Search results for Palmitic Acid

1003 hits were found for Palmitic Acid

#	Family	MCID	Name	MIFTS	Score
1		FTT001	Fatty Liver Disease	61	0.351

2	P	LVR013	Liver Disease	68	0.316

3		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.312

4		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.290

5	P	SCH015	Schizophrenia	74	0.280

6		LPD008	Lipid Metabolism Disorder	62	0.237

7	P	NRB001	Neuroblastoma	72	0.235

8	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.230

9	P	CLR023	Colorectal Cancer	99	0.228

10		48X005	48,xyyy	39	0.224

11		LVR012	Liver Cirrhosis	62	0.220

12		HLX001	Helix Syndrome	47	0.215

13		NNL006	Non-Alcoholic Steatohepatitis	54	0.214

14	P	KDN018	Kidney Disease	72	0.212

15		ACT119	Acute Promyelocytic Leukemia	63	0.211

16		HYP066	Hyperglycemia	61	0.210

17		HYP014	Hyperuricemia	52	0.204

18	P	SZR006	Seizure Disorder	56	0.202

19	P	CRN300	Coronary Heart Disease 1	63	0.198

20	c	NRF023	Neurofibromatosis, Type Ii	80	0.198

21		NRL016	Neural Tube Defects	82	0.198

22	P	DRR001	Diarrhea	55	0.197

23	P	HYP750	Hypertriglyceridemia, Familial	62	0.191

24		VSL002	Visual Epilepsy	59	0.191

25	P	BRS047	Breast Cancer	97	0.190

26		ALL026	Allergic Hypersensitivity Disease	62	0.190

27	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.189

28		ATH013	Atherosclerosis Susceptibility	65	0.187

29		DRM006	Dermatitis	61	0.185

30	c	GLL024	Gallbladder Disease 1	53	0.183

31		OST012	Osteoarthritis	78	0.182

32		ISC004	Ischemia	58	0.180

33		BNR002	Bone Resorption Disease	48	0.179

34	P	HPT023	Hepatocellular Carcinoma	100	0.178

35		HYP056	Hypoglycemia	66	0.177

36	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.174

37		GST092	Gastroesophageal Reflux	67	0.173

38	P	VSC007	Vascular Disease	63	0.172

39		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.170

40	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.170

41		HYP060	Hyperinsulinism	54	0.170

42		LPP008	Lipoprotein Quantitative Trait Locus	62	0.167

43		CYT002	Cytokine Deficiency	42	0.167

44	P	PRS040	Prostate Cancer	97	0.167

45		CLT003	Colitis	62	0.165

46	P	PSR002	Psoriasis	62	0.164

47	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.164

48	P	ENC018	Encephalopathy	61	0.164

49		KRT002	Keratomalacia	47	0.164

50	P	LKM002	Leukemia	68	0.164

51	P	INF037	Inflammatory Bowel Disease	54	0.163

52		PRT037	Pertussis	65	0.163

53		PST011	Pustulosis of Palm and Sole	52	0.163

54	P	GLM045	Glioma	63	0.162

55		GLL048	Glial Tumor	45	0.160

56	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.158

57		PPT005	Peptic Ulcer Disease	59	0.157

58		GLB015	Glioblastoma Multiforme	75	0.156

59	c	MCR120	Microvascular Complications of Diabetes 7	47	0.155

60		ATM095	Autoimmune Disease	62	0.155

61	c	MCR113	Microvascular Complications of Diabetes 3	52	0.155

62	c	MCR130	Microvascular Complications of Diabetes 6	41	0.155

63	c	MCR133	Microvascular Complications of Diabetes 4	41	0.155

64	P	BPL003	Bipolar Disorder	56	0.154

65	c	MJR024	Major Affective Disorder 9	41	0.154

66	c	MJR022	Major Affective Disorder 8	38	0.154

67	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.153

68	c	CHR684	Chronic Kidney Disease	70	0.153

69		ART140	Arteries, Anomalies of	52	0.152

70		DFC004	Deficiency Anemia	70	0.152

71		PSY004	Psychotic Disorder	67	0.152

72		CYS001	Cystic Fibrosis	81	0.151

73	c	PRC016	Pre-Eclampsia	63	0.151

74		INS001	Insulinoma	60	0.150

75		HMN044	Human Immunodeficiency Virus Type 1	71	0.149

76	P	DBT009	Diabetes Mellitus	64	0.148

77	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.148

78	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.148

79	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.148

80	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.148

81	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.148

82	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.148

83	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.148

84	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.148

85	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.148

86	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.148

87		ADN018	Adenoma	59	0.146

88	P	OST002	Osteoporosis	74	0.145

89	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.144

90	P	ADN016	Adenocarcinoma	64	0.144

91	P	MYL006	Myeloid Leukemia	60	0.143

92		HRW001	Hair Whorl	36	0.143

93	P	HRT032	Heart Disease	75	0.142

94		PLM001	Pulmonary Tuberculosis	69	0.141

95	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.140

96	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.140

97		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.138

98		47X002	47,xyy	49	0.137

99	P	PNC035	Pancreatic Cancer	84	0.137

100		IRN002	Iron Metabolism Disease	57	0.137

101	c	HYP595	Hypertension, Essential	84	0.136

102	P	NRP001	Neuropathy	56	0.135

103	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.135

104		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.134

105		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.134

106	P	BND020	Bone Disease	59	0.133

107	P	CRD246	Cardiovascular System Disease	57	0.133

108	P	LNG032	Lung Cancer	98	0.132

109	P	ALZ034	Alzheimer Disease	88	0.132

110	P	DRM053	Dermatitis, Atopic	66	0.131

111		BCT022	Bacterial Infectious Disease	56	0.131

112		DPR016	Depression	63	0.131

113	P	ESP024	Esophagitis	62	0.131

114		OCL069	Ocular Motor Apraxia	51	0.130

115		SKN016	Skin Disease	63	0.130

116		NTR005	Nutritional Deficiency Disease	62	0.130

117	c	LKM061	Leukemia, Acute Myeloid	84	0.130

118	P	ATS364	Autism	70	0.129

119	P	PRD008	Periodontitis	64	0.129

120		HYP266	Hypoxia	57	0.128

121		HPT004	Hepatic Coma	45	0.128

122		GLC003	Glucose Intolerance	54	0.127

123		END086	End Stage Renal Disease	51	0.127

124		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.126

125		MYL069	Myeloma, Multiple	85	0.126

126		CRB039	Cerebrovascular Disease	67	0.126

127	P	TRM003	Tremor	54	0.126

128	P	MYC007	Myocardial Infarction	70	0.126

129		DWN001	Down Syndrome	70	0.126

130		CNG034	Congestive Heart Failure	69	0.126

131	P	BCL017	B-Cell Lymphoma	58	0.125

132	c	HPT073	Hepatitis C Virus	72	0.125

133		STR067	Stroke, Ischemic	81	0.125

134	P	GST053	Gastric Cancer	83	0.125

135		PPL052	Papillomatosis, Confluent and Reticulated	33	0.125

136		SCH012	Schizoaffective Disorder	50	0.125

137		ANX004	Anoxia	40	0.124

138	P	BLD134	Bladder Cancer	79	0.124

139	P	HYP086	Hypothyroidism	69	0.123

140		CHL014	Cholera	59	0.123

141		STM007	Stomatitis	50	0.123

142		GST023	Gastric Ulcer	53	0.122

143		ALC007	Alcohol Dependence	66	0.122

144		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.122

145	P	CHL066	Cholangitis	51	0.122

146	P	ART022	Arthritis	69	0.122

147		ADL002	Adult Syndrome	70	0.121

148	c	ACT071	Acute Kidney Failure	60	0.120

149		OST159	Osteogenic Sarcoma	66	0.120

150		HPT019	Hepatic Encephalopathy	60	0.120

151	P	TRN020	Turner Syndrome	67	0.119

152	c	RHB024	Rhabdomyosarcoma 2	67	0.119

153	P	RHM011	Rheumatoid Arthritis	80	0.118

154		HYP781	Hypoascorbemia	51	0.118

155		HMC014	Homocysteinemia	53	0.118

156	P	MYP004	Myopathy	70	0.118

157		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.118

158	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.117

159		INS024	Insulin-Like Growth Factor I	79	0.117

160		DSS008	Disease of Mental Health	58	0.117

161		CNS004	Constipation	58	0.117

162		BRN071	Brain Injury	49	0.116

163	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.116

164	c	ACT075	Acute Myocardial Infarction	57	0.116

165	P	MCR115	Microvascular Complications of Diabetes 5	66	0.116

166		NPH009	Nephrolithiasis	55	0.116

167	P	LTR001	Lateral Sclerosis	54	0.116

168		MNT002	Mental Depression	58	0.115

169	c	DWL002	Dowling-Degos Disease 1	58	0.115

170	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.114

171	P	HRP006	Herpes Simplex	65	0.114

172	c	DBT099	Diabetes Mellitus, Type I	65	0.114

173		TRM010	Traumatic Brain Injury	51	0.114

174		THR024	Thrombosis	57	0.110

175	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.110

176		ANX010	Anxiety	73	0.110

177		CRV035	Cervical Cancer	76	0.109

178		KRT009	Keratosis	51	0.109

179	c	ACT027	Acute Pancreatitis	60	0.108

180	c	ATS007	Autism Spectrum Disorder	67	0.108

181		BRR014	Barrett Esophagus	65	0.108

182	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.108

183		CLF027	Cleft Palate, Isolated	64	0.108

184		GST033	Gestational Diabetes	61	0.108

185		RCK004	Rickets	68	0.108

186		ADR007	Adrenoleukodystrophy	75	0.107

187		SPN186	Spinal Cord Injury	60	0.107

188		OST003	Osteonecrosis	61	0.107

189		LNG099	Lung Disease	60	0.107

190		VTM002	Vitamin B12 Deficiency	48	0.107

191	P	MNN013	Meningitis	66	0.106

192	c	FTL070	Fetal Akinesia Deformation Sequence 2	36	0.106

193		CHL004	Cholelithiasis	49	0.106

194	P	EPL164	Epilepsy	71	0.106

195		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.105

196		EYD002	Eye Disease	58	0.105

197	P	SKN015	Skin Carcinoma	66	0.105

198	P	PRP019	Peripheral Nervous System Disease	58	0.105

199		SQM006	Squamous Cell Carcinoma	60	0.105

200		ADR022	Adrenomyeloneuropathy	38	0.105

201		CHL079	Children's Interstitial Lung Disease	26	0.105

202		MTH071	Methane Production	26	0.104

203	P	MLN008	Melanoma	69	0.104

204	c	SML038	Small Cell Cancer of the Lung	65	0.104

205	P	OVR082	Overgrowth Syndrome	50	0.103

206		TXC005	Toxic Shock Syndrome	62	0.103

207		PLM033	Pulmonary Embolism	59	0.103

208		HMP009	Haemophilus Influenzae	43	0.103

209	P	DMN002	Dementia	66	0.103

210		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.103

211	P	MJR001	Major Depressive Disorder	68	0.103

212	P	ENC004	Encephalitis	61	0.102

213		CRB004	Cerebral Artery Occlusion	45	0.102

214	c	MGR028	Migraine with or Without Aura 1	67	0.102

215	P	CTR002	Cataract	60	0.101

216		CHL123	Chlamydia	59	0.101

217		IMM167	Immune Deficiency Disease	78	0.101

218		CNT047	Contact Dermatitis	58	0.101

219		ATX019	Ataxia with Vitamin E Deficiency	42	0.101

220	c	ACT068	Acute Cystitis	63	0.100

221	c	SYS001	Systemic Lupus Erythematosus	86	0.100

222	P	HPT021	Hepatitis	67	0.100

223	P	FBR017	Fibrosarcoma	56	0.100

224	P	MSC005	Muscular Dystrophy	66	0.100

225		MDD011	Mood Disorder	62	0.100

226		DBT010	Diabetic Neuropathy	54	0.099

227		SCH003	Schizophreniform Disorder	56	0.099

228	P	PLM036	Pulmonary Fibrosis	65	0.099

229		DNT012	Dental Caries	53	0.099

230	c	HPT001	Hepatitis C	62	0.099

231	P	INF032	Infertility	57	0.099

232	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.099

233		PPL022	Papilloma	54	0.098

234		PLM010	Pulmonary Edema	54	0.098

235	P	MLT020	Multiple Sclerosis	72	0.098

236		TRD006	Tardive Dyskinesia	54	0.098

237		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.098

238	P	PNM007	Pneumonia	68	0.097

239		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.097

240		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.097

241		AGN016	Aging	56	0.097

242	P	ART021	Arteriosclerosis	54	0.097

243	c	INH020	Inherited Metabolic Disorder	47	0.097

244	P	ALC033	Alcohol Use Disorder	58	0.096

245	P	THR014	Thrombocytopenia	67	0.096

246	c	ATR087	Atrial Standstill 1	75	0.096

247	c	SVR001	Severe Acute Respiratory Syndrome	62	0.096

248		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.096

249	P	EXN002	Exanthem	57	0.095

250		ALL014	Allergic Encephalomyelitis	38	0.095

251		ANG054	Angina Pectoris	66	0.095

252		SQM002	Squamous Cell Papilloma	46	0.095

253		HYP005	Hypokalemia	55	0.095

254		LPT014	Leptin Deficiency or Dysfunction	74	0.095

255	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.094

256	P	HYP076	Hyperthyroidism	55	0.094

257		LYS012	Lysosomal Acid Lipase Deficiency	65	0.094

258	P	ATR011	Atrial Fibrillation	66	0.094

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

260	P	LPS004	Lupus Erythematosus	61	0.093

261	P	RSP003	Respiratory Failure	74	0.093

262		URL001	Urolithiasis	45	0.093

263	P	RHN004	Rhinitis	57	0.093

264	P	ECL001	Eclampsia	50	0.093

265	P	DYS154	Dystonia	65	0.093

266		BRN024	Bronchitis	68	0.093

267		MYL009	Myelodysplastic Syndrome	70	0.093

268	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.092

269	P	AST007	Astrocytoma	51	0.092

270		HNS001	Hansen's Disease	34	0.092

271	c	MLG068	Malignant Glioma	46	0.092

272	P	LPR021	Leprosy 3	69	0.092

273	P	CRD119	Cardiac Arrest	67	0.092

274		ACQ007	Acquired Immunodeficiency Syndrome	60	0.092

275	P	PNC044	Pancreatitis	61	0.091

276		ENT011	Enterocolitis	51	0.091

277	P	PHC003	Pheochromocytoma	71	0.090

278		CLN015	Colon Adenocarcinoma	65	0.090

279		ADR040	Adrenal Gland Pheochromocytoma	46	0.090

280	P	LNG064	Lung Cancer Susceptibility 3	78	0.090

281		SRC014	Sarcoma	65	0.090

282		SPN035	Spindle Cell Sarcoma	53	0.090

283	P	LYM118	Lymphoma	68	0.089

284	c	HPT016	Hepatitis B	59	0.089

285		ESP021	Esophageal Cancer	90	0.089

286	P	CYS018	Cystitis	59	0.089

287		MSL001	Measles	62	0.089

288		PNG002	Pain Agnosia	51	0.088

289	P	INF038	Influenza	68	0.088

290	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.088

291		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.088

292	P	ALP008	Alopecia	54	0.087

293	c	VRL010	Viral Hepatitis	52	0.087

294		TTN003	Tetanus	65	0.087

295	P	MYC084	Mycobacterium Tuberculosis 1	68	0.087

296	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.087

297	P	PLY019	Polyneuropathy	56	0.086

298		HYP081	Hypolipoproteinemia	51	0.086

299		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.086

300		BRN004	Brain Edema	56	0.086

301		PRP027	Peripheral Vascular Disease	71	0.085

302		DPH001	Diphtheria	60	0.085

303	P	ACT008	Actinic Keratosis	53	0.085

304		MTH009	Mouth Disease	56	0.085

305		OST115	Osteonecrosis of the Jaw	40	0.085

306	P	BRS044	Breast Adenocarcinoma	59	0.084

307	P	HDC001	Headache	57	0.084

308		MST005	Mastitis	53	0.084

309		AST005	Asthma	76	0.083

310	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.083

311		ALL010	Allergic Contact Dermatitis	56	0.083

312	P	NPH012	Nephrotic Syndrome	60	0.083

313	P	GLM040	Glioma Susceptibility 1	81	0.083

314	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.082

315	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.082

316	P	RTN016	Retinal Degeneration	53	0.082

317	P	MVM001	Movement Disease	63	0.082

318	P	CNR004	Cone-Rod Dystrophy 2	73	0.082

319		49X006	49, Xxxxy Syndrome	41	0.082

320	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.081

321		ZLL002	Zollinger-Ellison Syndrome	55	0.081

322		ALL003	Allergic Rhinitis	67	0.081

323		GST045	Gastroenteritis	59	0.081

324		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.081

325	P	MJR007	Major Affective Disorder 1	43	0.080

326		RYS001	Reye Syndrome	51	0.080

327	P	PLY011	Polycystic Ovary Syndrome	56	0.080

328	P	SBS003	Substance Abuse	55	0.080

329	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.080

330		CRV045	Cervical Intraepithelial Neoplasia	39	0.080

331	P	CND004	Candidiasis	58	0.080

332		NWC001	Newcastle Disease	45	0.080

333		ACY011	Acyl-Coa Dehydrogenase Deficiency	38	0.080

334	P	ART023	Arthropathy	62	0.080

335		PLC008	Placenta Disease	50	0.080

336	P	INT143	Interstitial Cystitis	61	0.079

337		RSC001	Rosacea	54	0.079

338	P	MLN007	Male Infertility	55	0.078

339	c	DRR009	Diarrhea 6	46	0.078

340	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.078

341		IRN001	Iron Deficiency Anemia	59	0.078

342		ORL011	Oral Cancer	60	0.078

343		PRN019	Perinatal Necrotizing Enterocolitis	59	0.077

344	P	NSP012	Nasopharyngeal Carcinoma	66	0.077

345		SBC016	Subacute Delirium	44	0.077

346	P	INT068	Intestinal Disease	53	0.077

347		LSH001	Leishmaniasis	63	0.077

348	P	CHR345	Chronic Pain	44	0.077

349	P	KLZ004	Kala-Azar 1	41	0.077

350	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.077

351	P	GRF003	Graft-Versus-Host Disease	72	0.076

352		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.076

353		SCH014	Schistosomiasis	57	0.076

354		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.076

355	P	HYP069	Hyperparathyroidism	63	0.076

356	P	THL005	Thalassemia	60	0.076

357	P	HYD006	Hydrocephalus	66	0.076

358		CYS013	Cystinuria	63	0.076

359		RTN023	Retinitis	46	0.076

360		NRR001	Neuroretinitis	42	0.076

361		LNG031	Lung Benign Neoplasm	51	0.075

362		DRY001	Dry Eye Syndrome	47	0.075

363	P	PLM037	Pulmonary Hypertension	67	0.075

364		OTT002	Otitis Media	72	0.075

365		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.075

366		LYM019	Lymphosarcoma	46	0.075

367		BRN028	Brain Cancer	74	0.074

368	P	SHR001	Short Bowel Syndrome	53	0.074

369	c	BSL007	Basal Cell Carcinoma	68	0.074

370		PRP030	Purpura	54	0.074

371		PRT013	Portal Hypertension	59	0.074

372	P	RTN008	Retinitis Pigmentosa	79	0.073

373		CLR108	Colorectal Adenoma	64	0.073

374	P	HYP265	Hypotonia	43	0.073

375		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.073

376		PLS009	Plasma Cell Neoplasm	51	0.073

377		CVD001	Covid-19	44	0.073

378		KRT013	Keratolytic Winter Erythema	46	0.073

379	c	MJR003	Major Affective Disorder 6	33	0.073

380	c	MJR006	Major Affective Disorder 5	33	0.073

381	P	PRK057	Parkinson Disease, Late-Onset	78	0.073

382	P	MNC007	Monocytic Leukemia	53	0.073

383		HMS001	Hemosiderosis	54	0.073

384	c	FML035	Familial Hyperlipidemia	55	0.073

385		MLR004	Malaria	81	0.073

386	c	HPT003	Hepatitis a	62	0.072

387	P	URT039	Urticaria	58	0.072

388	c	MJR008	Major Affective Disorder 2	35	0.072

389	c	MJR023	Major Affective Disorder 7	33	0.072

390	c	MJR004	Major Affective Disorder 4	28	0.072

391		BLR001	Biliary Atresia	50	0.072

392		CMM005	Common Cold	57	0.072

393		BCT002	Bacterial Vaginosis	53	0.072

394	P	END044	Endometriosis	63	0.071

395		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.071

396	P	RRH023	Rare Hereditary Hemochromatosis	41	0.071

397		MSC007	Muscle Hypertrophy	64	0.071

398		CHR074	Choriocarcinoma	47	0.071

399		IGR001	Ige Responsiveness, Atopic	59	0.070

400	P	RCT021	Rectum Cancer	52	0.070

401	P	BNG032	Benign Mesothelioma	46	0.070

402		GLS018	Glass Syndrome	57	0.070

403	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.070

404	P	MDL005	Medulloblastoma	77	0.070

405		MSC157	Muscular Dystrophy, Duchenne Type	72	0.070

406		TRN015	Transient Cerebral Ischemia	63	0.070

407		KRT019	Keratitis, Hereditary	65	0.069

408		BRN056	Bronchopulmonary Dysplasia	57	0.069

409	P	SCK005	Sickle Cell Disease	50	0.069

410	P	OPN001	Open-Angle Glaucoma	49	0.069

411		FDL002	Food Allergy	51	0.069

412	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.069

413		KRT001	Keratoconjunctivitis Sicca	49	0.069

414		KHL003	Kohlschutter-Tonz Syndrome	65	0.069

415		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.068

416		GTR002	Goiter	53	0.068

417	P	CNJ013	Conjunctivitis	65	0.068

418		TYP007	Typhoid Fever	63	0.068

419	c	DLT002	Dilated Cardiomyopathy	79	0.067

420		DYS073	Dysphagia	50	0.067

421	P	ADL010	Adult Respiratory Distress Syndrome	65	0.067

422		GNG013	Gingivitis	59	0.067

423		ANR040	Aneurysm	59	0.067

424		CLF001	Cleft Lip	53	0.067

425		SCK003	Sickle Cell Anemia	74	0.066

426		PLM031	Poliomyelitis	64	0.066

427		END040	Endogenous Depression	55	0.066

428	c	PRD040	Periodontitis, Chronic	53	0.066

429	c	PRM038	Primary Agammaglobulinemia	44	0.066

430	c	PNS012	Paine Syndrome	61	0.066

431		PRT038	Protein-Energy Malnutrition	54	0.066

432		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.066

433		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.065

434		PST092	Posttransplant Acute Limbic Encephalitis	29	0.065

435		NWB001	Newborn Respiratory Distress Syndrome	58	0.065

436	P	PRS038	Personality Disorder	65	0.065

437		PHR003	Pharyngitis	57	0.065

438		CHL067	Cholecystitis	57	0.065

439		HDN002	Head Injury	46	0.065

440		VRC005	Varicose Veins	60	0.065

441		DYS015	Dysentery	52	0.065

442		EXN003	Exencephaly	31	0.065

443	P	END033	Endocarditis	57	0.064

444		ILS001	Ileus	51	0.064

445		KRT006	Keratoconjunctivitis	53	0.064

446	P	HYP061	Hypertrophic Cardiomyopathy	70	0.064

447	P	SLP006	Sleep Apnea	69	0.064

448	c	MCR129	Microvascular Complications of Diabetes 1	66	0.064

449		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.064

450		SKN019	Skin Melanoma	68	0.064

451		CRN030	Coronary Stenosis	50	0.064

452		PLG002	Plague	63	0.063

453	c	FML001	Familial Atrial Fibrillation	65	0.063

454		CRC021	Carcinosarcoma	62	0.063

455		MDM001	Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency	33	0.063

456	P	FML011	Familial Adenomatous Polyposis	72	0.063

457	c	BRN108	Branchiootic Syndrome 1	62	0.063

458	P	UVT001	Uveitis	57	0.063

459		LYM133	Lymphoma, Hodgkin, Classic	69	0.063

460		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.063

461		ANR007	Anorexia Nervosa	63	0.063

462		NRT001	Neurotic Disorder	53	0.063

463	c	SPN225	Spondyloarthropathy 1	73	0.062

464		KWS001	Kwashiorkor	44	0.062

465		LKP003	Leukoplakia	39	0.062

466	P	RTN018	Retinal Disease	53	0.062

467		SPL018	Splenomegaly	48	0.062

468	P	THY023	Thymoma	65	0.062

469	c	THY107	Thymoma, Familial	52	0.062

470	P	CLC063	Celiac Disease 1	66	0.062

471	P	VSC011	Vasculitis	62	0.062

472		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.062

473		MXD026	Mixed Glioma	45	0.062

474		SFT003	Soft Tissue Sarcoma	56	0.061

475		PRP080	Peripheral Artery Disease	53	0.061

476	c	HNT004	Huntington Disease-Like 2	50	0.061

477		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.061

478		PTT037	Pituitary Tumors	44	0.061

479	c	GLC092	Glaucoma, Primary Open Angle	62	0.061

480		CRD223	Cardiac Arrhythmia	60	0.061

481		RTN017	Retinal Detachment	61	0.061

482		NSP002	Nasopharyngitis	43	0.061

483		BRK010	Burkitt Lymphoma	67	0.061

484		CRH005	Crohn's Colitis	53	0.061

485	P	SLP005	Sleep Disorder	59	0.061

486		CRT015	Carotid Artery Occlusion	45	0.061

487		HYP020	Hyperprolactinemia	64	0.061

488		OST017	Osteomyelitis	64	0.060

489	P	MYC008	Myocarditis	59	0.060

490	P	HYP058	Hypervitaminosis a	48	0.060

491		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.060

492	P	ALP009	Alopecia Areata	60	0.060

493		HYP025	Hyperphosphatemia	48	0.060

494		PST021	Postpartum Depression	50	0.059

495		PNM008	Pneumothorax	56	0.059

496	P	NRV007	Nervous System Disease	66	0.059

497		SPS057	Spasticity	45	0.059

498		HND015	Hand Skill, Relative	33	0.059

499		SXL003	Sexual Disorder	47	0.059

500		GLS001	Gliosarcoma	54	0.059

501		HPT022	Hepatoblastoma	56	0.058

502	P	OCL013	Oculodentodigital Dysplasia	69	0.058

503		AMN001	Amenorrhea	54	0.058

504	P	ANG015	Angioedema	57	0.058

505		DMY004	Demyelinating Disease	52	0.058

506		SPN051	Spondylitis	51	0.058

507		INF009	Inflammatory Spondylopathy	31	0.058

508		TRP004	Tropical Sprue	41	0.058

509		VRL011	Viral Infectious Disease	61	0.058

510		HYD002	Hydronephrosis	60	0.057

511		MCR013	Microphthalmia	57	0.057

512		ACT084	Acute Stress Disorder	47	0.057

513		CRB037	Cerebral Palsy	69	0.057

514		PPL001	Papillary Adenoma	44	0.057

515	P	NGH001	Night Blindness	48	0.057

516		PST028	Post-Traumatic Stress Disorder	58	0.056

517		RBS001	Rabies	58	0.056

518	c	SVR005	Severe Pre-Eclampsia	50	0.056

519		ATN005	Autonomic Dysfunction	46	0.056

520		RDN001	Reading Disorder	40	0.056

521	P	GRV001	Graves' Disease	55	0.056

522		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.056

523		FBR047	Fibromyalgia	58	0.056

524		ACY009	Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of	58	0.056

525		VSC003	Visceral Leishmaniasis	55	0.056

526		LMY002	Leiomyoma	52	0.056

527		ART016	Aortic Aneurysm	69	0.055

528	P	OLG002	Oligodendroglioma	67	0.055

529	P	PTT006	Pituitary Adenoma	55	0.055

530		SLC006	Silicosis	56	0.055

531		ATN004	Autonomic Neuropathy	45	0.055

532		TNS005	Tonsillitis	57	0.055

533		MCL006	Macular Retinal Edema	55	0.054

534		YLL002	Yellow Fever	61	0.054

535		HMT002	Hematologic Cancer	62	0.054

536	P	VSC018	Visceral Steatosis	33	0.054

537		XRP001	Xerophthalmia	41	0.054

538	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.054

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

540		INT002	Intermittent Claudication	61	0.053

541	c	PSR017	Psoriasis 2	53	0.053

542	c	PSR023	Psoriasis 1	52	0.053

543	c	SCN007	Secondary Hyperparathyroidism	51	0.053

544		LNT004	Lentigines	50	0.053

545	c	PSR032	Psoriasis 11	47	0.053

546	c	PSR028	Psoriasis 7	42	0.053

547	c	PSR018	Psoriasis 13	41	0.053

548	P	MLG074	Malignant Mesenchymoma	40	0.053

549		OBS002	Obsessive-Compulsive Disorder	68	0.053

550		WST001	West Syndrome	61	0.053

551		PLC005	Placental Insufficiency	57	0.053

552		TRP009	Triple X Syndrome	42	0.053

553		FCT007	Factor Vii Deficiency	67	0.053

554		VGN023	Vaginitis	54	0.053

555		INT075	Intracranial Hypertension	53	0.053

556		PLR008	Pleurisy	50	0.053

557		CRN296	Carnitine Palmitoyltransferase Ii Deficiency, Infantile	65	0.052

558	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.052

559	P	TRT010	Teratoma	52	0.052

560	c	INF145	Infantile Liver Failure Syndrome 1	50	0.052

561		INF034	Infective Endocarditis	53	0.052

562	c	EXD008	Exudative Vitreoretinopathy 1	71	0.052

563	P	TBR001	Tuberous Sclerosis	70	0.052

564		STN013	Stenotrophomonas Maltophilia Infection	25	0.052

565		CYT018	Cytochrome P450 2d6 Variant	27	0.052

566		MNT001	Mantle Cell Lymphoma	69	0.052

567	P	MTC069	Mitochondrial Disorders	56	0.052

568	P	PNC025	Panic Disorder	53	0.052

569	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.052

570		CHR178	Chromosomal Triplication	35	0.052

571		NPH098	Nephrolithiasis, X-Linked Recessive, with Renal Failure	41	0.052

572	c	HMC039	Hemochromatosis, Type 1	74	0.051

573	P	TXP001	Toxoplasmosis	60	0.051

574		LNG073	Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency	60	0.051

575	c	MCR112	Microvascular Complications of Diabetes 2	41	0.051

576	P	FLL037	Follicular Lymphoma	67	0.051

577		CHR066	Chronic Fatigue Syndrome	61	0.051

578	P	LRY044	Larynx Cancer	55	0.051

579		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.051

580		ACR007	Acromegaly	71	0.050

581		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.050

582	P	OPT006	Optic Nerve Disease	60	0.050

583		NRN004	Neuroendocrine Tumor	55	0.050

584		BCK006	Back Pain	42	0.050

585		SPT004	Septic Arthritis	58	0.050

586		PRD004	Prediabetes Syndrome	47	0.050

587		EXC002	Exocrine Pancreatic Insufficiency	42	0.050

588		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.050

589	c	MST023	Mesothelioma, Malignant	57	0.050

590		DFF005	Diffuse Large B-Cell Lymphoma	55	0.050

591		LYM040	Lymphoblastic Lymphoma	54	0.050

592	P	BLR006	Biliary Tract Disease	47	0.050

593		DBT002	Diabetic Autonomic Neuropathy	41	0.050

594		CMR002	Coumarin Resistance	56	0.050

595		EWN003	Ewing Sarcoma	69	0.049

596	P	RBL001	Rubella	59	0.049

597		PLS007	Plasmodium Falciparum Malaria	52	0.049

598		MLT157	Multiple System Atrophy 1	70	0.049

599		CHY002	Chylomicron Retention Disease	65	0.049

600	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.049

601		BRN002	Bronchiolitis	59	0.049

602		ESP002	Esophageal Varix	51	0.049

603		ASP007	Aspiration Pneumonia	48	0.049

604		FSC004	Fasciitis	50	0.049

605	P	INT070	Intestinal Obstruction	58	0.049

606	P	HYP726	Hypercalcemia, Infantile, 1	58	0.049

607	P	BNG030	Benign Ependymoma	60	0.048

608	P	SYP003	Syphilis	58	0.048

609		MCR004	Macroglobulinemia	49	0.048

610	P	PRC031	Preeclampsia/eclampsia 1	38	0.048

611		NRM005	Neuromuscular Disease	64	0.048

612		APP008	Appendicitis	61	0.048

613		TND005	Tendinitis	54	0.048

614		RTN020	Retinal Vascular Disease	46	0.048

615		GNG003	Gingival Recession	44	0.048

616		HYP457	Hypertrophic Scars	42	0.048

617		GST020	Gastric Antral Vascular Ectasia	41	0.048

618	P	SJG008	Sjogren Syndrome	61	0.047

619		CLL010	Cellular Ependymoma	54	0.047

620	P	PTS002	Ptosis	53	0.047

621	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.047

622		PLR007	Pleural Empyema	50	0.047

623		VTM033	Vitamin K Deficiency Bleeding	48	0.047

624		LPT006	Leptin Receptor Deficiency	48	0.047

625		GST030	Gastrinoma	45	0.047

626		ASP008	Aspiration Pneumonitis	45	0.047

627	c	BPL002	Bipolar I Disorder	49	0.047

628		PPL049	Papillon-Lefevre Syndrome	65	0.047

629		HYP080	Hypogonadism	50	0.047

630	c	LKM070	Leukemia, Acute Monocytic	57	0.046

631		FLL008	Folliculitis	46	0.046

632		MYM001	Myoma	54	0.046

633		CLL003	Cellulitis	54	0.046

634	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.046

635		BRS051	Breast Disease	58	0.046

636		ACD008	Acid-Labile Subunit Deficiency	54	0.046

637		PRS063	Paresthesia	41	0.046

638		PRN009	Paranoid Schizophrenia	50	0.045

639		CRP001	Carpal Tunnel Syndrome	67	0.045

640		HLL004	Hellp Syndrome	54	0.045

641		CHL013	Cholecystolithiasis	37	0.045

642		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.045

643		PRT058	Pure Autonomic Failure	59	0.045

644		SYN036	Syncope	45	0.045

645	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.045

646		CRC006	Carcinoid Syndrome	55	0.045

647		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.045

648	c	FLL041	Follicular Lymphoma 1	49	0.045

649		CLN045	Colonic Benign Neoplasm	46	0.045

650		CHL045	Choline Deficiency Disease	39	0.045

651		ANG049	Angioedema Induced by Ace Inhibitors	40	0.045

652	c	TBR025	Tuberous Sclerosis 1	77	0.044

653		WLS001	Wilson Disease	71	0.044

654	c	ALP101	Alpha-Thalassemia	62	0.044

655		MTC027	Mitochondrial Trifunctional Protein Deficiency	58	0.044

656	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.044

657	P	HMR005	Hemorrhoid	46	0.044

658	c	SYS043	Systemic Lupus Erythematosus 1	38	0.044

659		APN008	Apnea, Obstructive Sleep	64	0.044

660		GST071	Gastrointestinal Carcinoma	47	0.044

661		LPD009	Lipid Storage Disease	46	0.044

662		PLL012	Pollen Allergy	46	0.044

663		ATM052	Autoimmune Disease 1	37	0.044

664		TXC020	Toxic Oil Syndrome	33	0.044

665		AYM001	Ayme-Gripp Syndrome	57	0.044

666		ACT200	Acute Monoblastic Leukemia	52	0.044

667	P	PHT010	Photoparoxysmal Response 1	42	0.044

668	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.044

669		INT303	Intracranial Hypertension, Idiopathic	57	0.044

670		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.044

671		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.044

672	P	STR092	Striatal Degeneration, Autosomal Dominant 2	42	0.044

673		SHG001	Shigellosis	60	0.043

674		ORL005	Oral Candidiasis	56	0.043

675		OST011	Osteomalacia	52	0.043

676		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.043

677		CNT033	Central Nervous System Cancer	47	0.043

678	P	HYP733	Hypercalciuria, Absorptive, 2	45	0.043

679		CRB090	Cerebral Hypoxia	44	0.043

680		TND004	Tendinopathy	43	0.043

681	P	CRB088	Cerebral Atrophy	37	0.043

682		VGN020	Vaginal Disease	49	0.043

683		LNG015	Lingual-Facial-Buccal Dyskinesia	50	0.043

684		SYS003	Systolic Heart Failure	49	0.043

685		LMY014	Leiomyoma, Uterine	56	0.043

686		CLF004	Cleft Lip/palate	54	0.043

687		PRP036	Peripheral T-Cell Lymphoma	53	0.043

688	c	PRM092	Primary Lateral Sclerosis, Adult, 1	53	0.043

689		GNT002	Giant Cell Glioblastoma	50	0.043

690		VLV011	Vulvovaginal Candidiasis	49	0.043

691		CYN002	Cyanosis, Transient Neonatal	45	0.043

692		MYF001	Myofibroma	45	0.043

693		LWC001	Low Compliance Bladder	43	0.043

694		VSL013	Visual Impairment and Progressive Phthisis Bulbi	41	0.043

695		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.043

696		HMR039	Hemorrhage, Intracerebral	57	0.042

697		ALL009	Allergic Conjunctivitis	50	0.042

698	P	END046	Endometritis	49	0.042

699		IRR003	Irritant Dermatitis	49	0.042

700	c	XNT010	Xanthinuria, Type I	53	0.042

701		RTC005	Reticulosarcoma	47	0.042

702	c	ACT004	Acute Diarrhea	39	0.042

703		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	43	0.041

704		TRC003	Trichomoniasis	53	0.041

705		THR016	Thrombophlebitis	51	0.041

706		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.041

707		VGN019	Vaginal Discharge	46	0.041

708		NNT033	Neonatal Hypoxic and Ischemic Brain Injury	43	0.041

709		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.041

710		SPR126	Superior Semicircular Canal Dehiscence	40	0.041

711	c	HMG029	Hemoglobin Se Disease	39	0.041

712	c	NGH026	Night Blindness, Congenital Stationary, Type 1a	52	0.041

713		APH001	Aphthous Stomatitis	57	0.041

714	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.041

715		BRD004	Borderline Personality Disorder	53	0.041

716	P	HYP040	Hypospadias	51	0.041

717		ART004	Aortic Atherosclerosis	47	0.041

718	P	AVS003	Avascular Necrosis	42	0.041

719		CHL039	Choledocholithiasis	38	0.041

720	c	PNC108	Pancreatitis, Hereditary	70	0.040

721		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.040

722	c	BSL024	Basal Cell Carcinoma 1	56	0.040

723		GST049	Gastrointestinal System Cancer	49	0.040

724	c	BCT013	Bacterial Pneumonia	48	0.040

725		PLS025	Plasmablastic Lymphoma	47	0.040

726		GLC036	Glucagonoma	45	0.040

727		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.040

728		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	65	0.040

729	P	END047	Endophthalmitis	53	0.040

730		SMT001	Somatization Disorder	46	0.040

731		ENT001	Enterocele	39	0.040

732		RSP007	Respiratory Distress Syndrome, Infant	30	0.040

733		CNN003	Conn's Syndrome	79	0.040

734		FBR012	Fabry Disease	72	0.040

735		ACR041	Acromelic Frontonasal Dysostosis	52	0.040

736		DBT006	Diabetic Macular Edema	48	0.040

737		SKN005	Skin Atrophy	43	0.040

738		HML018	Homologous Wasting Disease	22	0.040

739	c	OPT053	Optic Atrophy 1	63	0.039

740	c	CNG216	Congenital Hydrocephalus	47	0.039

741		MNC019	Monocarboxylate Transporter 1 Deficiency	47	0.039

742		TBC004	Tobacco Addiction	64	0.039

743		WLD007	Waldenstroem's Macroglobulinemia	61	0.039

744	P	LCT002	Lactose Intolerance	53	0.039

745		MCN017	Meconium Ileus	52	0.039

746		CRN027	Corneal Neovascularization	47	0.039

747		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.039

748		MYF002	Myofascial Pain Syndrome	42	0.039

749		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.038

750	c	LTN004	Late-Onset Retinal Degeneration	59	0.038

751		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.038

752	P	KRT007	Keratoconus	50	0.038

753		INT017	Intestinal Schistosomiasis	48	0.038

754	P	BLD051	Blood Coagulation Disease	46	0.038

755		GRM010	Germ Cells Tumors	34	0.038

756		GNT167	Genetic Obesity	33	0.038

757		BWN001	Bowen-Conradi Syndrome	52	0.038

758		CRC014	Carcinoid Tumors, Intestinal	47	0.038

759		CRB086	Cerebral Aneurysms	40	0.038

760		ABT001	Abetalipoproteinemia	69	0.037

761		CRN036	Craniopharyngioma	65	0.037

762		FRZ001	Frozen Shoulder	53	0.037

763		NTR018	Neutrophilia, Hereditary	52	0.037

764	P	BRN035	Brain Stem Glioma	52	0.037

765		HND002	Hand, Foot and Mouth Disease	51	0.037

766	c	HRD202	Hereditary Lymphedema I	50	0.037

767		CLS016	Clostridium Difficile Colitis	48	0.037

768	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.037

769		GLB021	Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies	38	0.037

770		PTT009	Pituitary Gland Disease	54	0.037

771		CRT016	Carotid Artery Disease	52	0.037

772	P	LBR014	Leber Congenital Amaurosis 4	56	0.037

773	P	ORL007	Oral Cavity Cancer	53	0.037

774		PRV004	Periventricular Leukomalacia	52	0.037

775		LYM012	Lymphoplasmacytic Lymphoma	47	0.037

776	c	DRM054	Dermatitis, Atopic, 2	44	0.037

777		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	35	0.037

778		CLS047	Classic Progressive Supranuclear Palsy Syndrome	31	0.037

779	P	TTR001	Tetralogy of Fallot	70	0.036

780	c	PLY162	Polyposis Syndrome, Hereditary Mixed, 1	63	0.036

781		PNM010	Pneumothorax, Primary Spontaneous	60	0.036

782	P	PTN014	Patent Ductus Arteriosus 1	60	0.036

783		IFP001	Ifap Syndrome with or Without Bresheck Syndrome	51	0.036

784		CHR005	Chorioamnionitis	51	0.036

785		DRG024	Drug Allergy	42	0.036

786		STT009	Sutton Disease 2	30	0.036

787		OBS003	Obsessive-Compulsive Personality Disorder	46	0.036

788	P	MTR004	Maturity-Onset Diabetes of the Young	65	0.035

789	P	PLV020	Pelvic Organ Prolapse	57	0.035

790		FND002	Fundus Dystrophy	55	0.035

791		BRN045	Brunner Syndrome	55	0.035

792		APR001	Apraxia	52	0.035

793		BHR001	Behr Syndrome	51	0.035

794		ADR016	Adrenal Cortical Carcinoma	48	0.035

795		NCR007	Necrotizing Fasciitis	48	0.035

796		BRS064	Bursitis	48	0.035

797		MNN020	Meningococcal Infection	46	0.035

798		LYM051	Lymphomatoid Granulomatosis	45	0.035

799	P	CRN024	Corneal Disease	44	0.035

800		MGK001	Megakaryocytic Leukemia	64	0.035

801	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.035

802		APH002	Aphasia	57	0.035

803		ISL001	Islet Cell Tumor	56	0.035

804		HYP063	Hypersplenism	53	0.035

805		SPS003	Spastic Diplegia	51	0.035

806		HDR003	Hidradenitis	49	0.035

807		NRN001	Neuroendocrine Carcinoma	47	0.035

808		MNN028	Mononeuropathy of the Median Nerve, Mild	46	0.035

809		CRN322	Coronavirus Infectious Disease	40	0.035

810		MCL003	Macular Holes	40	0.035

811	c	PRG020	Paragangliomas 3	39	0.035

812		ADR004	Adrenal Cortical Adenocarcinoma	39	0.035

813		PTT048	Pituitary Adenoma, Prolactin-Secreting	65	0.034

814		IDP011	Idiopathic Interstitial Pneumonia	59	0.034

815		ERY004	Erysipelas	49	0.034

816		CLC006	Calcinosis	48	0.034

817		BCK003	Background Diabetic Retinopathy	46	0.034

818		ANL022	Anal Fistula	46	0.034

819	c	FML346	Familial Adenomatous Polyposis 1	66	0.033

820	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	60	0.033

821	P	STR022	Stargardt Disease	58	0.033

822		HDR002	Hidradenitis Suppurativa	55	0.033

823		ECH003	Echinococcosis	53	0.033

824		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	0.033

825		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.033

826		NSS002	Neisseria Meningitidis Infection	47	0.033

827		PRP017	Periapical Periodontitis	46	0.033

828		ATN011	Autoinflammation with Infantile Enterocolitis	44	0.033

829		CLN044	Colon Adenoma	44	0.033

830		VLV010	Vulvovaginitis	41	0.033

831		HYP344	Hyperthyroidism, Familial Gestational	39	0.033

832		CVT001	Cavitary Optic Disc Anomalies	38	0.033

833		JVN026	Jeavons Syndrome	24	0.033

834		MYP159	Myopathy, Proximal, with Ophthalmoplegia	55	0.033

835		MSM014	Mismatch Repair Cancer Syndrome	65	0.033

836		ADN009	Adenosquamous Carcinoma	47	0.033

837		PRL017	Prolymphocytic Leukemia	47	0.033

838	P	OCY003	Oocyte Maturation Defect 1	45	0.033

839		CLL014	Cll/sll	45	0.033

840		SPR008	Supratentorial Primitive Neuroectodermal Tumor	43	0.033

841	P	CLS010	Cluster Headache	42	0.033

842		ACT011	Acute Contagious Conjunctivitis	40	0.033

843	P	DYS021	Dysautonomia	39	0.033

844		ANT066	Anterior Cutaneous Nerve Entrapment Syndrome	34	0.033

845		HRP008	Herpes Simiae	25	0.033

846		PNM001	Pneumocystosis	59	0.032

847		LNN001	Lennox-Gastaut Syndrome	57	0.032

848		FRY006	Fryns Microphthalmia Syndrome	52	0.032

849	P	HYP730	Hypogonadotropic Hypogonadism	52	0.032

850	P	AGG001	Aggressive Periodontitis	50	0.032

851	c	DYS119	Dystonia 9	50	0.032

852		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.032

853		ACT055	Actinomycosis	47	0.032

854		SRT004	Serotonin Syndrome	47	0.032

855		CYS009	Cystadenoma	44	0.032

856	P	EPN001	Ependymoblastoma	44	0.032

857	P	ECT045	Ectodermal Dysplasia-Syndactyly Syndrome 1	39	0.032

858		ACL001	Acalculous Cholecystitis	35	0.032

859		CRN302	Carnitine Palmitoyltransferase Ii Deficiency, Lethal Neonatal	34	0.032

860		PSD063	Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak	56	0.031

861	P	HMP002	Hemophagocytic Lymphohistiocytosis	54	0.031

862	c	HYP740	Hyperlipoproteinemia, Type V	53	0.031

863		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.031

864	P	PNB001	Pineoblastoma	50	0.031

865		DFN270	Deafness, Dystonia, and Cerebral Hypomyelination	48	0.031

866		PLY068	Polysubstance Abuse	43	0.031

867		ULC007	Ulcerative Stomatitis	39	0.031

868		CRB026	Cerebellar Astrocytoma	37	0.031

869		BNN005	Bunion	33	0.031

870		THY020	Thyroid Hyalinizing Trabecular Adenoma	21	0.031

871		DMN031	Dementia, Lewy Body	65	0.030

872	P	ORT004	Orthostatic Intolerance	62	0.030

873		ADR005	Adrenal Carcinoma	58	0.030

874		CRT033	Corticobasal Degeneration	57	0.030

875		ORP003	Oropharynx Cancer	55	0.030

876	P	ACT105	Acute Mountain Sickness	52	0.030

877		FML037	Female Breast Cancer	52	0.030

878	c	PYR010	Peyronie's Disease	50	0.030

879	c	HYP739	Hyperlipoproteinemia, Type Iv	50	0.030

880		CHL018	Childhood Medulloblastoma	49	0.030

881	P	SCL015	Scleritis	48	0.030

882	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	46	0.030

883	P	PRD037	Periodontal Ehlers-Danlos Syndrome	45	0.030

884		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	45	0.030

885		PNC085	Penicillin Allergy	45	0.030

886		MMM006	Mammographic Density	41	0.030

887	c	MCR312	Microphthalmia, Syndromic 10	35	0.030

888		CHL057	Childhood Brain Stem Glioma	32	0.030

889		PDT014	Pediatric Ependymoma	32	0.030

890		PLN007	Plantar Fasciitis	32	0.030

891		BRN049	Brain Tumor, Childhood	29	0.030

892		CGN007	Cognitive Function 1, Social	27	0.030

893		LRY027	Laryngeal Papillomatosis	23	0.030

894		CHL009	Childhood Cerebral Astrocytoma	14	0.030

895	c	SCH082	Schizophrenia 5	31	0.030

896		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	65	0.029

897	P	TST021	Testicular Germ Cell Tumor	60	0.029

898	c	HYP260	Hypophosphatemic Rickets, Autosomal Dominant	60	0.029

899	P	SPN052	Spondyloarthropathy	54	0.029

900		PTH002	Pathological Gambling	49	0.029

901	P	GND004	Gonadal Dysgenesis	48	0.029

902		PRS115	Prosthetic Joint Infection	42	0.029

903		CNT060	Central Serous Chorioretinopathy	38	0.029

904		LBR036	Leber Plus Disease	66	0.028

905	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	66	0.028

906		PND002	Pendred Syndrome	65	0.028

907	P	SCK002	Sick Sinus Syndrome	55	0.028

908		RCT017	Rectal Disease	46	0.028

909		OBS004	Obstructive Hydrocephalus	46	0.028

910		PNC056	Pineocytoma	45	0.028

911	P	BCT020	Bacteremia 2	44	0.028

912	c	HYP841	Hypoalphalipoproteinemia, Primary, 1	41	0.028

913		PDT015	Pediatric Supratentorial Ependymoma	24	0.028

914		INT053	Intracranial Vasospasm	24	0.028

915		PDT016	Pediatric Infratentorial Ependymoma	22	0.028

916	P	MLN066	Melanoma, Cutaneous Malignant 1	70	0.027

917		DRR016	Diarrhea 2, with Microvillus Atrophy	60	0.027

918	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.027

919		ERY029	Erythermalgia, Primary	58	0.027

920		VTM028	Vitamin E, Familial Isolated Deficiency of	52	0.027

921		CHR078	Chorioretinitis	50	0.027

922	P	CRN028	Corneal Ulcer	47	0.027

923		CNT017	Central Nervous System Origin Vertigo	45	0.027

924		DNT014	Dental Pulp Disease	42	0.027

925	c	HYP057	Hypervitaminosis D	42	0.027

926		DNT006	Dental Pulp Necrosis	41	0.027

927		CLD014	Cole Disease	40	0.027

928	c	PLM022	Pulmonary Valve Insufficiency	39	0.027

929		RTN002	Retinal Perforation	38	0.027

930		BLN010	Balanitis	37	0.027

931		TQP001	Taqi Polymorphism	32	0.027

932		DLT018	Dilution, Pigmentary	28	0.027

933		HYP213	Hypomelanotic Disorder	23	0.027

934		SDD004	Sudden Arrhythmia Death Syndrome	22	0.027

935	P	USH001	Usher Syndrome	60	0.026

936		BRD001	Brody Myopathy	57	0.026

937	P	AGN002	Agnosia	55	0.026

938	c	PRG043	Progressive Familial Heart Block, Type Ib	54	0.026

939	P	NRD007	Neurodegeneration with Brain Iron Accumulation	52	0.026

940		CHR515	Chronic Atrial and Intestinal Dysrhythmia	50	0.026

941		GYN001	Gynecomastia	49	0.026

942	P	RCR004	Recurrent Respiratory Papillomatosis	49	0.026

943		GNG008	Ganglioneuroblastoma	48	0.026

944	P	ATT003	Attenuated Familial Adenomatous Polyposis	48	0.026

945		MTS001	Mutism	46	0.026

946	P	HRN001	Horner's Syndrome	45	0.026

947	P	END039	Endodermal Sinus Tumor	44	0.026

948		PNL014	Pineal Gland Cancer	41	0.026

949		GRM004	Germinoma	40	0.026

950		CNN010	Connective Tissue Benign Neoplasm	40	0.026

951		TST018	Testicular Yolk Sac Tumor	39	0.026

952	c	SCH080	Schizophrenia 3	32	0.026

953		CHL006	Childhood Oligodendroglioma	31	0.026

954		INF021	Infant Gynecomastia	31	0.026

955	P	CNT036	Central Nervous System Germ Cell Tumor	28	0.026

956		HMR014	Hemorrhagic Shock and Encephalopathy Syndrome	17	0.026

957		LCT022	Lecithin:cholesterol Acyltransferase Deficiency	58	0.025

958		NRL004	Neuroleptic Malignant Syndrome	56	0.025

959	c	MYP132	Myopathy, Congenital	55	0.025

960		SMT003	Somatostatinoma	52	0.025

961		SMT006	Somatoform Disorder	50	0.025

962	P	CRC039	Coarctation of Aorta	47	0.025

963		PST048	Postural Orthostatic Tachycardia Syndrome	45	0.025

964		CHL012	Childhood Disintegrative Disease	44	0.025

965		SPN119	Spondylarthropathy	44	0.025

966	P	INT260	Intracranial Berry Aneurysm	39	0.025

967		STR046	Stargardt Macular Degeneration	31	0.025

968		CRB054	Cerebellar Astrocytoma, Childhood	9	0.025

969	c	NRD017	Neurodegeneration with Brain Iron Accumulation 1	61	0.023

970		CHR288	Chronic Recurrent Multifocal Osteomyelitis	60	0.023

971		VLV032	Vulva Cancer	59	0.023

972		VPM001	Vipoma	50	0.023

973	c	FCL025	Focal Segmental Glomerulosclerosis 1	46	0.023

974		ANS012	Anus Disease	45	0.023

975		LRY022	Laryngoonychocutaneous Syndrome	44	0.023

976		TND006	Tendinosis	42	0.023

977		MDS018	Mediastinal Cancer	41	0.023

978		RGD002	Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal	40	0.023

979		PNC008	Pancreatic Endocrine Carcinoma	39	0.023

980		PNC016	Pancreatic Cholera	37	0.023

981		PRR004	Preretinal Fibrosis	37	0.023

982		SPP003	Suppurative Periapical Periodontitis	34	0.023

983		BLN002	Balanitis Xerotica Obliterans	29	0.023

984		MLR020	Malaria, Mild	27	0.023

985		ISL004	Isolated Gonadotropin-Releasing Hormone Deficiency	26	0.023

986		LKP001	Leukoplakia of Penis	25	0.023

987		ACT133	Acetylation, Slow	23	0.023

988	P	HRD012	Hereditary Elliptocytosis	51	0.021

989	P	PRS049	Persistent Mullerian Duct Syndrome	50	0.021

990	P	DPY001	Dupuytren Contracture	48	0.021

991		SYM002	Sympathetic Ophthalmia	47	0.021

992		RMS001	Rem Sleep Behavior Disorder	46	0.021

993		LMR001	Lemierre's Syndrome	42	0.021

994		GLC096	Galactorrhea	42	0.021

995		DDN003	Duodenum Adenocarcinoma	41	0.021

996		PHM001	Phimosis	37	0.021

997	c	GLC041	Glaucoma 1, Open Angle, a	34	0.021

998		HMP003	Hemopneumothorax	33	0.021

999	c	SCH081	Schizophrenia 6	31	0.021

1000		ENG004	Engraftment Syndrome	30	0.021

1001		PPM002	Ppoma	29	0.021

1002	c	ADL080	Adult Acute Respiratory Distress Syndrome	26	0.021

1003		ACT206	Acitretin/etretinate Embryopathy	18	0.021