Search results for erg

446 hits were found for erg

#	Family	MCID	Name	MIFTS	Score
1	P	PRS040	Prostate Cancer	97	6.279

2		EWN003	Ewing Sarcoma	69	6.214

3	P	MYL006	Myeloid Leukemia	60	5.909

4	P	LKM002	Leukemia	68	5.786

5		SRC014	Sarcoma	65	5.205

6		MYX005	Myxoid Liposarcoma	66	3.278

7	c	RTN035	Retinal Cone Dystrophy 3b	32	3.151

8		PRS006	Prostatic Acinar Adenocarcinoma	27	2.346

9		EXT052	Extraskeletal Ewing Sarcoma	33	2.306

10		RTN023	Retinitis	46	0.268

11		NRR001	Neuroretinitis	42	0.268

12	P	RTN008	Retinitis Pigmentosa	79	0.266

13	c	LKM061	Leukemia, Acute Myeloid	84	0.257

14	P	RTN016	Retinal Degeneration	53	0.226

15		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.215

16	P	MCR115	Microvascular Complications of Diabetes 5	66	0.204

17		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.201

18	P	NGH001	Night Blindness	48	0.201

19	P	RTN018	Retinal Disease	53	0.198

20		RTN017	Retinal Detachment	61	0.173

21	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.160

22	P	ADN016	Adenocarcinoma	64	0.160

23	P	CNG010	Congenital Stationary Night Blindness	54	0.160

24	P	CND005	Cone Dystrophy	43	0.152

25	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.148

26	P	CTR002	Cataract	60	0.140

27	c	ACT073	Acute Leukemia	58	0.136

28		DWN001	Down Syndrome	70	0.132

29		RTN209	Retinoschisis 1, X-Linked, Juvenile	62	0.132

30		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.127

31	P	MYP006	Myopia	55	0.123

32		PTH003	Pathologic Nystagmus	52	0.123

33		AMB002	Amblyopia	49	0.118

34		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.118

35		SPP007	Suppression Amblyopia	39	0.118

36	P	LNG028	Long Qt Syndrome	66	0.113

37	P	OPT006	Optic Nerve Disease	60	0.113

38	P	OPN001	Open-Angle Glaucoma	49	0.113

39	P	ACH003	Achromatopsia	61	0.108

40	c	CNT016	Central Retinal Vein Occlusion	53	0.108

41		SPN035	Spindle Cell Sarcoma	53	0.108

42	P	RTN022	Retinal Vein Occlusion	53	0.108

43		SCT002	Scotoma	44	0.108

44	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.102

45	P	OPT009	Optic Neuritis	57	0.102

46		NRT004	Neuritis	52	0.102

47		OCC002	Occult Macular Dystrophy	43	0.102

48		CHR178	Chromosomal Triplication	35	0.102

49		CYT019	Cytogenetically Normal Acute Myeloid Leukemia	33	0.102

50	P	MSC005	Muscular Dystrophy	66	0.096

51		MGK001	Megakaryocytic Leukemia	64	0.096

52		FND002	Fundus Dystrophy	55	0.096

53		PRS045	Prostatic Hypertrophy	53	0.096

54		OCL006	Ocular Hypertension	53	0.096

55	c	INH030	Inherited Retinal Disorder	51	0.096

56		RTN003	Retinal Ischemia	50	0.096

57	P	OGC005	Oguchi Disease	39	0.096

58	P	CNR004	Cone-Rod Dystrophy 2	73	0.090

59		MSC157	Muscular Dystrophy, Duchenne Type	72	0.090

60		SPP011	Suppression of Tumorigenicity 12	59	0.090

61		PRS021	Prostatic Adenoma	51	0.090

62	P	RTN014	Retinal Artery Occlusion	47	0.090

63		MCL003	Macular Holes	40	0.090

64		BRN026	Branch Retinal Artery Occlusion	40	0.090

65	c	NGH029	Night Blindness, Congenital Stationary, Type 1e	37	0.090

66		ANG020	Angiosarcoma	64	0.083

67		FND001	Fundus Albipunctatus	60	0.083

68	P	UVT001	Uveitis	57	0.083

69		MCL006	Macular Retinal Edema	55	0.083

70		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.083

71		KRT002	Keratomalacia	47	0.083

72	c	CNT028	Central Retinal Artery Occlusion	43	0.083

73		PPL052	Papillomatosis, Confluent and Reticulated	33	0.083

74	c	EXD008	Exudative Vitreoretinopathy 1	71	0.076

75	P	LPS002	Liposarcoma	65	0.076

76		ENH001	Enhanced S-Cone Syndrome	57	0.076

77		PRS129	Prostatic Hyperplasia, Benign	49	0.076

78		47X002	47,xyy	49	0.076

79		ALB002	Albinism	46	0.076

80		RFR003	Refractive Error	43	0.076

81	P	CNG024	Congenital Nystagmus	36	0.076

82		MLN046	Melanoma-Associated Retinopathy	24	0.076

83	P	RTN024	Retinoblastoma	73	0.068

84	P	NRB001	Neuroblastoma	72	0.068

85	c	LNG047	Long Qt Syndrome 2	58	0.068

86	P	NRP001	Neuropathy	56	0.068

87		OPT070	Optic Nerve Hypoplasia, Bilateral	56	0.068

88	c	FML008	Familial Retinoblastoma	53	0.068

89		DBT006	Diabetic Macular Edema	48	0.068

90		RTN020	Retinal Vascular Disease	46	0.068

91	P	EPT012	Epithelioid Sarcoma	44	0.068

92		CHL149	Childhood Acute Myeloid Leukemia	44	0.068

93	P	SDR002	Siderosis	44	0.068

94		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.068

95		SMT004	Smith-Lemli-Opitz Syndrome	70	0.059

96		OST159	Osteogenic Sarcoma	66	0.059

97		MYL031	Myeloproliferative Neoplasm	66	0.059

98		KRN002	Kearns-Sayre Syndrome	63	0.059

99	P	ANR048	Aniridia 1	63	0.059

100	P	VSC007	Vascular Disease	63	0.059

101	P	USH001	Usher Syndrome	60	0.059

102		ISC004	Ischemia	58	0.059

103	P	STR022	Stargardt Disease	58	0.059

104		EYD002	Eye Disease	58	0.059

105		HYP266	Hypoxia	57	0.059

106		HPT046	Hepatic Veno-Occlusive Disease	56	0.059

107		ERY051	Erythroleukemia, Familial	56	0.059

108	P	END047	Endophthalmitis	53	0.059

109	c	CNR007	Cone-Rod Dystrophy 6	53	0.059

110	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	52	0.059

111		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.059

112	c	LBR012	Leber Congenital Amaurosis 2	51	0.059

113	P	HYP058	Hypervitaminosis a	48	0.059

114		KHN001	Kuhnt-Junius Degeneration	47	0.059

115		BST008	Bestrophinopathy, Autosomal Recessive	46	0.059

116	c	CHR095	Chronic Progressive External Ophthalmoplegia	46	0.059

117	c	RTN150	Retinitis Pigmentosa 10	45	0.059

118	c	PLM170	Pulmonary Venoocclusive Disease 1, Autosomal Dominant	45	0.059

119	c	PCH010	Pachyonychia Congenita 3	44	0.059

120		RTN187	Retinitis Pigmentosa-Deafness Syndrome	42	0.059

121	P	PLM025	Pulmonary Venoocclusive Disease	42	0.059

122		MSN004	Mesenchymal Cell Neoplasm	41	0.059

123		ANX004	Anoxia	40	0.059

124	c	MCR122	Microphthalmia, Isolated 5	39	0.059

125		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.059

126	c	OGC001	Oguchi Disease 1	38	0.059

127		FST001	Foster-Kennedy Syndrome	36	0.059

128		CNC014	Cancer-Associated Retinopathy	34	0.059

129		MCL057	Macular Dystrophy with Central Cone Involvement	31	0.059

130	c	CND012	Cone Dystrophy 4	30	0.059

131	P	MCL035	Macular Dystrophy, Retinal, 2	26	0.059

132	P	CNR040	Cone-Rod Dystrophy and Hearing Loss 1	25	0.059

133	c	USH046	Usher Syndrome, Type 1m	15	0.059

134	P	LNG032	Lung Cancer	98	0.048

135		MYL069	Myeloma, Multiple	85	0.048

136		CYS001	Cystic Fibrosis	81	0.048

137		OST012	Osteoarthritis	78	0.048

138	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.048

139	P	SCH015	Schizophrenia	74	0.048

140	P	MLT020	Multiple Sclerosis	72	0.048

141	P	GRF003	Graft-Versus-Host Disease	72	0.048

142		MYL009	Myelodysplastic Syndrome	70	0.048

143	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.048

144		ART016	Aortic Aneurysm	69	0.048

145	P	CRD119	Cardiac Arrest	67	0.048

146	P	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	65	0.048

147		ALS001	Alstrom Syndrome	64	0.048

148	P	RHB003	Rhabdomyosarcoma	63	0.048

149		MSC152	Muscular Dystrophy, Becker Type	63	0.048

150		ACT119	Acute Promyelocytic Leukemia	63	0.048

151		RHB001	Rhabdoid Cancer	63	0.048

152	c	GLC092	Glaucoma, Primary Open Angle	62	0.048

153	P	ENC018	Encephalopathy	61	0.048

154	P	HMN010	Hemangioma	61	0.048

155	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	60	0.048

156	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.048

157		SRC027	Sarcoma, Synovial	58	0.048

158		GYR004	Gyrate Atrophy of Choroid and Retina	57	0.048

159		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.048

160	P	CHN012	Chondrosarcoma	56	0.048

161	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.048

162	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	55	0.048

163	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	54	0.048

164		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.048

165	P	SML001	Small Cell Carcinoma	52	0.048

166		IMP005	Impotence	52	0.048

167	c	LBR004	Leber Congenital Amaurosis 1	52	0.048

168	c	ACT135	Acute Graft Versus Host Disease	52	0.048

169		OCL069	Ocular Motor Apraxia	51	0.048

170	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	50	0.048

171		TRT020	Tritanopia	49	0.048

172		CHL061	Childhood Leukemia	48	0.048

173		BRD025	Birdshot Chorioretinopathy	48	0.048

174	P	CLR019	Color Blindness	48	0.048

175		MYP002	Myoepithelial Carcinoma	47	0.048

176		ATN005	Autonomic Dysfunction	46	0.048

177	c	KNB006	Knobloch Syndrome 1	46	0.048

178		PTT037	Pituitary Tumors	44	0.048

179	c	RTN172	Retinitis Pigmentosa 1	44	0.048

180	c	NGH010	Night Blindness, Congenital Stationary, Autosomal Dominant 2	44	0.048

181		PRL047	Prolonged Electroretinal Response Suppression	42	0.048

182		SPN050	Spinocerebellar Degeneration	42	0.048

183	P	VTL001	Vitelliform Macular Dystrophy	42	0.048

184		CLR033	Color Vision Deficiency	41	0.048

185	c	ACH038	Achromatopsia 7	39	0.048

186	c	RTN054	Retinitis Pigmentosa 25	39	0.048

187	c	RTN048	Retinitis Pigmentosa 19	38	0.048

188	c	CNR038	Cone-Rod Dystrophy, X-Linked, 3	38	0.048

189	c	CND011	Cone Dystrophy 3	38	0.048

190	c	NGH008	Night Blindness, Congenital Stationary, Autosomal Dominant 3	37	0.048

191	c	RTN157	Retinitis Pigmentosa 37	36	0.048

192	P	HRD217	Hereditary Optic Neuropathy	36	0.048

193	c	RTN036	Retinal Cone Dystrophy 4	35	0.048

194		CNR033	Cone-Rod Synaptic Disorder, Congenital Nonprogressive	35	0.048

195		HRD016	Hereditary Retinal Dystrophy	35	0.048

196		BST007	Best Vitelliform Macular Dystrophy	34	0.048

197		BRN041	Bornholm Eye Disease	34	0.048

198	c	NGH007	Night Blindness, Congenital Stationary, Type 1b	33	0.048

199	c	CNR012	Cone-Rod Dystrophy 11	28	0.048

200	P	ATM076	Autoimmune Retinopathy	27	0.048

201	c	RTN213	Retinitis Pigmentosa 80	27	0.048

202	c	RTN192	Retinitis Pigmentosa 77	23	0.048

203	c	RTN230	Retinitis Pigmentosa 88	21	0.048

204	c	RTN196	Retinitis Pigmentosa 78	21	0.048

205	c	RTN217	Retinitis Pigmentosa 83	20	0.048

206	c	NGH022	Night Blindness, Congenital Stationary, Type 1g	20	0.048

207	c	RTN227	Retinitis Pigmentosa 86	19	0.048

208		RTN191	Retinal Dystrophy with or Without Extraocular Anomalies	19	0.048

209	c	RTN219	Retinitis Pigmentosa 85	19	0.048

210	c	CNR041	Cone-Rod Dystrophy and Hearing Loss 2	18	0.048

211		ACT186	Acute Megakaryoblastic Leukemia in Down Syndrome	16	0.048

212		MCL029	Macular Degeneration, X-Linked Atrophic	14	0.048

213	P	OVR042	Ovarian Cancer	88	0.034

214	P	GST053	Gastric Cancer	83	0.034

215		MLR004	Malaria	81	0.034

216		GST019	Gastrointestinal Stromal Tumor	78	0.034

217	P	PRK057	Parkinson Disease, Late-Onset	78	0.034

218	c	NRF024	Neurofibromatosis, Type I	77	0.034

219		CRV035	Cervical Cancer	76	0.034

220		KPS004	Kaposi Sarcoma	75	0.034

221		GLB015	Glioblastoma Multiforme	75	0.034

222	P	NJM001	Nijmegen Breakage Syndrome	74	0.034

223		SVR004	Severe Combined Immunodeficiency	73	0.034

224		SCH036	Scheie Syndrome	72	0.034

225	P	FML011	Familial Adenomatous Polyposis	72	0.034

226		BHC003	Behcet Syndrome	71	0.034

227	P	ATS364	Autism	70	0.034

228		MLT157	Multiple System Atrophy 1	70	0.034

229	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	70	0.034

230	P	OST001	Osteopetrosis	70	0.034

231	P	MYP004	Myopathy	70	0.034

232	P	ASP006	Aspergillosis	69	0.034

233	P	MLN008	Melanoma	69	0.034

234	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.034

235	P	HYP086	Hypothyroidism	69	0.034

236	P	LYM118	Lymphoma	68	0.034

237	P	TMP003	Temporal Arteritis	68	0.034

238		SKN019	Skin Melanoma	68	0.034

239	P	THR014	Thrombocytopenia	67	0.034

240	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.034

241	P	PLM037	Pulmonary Hypertension	67	0.034

242	c	RHB024	Rhabdomyosarcoma 2	67	0.034

243		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.034

244	c	MCR129	Microvascular Complications of Diabetes 1	66	0.034

245	c	MCL013	Mucolipidosis Iv	66	0.034

246	P	BRD002	Bardet-Biedl Syndrome	66	0.034

247	P	ART005	Arteriovenous Malformation	65	0.034

248		KRT019	Keratitis, Hereditary	65	0.034

249		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.034

250		HRL003	Hurler Syndrome	65	0.034

251	c	WLM013	Wilms Tumor 1	65	0.034

252	P	CHR071	Charcot-Marie-Tooth Disease	65	0.034

253	P	DBT009	Diabetes Mellitus	64	0.034

254	P	HRM001	Hermansky-Pudlak Syndrome	64	0.034

255		MSC007	Muscle Hypertrophy	64	0.034

256		HYP020	Hyperprolactinemia	64	0.034

257	P	GLM045	Glioma	63	0.034

258	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.034

259		DPR016	Depression	63	0.034

260		IMM174	Immunodeficiency with Hyper-Igm, Type 1	63	0.034

261	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	62	0.034

262	P	VSC011	Vasculitis	62	0.034

263		ATM095	Autoimmune Disease	62	0.034

264		ALL026	Allergic Hypersensitivity Disease	62	0.034

265		ATY005	Atypical Teratoid Rhabdoid Tumor	61	0.034

266		HYP066	Hyperglycemia	61	0.034

267		WST001	West Syndrome	61	0.034

268	c	WLM018	Wilms Tumor 5	61	0.034

269	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.034

270		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.034

271		CRD223	Cardiac Arrhythmia	60	0.034

272	P	SNS001	Sensorineural Hearing Loss	60	0.034

273	P	OCL002	Oculocutaneous Albinism	60	0.034

274	P	THL005	Thalassemia	60	0.034

275	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.034

276		CHL014	Cholera	59	0.034

277		PRT058	Pure Autonomic Failure	59	0.034

278	c	LTN004	Late-Onset Retinal Degeneration	59	0.034

279		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.034

280		ANR040	Aneurysm	59	0.034

281	P	BCL017	B-Cell Lymphoma	58	0.034

282		CRD132	Cardiac Conduction Defect	58	0.034

283		CHR072	Chordoma	58	0.034

284		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.034

285		CHR081	Choroideremia	57	0.034

286	c	LKM070	Leukemia, Acute Monocytic	57	0.034

287		AYM001	Ayme-Gripp Syndrome	57	0.034

288	P	BPL003	Bipolar Disorder	56	0.034

289	P	SNR003	Senior-Loken Syndrome 1	56	0.034

290		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.034

291	P	ISL078	Isolated Ectopia Lentis	56	0.034

292	P	LBR014	Leber Congenital Amaurosis 4	56	0.034

293	c	FRS014	Fraser Syndrome 1	56	0.034

294		AGN016	Aging	56	0.034

295	c	CRD183	Ceroid Lipofuscinosis, Neuronal, 2	55	0.034

296		DFF005	Diffuse Large B-Cell Lymphoma	55	0.034

297	P	STR020	Strabismus	55	0.034

298		HRL004	Hurler-Scheie Syndrome	55	0.034

299	P	HYP076	Hyperthyroidism	55	0.034

300		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.034

301		DBF001	D-Bifunctional Protein Deficiency	54	0.034

302	c	PST005	Posterior Uveitis	54	0.034

303		PNC001	Pancytopenia	54	0.034

304	c	SPN294	Spinocerebellar Ataxia 1	53	0.034

305	c	JBR041	Joubert Syndrome 3	53	0.034

306	P	MNC007	Monocytic Leukemia	53	0.034

307		NVS001	Neovascular Glaucoma	53	0.034

308		INT075	Intracranial Hypertension	53	0.034

309	c	FML191	Familial Long Qt Syndrome	53	0.034

310		OST011	Osteomalacia	52	0.034

311		APR001	Apraxia	52	0.034

312		ACT200	Acute Monoblastic Leukemia	52	0.034

313		DSM007	Desmoplastic Small Round Cell Tumor	52	0.034

314		ONC002	Onchocerciasis	52	0.034

315	P	SPP010	Suppressor of Tumorigenicity 3	51	0.034

316		SRS007	Sorsby Fundus Dystrophy	51	0.034

317		ILS001	Ileus	51	0.034

318	P	PRC012	Pericardial Effusion	51	0.034

319		HYP781	Hypoascorbemia	51	0.034

320		ALN001	Aland Island Eye Disease	50	0.034

321		CHR078	Chorioretinitis	50	0.034

322		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.034

323		CYT005	Cytomegalovirus Retinitis	50	0.034

324	P	OBS001	Obstructive Jaundice	50	0.034

325	P	CHR637	Choroidal Dystrophy, Central Areolar, 1	50	0.034

326	P	MYT002	Myotonic Dystrophy	49	0.034

327	P	MTC133	Mitochondrial Myopathy	49	0.034

328		MYL003	Myeloid Sarcoma	49	0.034

329	c	BPL002	Bipolar I Disorder	49	0.034

330		INT054	Intraocular Lymphoma	48	0.034

331		ATS010	Autosomal Recessive Disease	48	0.034

332	c	USH035	Usher Syndrome Type 2	48	0.034

333		SPL018	Splenomegaly	48	0.034

334		HMP001	Hemopericardium	48	0.034

335		AST006	Astigmatism	47	0.034

336		LNG020	Lung Oat Cell Carcinoma	47	0.034

337		RTN001	Retinal Vasculitis	47	0.034

338		PRX028	Peroxisomal Acyl-Coa Oxidase Deficiency	47	0.034

339	c	STR084	Stargardt Disease 1	47	0.034

340	c	OPT051	Opitz Gbbb Syndrome, Type I	47	0.034

341		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.034

342		CD4003	Cd40 Ligand Deficiency	46	0.034

343		BCK003	Background Diabetic Retinopathy	46	0.034

344	c	LBR005	Leber Congenital Amaurosis 10	45	0.034

345		PST048	Postural Orthostatic Tachycardia Syndrome	45	0.034

346	c	LBR018	Leber Congenital Amaurosis 8	45	0.034

347	P	MNT185	Mental Retardation, Autosomal Dominant 7	45	0.034

348		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.034

349	c	LBR016	Leber Congenital Amaurosis 6	44	0.034

350		SPN032	Spindle Cell Carcinoma	44	0.034

351		FBR054	Fibroma	44	0.034

352		CHN010	Chondroma	43	0.034

353		MYX004	Myxedema	43	0.034

354	P	EPT020	Epithelioid Hemangioendothelioma	43	0.034

355		PRS042	Prostate Disease	43	0.034

356	P	HYP265	Hypotonia	43	0.034

357	P	MJR007	Major Affective Disorder 1	43	0.034

358		ONC003	Oncogenic Osteomalacia	42	0.034

359	c	MCL066	Macular Dystrophy, Vitelliform, 2	42	0.034

360	c	JBR013	Joubert Syndrome 8	42	0.034

361		EST005	Esotropia	42	0.034

362	c	LBR009	Leber Congenital Amaurosis 14	42	0.034

363	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.034

364		MCH006	Mechanical Strabismus	42	0.034

365	P	MSN005	Mesenchymal Chondrosarcoma	41	0.034

366		EST007	Estrogen Resistance	41	0.034

367	c	MJR024	Major Affective Disorder 9	41	0.034

368		LYM116	Lymph Node Disease	41	0.034

369	c	MCR112	Microvascular Complications of Diabetes 2	41	0.034

370	c	CNG195	Congenital Disorder of Glycosylation, Type Id	40	0.034

371	c	CNR014	Cone-Rod Dystrophy 16	40	0.034

372	c	RTN114	Retinitis Pigmentosa 58	40	0.034

373		CHN053	Chondromyxoid Fibroma	39	0.034

374		BLT001	Bilateral Retinoblastoma	39	0.034

375	c	RTN056	Retinitis Pigmentosa 28	39	0.034

376	c	CNR005	Cone-Rod Dystrophy 3	39	0.034

377	c	LBR017	Leber Congenital Amaurosis 7	38	0.034

378	c	MJR022	Major Affective Disorder 8	38	0.034

379		HPT070	Hepatosplenic T-Cell Lymphoma	38	0.034

380		MCP033	Mucopolysaccharidoses	38	0.034

381		CNT060	Central Serous Chorioretinopathy	38	0.034

382		PST036	Posterior Column Ataxia with Retinitis Pigmentosa	38	0.034

383	P	CNR031	Cone-Rod Dystrophy, X-Linked, 1	37	0.034

384		CRT012	Cortical Blindness	37	0.034

385	c	LBR011	Leber Congenital Amaurosis 16	37	0.034

386		PRR004	Preretinal Fibrosis	37	0.034

387	P	CRB059	Cerebellar Degeneration	37	0.034

388		SVR002	Severe Nonproliferative Diabetic Retinopathy	37	0.034

389	c	LBR006	Leber Congenital Amaurosis 11	36	0.034

390	c	CNR013	Cone-Rod Dystrophy 12	36	0.034

391		CRB159	Cerebral Visual Impairment	35	0.034

392	c	RTN180	Retinitis Pigmentosa 74	35	0.034

393		ASK001	Askin's Tumor	35	0.034

394		BTH002	Bothnia Retinal Dystrophy	35	0.034

395		RFM001	Roifman Syndrome	35	0.034

396	c	CRD216	Ceroid Lipofuscinosis, Neuronal, 9	35	0.034

397	c	MJR008	Major Affective Disorder 2	35	0.034

398	c	MNS014	Monosomy 22	35	0.034

399		AMR003	Amaurosis Fugax	34	0.034

400	c	CNR017	Cone-Rod Dystrophy 9	34	0.034

401		ACT177	Acute Basophilic Leukemia	34	0.034

402		CLR005	Clear Cell Chondrosarcoma	34	0.034

403		OPT001	Optic Disk Drusen	34	0.034

404		HMN016	Hemangioendothelioma	34	0.034

405		CRB006	Cribriform Carcinoma	33	0.034

406	c	MJR023	Major Affective Disorder 7	33	0.034

407	c	MSC045	Muscular Dystrophy-Dystroglycanopathy , Type a, 3	33	0.034

408	c	MJR003	Major Affective Disorder 6	33	0.034

409	c	MJR006	Major Affective Disorder 5	33	0.034

410		SSC001	Susac Syndrome	32	0.034

411	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.034

412		PLY150	Polykaryocytosis Inducer	31	0.034

413		CLR132	Colorblindness, Partial, Deutan Series	30	0.034

414		MNC001	Monocular Esotropia	30	0.034

415		CHN003	Chondroblastic Osteosarcoma	29	0.034

416		ISC001	Ischemic Neuropathy	29	0.034

417	c	MCL030	Macular Degeneration, Age-Related, 10	29	0.034

418		PST092	Posttransplant Acute Limbic Encephalitis	29	0.034

419	c	MJR004	Major Affective Disorder 4	28	0.034

420		MYP067	Myopathy, Distal, Tateyama Type	28	0.034

421	c	NNS043	Nonsyndromic Retinitis Pigmentosa	27	0.034

422		AMT001	Ametropic Amblyopia	27	0.034

423	c	SNR004	Senior-Loken Syndrome 4	26	0.034

424	c	PRX066	Peroxisome Biogenesis Disorder 3b	26	0.034

425		XLN012	X-Linked Congenital Stationary Night Blindness	26	0.034

426		CRY010	Cryptophthalmos	25	0.034

427		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.034

428	c	NGH030	Night Blindness, Congenital Stationary, Type 1f	25	0.034

429	c	RTN032	Retinal Cone Dystrophy 1	24	0.034

430	c	PRS134	Prostate Cancer, Hereditary, 3	24	0.034

431		SYN149	Syndromic Rod-Cone Dystrophy	22	0.034

432	c	MCL061	Macular Dystrophy, Vitelliform, 4	21	0.034

433		RRV005	Rare Vascular Tumor	20	0.034

434		RTN037	Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma	19	0.034

435		LTT006	Littoral Cell Angioma of the Spleen	19	0.034

436		INT334	Intellectual Developmental Disorder and Retinitis Pigmentosa	19	0.034

437		PHC015	Phacoanaphylactic Uveitis	19	0.034

438		MYP155	Myopathy, Congenital, with Tremor	19	0.034

439		ACT235	Acute Macular Neuroretinopathy	19	0.034

440		EXT012	Extraskeletal Chondroma	19	0.034

441		RTC011	Reticular Dystrophy of Retinal Pigment Epithelium	18	0.034

442		NGH031	Night Blindness, Congenital Stationary, Type1i	18	0.034

443		RTN229	Retinitis Pigmentosa 87 with Choroidal Involvement	17	0.034

444		PRP099	Peripheral Cone Dystrophy	15	0.034

445	c	CV3001	Cav3-Related Distal Myopathy	15	0.034

446		OPT069	Optic Atrophy with Negative Electroretinograms	9	0.034