Search results for Succinic acid

834 hits were found for Succinic acid

#	Family	MCID	Name	MIFTS	Score
1		ARG002	Argininosuccinic Aciduria	60	3.441

2		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.315

3	P	LVR013	Liver Disease	68	0.293

4		CHL068	Cholestasis	60	0.277

5	P	NRB001	Neuroblastoma	71	0.274

6		DPR016	Depression	63	0.265

7		FTT001	Fatty Liver Disease	61	0.263

8		48X005	48,xyyy	39	0.263

9		SCC001	Succinic Semialdehyde Dehydrogenase Deficiency	58	0.256

10	P	CLR023	Colorectal Cancer	98	0.254

11		MNT002	Mental Depression	57	0.251

12	P	KDN018	Kidney Disease	70	0.250

13	P	SZR006	Seizure Disorder	58	0.250

14		ISC004	Ischemia	60	0.246

15	P	BRS047	Breast Cancer	96	0.243

16		LVR012	Liver Cirrhosis	63	0.243

17		NRL016	Neural Tube Defects	82	0.241

18		VSL002	Visual Epilepsy	58	0.241

19	c	HYP595	Hypertension, Essential	84	0.240

20	P	DRR001	Diarrhea	57	0.231

21	P	PRG013	Paraganglioma	52	0.230

22		MTB004	Metabolic Acidosis	50	0.229

23	P	PHC003	Pheochromocytoma	71	0.229

24	P	MJR001	Major Depressive Disorder	68	0.229

25		ACT119	Acute Promyelocytic Leukemia	63	0.227

26		HYP266	Hypoxia	56	0.224

27		HLX001	Helix Syndrome	47	0.222

28		ADR040	Adrenal Gland Pheochromocytoma	46	0.221

29	P	PRS040	Prostate Cancer	97	0.220

30	c	MGR028	Migraine with or Without Aura 1	69	0.219

31		LWC001	Low Compliance Bladder	42	0.218

32		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.217

33		HYP014	Hyperuricemia	51	0.216

34	P	HRT032	Heart Disease	75	0.214

35		CLT003	Colitis	62	0.213

36		HYP066	Hyperglycemia	61	0.209

37	P	ENC018	Encephalopathy	61	0.207

38		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.207

39	P	LKM002	Leukemia	66	0.206

40		HYP056	Hypoglycemia	66	0.204

41	P	DDN001	Duodenal Ulcer	50	0.204

42		ALL026	Allergic Hypersensitivity Disease	64	0.203

43		LPD008	Lipid Metabolism Disorder	62	0.200

44		CNG034	Congestive Heart Failure	70	0.200

45	P	HPT023	Hepatocellular Carcinoma	100	0.199

46	P	GLM045	Glioma	63	0.197

47		ULC004	Ulcerative Colitis	73	0.197

48		GLL048	Glial Tumor	45	0.195

49		OST012	Osteoarthritis	78	0.194

50		ADL002	Adult Syndrome	69	0.194

51		ADN018	Adenoma	58	0.193

52		DRM006	Dermatitis	61	0.190

53	P	CRN300	Coronary Heart Disease 1	63	0.189

54		DFC004	Deficiency Anemia	75	0.189

55	P	MYP004	Myopathy	64	0.189

56	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.188

57		BNR002	Bone Resorption Disease	48	0.187

58	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	57	0.187

59		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.186

60		GLB015	Glioblastoma Multiforme	75	0.185

61		IRN002	Iron Metabolism Disease	57	0.185

62		CRB039	Cerebrovascular Disease	69	0.181

63		END040	Endogenous Depression	54	0.181

64		PPT005	Peptic Ulcer Disease	58	0.181

65		GT001	Gout	63	0.179

66		ATM095	Autoimmune Disease	61	0.179

67		NRT001	Neurotic Disorder	52	0.178

68		STT001	Status Epilepticus	59	0.178

69		ATX038	Ataxia and Polyneuropathy, Adult-Onset	44	0.177

70	P	VSC007	Vascular Disease	63	0.177

71		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.176

72	P	INF037	Inflammatory Bowel Disease	56	0.173

73		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.172

74		OCL069	Ocular Motor Apraxia	51	0.172

75		PRT037	Pertussis	65	0.172

76	P	OVR042	Ovarian Cancer	89	0.172

77	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	89	0.171

78		SPN186	Spinal Cord Injury	60	0.171

79	c	RHB024	Rhabdomyosarcoma 2	65	0.171

80	P	MYC007	Myocardial Infarction	70	0.171

81		STR067	Stroke, Ischemic	80	0.171

82		ATH013	Atherosclerosis Susceptibility	66	0.171

83	P	HNT016	Huntington Disease	71	0.170

84	P	ALZ034	Alzheimer Disease	88	0.170

85	P	ADN016	Adenocarcinoma	64	0.170

86	P	PSR002	Psoriasis	62	0.169

87	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.169

88	P	GST053	Gastric Cancer	83	0.168

89	P	LYM031	Lymphocytic Leukemia	55	0.168

90	P	HYP750	Hypertriglyceridemia, Familial	61	0.168

91		PST011	Pustulosis of Palm and Sole	52	0.168

92	P	CRN018	Coronary Artery Anomaly	63	0.167

93	c	CHR684	Chronic Kidney Disease	66	0.167

94	P	HYP265	Hypotonia	42	0.166

95		PLM001	Pulmonary Tuberculosis	70	0.165

96		47X002	47,xyy	49	0.164

97	c	GLL024	Gallbladder Disease 1	52	0.162

98	P	DBT009	Diabetes Mellitus	64	0.161

99		PRS045	Prostatic Hypertrophy	52	0.161

100	c	ACT068	Acute Cystitis	63	0.161

101	P	TRN020	Turner Syndrome	65	0.160

102	c	PCH010	Pachyonychia Congenita 3	43	0.159

103	P	LNG032	Lung Cancer	97	0.158

104		NNL006	Non-Alcoholic Steatohepatitis	51	0.157

105		CNS004	Constipation	57	0.156

106	P	NRP001	Neuropathy	56	0.155

107	P	HYP724	Hyperlipoproteinemia, Type Iii	72	0.155

108	P	MYL006	Myeloid Leukemia	60	0.154

109	P	PNC035	Pancreatic Cancer	84	0.153

110		CYS001	Cystic Fibrosis	80	0.153

111	P	HDC001	Headache	57	0.153

112	P	CRD246	Cardiovascular System Disease	56	0.152

113		NTR005	Nutritional Deficiency Disease	61	0.152

114	P	LCT001	Lactic Acidosis	51	0.152

115		PRS021	Prostatic Adenoma	51	0.151

116	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.150

117		ART140	Arteries, Anomalies of	53	0.150

118	c	LKM061	Leukemia, Acute Myeloid	83	0.150

119		DWN001	Down Syndrome	70	0.149

120		HRW001	Hair Whorl	36	0.149

121		PRS129	Prostatic Hyperplasia, Benign	49	0.149

122	P	BLD134	Bladder Cancer	78	0.147

123		OST159	Osteogenic Sarcoma	66	0.147

124	c	VSC019	Vesicoureteral Reflux 1	59	0.146

125		HYP060	Hyperinsulinism	54	0.146

126	P	EPL164	Epilepsy	71	0.145

127		HYP781	Hypoascorbemia	50	0.145

128		CHL079	Children's Interstitial Lung Disease	27	0.144

129	c	DNT047	Dentinogenesis Imperfecta Type 2	33	0.144

130	P	BLD124	Bleeding Disorder, Platelet-Type, 11	61	0.143

131		BRN071	Brain Injury	49	0.142

132		CYT002	Cytokine Deficiency	44	0.142

133	P	MLT020	Multiple Sclerosis	72	0.141

134	P	LYM118	Lymphoma	68	0.141

135		GST019	Gastrointestinal Stromal Tumor	76	0.140

136		URT049	Urate Oxidase, Pseudogene	25	0.139

137		END030	End Stage Renal Failure	58	0.139

138		GST023	Gastric Ulcer	53	0.139

139		ATS010	Autosomal Recessive Disease	48	0.138

140	P	BPL003	Bipolar Disorder	56	0.137

141		CRV035	Cervical Cancer	76	0.137

142	c	ACT075	Acute Myocardial Infarction	56	0.137

143	c	INH020	Inherited Metabolic Disorder	46	0.137

144	c	ACT071	Acute Kidney Failure	59	0.136

145	c	MJR024	Major Affective Disorder 9	41	0.136

146	c	MJR022	Major Affective Disorder 8	38	0.136

147		ANX004	Anoxia	42	0.136

148		DBT010	Diabetic Neuropathy	55	0.136

149		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.135

150	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.135

151	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.135

152	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.135

153	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.135

154	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.135

155	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.135

156	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.135

157	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.135

158	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.135

159	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.135

160	P	HYP086	Hypothyroidism	68	0.135

161	P	NTR004	Neutropenia	63	0.135

162		SKN016	Skin Disease	63	0.135

163	P	ATS364	Autism	65	0.134

164		AGN016	Aging	56	0.134

165	P	CNR004	Cone-Rod Dystrophy 2	71	0.134

166		TRM010	Traumatic Brain Injury	53	0.134

167		THY029	Thyroid Carcinoma	59	0.133

168		SQM006	Squamous Cell Carcinoma	60	0.132

169		LNG099	Lung Disease	61	0.132

170		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.132

171		TXC005	Toxic Shock Syndrome	61	0.132

172		ATX019	Ataxia with Vitamin E Deficiency	48	0.130

173		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.129

174		MYL069	Myeloma, Multiple	85	0.129

175	P	SCH015	Schizophrenia	75	0.129

176		PHN003	Phenylketonuria	75	0.129

177	c	MCR120	Microvascular Complications of Diabetes 7	47	0.128

178	c	MCR113	Microvascular Complications of Diabetes 3	52	0.128

179	c	MCR130	Microvascular Complications of Diabetes 6	41	0.127

180	c	MCR133	Microvascular Complications of Diabetes 4	41	0.127

181		ALC007	Alcohol Dependence	66	0.127

182		URM002	Uremia	49	0.127

183	P	RHM011	Rheumatoid Arthritis	80	0.126

184		CRH001	Crohn's Disease	74	0.126

185	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.125

186	c	ATR087	Atrial Standstill 1	74	0.124

187		RCK004	Rickets	69	0.123

188	P	CTR002	Cataract	60	0.123

189	P	PRD008	Periodontitis	62	0.123

190	P	PYL005	Pyelonephritis	56	0.123

191		VTM002	Vitamin B12 Deficiency	48	0.123

192	P	ART022	Arthritis	70	0.122

193	c	ATS007	Autism Spectrum Disorder	67	0.122

194	P	GLM007	Glomerulonephritis	57	0.121

195		PRT036	Peritonitis	65	0.121

196	P	KDN017	Kidney Cancer	61	0.120

197	P	PRP019	Peripheral Nervous System Disease	57	0.119

198		HMP009	Haemophilus Influenzae	42	0.119

199	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.119

200	P	MSC005	Muscular Dystrophy	66	0.119

201	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.118

202		ESP021	Esophageal Cancer	90	0.118

203	P	ATR011	Atrial Fibrillation	66	0.118

204	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.118

205		LYM019	Lymphosarcoma	47	0.117

206		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.117

207		BRR014	Barrett Esophagus	64	0.117

208		CHL123	Chlamydia	59	0.116

209		CRB004	Cerebral Artery Occlusion	44	0.116

210	P	BNG032	Benign Mesothelioma	45	0.116

211	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	66	0.116

212		TTN003	Tetanus	64	0.116

213	P	BRS044	Breast Adenocarcinoma	59	0.116

214	P	RTN024	Retinoblastoma	72	0.116

215	P	RHN004	Rhinitis	57	0.116

216	c	FML008	Familial Retinoblastoma	53	0.115

217	P	PNM007	Pneumonia	68	0.115

218		OST003	Osteonecrosis	61	0.115

219	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.115

220	c	ACT073	Acute Leukemia	58	0.114

221		ANG054	Angina Pectoris	66	0.114

222	P	RSP003	Respiratory Failure	74	0.114

223		ANX010	Anxiety	72	0.114

224		PLM010	Pulmonary Edema	55	0.114

225		BRN024	Bronchitis	68	0.113

226		BCT022	Bacterial Infectious Disease	56	0.113

227	P	PRK057	Parkinson Disease, Late-Onset	76	0.113

228	P	DMN002	Dementia	67	0.113

229	P	ALP008	Alopecia	56	0.112

230		RHM027	Rheumatic Disease	56	0.112

231		IRN001	Iron Deficiency Anemia	58	0.111

232	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.111

233	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.111

234		THR024	Thrombosis	56	0.111

235		PLM033	Pulmonary Embolism	59	0.111

236		ALL014	Allergic Encephalomyelitis	39	0.110

237	P	MCR115	Microvascular Complications of Diabetes 5	66	0.110

238	P	NSP012	Nasopharyngeal Carcinoma	67	0.110

239		SCH014	Schistosomiasis	56	0.109

240		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.109

241	P	HYP076	Hyperthyroidism	55	0.108

242	P	LPS004	Lupus Erythematosus	61	0.108

243	P	FBR017	Fibrosarcoma	56	0.108

244	c	ACT027	Acute Pancreatitis	59	0.108

245		SVR004	Severe Combined Immunodeficiency	73	0.108

246	c	SYS001	Systemic Lupus Erythematosus	86	0.107

247		CLN015	Colon Adenocarcinoma	63	0.107

248	P	PNC044	Pancreatitis	61	0.107

249		DNT012	Dental Caries	51	0.107

250	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.106

251		VCC001	Vaccinia	49	0.106

252		MTH071	Methane Production	26	0.106

253		CRD132	Cardiac Conduction Defect	59	0.105

254		SPP010	Suppressor of Tumorigenicity 3	51	0.105

255		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.105

256	P	THR014	Thrombocytopenia	68	0.104

257	P	OVR082	Overgrowth Syndrome	50	0.104

258	P	SKN015	Skin Carcinoma	67	0.104

259	P	TRM003	Tremor	53	0.104

260	P	ART021	Arteriosclerosis	54	0.104

261		AST005	Asthma	77	0.104

262	P	EXN002	Exanthem	57	0.104

263		MLN008	Melanoma	69	0.103

264	P	MNN013	Meningitis	65	0.102

265	P	DYS154	Dystonia	65	0.102

266	c	VRL010	Viral Hepatitis	51	0.102

267		IMM167	Immune Deficiency Disease	78	0.102

268	P	PRP029	Porphyria	62	0.102

269		PNG002	Pain Agnosia	51	0.102

270	c	SML038	Small Cell Cancer of the Lung	65	0.101

271	P	INF032	Infertility	57	0.101

272		SBC016	Subacute Delirium	44	0.101

273	P	GLM040	Glioma Susceptibility 1	81	0.101

274	P	CRD119	Cardiac Arrest	67	0.100

275		ALL003	Allergic Rhinitis	67	0.100

276		URN010	Urinary Tract Obstruction	57	0.100

277	P	AST007	Astrocytoma	50	0.099

278		MSC007	Muscle Hypertrophy	63	0.099

279		MDD011	Mood Disorder	62	0.099

280		CLF027	Cleft Palate, Isolated	64	0.099

281		BRN004	Brain Edema	55	0.098

282	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.098

283	P	MTC133	Mitochondrial Myopathy	49	0.098

284		CHL004	Cholelithiasis	49	0.097

285		PSY004	Psychotic Disorder	67	0.097

286		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.096

287	P	CYS018	Cystitis	59	0.096

288		GLS018	Glass Syndrome	53	0.096

289	c	DLT002	Dilated Cardiomyopathy	79	0.095

290	c	PNS012	Paine Syndrome	61	0.095

291		CNT047	Contact Dermatitis	57	0.095

292		PRG017	Paraganglioma and Gastric Stromal Sarcoma	52	0.095

293	P	MTH008	Methylmalonic Acidemia	51	0.094

294	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.094

295		BRN028	Brain Cancer	73	0.093

296		PRP027	Peripheral Vascular Disease	71	0.093

297	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.093

298		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.093

299	P	MYC008	Myocarditis	59	0.092

300		DPH001	Diphtheria	60	0.092

301		RNL077	Renal Fibrosis	47	0.092

302	P	URT039	Urticaria	58	0.092

303		EYD002	Eye Disease	58	0.092

304		MLR004	Malaria	80	0.091

305		HMS001	Hemosiderosis	54	0.091

306	c	MST023	Mesothelioma, Malignant	57	0.091

307	P	MTC069	Mitochondrial Disorders	56	0.091

308	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.091

309	c	BRN108	Branchiootic Syndrome 1	61	0.091

310	c	LKM071	Leukemia, Chronic Lymphocytic	79	0.091

311	P	PLM037	Pulmonary Hypertension	68	0.091

312	P	MLN007	Male Infertility	56	0.091

313		CMM005	Common Cold	56	0.090

314	P	PTT006	Pituitary Adenoma	54	0.090

315	P	MYC033	Myoclonus	46	0.090

316		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.090

317	P	RRH023	Rare Hereditary Hemochromatosis	41	0.090

318		MTC020	Mitochondrial Complex Ii Deficiency	54	0.089

319		PRN011	Pernicious Anemia	52	0.089

320	P	LNG064	Lung Cancer Susceptibility 3	77	0.088

321		NRF026	Neurofibromatosis, Type Iv, of Riccardi	63	0.088

322		LYM040	Lymphoblastic Lymphoma	54	0.088

323	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	66	0.088

324		GST050	Gastrointestinal System Disease	56	0.088

325	P	ADL010	Adult Respiratory Distress Syndrome	63	0.088

326	P	GRF003	Graft-Versus-Host Disease	71	0.088

327		ORL015	Oral Squamous Cell Carcinoma	43	0.087

328		GST045	Gastroenteritis	59	0.087

329	P	HYP061	Hypertrophic Cardiomyopathy	66	0.087

330	c	MCR129	Microvascular Complications of Diabetes 1	66	0.087

331		ENT004	Enthesopathy	48	0.087

332		BLD044	Bladder Disease	48	0.087

333	P	MYC084	Mycobacterium Tuberculosis 1	68	0.087

334		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.086

335		NWC001	Newcastle Disease	44	0.086

336	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	60	0.085

337		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.085

338		HYD002	Hydronephrosis	59	0.085

339	P	SLP005	Sleep Disorder	59	0.085

340	P	HML002	Hemolytic Anemia	62	0.085

341		INT007	Intermediate Coronary Syndrome	55	0.084

342		CHL067	Cholecystitis	58	0.084

343	P	CHR345	Chronic Pain	50	0.084

344	c	MTC059	Mitochondrial Dna Depletion Syndrome 5	43	0.084

345		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.084

346		ENT011	Enterocolitis	50	0.084

347	P	SBR004	Seborrheic Dermatitis	45	0.083

348	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	35	0.083

349		TRN015	Transient Cerebral Ischemia	62	0.083

350		HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	56	0.083

351	P	INS002	in Situ Carcinoma	52	0.083

352	P	HYP098	Hypereosinophilic Syndrome	66	0.083

353	P	NPH012	Nephrotic Syndrome	63	0.083

354		MST005	Mastitis	53	0.083

355		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.082

356		LSH001	Leishmaniasis	63	0.082

357	P	KLZ004	Kala-Azar 1	41	0.082

358		LYM133	Lymphoma, Hodgkin, Classic	69	0.082

359		GTR002	Goiter	52	0.082

360	P	OBS001	Obstructive Jaundice	48	0.082

361	c	CHR682	Chronic Bilirubin Encephalopathy	38	0.082

362		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.081

363	P	URF003	Urofacial Syndrome 1	57	0.081

364		URN009	Urinary System Disease	48	0.081

365	P	THL005	Thalassemia	60	0.081

366		TYP007	Typhoid Fever	63	0.080

367		END057	Endometrial Cancer	74	0.080

368		VSC002	Vascular Dementia	57	0.080

369		PRP030	Purpura	55	0.080

370	c	HPT003	Hepatitis a	63	0.079

371	c	BSL007	Basal Cell Carcinoma	68	0.079

372	c	INF071	Inflammatory Bowel Disease 1	68	0.079

373	P	PLY014	Polycystic Kidney Disease	59	0.079

374	P	CND004	Candidiasis	57	0.078

375	c	CHR064	Chronic Monocytic Leukemia	34	0.078

376		MSL001	Measles	61	0.078

377		ACY011	Acyl-Coa Dehydrogenase Deficiency	37	0.078

378	c	PRD040	Periodontitis, Chronic	54	0.078

379		HDN002	Head Injury	45	0.078

380	P	ALP009	Alopecia Areata	60	0.078

381	c	ATS307	Autosomal Recessive Cerebellar Ataxia	41	0.078

382		BLR001	Biliary Atresia	50	0.078

383		ALL010	Allergic Contact Dermatitis	55	0.077

384		MMM001	Mammary Paget's Disease	53	0.077

385	P	TCL004	T-Cell Leukemia	47	0.077

386		IGR001	Ige Responsiveness, Atopic	59	0.076

387	P	RCT021	Rectum Cancer	53	0.076

388		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	57	0.076

389		ORG002	Organic Acidemia	43	0.076

390		PNC001	Pancytopenia	54	0.076

391	c	ACT042	Acute Pyelonephritis	44	0.076

392		RHM001	Rheumatic Fever	61	0.076

393	c	FML001	Familial Atrial Fibrillation	66	0.075

394	P	SCK005	Sickle Cell Disease	50	0.075

395		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.075

396		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.074

397		FBR047	Fibromyalgia	59	0.074

398		RTN017	Retinal Detachment	60	0.074

399		PTT037	Pituitary Tumors	44	0.074

400		CHG001	Chagas Disease	66	0.074

401		SPN041	Spinal Cord Disease	56	0.074

402		PRP080	Peripheral Artery Disease	53	0.074

403		URT010	Ureteral Obstruction	46	0.074

404	P	SHR001	Short Bowel Syndrome	52	0.073

405		KHL003	Kohlschutter-Tonz Syndrome	64	0.073

406	c	PRG021	Paragangliomas 4	37	0.073

407		MLK006	Milk Allergy	48	0.072

408		AMN003	Amnestic Disorder	54	0.072

409		DBT002	Diabetic Autonomic Neuropathy	41	0.072

410	P	NRV007	Nervous System Disease	66	0.072

411		DSS008	Disease of Mental Health	57	0.072

412		AMN006	Aminoaciduria	38	0.072

413		GNG013	Gingivitis	59	0.071

414	P	THY032	Thyroiditis	53	0.071

415		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.071

416	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.071

417	P	FRD001	Friedreich Ataxia	63	0.071

418		CYT018	Cytochrome P450 2d6 Variant	27	0.071

419	P	HYD006	Hydrocephalus	65	0.070

420		MTC005	Mitochondrial Metabolism Disease	48	0.069

421		SCR011	Scrapie	38	0.069

422		LMY003	Leiomyomatosis	43	0.069

423		INT020	Intravenous Leiomyomatosis	36	0.069

424	c	BCT007	Bacterial Meningitis	55	0.069

425		49X006	49, Xxxxy Syndrome	41	0.069

426	P	MVM001	Movement Disease	61	0.068

427		ANR007	Anorexia Nervosa	63	0.068

428		ACT058	Active Peptic Ulcer Disease	55	0.068

429		BTN004	Biotin Deficiency	38	0.068

430		LGH007	Leigh Syndrome	70	0.068

431		PLC008	Placenta Disease	49	0.067

432	c	SPN225	Spondyloarthropathy 1	73	0.067

433		BRK010	Burkitt Lymphoma	67	0.067

434	P	RHB003	Rhabdomyosarcoma	62	0.067

435	P	VSC011	Vasculitis	62	0.067

436	c	HNT011	Huntington Disease-Like 3	38	0.067

437	P	PRS038	Personality Disorder	65	0.066

438	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	50	0.066

439		NRG002	Neurogenic Bladder	54	0.066

440	c	GRV008	Graves Disease 1	55	0.066

441		NRM022	Neurometabolic Disease	25	0.066

442		OST017	Osteomyelitis	64	0.065

443		BCT002	Bacterial Vaginosis	52	0.065

444	P	MJR007	Major Affective Disorder 1	43	0.065

445		SCK003	Sickle Cell Anemia	72	0.065

446	P	NRC002	Narcolepsy	51	0.065

447		PST021	Postpartum Depression	50	0.065

448		RTC012	Reticuloendotheliosis, X-Linked	40	0.064

449		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.064

450		OBS002	Obsessive-Compulsive Disorder	68	0.064

451		RST023	Resting Heart Rate, Variation in	41	0.064

452		AMN002	Amino Acid Metabolic Disorder	40	0.064

453		LYM027	Lymphopenia	57	0.064

454		PRP016	Paraplegia	53	0.064

455		ACT228	Acute Radiation Syndrome	29	0.064

456	P	FNC004	Fanconi Syndrome	50	0.064

457		HPT014	Hepatorenal Syndrome	50	0.063

458	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	65	0.063

459	P	OPN001	Open-Angle Glaucoma	49	0.063

460		HYP141	Hyperphenylalaninemia	38	0.063

461		NRN004	Neuroendocrine Tumor	55	0.062

462	P	MYG005	Myoglobinuria	43	0.062

463		CRB037	Cerebral Palsy	68	0.062

464		CRC021	Carcinosarcoma	61	0.062

465	c	MJR003	Major Affective Disorder 6	33	0.061

466	c	MJR006	Major Affective Disorder 5	33	0.061

467	P	STR092	Striatal Degeneration, Autosomal Dominant 2	43	0.061

468	P	GRV001	Graves' Disease	55	0.061

469	P	BRB001	Beriberi	44	0.061

470		NRM005	Neuromuscular Disease	63	0.061

471	c	MJR008	Major Affective Disorder 2	34	0.060

472	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.060

473	c	MJR023	Major Affective Disorder 7	33	0.060

474	c	MJR004	Major Affective Disorder 4	28	0.060

475		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.060

476	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.060

477		BCT004	Bacteriuria	48	0.060

478	P	VTR007	Vitreoretinopathy	46	0.060

479		TNS005	Tonsillitis	57	0.060

480		SLC006	Silicosis	56	0.060

481		TRY001	Trypanosomiasis	50	0.060

482	P	ATX030	Ataxia-Telangiectasia	83	0.060

483		GRD007	Grade Iii Astrocytoma	59	0.060

484	c	ADL017	Adult T-Cell Leukemia	57	0.060

485	P	LCH002	Lichen Planus	54	0.060

486		RRD056	Rare Disease in Surgical Orthopedic	28	0.060

487	P	CLS010	Cluster Headache	43	0.059

488		THY111	Thyroid Carcinoma, Familial Medullary	67	0.059

489	c	PRG018	Paragangliomas 1	57	0.059

490	c	WLM018	Wilms Tumor 5	62	0.059

491	P	LKD001	Leukodystrophy	59	0.059

492		VSC003	Visceral Leishmaniasis	55	0.059

493		CRT015	Carotid Artery Occlusion	44	0.059

494		AMN001	Amenorrhea	54	0.059

495		LRN003	Learning Disability	49	0.059

496		SLP001	Sleeping Sickness	48	0.059

497		PHR003	Pharyngitis	56	0.058

498	P	SLM003	Salmonellosis	54	0.058

499		EXT006	Extrahepatic Cholestasis	40	0.058

500		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.058

501		VGN023	Vaginitis	55	0.057

502	c	ACT135	Acute Graft Versus Host Disease	51	0.057

503		NTR046	Neutrophil Migration	50	0.057

504		THY125	Thyroid Gland Medullary Carcinoma	51	0.057

505	c	PRG106	Progressive Muscular Dystrophy	33	0.057

506		AMN012	Aminoacidopathies	21	0.057

507		SCC003	Succinic Acidemia	10	0.057

508		ENC005	Encephalomalacia	38	0.057

509	c	CHR098	Chronic Pyelonephritis	35	0.057

510	P	ANR048	Aniridia 1	63	0.057

511	P	PNC025	Panic Disorder	53	0.057

512		ANP008	Anaplastic Oligoastrocytoma	30	0.057

513		ACN002	Acanthosis Nigricans	60	0.056

514		SCH003	Schizophreniform Disorder	56	0.056

515		HSH003	Hashimoto Thyroiditis	62	0.056

516	P	MLT074	Multiple Endocrine Neoplasia	55	0.056

517		HML018	Homologous Wasting Disease	22	0.056

518		RTN003	Retinal Ischemia	50	0.056

519	c	HMC039	Hemochromatosis, Type 1	74	0.056

520	P	ANG015	Angioedema	54	0.056

521	P	RTT002	Rett Syndrome	80	0.056

522		PRM329	Premature Aging	39	0.056

523	P	TRC086	Trichohepatoenteric Syndrome 1	59	0.056

524	c	MCR112	Microvascular Complications of Diabetes 2	41	0.056

525		KRN002	Kearns-Sayre Syndrome	63	0.055

526		ACR007	Acromegaly	71	0.055

527		CMR002	Coumarin Resistance	56	0.055

528	P	ASP006	Aspergillosis	66	0.055

529		MSC190	Muscular Disease	51	0.055

530	P	RRT020	Rare Tumor	41	0.054

531		GMM004	Gamma-Amino Butyric Acid Metabolism Disorder	27	0.054

532		DFF005	Diffuse Large B-Cell Lymphoma	56	0.054

533	c	CNT035	Central Nervous System Disease	54	0.054

534	c	GLC092	Glaucoma, Primary Open Angle	62	0.054

535		SPT004	Septic Arthritis	57	0.054

536		CHN010	Chondroma	44	0.054

537		MYP097	Myopathy with Lactic Acidosis, Hereditary	32	0.054

538		LST001	Listeriosis	54	0.054

539		ACT084	Acute Stress Disorder	48	0.054

540		SYS003	Systolic Heart Failure	50	0.053

541		ERL001	Early Myoclonic Encephalopathy	61	0.053

542		BRN002	Bronchiolitis	59	0.053

543	P	INT070	Intestinal Obstruction	58	0.053

544		PST028	Post-Traumatic Stress Disorder	58	0.053

545		ORL005	Oral Candidiasis	56	0.053

546	P	SNS001	Sensorineural Hearing Loss	61	0.053

547	P	BNG030	Benign Ependymoma	60	0.053

548	P	VNT002	Ventricular Septal Defect	60	0.053

549		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.053

550	P	GNT008	Giant Cell Tumor	44	0.053

551		MCL006	Macular Retinal Edema	55	0.052

552		HRT011	Heart Septal Defect	50	0.052

553		THY124	Thyroid Gland Papillary Carcinoma	52	0.052

554		PPL002	Papillary Carcinoma	47	0.052

555	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	59	0.052

556		THR013	Thoracic Outlet Syndrome	53	0.052

557		CLL010	Cellular Ependymoma	53	0.052

558	P	CWD010	Cowden Syndrome	66	0.052

559		WST001	West Syndrome	60	0.051

560		SXL003	Sexual Disorder	48	0.051

561		MYF002	Myofascial Pain Syndrome	42	0.051

562		GNG005	Gangliocytoma	55	0.051

563		GNG002	Ganglioneuroma	53	0.051

564		NWB001	Newborn Respiratory Distress Syndrome	58	0.051

565	P	RNL015	Renal Hypertension	48	0.051

566	P	MTH007	Methemoglobinemia	46	0.051

567		LMB062	Limb Ischemia	55	0.051

568		CLL003	Cellulitis	54	0.051

569		PRS063	Paresthesia	43	0.051

570	P	MTC004	Mitochondrial Encephalomyopathy	43	0.050

571	c	DFN360	Deafness, Autosomal Dominant 69	37	0.050

572		AND002	Androgen Insensitivity Syndrome	66	0.050

573	P	MST009	Mastocytosis	63	0.050

574		TRP009	Triple X Syndrome	42	0.050

575	P	CHL002	Childhood Absence Epilepsy	60	0.050

576		CRC014	Carcinoid Tumors, Intestinal	48	0.050

577		GSG001	Gas Gangrene	50	0.050

578	P	ANG001	Angelman Syndrome	67	0.049

579	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.049

580	P	HMR005	Hemorrhoid	46	0.049

581		MNG007	Manganese Poisoning	29	0.049

582	P	MYT002	Myotonic Dystrophy	49	0.049

583	P	MGR001	Migraine Without Aura	48	0.049

584		DRG024	Drug Allergy	43	0.049

585		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	37	0.049

586		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	64	0.049

587		CHL152	Childhood Acute Lymphocytic Leukemia	43	0.048

588	c	ACT020	Acute T Cell Leukemia	53	0.048

589	c	MCL013	Mucolipidosis Iv	64	0.048

590		ERY003	Erythema Multiforme	57	0.048

591	P	HML001	Hemolytic-Uremic Syndrome	52	0.048

592		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	34	0.048

593	P	MTR003	Mitral Valve Stenosis	50	0.047

594	c	ALP101	Alpha-Thalassemia	62	0.047

595		SHG001	Shigellosis	55	0.047

596		OST011	Osteomalacia	52	0.047

597		CRB090	Cerebral Hypoxia	43	0.047

598		ATM052	Autoimmune Disease 1	37	0.047

599		LWC002	Lowe Oculocerebrorenal Syndrome	66	0.047

600		HMP001	Hemopericardium	46	0.047

601		CHL147	Chlamydia Pneumonia	45	0.047

602		CYN002	Cyanosis, Transient Neonatal	45	0.047

603	P	CRB088	Cerebral Atrophy	38	0.047

604		ATX010	Ataxia Neuropathy Spectrum	38	0.047

605		ACT064	Acute Necrotizing Encephalitis	32	0.047

606		BLD137	Blood Group--Ahonen	19	0.047

607		MRP001	Morphine Dependence	41	0.047

608		CNV004	Canavan Disease	60	0.046

609		DFF036	Differentiated Thyroid Carcinoma	51	0.046

610		STT002	Status Asthmaticus	49	0.046

611	c	PRG020	Paragangliomas 3	38	0.046

612		ALP048	Alopecia Totalis	31	0.046

613		THY006	Thymus Lymphoma	26	0.046

614		CLR030	Clear Cell Renal Cell Carcinoma	53	0.046

615		HRT012	Heart Valve Disease	53	0.046

616		THR016	Thrombophlebitis	51	0.046

617		BLP005	Blepharitis	49	0.046

618		RTC005	Reticulosarcoma	49	0.046

619	c	NRF024	Neurofibromatosis, Type I	71	0.045

620		MSN004	Mesenchymal Cell Neoplasm	41	0.045

621	P	INB001	Inborn Amino Acid Metabolism Disorder	10	0.045

622		VLV047	Volvulus of Midgut	50	0.045

623		SPT005	Spotted Fever	49	0.045

624		PLS025	Plasmablastic Lymphoma	47	0.045

625		VGN019	Vaginal Discharge	44	0.045

626	P	AVS003	Avascular Necrosis	42	0.045

627		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.045

628	c	PRG019	Paragangliomas 2	31	0.045

629	P	TCD001	Tic Disorder	54	0.045

630		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.045

631		ORL013	Oral Lichen Planus	45	0.045

632		GST020	Gastric Antral Vascular Ectasia	41	0.045

633		LPD012	Lipoid Congenital Adrenal Hyperplasia	71	0.044

634	P	EPL140	Epilepsy, Idiopathic Generalized	61	0.044

635		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	49	0.044

636		FMR004	Fumarase Deficiency	41	0.044

637		CHR176	Chromophil Renal Cell Carcinoma	23	0.044

638	P	CYS039	Cystic Kidney Disease	54	0.044

639		ACR041	Acromelic Frontonasal Dysostosis	52	0.044

640		CRV040	Cervix Carcinoma	50	0.044

641	c	INV001	Invasive Aspergillosis	48	0.044

642		DBT006	Diabetic Macular Edema	48	0.044

643	c	BCT013	Bacterial Pneumonia	47	0.044

644	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.044

645		CNN003	Conn's Syndrome	79	0.044

646		RSP019	Respiratory Distress Syndrome in Premature Infants	57	0.044

647		GLL018	Gallbladder Cancer	56	0.044

648	P	HYP111	Hyperprolinemia	39	0.044

649		NSP002	Nasopharyngitis	41	0.043

650		GBM001	Gaba Aminotransferase Deficiency	19	0.043

651		CLB002	Clubfoot	47	0.042

652		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.042

653	P	AXN002	Axenfeld-Rieger Syndrome	58	0.042

654		SJG002	Sjogren-Larsson Syndrome	57	0.042

655		ARG007	Argininemia	57	0.042

656		URT001	Urethritis	48	0.042

657		INT017	Intestinal Schistosomiasis	47	0.042

658	P	SPR086	Spermatogenic Failure 3	44	0.042

659		UND005	Undifferentiated Pleomorphic Sarcoma	66	0.041

660	P	EPL198	Epilepsy, Myoclonic Juvenile	62	0.041

661		GNR004	Generalized Anxiety Disorder	56	0.041

662		BRT005	Barth Syndrome	53	0.041

663		EXP004	Exophthalmos	52	0.041

664		OPT003	Opiate Dependence	50	0.041

665		RCK002	Rocky Mountain Spotted Fever	40	0.041

666		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.041

667		SMN007	Seminoma	44	0.041

668	c	CWD006	Cowden Syndrome 1	77	0.041

669	P	ALG028	Alagille Syndrome 1	73	0.040

670		ATR057	Atrioventricular Block	55	0.040

671		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.040

672		LNG015	Lingual-Facial-Buccal Dyskinesia	47	0.040

673		ALR002	Al-Raqad Syndrome	34	0.040

674	P	PLV020	Pelvic Organ Prolapse	59	0.040

675		BHR001	Behr Syndrome	49	0.040

676		TST015	Testicular Disease	43	0.040

677	P	HYP263	Hypersomnia	41	0.040

678		GBT001	Gaba-Transaminase Deficiency	39	0.040

679	P	OTT001	Otitis Externa	39	0.040

680		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.040

681		ALP097	Alopecia Universalis Congenita	56	0.039

682		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	58	0.039

683		APH002	Aphasia	57	0.039

684		TNG003	Tongue Cancer	55	0.039

685		APR001	Apraxia	51	0.039

686		HPT082	Hepatic Adenomas, Familial	37	0.039

687		HNM002	Hinman Syndrome	29	0.039

688	c	MTC060	Mitochondrial Dna Depletion Syndrome 9	48	0.039

689		ONC007	Oncocytoma	48	0.039

690	c	MTR002	Mitral Valve Insufficiency	47	0.039

691		MLN003	Melancholia	39	0.039

692		ART001	Arterial Tortuosity Syndrome	66	0.038

693		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	64	0.038

694		ISL001	Islet Cell Tumor	56	0.038

695	P	ALP106	Alport Syndrome 1, X-Linked	55	0.038

696		HMT008	Hematuria, Benign Familial	53	0.038

697		ADR016	Adrenal Cortical Carcinoma	48	0.038

698		ADP007	Adie Pupil	39	0.038

699		VTM028	Vitamin E, Familial Isolated Deficiency of	52	0.038

700		CRR012	Cirrhotic Cardiomyopathy	23	0.038

701		PTT048	Pituitary Adenoma, Prolactin-Secreting	64	0.038

702		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	58	0.038

703		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.038

704		CGN005	Cognitive Impairment with or Without Cerebellar Ataxia	39	0.038

705		ADR004	Adrenal Cortical Adenocarcinoma	38	0.038

706		DRM009	Dermatomycosis	36	0.038

707		RSP007	Respiratory Distress Syndrome, Infant	30	0.038

708		LYM053	Lymphomatous Thyroiditis	22	0.037

709	P	SCL055	Suclg1-Related Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria	10	0.037

710	P	END047	Endophthalmitis	52	0.037

711	P	MGR003	Migraine with Aura	50	0.037

712	P	PRT026	Parotitis	42	0.037

713		CVT001	Cavitary Optic Disc Anomalies	38	0.037

714		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.036

715		CHR072	Chordoma	59	0.036

716	P	RNL017	Renal Oncocytoma	53	0.036

717		DYS009	Dysthymic Disorder	48	0.036

718		CRN019	Coronary Artery Vasospasm	46	0.036

719	c	RNG019	Ring Chromosome 3	21	0.036

720		OBS524	Obsolete: Benign Exophthalmos Syndrome	15	0.036

721	P	ACR001	Aicardi-Goutieres Syndrome	65	0.035

722		PNM001	Pneumocystosis	54	0.035

723	c	SPN294	Spinocerebellar Ataxia 1	52	0.035

724	c	ACR116	Aicardi-Goutieres Syndrome 1	51	0.035

725		APL002	Aplasia of Lacrimal and Salivary Glands	50	0.035

726		SCL003	Social Phobia	48	0.035

727		CRB196	Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome	43	0.035

728		BRK012	Broken Heart Syndrome	35	0.035

729		TRC120	Tricarboxylic Acid Cycle, Defect of	16	0.035

730	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	69	0.035

731		NRL004	Neuroleptic Malignant Syndrome	55	0.035

732		EPT021	Epithelial Recurrent Erosion Dystrophy	37	0.035

733		PRX097	Paroxysmal Dystonia	31	0.035

734		TST003	Testicular Leukemia	26	0.035

735		MTC015	Mitochondrial Dna-Associated Leigh Syndrome and Narp	24	0.035

736		DRG016	Drug Induced Dyskinesia	24	0.035

737	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	67	0.034

738		HMN009	Hemangioblastoma	54	0.034

739		ENC055	Encephalopathy, Ethylmalonic	52	0.034

740		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	50	0.034

741		MNN020	Meningococcal Infection	45	0.034

742		SDD008	Sudden Sensorineural Hearing Loss	43	0.034

743		RHM035	Rheumatic Fever-Related Antigen	39	0.034

744		HYP026	Hypoglycemic Coma	38	0.034

745		HYP189	Hypoadrenalism	37	0.034

746		MYC088	Mycobacterium Avium Complex Infections	29	0.034

747	P	MTR012	Mitral Valve Disease	57	0.033

748	P	ART018	Aortic Valve Insufficiency	53	0.033

749	P	ACT105	Acute Mountain Sickness	52	0.033

750		WRN003	Wernicke Encephalopathy	47	0.033

751		OPD001	Opioid Abuse	45	0.033

752		PNC085	Penicillin Allergy	44	0.033

753	P	PHT010	Photoparoxysmal Response 1	42	0.033

754	P	MYC026	Myoclonus Epilepsy	35	0.033

755		NRP027	Neuropathy, Painful	24	0.033

756		NCL007	Nuclear Gene-Encoded Leigh Syndrome	23	0.033

757	c	SCL054	Sucla2-Related Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form with Methylmalonic Aciduria	10	0.033

758		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.033

759		MNN032	Meningococcal Meningitis	46	0.033

760		DNT006	Dental Pulp Necrosis	40	0.033

761		CRB009	Cerebritis	36	0.033

762	c	BLD140	Blood Group, I System	30	0.033

763		DFF015	Diffuse Glomerulonephritis	27	0.033

764		AND005	Androgen Insensitivity Syndrome, Mild	22	0.033

765		HYP780	Hypoadrenocorticism, Familial	62	0.031

766	P	OST009	Osteochondritis Dissecans	60	0.031

767	P	JVN007	Juvenile Absence Epilepsy	48	0.031

768		MCR037	Macroglossia	45	0.031

769		URN003	Urinary Schistosomiasis	44	0.031

770		ADR041	Adrenal Cortical Adenoma	43	0.031

771		BSL008	Basal Ganglia Disease	43	0.031

772		PTY002	Pityriasis Versicolor	37	0.031

773		PRS025	Presbyopia	37	0.031

774	P	BCL013	B-Cell Adult Acute Lymphocytic Leukemia	32	0.031

775		ACT216	Acute Leukemia of Ambiguous Lineage	32	0.031

776		FCL001	Facial Dermatosis	29	0.031

777		WLM014	Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome	49	0.031

778		FML304	Familial Isolated Dilated Cardiomyopathy	40	0.031

779	c	MLG157	Malignant Pheochromocytoma	39	0.031

780		WLM019	Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome	17	0.031

781		CHR001	Churg-Strauss Syndrome	60	0.030

782	P	CRN028	Corneal Ulcer	47	0.030

783	c	CHR095	Chronic Progressive External Ophthalmoplegia	46	0.030

784	c	EPL133	Epilepsy, Juvenile Absence 1	39	0.030

785		GLT028	Glutaric Aciduria Iii	28	0.030

786		ALL012	Allergic Angiitis	24	0.030

787	P	CNG499	Congenital Anomalies of Kidney and Urinary Tract 2	49	0.029

788	c	TCL001	T-Cell Adult Acute Lymphocytic Leukemia	43	0.029

789	P	CRB045	Cerebellar Hypoplasia	37	0.029

790	P	SYR003	Syringoma	37	0.029

791	c	GST103	Gastric Cancer, Hereditary Diffuse	64	0.028

792	P	DYS193	Dystonia 11, Myoclonic	56	0.028

793	c	VRL005	Viral Pneumonia	49	0.028

794	P	PRG130	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1	48	0.028

795	P	CPL014	Capillary Malformation-Arteriovenous Malformation 1	47	0.028

796	c	ATM092	Autoimmune Polyendocrine Syndrome, Type Ii	46	0.028

797	c	HYP793	Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1	44	0.028

798	c	PRG039	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3	44	0.028

799	c	PRG040	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4	42	0.028

800	P	CRN035	Cranial Nerve Palsy	41	0.028

801	c	PRG038	Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2	40	0.028

802		TST043	Testicular Seminoma	35	0.028

803		FMR011	Fumarate Hydratase Deficiency	30	0.028

804	P	JBR020	Joubert Syndrome 1	72	0.026

805		MLT163	Multiple Pterygium Syndrome, Escobar Variant	64	0.026

806	P	CHR640	Charcot-Marie-Tooth Disease, X-Linked Dominant, 1	56	0.026

807		ADR056	Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete	56	0.026

808		CLL002	Collecting Duct Carcinoma	54	0.026

809		SPS007	Spastic Cerebral Palsy	45	0.026

810		EMP001	Empty Sella Syndrome	44	0.026

811	c	XLN110	X-Linked Charcot-Marie-Tooth Disease	43	0.026

812		ANG011	Angiodysplasia	43	0.026

813		PSD001	Pseudobulbar Palsy	40	0.026

814		MCC013	Mucocutaneous Ulceration, Chronic	39	0.026

815		SCL001	Scalp Dermatosis	37	0.026

816		CNT001	Contagious Pustular Dermatitis	29	0.026

817		LKN027	Leukoencephalopathy, Acute Reversible, with Increased Urinary Alpha-Ketoglutarate	18	0.026

818		WLL001	Williams-Beuren Syndrome	62	0.024

819		MTC146	Mitochondrial Complex I Deficiency, Nuclear Type 1	59	0.024

820	c	CTS029	Cutis Laxa, Autosomal Recessive, Type Iiia	54	0.024

821		HYP134	Hypoparathyroidism-Retardation-Dysmorphism Syndrome	52	0.024

822		FCL022	Focal Dystonia	42	0.024

823		MRN002	Mooren's Ulcer	38	0.024

824		HRM003	Hormone Producing Pituitary Cancer	37	0.024

825		PHT003	Phototoxic Dermatitis	34	0.024

826		INT040	Intrinsic Asthma	34	0.024

827		PRN007	Perinephritis	33	0.024

828	c	INF086	Inflammatory Bowel Disease 3	32	0.024

829	c	SPR094	Sporadic Pheochromocytoma	32	0.024

830		CTC004	Catecholamine-Producing Tumor	30	0.024

831		MSC004	Muscle Tissue Disease	25	0.024

832		HND001	Hand Dermatosis	22	0.024

833		CHL135	Chloramphenicol Toxicity	18	0.024

834		STN005	St Anthony's Fire	17	0.024