Search results for ACADS

954 hits were found for ACADS

#	Family	MCID	Name	MIFTS	Score
1		ACY005	Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of	55	88.795

2	P	MYP004	Myopathy	67	17.188

3	P	DBT009	Diabetes Mellitus	67	13.200

4		ACY009	Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of	59	11.531

5		MLT118	Multiple Acyl-Coa Dehydrogenase Deficiency	65	10.614

6		ENC055	Encephalopathy, Ethylmalonic	51	10.218

7		ISV001	Isovaleric Acidemia	54	10.218

8		RBF001	Riboflavin Deficiency	49	10.218

9		ORG002	Organic Acidemia	44	10.218

10		ACY010	Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of	64	9.669

11	P	PRD006	Prader-Willi Syndrome	61	8.017

12		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	61	7.621

13		3MT001	3-Methylcrotonyl-Coa Carboxylase Deficiency	52	7.621

14	P	MLG056	Malignant Hyperthermia	66	7.621

15	c	SPN295	Spinocerebellar Ataxia, Autosomal Recessive 3	37	7.225

16	P	SHR074	Short-Rib Thoracic Dysplasia 1 with or Without Polydactyly	60	7.225

17		FZL002	Fazio-Londe Disease	39	7.225

18		CRN239	Carnitine Deficiency, Systemic Primary	61	7.225

19	c	SHR067	Short-Rib Thoracic Dysplasia 2 with or Without Polydactyly	44	7.225

20	P	SPN202	Spinocerebellar Ataxia, X-Linked 1	41	7.225

21	c	SPN403	Spinocerebellar Ataxia, X-Linked 2	20	7.225

22		MTC027	Mitochondrial Trifunctional Protein Deficiency	57	7.225

23		CRN295	Carnitine Palmitoyltransferase I Deficiency	55	7.225

24		XLN076	X-Linked Cerebellar Ataxia	21	7.225

25		MSC193	Muscular Lipidosis	22	7.225

26		INF065	Infantile Hypotonia	21	7.225

27		HLX001	Helix Syndrome	48	4.445

28		ACY011	Acyl-Coa Dehydrogenase Deficiency	30	4.233

29		HMN044	Human Immunodeficiency Virus Type 1	78	3.041

30		LPP008	Lipoprotein Quantitative Trait Locus	65	3.016

31		ART140	Arteries, Anomalies of	53	2.937

32	P	HRP006	Herpes Simplex	65	2.828

33		HYP056	Hypoglycemia	65	2.575

34		PRT037	Pertussis	65	2.535

35		IMM167	Immune Deficiency Disease	78	2.489

36		VCC001	Vaccinia	47	2.441

37		STM007	Stomatitis	54	2.441

38	P	ENC018	Encephalopathy	62	2.398

39		MTB004	Metabolic Acidosis	48	2.351

40	P	HYP265	Hypotonia	42	2.351

41	c	TYP009	Type 2 Diabetes Mellitus	92	2.331

42		ATS010	Autosomal Recessive Disease	42	2.252

43		GLM045	Glioma	63	2.137

44		HPT004	Hepatic Coma	43	2.090

45		HPT019	Hepatic Encephalopathy	59	2.090

46		47X002	47,xyy	48	1.980

47	P	NRB001	Neuroblastoma	66	1.940

48	c	INH020	Inherited Metabolic Disorder	48	1.906

49		ACT098	Acute Erythroid Leukemia	55	1.899

50		CHL014	Cholera	62	1.899

51		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	1.815

52		ART002	Arts Syndrome	66	1.807

53	P	GLM040	Glioma Susceptibility 1	71	1.776

54		MDM001	Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency	34	1.726

55		PLM129	Pulmonary Disease, Chronic Obstructive	74	1.688

56		HRW001	Hair Whorl	35	1.680

57		CLT003	Colitis	63	1.603

58	P	HNT016	Huntington Disease	73	1.584

59		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	1.584

60	c	LKM005	Leukemia, T-Cell, Chronic	34	1.584

61	P	ALZ034	Alzheimer Disease	87	1.534

62		PLY150	Polykaryocytosis Inducer	29	1.534

63		RPD005	Rapidly Involuting Congenital Hemangioma	46	1.534

64		ULC004	Ulcerative Colitis	74	1.510

65		CNT047	Contact Dermatitis	57	1.510

66		DRM006	Dermatitis	62	1.510

67		KPS004	Kaposi Sarcoma	77	1.482

68		SPN035	Spindle Cell Sarcoma	54	1.482

69		SRC014	Sarcoma	65	1.482

70		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	1.428

71		NNL005	Non-Alcoholic Fatty Liver Disease	63	1.428

72		SCR011	Scrapie	39	1.428

73		FTT001	Fatty Liver Disease	62	1.428

74		DPH001	Diphtheria	59	1.428

75		CHL123	Chlamydia	58	1.428

76		ACT088	Acute Insulin Response	39	1.404

77		PMP014	Pemphigoid	51	1.404

78		EXT007	Extracutaneous Mastocytoma	38	1.404

79		MST004	Mast Cell Neoplasm	42	1.404

80	P	PHC003	Pheochromocytoma	69	1.372

81	P	RTN024	Retinoblastoma	73	1.372

82		HND015	Hand Skill, Relative	30	1.372

83		LPD008	Lipid Metabolism Disorder	62	1.372

84	P	OVR042	Ovarian Cancer	88	1.343

85		XRD010	Xeroderma Pigmentosum, Variant Type	73	1.313

86	c	HPT073	Hepatitis C Virus	71	1.313

87		ADR040	Adrenal Gland Pheochromocytoma	46	1.313

88		PST092	Posttransplant Acute Limbic Encephalitis	28	1.313

89		GLL048	Glial Tumor	52	1.313

90	P	SKN015	Skin Carcinoma	71	1.313

91		CRT016	Carotid Artery Disease	52	1.313

92	c	MGR028	Migraine with or Without Aura 1	64	1.278

93		BLL006	Bullous Pemphigoid	61	1.278

94		ATH013	Atherosclerosis Susceptibility	63	1.252

95		ANG054	Angina Pectoris	66	1.252

96		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	1.252

97		OST159	Osteogenic Sarcoma	66	1.252

98		TRT001	Teratocarcinoma	42	1.252

99	P	FBR017	Fibrosarcoma	56	1.252

100	P	PRN023	Prion Disease	60	1.252

101		SVR004	Severe Combined Immunodeficiency	72	1.252

102		EMB004	Embryonal Carcinoma	56	1.252

103	P	PNC035	Pancreatic Cancer	86	1.237

104	P	OLG002	Oligodendroglioma	66	1.216

105		ANX004	Anoxia	40	1.188

106	P	THL005	Thalassemia	56	1.188

107	P	MYC084	Mycobacterium Tuberculosis 1	68	1.188

108	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	1.188

109		BRK010	Burkitt Lymphoma	66	1.188

110		CYS001	Cystic Fibrosis	78	1.188

111	P	FRD001	Friedreich Ataxia	61	1.188

112	c	MCL042	Macular Degeneration, Age-Related, 1	85	1.188

113	c	HYP836	Hypercholesterolemia, Familial, 1	73	1.188

114	P	SPS008	Spastic Ataxia	41	1.188

115	P	BPL003	Bipolar Disorder	56	1.188

116	P	LTR001	Lateral Sclerosis	58	1.188

117		PPL022	Papilloma	53	1.188

118	c	HPT016	Hepatitis B	62	1.188

119		48X005	48,xyyy	39	1.188

120		HMP009	Haemophilus Influenzae	41	1.188

121	P	LNG032	Lung Cancer	98	1.120

122		INS024	Insulin-Like Growth Factor I	78	1.120

123	c	MJR022	Major Affective Disorder 8	38	1.120

124	c	BTT014	Beta-Thalassemia	72	1.120

125	c	MJR024	Major Affective Disorder 9	41	1.120

126		2MT003	2-Methylbutyryl-Coa Dehydrogenase Deficiency	39	1.120

127	c	HPT003	Hepatitis a	63	1.120

128		CHL147	Chlamydia Pneumonia	47	1.120

129		SQM002	Squamous Cell Papilloma	46	1.120

130	P	STR020	Strabismus	56	1.114

131		PMP006	Pemphigus Vulgaris, Familial	58	1.114

132	P	HPT023	Hepatocellular Carcinoma	96	1.114

133	P	PMP001	Pemphigus	55	1.114

134		MCH006	Mechanical Strabismus	40	1.114

135	P	BRS047	Breast Cancer	98	1.111

136	P	BCK002	Beckwith-Wiedemann Syndrome	62	1.111

137		AGN016	Aging	54	1.048

138		ADR041	Adrenal Cortical Adenoma	49	1.048

139		MTC151	Mitochondrial Complex I Deficiency, Nuclear Type 20	36	1.048

140	P	VSC011	Vasculitis	61	1.048

141	P	INF038	Influenza	68	1.048

142		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	1.048

143	P	LKM002	Leukemia	67	1.048

144		CRT013	Carotid Stenosis	51	1.048

145		CLN015	Colon Adenocarcinoma	65	1.048

146		MLG169	Malignant Astrocytoma	57	1.048

147		TTN003	Tetanus	65	1.048

148		MDD011	Mood Disorder	62	1.048

149	P	ENC004	Encephalitis	61	1.048

150	P	NSP012	Nasopharyngeal Carcinoma	61	0.970

151	P	FRG001	Fragile X Syndrome	70	0.970

152	P	ADL017	Adult T-Cell Leukemia	56	0.970

153	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	0.970

154	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.970

155		MDD018	Middle East Respiratory Syndrome	44	0.970

156	P	AMY004	Amyloidosis	70	0.970

157	P	DYS154	Dystonia	64	0.970

158	P	TRM003	Tremor	48	0.970

159		MTH009	Mouth Disease	57	0.970

160		LNG039	Lung Squamous Cell Carcinoma	57	0.970

161	P	CTR002	Cataract	60	0.970

162	P	MLN008	Melanoma	76	0.970

163		RBS001	Rabies	58	0.970

164		PLM031	Poliomyelitis	63	0.970

165		LYS002	Lysosomal Storage Disease	51	0.970

166	P	SCK005	Sickle Cell Disease	56	0.970

167		PTT037	Pituitary Tumors	44	0.970

168		MSL001	Measles	61	0.970

169		SPN186	Spinal Cord Injury	61	0.885

170	P	BLD134	Bladder Cancer	79	0.885

171		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.885

172	P	RTN008	Retinitis Pigmentosa	80	0.885

173	P	SCH015	Schizophrenia	74	0.885

174	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.885

175		ATM095	Autoimmune Disease	61	0.885

176	P	FML011	Familial Adenomatous Polyposis	71	0.885

177		MLR004	Malaria	80	0.885

178		DFC004	Deficiency Anemia	74	0.885

179		SCK003	Sickle Cell Anemia	74	0.885

180		DWN001	Down Syndrome	70	0.885

181		DSS032	Disease by Infectious Agent	55	0.885

182		NRR001	Neuroretinitis	42	0.885

183	P	PRK039	Parkinsonism	55	0.885

184		CRN030	Coronary Stenosis	50	0.885

185		RTN023	Retinitis	46	0.885

186	P	EPL164	Epilepsy	68	0.885

187		ADN018	Adenoma	59	0.885

188	P	RTN016	Retinal Degeneration	52	0.885

189	P	LNG064	Lung Cancer Susceptibility 3	70	0.885

190		PLG002	Plague	58	0.885

191		NWC001	Newcastle Disease	47	0.885

192	c	DNT047	Dentinogenesis Imperfecta Type 2	35	0.885

193	P	ATS364	Autism	69	0.792

194	c	HMC039	Hemochromatosis, Type 1	73	0.792

195		OBN001	Ouabain Resistance	16	0.792

196		RTC012	Reticuloendotheliosis, X-Linked	35	0.792

197		ANX010	Anxiety	70	0.792

198		PPL052	Papillomatosis, Confluent and Reticulated	34	0.792

199		MYL009	Myelodysplastic Syndrome	67	0.792

200	P	CHN012	Chondrosarcoma	57	0.792

201	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	0.792

202	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	63	0.792

203		KWS002	Kawasaki Disease	65	0.792

204		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	0.792

205		CRN270	Coronary Artery Dissection, Spontaneous	32	0.792

206		FBR054	Fibroma	44	0.792

207	c	ACT073	Acute Leukemia	58	0.792

208	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	27	0.792

209	P	RHB003	Rhabdomyosarcoma	66	0.792

210	P	MYL006	Myeloid Leukemia	61	0.792

211	P	HML002	Hemolytic Anemia	62	0.792

212		SKN016	Skin Disease	63	0.792

213	P	LVR013	Liver Disease	69	0.792

214	c	HPT001	Hepatitis C	62	0.792

215		MNT002	Mental Depression	57	0.792

216		MRK001	Merkel Cell Carcinoma	64	0.792

217		ANT024	Anthrax Disease	58	0.792

218		BRN028	Brain Cancer	74	0.792

219		CHG001	Chagas Disease	66	0.792

220		ALL029	Allergic Disease	59	0.792

221		MLN003	Melancholia	41	0.792

222	P	ADN016	Adenocarcinoma	63	0.792

223		BRC012	Brucellosis	66	0.792

224	P	RSP003	Respiratory Failure	74	0.792

225		ISC004	Ischemia	61	0.792

226	P	SBS003	Substance Abuse	54	0.792

227	P	KDN017	Kidney Cancer	61	0.792

228	c	FML021	Familial Hypercholesterolemia	72	0.792

229		SQM006	Squamous Cell Carcinoma	60	0.792

230		WLL004	Wallerian Degeneration	38	0.792

231	P	CRN074	Coronary Artery Aneurysm	42	0.792

232		VRL003	Variola Major	43	0.718

233		CVD001	Covid-19	57	0.718

234		PNG002	Pain Agnosia	51	0.718

235	c	CHR708	Chronic Urticaria	42	0.718

236		SML019	Smallpox	55	0.718

237		IRR003	Irritant Dermatitis	47	0.718

238	P	URT039	Urticaria	58	0.718

239	c	TYP008	Type 1 Diabetes Mellitus	70	0.686

240		PLY100	Polyploidy	36	0.686

241		INT358	Intestinal Polyposis Syndrome	25	0.686

242	P	OVR082	Overgrowth Syndrome	49	0.686

243	P	MCH002	Machado-Joseph Disease	62	0.686

244	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.686

245	P	LPR021	Leprosy 3	71	0.686

246	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.686

247		MSC157	Muscular Dystrophy, Duchenne Type	79	0.686

248	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	0.686

249		BRT054	Brittle Bone Disorder	74	0.686

250		MLN071	Melanoma Tumor Antigen Gp90	17	0.686

251	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.686

252	c	ATR087	Atrial Standstill 1	74	0.686

253		FBR032	Fibromuscular Dysplasia	48	0.686

254		WLL001	Williams-Beuren Syndrome	61	0.686

255	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.686

256		ADR016	Adrenal Cortical Carcinoma	62	0.686

257	P	EXN002	Exanthem	58	0.686

258	c	FTL067	Fetal Hemoglobin Quantitative Trait Locus 6	25	0.686

259	P	INF037	Inflammatory Bowel Disease	53	0.686

260		MSC007	Muscle Hypertrophy	64	0.686

261		END062	Endometrial Hyperplasia	48	0.686

262		NNL006	Non-Alcoholic Steatohepatitis	54	0.686

263	c	LKM061	Leukemia, Acute Myeloid	83	0.686

264	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	0.686

265	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	56	0.686

266	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.686

267	c	BRN108	Branchiootic Syndrome 1	62	0.686

268	c	HNT011	Huntington Disease-Like 3	34	0.686

269	P	GST053	Gastric Cancer	83	0.686

270	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.686

271	c	PCH010	Pachyonychia Congenita 3	43	0.686

272	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.686

273	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.686

274		ADR054	Adrenocortical Carcinoma, Hereditary	47	0.686

275		OCL069	Ocular Motor Apraxia	57	0.686

276		PHN003	Phenylketonuria	76	0.686

277	P	SPP010	Suppressor of Tumorigenicity 3	51	0.686

278	P	PRS040	Prostate Cancer	95	0.686

279		HMF008	Hemifacial Atrophy, Progressive	38	0.686

280	P	HMN032	Human Herpesvirus 8	48	0.686

281		BCT022	Bacterial Infectious Disease	56	0.686

282		ARG004	Argyria	26	0.686

283		THY029	Thyroid Carcinoma	51	0.686

284		TRM010	Traumatic Brain Injury	51	0.686

285		CRH001	Crohn's Disease	80	0.686

286	P	PSR002	Psoriasis	63	0.686

287		CHC001	Chickenpox	57	0.686

288		CHR074	Choriocarcinoma	46	0.686

289		HPT022	Hepatoblastoma	54	0.686

290	P	ALP008	Alopecia	54	0.686

291	P	MSC005	Muscular Dystrophy	67	0.686

292	P	ALC033	Alcohol Use Disorder	61	0.686

293		ADR004	Adrenal Cortical Adenocarcinoma	38	0.686

294	c	VRL010	Viral Hepatitis	53	0.686

295	P	BRS044	Breast Adenocarcinoma	58	0.686

296	P	LCT001	Lactic Acidosis	51	0.686

297	P	SYS005	Systemic Scleroderma	74	0.686

298		ACQ007	Acquired Immunodeficiency Syndrome	59	0.686

299	P	ACN011	Acne	57	0.686

300		PST011	Pustulosis of Palm and Sole	52	0.686

301	c	LCL006	Localized Scleroderma	65	0.686

302		FCL003	Facial Hemiatrophy	29	0.686

303	P	PRD008	Periodontitis	64	0.686

304	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.686

305		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	0.686

306	P	DNG005	Dengue Virus	56	0.686

307	P	CHR071	Charcot-Marie-Tooth Disease	64	0.686

308	P	HYP061	Hypertrophic Cardiomyopathy	69	0.686

309		CNN003	Conn's Syndrome	79	0.686

310	c	ACT027	Acute Pancreatitis	60	0.686

311		SNS003	Sensory Peripheral Neuropathy	52	0.686

312	c	BSL007	Basal Cell Carcinoma	68	0.686

313	P	GCH001	Gaucher's Disease	70	0.686

314		KRT009	Keratosis	53	0.686

315	P	HPT021	Hepatitis	69	0.686

316		HGH043	High Grade Glioma	45	0.686

317		TTH006	Tooth Disease	51	0.686

318		CNG034	Congestive Heart Failure	69	0.686

319		CRB039	Cerebrovascular Disease	66	0.686

320		LVR012	Liver Cirrhosis	63	0.686

321	P	PNC044	Pancreatitis	61	0.686

322	P	OVR046	Ovarian Cyst	46	0.686

323		GST045	Gastroenteritis	58	0.686

324	P	BNG032	Benign Mesothelioma	53	0.686

325		DMY004	Demyelinating Disease	50	0.686

326	P	PTS002	Ptosis	52	0.686

327	P	DRR001	Diarrhea	55	0.686

328		ENT004	Enthesopathy	51	0.686

329		PST028	Post-Traumatic Stress Disorder	59	0.686

330	P	RCT021	Rectum Cancer	54	0.686

331		SNL007	Senile Cataract	40	0.686

332	P	NRF002	Neurofibromatosis	57	0.686

333		HNS001	Hansen's Disease	32	0.686

334		SPL018	Splenomegaly	49	0.686

335		HYP266	Hypoxia	57	0.686

336		BRK012	Broken Heart Syndrome	42	0.686

337		CHR178	Chromosomal Triplication	34	0.686

338		LNR005	Linear Scleroderma	21	0.686

339		ALL014	Allergic Encephalomyelitis	34	0.686

340	c	GLM047	Glioma Susceptibility 3	33	0.656

341	c	MSM022	Mismatch Repair Cancer Syndrome 1	70	0.656

342	c	GLM025	Glioma Susceptibility 2	30	0.656

343	c	GLM043	Glioma Susceptibility 9	30	0.656

344		MNN043	Meningioma, Familial	79	0.656

345		VNZ002	Venezuelan Equine Encephalitis	46	0.560

346		ADR022	Adrenomyeloneuropathy	39	0.560

347		HMZ003	Homozygous Familial Hypercholesterolemia	60	0.560

348		SPS019	Spastic Paraparesis	38	0.560

349		CBP002	Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome	19	0.560

350		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	0.560

351	P	ALP061	Alopecia, Androgenetic, 1	49	0.560

352		FRN006	Frontotemporal Dementia	68	0.560

353	c	DWL002	Dowling-Degos Disease 1	58	0.560

354	P	MYS003	Myasthenia Gravis	68	0.560

355	c	XRD022	Xeroderma Pigmentosum, Complementation Group D	56	0.560

356		ADR007	Adrenoleukodystrophy	73	0.560

357	c	THY107	Thymoma, Familial	42	0.560

358		SDD001	Sudden Infant Death Syndrome	60	0.560

359		TNG002	Tangier Disease	64	0.560

360	c	LSS005	Lissencephaly 1	57	0.560

361		ALZ029	Alzheimer Disease Mitochondrial	24	0.560

362	P	DRM053	Dermatitis, Atopic	65	0.560

363		END057	Endometrial Cancer	72	0.560

364		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	0.560

365		MRF001	Marfan Syndrome	76	0.560

366		OBS002	Obsessive-Compulsive Disorder	68	0.560

367		PHS027	Phosphoglycoprotein 1	15	0.560

368		NND010	Nondisjunction	34	0.560

369		CLF027	Cleft Palate, Isolated	64	0.560

370		CRT072	Creutzfeldt-Jakob Disease	68	0.560

371	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	0.560

372		ALC007	Alcohol Dependence	66	0.560

373		ABT001	Abetalipoproteinemia	68	0.560

374	c	OST080	Osteogenesis Imperfecta, Type Ii	56	0.560

375	P	PRK057	Parkinson Disease, Late-Onset	80	0.560

376		ASP002	Aspartylglucosaminuria	58	0.560

377	P	HYP605	Hyperphenylalaninemia, Bh4-Deficient, B	44	0.560

378		FDB001	Foodborne Botulism	55	0.560

379		ISB001	Isobutyryl-Coa Dehydrogenase Deficiency	36	0.560

380		WST001	West Syndrome	59	0.560

381	P	MCL001	Mucolipidosis	49	0.560

382	c	ATS007	Autism Spectrum Disorder	72	0.560

383	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.560

384		AND014	Androgenic Alopecia	47	0.560

385		KRN002	Kearns-Sayre Syndrome	63	0.560

386		HLC007	Helicobacter Pylori Infection	67	0.560

387		NRL016	Neural Tube Defects	81	0.560

388	P	CHR625	Charcot-Marie-Tooth Disease, Demyelinating, Type 1b	57	0.560

389	P	PRP003	Porphyria Cutanea Tarda	66	0.560

390		LTN004	Late-Onset Retinal Degeneration	60	0.560

391		CVT001	Cavitary Optic Disc Anomalies	37	0.560

392		CYS013	Cystinuria	66	0.560

393		NTH001	Netherton Syndrome	61	0.560

394		LRN002	Laron Syndrome	63	0.560

395	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.560

396	c	NMN015	Niemann-Pick Disease, Type C1	68	0.560

397	P	MJR007	Major Affective Disorder 1	42	0.560

398	P	HYP750	Hypertriglyceridemia, Familial	62	0.560

399	P	CRY007	Cryoglobulinemia, Familial Mixed	49	0.560

400		DYS192	Dystonia, Dopa-Responsive	55	0.560

401		THY111	Thyroid Carcinoma, Familial Medullary	67	0.560

402		MYL057	Myelopathy, Htlv-1-Associated	38	0.560

403	c	NRF024	Neurofibromatosis, Type I	72	0.560

404		OCL052	Ocular Dominance	40	0.560

405		PCK003	Pick Disease of Brain	69	0.560

406		ARB004	Arbitrary Restriction Polymorphism 1	14	0.560

407		CHR431	Chronic Venous Insufficiency	48	0.560

408	P	FLL037	Follicular Lymphoma	74	0.560

409	P	VNW001	Von Willebrand's Disease	65	0.560

410	c	CHR095	Chronic Progressive External Ophthalmoplegia	49	0.560

411		CWP001	Cowpox	45	0.560

412	P	ZLL001	Zellweger Syndrome	65	0.560

413		PRX001	Peroxisomal Disease	46	0.560

414	P	BCL017	B-Cell Lymphoma	59	0.560

415	P	MSC003	Muscular Atrophy	52	0.560

416		AVN001	Avian Influenza	61	0.560

417		DRM011	Dermatophytosis	52	0.560

418	P	LCH002	Lichen Planus	54	0.560

419		VRL011	Viral Infectious Disease	61	0.560

420	P	RRH023	Rare Hereditary Hemochromatosis	54	0.560

421	P	MTH008	Methylmalonic Acidemia	52	0.560

422		ALL010	Allergic Contact Dermatitis	56	0.560

423		NRN001	Neuroendocrine Carcinoma	47	0.560

424	P	CHR012	Chronic Granulomatous Disease	69	0.560

425	P	GST044	Gastritis	55	0.560

426		ART016	Aortic Aneurysm	68	0.560

427		GST040	Gastric Adenocarcinoma	67	0.560

428		THY125	Thyroid Gland Medullary Carcinoma	48	0.560

429		PLS011	Plasmacytoma	56	0.560

430		CNN005	Connective Tissue Disease	67	0.560

431		PRT036	Peritonitis	65	0.560

432		OCC001	Occupational Dermatitis	28	0.560

433		END086	End Stage Renal Disease	52	0.560

434		ACT084	Acute Stress Disorder	54	0.560

435		SCB001	Scabies	50	0.560

436		CMB007	Combined Immunodeficiency	57	0.560

437	P	VNS003	Venous Insufficiency	55	0.560

438	P	GRF003	Graft-Versus-Host Disease	71	0.560

439		TCK001	Tick-Borne Encephalitis	59	0.560

440		SWN001	Swine Influenza	46	0.560

441	c	DLT002	Dilated Cardiomyopathy	78	0.560

442	P	DMN002	Dementia	66	0.560

443		HMS001	Hemosiderosis	48	0.560

444	P	NTR004	Neutropenia	63	0.560

445		PCD001	Pica Disease	38	0.560

446	P	HMN010	Hemangioma	62	0.560

447	P	VSC007	Vascular Disease	63	0.560

448		IMP005	Impotence	52	0.560

449		RTN020	Retinal Vascular Disease	46	0.560

450		NRT004	Neuritis	53	0.560

451	c	HPT015	Hepatitis D	49	0.560

452	P	ECT006	Ectodermal Dysplasia	63	0.560

453		SCH014	Schistosomiasis	56	0.560

454	P	HRT032	Heart Disease	81	0.560

455		LPR001	Lepromatous Leprosy	49	0.560

456	P	MCR010	Microcephaly	60	0.560

457		LYM017	Lyme Disease	62	0.560

458		WST002	Western Equine Encephalitis	40	0.560

459		QFV001	Q Fever	62	0.560

460		KRT002	Keratomalacia	55	0.560

461	P	END033	Endocarditis	58	0.560

462	P	DYS005	Dyslexia	41	0.560

463	P	TRT010	Teratoma	51	0.560

464	P	THY023	Thymoma	64	0.560

465	P	MTR014	Motor Neuron Disease	65	0.560

466	P	ART021	Arteriosclerosis	54	0.560

467		CRY004	Cryoglobulinemia	48	0.560

468		TRP002	Tropical Spastic Paraparesis	49	0.560

469		TYP007	Typhoid Fever	64	0.560

470	P	PRP029	Porphyria	60	0.560

471	P	ADL010	Adult Respiratory Distress Syndrome	71	0.560

472		LST001	Listeriosis	59	0.560

473	P	CRD246	Cardiovascular System Disease	56	0.560

474	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	0.560

475		HYP014	Hyperuricemia	51	0.560

476		HYP060	Hyperinsulinism	54	0.560

477	P	MYT002	Myotonic Dystrophy	51	0.560

478		ISL099	Isolated Methylmalonic Acidemia	36	0.560

479		GRN017	Granulocytopenia	42	0.560

480		HTL001	Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis	38	0.560

481		MLT028	Multiminicore Disease	43	0.560

482		ANR040	Aneurysm	61	0.560

483		CHL078	Childhood-Onset Schizophrenia	29	0.560

484		CYT002	Cytokine Deficiency	43	0.560

485		CRC034	Carcinoma Showing Thymus-Like Differentiation	22	0.560

486		MYC019	Mycobacterium Marinum	29	0.560

487		HMR014	Hemorrhagic Shock and Encephalopathy Syndrome	19	0.560

488		LYM126	Lymphoma Aids Related	44	0.560

489		ETN001	Eating Disorder	59	0.560

490		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.396

491		SPN050	Spinocerebellar Degeneration	39	0.396

492	P	PRG139	Progeroid Syndrome	27	0.396

493		CMP097	Complex Chromosomal Rearrangement	23	0.396

494		PST021	Postpartum Depression	50	0.396

495	P	DBT005	Diabetes Insipidus	54	0.396

496	P	SMP003	Simpson-Golabi-Behmel Syndrome	49	0.396

497		SLP010	Slipped Capital Femoral Epiphysis	38	0.396

498		MTC005	Mitochondrial Metabolism Disease	45	0.396

499		CNN002	Cannabis Abuse	45	0.396

500		CNC014	Cancer-Associated Retinopathy	42	0.396

501		STP007	Staphylococcal Scarlet Fever	16	0.396

502		CYT017	Cytophagic Histiocytic Panniculitis	18	0.396

503	P	SZR006	Seizure Disorder	70	0.396

504		CHR603	Chronic Enteropathy Associated with Slco2a1 Gene	25	0.396

505		OST115	Osteonecrosis of the Jaw	41	0.396

506	P	AVS003	Avascular Necrosis	41	0.396

507		STP004	Staphylococcal Toxic Shock Syndrome	45	0.396

508		SPS057	Spasticity	42	0.396

509		MTH086	Methotrexate Toxicity	32	0.396

510	c	B4G002	B4galt7-Related Spondylodysplastic Ehlers-Danlos Syndrome	35	0.396

511	c	ACT134	Acute Liver Failure	59	0.396

512		CLS049	Classic Phenylketonuria	41	0.396

513		THY128	Thyroid Tumor	35	0.396

514		PFF001	Pfeiffer Syndrome	77	0.396

515	c	ALZ049	Alzheimer Disease 2	48	0.396

516	c	EPS035	Episodic Ataxia, Type 2	63	0.396

517	P	BLR024	Biliary Cirrhosis, Primary, 1	28	0.396

518		RST023	Resting Heart Rate, Variation in	40	0.396

519	P	CRN300	Coronary Heart Disease 1	73	0.396

520		NCL008	Nuclear Ribonucleic Acid	15	0.396

521		ORN008	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to	62	0.396

522	P	RTT002	Rett Syndrome	79	0.396

523	c	MCP045	Mucopolysaccharidosis, Type Iiic	59	0.396

524		SMT004	Smith-Lemli-Opitz Syndrome	70	0.396

525	c	OPT051	Opitz Gbbb Syndrome, Type I	46	0.396

526		SQM013	Squamous Cell Carcinoma, Head and Neck	73	0.396

527		HMT020	Hematopoietic Stem Cell Kinetics, Control of	8	0.396

528	P	LSS036	Lissencephaly, X-Linked, 1	47	0.396

529		HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.396

530		CRD223	Cardiac Arrhythmia	63	0.396

531	c	MCR247	Microcephaly 1, Primary, Autosomal Recessive	42	0.396

532	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.396

533	c	MCL046	Mucolipidosis Iii Alpha/beta	60	0.396

534	c	MCL016	Mucolipidosis Iii Gamma	50	0.396

535		ACR009	Acromesomelic Dysplasia, Hunter-Thompson Type	41	0.396

536		ANN002	Anencephaly	57	0.396

537		FBR012	Fabry Disease	70	0.396

538		CRN296	Carnitine Palmitoyltransferase Ii Deficiency, Infantile	64	0.396

539	P	SPR120	Supranuclear Palsy, Progressive, 1	69	0.396

540	c	MTR020	Maturity-Onset Diabetes of the Young, Type 3	54	0.396

541	c	SCH051	Schizophrenia 4	32	0.396

542	P	MTR004	Maturity-Onset Diabetes of the Young	68	0.396

543	P	KLZ004	Kala-Azar 1	41	0.396

544	c	RBN018	Robinow Syndrome, Autosomal Dominant 1	50	0.396

545	P	LFR001	Li-Fraumeni Syndrome	73	0.396

546		LPM012	Lipomatosis, Multiple	60	0.396

547		MCR037	Macroglossia	44	0.396

548	P	MLN066	Melanoma, Cutaneous Malignant 1	66	0.396

549		PRN011	Pernicious Anemia	53	0.396

550		LNT004	Lentigines	46	0.396

551	c	SYS001	Systemic Lupus Erythematosus	87	0.396

552		CRD002	Cri-Du-Chat Syndrome	49	0.396

553	P	EST010	Esterase B	13	0.396

554	P	CLR023	Colorectal Cancer	100	0.396

555		FCT001	Factor Viii Deficiency	60	0.396

556		GLL008	Gilles De La Tourette Syndrome	65	0.396

557		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.396

558	c	MST023	Mesothelioma, Malignant	56	0.396

559	c	OST135	Osteogenesis Imperfecta, Type I	53	0.396

560		OTT002	Otitis Media	71	0.396

561		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	61	0.396

562		HYP781	Hypoascorbemia	52	0.396

563	c	LKM063	Leukemia, Chronic Myeloid	71	0.396

564		MND002	Mandibuloacral Dysplasia with Type B Lipodystrophy	37	0.396

565	P	APL001	Aplastic Anemia	73	0.396

566		CHR100	Chronic Ulcer of Skin	57	0.396

567		PRP027	Peripheral Vascular Disease	71	0.396

568	P	LSS002	Lissencephaly	50	0.396

569		EPD015	Epidemic Typhus	44	0.396

570	P	ADV001	Advanced Sleep Phase Syndrome	41	0.396

571	P	OCL002	Oculocutaneous Albinism	59	0.396

572		FTL006	Fetal Alcohol Spectrum Disorder	43	0.396

573		OPP004	Oppositional Defiant Disorder	49	0.396

574	c	MCR115	Microvascular Complications of Diabetes 5	65	0.396

575	c	MCR130	Microvascular Complications of Diabetes 6	41	0.396

576		MYX005	Myxoid Liposarcoma	65	0.396

577		HYP814	Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency	34	0.396

578	c	RTN134	Retinitis Pigmentosa 40	33	0.396

579	c	CRN110	Cranioectodermal Dysplasia 3	27	0.396

580		HYP003	Hypermethioninemia	51	0.396

581	P	HRD021	Hereditary Sensory Neuropathy	48	0.396

582	c	SVR003	Severe Congenital Neutropenia	59	0.396

583		DFF005	Diffuse Large B-Cell Lymphoma	54	0.396

584		TRC010	Trichotillomania	50	0.396

585	c	RTN106	Retinitis Pigmentosa 51	36	0.396

586		PMP013	Pemphigus Gestationis	19	0.396

587		CHK001	Chikungunya	60	0.396

588	c	SLV029	Silver-Russell Syndrome 2	26	0.396

589		PRT251	Proteinuria, Chronic Benign	57	0.396

590	c	ATM101	Autoimmune Gastritis	40	0.396

591	P	ERY036	Erythema Nodosum	49	0.396

592	P	URN019	Urinary Tract Infection	49	0.396

593		INF034	Infective Endocarditis	54	0.396

594		AMS001	Amusia	24	0.396

595	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.396

596		HMN047	Human Cytomegalovirus Infection	57	0.396

597		WTH001	Withdrawal Disorder	48	0.396

598	P	CTN015	Cutaneous T Cell Lymphoma	48	0.396

599		APR001	Apraxia	52	0.396

600		RSP021	Respiratory Allergy	41	0.396

601		BNR002	Bone Resorption Disease	47	0.396

602	P	SLM003	Salmonellosis	54	0.396

603	c	ERL056	Early-Onset Parkinson's Disease	40	0.396

604		PHY002	Physical Disorder	41	0.396

605		MNN032	Meningococcal Meningitis	53	0.396

606	P	FML023	Familial Hemiplegic Migraine	53	0.396

607		CRH005	Crohn's Colitis	53	0.396

608		PRL013	Paralytic Poliomyelitis	30	0.396

609	c	FML001	Familial Atrial Fibrillation	65	0.396

610	P	FTL001	Fetal Alcohol Syndrome	55	0.396

611		ZLL002	Zollinger-Ellison Syndrome	55	0.396

612		URL001	Urolithiasis	46	0.396

613		BTT017	Beta-Thalassemia Major	51	0.396

614		PMP004	Pemphigus Foliaceus	43	0.396

615	c	RTN041	Retinitis Pigmentosa 11	42	0.396

616		DDN011	Duodenal Atresia	48	0.396

617		TRD006	Tardive Dyskinesia	53	0.396

618	P	TYS001	Tay-Sachs Disease	69	0.396

619	c	TYR012	Tyrosinemia, Type I	61	0.396

620		WRN001	Werner Syndrome	69	0.396

621	c	XRD030	Xeroderma Pigmentosum, Complementation Group C	55	0.396

622		LGH007	Leigh Syndrome	70	0.396

623		SPN360	Spondylometaphyseal Dysplasia, Corner Fracture Type	38	0.396

624		CNT105	Central Core Disease of Muscle	59	0.396

625	c	SPN309	Spinocerebellar Ataxia 6	58	0.396

626	c	PRG020	Paragangliomas 3	39	0.396

627	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.396

628		ALV005	Alveolar Soft Part Sarcoma	61	0.396

629		PRS131	Prostate Cancer/brain Cancer Susceptibility	23	0.396

630		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.396

631		AST006	Astigmatism	47	0.396

632	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.396

633		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	66	0.396

634		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.396

635		ANL018	Analbuminemia	53	0.396

636		HYP110	Hyperproinsulinemia	37	0.396

637	c	LYM150	Lymphatic Malformation 7	38	0.396

638		EWN003	Ewing Sarcoma	70	0.396

639	P	HYP818	Hypobetalipoproteinemia, Familial, 1	60	0.396

640	P	MJR001	Major Depressive Disorder	68	0.396

641		HMM004	Hamamy Syndrome	39	0.396

642	c	MCR312	Microphthalmia, Syndromic 10	40	0.396

643	c	MJR006	Major Affective Disorder 5	32	0.396

644		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	43	0.396

645		ACT119	Acute Promyelocytic Leukemia	62	0.396

646	c	MCR120	Microvascular Complications of Diabetes 7	47	0.396

647		HRN029	Hearing Loss, Noise-Induced	37	0.396

648	c	LPD035	Lipodystrophy, Congenital Generalized, Type 4	45	0.396

649		ALP103	Alpha-1-Antitrypsin Deficiency	68	0.396

650	c	MJR003	Major Affective Disorder 6	32	0.396

651	c	GLY043	Glycogen Storage Disease Xii	30	0.396

652	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.396

653		WST005	West Nile Virus	57	0.396

654	c	PSD048	Pseudo-Von Willebrand Disease	39	0.396

655	c	SCH079	Schizophrenia 1	44	0.396

656		TBL029	Tubulin, Beta	28	0.396

657		GLT038	Glutamyl Ribose-5-Phosphate Storage Disease	8	0.396

658		MNN047	Mannosidosis, Alpha B, Lysosomal	67	0.396

659	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.396

660		PLY068	Polysubstance Abuse	41	0.396

661	c	ALB019	Albinism, Oculocutaneous, Type Iv	48	0.396

662	c	RTN036	Retinal Cone Dystrophy 4	35	0.396

663		RHM035	Rheumatic Fever-Related Antigen	37	0.396

664		ALS001	Alstrom Syndrome	65	0.396

665	c	HMP029	Hemophilia a	68	0.396

666		INC021	Incontinentia Pigmenti	63	0.396

667		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.396

668	c	LFR007	Li-Fraumeni Syndrome 2	46	0.396

669	c	PLN018	Peeling Skin Syndrome 2	38	0.396

670	P	CMP072	Camptodactyly Syndrome, Guadalajara, Type I	31	0.396

671	P	CHN044	Chondrodysplasia Punctata Syndrome	43	0.396

672		PLS030	Plasminogen Deficiency, Type I	51	0.396

673		DYS179	Dyssegmental Dysplasia, Rolland-Desbuquois Type	25	0.396

674	P	GLC113	Galactosemia I	66	0.396

675	c	WLM013	Wilms Tumor 1	66	0.396

676		BTT016	Batten-Turner Congenital Myopathy	53	0.396

677	c	PRD040	Periodontitis, Chronic	52	0.396

678		EPL131	Epilepsy, Pyridoxine-Dependent	45	0.396

679	c	PNC106	Pancreatic Agenesis 1	51	0.396

680		SBC001	Subacute Sclerosing Panencephalitis	53	0.396

681	P	IMR002	Imerslund-Grasbeck Syndrome 1	42	0.396

682		VLC001	Velocardiofacial Syndrome	57	0.396

683		YST001	Yeast Factor	6	0.396

684	P	SRC025	Sarcoidosis 1	71	0.396

685		KRT071	Keratosis, Seborrheic	56	0.396

686	c	NRB010	Neuroblastoma 1	59	0.396

687		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	0.396

688	c	INF071	Inflammatory Bowel Disease 1	65	0.396

689		TBC004	Tobacco Addiction	63	0.396

690	c	TBR025	Tuberous Sclerosis 1	84	0.396

691		HYP732	Hyperalphalipoproteinemia 1	52	0.396

692	c	MLG147	Malignant Hyperthermia 1	45	0.396

693		DFC006	Defective Interfering Particle Induction, Control of	15	0.396

694		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.396

695	c	EXS020	Exostoses, Multiple, Type Ii	38	0.396

696		RNL114	Renal Cell Carcinoma, Nonpapillary	80	0.396

697		HYP042	Hypochondroplasia	59	0.396

698	c	CND033	Candidiasis, Familial, 1	27	0.396

699		CLB010	Coloboma of Macula	53	0.396

700		PPL048	Papillorenal Syndrome	58	0.396

701		DRM046	Dermal Ridges-off-the-End	20	0.396

702	c	EHL076	Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1	33	0.396

703		EPD023	Epidermolysis Bullosa Simplex with Mottled Pigmentation	45	0.396

704	c	EXS019	Exostoses, Multiple, Type I	54	0.396

705		NVS017	Nevus, Epidermal	66	0.396

706		PLT016	Platelet Adenylate Cyclase Activity	16	0.396

707		NPH091	Nephrolithiasis, Calcium Oxalate	61	0.396

708	c	MGR032	Migraine, Familial Hemiplegic, 1	54	0.396

709	P	FTL033	Fetal Hemoglobin Quantitative Trait Locus 1	42	0.396

710	c	FTL065	Fetal Hemoglobin Quantitative Trait Locus 5	16	0.396

711	c	FTL036	Fetal Hemoglobin Quantitative Trait Locus 2	16	0.396

712		ACH004	Achondroplasia	66	0.396

713		SVR095	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency	47	0.396

714		ADP007	Adie Pupil	40	0.396

715	c	OST125	Osteopetrosis, Autosomal Dominant 1	34	0.396

716	P	MYC007	Myocardial Infarction	70	0.396

717	c	EHL085	Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2	46	0.396

718		HYP020	Hyperprolactinemia	63	0.396

719	c	RBN017	Robinow Syndrome, Autosomal Dominant 2	45	0.396

720		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	0.396

721		EST002	Estrogen-Receptor Negative Breast Cancer	45	0.396

722	P	PTN014	Patent Ductus Arteriosus 1	59	0.396

723	c	ATS307	Autosomal Recessive Cerebellar Ataxia	39	0.396

724		GLC003	Glucose Intolerance	54	0.396

725		PRM329	Premature Aging	36	0.396

726		MLD011	Mild Hyperphenylalaninemia	24	0.396

727	P	PLN008	Peeling Skin Syndrome	43	0.396

728	P	HYP730	Hypogonadotropic Hypogonadism	53	0.396

729		LBR036	Leber Plus Disease	66	0.396

730	c	HMP004	Hemophilia B	68	0.396

731	c	MLT095	Multiple Sclerosis 4	18	0.396

732	c	CRN111	Cranioectodermal Dysplasia 4	31	0.396

733		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.396

734		LTX001	Latex Allergy	42	0.396

735		SPN250	Spondyloepimetaphyseal Dysplasia	36	0.396

736	P	LPS004	Lupus Erythematosus	61	0.396

737	c	ACT075	Acute Myocardial Infarction	56	0.396

738		CTN004	Cutaneous Fibrous Histiocytoma	39	0.396

739		CLC001	Calciphylaxis	51	0.396

740		ANG016	Angiokeratoma	37	0.396

741		GST030	Gastrinoma	45	0.396

742		SCH012	Schizoaffective Disorder	50	0.396

743		LCN001	Lice Infestation	41	0.396

744		BRN018	Borna Disease	36	0.396

745		URT010	Ureteral Obstruction	45	0.396

746		CRC021	Carcinosarcoma	64	0.396

747		MLL001	Molluscum Contagiosum	48	0.396

748		NRM001	Neuromyelitis Optica	61	0.396

749		SKN019	Skin Melanoma	71	0.396

750	P	NRC002	Narcolepsy	56	0.396

751		CRV002	Cervix Uteri Carcinoma in Situ	47	0.396

752		VSC003	Visceral Leishmaniasis	55	0.396

753	P	HMC002	Homocystinuria	53	0.396

754	P	TYR004	Tyrosinemia	50	0.396

755	c	BRS049	Breast Carcinoma in Situ	50	0.396

756	P	ACT008	Actinic Keratosis	54	0.396

757		KRT006	Keratoconjunctivitis	53	0.396

758	P	NRP001	Neuropathy	60	0.396

759		LRN003	Learning Disability	49	0.396

760		LSH001	Leishmaniasis	64	0.396

761	P	VND001	Vein Disease	42	0.396

762	P	MVM001	Movement Disease	61	0.396

763		ADN001	Adenosine Deaminase Deficiency	59	0.396

764		ADG002	Audiogenic Seizures	25	0.396

765		NM001	Noma	38	0.396

766		YLL002	Yellow Fever	61	0.396

767	P	HYP098	Hypereosinophilic Syndrome	66	0.396

768		SYN036	Syncope	45	0.396

769	c	FML191	Familial Long Qt Syndrome	55	0.396

770		IMM206	Immune Complex Mediated Vasculitis	13	0.396

771		MNG007	Manganese Poisoning	28	0.396

772	P	PRS038	Personality Disorder	65	0.396

773	P	PTT006	Pituitary Adenoma	55	0.396

774		PNC129	Pancreatic Adenocarcinoma	65	0.396

775		SVR001	Severe Acute Respiratory Syndrome	67	0.396

776	P	ANT006	Antiphospholipid Syndrome	55	0.396

777		CHR001	Churg-Strauss Syndrome	61	0.396

778		GLB002	Glioblastoma	67	0.396

779		CNN001	Cannabis Dependence	38	0.396

780	P	BRD002	Bardet-Biedl Syndrome	66	0.396

781		CLL003	Cellulitis	53	0.396

782	P	TRN020	Turner Syndrome	67	0.396

783	P	CNT009	Central Core Myopathy	43	0.396

784	P	CND004	Candidiasis	58	0.396

785		END040	Endogenous Depression	55	0.396

786	P	PLM036	Pulmonary Fibrosis	66	0.396

787		INS001	Insulinoma	59	0.396

788		SMN006	Seminal Vesicle Tumor	19	0.396

789		ADR005	Adrenal Carcinoma	62	0.396

790		BLD131	Bladder Urothelial Carcinoma	60	0.396

791		TCK004	Tick Infestation	30	0.396

792	P	PNC025	Panic Disorder	52	0.396

793		CLL014	Cll/sll	45	0.396

794		NPH009	Nephrolithiasis	54	0.396

795		ESP023	Esophageal Disease	52	0.396

796		CYC005	Cyclothymic Disorder	40	0.396

797		OST012	Osteoarthritis	77	0.396

798		SBC011	Sebaceous Adenocarcinoma	43	0.396

799		TNC002	Tinea Capitis	42	0.396

800	P	HRD001	Hereditary Multiple Exostoses	48	0.396

801	P	INT070	Intestinal Obstruction	57	0.396

802	P	NGH001	Night Blindness	52	0.396

803	P	MNC007	Monocytic Leukemia	47	0.396

804	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.396

805		SLP001	Sleeping Sickness	56	0.396

806		TRY001	Trypanosomiasis	50	0.396

807		CRB004	Cerebral Artery Occlusion	45	0.396

808		PLM005	Pleomorphic Lipoma	40	0.396

809	P	DRM010	Dermatomyositis	61	0.396

810		RCK004	Rickets	68	0.396

811	c	MCR113	Microvascular Complications of Diabetes 3	52	0.396

812	c	MCR133	Microvascular Complications of Diabetes 4	41	0.396

813		LMB002	Lambert-Eaton Myasthenic Syndrome	52	0.396

814		INH001	Inhalation Anthrax	42	0.396

815	P	MGR003	Migraine with Aura	52	0.396

816		OST003	Osteonecrosis	61	0.396

817	c	PRC016	Pre-Eclampsia	65	0.396

818		GT001	Gout	64	0.396

819		TNC003	Tinea Corporis	40	0.396

820		LYM009	Lymphocytic Choriomeningitis	46	0.396

821	P	MLN007	Male Infertility	56	0.396

822	P	ESP024	Esophagitis	60	0.396

823	P	OPT009	Optic Neuritis	57	0.396

824		SHG001	Shigellosis	63	0.396

825		PRM236	Primary Biliary Cholangitis	60	0.396

826		ALC006	Alcoholic Hepatitis	61	0.396

827	P	SPN046	Spinal Muscular Atrophy	63	0.396

828		PRV004	Periventricular Leukomalacia	52	0.396

829	c	ACT068	Acute Cystitis	61	0.396

830	P	WST004	West Nile Encephalitis	44	0.396

831		WST003	West Nile Fever	40	0.396

832		HRY003	Hairy Cell Leukemia	61	0.396

833		CRD003	Cardiac Sarcoidosis	44	0.396

834	P	HYP069	Hyperparathyroidism	62	0.396

835		CHN002	Chancroid	36	0.396

836		TXC005	Toxic Shock Syndrome	62	0.396

837	P	HYP035	Hypophosphatasia	62	0.396

838		PSY004	Psychotic Disorder	66	0.396

839	P	NMN002	Niemann-Pick Disease	60	0.396

840		PMP002	Pemphigoid Gestationis	38	0.396

841	P	BRS053	Breast Fibroadenoma	49	0.396

842		PPL002	Papillary Carcinoma	46	0.396

843	P	TBR001	Tuberous Sclerosis	69	0.396

844		HYP081	Hypolipoproteinemia	49	0.396

845	P	RHZ001	Rhizomelic Chondrodysplasia Punctata	57	0.396

846		TRN018	Transitional Cell Carcinoma	56	0.396

847	P	LNG028	Long Qt Syndrome	64	0.396

848		HMG005	Hemoglobinopathy	56	0.396

849	P	HYD006	Hydrocephalus	61	0.396

850		HYD002	Hydronephrosis	58	0.396

851	P	CRD119	Cardiac Arrest	67	0.396

852		SPN369	Spinal Disease	44	0.396

853	P	BND020	Bone Disease	59	0.396

854		HYP041	Hypochondrogenesis	35	0.396

855		MCS002	Mucositis	56	0.396

856		PRT013	Portal Hypertension	59	0.396

857		CCT002	Cicatricial Pemphigoid	53	0.396

858		EST003	Eastern Equine Encephalitis	38	0.396

859		BRD004	Borderline Personality Disorder	53	0.396

860		ANH002	Anhidrosis	46	0.396

861	c	PRM005	Primary Hyperparathyroidism	59	0.396

862	P	HRN001	Horner's Syndrome	46	0.396

863	P	NNT058	Neonatal Diabetes	52	0.396

864		TBR006	Tuberculoid Leprosy	43	0.396

865	c	VRL005	Viral Pneumonia	53	0.396

866		MCR013	Microphthalmia	60	0.396

867		CYS010	Cystinosis	62	0.396

868		BRN024	Bronchitis	67	0.396

869		PRG009	Progressive Multifocal Leukoencephalopathy	58	0.396

870	c	HPT007	Hepatitis E	51	0.396

871	P	BRT004	Bartter Disease	58	0.396

872		TST018	Testicular Yolk Sac Tumor	39	0.396

873		ART017	Aortic Disease	49	0.396

874	P	INF032	Infertility	57	0.396

875	P	PRP019	Peripheral Nervous System Disease	58	0.396

876		CHS002	Chiasmal Syndrome	24	0.396

877	P	RTN018	Retinal Disease	53	0.396

878		ANP009	Anaplastic Oligodendroglioma	41	0.396

879		CCN002	Cocaine Abuse	49	0.396

880		PRP030	Purpura	54	0.396

881		BRS099	Breast Ductal Carcinoma	61	0.396

882		GNG013	Gingivitis	59	0.396

883		ANP005	Anaplastic Astrocytoma	57	0.396

884		RCT009	Rectosigmoid Cancer	37	0.396

885		MSN004	Mesenchymal Cell Neoplasm	42	0.396

886	P	LPS002	Liposarcoma	64	0.396

887		NCR004	Nocardiosis	53	0.396

888		PNC034	Pancreas Disease	50	0.396

889	P	HYP073	Hypersensitivity Reaction Type Iv Disease	43	0.396

890		NCR002	Necrobiosis Lipoidica	38	0.396

891		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.396

892		KLB003	Klebsiella Pneumonia	50	0.396

893	P	GND004	Gonadal Dysgenesis	47	0.396

894		HMN048	Human Papillomavirus Infectious Disease	46	0.396

895	P	EHL001	Ehlers-Danlos Syndrome	58	0.396

896		PLS007	Plasmodium Falciparum Malaria	52	0.396

897		GNG003	Gingival Recession	49	0.396

898		PNN001	Panniculitis	52	0.396

899		RHM001	Rheumatic Fever	59	0.396

900		HND002	Hand, Foot and Mouth Disease	50	0.396

901		AMN003	Amnestic Disorder	54	0.396

902		GNR004	Generalized Anxiety Disorder	55	0.396

903		IRN002	Iron Metabolism Disease	57	0.396

904	P	END039	Endodermal Sinus Tumor	41	0.396

905		HYP080	Hypogonadism	50	0.396

906		GST052	Gestational Choriocarcinoma	35	0.396

907	P	ICH004	Ichthyosis	56	0.396

908		UPP004	Upper Respiratory Tract Disease	33	0.396

909		SBS004	Substance Dependence	47	0.396

910		HYP141	Hyperphenylalaninemia	42	0.396

911	P	LMB006	Limb-Girdle Muscular Dystrophy	52	0.396

912		ALB002	Albinism	47	0.396

913	P	INS002	in Situ Carcinoma	53	0.396

914		INV005	Inverted Follicular Keratosis	32	0.396

915	c	ACT135	Acute Graft Versus Host Disease	51	0.396

916		ADS004	Aids Dementia Complex	40	0.396

917	P	CLL015	Collagen Disease	48	0.396

918		GRM010	Germ Cells Tumors	33	0.396

919		NRF007	Neurofibroma	64	0.396

920	P	EPS003	Episodic Ataxia	59	0.396

921		TRC023	Trichinosis	53	0.396

922	P	HMP007	Hemophilia	52	0.396

923		TTR005	Tetrahydrobiopterin Deficiency	48	0.396

924		MYX011	Myxozoa	18	0.396

925		NSS002	Neisseria Meningitidis Infection	47	0.396

926		TRC096	Trichothiodystrophy	55	0.396

927		DPR016	Depression	65	0.396

928		CMP083	Complete Plasminogen Activator Inhibitor 1 Deficiency	27	0.396

929		HRD104	Hereditary Multiple Osteochondromas	43	0.396

930	P	MTC069	Mitochondrial Disorders	57	0.396

931		RP6003	Rpe65-Related Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy	9	0.396

932	P	CRB088	Cerebral Atrophy	33	0.396

933	P	CHR345	Chronic Pain	50	0.396

934		TRP014	Triploidy	38	0.396

935		WLL006	Wells Syndrome	49	0.396

936		AGR019	Age-Related Hearing Loss	41	0.396

937		SRF006	Surfactant Dysfunction	33	0.396

938		CNG069	Congenital Cytomegalovirus	51	0.396

939		ALL012	Allergic Angiitis	24	0.396

940		CRV045	Cervical Intraepithelial Neoplasia	39	0.396

941		CRT033	Corticobasal Degeneration	47	0.396

942	P	OGC005	Oguchi Disease	45	0.396

943		PRS119	Persistent Genital Arousal Disorder	18	0.396

944	c	RNG024	Ring Chromosome 8	28	0.396

945	c	ERL029	Early-Onset, Autosomal Dominant Alzheimer Disease	59	0.396

946		EXN003	Exencephaly	30	0.396

947	c	HMG029	Hemoglobin Se Disease	40	0.396

948		AMN006	Aminoaciduria	37	0.396

949		DWR001	Dwarfism	44	0.396

950	c	FML053	Familial Colorectal Cancer	48	0.396

951	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.396

952