Search results for (2E)-Decenoyl-CoA

789 hits were found for (2E)-Decenoyl-CoA

#	Family	MCID	Name	MIFTS	Score
1	P	CHR654	Charcot-Marie-Tooth Disease, Axonal, Type 2e	58	42.633

2	c	WRD033	Waardenburg Syndrome, Type 2e	53	32.084

3	c	MSC176	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 4	48	28.406

4	c	PNT034	Pontocerebellar Hypoplasia, Type 2e	52	24.797

5	c	MSC170	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 2	66	22.497

6	c	PSD092	Pseudohypoaldosteronism, Type Iie	48	20.020

7	c	MSC169	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1	61	18.415

8		IMM140	Immunodeficiency 47	56	15.692

9		GNY003	Guanylate Cyclase 2e, Pseudogene	12	10.141

10	c	ART054	Arthrogryposis, Distal, Type 2e	14	9.506

11	P	LMB006	Limb-Girdle Muscular Dystrophy	52	6.612

12	P	MSC005	Muscular Dystrophy	67	6.458

13	P	ICH004	Ichthyosis	56	4.366

14		ICH002	Ichthyosis Bullosa of Siemens	41	4.313

15	P	CHR071	Charcot-Marie-Tooth Disease	64	4.155

16		TTH006	Tooth Disease	51	4.155

17		KRT009	Keratosis	53	4.050

18	P	NRP001	Neuropathy	60	3.944

19		EPD002	Epidermolytic Hyperkeratosis	56	3.731

20		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	3.729

21	P	ATS411	Autosomal Dominant Epidermolytic Ichthyosis	36	3.673

22	P	QLT011	Qualitative or Quantitative Defects of Sarcoglycan	26	3.474

23	c	PLM127	Pulmonary Hypertension, Primary, 3	34	3.093

24	P	VNW001	Von Willebrand's Disease	65	3.039

25	P	HML001	Hemolytic-Uremic Syndrome	52	2.808

26	c	HYP836	Hypercholesterolemia, Familial, 1	73	2.780

27	c	FML021	Familial Hypercholesterolemia	72	2.780

28	P	PRP019	Peripheral Nervous System Disease	58	2.679

29		HLX001	Helix Syndrome	48	2.342

30		NRL005	Neurilemmoma	60	2.342

31		EXF002	Exfoliative Ichthyosis	25	2.291

32		ATM095	Autoimmune Disease	61	2.281

33		HRW001	Hair Whorl	35	2.281

34		SNS003	Sensory Peripheral Neuropathy	52	2.241

35		GLM045	Glioma	63	2.217

36		MSC157	Muscular Dystrophy, Duchenne Type	79	2.189

37	c	CHR656	Charcot-Marie-Tooth Disease, Demyelinating, Type 1f	46	2.184

38	c	DWL002	Dowling-Degos Disease 1	58	2.044

39		SJG002	Sjogren-Larsson Syndrome	54	2.005

40	c	HPT073	Hepatitis C Virus	71	2.005

41		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	2.005

42	P	NRB001	Neuroblastoma	66	2.005

43		ACT098	Acute Erythroid Leukemia	55	1.926

44	c	VNW005	Von Willebrand Disease, Type 1	45	1.926

45		LPD008	Lipid Metabolism Disorder	62	1.926

46		NRR001	Neuroretinitis	42	1.921

47		RTN023	Retinitis	46	1.921

48		RPD005	Rapidly Involuting Congenital Hemangioma	46	1.882

49		HYP066	Hyperglycemia	61	1.882

50	P	SCH015	Schizophrenia	74	1.843

51	P	HYP750	Hypertriglyceridemia, Familial	62	1.843

52		ALL014	Allergic Encephalomyelitis	34	1.843

53	P	SZR006	Seizure Disorder	70	1.792

54		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	1.776

55	P	RTN008	Retinitis Pigmentosa	80	1.776

56	P	CLR023	Colorectal Cancer	100	1.768

57	P	PNC035	Pancreatic Cancer	86	1.753

58	c	PCH010	Pachyonychia Congenita 3	43	1.753

59	P	BCL017	B-Cell Lymphoma	59	1.753

60	P	TRM003	Tremor	48	1.753

61	P	HPT023	Hepatocellular Carcinoma	96	1.656

62	P	LNG064	Lung Cancer Susceptibility 3	70	1.646

63	c	MSC171	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5	42	1.624

64	P	AXN001	Axonal Neuropathy	35	1.587

65		MNN043	Meningioma, Familial	79	1.548

66		SCR001	Secretory Meningioma	40	1.548

67		LYM002	Lymphoplasmacyte-Rich Meningioma	35	1.548

68		SPN021	Spinal Meningioma	50	1.548

69		CHR178	Chromosomal Triplication	34	1.548

70	P	LKM062	Leukemia, Acute Lymphoblastic	69	1.544

71	P	OPT006	Optic Nerve Disease	58	1.514

72	P	BRS047	Breast Cancer	98	1.444

73	P	DRR001	Diarrhea	55	1.444

74		ESP021	Esophageal Cancer	83	1.426

75		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	1.408

76	c	MCL042	Macular Degeneration, Age-Related, 1	85	1.370

77	c	MSC177	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 3	42	1.356

78	c	CHR676	Charcot-Marie-Tooth Disease, Dominant Intermediate G	24	1.355

79	c	WRD029	Waardenburg Syndrome, Type 2b	29	1.315

80	c	WRD031	Waardenburg Syndrome, Type 3	45	1.315

81	c	WRD032	Waardenburg Syndrome, Type 2a	47	1.315

82	P	WRD001	Waardenburg's Syndrome	60	1.315

83		ANS002	Aniseikonia	32	1.291

84		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	1.291

85		SCT002	Scotoma	42	1.291

86	c	HPT001	Hepatitis C	62	1.291

87		ANX004	Anoxia	40	1.281

88		HGH043	High Grade Glioma	45	1.281

89		PRG009	Progressive Multifocal Leukoencephalopathy	58	1.281

90		GST045	Gastroenteritis	58	1.281

91		EPD050	Epidermolysis Bullosa Simplex with Muscular Dystrophy	56	1.231

92		BNG077	Benign Idiopathic Neonatal Seizures	23	1.208

93	P	KLZ004	Kala-Azar 1	41	1.208

94		LSH001	Leishmaniasis	64	1.208

95		SVR001	Severe Acute Respiratory Syndrome	67	1.208

96		CLN015	Colon Adenocarcinoma	65	1.208

97		HMN044	Human Immunodeficiency Virus Type 1	78	1.141

98		LBR036	Leber Plus Disease	66	1.141

99	P	MSC003	Muscular Atrophy	52	1.141

100		ACQ007	Acquired Immunodeficiency Syndrome	59	1.141

101		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	1.141

102	P	SPN046	Spinal Muscular Atrophy	63	1.141

103		NRT004	Neuritis	53	1.141

104		NRF007	Neurofibroma	64	1.141

105	c	BRN108	Branchiootic Syndrome 1	62	1.131

106	P	EPL164	Epilepsy	68	1.131

107		MCR013	Microphthalmia	60	1.131

108	P	LNG032	Lung Cancer	98	1.118

109	P	RTN209	Retinoschisis 1, X-Linked, Juvenile	60	1.118

110		CLR109	Colorectal Adenocarcinoma	50	1.118

111		CMB039	Combined Pulmonary Fibrosis-Emphysema Syndrome	18	1.118

112		GLL048	Glial Tumor	52	1.118

113	P	FBR017	Fibrosarcoma	56	1.118

114	P	RTN018	Retinal Disease	53	1.118

115		XLN247	X-Linked Congenital Retinoschisis	20	1.118

116	P	JVN042	Juvenile Retinoschisis	39	1.118

117		MTR087	Maternal Uniparental Disomy	28	1.092

118	c	MTR062	Maternal Uniparental Disomy of Chromosome 4	18	1.092

119	c	ATR087	Atrial Standstill 1	74	1.092

120	c	LKM063	Leukemia, Chronic Myeloid	71	1.092

121	c	PLM121	Pulmonary Hypertension, Primary, 4	28	1.092

122	c	TYP009	Type 2 Diabetes Mellitus	92	1.092

123	P	HYP077	Hypertrichosis	46	1.092

124		DBT010	Diabetic Neuropathy	54	1.092

125		GLB002	Glioblastoma	67	1.092

126	P	THY032	Thyroiditis	57	1.092

127		BRN028	Brain Cancer	74	1.092

128	P	MLN008	Melanoma	76	1.092

129		STT001	Status Epilepticus	59	1.092

130		BRN071	Brain Injury	50	1.092

131	P	ALZ034	Alzheimer Disease	87	1.021

132		SCH060	Schistosoma Mansoni Infection, Susceptibility/	38	1.021

133	P	SRC025	Sarcoidosis 1	71	1.021

134		BCT022	Bacterial Infectious Disease	56	1.021

135	P	MYP006	Myopia	56	1.021

136		DRM011	Dermatophytosis	52	1.021

137		VSC003	Visceral Leishmaniasis	55	1.021

138	P	BRS044	Breast Adenocarcinoma	58	1.021

139		CMM005	Common Cold	56	1.021

140		GLS001	Gliosarcoma	64	1.021

141		SCH014	Schistosomiasis	56	1.021

142	P	HRT032	Heart Disease	81	1.021

143	c	HPT016	Hepatitis B	62	1.021

144	c	RNG007	Ring Chromosome 12	27	1.021

145		DSS012	Disseminated Infection with Mycobacterium Avium Complex	19	1.021

146	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	0.952

147	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.952

148	c	CHR352	Charcot-Marie-Tooth Disease, Axonal, Type 2f	45	0.952

149	c	NRN041	Neuronopathy, Distal Hereditary Motor, Type Iib	33	0.952

150	c	DST106	Distal Hereditary Motor Neuronopathy Type 2	41	0.952

151	c	CHR699	Charcot-Marie-Tooth Disease Type 2a2a	28	0.952

152	P	MVM001	Movement Disease	61	0.952

153		MFN001	Mfn2 Hereditary Motor and Sensory Neuropathy	13	0.952

154		DYS073	Dysphagia	53	0.952

155	P	PSR002	Psoriasis	63	0.927

156	P	CRN300	Coronary Heart Disease 1	73	0.913

157		END057	Endometrial Cancer	72	0.913

158	P	MLT020	Multiple Sclerosis	79	0.913

159	P	PRK057	Parkinson Disease, Late-Onset	80	0.913

160	P	ANP001	Anaplastic Large Cell Lymphoma	61	0.913

161		LWG006	Low Grade Glioma	41	0.913

162	P	LYM118	Lymphoma	67	0.913

163		NNL005	Non-Alcoholic Fatty Liver Disease	63	0.913

164		IMM167	Immune Deficiency Disease	78	0.913

165	P	GST053	Gastric Cancer	83	0.913

166		SZR028	Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome	36	0.913

167	P	PRK039	Parkinsonism	55	0.913

168		TRM010	Traumatic Brain Injury	51	0.913

169	P	DBT009	Diabetes Mellitus	67	0.913

170		CRB004	Cerebral Artery Occlusion	45	0.913

171		CNT016	Central Retinal Vein Occlusion	54	0.913

172	P	HPT021	Hepatitis	69	0.913

173		SVR004	Severe Combined Immunodeficiency	72	0.913

174		LVR012	Liver Cirrhosis	63	0.913

175	P	GLM007	Glomerulonephritis	60	0.913

176	P	HMP007	Hemophilia	52	0.913

177		HNM002	Hinman Syndrome	27	0.858

178	c	BLD140	Blood Group, I System	46	0.858

179		ADP007	Adie Pupil	40	0.858

180	P	NSP012	Nasopharyngeal Carcinoma	61	0.791

181		CRV035	Cervical Cancer	73	0.791

182		ANX010	Anxiety	70	0.791

183		PLY150	Polykaryocytosis Inducer	29	0.791

184	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.791

185	P	URN019	Urinary Tract Infection	49	0.791

186	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	0.791

187	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	80	0.791

188		NRL016	Neural Tube Defects	81	0.791

189		DWN001	Down Syndrome	70	0.791

190	c	SML038	Small Cell Cancer of the Lung	69	0.791

191		HND015	Hand Skill, Relative	30	0.791

192	P	MYP004	Myopathy	67	0.791

193		PRM133	Primary Pulmonary Lymphoma	16	0.791

194	P	LVR013	Liver Disease	69	0.791

195		PRT036	Peritonitis	65	0.791

196		ANT024	Anthrax Disease	58	0.791

197	c	PLM128	Pulmonary Hypertension, Primary, 2	28	0.791

198		TRY001	Trypanosomiasis	50	0.791

199		GST027	Gastric Lymphoma	46	0.791

200		CHG001	Chagas Disease	66	0.791

201		PTS001	Patau Syndrome	56	0.791

202		STM006	Stomach Disease	47	0.791

203	c	ACT071	Acute Kidney Failure	60	0.791

204		LNG013	Lung Lymphoma	31	0.791

205	c	ATS246	Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2c	33	0.711

206	c	ATS277	Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2d	41	0.711

207	P	CLP009	Calpain-3-Related Limb-Girdle Muscular Dystrophy R1	30	0.711

208	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.701

209		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	58	0.701

210		VSL002	Visual Epilepsy	39	0.701

211		CLF004	Cleft Lip/palate	57	0.646

212	P	HRD217	Hereditary Optic Neuropathy	36	0.646

213		OBN001	Ouabain Resistance	16	0.646

214		AMN014	Aminopterin Syndrome Sine Aminopterin	32	0.646

215	c	SCL052	Scleroderma, Familial Progressive	61	0.646

216	c	MSC172	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 8	44	0.646

217	c	MYS033	Miyoshi Muscular Dystrophy 1	52	0.646

218		INS024	Insulin-Like Growth Factor I	78	0.646

219		ART002	Arts Syndrome	66	0.646

220		AGN016	Aging	54	0.646

221		NRP045	Neuropathy, Ataxia, and Retinitis Pigmentosa	47	0.646

222	c	MSC174	Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 7	42	0.646

223	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.646

224		CHR005	Chorioamnionitis	50	0.646

225	c	VNW010	Von Willebrand Disease, Type 2	48	0.646

226		TTH002	Tooth Agenesis	61	0.646

227		DFF005	Diffuse Large B-Cell Lymphoma	54	0.646

228	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	48	0.646

229	P	STR022	Stargardt Disease	61	0.646

230		CLT003	Colitis	63	0.646

231		BNR002	Bone Resorption Disease	47	0.646

232		THR024	Thrombosis	56	0.646

233	P	CNG010	Congenital Stationary Night Blindness	56	0.646

234		INT017	Intestinal Schistosomiasis	51	0.646

235	c	LKM061	Leukemia, Acute Myeloid	83	0.646

236		MLC004	Mulchandani-Bhoj-Conlin Syndrome	51	0.646

237		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.646

238	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	65	0.646

239		LBR038	Leber Hereditary Optic Neuropathy, Modifier of	62	0.646

240		TTH030	Teeth, Supernumerary	33	0.646

241	P	PRS040	Prostate Cancer	95	0.646

242	c	GLC092	Glaucoma, Primary Open Angle	62	0.646

243		PRT112	Portal Hypertension, Noncirrhotic	30	0.646

244		ORL015	Oral Squamous Cell Carcinoma	43	0.646

245	P	OPN001	Open-Angle Glaucoma	55	0.646

246		BRN004	Brain Edema	54	0.646

247	P	EPD003	Epidermolysis Bullosa Simplex	57	0.646

248		BNM001	Bone Marrow Cancer	46	0.646

249		NRM001	Neuromyelitis Optica	61	0.646

250	P	NRC002	Narcolepsy	56	0.646

251		CLF001	Cleft Lip	53	0.646

252		CHC001	Chickenpox	57	0.646

253		YLL002	Yellow Fever	61	0.646

254		47X002	47,xyy	48	0.646

255		SKN016	Skin Disease	63	0.646

256	P	SKN015	Skin Carcinoma	71	0.646

257	P	RTN016	Retinal Degeneration	52	0.646

258		PPT005	Peptic Ulcer Disease	58	0.646

259	P	ART022	Arthritis	71	0.646

260		OST012	Osteoarthritis	77	0.646

261	P	NGH001	Night Blindness	52	0.646

262		SLP001	Sleeping Sickness	56	0.646

263	P	DNG005	Dengue Virus	56	0.646

264	P	DMN002	Dementia	66	0.646

265	P	UVT001	Uveitis	57	0.646

266		GT001	Gout	64	0.646

267		ALL029	Allergic Disease	59	0.646

268		CRY005	Cryptococcosis	60	0.646

269	P	OPT009	Optic Neuritis	57	0.646

270	P	LKM002	Leukemia	67	0.646

271		DNT012	Dental Caries	53	0.646

272	P	ACH003	Achromatopsia	62	0.646

273		GST033	Gestational Diabetes	61	0.646

274		CNG034	Congestive Heart Failure	69	0.646

275		ISC004	Ischemia	61	0.646

276		EMB004	Embryonal Carcinoma	56	0.646

277	P	EPD016	Epidermolysis Bullosa	53	0.646

278		DRM006	Dermatitis	62	0.646

279	P	PTS002	Ptosis	52	0.646

280		GST023	Gastric Ulcer	52	0.646

281		IRN002	Iron Metabolism Disease	57	0.646

282	P	BNC003	Bone Cancer	58	0.646

283		DYS032	Dystrophinopathies	47	0.646

284		RFR003	Refractive Error	41	0.646

285		DPR016	Depression	65	0.646

286	P	CHR345	Chronic Pain	50	0.646

287		CRD132	Cardiac Conduction Defect	60	0.635

288		ADG002	Audiogenic Seizures	25	0.635

289		INS001	Insulinoma	59	0.635

290		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.495

291		GNT176	Genetic Motor Neuron Disease	20	0.495

292	c	ATS452	Autosomal Recessive Axonal Hereditary Motor and Sensory Neuropathy	18	0.495

293		SPS019	Spastic Paraparesis	38	0.495

294	c	WRD010	Waardenburg Syndrome Type 4	30	0.495

295	c	AXN013	Axonal Hereditary Motor and Sensory Neuropathy	13	0.495

296	c	SPS128	Spastic Paraplegia 7, Autosomal Recessive	58	0.495

297	P	SPS133	Spastic Paraplegia 2, X-Linked	50	0.495

298	c	CHR646	Charcot-Marie-Tooth Disease, Axonal, Type 2b	50	0.495

299		MST006	Mast Syndrome	40	0.495

300	c	SPS108	Spastic Paraplegia 5a, Autosomal Recessive	42	0.495

301	c	PNT044	Pontocerebellar Hypoplasia, Type 2a	41	0.495

302		ALB025	Albinism, Ocular, with Late-Onset Sensorineural Deafness	49	0.495

303	c	SPS222	Spastic Paraplegia 20, Autosomal Recessive	56	0.495

304		ATX047	Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, with Optic Atrophy and Mental Retardation	23	0.495

305	c	SPS219	Spastic Paraplegia 17, Autosomal Dominant	42	0.495

306	c	SPS125	Spastic Paraplegia 15, Autosomal Recessive	49	0.495

307	c	NRP053	Neuropathy, Hereditary Sensory and Autonomic, Type Iia	67	0.495

308	c	AMY058	Amyotrophic Lateral Sclerosis 2, Juvenile	41	0.495

309	c	WRD026	Waardenburg Syndrome, Type 2c	26	0.495

310	c	SPS110	Spastic Paraplegia 19, Autosomal Dominant	29	0.495

311		MYP136	Myopathy, Centronuclear, X-Linked	59	0.495

312	c	AMY045	Amyotrophic Lateral Sclerosis 4, Juvenile	49	0.495

313	c	SPS127	Spastic Paraplegia 6, Autosomal Dominant	48	0.495

314	c	NRN037	Neuronopathy, Distal Hereditary Motor, Type Va	49	0.495

315	c	CHR649	Charcot-Marie-Tooth Disease, Axonal, Type 2d	46	0.495

316	c	SPS151	Spastic Paraplegia 11, Autosomal Recessive	49	0.495

317		NRP049	Neuropathy, Hereditary Sensory and Autonomic, Type I, with Cough and Gastroesophageal Reflux	32	0.495

318	c	CHR350	Charcot-Marie-Tooth Disease, Axonal, Type 2k	47	0.495

319	P	DYS193	Dystonia 11, Myoclonic	55	0.495

320		NRP051	Neuropathy, Hereditary, with Liability to Pressure Palsies	54	0.495

321	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.495

322		MLN065	Melanocytic Nevus Syndrome, Congenital	62	0.495

323		TTZ003	Tietz Albinism-Deafness Syndrome	59	0.495

324		PPL049	Papillon-Lefevre Syndrome	66	0.495

325		SLW005	Slowed Nerve Conduction Velocity, Autosomal Dominant	35	0.495

326	c	CHR353	Charcot-Marie-Tooth Disease, Axonal, Type 2l	41	0.495

327		PRP066	Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease	50	0.495

328		GLD006	Goldberg-Shprintzen Syndrome	49	0.495

329	P	OCL001	Ocular Albinism	48	0.495

330	P	DST002	Distal Arthrogryposis	65	0.495

331		DYS001	Dyskinetic Cerebral Palsy	31	0.495

332	P	PRR025	Perrault Syndrome	42	0.495

333	c	SPS123	Spastic Paraplegia 32, Autosomal Recessive	33	0.495

334	c	NRP039	Neuropathy, Hereditary Sensory, Type Id	39	0.495

335	c	NRP029	Neuropathy, Hereditary Sensory, Type Iic	36	0.495

336	c	CHR026	Charcot-Marie-Tooth Disease Type X	25	0.495

337	c	CHR025	Charcot-Marie-Tooth Disease Intermediate Type	29	0.495

338	P	HRD021	Hereditary Sensory Neuropathy	48	0.495

339	c	SPN444	Spinal Muscular Atrophy Type 0	22	0.495

340	c	AMY081	Amyotrophic Lateral Sclerosis Type 12	28	0.495

341	c	AMY074	Amyotrophic Lateral Sclerosis Type 14	21	0.495

342	c	AMY079	Amyotrophic Lateral Sclerosis Type 15	26	0.495

343		INT072	Intestinal Pseudo-Obstruction	62	0.495

344	c	AMY022	Amyotrophic Lateral Sclerosis Type 5	33	0.495

345	c	AMY023	Amyotrophic Lateral Sclerosis Type 6	34	0.495

346	c	OPT023	Optic Atrophy 2	32	0.495

347	c	CHR647	Charcot-Marie-Tooth Disease, Demyelinating, Type 1c	46	0.495

348	c	CHR521	Charcot-Marie-Tooth Disease, Type 4b1	47	0.495

349	c	CHR376	Charcot-Marie-Tooth Disease, Type 4d	47	0.495

350	c	CHR516	Charcot-Marie-Tooth Disease, Type 4c	48	0.495

351	c	AMY094	Amyotrophic Lateral Sclerosis 5, Juvenile	31	0.495

352	c	PNT043	Pontocerebellar Hypoplasia, Type 4	41	0.495

353	c	WRD020	Waardenburg Syndrome, Type 4a	49	0.495

354	c	SPS198	Spastic Paraplegia 16, X-Linked	30	0.495

355	P	PHS005	Peho Syndrome	44	0.495

356	P	CHR625	Charcot-Marie-Tooth Disease, Demyelinating, Type 1b	57	0.495

357	c	CHR626	Charcot-Marie-Tooth Disease, Axonal, Type 2a1	36	0.495

358	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	56	0.495

359		CHR629	Charcot-Marie-Tooth Disease and Deafness	50	0.495

360	c	SPS117	Spastic Paraplegia 10, Autosomal Dominant	48	0.495

361	c	CHR650	Charcot-Marie-Tooth Disease, Axonal, Type 2b1	45	0.495

362	c	CHR651	Charcot-Marie-Tooth Disease, Axonal, Type 2b2	39	0.495

363	P	HRD094	Hereditary Motor and Sensory Neuropathy, Type Iic	48	0.495

364	c	SPS149	Spastic Paraplegia 8, Autosomal Dominant	48	0.495

365	P	SPN408	Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1	51	0.495

366		NRP009	Neuropathy, Hereditary Motor and Sensory, Okinawa Type	32	0.495

367	c	SPS068	Spastic Paraplegia 14, Autosomal Recessive	29	0.495

368	P	NRP063	Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive	58	0.495

369	c	SPS097	Spastic Paraplegia 13, Autosomal Dominant	41	0.495

370		NRP010	Neuropathy, Hereditary Motor and Sensory, Russe Type	36	0.495

371	c	SPN326	Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2	38	0.495

372	c	ALZ053	Alzheimer Disease 7	32	0.495

373	c	CHR519	Charcot-Marie-Tooth Disease, Type 4b2	48	0.495

374	c	SPS131	Spastic Paraplegia 12, Autosomal Dominant	41	0.495

375	c	SPS103	Spastic Paraplegia 50, Autosomal Recessive	41	0.495

376	c	MYP081	Myopathy, Myofibrillar, 6	41	0.495

377	c	SPS071	Spastic Paraplegia 48, Autosomal Recessive	44	0.495

378	c	CHR671	Charcot-Marie-Tooth Disease, Axonal, Type 2r	37	0.495

379		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	0.495

380	c	CRT074	Cortical Dysplasia, Complex, with Other Brain Malformations 6	32	0.495

381		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	55	0.495

382	c	CHR514	Charcot-Marie-Tooth Disease, Recessive Intermediate D	27	0.495

383	c	CHR544	Charcot-Marie-Tooth Disease, Axonal, Type 2w	34	0.495

384	c	CHR618	Charcot-Marie-Tooth Disease, Axonal, Type 2cc	28	0.495

385		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	0.495

386	c	PNT036	Pontocerebellar Hypoplasia, Type 6	46	0.495

387		GLC105	Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency	33	0.495

388	c	CHR670	Charcot-Marie-Tooth Disease, Demyelinating, Type 4f	43	0.495

389	c	SPS106	Spastic Paraplegia 54, Autosomal Recessive	42	0.495

390	c	SPS119	Spastic Paraplegia 55, Autosomal Recessive	39	0.495

391		CLD014	Cole Disease	38	0.495

392	c	SPS137	Spastic Paraplegia 57, Autosomal Recessive	39	0.495

393	c	SPS157	Spastic Paraplegia 64, Autosomal Recessive	40	0.495

394	c	SPS141	Spastic Paraplegia 61, Autosomal Recessive	37	0.495

395	c	SPS228	Spastic Paraplegia 63, Autosomal Recessive	35	0.495

396	c	SPS107	Spastic Paraplegia 18, Autosomal Recessive	41	0.495

397	P	AMY106	Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia	44	0.495

398	c	SPS096	Spastic Paraplegia 44, Autosomal Recessive	38	0.495

399	c	WRD024	Waardenburg Syndrome, Type 4c	43	0.495

400	c	WRD019	Waardenburg Syndrome, Type 4b	45	0.495

401	c	CHR351	Charcot-Marie-Tooth Disease, Axonal, Type 2n	41	0.495

402	c	SPS115	Spastic Paraplegia 41, Autosomal Dominant	29	0.495

403	c	NRN018	Neuronopathy, Distal Hereditary Motor, Type Iic	34	0.495

404	c	NRP040	Neuropathy, Hereditary Sensory and Autonomic, Type Ic	42	0.495

405	c	CHR666	Charcot-Marie-Tooth Disease, Recessive Intermediate B	36	0.495

406	c	PNT049	Pontocerebellar Hypoplasia, Type 2d	43	0.495

407	c	SPS095	Spastic Paraplegia 47, Autosomal Recessive	43	0.495

408	c	SPS122	Spastic Paraplegia 52, Autosomal Recessive	39	0.495

409	c	CHR420	Charcot-Marie-Tooth Disease, Type 4j	48	0.495

410	c	AMY085	Amyotrophic Lateral Sclerosis 9	36	0.495

411	c	SPS129	Spastic Paraplegia 39, Autosomal Recessive	44	0.495

412	c	SPS153	Spastic Paraplegia 35, Autosomal Recessive	50	0.495

413	c	SPS099	Spastic Paraplegia 42, Autosomal Dominant	40	0.495

414	c	SPS113	Spastic Paraplegia 33, Autosomal Dominant	37	0.495

415		PHS023	Phosphoserine Aminotransferase Deficiency	41	0.495

416	P	CHR640	Charcot-Marie-Tooth Disease, X-Linked Dominant, 1	51	0.495

417	c	CHR641	Charcot-Marie-Tooth Disease, X-Linked Recessive, 2	33	0.495

418		MSS001	Masa Syndrome	60	0.495

419		SPN402	Spinal Muscular Atrophy, X-Linked 2	48	0.495

420	c	PNT046	Pontocerebellar Hypoplasia, Type 5	30	0.495

421	c	SPS148	Spastic Paraplegia 31, Autosomal Dominant	47	0.495

422	c	SPN191	Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4	46	0.495

423		ALX003	Alexander Disease	61	0.495

424	c	LBR004	Leber Congenital Amaurosis 1	52	0.495

425	c	AMY090	Amyotrophic Lateral Sclerosis 8	43	0.495

426	c	NRP037	Neuropathy, Hereditary Sensory and Autonomic, Type V	55	0.495

427	c	WRD022	Waardenburg Syndrome, Type 2d	33	0.495

428	c	SPS116	Spastic Paraplegia 26, Autosomal Recessive	40	0.495

429	c	CHR421	Charcot-Marie-Tooth Disease, Type 4h	46	0.495

430	c	SPS124	Spastic Paraplegia 28, Autosomal Recessive	41	0.495

431		BHR001	Behr Syndrome	51	0.495

432	c	CHR517	Charcot-Marie-Tooth Disease, Type 4a	45	0.495

433		YNS002	Yunis-Varon Syndrome	50	0.495

434		HLN001	Halo Nevi	27	0.495

435	c	WRD030	Waardenburg Syndrome, Type 1	53	0.495

436	c	GNT049	Giant Axonal Neuropathy 1, Autosomal Recessive	48	0.495

437		PYC001	Pycnodysostosis	55	0.495

438		TLC001	Telecanthus	35	0.495

439		SCP002	Scapuloperoneal Spinal Muscular Atrophy	55	0.495

440	c	SPS147	Spastic Paraplegia 4, Autosomal Dominant	55	0.495

441		RSS026	Roussy-Levy Hereditary Areflexic Dystasia	46	0.495

442		DLT018	Dilution, Pigmentary	25	0.495

443		HYP186	Hypertrophic Neuropathy of Dejerine-Sottas	51	0.495

444	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	57	0.495

445		PBL005	Piebald Trait	59	0.495

446		HTR005	Heterochromia Iridis	21	0.495

447	P	HRS035	Hirschsprung Disease 1	66	0.495

448	P	CMP005	Campomelic Dysplasia	65	0.495

449	c	NRN040	Neuronopathy, Distal Hereditary Motor, Type Viib	45	0.495

450	c	CHR371	Charcot-Marie-Tooth Disease, Dominant Intermediate C	41	0.495

451	c	CHR658	Charcot-Marie-Tooth Disease, Recessive Intermediate a	38	0.495

452	c	AMY063	Amyotrophic Lateral Sclerosis 20	31	0.495

453	c	CHR547	Charcot-Marie-Tooth Disease, Axonal, Type 2u	38	0.495

454	c	DVL055	Developmental and Epileptic Encephalopathy 29	37	0.495

455	c	LKD023	Leukodystrophy, Hypomyelinating, 12	38	0.495

456	c	CHR542	Charcot-Marie-Tooth Disease, Axonal, Type 2t	36	0.495

457		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	60	0.495

458	c	CHR652	Charcot-Marie-Tooth Disease, Axonal, Type 2i	38	0.495

459	c	CHR653	Charcot-Marie-Tooth Disease, Demyelinating, Type 1d	39	0.495

460		CHR655	Charcot-Marie-Tooth Disease, Axonal, with Vocal Cord Paresis, Autosomal Recessive	32	0.495

461	c	CHR545	Charcot-Marie-Tooth Disease, Axonal, Type 2h	27	0.495

462	c	CHR657	Charcot-Marie-Tooth Disease, Axonal, Type 2j	39	0.495

463	c	CHR481	Charcot-Marie-Tooth Disease, Dominant Intermediate D	32	0.495

464	c	DNJ004	Dnajb2-Related Charcot-Marie-Tooth Disease Type 2	15	0.495

465		NNS061	Non-Syndromic Pontocerebellar Hypoplasia	20	0.495

466	P	PNT019	Pontocerebellar Hypoplasia	46	0.495

467	P	HYP730	Hypogonadotropic Hypogonadism	53	0.495

468	c	GNT045	Giant Axonal Neuropathy 2	24	0.495

469	c	HRD210	Hereditary Spastic Paraplegia 23	22	0.495

470	c	ATS425	Autosomal Recessive Distal Hereditary Motor Neuronopathy	20	0.495

471	P	ATS426	Autosomal Dominant Distal Hereditary Motor Neuronopathy	33	0.495

472	c	HRD220	Hereditary Spastic Paraplegia 30	32	0.495

473	c	HRD186	Hereditary Spastic Paraplegia 51	29	0.495

474	c	HRD188	Hereditary Spastic Paraplegia 72	28	0.495

475	c	CHR422	Charcot-Marie-Tooth Disease, Dominant Intermediate B	46	0.495

476	c	CHR491	Charcot-Marie-Tooth Disease, Dominant Intermediate a	30	0.495

477	c	CHR608	Charcot-Marie-Tooth Disease, Axonal, Type 2p	45	0.495

478		LSN001	Lesion of Sciatic Nerve	22	0.495

479	P	SPN423	Spinal Muscular Atrophy with Lower Extremity Predominance	26	0.495

480	P	OCL062	Ocular Albinism with Congenital Sensorineural Deafness	23	0.495

481	P	DYS154	Dystonia	64	0.495

482	P	KLL001	Kallmann Syndrome	65	0.495

483	P	ACT008	Actinic Keratosis	54	0.495

484		CCH001	Cochlear Disease	28	0.495

485	P	DST101	Distal Hereditary Motor Neuropathies	23	0.495

486		BRC011	Brachial Plexus Neuropathy	38	0.495

487		PRG001	Progressive Muscular Atrophy	41	0.495

488		ANG018	Angiomyolipoma	46	0.495

489	P	CNT004	Centronuclear Myopathy	57	0.495

490		NRM005	Neuromuscular Disease	63	0.495

491		PRP016	Paraplegia	52	0.495

492		DFF013	Diffuse Meningeal Melanocytosis	20	0.495

493	c	CHR522	Charcot-Marie-Tooth Disease, Dominant Intermediate E	40	0.495

494	c	MLN043	Melanoma, Cutaneous Malignant 8	37	0.495

495		EPT001	Epithelioid Cell Melanoma	21	0.495

496	c	SPS101	Spastic Paraplegia 56, Autosomal Recessive	39	0.495

497	c	SPS126	Spastic Paraplegia 49, Autosomal Recessive	44	0.495

498	c	CHR504	Charcot-Marie-Tooth Disease, Type 4b3	45	0.495

499		ALK024	Alkuraya-Kucinskas Syndrome	45	0.495

500		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	0.495

501	P	SNS001	Sensorineural Hearing Loss	59	0.495

502	c	AMY083	Amyotrophic Lateral Sclerosis 11	39	0.495

503	c	SPS109	Spastic Paraplegia 46, Autosomal Recessive	42	0.495

504	c	AMY057	Amyotrophic Lateral Sclerosis 16, Juvenile	38	0.495

505	P	LTR001	Lateral Sclerosis	58	0.495

506		MTR007	Motor Peripheral Neuropathy	40	0.495

507		ARG003	Argyll Robertson Pupil	23	0.495

508	c	HRD010	Hereditary Spastic Paraplegia	66	0.495

509	P	PPL023	Pupil Disease	26	0.495

510		MLG005	Malignant Spindle Cell Melanoma	39	0.495

511		MLN079	Melanoma in Congenital Melanocytic Nevus	37	0.495

512	c	CHR571	Charcot-Marie-Tooth Disease Type 5	23	0.495

513	P	MCR010	Microcephaly	60	0.495

514		SPS004	Spastic Quadriplegia	40	0.495

515		ABN004	Abnormal Pupillary Function	15	0.495

516		MLG061	Malignant Choroid Melanoma	33	0.495

517		CHL010	Childhood Kidney Cell Carcinoma	38	0.495

518		GLL012	Gallbladder Melanoma	25	0.495

519	P	MTR014	Motor Neuron Disease	65	0.495

520	P	PLY019	Polyneuropathy	52	0.495

521		MNN017	Mononeuropathy	41	0.495

522		MLN005	Melanoacanthoma	22	0.495

523		MGC001	Megacolon	48	0.495

524		SPS003	Spastic Diplegia	53	0.495

525		QDR001	Quadriplegia	50	0.495

526		CHR073	Choreatic Disease	54	0.495

527		OCH001	Ochronosis	40	0.495

528		HYP080	Hypogonadism	50	0.495

529		CRB037	Cerebral Palsy	67	0.495

530		BSC002	Bscl2-Related Neurologic Disorders/seipinopathy	10	0.495

531		ALB002	Albinism	47	0.495

532	c	SPS092	Spastic Paraplegia 11	33	0.495

533		TSN004	Tsen54 Pontocerebellar Hypoplasia	15	0.495

534	P	PRX014	Proximal Spinal Muscular Atrophy	42	0.495

535	c	ERL012	Early-Onset Glaucoma	24	0.495

536	P	ENC018	Encephalopathy	62	0.495

537	P	CHR453	Charcot-Marie-Tooth Hereditary Neuropathy	39	0.495

538	P	GNT009	Giant Axonal Neuropathy	46	0.495

539	P	CRB088	Cerebral Atrophy	33	0.495

540		ATN005	Autonomic Dysfunction	46	0.495

541	c	HRD088	Hereditary Neuropathies	33	0.495

542	P	MYC033	Myoclonus	47	0.495

543		HYP213	Hypomelanotic Disorder	22	0.495

544		ANC002	Anca-Associated Vasculitis	44	0.495

545	c	ATS272	Autosomal Dominant Intermediate Charcot-Marie-Tooth	19	0.495

546	c	CHR135	Charcot-Marie-Tooth Disease Type 2a	23	0.495

547		PRX008	Paroxysmal Cold Hemoglobinuria	26	0.495

548		ARC025	Arachnoid Cysts, Intracranial	37	0.457

549	c	TYP008	Type 1 Diabetes Mellitus	70	0.457

550		LYM133	Lymphoma, Hodgkin, Classic	74	0.457

551		QLT002	Qualitative or Quantitative Defects of Dystrophin	19	0.457

552		ERY002	Erythema Infectiosum	35	0.457

553		APN006	Apnea of Prematurity	24	0.457

554		CYN003	Cyanide Poisoning	22	0.457

555	P	OVR082	Overgrowth Syndrome	49	0.457

556		ATH013	Atherosclerosis Susceptibility	63	0.457

557	P	BLD134	Bladder Cancer	79	0.457

558	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.457

559		PLM134	Pulmonary Fibrosis, Idiopathic	76	0.457

560	P	ULL002	Ullrich Congenital Muscular Dystrophy 1	57	0.457

561	P	MYS003	Myasthenia Gravis	68	0.457

562		MSC152	Muscular Dystrophy, Becker Type	69	0.457

563	c	MSC036	Muscular Dystrophy-Dystroglycanopathy , Type C, 5	64	0.457

564		PSR001	Psoriatic Arthritis	62	0.457

565	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.457

566		SHR097	Short Tarsus with Absence of Lower Eyelashes	25	0.457

567	c	HRD138	Hereditary Motor and Sensory Neuropathy V	32	0.457

568		STR067	Stroke, Ischemic	80	0.457

569	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	0.457

570	P	DRM053	Dermatitis, Atopic	65	0.457

571	c	PLM164	Pulmonary Hypertension, Primary, 1	76	0.457

572		RTN017	Retinal Detachment	60	0.457

573	P	RHM011	Rheumatoid Arthritis	82	0.457

574		LTH043	Lithium Transport	17	0.457

575		MRF001	Marfan Syndrome	76	0.457

576	P	BTH005	Bethlem Myopathy 1	62	0.457

577	P	OST002	Osteoporosis	76	0.457

578		TRT017	Teratoma, Ovarian	28	0.457

579	c	PCH015	Pachyonychia Congenita 1	60	0.457

580	P	LKM071	Leukemia, Chronic Lymphocytic	75	0.457

581	c	SYS001	Systemic Lupus Erythematosus	87	0.457

582	P	OVR042	Ovarian Cancer	88	0.457

583		MNT107	Mental Retardation, Fra12a Type	20	0.457

584		GLL008	Gilles De La Tourette Syndrome	65	0.457

585		ALC007	Alcohol Dependence	66	0.457

586	c	SPN225	Spondyloarthropathy 1	70	0.457

587		GST092	Gastroesophageal Reflux	61	0.457

588	c	SYN084	Synpolydactyly 1	36	0.457

589		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.457

590	P	CLC063	Celiac Disease 1	66	0.457

591		HYD038	Hydrops Fetalis, Nonimmune	59	0.457

592	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.457

593	P	PLM037	Pulmonary Hypertension	72	0.457

594		MTR088	Mature T-Cell and Nk-Cell Lymphoma	42	0.457

595	P	SLP006	Sleep Apnea	69	0.457

596		FTL006	Fetal Alcohol Spectrum Disorder	43	0.457

597		PRP036	Peripheral T-Cell Lymphoma	53	0.457

598		MLR004	Malaria	80	0.457

599	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	45	0.457

600	c	MJR022	Major Affective Disorder 8	38	0.457

601	c	MCR130	Microvascular Complications of Diabetes 6	41	0.457

602		HYP561	Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness	27	0.457

603	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.457

604		CYN002	Cyanosis, Transient Neonatal	43	0.457

605		NDL024	Nodal Marginal Zone Lymphoma	37	0.457

606	c	ATS007	Autism Spectrum Disorder	72	0.457

607		ART074	Aortic Dissection	53	0.457

608		HMN047	Human Cytomegalovirus Infection	57	0.457

609	P	CTN015	Cutaneous T Cell Lymphoma	48	0.457

610	P	SYN012	Synpolydactyly	38	0.457

611	P	ATR011	Atrial Fibrillation	66	0.457

612	P	FTL001	Fetal Alcohol Syndrome	55	0.457

613	P	SML001	Small Cell Carcinoma	52	0.457

614	P	BSL038	Basal Ganglia Calcification, Idiopathic, 1	53	0.457

615		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.457

616	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	0.457

617		CNT105	Central Core Disease of Muscle	59	0.457

618		HSH003	Hashimoto Thyroiditis	60	0.457

619	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.457

620		RNL065	Renal Cell Carcinoma, Papillary, 1	79	0.457

621		ALV005	Alveolar Soft Part Sarcoma	61	0.457

622		LYM143	Lymphoma, Non-Hodgkin, Familial	75	0.457

623		AST006	Astigmatism	47	0.457

624		EWN003	Ewing Sarcoma	70	0.457

625	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.457

626	c	LSS030	Lissencephaly 7 with Cerebellar Hypoplasia	21	0.457

627	c	CHR617	Charcot-Marie-Tooth Disease, Axonal, Type 2z	35	0.457

628	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.457

629	P	MJR001	Major Depressive Disorder	68	0.457

630	c	MJR024	Major Affective Disorder 9	41	0.457

631		ACT119	Acute Promyelocytic Leukemia	62	0.457

632	c	MCR120	Microvascular Complications of Diabetes 7	47	0.457

633	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.457

634	P	DVL012	Developmental Dysplasia of the Hip 1	46	0.457

635		TBL029	Tubulin, Beta	28	0.457

636	c	CHR660	Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2a2a	35	0.457

637	P	HMN036	Hemangiopericytoma, Malignant	58	0.457

638		MYL005	Myelofibrosis	71	0.457

639		OCL069	Ocular Motor Apraxia	57	0.457

640	P	RTN024	Retinoblastoma	73	0.457

641		OST159	Osteogenic Sarcoma	66	0.457

642	P	STR020	Strabismus	56	0.457

643	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.457

644	c	HYP595	Hypertension, Essential	85	0.457

645		CRN238	Corneal Dystrophy, Epithelial Basement Membrane	32	0.457

646		RNL114	Renal Cell Carcinoma, Nonpapillary	80	0.457

647		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	55	0.457

648		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	72	0.457

649	P	MDL005	Medulloblastoma	75	0.457

650	P	GLM040	Glioma Susceptibility 1	71	0.457

651		MMM006	Mammographic Density	39	0.457

652		CHL065	Cholangiocarcinoma	58	0.457

653		DCT002	Ductal Carcinoma in Situ	58	0.457

654		PNG002	Pain Agnosia	51	0.457

655	P	PTN014	Patent Ductus Arteriosus 1	59	0.457

656		DSS032	Disease by Infectious Agent	55	0.457

657		TNG009	Tongue Squamous Cell Carcinoma	43	0.457

658		ARG004	Argyria	26	0.457

659	c	ATS331	Autosomal Recessive Limb-Girdle Muscular Dystrophy	40	0.457

660		TNG007	Tongue Carcinoma	52	0.457

661		MDD018	Middle East Respiratory Syndrome	44	0.457

662		PRT037	Pertussis	65	0.457

663	P	LPS004	Lupus Erythematosus	61	0.457

664	P	AMY004	Amyloidosis	70	0.457

665	c	ACT075	Acute Myocardial Infarction	56	0.457

666	P	FBR003	Fibrous Histiocytoma	43	0.457

667		CLR011	Clear Cell Ependymoma	31	0.457

668	P	EPD009	Epidermolysis Bullosa Dystrophica	66	0.457

669		NTR005	Nutritional Deficiency Disease	61	0.457

670		NRL001	Neurilemmoma of the Fifth Cranial Nerve	26	0.457

671	P	RHB003	Rhabdomyosarcoma	66	0.457

672		CRV002	Cervix Uteri Carcinoma in Situ	47	0.457

673		IRD001	Iridocyclitis	53	0.457

674		MCH006	Mechanical Strabismus	40	0.457

675	P	HRP006	Herpes Simplex	65	0.457

676		LRN003	Learning Disability	49	0.457

677		ULC004	Ulcerative Colitis	74	0.457

678		FTT001	Fatty Liver Disease	62	0.457

679	P	HML002	Hemolytic Anemia	62	0.457

680		CLL010	Cellular Ependymoma	57	0.457

681		PST092	Posttransplant Acute Limbic Encephalitis	28	0.457

682		LMN005	Lmna-Related Cardiocutaneous Progeria Syndrome	28	0.457

683	P	ALP008	Alopecia	54	0.457

684	c	PRG106	Progressive Muscular Dystrophy	32	0.457

685	P	ALC033	Alcohol Use Disorder	61	0.457

686	P	THR014	Thrombocytopenia	66	0.457

687	P	CYS018	Cystitis	59	0.457

688		SKN022	Skin Squamous Cell Carcinoma	54	0.457

689	P	OLG002	Oligodendroglioma	66	0.457

690		TRC003	Trichomoniasis	53	0.457

691		VCC001	Vaccinia	47	0.457

692	P	BPL003	Bipolar Disorder	56	0.457

693		MNT002	Mental Depression	57	0.457

694	P	PLM036	Pulmonary Fibrosis	66	0.457

695	P	ART023	Arthropathy	61	0.457

696	P	INF038	Influenza	68	0.457

697		PST011	Pustulosis of Palm and Sole	52	0.457

698		PPT002	Peptic Ulcer Perforation	34	0.457

699		SPN051	Spondylitis	51	0.457

700		EXT034	Extrinsic Allergic Alveolitis	57	0.457

701		LNG099	Lung Disease	62	0.457

702	P	BNG030	Benign Ependymoma	51	0.457

703		MYL001	Myelitis	50	0.457

704	P	PLY020	Polyradiculoneuropathy	46	0.457

705		DFF016	Diffuse Astrocytoma	45	0.457

706	P	PRD008	Periodontitis	64	0.457

707	P	INT070	Intestinal Obstruction	57	0.457

708	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.457

709		PGM003	Pigmentation Disease	45	0.457

710	P	KRT007	Keratoconus	50	0.457

711		NSP002	Nasopharyngitis	45	0.457

712	P	GRF003	Graft-Versus-Host Disease	71	0.457

713	c	MCR113	Microvascular Complications of Diabetes 3	52	0.457

714	c	MCR133	Microvascular Complications of Diabetes 4	41	0.457

715		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	65	0.457

716		THY006	Thymus Lymphoma	27	0.457

717	c	DLT002	Dilated Cardiomyopathy	78	0.457

718		DNG003	Dengue Disease	65	0.457

719	P	MLN007	Male Infertility	56	0.457

720	P	ESP024	Esophagitis	60	0.457

721		INF009	Inflammatory Spondylopathy	30	0.457

722		DYS015	Dysentery	50	0.457

723		TST004	Testicular Lymphoma	39	0.457

724		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.457

725	P	HMN010	Hemangioma	62	0.457

726		BLR008	Bilirubin Metabolic Disorder	57	0.457

727		RTN020	Retinal Vascular Disease	46	0.457

728	P	HYP086	Hypothyroidism	69	0.457

729	P	ADN016	Adenocarcinoma	63	0.457

730		MLG169	Malignant Astrocytoma	57	0.457

731		URT001	Urethritis	53	0.457

732		BCT004	Bacteriuria	47	0.457

733		BRC012	Brucellosis	66	0.457

734	P	MYG005	Myoglobinuria	40	0.457

735		CYT005	Cytomegalovirus Retinitis	50	0.457

736		MST005	Mastitis	53	0.457

737		HMP005	Hemiplegia	54	0.457

738	P	RSP003	Respiratory Failure	74	0.457

739		RBS001	Rabies	58	0.457

740	P	PYL005	Pyelonephritis	57	0.457

741		PRT038	Protein-Energy Malnutrition	53	0.457

742		RCT015	Reactive Arthritis	61	0.457

743	c	INF023	Inflammatory Breast Carcinoma	49	0.457

744		INT079	Intrahepatic Cholangiocarcinoma	51	0.457

745	c	ESS001	Essential Tremor	57	0.457

746		CHR070	Chronic Inflammatory Demyelinating Polyradiculoneuropathy	57	0.457

747		HMN014	Human Immunodeficiency Virus Infectious Disease	54	0.457

748	P	INT068	Intestinal Disease	53	0.457

749		OVR109	Ovarian Germ Cell Teratoma	32	0.457

750	P	PNM007	Pneumonia	67	0.457

751		CCN002	Cocaine Abuse	49	0.457

752	P	TRT010	Teratoma	51	0.457

753		PLM029	Palmoplantar Keratosis	48	0.457

754		INT066	Interstitial Lung Disease	60	0.457

755	P	LRY044	Larynx Cancer	54	0.457

756	P	KDN017	Kidney Cancer	61	0.457

757	P	TCD001	Tic Disorder	49	0.457

758		BRS051	Breast Disease	58	0.457

759	P	JNC001	Junctional Epidermolysis Bullosa	53	0.457

760		DMY004	Demyelinating Disease	50	0.457

761		PLR005	Pleuropneumonia	33	0.457

762	P	EHL001	Ehlers-Danlos Syndrome	58	0.457

763		PLS007	Plasmodium Falciparum Malaria	52	0.457

764		AZS001	Azoospermia	45	0.457

765		ENT004	Enthesopathy	51	0.457

766		HYP014	Hyperuricemia	51	0.457

767		RTN021	Retinal Vascular Occlusion	45	0.457

768		SQM006	Squamous Cell Carcinoma	60	0.457

769		NRN004	Neuroendocrine Tumor	59	0.457

770	P	RTN022	Retinal Vein Occlusion	54	0.457

771		PLM033	Pulmonary Embolism	58	0.457

772	P	INS002	in Situ Carcinoma	53	0.457

773		HYP706	Hypermobile Ehlers-Danlos Syndrome	55	0.457

774	P	MYC008	Myocarditis	59	0.457

775		HRP004	Herpes Zoster	61	0.457

776		PTH003	Pathologic Nystagmus	52	0.457

777		SFT003	Soft Tissue Sarcoma	57	0.457

778		SPL018	Splenomegaly	49	0.457

779		48X005	48,xyyy	39	0.457

780		PRN039	Paraneoplastic Syndromes	37	0.457

781		CND006	Candida Glabrata	30	0.457

782		CYT002	Cytokine Deficiency	43	0.457

783		CRV045	Cervical Intraepithelial Neoplasia	39	0.457

784		HMP009	Haemophilus Influenzae	41	0.457

785		MYC019	Mycobacterium Marinum	29	0.457

786		CHR176	Chromophil Renal Cell Carcinoma	23	0.457

787	c	LMB030	Limb-Girdle Muscular Dystrophy Type 1c	27	0.457

788		LYM051	Lymphomatoid Granulomatosis	45	0.457

789		MYC015	Mycobacterium Fortuitum	28	0.457