomiasis	56	0.907

369	P	RSP003	Respiratory Failure	74	0.907

370		CHL123	Chlamydia	58	0.907

371	P	PRN023	Prion Disease	60	0.907

372		SVR004	Severe Combined Immunodeficiency	72	0.907

373		HRT015	Heritable Pulmonary Arterial Hypertension	46	0.907

374	P	TXP001	Toxoplasmosis	60	0.907

375		CCN001	Cocaine Dependence	48	0.907

376		LKP003	Leukoplakia	39	0.907

377		IDP022	Idiopathic Spinal Cord Herniation	17	0.907

378	P	LNG032	Lung Cancer	98	0.811

379		HTT002	Hutterite Cerebroosteonephrodysplasia Syndrome	25	0.811

380		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.811

381		SMN008	Semantic Dementia	47	0.811

382		SDD001	Sudden Infant Death Syndrome	60	0.811

383		CMB017	Combined Oxidative Phosphorylation Deficiency 6	41	0.811

384	P	MYS005	Myositis	56	0.811

385		OBS002	Obsessive-Compulsive Disorder	68	0.811

386	P	ATX030	Ataxia-Telangiectasia	80	0.811

387		ISV001	Isovaleric Acidemia	54	0.811

388		AGN018	Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome	57	0.811

389		OPP004	Oppositional Defiant Disorder	49	0.811

390		DSR012	Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency	39	0.811

391	P	ATR011	Atrial Fibrillation	66	0.811

392		CRP032	Corpus Callosum, Agenesis of	49	0.811

393	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	0.811

394		CNT105	Central Core Disease of Muscle	59	0.811

395		IGR001	Ige Responsiveness, Atopic	59	0.811

396		DMT001	Dimethylglycine Dehydrogenase Deficiency	27	0.811

397		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.811

398	c	MCR312	Microphthalmia, Syndromic 10	40	0.811

399		MTH026	Methemoglobinemia Due to Deficiency of Methemoglobin Reductase	35	0.811

400		OST159	Osteogenic Sarcoma	66	0.811

401	P	HYP750	Hypertriglyceridemia, Familial	62	0.811

402		HRW001	Hair Whorl	35	0.811

403	c	CRT081	Cortical Dysplasia, Complex, with Other Brain Malformations 7	31	0.811

404		PLY183	Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome	41	0.811

405	P	MLG056	Malignant Hyperthermia	66	0.811

406	P	MYL006	Myeloid Leukemia	61	0.811

407	P	TRM003	Tremor	48	0.811

408		MCR099	Microlissencephaly	37	0.811

409		SVR001	Severe Acute Respiratory Syndrome	67	0.811

410	P	KRT005	Keratoacanthoma	47	0.811

411		OVR063	Overnutrition	42	0.811

412		HYP005	Hypokalemia	55	0.811

413		ANT007	Anterior Horn Cell Disease	31	0.811

414		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.811

415		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	0.811

416		CHL004	Cholelithiasis	49	0.811

417		OLG003	Oligohydramnios	51	0.811

418		CRT015	Carotid Artery Occlusion	45	0.811

419		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.811

420		PLR005	Pleuropneumonia	33	0.811

421		PLS007	Plasmodium Falciparum Malaria	52	0.811

422	P	ART005	Arteriovenous Malformation	65	0.811

423		NNT010	Nontoxic Goiter	32	0.811

424		SNL007	Senile Cataract	40	0.811

425		TBL023	Tubulinopathies	31	0.811

426		PLY024	Polymicrogyria	47	0.811

427	P	HDC001	Headache	57	0.811

428	P	HYP120	Hypoaldosteronism	35	0.811

429		PRN039	Paraneoplastic Syndromes	37	0.766

430		MCL027	Macular Dystrophy, Dominant Cystoid	51	0.719

431	c	DRM054	Dermatitis, Atopic, 2	46	0.719

432		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	0.719

433		MTC005	Mitochondrial Metabolism Disease	45	0.702

434	P	SZR006	Seizure Disorder	70	0.702

435	c	DWL002	Dowling-Degos Disease 1	58	0.702

436		DHY002	Dihydropyrimidine Dehydrogenase Deficiency	57	0.702

437		MSC157	Muscular Dystrophy, Duchenne Type	79	0.702

438		DSM002	Desmosterolosis	39	0.702

439		ACR020	Acropectorovertebral Dysplasia	23	0.702

440		ALC007	Alcohol Dependence	66	0.702

441	P	PRK057	Parkinson Disease, Late-Onset	80	0.702

442	P	FML011	Familial Adenomatous Polyposis	71	0.702

443		MLR004	Malaria	80	0.702

444	P	HYP111	Hyperprolinemia	45	0.702

445	P	PLY014	Polycystic Kidney Disease	69	0.702

446		HMN047	Human Cytomegalovirus Infection	57	0.702

447		SBJ001	Subjective Cognitive Decline	30	0.702

448	c	RHZ004	Rhizomelic Chondrodysplasia Punctata, Type 3	42	0.702

449		PRL023	Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome	46	0.702

450	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	0.702

451	P	PNC035	Pancreatic Cancer	86	0.702

452	c	CRB176	Cerebral Amyloid Angiopathy, Itm2b-Related, 1	43	0.702

453		KRT019	Keratitis, Hereditary	66	0.702

454	c	SPN284	Spinocerebellar Ataxia 38	40	0.702

455	P	ASP006	Aspergillosis	72	0.702

456		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	47	0.702

457		RNL114	Renal Cell Carcinoma, Nonpapillary	80	0.702

458		DMN031	Dementia, Lewy Body	65	0.702

459		PCK003	Pick Disease of Brain	69	0.702

460	c	NMN014	Niemann-Pick Disease, Type C2	49	0.702

461	P	HRD008	Hereditary Hemorrhagic Telangiectasia	65	0.702

462	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	66	0.702

463	P	ZLL001	Zellweger Syndrome	65	0.702

464	P	BCL017	B-Cell Lymphoma	59	0.702

465	c	CHR684	Chronic Kidney Disease	69	0.702

466		URM002	Uremia	47	0.702

467	P	HRP006	Herpes Simplex	65	0.702

468	P	MSC005	Muscular Dystrophy	67	0.702

469	P	MTH008	Methylmalonic Acidemia	52	0.702

470	P	ALC033	Alcohol Use Disorder	61	0.702

471		VCC001	Vaccinia	47	0.702

472		LCL004	Localized Osteosarcoma	34	0.702

473	P	SKN015	Skin Carcinoma	71	0.702

474		END040	Endogenous Depression	55	0.702

475		SPN035	Spindle Cell Sarcoma	54	0.702

476	P	INF038	Influenza	68	0.702

477		LNG099	Lung Disease	62	0.702

478		TRY001	Trypanosomiasis	50	0.702

479	P	DNG005	Dengue Virus	56	0.702

480	P	KLP003	Klippel-Feil Syndrome	47	0.702

481	P	NTR004	Neutropenia	63	0.702

482	c	SCN007	Secondary Hyperparathyroidism	51	0.702

483	c	ACT027	Acute Pancreatitis	60	0.702

484		THY122	Thyroid Gland Cancer	59	0.702

485		CLB002	Clubfoot	51	0.702

486		CCC002	Coccidiosis	50	0.702

487	P	ECL001	Eclampsia	52	0.702

488		SRC014	Sarcoma	65	0.702

489	P	HYP040	Hypospadias	51	0.702

490	P	HYP024	Hypoparathyroidism	55	0.702

491		HYD001	Hydranencephaly	43	0.702

492		PLG002	Plague	58	0.702

493		CRB033	Cerebral Degeneration	39	0.702

494	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	0.702

495		KRT008	Keratopathy	46	0.702

496		CRB037	Cerebral Palsy	67	0.702

497	P	INS002	in Situ Carcinoma	53	0.702

498		HRN003	Heroin Dependence	44	0.702

499	P	SCK005	Sickle Cell Disease	56	0.702

500		ERY069	Erythrokeratoderma ''en Cocardes''	27	0.702

501		ADR022	Adrenomyeloneuropathy	39	0.574

502		PLY100	Polyploidy	36	0.574

503	P	AVS003	Avascular Necrosis	41	0.574

504		CHR696	Charcot-Marie-Tooth Disease, X-Linked Recessive, 4, with or Without Cerebellar Ataxia	32	0.574

505	P	RTT002	Rett Syndrome	79	0.574

506		ADR007	Adrenoleukodystrophy	73	0.574

507		LSC001	Lesch-Nyhan Syndrome	62	0.574

508		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	50	0.574

509	P	FRG001	Fragile X Syndrome	70	0.574

510		SRC015	Sarcosinemia	38	0.574

511		MYP035	Myopathy, Distal, with Anterior Tibial Onset	33	0.574

512	c	CTR132	Cataract 3, Multiple Types	42	0.574

513		BRT054	Brittle Bone Disorder	74	0.574

514		CRV035	Cervical Cancer	73	0.574

515		END057	Endometrial Cancer	72	0.574

516		CRT072	Creutzfeldt-Jakob Disease	68	0.574

517		GRS011	Gerstmann-Straussler Disease	56	0.574

518	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	0.574

519		CRN287	Carnitine Deficiency, Myopathic	17	0.574

520		CYS001	Cystic Fibrosis	78	0.574

521	c	GLY007	Glycogen Storage Disease Iv	58	0.574

522		CHR100	Chronic Ulcer of Skin	57	0.574

523	P	LSS002	Lissencephaly	50	0.574

524		FML037	Female Breast Cancer	51	0.574

525		VTM002	Vitamin B12 Deficiency	48	0.574

526	c	BTT014	Beta-Thalassemia	72	0.574

527		DFF005	Diffuse Large B-Cell Lymphoma	54	0.574

528		NNL006	Non-Alcoholic Steatohepatitis	54	0.574

529		AGR018	Agraphia	37	0.574

530		SXL003	Sexual Disorder	49	0.574

531	c	CNG006	Congenital Hypothyroidism	63	0.574

532		CLR108	Colorectal Adenoma	64	0.574

533		PYR022	Pyruvate Dehydrogenase E1-Alpha Deficiency	64	0.574

534		IMM167	Immune Deficiency Disease	78	0.574

535	c	GRV008	Graves Disease 1	54	0.574

536		PRN056	Parana Hard-Skin Syndrome	17	0.574

537	c	SPH013	Spherocytosis, Type 1	42	0.574

538		PRS012	Pars Planitis	47	0.574

539	c	BRN108	Branchiootic Syndrome 1	62	0.574

540	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.574

541		LPT014	Leptin Deficiency or Dysfunction	78	0.574

542	c	PNT034	Pontocerebellar Hypoplasia, Type 2e	52	0.574

543		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	0.574

544		MYP163	Myopathy, Mitochondrial Progressive, with Congenital Cataract and Developmental Delay	27	0.574

545	P	DVL012	Developmental Dysplasia of the Hip 1	46	0.574

546	c	CRB098	Cerebrooculofacioskeletal Syndrome 2	30	0.574

547	c	CRB100	Cerebrooculofacioskeletal Syndrome 4	33	0.574

548	P	CRB101	Cerebrooculofacioskeletal Syndrome 1	53	0.574

549	c	RHZ011	Rhizomelic Chondrodysplasia Punctata, Type 1	53	0.574

550		HMC042	Homocystinuria-Megaloblastic Anemia, Cble Complementation Type	33	0.574

551		BTT016	Batten-Turner Congenital Myopathy	53	0.574

552		MYL005	Myelofibrosis	71	0.574

553		OCL069	Ocular Motor Apraxia	57	0.574

554		TLC001	Telecanthus	35	0.574

555	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.574

556	P	SRC025	Sarcoidosis 1	71	0.574

557	P	SCL057	Scoliosis, Isolated 1	40	0.574

558		RFS006	Refsum Disease, Classic	63	0.574

559	P	RNL100	Renal Hypodysplasia/aplasia 1	63	0.574

560	P	PTN014	Patent Ductus Arteriosus 1	59	0.574

561		OST017	Osteomyelitis	63	0.574

562	P	PNT019	Pontocerebellar Hypoplasia	46	0.574

563	P	NRD007	Neurodegeneration with Brain Iron Accumulation	52	0.574

564	c	CHR697	Charcot-Marie-Tooth Disease X-Linked Recessive 4	31	0.574

565		DST103	Distal Muscular Dystrophy with Anterior Tibial Onset	29	0.574

566		GRN051	Granulomatous Disease, Chronic, X-Linked	57	0.574

567		HPT004	Hepatic Coma	43	0.574

568		BLS002	Blastomycosis	47	0.574

569		IDP073	Idiopathic Hypercalciuria	40	0.574

570		CNG393	Congenital Muscular Dystrophy with Hyperlaxity	12	0.574

571		DYS003	Dysgraphia	35	0.574

572		SCH012	Schizoaffective Disorder	50	0.574

573	P	DYS154	Dystonia	64	0.574

574		VLK001	Volkmann Contracture	23	0.574

575	P	MVM001	Movement Disease	61	0.574

576	P	HML002	Hemolytic Anemia	62	0.574

577		HMG002	Hemoglobinuria	50	0.574

578		GLL048	Glial Tumor	52	0.574

579	P	HMR005	Hemorrhoid	49	0.574

580		GLY078	Glycogen Storage Disease Due to Glycogen Branching Enzyme Deficiency	38	0.574

581	P	THR014	Thrombocytopenia	66	0.574

582	P	BRS044	Breast Adenocarcinoma	58	0.574

583		ART016	Aortic Aneurysm	68	0.574

584	P	SYS005	Systemic Scleroderma	74	0.574

585		MTS001	Mutism	44	0.574

586	c	SBC007	Subacute Thyroiditis	43	0.574

587		INH003	Inhibited Female Orgasm	27	0.574

588	P	SNS001	Sensorineural Hearing Loss	59	0.574

589		SLP001	Sleeping Sickness	56	0.574

590		RCK004	Rickets	68	0.574

591		MYP164	Myopathy, Congenital, with Diaphragmatic Defects, Respiratory Insufficiency, and Dysmorphic Facies	24	0.574

592	P	UVT001	Uveitis	57	0.574

593		BRN028	Brain Cancer	74	0.574

594		MRS001	Marasmus	42	0.574

595	P	GRV001	Graves' Disease	55	0.574

596		PCD001	Pica Disease	38	0.574

597		ATY001	Atypical Depressive Disorder	45	0.574

598	P	GLL022	Guillain-Barre Syndrome	60	0.574

599		IMP005	Impotence	52	0.574

600	c	BSL007	Basal Cell Carcinoma	68	0.574

601		NRT004	Neuritis	53	0.574

602		NNT012	Neonatal Jaundice	53	0.574

603	P	ADN016	Adenocarcinoma	63	0.574

604		MGL001	Megaloblastic Anemia	58	0.574

605		HYP030	Hypoactive Sexual Desire Disorder	41	0.574

606	P	GLY013	Glycogen Storage Disease	60	0.574

607	P	END044	Endometriosis	62	0.574

608	P	HRT032	Heart Disease	81	0.574

609		PRM013	Premature Menopause	58	0.574

610		BRD004	Borderline Personality Disorder	53	0.574

611		MNN009	Meningoencephalitis	48	0.574

612	P	PNC044	Pancreatitis	61	0.574

613	P	INF032	Infertility	57	0.574

614	P	RTN018	Retinal Disease	53	0.574

615	P	AXN001	Axonal Neuropathy	35	0.574

616	P	PRM002	Primary Hyperoxaluria	65	0.574

617	P	KDN017	Kidney Cancer	61	0.574

618	P	MTR014	Motor Neuron Disease	65	0.574

619		PHM001	Phimosis	38	0.574

620		BRS051	Breast Disease	58	0.574

621		DMY004	Demyelinating Disease	50	0.574

622		IDP070	Idiopathic Scoliosis	42	0.574

623		LST001	Listeriosis	59	0.574

624		CHR073	Choreatic Disease	54	0.574

625	P	HRD011	Hereditary Spherocytosis	64	0.574

626		CND002	Conduct Disorder	51	0.574

627		HST011	Histoplasmosis	55	0.574

628		SBS004	Substance Dependence	47	0.574

629	P	TRC031	Trichorhinophalangeal Syndrome	38	0.574

630		DCB001	Decubitus Ulcer	62	0.574

631		FSC004	Fasciitis	49	0.574

632		PRL005	Proliferative Fasciitis	20	0.574

633		ISC003	Ischemic Fasciitis	28	0.574

634		MYP017	Myopathy, Mitochondrial Progressive, with Congenital Cataract, Hearing Loss, and Developmental Delay	14	0.574

635		GB1002	Gbe1 Adult Polyglucosan Body Disease	7	0.574

636		ANR040	Aneurysm	61	0.574

637		BRN056	Bronchopulmonary Dysplasia	56	0.574

638		MTH046	Methylmalonic Acidemia Without Homocystinuria	39	0.574

639		CCC003	Coccygodynia	18	0.574

640		GLM045	Glioma	63	0.574

641		SPT023	Septate Uterus	30	0.541

642		URM005	Uremic Pruritus	45	0.541

643	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.541

644		ATM095	Autoimmune Disease	61	0.541

645	P	RST001	Restless Legs Syndrome	52	0.541

646	P	CRP001	Carpal Tunnel Syndrome	66	0.541

647	c	PCH010	Pachyonychia Congenita 3	43	0.541

648		PLY105	Polycystic Ovary Syndrome 1	39	0.541

649	c	CWD006	Cowden Syndrome 1	78	0.541

650	P	VSC011	Vasculitis	61	0.541

651		CHR066	Chronic Fatigue Syndrome	60	0.541

652		WHT017	Wheat Allergy	31	0.541

653		CHR001	Churg-Strauss Syndrome	61	0.541

654		APP008	Appendicitis	62	0.541

655		PPT005	Peptic Ulcer Disease	58	0.541

656	P	DRM007	Dermatitis Herpetiformis	54	0.541

657	P	VNS003	Venous Insufficiency	55	0.541

658		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	0.541

659		TBS001	Tabes Dorsalis	31	0.541

660		CNS004	Constipation	56	0.541

661	P	CWD010	Cowden Syndrome	70	0.541

662		FLL008	Folliculitis	46	0.541

663	P	SLP005	Sleep Disorder	61	0.541

664	P	ADL010	Adult Respiratory Distress Syndrome	71	0.541

665		PTL002	Patellofemoral Pain Syndrome	34	0.541

666		ALL012	Allergic Angiitis	24	0.541

667	P	CLS010	Cluster Headache	42	0.541

668		ESN016	Eosinophilic Pustular Folliculitis	24	0.541

669		MCR088	Microscopic Polyangiitis	51	0.541

670		ANC002	Anca-Associated Vasculitis	44	0.541

671	c	GRN062	Granulomatous Disease, Chronic, Autosomal Recessive, 1	46	0.406

672		PST021	Postpartum Depression	50	0.406

673		DMN026	Dementia Pugilistica	27	0.406

674		RFR010	Refractory Anemia	49	0.406

675		SNK001	Snakebite Envenomation	22	0.406

676		CYN003	Cyanide Poisoning	22	0.406

677		OST115	Osteonecrosis of the Jaw	41	0.406

678		SPS057	Spasticity	42	0.406

679		ARG006	Aregenerative Anemia	28	0.406

680		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	0.406

681	c	STC015	Stickler Syndrome, Type I	51	0.406

682	P	BLD134	Bladder Cancer	79	0.406

683	P	NSP012	Nasopharyngeal Carcinoma	61	0.406

684		GND001	Gonadoblastoma	43	0.406

685		MRD002	Marden-Walker Syndrome	56	0.406

686		FRG010	Fragile X Tremor/ataxia Syndrome	44	0.406

687		SQM013	Squamous Cell Carcinoma, Head and Neck	73	0.406

688		MND023	Mend Syndrome	49	0.406

689		MST021	Meester-Loeys Syndrome	42	0.406

690	P	LPR021	Leprosy 3	71	0.406

691		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	61	0.406

692		ALL003	Allergic Rhinitis	67	0.406

693	P	LNR013	Linear Skin Defects with Multiple Congenital Anomalies 1	52	0.406

694		STR067	Stroke, Ischemic	80	0.406

695	c	PLM164	Pulmonary Hypertension, Primary, 1	76	0.406

696	P	PHC003	Pheochromocytoma	69	0.406

697	c	SYS001	Systemic Lupus Erythematosus	87	0.406

698	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	54	0.406

699		PLY150	Polykaryocytosis Inducer	29	0.406

700	P	CNR004	Cone-Rod Dystrophy 2	74	0.406

701		CRD002	Cri-Du-Chat Syndrome	49	0.406

702	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.406

703		HYP781	Hypoascorbemia	52	0.406

704		PLL017	Pallister-Hall-Like Syndrome	37	0.406

705	c	LKM063	Leukemia, Chronic Myeloid	71	0.406

706		EPD015	Epidemic Typhus	44	0.406

707		END014	Endemic Typhus	32	0.406

708		CNZ001	Coenzyme Q10 Deficiency Disease	41	0.406

709	c	FTL067	Fetal Hemoglobin Quantitative Trait Locus 6	25	0.406

710		DLY008	Delayed Sleep Phase Disorder	44	0.406

711		HRS016	Hirschsprung Disease, Cardiac Defects, and Autonomic Dysfunction	26	0.406

712		INV001	Invasive Aspergillosis	49	0.406

713	P	URN019	Urinary Tract Infection	49	0.406

714		ALX002	Alexithymia	37	0.406

715		ASS001	Associative Agnosia	24	0.406

716		MCR191	Microscopic Colitis	46	0.406

717	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.406

718		LWG006	Low Grade Glioma	41	0.406

719	P	CTN015	Cutaneous T Cell Lymphoma	48	0.406

720		CRH005	Crohn's Colitis	53	0.406

721		FSR001	Fusariosis	45	0.406

722		NRL018	Neural Tube Defects, Folate-Sensitive	45	0.406

723	P	HYP768	Hyperlipoproteinemia, Type I	67	0.406

724		GST108	Gist-Plus Syndrome	22	0.406

725		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.406

726		PRS131	Prostate Cancer/brain Cancer Susceptibility	23	0.406

727		SCK003	Sickle Cell Anemia	74	0.406

728		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.406

729		HMM004	Hamamy Syndrome	39	0.406

730		ACT119	Acute Promyelocytic Leukemia	62	0.406

731		TBL029	Tubulin, Beta	28	0.406

732	P	MPL001	Maple Syrup Urine Disease	70	0.406

733		SPN362	Spondylometaphyseal Dysplasia, Sedaghatian Type	42	0.406

734		MTC207	Mitochondrial Complex Ii Deficiency, Nuclear Type 1	55	0.406

735	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	49	0.406

736	c	CLR041	Colorectal Cancer, Hereditary Nonpolyposis, Type 2	35	0.406

737	c	HYD064	Hydrocephalus, Congenital, 1	51	0.406

738	c	HYP248	Hyperprolinemia, Type I	42	0.406

739		VRC005	Varicose Veins	60	0.406

740		VLC001	Velocardiofacial Syndrome	57	0.406

741		RTN179	Retinal Arteries, Tortuosity of	41	0.406

742		KRT071	Keratosis, Seborrheic	56	0.406

743	P	STR020	Strabismus	56	0.406

744		DGR001	Digeorge Syndrome	62	0.406

745		CRN238	Corneal Dystrophy, Epithelial Basement Membrane	32	0.406

746	P	MJR007	Major Affective Disorder 1	42	0.406

747		MLT157	Multiple System Atrophy 1	69	0.406

748	P	FTL033	Fetal Hemoglobin Quantitative Trait Locus 1	42	0.406

749	P	ANG001	Angelman Syndrome	65	0.406

750		ANT078	Antipyrine Metabolism	23	0.406

751	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	53	0.406

752	c	MYP118	Myopathy, Myofibrillar, 8	30	0.406

753		PNG002	Pain Agnosia	51	0.406

754		GST019	Gastrointestinal Stromal Tumor	78	0.406

755		CLR109	Colorectal Adenocarcinoma	50	0.406

756		FRG008	Fragile X-Associated Tremor/ataxia Syndrome	44	0.406

757		ADR040	Adrenal Gland Pheochromocytoma	46	0.406

758		BLP004	Blepharophimosis	36	0.406

759	P	LCT002	Lactose Intolerance	52	0.406

760		ADN072	Adenoma of Pancreas	17	0.406

761	c	CHR695	Chronic Primary Adrenal Insufficiency	15	0.406

762	P	PRN026	Porencephaly	55	0.406

763		MTC151	Mitochondrial Complex I Deficiency, Nuclear Type 20	36	0.406

764		PRC002	Paracoccidioidomycosis	54	0.406

765	c	CHR095	Chronic Progressive External Ophthalmoplegia	49	0.406

766	c	ACT073	Acute Leukemia	58	0.406

767	P	MYP006	Myopia	56	0.406

768		FSC002	Fascioliasis	44	0.406

769	P	SDR003	Sideroblastic Anemia	51	0.406

770		PRX001	Peroxisomal Disease	46	0.406

771	P	HYP083	Hypopituitarism	52	0.406

772		NTR005	Nutritional Deficiency Disease	61	0.406

773	P	HRD200	Hereditary Breast Ovarian Cancer Syndrome	67	0.406

774		INT075	Intracranial Hypertension	53	0.406

775		GSG001	Gas Gangrene	52	0.406

776		MCH006	Mechanical Strabismus	40	0.406

777	P	NRP001	Neuropathy	60	0.406

778		AMB001	Amebiasis	57	0.406

779	P	MTC133	Mitochondrial Myopathy	50	0.406

780		PST092	Posttransplant Acute Limbic Encephalitis	28	0.406

781		INF118	Inflammatory Myopathy with Abundant Macrophages	27	0.406

782		FWL003	Fowler Urethral Sphincter Dysfunction Syndrome	22	0.406

783		YLL002	Yellow Fever	61	0.406

784		HRD180	Hereditary Persistence of Fetal Hemoglobin-Sickle Cell Disease Syndrome	26	0.406

785		PNC129	Pancreatic Adenocarcinoma	65	0.406

786	c	HPT001	Hepatitis C	62	0.406

787		SYS004	Systemic Mastocytosis	63	0.406

788	P	TRN020	Turner Syndrome	67	0.406

789	P	MST009	Mastocytosis	64	0.406

790		AVD001	Avoidant Personality Disorder	49	0.406

791	P	GST044	Gastritis	55	0.406

792		ACQ007	Acquired Immunodeficiency Syndrome	59	0.406

793		ILS001	Ileus	50	0.406

794		CLR030	Clear Cell Renal Cell Carcinoma	54	0.406

795		ANT024	Anthrax Disease	58	0.406

796		CHL061	Childhood Leukemia	47	0.406

797	P	PLL002	Pellagra	46	0.406

798	P	ART022	Arthritis	71	0.406

799	P	RTN014	Retinal Artery Occlusion	47	0.406

800	P	MNC007	Monocytic Leukemia	47	0.406

801		ASY002	Asymptomatic Neurosyphilis	41	0.406

802		SLC006	Silicosis	56	0.406

803		CMM005	Common Cold	56	0.406

804	c	SPR162	Spermatogenic Failure 50	42	0.406

805		CHL147	Chlamydia Pneumonia	47	0.406

806		STR103	Streptococcus Pneumonia	47	0.406

807		OST003	Osteonecrosis	61	0.406

808		DNG003	Dengue Disease	65	0.406

809	P	MLN007	Male Infertility	56	0.406

810	P	ESP024	Esophagitis	60	0.406

811		SYN005	Synostosis	43	0.406

812	P	LKM002	Leukemia	67	0.406

813		BRN026	Branch Retinal Artery Occlusion	41	0.406

814		PPL022	Papilloma	53	0.406

815		BLR008	Bilirubin Metabolic Disorder	57	0.406

816	P	BRB001	Beriberi	44	0.406

817		SQM002	Squamous Cell Papilloma	46	0.406

818		TXC005	Toxic Shock Syndrome	62	0.406

819	P	MLN008	Melanoma	76	0.406

820		RTN020	Retinal Vascular Disease	46	0.406

821	P	NPH012	Nephrotic Syndrome	60	0.406

822	P	CRN037	Craniosynostosis	68	0.406

823		HPT014	Hepatorenal Syndrome	49	0.406

824	P	MCR010	Microcephaly	60	0.406

825		RBS001	Rabies	58	0.406

826		SPT005	Spotted Fever	49	0.406

827		KRT002	Keratomalacia	55	0.406

828		TTN003	Tetanus	65	0.406

829		HYP006	Hypertensive Heart Disease	49	0.406

830	P	RHN004	Rhinitis	57	0.406

831		THY030	Thyroid Gland Disease	50	0.406

832		ADJ001	Adjustment Disorder	47	0.406

833	P	PRP019	Peripheral Nervous System Disease	58	0.406

834		PRM020	Premenstrual Tension	39	0.406

835		GNG013	Gingivitis	59	0.406

836	c	CNT035	Central Nervous System Disease	54	0.406

837		GST045	Gastroenteritis	58	0.406

838	P	ART021	Arteriosclerosis	54	0.406

839	P	THR015	Thrombophilia	51	0.406

840	c	FML021	Familial Hypercholesterolemia	72	0.406

841	P	PLY019	Polyneuropathy	52	0.406

842		TYP007	Typhoid Fever	64	0.406

843		ERY004	Erysipelas	47	0.406

844		CHL035	Cholinergic Urticaria	29	0.406

845	P	GND004	Gonadal Dysgenesis	47	0.406

846		NCR001	Necrotizing Ulcerative Gingivitis	26	0.406

847		PLM010	Pulmonary Edema	55	0.406

848		GNG011	Gingival Disease	54	0.406

849	P	URT039	Urticaria	58	0.406

850		AZS001	Azoospermia	45	0.406

851		HDR002	Hidradenitis Suppurativa	54	0.406

852	P	BNC003	Bone Cancer	58	0.406

853	c	SVR005	Severe Pre-Eclampsia	50	0.406

854		DVL001	Developmental Coordination Disorder	34	0.406

855	P	MNN013	Meningitis	65	0.406

856		INV005	Inverted Follicular Keratosis	32	0.406

857	P	ACT105	Acute Mountain Sickness	52	0.406

858		ADS004	Aids Dementia Complex	40	0.406

859	P	ENC004	Encephalitis	61	0.406

860		ATS301	Autosomal Dominant Epilepsy with Auditory Features	36	0.406

861		HNS001	Hansen's Disease	32	0.406

862		MNN020	Meningococcal Infection	45	0.406

863		NNT017	Neonatal Adrenoleukodystrophy	54	0.406

864		ORL012	Oral Leukoplakia	36	0.406

865		WLL004	Wallerian Degeneration	38	0.406

866		CHR121	Charcot-Marie-Tooth Neuropathy X Type 5	17	0.406

867		DSR002	Disorders of Intracellular Cobalamin Metabolism	29	0.406

868	P	MTC069	Mitochondrial Disorders	57	0.406

869		CRB086	Cerebral Aneurysms	40	0.406

870		DVL005	Developmental Dyspraxia	22	0.406

871		CTS005	Catastrophic Antiphospholipid Syndrome	43	0.406

872		CYT002	Cytokine Deficiency	43	0.406

873	P	ADT009	Auditory Neuropathy Spectrum Disorder	34	0.406

874		EXR007	Exercise-Induced Anaphylaxis	23	0.406

875		NRS003	Neurosyphilis	45	0.406

876		PNC049	Pancreatic Adenoma	14	0.406

877		PST046	Post-Transplant Lymphoproliferative Disease	53	0.406

878		DWR001	Dwarfism	44	0.406

879		MSL001	Measles	61	0.406

880	P	NRV007	Nervous System Disease	67	0.406