Search results for erg

1558 hits were found for erg

#	Family	MCID	Name	MIFTS	Score
1	P	PRS040	Prostate Cancer	95	49.298

2		EWN003	Ewing Sarcoma	70	41.052

3	P	LKM002	Leukemia	67	29.932

4	P	MYL006	Myeloid Leukemia	61	29.638

5		SRC014	Sarcoma	65	26.962

6		NRR001	Neuroretinitis	42	18.591

7		RTN023	Retinitis	46	18.591

8	P	RTN008	Retinitis Pigmentosa	80	17.912

9	P	RTN016	Retinal Degeneration	52	16.377

10		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	16.138

11		MYX005	Myxoid Liposarcoma	65	14.504

12	P	NGH001	Night Blindness	52	14.412

13	P	RTN018	Retinal Disease	53	13.325

14	c	MCR115	Microvascular Complications of Diabetes 5	65	12.714

15	c	RTN035	Retinal Cone Dystrophy 3b	32	12.472

16		PRS006	Prostatic Acinar Adenocarcinoma	25	11.782

17	P	CNG010	Congenital Stationary Night Blindness	56	11.773

18	c	LKM061	Leukemia, Acute Myeloid	83	11.615

19	c	MCL042	Macular Degeneration, Age-Related, 1	85	11.150

20	P	CND005	Cone Dystrophy	47	9.986

21		INT323	Intraocular Pressure Quantitative Trait Locus	64	9.883

22		RTN017	Retinal Detachment	60	9.616

23	c	NRF024	Neurofibromatosis, Type I	72	9.599

24	P	RTN209	Retinoschisis 1, X-Linked, Juvenile	60	9.513

25		EXT052	Extraskeletal Ewing Sarcoma	30	9.210

26		PTH003	Pathologic Nystagmus	52	8.952

27	P	JVN042	Juvenile Retinoschisis	39	8.702

28	P	MYP006	Myopia	56	8.157

29		SPN035	Spindle Cell Sarcoma	54	8.086

30	P	CNR004	Cone-Rod Dystrophy 2	74	7.868

31	P	LKM062	Leukemia, Acute Lymphoblastic	69	7.778

32		SCT002	Scotoma	42	7.763

33		RTN003	Retinal Ischemia	49	7.728

34	c	INH030	Inherited Retinal Disorder	28	7.359

35		FND002	Fundus Dystrophy	55	7.338

36	P	RTN022	Retinal Vein Occlusion	54	7.027

37		CNT016	Central Retinal Vein Occlusion	54	6.982

38		XLN247	X-Linked Congenital Retinoschisis	20	6.790

39		MCL006	Macular Retinal Edema	57	6.779

40	P	OPT006	Optic Nerve Disease	58	6.774

41	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	68	6.754

42	P	ACH003	Achromatopsia	62	6.691

43	P	ADN016	Adenocarcinoma	63	6.664

44	P	UVT001	Uveitis	57	6.475

45	c	ACT073	Acute Leukemia	58	6.469

46		RFR003	Refractive Error	41	6.246

47		OCL006	Ocular Hypertension	53	6.244

48	P	LNG032	Lung Cancer	98	6.241

49	P	CTR002	Cataract	60	6.041

50	P	MSC005	Muscular Dystrophy	67	5.945

51	P	OPN001	Open-Angle Glaucoma	55	5.934

52		DWN001	Down Syndrome	70	5.910

53		SPP007	Suppression Amblyopia	38	5.756

54		AMB002	Amblyopia	50	5.756

55		NRT004	Neuritis	53	5.750

56	P	OGC005	Oguchi Disease	45	5.748

57		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	45	5.737

58		SPP011	Suppression of Tumorigenicity 12	61	5.554

59	c	NGH029	Night Blindness, Congenital Stationary, Type 1e	37	5.530

60	P	STR022	Stargardt Disease	61	5.528

61		SML031	Small Cell Carcinoma of the Bladder	46	5.493

62		RTN020	Retinal Vascular Disease	46	5.485

63		OCC002	Occult Macular Dystrophy	46	5.430

64		LBR036	Leber Plus Disease	66	5.345

65	P	OPT009	Optic Neuritis	57	5.327

66		MSC157	Muscular Dystrophy, Duchenne Type	79	5.325

67		KRT002	Keratomalacia	55	5.319

68	P	RTN024	Retinoblastoma	73	5.318

69	P	GST053	Gastric Cancer	83	5.263

70		ENH001	Enhanced S-Cone Syndrome	58	5.245

71		FND001	Fundus Albipunctatus	55	5.182

72		PRS045	Prostatic Hypertrophy	53	5.150

73	P	BLD134	Bladder Cancer	79	5.117

74	c	EXD008	Exudative Vitreoretinopathy 1	71	5.016

75	P	USH001	Usher Syndrome	64	4.999

76		MCL003	Macular Holes	44	4.993

77	P	EYD002	Eye Disease	57	4.984

78	P	SML001	Small Cell Carcinoma	52	4.976

79		PRS021	Prostatic Adenoma	43	4.913

80	P	RTN014	Retinal Artery Occlusion	47	4.889

81		BRN026	Branch Retinal Artery Occlusion	41	4.889

82		MLN046	Melanoma-Associated Retinopathy	24	4.757

83		RTN187	Retinitis Pigmentosa-Deafness Syndrome	48	4.754

84		ANG020	Angiosarcoma	64	4.742

85		END057	Endometrial Cancer	72	4.737

86		47X002	47,xyy	48	4.672

87		CHR178	Chromosomal Triplication	34	4.625

88	P	LNG028	Long Qt Syndrome	64	4.620

89	P	NRP001	Neuropathy	60	4.504

90		CNC014	Cancer-Associated Retinopathy	42	4.469

91		CYT019	Cytogenetically Normal Acute Myeloid Leukemia	30	4.424

92	P	MCR129	Microvascular Complications of Diabetes 1	68	4.422

93	c	MCR112	Microvascular Complications of Diabetes 2	42	4.422

94	P	END047	Endophthalmitis	53	4.408

95		BST008	Bestrophinopathy, Autosomal Recessive	46	4.377

96		CNT028	Central Retinal Artery Occlusion	43	4.356

97		PRS129	Prostatic Hyperplasia, Benign	49	4.255

98		MNN043	Meningioma, Familial	79	4.108

99		ALB002	Albinism	47	4.008

100		OPT070	Optic Nerve Hypoplasia, Bilateral	56	3.976

101		GST040	Gastric Adenocarcinoma	67	3.875

102	P	LNG064	Lung Cancer Susceptibility 3	70	3.875

103		ADN011	Adenoid Cystic Carcinoma	68	3.863

104	P	LPS002	Liposarcoma	64	3.834

105	c	GLC092	Glaucoma, Primary Open Angle	62	3.830

106		BRD025	Birdshot Chorioretinopathy	48	3.810

107		SVR004	Severe Combined Immunodeficiency	72	3.807

108	c	OGC001	Oguchi Disease 1	39	3.740

109	P	CNG024	Congenital Nystagmus	36	3.696

110		GST103	Gastric Cancer, Hereditary Diffuse	68	3.689

111	P	OVR042	Ovarian Cancer	88	3.629

112		CHR081	Choroideremia	58	3.568

113		ATM076	Autoimmune Retinopathy	27	3.564

114		ISC004	Ischemia	61	3.561

115	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	63	3.559

116	P	EPT012	Epithelioid Sarcoma	41	3.557

117	P	SCH015	Schizophrenia	74	3.550

118		ATX038	Ataxia and Polyneuropathy, Adult-Onset	46	3.548

119	P	LYM118	Lymphoma	67	3.521

120		HYP066	Hyperglycemia	61	3.499

121		GLM045	Glioma	63	3.495

122	P	NRN021	Neuronal Ceroid Lipofuscinosis	65	3.474

123		KHN001	Kuhnt-Junius Degeneration	48	3.473

124		ACT250	Acute Megakaryocytic Leukemia	60	3.457

125		DBT006	Diabetic Macular Edema	48	3.401

126		HYP266	Hypoxia	57	3.398

127	P	VTL001	Vitelliform Macular Dystrophy	46	3.364

128	P	STR020	Strabismus	56	3.361

129		MCH006	Mechanical Strabismus	40	3.361

130		SKN019	Skin Melanoma	71	3.358

131	P	GLM040	Glioma Susceptibility 1	71	3.351

132	P	MLT020	Multiple Sclerosis	79	3.317

133	P	CLR019	Color Blindness	48	3.317

134		OST159	Osteogenic Sarcoma	66	3.313

135		MSN004	Mesenchymal Cell Neoplasm	42	3.306

136	P	VTR007	Vitreoretinopathy	46	3.292

137	c	PCH010	Pachyonychia Congenita 3	43	3.279

138	P	SDR002	Siderosis	43	3.279

139		RPD005	Rapidly Involuting Congenital Hemangioma	46	3.197

140		HMN016	Hemangioendothelioma	34	3.184

141		PPL052	Papillomatosis, Confluent and Reticulated	34	3.183

142		BCK003	Background Diabetic Retinopathy	47	3.173

143		ACT098	Acute Erythroid Leukemia	55	3.148

144		MSC152	Muscular Dystrophy, Becker Type	69	3.148

145		SML009	Small Intestine Adenocarcinoma	57	3.144

146	P	BRS047	Breast Cancer	98	3.097

147	c	STR084	Stargardt Disease 1	53	3.067

148		XLN012	X-Linked Congenital Stationary Night Blindness	28	3.067

149		FST001	Foster-Kennedy Syndrome	39	3.066

150		ACT120	Acute Zonal Occult Outer Retinopathy	24	3.059

151		AGN016	Aging	54	3.054

152		AST006	Astigmatism	47	3.044

153		CHL152	Childhood Acute Lymphocytic Leukemia	50	3.024

154	P	BRD002	Bardet-Biedl Syndrome	66	3.019

155		CLR033	Color Vision Deficiency	40	3.019

156		LNG039	Lung Squamous Cell Carcinoma	57	3.004

157		CLN015	Colon Adenocarcinoma	65	2.973

158		PTT037	Pituitary Tumors	44	2.952

159		ATS010	Autosomal Recessive Disease	42	2.920

160		RNL114	Renal Cell Carcinoma, Nonpapillary	80	2.906

161		CNT060	Central Serous Chorioretinopathy	38	2.895

162	P	TMR010	Tumor Predisposition Syndrome	67	2.882

163		ADN089	Adenosquamous Lung Carcinoma	49	2.882

164		BRN015	Bronchiolo-Alveolar Adenocarcinoma	55	2.882

165	c	BRN108	Branchiootic Syndrome 1	62	2.872

166	P	EPT020	Epithelioid Hemangioendothelioma	44	2.843

167		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	2.832

168	c	NNS043	Nonsyndromic Retinitis Pigmentosa	27	2.817

169	c	NGH007	Night Blindness, Congenital Stationary, Type 1b	42	2.813

170		TRT020	Tritanopia	50	2.801

171	c	SML038	Small Cell Cancer of the Lung	69	2.797

172		KRN002	Kearns-Sayre Syndrome	63	2.769

173	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	60	2.768

174	c	CLR087	Colorectal Cancer 12	34	2.768

175	P	HMN010	Hemangioma	62	2.767

176	c	LBR004	Leber Congenital Amaurosis 1	52	2.764

177		PRL047	Prolonged Electroretinal Response Suppression	43	2.738

178	c	USH035	Usher Syndrome Type 2	52	2.708

179	c	PST005	Posterior Uveitis	54	2.708

180	P	SNS001	Sensorineural Hearing Loss	59	2.708

181		MYL031	Myeloproliferative Neoplasm	66	2.704

182		CHL149	Childhood Acute Myeloid Leukemia	43	2.697

183	c	RTN150	Retinitis Pigmentosa 10	44	2.693

184		48X005	48,xyyy	39	2.680

185	c	LNG047	Long Qt Syndrome 2	59	2.661

186		WST001	West Syndrome	59	2.652

187		PST092	Posttransplant Acute Limbic Encephalitis	28	2.652

188		BLC001	Blue Cone Monochromacy	45	2.649

189	P	BLY001	B-Lymphoblastic Leukemia/lymphoma	52	2.645

190	P	RHB003	Rhabdomyosarcoma	66	2.645

191	P	VSC007	Vascular Disease	63	2.645

192	c	LBR012	Leber Congenital Amaurosis 2	52	2.615

193	c	MJR022	Major Affective Disorder 8	38	2.615

194	c	MJR024	Major Affective Disorder 9	41	2.615

195	P	BPL003	Bipolar Disorder	56	2.615

196	c	GLM047	Glioma Susceptibility 3	33	2.567

197	c	MSM022	Mismatch Repair Cancer Syndrome 1	70	2.567

198	c	GLM025	Glioma Susceptibility 2	30	2.567

199	c	GLM043	Glioma Susceptibility 9	30	2.567

200	P	OLG002	Oligodendroglioma	66	2.567

201		CYT005	Cytomegalovirus Retinitis	50	2.565

202		NRN005	Neuronal Ceroid-Lipofuscinoses	61	2.554

203	P	HRD217	Hereditary Optic Neuropathy	36	2.548

204	P	MLN008	Melanoma	76	2.530

205		STR046	Stargardt Macular Degeneration	27	2.530

206	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	2.515

207	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	2.515

208	c	BDY005	Body Mass Index Quantitative Trait Locus 9	47	2.515

209		PLY150	Polykaryocytosis Inducer	29	2.515

210	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	2.515

211		MYL009	Myelodysplastic Syndrome	67	2.515

212	P	BDY004	Body Mass Index Quantitative Trait Locus 11	83	2.515

213	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	2.515

214	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	2.515

215	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	2.515

216	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	2.515

217	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	2.515

218	P	VSC011	Vasculitis	61	2.505

219	P	HYP265	Hypotonia	42	2.505

220		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	2.456

221	c	NGH010	Night Blindness, Congenital Stationary, Autosomal Dominant 2	46	2.446

222	P	NRB001	Neuroblastoma	66	2.446

223		IMP005	Impotence	52	2.446

224		CHR078	Chorioretinitis	51	2.443

225	c	RTN172	Retinitis Pigmentosa 1	44	2.441

226		ALN001	Aland Island Eye Disease	55	2.411

227	P	MJR001	Major Depressive Disorder	68	2.406

228		CRB159	Cerebral Visual Impairment	34	2.379

229	P	CHN012	Chondrosarcoma	57	2.374

230		GYR004	Gyrate Atrophy of Choroid and Retina	58	2.374

231		RHB024	Rhabdomyosarcoma 2	67	2.373

232	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	47	2.307

233		SRC027	Sarcoma, Synovial	58	2.300

234		OCL069	Ocular Motor Apraxia	57	2.294

235	c	MCL066	Macular Dystrophy, Vitelliform, 2	48	2.293

236		BRS099	Breast Ductal Carcinoma	61	2.286

237		MNC001	Monocular Esotropia	30	2.278

238		EST005	Esotropia	43	2.278

239		ALL029	Allergic Disease	59	2.278

240	P	ATS308	Autosomal Dominant Cerebellar Ataxia	64	2.278

241	c	MCR122	Microphthalmia, Isolated 5	39	2.264

242		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	2.261

243	P	ANR048	Aniridia 1	64	2.251

244	c	CHR095	Chronic Progressive External Ophthalmoplegia	49	2.251

245		NVS001	Neovascular Glaucoma	52	2.243

246		PHC015	Phacoanaphylactic Uveitis	18	2.221

247		VTR003	Vitreous Detachment	41	2.219

248	P	THL005	Thalassemia	56	2.208

249	P	BCL017	B-Cell Lymphoma	59	2.208

250		HYP056	Hypoglycemia	65	2.208

251		LTN004	Late-Onset Retinal Degeneration	60	2.201

252	c	PLM164	Pulmonary Hypertension, Primary, 1	76	2.180

253		ACT119	Acute Promyelocytic Leukemia	62	2.180

254	P	EPL164	Epilepsy	68	2.172

255	P	FLL037	Follicular Lymphoma	74	2.153

256	P	OCL002	Oculocutaneous Albinism	59	2.135

257		MCP033	Mucopolysaccharidoses	44	2.135

258	P	DBT009	Diabetes Mellitus	67	2.134

259		PRP099	Peripheral Cone Dystrophy	14	2.122

260		ACT235	Acute Macular Neuroretinopathy	16	2.097

261	P	MYP004	Myopathy	67	2.097

262		CMB007	Combined Immunodeficiency	57	2.097

263		SPN050	Spinocerebellar Degeneration	39	2.095

264	c	PRS134	Prostate Cancer, Hereditary, 3	20	2.095

265	c	USH036	Usher Syndrome, Type I	61	2.076

266		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	2.076

267		ANX004	Anoxia	40	2.063

268	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	70	2.058

269		SPL018	Splenomegaly	49	2.058

270		ART016	Aortic Aneurysm	68	2.051

271		RHB001	Rhabdoid Cancer	68	2.051

272		OST012	Osteoarthritis	77	2.051

273	P	ART022	Arthritis	71	2.046

274	c	CNR007	Cone-Rod Dystrophy 6	52	2.029

275		BRN041	Bornholm Eye Disease	34	2.019

276	c	RTN032	Retinal Cone Dystrophy 1	24	2.018

277		DSM007	Desmoplastic Small Round Cell Tumor	54	2.018

278	c	RNG015	Ring Chromosome 2	22	2.016

279		SMT004	Smith-Lemli-Opitz Syndrome	70	2.011

280		ANR040	Aneurysm	61	2.004

281		ALS001	Alstrom Syndrome	65	2.002

282	c	BRD010	Bardet-Biedl Syndrome 1	64	1.985

283		INT082	Intraocular Retinoblastoma	29	1.985

284	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	1.978

285		VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	1.978

286		DFF005	Diffuse Large B-Cell Lymphoma	54	1.978

287	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	1.978

288	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	61	1.957

289		MYL069	Myeloma, Multiple	77	1.957

290		ATN005	Autonomic Dysfunction	46	1.957

291	P	CLR023	Colorectal Cancer	100	1.954

292		KRT019	Keratitis, Hereditary	66	1.936

293		KPS004	Kaposi Sarcoma	77	1.936

294	c	NGH025	Night Blindness, Congenital Stationary, Type 2a	44	1.922

295	P	PNC035	Pancreatic Cancer	86	1.920

296		HRD016	Hereditary Retinal Dystrophy	34	1.907

297		PRS047	Prostatitis	58	1.906

298		HPT046	Hepatic Veno-Occlusive Disease	62	1.900

299		ADN018	Adenoma	59	1.893

300		INT054	Intraocular Lymphoma	48	1.893

301		RTN001	Retinal Vasculitis	46	1.893

302	P	MYT002	Myotonic Dystrophy	51	1.893

303	c	CND011	Cone Dystrophy 3	40	1.891

304	c	TYP008	Type 1 Diabetes Mellitus	70	1.890

305		HLX001	Helix Syndrome	48	1.890

306	P	RHM011	Rheumatoid Arthritis	82	1.857

307	c	OPT053	Optic Atrophy 1	62	1.857

308		CLB010	Coloboma of Macula	53	1.857

309		CYS001	Cystic Fibrosis	78	1.855

310		MYP002	Myoepithelial Carcinoma	46	1.855

311	P	CHR637	Choroidal Dystrophy, Central Areolar, 1	49	1.848

312		CHL014	Cholera	62	1.848

313	c	LBR016	Leber Congenital Amaurosis 6	42	1.834

314		BTT001	Bietti Crystalline Corneoretinal Dystrophy	48	1.823

315		ACT038	Acute Retrobulbar Neuritis	24	1.823

316	c	CRD183	Ceroid Lipofuscinosis, Neuronal, 2	56	1.808

317	c	RTN054	Retinitis Pigmentosa 25	42	1.806

318		CLR132	Colorblindness, Partial, Deutan Series	30	1.802

319		LNG073	Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency	58	1.802

320	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	54	1.801

321		MLR004	Malaria	80	1.801

322	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	49	1.801

323	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	53	1.801

324		CHL061	Childhood Leukemia	47	1.801

325	c	MGR028	Migraine with or Without Aura 1	64	1.789

326		SFT003	Soft Tissue Sarcoma	57	1.789

327	c	RTN162	Retinitis Pigmentosa 2	45	1.754

328		MCR013	Microphthalmia	60	1.754

329		MTR001	Mature Cataract	29	1.754

330		MSC012	Muscular Dystrophy, Duchenne and Becker Type	33	1.754

331		SYN149	Syndromic Rod-Cone Dystrophy	21	1.754

332		RLP002	Relapsing-Remitting Multiple Sclerosis	56	1.754

333		OPT001	Optic Disk Drusen	34	1.754

334		CHN010	Chondroma	43	1.754

335	P	BNC003	Bone Cancer	58	1.754

336		CND006	Candida Glabrata	30	1.754

337		ACT186	Acute Megakaryoblastic Leukemia in Down Syndrome	15	1.744

338		MCL057	Macular Dystrophy with Central Cone Involvement	28	1.729

339	P	PLM025	Pulmonary Venoocclusive Disease	44	1.707

340		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	1.705

341		CHN053	Chondromyxoid Fibroma	39	1.705

342		HRL003	Hurler Syndrome	66	1.705

343		CRD223	Cardiac Arrhythmia	63	1.705

344		CHR072	Chordoma	57	1.705

345		FBR054	Fibroma	44	1.705

346	P	MSN005	Mesenchymal Chondrosarcoma	47	1.705

347	P	ENC018	Encephalopathy	62	1.705

348		CNR033	Cone-Rod Synaptic Disorder, Congenital Nonprogressive	35	1.698

349		LNG111	Lung Non-Squamous Non-Small Cell Carcinoma	56	1.693

350	c	ATM099	Autoimmune Uveitis	45	1.683

351	P	PLY006	Polydactyly	59	1.683

352		CRH001	Crohn's Disease	80	1.683

353		CRN030	Coronary Stenosis	50	1.683

354		IRD001	Iridocyclitis	53	1.683

355		VNH007	Von Hippel-Lindau Syndrome	73	1.672

356		MCL029	Macular Degeneration, X-Linked Atrophic	17	1.668

357		SHR107	Short Stature-Obesity Syndrome	25	1.653

358	c	SPN294	Spinocerebellar Ataxia 1	53	1.653

359		HYP020	Hyperprolactinemia	63	1.653

360	P	THR014	Thrombocytopenia	66	1.653

361		EXT012	Extraskeletal Chondroma	17	1.653

362		CLR005	Clear Cell Chondrosarcoma	37	1.653

363		OST011	Osteomalacia	52	1.653

364		BLT001	Bilateral Retinoblastoma	35	1.653

365		CHN003	Chondroblastic Osteosarcoma	30	1.653

366		PSR001	Psoriatic Arthritis	62	1.646

367	c	ATS169	Autosomal Recessive Congenital Stationary Night Blindness	30	1.646

368	c	MCL013	Mucolipidosis Iv	65	1.646

369	c	CNR038	Cone-Rod Dystrophy, X-Linked, 3	36	1.623

370	c	NGH008	Night Blindness, Congenital Stationary, Autosomal Dominant 3	36	1.623

371	c	DWL002	Dowling-Degos Disease 1	58	1.608

372	P	MYC084	Mycobacterium Tuberculosis 1	68	1.608

373		CLT003	Colitis	63	1.608

374	P	HNT016	Huntington Disease	73	1.608

375	P	KRT007	Keratoconus	50	1.608

376		VGT001	Vogt-Koyanagi-Harada Disease	56	1.608

377	P	PLM037	Pulmonary Hypertension	72	1.599

378		SVR002	Severe Nonproliferative Diabetic Retinopathy	36	1.599

379		RRV005	Rare Vascular Tumor	17	1.599

380		ILS001	Ileus	50	1.599

381	P	CRN026	Corneal Edema	42	1.599

382		ONC003	Oncogenic Osteomalacia	42	1.599

383		SKN022	Skin Squamous Cell Carcinoma	54	1.577

384		LBL001	Lobular Neoplasia	55	1.577

385		MYL005	Myelofibrosis	71	1.573

386	P	RRT020	Rare Tumor	39	1.569

387	P	JBR020	Joubert Syndrome 1	74	1.569

388	c	TYP009	Type 2 Diabetes Mellitus	92	1.569

389		DGN002	Degenerative Myopia	31	1.569

390	c	INT064	Intermediate Uveitis	54	1.569

391		PTT063	Pattern Dystrophy	36	1.569

392	c	CND012	Cone Dystrophy 4	30	1.563

393		TTR011	Tetraploidy	43	1.542

394	c	LKM070	Leukemia, Acute Monocytic	56	1.542

395		MLT157	Multiple System Atrophy 1	69	1.542

396		SCH036	Scheie Syndrome	73	1.542

397	P	ISL078	Isolated Ectopia Lentis	58	1.542

398		PRS042	Prostate Disease	42	1.542

399		INT075	Intracranial Hypertension	53	1.542

400	P	MTC133	Mitochondrial Myopathy	50	1.542

401		SRC030	Sarcomatoid Carcinoma	42	1.542

402		SCR001	Secretory Meningioma	40	1.542

403		LYM002	Lymphoplasmacyte-Rich Meningioma	35	1.542

404	P	MNC007	Monocytic Leukemia	47	1.542

405		PNC001	Pancytopenia	53	1.542

406		ATY005	Atypical Teratoid Rhabdoid Tumor	69	1.542

407		SPN021	Spinal Meningioma	50	1.542

408		ACT200	Acute Monoblastic Leukemia	41	1.542

409	c	ATS007	Autism Spectrum Disorder	72	1.529

410	P	MGR001	Migraine Without Aura	49	1.529

411	P	PNV001	Panuveitis	49	1.529

412		LKS001	Leukostasis	41	1.529

413		RTN021	Retinal Vascular Occlusion	45	1.529

414		ESP021	Esophageal Cancer	83	1.514

415		END041	Endometrial Adenocarcinoma	64	1.514

416	c	PRS097	Prostate Cancer, Hereditary, 1	39	1.490

417	c	PRS070	Prostate Cancer, Hereditary, 12	22	1.490

418	c	PRS071	Prostate Cancer, Hereditary, 13	25	1.490

419	c	PRS117	Prostate Cancer, Hereditary, 11	24	1.490

420	c	PRS114	Prostate Cancer, Hereditary, 2	33	1.490

421		PRS015	Prostate Signet Ring Cell Adenocarcinoma	25	1.490

422		PRP030	Purpura	54	1.489

423		LYS002	Lysosomal Storage Disease	51	1.489

424	P	PTS002	Ptosis	52	1.489

425	c	ATS168	Autosomal Dominant Congenital Stationary Night Blindness	24	1.489

426		ONC007	Oncocytoma	50	1.481

427		APR001	Apraxia	52	1.481

428		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	65	1.481

429	P	CHR071	Charcot-Marie-Tooth Disease	64	1.481

430	P	HYP086	Hypothyroidism	69	1.481

431	P	ART005	Arteriovenous Malformation	65	1.481

432	c	DNT047	Dentinogenesis Imperfecta Type 2	35	1.481

433		BTH002	Bothnia Retinal Dystrophy	35	1.452

434		FML292	Familial Drusen	34	1.447

435		RTN078	Retinoschisis of Fovea	19	1.447

436	P	AST005	Asthma	76	1.447

437	c	CNG411	Congenital Disorder of Glycosylation, Type in	67	1.447

438		PPL021	Papilledema	49	1.447

439		MNT002	Mental Depression	57	1.447

440		ALT003	Alternating Exotropia	33	1.447

441	P	MCR010	Microcephaly	60	1.447

442		EXT022	Exotropia	42	1.447

443		DPR016	Depression	65	1.447

444		CRV035	Cervical Cancer	73	1.417

445		ASK001	Askin's Tumor	32	1.417

446	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	1.417

447		GST019	Gastrointestinal Stromal Tumor	78	1.417

448		PST048	Postural Orthostatic Tachycardia Syndrome	46	1.417

449		CRT012	Cortical Blindness	42	1.417

450	P	CRB059	Cerebellar Degeneration	36	1.417

451	c	PRS136	Prostate Cancer, Hereditary, 6	33	1.409

452	c	PRS130	Prostate Cancer, Hereditary, 8	32	1.409

453	c	STR040	Stargardt Disease 3	34	1.404

454	c	THY107	Thymoma, Familial	42	1.404

455	c	RTN058	Retinitis Pigmentosa 3	43	1.404

456		ANG054	Angina Pectoris	66	1.404

457	P	OCL001	Ocular Albinism	48	1.404

458	c	RTN066	Retinitis Pigmentosa 4	42	1.404

459	P	EXD001	Exudative Vitreoretinopathy	56	1.404

460	P	ATR011	Atrial Fibrillation	66	1.404

461	c	SPN291	Spinocerebellar Ataxia 7	53	1.404

462	P	MYC007	Myocardial Infarction	70	1.404

463		CRN019	Coronary Artery Vasospasm	47	1.404

464	P	THY023	Thymoma	64	1.404

465	P	MCL035	Macular Dystrophy, Retinal, 2	27	1.378

466	c	USH046	Usher Syndrome, Type 1m	17	1.378

467		ATM095	Autoimmune Disease	61	1.359

468		PRS012	Pars Planitis	47	1.359

469		THR100	Thrombocytopenic Purpura, Autoimmune	61	1.359

470	P	PSR002	Psoriasis	63	1.359

471		PST011	Pustulosis of Palm and Sole	52	1.359

472		TLN003	Telangiectasis	51	1.359

473	P	NPH005	Nephronophthisis	56	1.359

474	P	LBR033	Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy	22	1.359

475		MSC007	Muscle Hypertrophy	64	1.349

476	c	MCL030	Macular Degeneration, Age-Related, 10	24	1.349

477	P	NJM001	Nijmegen Breakage Syndrome	76	1.349

478	c	WLM013	Wilms Tumor 1	66	1.349

479	P	SPP010	Suppressor of Tumorigenicity 3	51	1.349

480		CRB006	Cribriform Carcinoma	34	1.349

481		GLB002	Glioblastoma	67	1.349

482		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	50	1.349

483		ACT113	Acute Myeloblastic Leukemia with Maturation	46	1.349

484		LYM116	Lymph Node Disease	42	1.349

485		CHR167	Chorioretinal Atrophy, Progressive Bifocal	27	1.335

486	c	RTN036	Retinal Cone Dystrophy 4	35	1.335

487		RTN191	Retinal Dystrophy with or Without Extraocular Anomalies	19	1.317

488	P	SZR006	Seizure Disorder	70	1.313

489		CRT072	Creutzfeldt-Jakob Disease	68	1.313

490	c	MCR130	Microvascular Complications of Diabetes 6	41	1.313

491	P	FTL001	Fetal Alcohol Syndrome	55	1.313

492		IMM167	Immune Deficiency Disease	78	1.313

493	c	MCR120	Microvascular Complications of Diabetes 7	47	1.313

494	P	HMC002	Homocystinuria	53	1.313

495	c	MCR113	Microvascular Complications of Diabetes 3	52	1.313

496	c	MCR133	Microvascular Complications of Diabetes 4	41	1.313

497	c	PRC016	Pre-Eclampsia	65	1.313

498	P	PLY019	Polyneuropathy	52	1.313

499		SQM006	Squamous Cell Carcinoma	60	1.313

500		RP6003	Rpe65-Related Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy	9	1.313

501	P	GRF003	Graft-Versus-Host Disease	71	1.299

502	c	CNR013	Cone-Rod Dystrophy 12	36	1.295

503	P	SNR003	Senior-Loken Syndrome 1	58	1.295

504		CRD132	Cardiac Conduction Defect	60	1.274

505		HRL004	Hurler-Scheie Syndrome	57	1.274

506		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	61	1.274

507		SVR001	Severe Acute Respiratory Syndrome	67	1.274

508	P	HRM001	Hermansky-Pudlak Syndrome	65	1.274

509	P	NPH012	Nephrotic Syndrome	60	1.274

510	P	OST001	Osteopetrosis	71	1.274

511		LTT006	Littoral Cell Angioma of the Spleen	18	1.274

512		PRT058	Pure Autonomic Failure	58	1.274

513	P	ATS364	Autism	69	1.265

514		RTN208	Retinopathy, Pericentral Pigmentary, Autosomal Recessive	16	1.265

515		ALC007	Alcohol Dependence	66	1.265

516		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	68	1.265

517	P	RTN034	Retinal Cone Dystrophy 3a	28	1.265

518		TRM010	Traumatic Brain Injury	51	1.265

519	P	HYP087	Hypotrichosis	42	1.265

520	c	HPT001	Hepatitis C	62	1.265

521		CRT015	Carotid Artery Occlusion	45	1.265

522	P	TRT010	Teratoma	51	1.265

523		KRT001	Keratoconjunctivitis Sicca	50	1.265

524		CLR030	Clear Cell Renal Cell Carcinoma	54	1.238

525		PLM173	Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal	34	1.226

526		PSD011	Pseudovascular Skin Squamous Cell Carcinoma	16	1.226

527		SQM013	Squamous Cell Carcinoma, Head and Neck	73	1.215

528	c	CNR003	Cone-Rod Dystrophy 1	31	1.215

529		ALC001	Alcohol-Related Birth Defect	36	1.215

530	c	BTT014	Beta-Thalassemia	72	1.215

531	P	NNP021	Nanophthalmos	39	1.215

532	P	MTH008	Methylmalonic Acidemia	52	1.215

533	P	ANT006	Antiphospholipid Syndrome	55	1.215

534		XRP001	Xerophthalmia	41	1.215

535		GT001	Gout	64	1.215

536		HYP008	Hypertensive Retinopathy	39	1.215

537		STT001	Status Epilepticus	59	1.215

538		SNL007	Senile Cataract	40	1.215

539	P	VTR008	Vitreoretinal Degeneration	29	1.215

540	P	HDC001	Headache	57	1.215

541	P	GNG009	Gangliosidosis	44	1.215

542	P	CNR031	Cone-Rod Dystrophy, X-Linked, 1	37	1.201

543		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	1.201

544	P	LBR014	Leber Congenital Amaurosis 4	56	1.201

545	c	NGH030	Night Blindness, Congenital Stationary, Type 1f	25	1.201

546	P	BLD062	Bile Duct Cancer	67	1.197

547	P	LNG021	Lung Occult Small Cell Carcinoma	20	1.197

548		LNG019	Lung Combined Type Small Cell Carcinoma	32	1.197

549		CVD001	Covid-19	57	1.191

550	P	GLL032	Galloway-Mowat Syndrome	46	1.191

551		EST007	Estrogen Resistance	41	1.191

552	P	HMN036	Hemangiopericytoma, Malignant	58	1.191

553		MYL003	Myeloid Sarcoma	48	1.191

554	c	RTN048	Retinitis Pigmentosa 19	39	1.189

555	c	RTN230	Retinitis Pigmentosa 88	23	1.189

556	c	RTN233	Retinitis Pigmentosa 89	20	1.189

557		NRR002	Norrie Disease	61	1.164

558	c	USH037	Usher Syndrome, Type Iia	48	1.164

559	P	LKM071	Leukemia, Chronic Lymphocytic	75	1.164

560		MCL069	Macular Dystrophy, Retinal, 1, North Carolina Type	38	1.164

561	P	LSS002	Lissencephaly	50	1.164

562		DFC004	Deficiency Anemia	74	1.164

563	P	MCL001	Mucolipidosis	49	1.164

564	P	RBL001	Rubella	58	1.164

565	P	CHL066	Cholangitis	52	1.164

566		SKN016	Skin Disease	63	1.164

567		CRT013	Carotid Stenosis	51	1.164

568	P	SCL009	Sclerosing Cholangitis	48	1.164

569		THR004	Thrombocytosis	53	1.164

570	P	BLP003	Blepharospasm	46	1.164

571		HYP080	Hypogonadism	50	1.164

572	P	LMY004	Leiomyosarcoma	62	1.164

573	c	RNG021	Ring Chromosome 5	20	1.164

574		MTH021	Methylmalonic Acidemia with Homocystinuria	44	1.164

575		PRR004	Preretinal Fibrosis	34	1.127

576		HYP781	Hypoascorbemia	52	1.119

577		MTH047	Methanol Poisoning	37	1.110

578	P	ALZ034	Alzheimer Disease	87	1.110

579	P	PHC003	Pheochromocytoma	69	1.110

580		ATR057	Atrioventricular Block	54	1.110

581		DBT090	Diabetes and Deafness, Maternally Inherited	45	1.110

582		NRN008	Neuronal Intranuclear Inclusion Disease	47	1.110

583		MYP106	Myopathy, Myosin Storage, Autosomal Recessive	33	1.110

584		ADR040	Adrenal Gland Pheochromocytoma	46	1.110

585		SCR011	Scrapie	39	1.110

586	P	ALP008	Alopecia	54	1.110

587	P	CRN024	Corneal Disease	44	1.110

588	P	NTR004	Neutropenia	63	1.110

589	P	SBS003	Substance Abuse	54	1.110

590		ABS022	Absolute Glaucoma	33	1.110

591		VCN001	Vcan-Related Vitreoretinopathy	20	1.110

592	c	MNS014	Monosomy 22	35	1.097

593	P	TMP003	Temporal Arteritis	69	1.097

594		LNG099	Lung Disease	62	1.097

595		DNG001	Dengue Shock Syndrome	40	1.097

596	P	DNG005	Dengue Virus	56	1.097

597		DNG002	Dengue Hemorrhagic Fever	60	1.097

598		HMP001	Hemopericardium	47	1.097

599	P	PRC012	Pericardial Effusion	50	1.097

600	P	HYP076	Hyperthyroidism	53	1.097

601		DBF001	D-Bifunctional Protein Deficiency	55	1.089

602		SRS007	Sorsby Fundus Dystrophy	51	1.089

603	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	1.089

604	c	LBR005	Leber Congenital Amaurosis 10	45	1.075

605	c	LBR018	Leber Congenital Amaurosis 8	47	1.075

606	c	LBR006	Leber Congenital Amaurosis 11	35	1.075

607	c	LBR017	Leber Congenital Amaurosis 7	37	1.075

608		LYM133	Lymphoma, Hodgkin, Classic	74	1.053

609		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	1.053

610	c	FML294	Familial Short Qt Syndrome	43	1.053

611		INS024	Insulin-Like Growth Factor I	78	1.053

612	c	USH038	Usher Syndrome, Type Iiia	51	1.053

613	c	SPN225	Spondyloarthropathy 1	70	1.053

614		FTL006	Fetal Alcohol Spectrum Disorder	43	1.053

615	c	SHR030	Short Qt Syndrome	44	1.053

616	c	BRD017	Bardet-Biedl Syndrome 5	38	1.053

617	c	CHL119	Cholangitis, Primary Sclerosing	58	1.053

618		ALL006	Allergic Asthma	56	1.053

619		ULC004	Ulcerative Colitis	74	1.053

620		SPN051	Spondylitis	51	1.053

621		ADN009	Adenosquamous Carcinoma	48	1.053

622	c	DLT002	Dilated Cardiomyopathy	78	1.053

623		DNG003	Dengue Disease	65	1.053

624		INF009	Inflammatory Spondylopathy	30	1.053

625		DBT008	Diabetic Angiopathy	45	1.053

626		DMY004	Demyelinating Disease	50	1.053

627		KRT008	Keratopathy	46	1.053

628		HYP060	Hyperinsulinism	54	1.053

629	P	NRF002	Neurofibromatosis	57	1.053

630	c	NNS007	Nonsyndromic Deafness	33	1.053

631	P	MTC069	Mitochondrial Disorders	57	1.053

632	c	ACT135	Acute Graft Versus Host Disease	51	1.042

633	P	CNR040	Cone-Rod Dystrophy and Hearing Loss 1	26	1.027

634		CLP005	Ciliopathy	41	0.992

635	c	MCP050	Mucopolysaccharidosis, Type Ii	74	0.992

636		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.992

637	c	ATR087	Atrial Standstill 1	74	0.992

638		TRD008	Triiodothyronine Receptor Auxiliary Protein	33	0.992

639		MNT001	Mantle Cell Lymphoma	67	0.992

640	c	NGH027	Night Blindness, Congenital Stationary, Type 1c	36	0.992

641	P	CTN015	Cutaneous T Cell Lymphoma	48	0.992

642		CRH005	Crohn's Colitis	53	0.992

643	c	LBR015	Leber Congenital Amaurosis 5	42	0.992

644	c	BRD011	Bardet-Biedl Syndrome 10	49	0.992

645		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	39	0.992

646		LBR038	Leber Hereditary Optic Neuropathy, Modifier of	62	0.992

647	c	ACH020	Achromatopsia 2	48	0.992

648	P	ATT013	Attention Deficit-Hyperactivity Disorder	64	0.992

649	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	0.992

650		OPT010	Optic Papillitis	38	0.992

651	c	CHR684	Chronic Kidney Disease	69	0.992

652		SCH012	Schizoaffective Disorder	50	0.992

653		NRM001	Neuromyelitis Optica	61	0.992

654		GLL048	Glial Tumor	52	0.992

655		DBT010	Diabetic Neuropathy	54	0.992

656		MYP060	Myopic Macular Degeneration	19	0.992

657	P	FBR017	Fibrosarcoma	56	0.992

658	P	CND004	Candidiasis	58	0.992

659	P	LCT001	Lactic Acidosis	51	0.992

660	P	SYP003	Syphilis	59	0.992

661	P	ACN011	Acne	57	0.992

662		RDG001	Red-Green Color Blindness	28	0.992

663		PRS025	Presbyopia	38	0.992

664		UNL002	Unilateral Retinoblastoma	37	0.992

665		DRM006	Dermatitis	62	0.992

666		TXC008	Toxic Optic Neuropathy	27	0.992

667		CHR073	Choreatic Disease	54	0.992

668		ENT004	Enthesopathy	51	0.992

669	c	HPT016	Hepatitis B	62	0.992

670	P	ACT105	Acute Mountain Sickness	52	0.992

671		BRN071	Brain Injury	50	0.992

672	P	MYC033	Myoclonus	47	0.992

673		ACT177	Acute Basophilic Leukemia	34	0.985

674		DRM014	Dermatofibrosarcoma Protuberans	65	0.985

675	P	SYS005	Systemic Scleroderma	74	0.985

676		AMT001	Ametropic Amblyopia	26	0.985

677		VSC002	Vascular Dementia	60	0.985

678		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.985

679		AMR003	Amaurosis Fugax	33	0.985

680	c	SNR004	Senior-Loken Syndrome 4	26	0.944

681	c	MSC045	Muscular Dystrophy-Dystroglycanopathy , Type a, 3	36	0.944

682	c	LBR011	Leber Congenital Amaurosis 16	38	0.944

683	c	LBR009	Leber Congenital Amaurosis 14	41	0.944

684		HPT070	Hepatosplenic T-Cell Lymphoma	36	0.940

685	P	DBT005	Diabetes Insipidus	54	0.928

686		PRM155	Primary Cutaneous Anaplastic Large Cell Lymphoma	34	0.928

687		SHK001	Shaken Baby Syndrome	21	0.928

688	c	MCP049	Mucopolysaccharidosis, Type Vii	63	0.928

689		DNN001	Danon Disease	59	0.928

690		MYC006	Mycosis Fungoides	65	0.928

691	c	USH041	Usher Syndrome, Type if	47	0.928

692		HMC014	Homocysteinemia	52	0.928

693		BRK010	Burkitt Lymphoma	66	0.928

694	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.928

695		HMN044	Human Immunodeficiency Virus Type 1	78	0.928

696	P	ANP001	Anaplastic Large Cell Lymphoma	61	0.928

697	P	SLP006	Sleep Apnea	69	0.928

698	P	INF037	Inflammatory Bowel Disease	53	0.928

699	c	RTN044	Retinitis Pigmentosa 14	37	0.928

700	P	TYS001	Tay-Sachs Disease	69	0.928

701		LGH007	Leigh Syndrome	70	0.928

702	c	USH020	Usher Syndrome, Type Iic	45	0.928

703	P	PRN026	Porencephaly	55	0.928

704		PRT037	Pertussis	65	0.928

705	P	PRK039	Parkinsonism	55	0.928

706		MTC004	Mitochondrial Encephalomyopathy	42	0.928

707	P	HYP098	Hypereosinophilic Syndrome	66	0.928

708	P	RRH023	Rare Hereditary Hemochromatosis	54	0.928

709		NRN001	Neuroendocrine Carcinoma	47	0.928

710	P	OLV001	Olivopontocerebellar Atrophy	51	0.928

711	P	PNC025	Panic Disorder	52	0.928

712	P	MGR003	Migraine with Aura	52	0.928

713		HMS001	Hemosiderosis	48	0.928

714		CHR008	Choroiditis	48	0.928

715		CYS010	Cystinosis	62	0.928

716		LVR012	Liver Cirrhosis	63	0.928

717		OPT007	Optic Nerve Glioma	40	0.928

718		MDD011	Mood Disorder	62	0.928

719		DSR002	Disorders of Intracellular Cobalamin Metabolism	29	0.928

720		PRS063	Paresthesia	39	0.928

721		ALL014	Allergic Encephalomyelitis	34	0.928

722		MLN065	Melanocytic Nevus Syndrome, Congenital	62	0.888

723		PLS025	Plasmablastic Lymphoma	56	0.888

724		MLT165	Multilocular Cystic Renal Neoplasm of Low Malignant Potential	28	0.888

725		MLT003	Multilocular Clear Cell Renal Cell Carcinoma	32	0.888

726		OVR062	Ovary Serous Adenocarcinoma	25	0.888

727		PRM126	Primary Peritoneal Carcinoma	62	0.888

728		NGH031	Night Blindness, Congenital Stationary, Type1i	19	0.862

729		CHR603	Chronic Enteropathy Associated with Slco2a1 Gene	25	0.859

730		CTS003	Coats Disease	53	0.859

731		ACR008	Acrocallosal Syndrome	70	0.859

732		ANG004	Angioid Streaks	40	0.859

733		MNK001	Menkes Disease	64	0.859

734		HYP332	Hypotrichosis, Congenital, with Juvenile Macular Dystrophy	41	0.859

735		KSH004	Kashin-Beck Disease	38	0.859

736		VTR010	Vitreoretinochoroidopathy	49	0.859

737	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.859

738	c	BRD013	Bardet-Biedl Syndrome 12	44	0.859

739		NRT011	Neurotrophic Keratopathy	36	0.859

740	c	LRG001	Large Cell Carcinoma	48	0.859

741		INT007	Intermediate Coronary Syndrome	54	0.859

742		LRN003	Learning Disability	49	0.859

743	P	SKN015	Skin Carcinoma	71	0.859

744	P	DMN002	Dementia	66	0.859

745		BLR001	Biliary Atresia	55	0.859

746		HYD002	Hydronephrosis	58	0.859

747	P	STC001	Stickler Syndrome	60	0.859

748		TRC008	Trachoma	53	0.859

749	P	SHR001	Short Bowel Syndrome	53	0.859

750		HYD001	Hydranencephaly	43	0.859

751		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	46	0.859

752	P	KDN017	Kidney Cancer	61	0.859

753	c	GM2006	Gm2 Gangliosidosis	46	0.859

754	P	TMP001	Temporal Lobe Epilepsy	49	0.859

755		LST001	Listeriosis	59	0.859

756	c	MCP001	Mucopolysaccharidosis Iii	69	0.859

757	c	LKM005	Leukemia, T-Cell, Chronic	34	0.859

758		MCL079	Macular Telangiectasia Type 2	27	0.859

759		MLT035	Multifocal Choroiditis	31	0.859

760		ORN004	Ornithinemia	13	0.859

761	P	KNB001	Knobloch Syndrome	38	0.859

762	P	HYP058	Hypervitaminosis a	47	0.847

763		CLL002	Collecting Duct Carcinoma	54	0.846

764		ACR014	Acral Lentiginous Melanoma	52	0.846

765		LNG012	Lung Occult Squamous Cell Carcinoma	20	0.846

766		PPL004	Papillary Squamous Carcinoma	39	0.846

767		PNS010	Penis Squamous Cell Carcinoma	45	0.846

768		LNG007	Lung Mixed Small Cell and Squamous Cell Carcinoma	21	0.846

769		PNS005	Penis Mixed Squamous Cell Carcinoma	12	0.846

770		SSC001	Susac Syndrome	32	0.840

771	c	OPT051	Opitz Gbbb Syndrome, Type I	46	0.840

772	P	PRK057	Parkinson Disease, Late-Onset	80	0.840

773	P	FML011	Familial Adenomatous Polyposis	71	0.840

774		MYP067	Myopathy, Distal, Tateyama Type	28	0.840

775		CD4003	Cd40 Ligand Deficiency	54	0.840

776	P	ASP006	Aspergillosis	72	0.840

777		IMM174	Immunodeficiency with Hyper-Igm, Type 1	64	0.840

778		ISC001	Ischemic Neuropathy	27	0.840

779	c	CV3001	Cav3-Related Distal Myopathy	17	0.840

780	c	ACH038	Achromatopsia 7	37	0.839

781	c	NGH022	Night Blindness, Congenital Stationary, Type 1g	20	0.839

782	c	CNR012	Cone-Rod Dystrophy 11	27	0.839

783		KNB006	Knobloch Syndrome 1	43	0.839

784		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.839

785	c	RTN192	Retinitis Pigmentosa 77	22	0.839

786	c	RTN196	Retinitis Pigmentosa 78	20	0.839

787	c	RTN219	Retinitis Pigmentosa 85	18	0.839

788		CNR041	Cone-Rod Dystrophy and Hearing Loss 2	19	0.839

789	c	RTN157	Retinitis Pigmentosa 37	34	0.839

790	c	RTN227	Retinitis Pigmentosa 86	21	0.839

791		RTN232	Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Migraine Headache Syndrome	25	0.839

792	c	RTN213	Retinitis Pigmentosa 80	27	0.839

793	c	RTN217	Retinitis Pigmentosa 83	20	0.839

794	c	RTN234	Retinitis Pigmentosa 90	23	0.839

795		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.814

796		ACT201	Acute Posterior Multifocal Placoid Pigment Epitheliopathy	21	0.785

797		OPT077	Optic Disc Pit	17	0.785

798	c	TRN053	Transient Pseudohypoaldosteronism	24	0.785

799		OCL015	Oculomotor Apraxia	39	0.785

800		SPS057	Spasticity	42	0.785

801	P	OVR082	Overgrowth Syndrome	49	0.785

802		LRY022	Laryngoonychocutaneous Syndrome	43	0.785

803		SCH018	Schizencephaly	52	0.785

804		EPD052	Epidermolysis Bullosa Simplex Superficialis	17	0.785

805	c	BRD015	Bardet-Biedl Syndrome 3	48	0.785

806	c	RTN069	Retinitis Pigmentosa 7	44	0.785

807		OCL008	Oculopharyngeal Muscular Dystrophy	53	0.785

808	c	MCL059	Macular Dystrophy, Patterned, 1	29	0.785

809	P	ATX030	Ataxia-Telangiectasia	80	0.785

810		LNN001	Lennox-Gastaut Syndrome	61	0.785

811	c	OGC002	Oguchi Disease 2	35	0.785

812		BRN032	Brain Glioma	45	0.785

813		GNY003	Guanylate Cyclase 2e, Pseudogene	12	0.785

814	c	BRD019	Bardet-Biedl Syndrome 7	43	0.785

815	c	DFN093	Deafness, Autosomal Recessive 23	38	0.785

816	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	65	0.785

817	c	ALB009	Albinism, Oculocutaneous, Type Ia	53	0.785

818		MTC027	Mitochondrial Trifunctional Protein Deficiency	57	0.785

819		NRM019	Neuraminidase Deficiency	48	0.785

820	P	PSD087	Pseudoxanthoma Elasticum	67	0.785

821		PTR032	Peters-Plus Syndrome	63	0.785

822	c	BRD014	Bardet-Biedl Syndrome 2	53	0.785

823		ADN001	Adenosine Deaminase Deficiency	59	0.785

824	P	HRD018	Hair Disease	44	0.785

825		CLR017	Clear Cell Sarcoma	44	0.785

826	P	PRD008	Periodontitis	64	0.785

827	P	HYP061	Hypertrophic Cardiomyopathy	69	0.785

828		CNS004	Constipation	56	0.785

829	P	DMN001	Diamond-Blackfan Anemia	71	0.785

830	c	BSL007	Basal Cell Carcinoma	68	0.785

831		MLG169	Malignant Astrocytoma	57	0.785

832		PRT018	Portal Vein Thrombosis	50	0.785

833		ASP004	Asphyxia Neonatorum	50	0.785

834		ACQ002	Acquired Night Blindness	20	0.785

835	P	PRP019	Peripheral Nervous System Disease	58	0.785

836	c	GM1007	Gm1 Gangliosidosis	65	0.785

837		GLY031	Glycoproteinosis	49	0.785

838	P	BNG032	Benign Mesothelioma	53	0.785

839		VSC006	Vascular Cancer	46	0.785

840		HST011	Histoplasmosis	55	0.785

841	P	INS002	in Situ Carcinoma	53	0.785

842		MSC077	Muscle Eye Brain Disease	52	0.785

843		MSL001	Measles	61	0.785

844		MCR055	Microcephaly Nonsyndromal	9	0.785

845		PCH002	Pachygyria	32	0.785

846		RTC011	Reticular Dystrophy of Retinal Pigment Epithelium	18	0.724

847	c	CNR005	Cone-Rod Dystrophy 3	40	0.724

848	c	CNR014	Cone-Rod Dystrophy 16	42	0.724

849		ADR022	Adrenomyeloneuropathy	39	0.702

850	c	RRR006	Rare Retinal Disorder	8	0.702

851		MTR087	Maternal Uniparental Disomy	28	0.702

852	c	JVN041	Juvenile Nephronophthisis	43	0.702

853		CNG506	Congenital Amyoplasia	27	0.702

854		BTT011	Butterfly-Shaped Pigment Dystrophy	31	0.702

855		ATX010	Ataxia Neuropathy Spectrum	34	0.702

856		OLG014	Oligocone Trichromacy	25	0.702

857	c	NRF023	Neurofibromatosis, Type Ii	71	0.702

858		ATH013	Atherosclerosis Susceptibility	63	0.702

859		DRV001	Dravet Syndrome	69	0.702

860		MST006	Mast Syndrome	40	0.702

861		ADR007	Adrenoleukodystrophy	73	0.702

862	c	RTN053	Retinitis Pigmentosa 24	27	0.702

863	c	DFN146	Deafness, X-Linked 3	27	0.702

864	c	MCL046	Mucolipidosis Iii Alpha/beta	60	0.702

865	c	MCL016	Mucolipidosis Iii Gamma	50	0.702

866		SNS008	Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis	60	0.702

867	c	RTN068	Retinitis Pigmentosa 6	27	0.702

868	P	SPR120	Supranuclear Palsy, Progressive, 1	69	0.702

869	c	CRD185	Ceroid Lipofuscinosis, Neuronal, 6	53	0.702

870		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	62	0.702

871	P	KLZ004	Kala-Azar 1	41	0.702

872		MCL027	Macular Dystrophy, Dominant Cystoid	51	0.702

873	c	NRD017	Neurodegeneration with Brain Iron Accumulation 1	63	0.702

874	P	DST002	Distal Arthrogryposis	65	0.702

875		MRG003	Marginal Zone B-Cell Lymphoma	52	0.702

876	c	LNG050	Long Qt Syndrome 5	46	0.702

877	c	RTN143	Retinitis Pigmentosa 47	41	0.702

878	c	NGH028	Night Blindness, Congenital Stationary, Type 1d	26	0.702

879		BTT017	Beta-Thalassemia Major	51	0.702

880	c	USH040	Usher Syndrome, Type Id	47	0.702

881	P	FRD001	Friedreich Ataxia	61	0.702

882		LYM143	Lymphoma, Non-Hodgkin, Familial	75	0.702

883		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	34	0.702

884	c	NNP011	Nanophthalmos 2	26	0.702

885	c	RTN133	Retinitis Pigmentosa 43	29	0.702

886		MGL003	Megalocornea	47	0.702

887		CHN016	Cohen Syndrome	60	0.702

888		GLC012	Galactosialidosis	56	0.702

889		PGM007	Pigmented Paravenous Chorioretinal Atrophy	42	0.702

890	c	BNM018	Bone Mineral Density Quantitative Trait Locus 3	33	0.702

891		GLC003	Glucose Intolerance	54	0.702

892		PRM329	Premature Aging	36	0.702

893		THY029	Thyroid Carcinoma	51	0.702

894		XLN228	X-Linked Recessive Disease	24	0.702

895	P	NRD007	Neurodegeneration with Brain Iron Accumulation	52	0.702

896	c	CRD179	Ceroid Lipofuscinosis, Neuronal, 7	49	0.702

897	P	RNG032	Ring Chromosome	39	0.702

898	P	ZLL001	Zellweger Syndrome	65	0.702

899	P	FBR003	Fibrous Histiocytoma	43	0.702

900		GLC001	Glaucomatocyclitic Crisis	27	0.702

901		KRT006	Keratoconjunctivitis	53	0.702

902	P	HRP006	Herpes Simplex	65	0.702

903		LSH001	Leishmaniasis	64	0.702

904	P	TRM003	Tremor	48	0.702

905	c	ATS025	Autosomal Dominant Progressive External Ophthalmoplegia	45	0.702

906	P	TXC009	Toxic Maculopathy	21	0.702

907		SPS087	Spasmus Nutans	21	0.702

908		PNM008	Pneumothorax	54	0.702

909		MLG077	Malignant Peripheral Nerve Sheath Tumor	54	0.702

910		SMN007	Seminoma	42	0.702

911	P	GRV001	Graves' Disease	55	0.702

912	c	SCN007	Secondary Hyperparathyroidism	51	0.702

913		PRP026	Peripheral Retinal Degeneration	29	0.702

914	P	HYP069	Hyperparathyroidism	62	0.702

915		RBS002	Rubeosis Iridis	32	0.702

916	P	ECL001	Eclampsia	52	0.702

917		ACC002	Accommodative Spasm	25	0.702

918	P	PRN023	Prion Disease	60	0.702

919	P	INT068	Intestinal Disease	53	0.702

920		ERL001	Early Myoclonic Encephalopathy	62	0.702

921	P	CPL006	Capillary Hemangioma	53	0.702

922		LNS001	Lens Subluxation	39	0.702

923		DBT007	Diabetic Cataract	36	0.702

924	P	ACT028	Acute Closed-Angle Glaucoma	32	0.702

925		LKC002	Leukocoria	33	0.702

926		SLR002	Solar Retinopathy	28	0.702

927		RTN004	Retinal Microaneurysm	33	0.702

928		DBT004	Diabetic Polyneuropathy	50	0.702

929		CRB033	Cerebral Degeneration	39	0.702

930		HDR002	Hidradenitis Suppurativa	54	0.702

931		HDR003	Hidradenitis	50	0.702

932		IRN002	Iron Metabolism Disease	57	0.702

933		NRN004	Neuroendocrine Tumor	59	0.702

934	P	MRQ003	Morquio Syndrome	35	0.702

935		PLM033	Pulmonary Embolism	58	0.702

936		DYS032	Dystrophinopathies	47	0.702

937		PLG003	Polg-Related Disorders	20	0.702

938		STM007	Stomatitis	54	0.702

939	P	SCK005	Sickle Cell Disease	56	0.702

940		MYT011	Myotonia	39	0.702

941		PRN039	Paraneoplastic Syndromes	37	0.702

942		FRS019	Farsightedness	36	0.702

943	P	NNS072	Nonsyndromic Hearing Loss