Search results for Palmitic Acid

996 hits were found for Palmitic Acid

#	Family	MCID	Name	MIFTS	Score
1		FTT001	Fatty Liver Disease	63	0.338

2		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.330

3	P	LVR013	Liver Disease	71	0.312

4	P	SCH015	Schizophrenia	76	0.285

5		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.273

6		PLM017	Pulmonary Alveolar Microlithiasis	54	0.271

7	P	NRB010	Neuroblastoma 1	66	0.242

8		LPD008	Lipid Metabolism Disorder	64	0.238

9		48X005	48,xyyy	37	0.231

10	P	CLR023	Colorectal Cancer	100	0.231

11		LVR012	Liver Cirrhosis	67	0.230

12	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	58	0.221

13		HLX001	Helix Syndrome	46	0.219

14		ACT119	Acute Promyelocytic Leukemia	63	0.217

15	P	KDN018	Kidney Disease	73	0.215

16		HYP066	Hyperglycemia	63	0.213

17	P	SZR006	Seizure Disorder	59	0.210

18		ALL026	Allergic Hypersensitivity Disease	65	0.206

19		HYP014	Hyperuricemia	52	0.204

20		NNL006	Non-Alcoholic Steatohepatitis	53	0.204

21		VSL002	Visual Epilepsy	58	0.204

22	P	DRR001	Diarrhea	55	0.204

23		NRL016	Neural Tube Defects	83	0.203

24	P	BRS047	Breast Cancer	99	0.198

25	P	CRN300	Coronary Heart Disease 1	59	0.197

26	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	91	0.196

27		ATH013	Atherosclerosis Susceptibility	68	0.195

28	P	NRF023	Neurofibromatosis, Type Ii	77	0.193

29	P	HYP750	Hypertriglyceridemia, Familial	62	0.190

30		DRM006	Dermatitis	63	0.189

31	c	GLL024	Gallbladder Disease 1	53	0.189

32		ISC004	Ischemia	62	0.189

33		OST012	Osteoarthritis	80	0.185

34		TRD008	Triiodothyronine Receptor Auxiliary Protein	35	0.183

35		HYP056	Hypoglycemia	68	0.182

36	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	82	0.178

37		BNR002	Bone Resorption Disease	51	0.178

38		GST092	Gastroesophageal Reflux	68	0.177

39		CLT003	Colitis	63	0.176

40	P	HPT023	Hepatocellular Carcinoma	99	0.176

41	P	BDY004	Body Mass Index Quantitative Trait Locus 11	78	0.175

42	P	VSC007	Vascular Disease	65	0.174

43		HYP060	Hyperinsulinism	55	0.172

44	P	ENC018	Encephalopathy	64	0.172

45	P	PSR002	Psoriasis	63	0.171

46	P	GLM045	Glioma	64	0.170

47		PST011	Pustulosis of Palm and Sole	51	0.169

48	P	LKM002	Leukemia	69	0.169

49		PRT037	Pertussis	66	0.168

50		GLL048	Glial Tumor	48	0.168

51	P	INF037	Inflammatory Bowel Disease	57	0.168

52		CYT002	Cytokine Deficiency	46	0.168

53	P	PRS040	Prostate Cancer	97	0.166

54		KRT002	Keratomalacia	47	0.166

55	P	CRN018	Coronary Artery Anomaly	67	0.164

56		PPT005	Peptic Ulcer Disease	60	0.163

57	P	HYP724	Hyperlipoproteinemia, Type Iii	74	0.161

58		GLB002	Glioblastoma	74	0.160

59		GLB015	Glioblastoma Multiforme	60	0.159

60		ART140	Arteries, Anomalies of	60	0.158

61		ATM095	Autoimmune Disease	62	0.158

62		DFC004	Deficiency Anemia	77	0.158

63	P	BPL003	Bipolar Disorder	59	0.157

64	c	HYP836	Hypercholesterolemia, Familial, 1	74	0.157

65		CYS001	Cystic Fibrosis	84	0.156

66	c	MJR024	Major Affective Disorder 9	42	0.156

67	c	MJR022	Major Affective Disorder 8	39	0.156

68	c	MCR120	Microvascular Complications of Diabetes 7	48	0.155

69		PSY004	Psychotic Disorder	68	0.155

70	c	MCR113	Microvascular Complications of Diabetes 3	55	0.155

71	c	MCR130	Microvascular Complications of Diabetes 6	42	0.155

72	c	MCR133	Microvascular Complications of Diabetes 4	42	0.155

73	P	HRT032	Heart Disease	78	0.154

74	P	DBT009	Diabetes Mellitus	66	0.154

75		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.154

76	c	CHR684	Chronic Kidney Disease	68	0.153

77		HMN044	Human Immunodeficiency Virus Type 1	73	0.153

78	c	BDY005	Body Mass Index Quantitative Trait Locus 9	49	0.153

79	c	BDY020	Body Mass Index Quantitative Trait Locus 19	51	0.152

80	c	BDY021	Body Mass Index Quantitative Trait Locus 20	50	0.152

81	c	BDY010	Body Mass Index Quantitative Trait Locus 4	48	0.152

82	c	BDY015	Body Mass Index Quantitative Trait Locus 12	48	0.152

83	c	BDY019	Body Mass Index Quantitative Trait Locus 18	48	0.152

84	c	BDY011	Body Mass Index Quantitative Trait Locus 10	47	0.152

85	c	BDY017	Body Mass Index Quantitative Trait Locus 14	46	0.152

86	c	BDY006	Body Mass Index Quantitative Trait Locus 8	45	0.152

87	c	BDY012	Body Mass Index Quantitative Trait Locus 7	45	0.152

88		ADN018	Adenoma	60	0.152

89	P	OST002	Osteoporosis	79	0.151

90	P	ADN016	Adenocarcinoma	65	0.150

91	c	BDY007	Body Mass Index Quantitative Trait Locus 1	43	0.150

92	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	59	0.149

93		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.148

94		INS001	Insulinoma	60	0.147

95	P	MYL006	Myeloid Leukemia	61	0.147

96		HRW001	Hair Whorl	36	0.147

97	c	ACT210	Acute Respiratory Distress Syndrome	59	0.146

98		PLM001	Pulmonary Tuberculosis	72	0.146

99	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	51	0.144

100	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	43	0.144

101	c	PRC016	Pre-Eclampsia	63	0.143

102	c	HYP595	Hypertension, Essential	87	0.143

103	P	PNC035	Pancreatic Cancer	86	0.143

104		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	55	0.142

105		47X002	47,xyy	49	0.141

106		IRN002	Iron Metabolism Disease	58	0.141

107	P	LNG032	Lung Cancer	99	0.139

108	P	NRP001	Neuropathy	57	0.139

109		OCL069	Ocular Motor Apraxia	53	0.137

110		CRB039	Cerebrovascular Disease	71	0.137

111	P	ALZ034	Alzheimer Disease	90	0.137

112	P	BLD134	Bladder Cancer	79	0.137

113	P	ATS364	Autism	68	0.136

114	P	ESP024	Esophagitis	62	0.136

115		HYP266	Hypoxia	58	0.135

116		DWN001	Down Syndrome	70	0.133

117		GLC003	Glucose Intolerance	55	0.133

118	P	DRM053	Dermatitis, Atopic	68	0.133

119	P	BLD124	Bleeding Disorder, Platelet-Type, 11	66	0.133

120	P	MYC007	Myocardial Infarction	74	0.133

121		HPT004	Hepatic Coma	42	0.132

122		NTR005	Nutritional Deficiency Disease	61	0.132

123		BND020	Bone Disease	60	0.132

124		SKN016	Skin Disease	64	0.131

125	c	LKM061	Leukemia, Acute Myeloid	84	0.131

126	c	RHB024	Rhabdomyosarcoma 2	64	0.131

127		MYL069	Myeloma, Multiple	85	0.131

128	c	HPT073	Hepatitis C Virus	74	0.131

129		STR067	Stroke, Ischemic	82	0.130

130		BCT022	Bacterial Infectious Disease	57	0.130

131	P	TRM003	Tremor	55	0.130

132	P	GST053	Gastric Cancer	85	0.129

133		ADL002	Adult Syndrome	62	0.129

134		ANX004	Anoxia	44	0.128

135	P	PRD008	Periodontitis	66	0.128

136		DPR016	Depression	64	0.128

137		CNG034	Congestive Heart Failure	69	0.128

138		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	41	0.128

139	P	HYP086	Hypothyroidism	70	0.127

140		SCH012	Schizoaffective Disorder	50	0.127

141		CHL014	Cholera	58	0.127

142	P	BCL017	B-Cell Lymphoma	61	0.127

143	P	LYM031	Lymphocytic Leukemia	56	0.127

144		STM007	Stomatitis	51	0.127

145		ALC007	Alcohol Dependence	68	0.126

146		END030	End Stage Renal Failure	60	0.126

147		GST023	Gastric Ulcer	53	0.125

148	c	ACT071	Acute Kidney Failure	60	0.125

149	P	RHM011	Rheumatoid Arthritis	82	0.124

150		BRN071	Brain Injury	51	0.124

151	P	TRN020	Turner Syndrome	66	0.124

152	P	ART022	Arthritis	71	0.124

153		HPT019	Hepatic Encephalopathy	60	0.123

154		ATX038	Ataxia and Polyneuropathy, Adult-Onset	51	0.123

155		TRM010	Traumatic Brain Injury	54	0.123

156		OST159	Osteogenic Sarcoma	67	0.122

157	P	MYP004	Myopathy	63	0.122

158	P	CHL066	Cholangitis	53	0.121

159		PPL052	Papillomatosis, Confluent and Reticulated	34	0.121

160		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	67	0.121

161		INS024	Insulin-Like Growth Factor I	79	0.120

162		HMC014	Homocysteinemia	54	0.120

163		DSS008	Disease of Mental Health	66	0.120

164		CNS004	Constipation	59	0.120

165		HYP781	Hypoascorbemia	48	0.120

166	c	ACT075	Acute Myocardial Infarction	59	0.119

167	P	HRP006	Herpes Simplex	66	0.119

168	c	AMY091	Amyotrophic Lateral Sclerosis 1	88	0.119

169	P	LTR001	Lateral Sclerosis	56	0.118

170	P	MCR115	Microvascular Complications of Diabetes 5	67	0.118

171	P	DBT085	Diabetes Mellitus, Insulin-Dependent	68	0.117

172	c	MCL042	Macular Degeneration, Age-Related, 1	88	0.117

173		THR024	Thrombosis	58	0.116

174	c	DWL002	Dowling-Degos Disease 1	59	0.115

175	P	EPL164	Epilepsy	73	0.115

176		CRV035	Cervical Cancer	77	0.114

177		DYS014	Dyspepsia	51	0.113

178		BRR014	Barrett Esophagus	67	0.111

179		AGN016	Aging	58	0.111

180		SQM006	Squamous Cell Carcinoma	60	0.111

181		ADR007	Adrenoleukodystrophy	72	0.111

182		SPN186	Spinal Cord Injury	63	0.111

183		KRT009	Keratosis	52	0.111

184	c	DNT047	Dentinogenesis Imperfecta Type 2	34	0.110

185		CLF027	Cleft Palate, Isolated	67	0.110

186		LNG099	Lung Disease	62	0.110

187	c	SML038	Small Cell Cancer of the Lung	67	0.110

188		VTM002	Vitamin B12 Deficiency	48	0.110

189		CHL004	Cholelithiasis	50	0.110

190		ADR022	Adrenomyeloneuropathy	39	0.109

191		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	56	0.108

192	c	HPT001	Hepatitis C	62	0.108

193	P	DMN002	Dementia	68	0.108

194	c	MGR028	Migraine with or Without Aura 1	70	0.108

195	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	65	0.107

196		CHL079	Children's Interstitial Lung Disease	27	0.107

197		HMP009	Haemophilus Influenzae	46	0.107

198		ANX010	Anxiety	75	0.107

199	P	PRP019	Peripheral Nervous System Disease	64	0.107

200	P	INF032	Infertility	60	0.106

201	P	ART021	Arteriosclerosis	56	0.106

202	P	MLT020	Multiple Sclerosis	73	0.106

203	P	SKN015	Skin Carcinoma	67	0.106

204	c	ATS007	Autism Spectrum Disorder	69	0.106

205	P	CTR002	Cataract	62	0.106

206		PLM033	Pulmonary Embolism	60	0.106

207		EYD002	Eye Disease	59	0.106

208		IMM167	Immune Deficiency Disease	79	0.106

209		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.105

210	P	ENC004	Encephalitis	64	0.105

211		PLM129	Pulmonary Disease, Chronic Obstructive	74	0.105

212	P	MNN013	Meningitis	67	0.105

213		TXC005	Toxic Shock Syndrome	63	0.105

214		CHL123	Chlamydia	60	0.104

215	c	FNC043	Fanconi Anemia, Complementation Group E	64	0.104

216	P	MJR001	Major Depressive Disorder	69	0.104

217	c	ACT068	Acute Cystitis	63	0.104

218		MTH071	Methane Production	26	0.104

219	c	FTL070	Fetal Akinesia Deformation Sequence 2	33	0.103

220	P	FBR017	Fibrosarcoma	57	0.103

221	P	MSC005	Muscular Dystrophy	68	0.103

222	c	SYS001	Systemic Lupus Erythematosus	88	0.103

223		CRB004	Cerebral Artery Occlusion	38	0.103

224	P	HPT021	Hepatitis	69	0.103

225		RCK004	Rickets	70	0.103

226		SCH003	Schizophreniform Disorder	49	0.103

227	P	EXN002	Exanthem	58	0.102

228		CNT047	Contact Dermatitis	58	0.102

229		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.102

230		SRC014	Sarcoma	67	0.102

231		SPN035	Spindle Cell Sarcoma	57	0.102

232	c	ACT027	Acute Pancreatitis	60	0.102

233		OST003	Osteonecrosis	62	0.102

234		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	26	0.102

235		MDD011	Mood Disorder	62	0.101

236		MLN008	Melanoma	68	0.101

237		TRD006	Tardive Dyskinesia	58	0.101

238	P	THR014	Thrombocytopenia	67	0.101

239		DBT010	Diabetic Neuropathy	56	0.101

240		PPL022	Papilloma	56	0.101

241		PLM010	Pulmonary Edema	56	0.101

242	c	THR092	Thrombophilia Due to Thrombin Defect	74	0.100

243	P	ALC033	Alcohol Use Disorder	58	0.100

244	c	INH020	Inherited Metabolic Disorder	51	0.099

245		DNT012	Dental Caries	52	0.099

246	P	PNM007	Pneumonia	71	0.099

247		OVR082	Overgrowth Syndrome	51	0.099

248		ATX019	Ataxia with Vitamin E Deficiency	46	0.099

249	P	DYS154	Dystonia	65	0.099

250		ANG054	Angina Pectoris	66	0.098

251		HYP005	Hypokalemia	55	0.098

252	P	HYP076	Hyperthyroidism	55	0.098

253	P	LPS004	Lupus Erythematosus	62	0.098

254	P	ATR011	Atrial Fibrillation	67	0.097

255		ALL014	Allergic Encephalomyelitis	40	0.097

256		SQM002	Squamous Cell Papilloma	49	0.097

257	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	62	0.097

258		LPT014	Leptin Deficiency or Dysfunction	72	0.097

259		LYS012	Lysosomal Acid Lipase Deficiency	63	0.097

260	c	LRG017	Large Intestine Cancer	53	0.097

261	P	ATT013	Attention Deficit-Hyperactivity Disorder	66	0.096

262	P	CRD119	Cardiac Arrest	71	0.096

263		MYL009	Myelodysplastic Syndrome	72	0.096

264	P	INF038	Influenza	69	0.096

265		HNS001	Hansen's Disease	35	0.096

266	P	PNC044	Pancreatitis	61	0.096

267	P	LPR021	Leprosy 3	67	0.095

268	c	ATR087	Atrial Standstill 1	76	0.095

269		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	66	0.095

270	P	RSP003	Respiratory Failure	75	0.095

271		CLN015	Colon Adenocarcinoma	65	0.095

272		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	36	0.095

273		BRN024	Bronchitis	70	0.095

274	P	AST007	Astrocytoma	52	0.095

275	c	MLG068	Malignant Glioma	46	0.095

276	P	ECL001	Eclampsia	53	0.094

277		ACQ007	Acquired Immunodeficiency Syndrome	61	0.094

278	P	RHN004	Rhinitis	59	0.094

279	P	LYM118	Lymphoma	70	0.094

280		MLR004	Malaria	82	0.093

281	c	HPT016	Hepatitis B	63	0.092

282		ESP021	Esophageal Cancer	90	0.092

283	P	CYS018	Cystitis	59	0.092

284		ENT011	Enterocolitis	51	0.091

285		PNG002	Pain Agnosia	52	0.091

286	c	VRL010	Viral Hepatitis	56	0.091

287		MSL001	Measles	61	0.090

288	P	MYC084	Mycobacterium Tuberculosis 1	69	0.090

289	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.090

290		GST033	Gestational Diabetes	58	0.090

291		TTN003	Tetanus	62	0.089

292		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	46	0.089

293	P	PLM036	Pulmonary Fibrosis	66	0.089

294		IDP011	Idiopathic Interstitial Pneumonia	65	0.089

295	P	HDC001	Headache	59	0.089

296	P	ALP008	Alopecia	58	0.089

297	P	PLY019	Polyneuropathy	55	0.088

298		PRP027	Peripheral Vascular Disease	72	0.088

299		DPH001	Diphtheria	61	0.088

300		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	56	0.087

301	P	ACT008	Actinic Keratosis	50	0.087

302	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.087

303		AST005	Asthma	80	0.087

304		MTH009	Mouth Disease	56	0.086

305		OST115	Osteonecrosis of the Jaw	40	0.086

306	P	NPH012	Nephrotic Syndrome	65	0.086

307		ALL010	Allergic Contact Dermatitis	56	0.085

308	P	MVM001	Movement Disease	63	0.085

309		MST005	Mastitis	55	0.085

310		49X002	49,xxxxy Syndrome	39	0.085

311		ZLL002	Zollinger-Ellison Syndrome	54	0.084

312	P	CNR004	Cone-Rod Dystrophy 2	72	0.084

313	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.084

314	P	BRS044	Breast Adenocarcinoma	59	0.084

315	P	SBS003	Substance Abuse	56	0.084

316	P	LNG064	Lung Cancer Susceptibility 3	79	0.084

317	c	PRS136	Prostate Cancer, Hereditary, 6	34	0.084

318	c	PRS130	Prostate Cancer, Hereditary, 8	33	0.084

319		ALL003	Allergic Rhinitis	69	0.084

320	P	RTN016	Retinal Degeneration	56	0.084

321	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	61	0.083

322	P	MJR007	Major Affective Disorder 1	44	0.083

323		RYS001	Reye Syndrome	49	0.083

324		GST045	Gastroenteritis	60	0.082

325	P	CHR345	Chronic Pain	52	0.082

326		STT004	Steatorrhea	39	0.082

327		NWC001	Newcastle Disease	45	0.082

328		HYP081	Hypolipoproteinemia	51	0.082

329	P	INT143	Interstitial Cystitis	62	0.081

330	c	CRV002	Cervix Uteri Carcinoma in Situ	47	0.081

331		CRV045	Cervical Intraepithelial Neoplasia	41	0.081

332	P	ART023	Arthropathy	61	0.081

333		BRN004	Brain Edema	57	0.081

334		IRN001	Iron Deficiency Anemia	59	0.080

335		ACY011	Acyl-Coa Dehydrogenase Deficiency	38	0.080

336	P	PLM037	Pulmonary Hypertension	69	0.080

337	P	PLY011	Polycystic Ovary Syndrome	58	0.080

338	c	LKM071	Leukemia, Chronic Lymphocytic	81	0.080

339		HMN014	Human Immunodeficiency Virus Infectious Disease	56	0.080

340		ORL011	Oral Cancer	62	0.080

341		RSC001	Rosacea	55	0.080

342		LNG031	Lung Benign Neoplasm	52	0.080

343	P	NSP012	Nasopharyngeal Carcinoma	67	0.079

344		SBC016	Subacute Delirium	43	0.079

345	P	HYD006	Hydrocephalus	68	0.078

346	c	CNG216	Congenital Hydrocephalus	55	0.078

347		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	63	0.078

348	P	INS002	in Situ Carcinoma	55	0.078

349		RTN023	Retinitis	46	0.078

350		NRR001	Neuroretinitis	46	0.078

351	P	HYP069	Hyperparathyroidism	64	0.078

352		OTT002	Otitis Media	71	0.078

353		CYS013	Cystinuria	66	0.078

354		LSH001	Leishmaniasis	64	0.078

355	P	KLZ004	Kala-Azar 1	43	0.078

356	P	INT068	Intestinal Disease	56	0.078

357		PRN019	Perinatal Necrotizing Enterocolitis	55	0.078

358		LYM019	Lymphosarcoma	48	0.077

359	c	LKM004	Leukemia, B-Cell, Chronic	35	0.077

360		SQM013	Squamous Cell Carcinoma, Head and Neck	81	0.077

361	P	GRF003	Graft-Versus-Host Disease	71	0.077

362	c	PNS012	Paine Syndrome	61	0.077

363		SCH014	Schistosomiasis	57	0.077

364		SCH060	Schistosoma Mansoni Infection, Susceptibility/	40	0.077

365	P	THL005	Thalassemia	62	0.077

366		INT323	Intraocular Pressure Quantitative Trait Locus	64	0.076

367	P	SHR001	Short Bowel Syndrome	50	0.076

368		PRT013	Portal Hypertension	61	0.076

369	P	RTN008	Retinitis Pigmentosa	77	0.076

370	P	PRK057	Parkinson Disease, Late-Onset	77	0.076

371		BRN028	Brain Cancer	75	0.076

372		CLR108	Colorectal Adenoma	64	0.076

373		PRP030	Purpura	56	0.076

374		RRS014	Rare Surgical Neurologic Disease	33	0.076

375		DRY001	Dry Eye Syndrome	50	0.076

376	c	BSL007	Basal Cell Carcinoma	68	0.075

377	c	FML035	Familial Hyperlipidemia	56	0.075

378		CMM005	Common Cold	57	0.075

379	c	HPT003	Hepatitis a	60	0.075

380	P	HYP265	Hypotonia	43	0.075

381	c	MJR003	Major Affective Disorder 6	34	0.075

382	c	MJR006	Major Affective Disorder 5	34	0.075

383	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.074

384		HMS001	Hemosiderosis	54	0.074

385	P	URT039	Urticaria	61	0.074

386	P	END033	Endocarditis	58	0.074

387	c	MJR008	Major Affective Disorder 2	35	0.074

388	c	MJR023	Major Affective Disorder 7	34	0.074

389	c	MJR004	Major Affective Disorder 4	29	0.074

390	P	CND004	Candidiasis	61	0.074

391		BLR001	Biliary Atresia	51	0.074

392		CHR074	Choriocarcinoma	47	0.073

393	P	BNG032	Benign Mesothelioma	47	0.073

394		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	58	0.073

395	P	RCT021	Rectum Cancer	54	0.073

396		TRN015	Transient Cerebral Ischemia	62	0.073

397		IGR001	Ige Responsiveness, Atopic	61	0.073

398		GLS018	Glass Syndrome	51	0.073

399		MSC007	Muscle Hypertrophy	65	0.072

400	P	RRH023	Rare Hereditary Hemochromatosis	41	0.072

401		MSC157	Muscular Dystrophy, Duchenne Type	70	0.072

402	P	END044	Endometriosis	63	0.072

403		KHL003	Kohlschutter-Tonz Syndrome	63	0.072

404		BCT002	Bacterial Vaginosis	52	0.072

405	P	MLN007	Male Infertility	57	0.072

406	c	SVR001	Severe Acute Respiratory Syndrome	56	0.072

407	c	HYP555	Hypertriglyceridemia, Transient Infantile	38	0.071

408	P	OPN001	Open-Angle Glaucoma	50	0.071

409	P	MDL005	Medulloblastoma	78	0.071

410		GTR002	Goiter	54	0.071

411	P	SCK005	Sickle Cell Disease	53	0.071

412		FDL002	Food Allergy	52	0.071

413		KRT019	Keratitis, Hereditary	69	0.070

414		PLC008	Placenta Disease	51	0.070

415	c	LKM060	Leukemia, Acute Lymphoblastic 3	57	0.070

416	P	GLM040	Glioma Susceptibility 1	68	0.070

417	P	CNJ013	Conjunctivitis	67	0.070

418		END040	Endogenous Depression	55	0.070

419		DYS073	Dysphagia	52	0.070

420		KRT001	Keratoconjunctivitis Sicca	53	0.070

421		TYP007	Typhoid Fever	61	0.070

422		PLM031	Poliomyelitis	58	0.069

423		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.069

424		GNG013	Gingivitis	60	0.068

425		PRT038	Protein-Energy Malnutrition	56	0.068

426		CHL067	Cholecystitis	60	0.068

427		SCK003	Sickle Cell Anemia	74	0.067

428		RLP002	Relapsing-Remitting Multiple Sclerosis	57	0.067

429		PHR003	Pharyngitis	56	0.067

430		DYS015	Dysentery	45	0.067

431	c	PRM038	Primary Agammaglobulinemia	45	0.067

432	c	CHR064	Chronic Monocytic Leukemia	43	0.067

433		LYM133	Lymphoma, Hodgkin, Classic	70	0.067

434		EXN003	Exencephaly	32	0.067

435	P	PRS038	Personality Disorder	66	0.067

436		VRC005	Varicose Veins	61	0.067

437		PST092	Posttransplant Acute Limbic Encephalitis	29	0.067

438		NRT001	Neurotic Disorder	53	0.066

439		BRN056	Bronchopulmonary Dysplasia	57	0.066

440	c	FML001	Familial Atrial Fibrillation	67	0.066

441		KRT006	Keratoconjunctivitis	53	0.066

442	c	PRD040	Periodontitis, Chronic	56	0.066

443		CRC021	Carcinosarcoma	62	0.066

444		KRT013	Keratolytic Winter Erythema	45	0.066

445		NWB001	Newborn Respiratory Distress Syndrome	58	0.065

446		PLG002	Plague	54	0.065

447	P	SLP006	Sleep Apnea	71	0.065

448	P	HYP061	Hypertrophic Cardiomyopathy	68	0.065

449		BRK010	Burkitt Lymphoma	68	0.065

450		CRN030	Coronary Stenosis	49	0.065

451		MDM001	Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency	36	0.065

452		KWS001	Kwashiorkor	46	0.065

453		MXD026	Mixed Glioma	36	0.065

454		SKN019	Skin Melanoma	68	0.065

455	P	FML011	Familial Adenomatous Polyposis	73	0.065

456	c	MCR129	Microvascular Complications of Diabetes 1	67	0.065

457	P	UVT001	Uveitis	58	0.065

458		LKP003	Leukoplakia	40	0.064

459		LYM143	Lymphoma, Non-Hodgkin, Familial	74	0.064

460	P	THY023	Thymoma	64	0.064

461	c	THY107	Thymoma, Familial	55	0.064

462		ANR007	Anorexia Nervosa	64	0.064

463	P	VSC011	Vasculitis	64	0.064

464	c	BRN108	Branchiootic Syndrome 1	62	0.064

465		HMT018	Hematopoietic Stem Cell Transplantation	54	0.064

466		SPL018	Splenomegaly	48	0.064

467	c	HNT004	Huntington Disease-Like 2	48	0.064

468	c	SPN225	Spondyloarthropathy 1	74	0.063

469		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.063

470		CRH005	Crohn's Colitis	56	0.063

471		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.063

472		PTT037	Pituitary Tumors	47	0.063

473	c	GLC092	Glaucoma, Primary Open Angle	63	0.063

474		ANR040	Aneurysm	60	0.063

475		PRP080	Peripheral Artery Disease	51	0.063

476		ACT113	Acute Myeloblastic Leukemia with Maturation	48	0.063

477		SFT003	Soft Tissue Sarcoma	57	0.062

478	P	RTN018	Retinal Disease	53	0.062

479		HYP020	Hyperprolactinemia	62	0.062

480	P	SLP005	Sleep Disorder	58	0.062

481	P	MNC007	Monocytic Leukemia	52	0.062

482		CRT015	Carotid Artery Occlusion	44	0.062

483		RRD056	Rare Disease in Surgical Orthopedic	29	0.062

484		OST017	Osteomyelitis	65	0.062

485	P	MYC008	Myocarditis	60	0.062

486	P	CLC063	Celiac Disease 1	66	0.062

487		RTN017	Retinal Detachment	62	0.062

488	P	ADL010	Adult Respiratory Distress Syndrome	61	0.062

489		CLF001	Cleft Lip	53	0.062

490	P	HYP058	Hypervitaminosis a	45	0.061

491		NSP002	Nasopharyngitis	41	0.061

492	P	OCL013	Oculodentodigital Dysplasia	65	0.061

493		PNM008	Pneumothorax	56	0.061

494		PST021	Postpartum Depression	51	0.061

495	P	ALP009	Alopecia Areata	61	0.061

496		GLS001	Gliosarcoma	56	0.061

497		SPS057	Spasticity	38	0.061

498		SXL003	Sexual Disorder	49	0.061

499		AMN001	Amenorrhea	54	0.061

500		HPT022	Hepatoblastoma	58	0.060

501	P	NRV007	Nervous System Disease	68	0.060

502		ILS001	Ileus	51	0.060

503	P	ANG015	Angioedema	54	0.060

504		HYD002	Hydronephrosis	58	0.059

505	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	49	0.059

506		TRP004	Tropical Sprue	41	0.059

507		DMY004	Demyelinating Disease	54	0.059

508		SPN051	Spondylitis	53	0.058

509		INF009	Inflammatory Spondylopathy	29	0.058

510		TRP009	Triple X Syndrome	42	0.058

511		MCR013	Microphthalmia	62	0.058

512	P	GRV001	Graves' Disease	57	0.058

513	P	OLG002	Oligodendroglioma	67	0.058

514		ATN005	Autonomic Dysfunction	48	0.058

515		CRB037	Cerebral Palsy	69	0.057

516		RBS001	Rabies	57	0.057

517		TNS005	Tonsillitis	58	0.057

518		ATN004	Autonomic Neuropathy	43	0.057

519		RDN001	Reading Disorder	42	0.057

520		SLC006	Silicosis	55	0.057

521	P	PTT006	Pituitary Adenoma	53	0.057

522		PPL001	Papillary Adenoma	42	0.057

523	c	SVR005	Severe Pre-Eclampsia	50	0.056

524		ACT084	Acute Stress Disorder	42	0.056

525		YLL002	Yellow Fever	58	0.056

526		ACY009	Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of	55	0.056

527	c	PSR017	Psoriasis 2	55	0.056

528	c	PSR023	Psoriasis 1	50	0.056

529	c	PSR028	Psoriasis 7	40	0.056

530	c	PSR018	Psoriasis 13	40	0.056

531	c	PSR032	Psoriasis 11	40	0.056

532		VRL011	Viral Infectious Disease	62	0.056

533		VSC003	Visceral Leishmaniasis	55	0.056

534		PST028	Post-Traumatic Stress Disorder	60	0.056

535		MCL006	Macular Retinal Edema	52	0.056

536		CRD223	Cardiac Arrhythmia	61	0.055

537		INT002	Intermittent Claudication	60	0.055

538	P	VSC018	Visceral Steatosis	34	0.055

539		LMY002	Leiomyoma	52	0.055

540		LNT004	Lentigines	47	0.055

541	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	61	0.055

542	P	NGH001	Night Blindness	48	0.055

543		XRP001	Xerophthalmia	37	0.055

544		FCT007	Factor Vii Deficiency	65	0.055

545		FBR047	Fibromyalgia	60	0.055

546	c	SCN007	Secondary Hyperparathyroidism	52	0.055

547	P	TRT010	Teratoma	52	0.055

548		CHR178	Chromosomal Triplication	36	0.055

549		CYT018	Cytochrome P450 2d6 Variant	28	0.055

550		WST001	West Syndrome	61	0.055

551		MNT001	Mantle Cell Lymphoma	69	0.054

552		INT075	Intracranial Hypertension	54	0.054

553		OBS002	Obsessive-Compulsive Disorder	69	0.054

554	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	61	0.054

555		VGN023	Vaginitis	54	0.054

556		PLR008	Pleurisy	50	0.054

557	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.054

558		PLC005	Placental Insufficiency	55	0.054

559	P	PNC025	Panic Disorder	53	0.054

560	c	INF145	Infantile Liver Failure Syndrome 1	50	0.054

561	c	MLG074	Malignant Mesenchymoma	50	0.054

562		CRN296	Carnitine Palmitoyltransferase Ii Deficiency, Infantile	62	0.054

563	c	HMC039	Hemochromatosis, Type 1	73	0.053

564	P	FLL037	Follicular Lymphoma	67	0.053

565	c	EXD008	Exudative Vitreoretinopathy 1	69	0.053

566	P	LRY044	Larynx Cancer	59	0.053

567		HYP025	Hyperphosphatemia	47	0.053

568		BCK006	Back Pain	44	0.053

569		STN013	Stenotrophomonas Maltophilia Infection	26	0.053

570		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.053

571		CMR002	Coumarin Resistance	56	0.053

572		CHR066	Chronic Fatigue Syndrome	61	0.053

573	P	TXP001	Toxoplasmosis	61	0.053

574	P	TBR001	Tuberous Sclerosis	72	0.052

575		ACR007	Acromegaly	70	0.052

576	c	MST023	Mesothelioma, Malignant	59	0.052

577	P	MTC069	Mitochondrial Disorders	57	0.052

578		SPT004	Septic Arthritis	55	0.052

579	c	MCR112	Microvascular Complications of Diabetes 2	42	0.052

580		EXC002	Exocrine Pancreatic Insufficiency	41	0.052

581		LYM040	Lymphoblastic Lymphoma	54	0.052

582	c	CHR682	Chronic Bilirubin Encephalopathy	36	0.052

583	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	46	0.052

584		MLT157	Multiple System Atrophy 1	71	0.051

585		EWN003	Ewing Sarcoma	69	0.051

586		HMT002	Hematologic Cancer	64	0.051

587		LNG073	Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.051

588		DFF005	Diffuse Large B-Cell Lymphoma	56	0.051

589		IMM064	Immunodeficiency, Common Variable, 10	51	0.051

590		PLS007	Plasmodium Falciparum Malaria	53	0.051

591	P	INT070	Intestinal Obstruction	60	0.051

592		NRN004	Neuroendocrine Tumor	59	0.051

593		PRD004	Prediabetes Syndrome	49	0.051

594		NRM005	Neuromuscular Disease	62	0.051

595	P	HYP726	Hypercalcemia, Infantile, 1	58	0.051

596	P	RBL001	Rubella	56	0.051

597		MCR004	Macroglobulinemia	50	0.051

598		RTC005	Reticulosarcoma	48	0.051

599		ASP007	Aspiration Pneumonia	46	0.051

600		FSC004	Fasciitis	47	0.050

601		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	37	0.050

602		CHY002	Chylomicron Retention Disease	63	0.050

603	P	EPN002	Ependymoma	61	0.050

604		DBT002	Diabetic Autonomic Neuropathy	45	0.050

605		THR100	Thrombocytopenic Purpura, Autoimmune	61	0.050

606		ESP002	Esophageal Varix	49	0.050

607	P	BLR006	Biliary Tract Disease	49	0.050

608		TND005	Tendinitis	45	0.050

609		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	65	0.049

610		APP008	Appendicitis	61	0.049

611		BRN002	Bronchiolitis	60	0.049

612	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	52	0.049

613	c	BNG030	Benign Ependymoma	48	0.049

614		GST020	Gastric Antral Vascular Ectasia	42	0.049

615	P	PTS002	Ptosis	53	0.049

616		LPT006	Leptin Receptor Deficiency	47	0.049

617		ASP008	Aspiration Pneumonitis	41	0.049

618	P	SYP003	Syphilis	59	0.049

619	P	SJG008	Sjogren Syndrome	57	0.049

620		GST030	Gastrinoma	43	0.049

621	P	PRC031	Preeclampsia/eclampsia 1	42	0.049

622	c	LKM070	Leukemia, Acute Monocytic	55	0.048

623		CLL003	Cellulitis	56	0.048

624		CLN045	Colonic Benign Neoplasm	52	0.048

625		VTM033	Vitamin K Deficiency Bleeding	47	0.048

626		HYP457	Hypertrophic Scars	44	0.048

627		BRS051	Breast Disease	59	0.048

628	P	PRV006	Pervasive Developmental Disorder	58	0.048

629		HYP080	Hypogonadism	51	0.048

630	c	FLL041	Follicular Lymphoma 1	50	0.048

631		PLR007	Pleural Empyema	44	0.048

632	P	PRC017	Precursor Lymphoblastic Lymphoma/leukemia	28	0.048

633	c	BPL002	Bipolar I Disorder	48	0.048

634		PPL049	Papillon-Lefevre Syndrome	63	0.047

635		RTN020	Retinal Vascular Disease	49	0.047

636		PRS063	Paresthesia	46	0.047

637		HYP064	Hypogonadotropism	40	0.047

638		CHL013	Cholecystolithiasis	37	0.047

639		CRP001	Carpal Tunnel Syndrome	68	0.047

640	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	54	0.047

641		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.047

642	c	LKM056	Leukemia, Chronic Lymphocytic 2	49	0.047

643		CRT084	Creatinine Clearance Quantitative Trait Locus	26	0.047

644		PRN009	Paranoid Schizophrenia	47	0.047

645		ACD008	Acid-Labile Subunit Deficiency	55	0.046

646		GNG003	Gingival Recession	43	0.046

647		GST071	Gastrointestinal Carcinoma	42	0.046

648		PRT058	Pure Autonomic Failure	60	0.046

649		ACT200	Acute Monoblastic Leukemia	56	0.046

650		SYN036	Syncope	46	0.046

651		APN008	Apnea, Obstructive Sleep	64	0.046

652	P	HMR005	Hemorrhoid	47	0.046

653		PLL012	Pollen Allergy	46	0.046

654	c	SYS043	Systemic Lupus Erythematosus 1	39	0.046

655	c	ALP101	Alpha-Thalassemia	63	0.045

656		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	57	0.045

657		CRC006	Carcinoid Syndrome	55	0.045

658	P	NRV006	Nervous System Cancer	55	0.045

659		PRP036	Peripheral T-Cell Lymphoma	53	0.045

660		INT303	Intracranial Hypertension, Idiopathic	52	0.045

661		MYM001	Myoma	52	0.045

662		TXC020	Toxic Oil Syndrome	34	0.045

663	P	NRN021	Neuronal Ceroid Lipofuscinosis	63	0.045

664		HMR039	Hemorrhage, Intracerebral	59	0.045

665		MTC027	Mitochondrial Trifunctional Protein Deficiency	55	0.045

666	c	PRM092	Primary Lateral Sclerosis, Adult, 1	54	0.045

667		NRL018	Neural Tube Defects, Folate-Sensitive	50	0.045

668		LPD009	Lipid Storage Disease	49	0.045

669	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.045

670	P	STR092	Striatal Degeneration, Autosomal Dominant 2	42	0.045

671	P	PHT010	Photoparoxysmal Response 1	39	0.045

672		FLL008	Folliculitis	46	0.045

673		WLS001	Wilson Disease	69	0.045

674	c	MCL013	Mucolipidosis Iv	60	0.045

675		SHG001	Shigellosis	54	0.045

676		INF034	Infective Endocarditis	53	0.045

677		GNT002	Giant Cell Glioblastoma	52	0.045

678		OST011	Osteomalacia	51	0.045

679	c	CNT033	Central Nervous System Cancer	51	0.045

680		CRB090	Cerebral Hypoxia	45	0.045

681		CHL045	Choline Deficiency Disease	39	0.045

682		LYM048	Lymphoma, Large-Cell, Immunoblastic	30	0.045

683		LNG015	Lingual-Facial-Buccal Dyskinesia	48	0.044

684		SYS003	Systolic Heart Failure	43	0.044

685	c	TBR025	Tuberous Sclerosis 1	74	0.044

686	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.044

687		PLS025	Plasmablastic Lymphoma	48	0.044

688		CYN002	Cyanosis, Transient Neonatal	45	0.044

689	P	CRB088	Cerebral Atrophy	43	0.044

690	c	XNT010	Xanthinuria, Type I	51	0.044

691		CRY008	Cryopyrin-Associated Periodic Syndrome	48	0.044

692		IRR003	Irritant Dermatitis	46	0.044

693		CTS005	Catastrophic Antiphospholipid Syndrome	44	0.044

694		TND004	Tendinopathy	44	0.044

695		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.044

696		ATM052	Autoimmune Disease 1	38	0.044

697		ALL009	Allergic Conjunctivitis	50	0.043

698		RSP007	Respiratory Distress Syndrome, Infant	31	0.043

699		ORL005	Oral Candidiasis	56	0.043

700		GST049	Gastrointestinal System Cancer	49	0.043

701		LWC001	Low Compliance Bladder	45	0.043

702	P	AVS003	Avascular Necrosis	43	0.043

703		URG005	Uruguay Faciocardiomusculoskeletal Syndrome	37	0.043

704		SMT001	Somatization Disorder	45	0.042

705		ENT001	Enterocele	44	0.042

706	c	PNC108	Pancreatitis, Hereditary	70	0.042

707		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.042

708	P	CNT110	Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a	61	0.042

709		LMY014	Leiomyoma, Uterine	57	0.042

710		ACR041	Acromelic Frontonasal Dysostosis	50	0.042

711		THR016	Thrombophlebitis	50	0.042

712	P	END046	Endometritis	49	0.042

713		ART004	Aortic Atherosclerosis	47	0.042

714		DBT006	Diabetic Macular Edema	46	0.042

715	c	ACT004	Acute Diarrhea	38	0.042

716		VGN019	Vaginal Discharge	35	0.042

717	P	HYP040	Hypospadias	54	0.041

718		BRD004	Borderline Personality Disorder	51	0.041

719	c	BCT013	Bacterial Pneumonia	49	0.041

720		RNL011	Renal Osteodystrophy	49	0.041

721		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	48	0.041

722		TRC003	Trichomoniasis	46	0.041

723		SKN005	Skin Atrophy	41	0.041

724		GRM010	Germ Cells Tumors	35	0.041

725	P	END047	Endophthalmitis	50	0.041

726		VGN020	Vaginal Disease	45	0.041

727		LYM012	Lymphoplasmacytic Lymphoma	62	0.041

728		APH001	Aphthous Stomatitis	56	0.041

729		STP011	Stapes Ankylosis with Broad Thumbs and Toes	50	0.041

730		GLC036	Glucagonoma	45	0.041

731	c	HMG029	Hemoglobin Se Disease	40	0.041

732		SPR126	Superior Semicircular Canal Dehiscence	39	0.041

733		PLY068	Polysubstance Abuse	44	0.041

734	P	LCT002	Lactose Intolerance	51	0.040

735		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	51	0.040

736		VLV011	Vulvovaginal Candidiasis	50	0.040

737	P	BLD051	Blood Coagulation Disease	48	0.040

738		MCL027	Macular Dystrophy, Dominant Cystoid	47	0.040

739		MYF001	Myofibroma	40	0.040

740		CHL039	Choledocholithiasis	37	0.040

741	P	BRN035	Brain Stem Glioma	51	0.040

742	c	LTN004	Late-Onset Retinal Degeneration	49	0.040

743		CRC014	Carcinoid Tumors, Intestinal	49	0.040

744		CRN027	Corneal Neovascularization	48	0.040

745	c	BSL024	Basal Cell Carcinoma 1	47	0.040

746		ADR054	Adrenocortical Carcinoma, Hereditary	68	0.039

747		CRN036	Craniopharyngioma	65	0.039

748		NTR018	Neutrophilia, Hereditary	53	0.039

749		FRZ001	Frozen Shoulder	53	0.039

750		OPT003	Opiate Dependence	50	0.039

751		INT017	Intestinal Schistosomiasis	49	0.039

752	c	DRM054	Dermatitis, Atopic, 2	45	0.039

753		MYF002	Myofascial Pain Syndrome	39	0.039

754		FBR012	Fabry Disease	68	0.039

755		ABT001	Abetalipoproteinemia	68	0.039

756	P	PTN014	Patent Ductus Arteriosus 1	60	0.039

757	P	ORL007	Oral Cavity Cancer	57	0.039

758	c	LBR014	Leber Congenital Amaurosis 4	55	0.039

759	P	KRT007	Keratoconus	51	0.039

760		PRV004	Periventricular Leukomalacia	50	0.039

761		CLS016	Clostridium Difficile Colitis	48	0.039

762		LYM051	Lymphomatoid Granulomatosis	47	0.039

763	P	HRD086	Hereditary Hypophosphatemic Rickets	41	0.039

764		CRB086	Cerebral Aneurysms	41	0.039

765		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	32	0.039

766		OBS003	Obsessive-Compulsive Personality Disorder	42	0.038

767	P	LYM025	Lymphedema	54	0.038

768		BWN001	Bowen-Conradi Syndrome	49	0.038

769		EWN002	Ewing's Family of Tumors	48	0.038

770		CLC006	Calcinosis	48	0.038

771	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.038

772		PNM010	Pneumothorax, Primary Spontaneous	60	0.037

773	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	58	0.037

774		SPS003	Spastic Diplegia	53	0.037

775		NRN001	Neuroendocrine Carcinoma	48	0.037

776		IFP001	Ifap Syndrome with or Without Bresheck Syndrome	48	0.037

777		BHR001	Behr Syndrome	47	0.037

778		CRT016	Carotid Artery Disease	53	0.037

779	P	TTR001	Tetralogy of Fallot	70	0.037

780	P	PLV020	Pelvic Organ Prolapse	61	0.037

781		BRN045	Brunner Syndrome	57	0.037

782		APH002	Aphasia	56	0.037

783		HND002	Hand, Foot and Mouth Disease	52	0.037

784		APR001	Apraxia	50	0.037

785		HDR003	Hidradenitis	48	0.037

786		NCR007	Necrotizing Fasciitis	47	0.037

787		BRS064	Bursitis	42	0.037

788		MNN028	Mononeuropathy of the Median Nerve, Mild	41	0.037

789		CLS047	Classic Progressive Supranuclear Palsy Syndrome	30	0.037

790		ANL022	Anal Fistula	47	0.036

791		MGK001	Megakaryocytic Leukemia	65	0.036

792	P	FCL005	Focal Segmental Glomerulosclerosis	63	0.036

793		FND002	Fundus Dystrophy	52	0.036

794		CHR005	Chorioamnionitis	51	0.036

795		HYP063	Hypersplenism	51	0.036

796		ERY004	Erysipelas	46	0.036

797		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	46	0.036

798		LCH009	Lichen Sclerosus	39	0.036

799	c	PRG020	Paragangliomas 3	36	0.036

800		JVN026	Jeavons Syndrome	24	0.036

801		PTT048	Pituitary Adenoma, Prolactin-Secreting	61	0.035

802		HDR002	Hidradenitis Suppurativa	58	0.035

803		ADR016	Adrenal Cortical Carcinoma	51	0.035

804		PRP017	Periapical Periodontitis	43	0.035

805	P	CRN024	Corneal Disease	42	0.035

806		ACL001	Acalculous Cholecystitis	35	0.035

807		STT009	Sutton Disease 2	31	0.035

808		PTT009	Pituitary Gland Disease	54	0.035

809	c	FML346	Familial Adenomatous Polyposis 1	71	0.034

810	P	STR022	Stargardt Disease	59	0.034

811	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	58	0.034

812		ECH003	Echinococcosis	54	0.034

813		SRT004	Serotonin Syndrome	48	0.034

814	P	PRD037	Periodontal Ehlers-Danlos Syndrome	45	0.034

815		PRL017	Prolymphocytic Leukemia	45	0.034

816		ATN011	Autoinflammation with Infantile Enterocolitis	45	0.034

817		CLL014	Cll/sll	44	0.034

818		ADR004	Adrenal Cortical Adenocarcinoma	44	0.034

819		VLV010	Vulvovaginitis	42	0.034

820		CLN044	Colon Adenoma	41	0.034

821		SPR008	Supratentorial Primitive Neuroectodermal Tumor	39	0.034

822		CVT001	Cavitary Optic Disc Anomalies	39	0.034

823		ACT011	Acute Contagious Conjunctivitis	35	0.034

824		MSM014	Mismatch Repair Cancer Syndrome	65	0.034

825	P	TST021	Testicular Germ Cell Tumor	63	0.034

826		PNM001	Pneumocystosis	53	0.034

827		ADN009	Adenosquamous Carcinoma	50	0.034

828		MTY001	Mutyh-Associated Polyposis	48	0.034

829		MNC019	Monocarboxylate Transporter 1 Deficiency	47	0.034

830	P	OCY003	Oocyte Maturation Defect 1	44	0.034

831		MCL003	Macular Holes	44	0.034

832		CYS009	Cystadenoma	43	0.034

833	P	DYS021	Dysautonomia	41	0.034

834		BCK003	Background Diabetic Retinopathy	37	0.034

835		CRB026	Cerebellar Astrocytoma	31	0.034

836		MYP139	Myopathy, Proximal, and Ophthalmoplegia	56	0.034

837	P	HMP002	Hemophagocytic Lymphohistiocytosis	68	0.033

838		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	58	0.033

839		LNN001	Lennox-Gastaut Syndrome	56	0.033

840		ORP003	Oropharynx Cancer	55	0.033

841	P	HYP730	Hypogonadotropic Hypogonadism	54	0.033

842	P	SPN052	Spondyloarthropathy	54	0.033

843		OPD006	Opioid Addiction	49	0.033

844		PNC119	Pancreatic Neuroendocrine Tumor	48	0.033

845		AYM001	Ayme-Gripp Syndrome	45	0.033

846	c	DYS119	Dystonia 9	45	0.033

847	P	CLS010	Cluster Headache	44	0.033

848		BNN005	Bunion	34	0.033

849		CRN302	Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal	32	0.033

850		ANT066	Anterior Cutaneous Nerve Entrapment Syndrome	28	0.033

851		CHL057	Childhood Brain Stem Glioma	19	0.033

852		CHL009	Childhood Cerebral Astrocytoma	15	0.033

853		NRL004	Neuroleptic Malignant Syndrome	48	0.032

854	c	PRG043	Progressive Familial Heart Block, Type Ib	48	0.032

855		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	58	0.032

856		FRY006	Fryns Microphthalmia Syndrome	55	0.032

857	c	HYP740	Hyperlipoproteinemia, Type V	53	0.032

858	P	PNB001	Pineoblastoma	52	0.032

859	P	AGG001	Aggressive Periodontitis	50	0.032

860	P	SCL015	Scleritis	49	0.032

861	P	GND004	Gonadal Dysgenesis	47	0.032

862		CHL018	Childhood Medulloblastoma	46	0.032

863		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	43	0.032

864	P	ECT045	Ectodermal Dysplasia-Syndactyly Syndrome 1	39	0.032

865		RCT017	Rectal Disease	39	0.032

866		HYP189	Hypoadrenalism	39	0.032

867		PDT014	Pediatric Ependymoma	33	0.032

868		EMB015	Embryonal Tumor with Multilayered Rosettes	29	0.032

869		CGN007	Cognitive Function 1, Social	28	0.032

870	P	ORT004	Orthostatic Intolerance	68	0.031

871		DMN031	Dementia, Lewy Body	66	0.031

872		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	65	0.031

873		ADR005	Adrenal Carcinoma	58	0.031

874		CRT033	Corticobasal Degeneration	55	0.031

875	P	ACT105	Acute Mountain Sickness	53	0.031

876	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	53	0.031

877		FML037	Female Breast Cancer	52	0.031

878	c	HYP739	Hyperlipoproteinemia, Type Iv	50	0.031

879		ISL001	Islet Cell Tumor	47	0.031

880	P	BCT020	Bacteremia 2	45	0.031

881		PNC085	Penicillin Allergy	44	0.031

882		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.031

883		PRS115	Prosthetic Joint Infection	43	0.031

884		MMM006	Mammographic Density	43	0.031

885	c	MCR312	Microphthalmia, Syndromic 10	34	0.031

886		BRN049	Brain Tumor, Childhood	30	0.031

887		LRY027	Laryngeal Papillomatosis	24	0.031

888	P	MLN066	Melanoma, Cutaneous Malignant 1	69	0.030

889	P	HYP609	Hypophosphatemic Rickets, X-Linked Dominant	62	0.030

890	P	SCK002	Sick Sinus Syndrome	56	0.030

891		VTM027	Vitamin D-Dependent Rickets, Type 2a	56	0.030

892	c	PYR010	Peyronie's Disease	51	0.030

893		PTH002	Pathological Gambling	48	0.030

894		PRS034	Parasitic Helminthiasis Infectious Disease	48	0.030

895		ULC007	Ulcerative Stomatitis	41	0.030

896		CNT060	Central Serous Chorioretinopathy	41	0.030

897		HRN003	Heroin Dependence	41	0.030

898		CNT017	Central Nervous System Origin Vertigo	38	0.030

899		PLN007	Plantar Fasciitis	32	0.030

900		PDT015	Pediatric Supratentorial Ependymoma	31	0.030

901		PDT016	Pediatric Infratentorial Ependymoma	29	0.030

902		SDD004	Sudden Arrhythmia Death Syndrome	23	0.030

903	P	LBR001	Leber Congenital Amaurosis	67	0.029

904		MSC165	Muscular Dystrophy, Congenital, Lmna-Related	66	0.029

905	c	HYP798	Hypophosphatemic Rickets, X-Linked Recessive	60	0.029

906	P	AGN002	Agnosia	56	0.029

907	P	CRN028	Corneal Ulcer	49	0.029

908		CLD014	Cole Disease	41	0.029

909		OBS004	Obstructive Hydrocephalus	39	0.029

910	c	JVN024	Juvenile Hereditary Hemochromatosis	32	0.029

911		INT053	Intracranial Vasospasm	32	0.029

912		CHL006	Childhood Oligodendroglioma	31	0.029

913		VNT037	Ventral Hernia	31	0.029

914		DLT018	Dilution, Pigmentary	28	0.029

915	P	CNT036	Central Nervous System Germ Cell Tumor	28	0.029

916		HYP213	Hypomelanotic Disorder	25	0.029

917		THY020	Thyroid Hyalinizing Trabecular Adenoma	23	0.029

918	c	SCH082	Schizophrenia 5	40	0.028

919		PNC012	Punctate Epithelial Keratoconjunctivitis	30	0.028

920	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.028

921		ERY029	Erythermalgia, Primary	58	0.028

922	P	HRN001	Horner's Syndrome	46	0.028

923		GRM004	Germinoma	45	0.028

924	P	END039	Endodermal Sinus Tumor	44	0.028

925		CNN010	Connective Tissue Benign Neoplasm	44	0.028

926		CHR078	Chorioretinitis	43	0.028

927	c	HYP057	Hypervitaminosis D	41	0.028

928		TST018	Testicular Yolk Sac Tumor	39	0.028

929		DNT014	Dental Pulp Disease	38	0.028

930		DNT006	Dental Pulp Necrosis	37	0.028

931		LCH016	Lichen Sclerosus Et Atrophicus	36	0.028

932	c	PLM022	Pulmonary Valve Insufficiency	35	0.028

933		BLN010	Balanitis	34	0.028

934		TQP001	Taqi Polymorphism	34	0.028

935		RTN002	Retinal Perforation	33	0.028

936	c	RTN181	Retinitis Pigmentosa 2, X-Linked	16	0.028

937	P	USH001	Usher Syndrome	58	0.027

938		DRR016	Diarrhea 2, with Microvillus Atrophy	54	0.027

939		SMT006	Somatoform Disorder	51	0.027

940		PST048	Postural Orthostatic Tachycardia Syndrome	49	0.027

941		ATT003	Attenuated Familial Adenomatous Polyposis	48	0.027

942		RCR004	Recurrent Respiratory Papillomatosis	48	0.027

943		GNG008	Ganglioneuroblastoma	47	0.027

944		SYM002	Sympathetic Ophthalmia	46	0.027

945		PNC056	Pineocytoma	46	0.027

946		MTS001	Mutism	43	0.027

947		CHL012	Childhood Disintegrative Disease	41	0.027

948	P	INT260	Intracranial Berry Aneurysm	38	0.027

949		ANS012	Anus Disease	37	0.027

950		CHN040	Choanal Atresia and Lymphedema	36	0.027

951		CRB054	Cerebellar Astrocytoma, Childhood	9	0.027

952		LCT022	Lecithin:cholesterol Acyltransferase Deficiency	60	0.025

953		VTM028	Vitamin E, Familial Isolated Deficiency of	57	0.025

954	c	MYP132	Myopathy, Congenital	55	0.025

955		BRD001	Brody Myopathy	55	0.025

956		SMT003	Somatostatinoma	49	0.025

957		SPN119	Spondylarthropathy	45	0.025

958		MDS018	Mediastinal Cancer	40	0.025

959		AMP007	Amphetamine Abuse	39	0.025

960		RGD002	Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal	38	0.025

961	c	SCH080	Schizophrenia 3	34	0.025

962		STR046	Stargardt Macular Degeneration	32	0.025

963		CHR288	Chronic Recurrent Multifocal Osteomyelitis	58	0.024

964		VLV032	Vulva Cancer	53	0.024

965		VPM001	Vipoma	47	0.024

966	c	FCL025	Focal Segmental Glomerulosclerosis 1	47	0.024

967		LRY022	Laryngoonychocutaneous Syndrome	45	0.024

968	P	CNT037	Central Nervous System Germinoma	43	0.024

969		RMS001	Rem Sleep Behavior Disorder	43	0.024

970		TND006	Tendinosis	42	0.024

971		PNL014	Pineal Gland Cancer	40	0.024

972		BLN002	Balanitis Xerotica Obliterans	38	0.024

973		PNC008	Pancreatic Endocrine Carcinoma	36	0.024

974		PRR004	Preretinal Fibrosis	36	0.024

975		SPP003	Suppurative Periapical Periodontitis	34	0.024

976		MXD032	Mixed Germ Cell Tumor	32	0.024

977		WDH001	Wdha Syndrome	32	0.024

978		PPM002	Ppoma	28	0.024

979		ISL004	Isolated Gonadotropin-Releasing Hormone Deficiency	27	0.024

980		MLR020	Malaria, Mild	27	0.024

981		MXD025	Mixed Germ Cell Cancer	26	0.024

982		ACT133	Acetylation, Slow	23	0.024

983		LKP001	Leukoplakia of Penis	19	0.024

984		CHL046	Childhood Central Nervous System Mixed Germ Cell Tumor	11	0.024

985		CHL027	Childhood Central Nervous System Germinoma	11	0.024

986	P	PRS049	Persistent Mullerian Duct Syndrome	53	0.022

987	P	HRD012	Hereditary Elliptocytosis	50	0.022

988	P	DPY001	Dupuytren Contracture	48	0.022

989	c	PRS128	Persistent Mullerian Duct Syndrome, Types I and Ii	45	0.022

990		GLC096	Galactorrhea	44	0.022

991		PHM001	Phimosis	39	0.022

992	c	GLC041	Glaucoma 1, Open Angle, a	33	0.022

993		ENG004	Engraftment Syndrome	30	0.022

994		HMP003	Hemopneumothorax	29	0.022

995	c	SCH081	Schizophrenia 6	27	0.022

996		ACT206	Acitretin/etretinate Embryopathy	16	0.022