Search results for B2

781 hits were found for B2

#	Family	MCID	Name	MIFTS	Score
1	c	BRC052	Brachydactyly, Type B2	41	7.579

2	c	MSC044	Muscular Dystrophy-Dystroglycanopathy , Type B, 2	30	4.149

3	c	CHR651	Charcot-Marie-Tooth Disease, Axonal, Type 2b2	39	3.376

4		RBF001	Riboflavin Deficiency	49	2.535

5		CRT005	Cortical Thymoma	24	2.387

6	P	CLR023	Colorectal Cancer	99	0.123

7		BRN004	Brain Edema	56	0.121

8	c	MCR113	Microvascular Complications of Diabetes 3	52	0.115

9	c	MCR120	Microvascular Complications of Diabetes 7	47	0.115

10	c	MCR130	Microvascular Complications of Diabetes 6	41	0.115

11	c	MCR133	Microvascular Complications of Diabetes 4	41	0.115

12	c	PRC016	Pre-Eclampsia	63	0.109

13	P	MYC008	Myocarditis	59	0.109

14		PRT037	Pertussis	65	0.106

15	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.100

16		ISC004	Ischemia	58	0.100

17	c	HYP595	Hypertension, Essential	84	0.093

18	P	LVR013	Liver Disease	68	0.093

19		HLX001	Helix Syndrome	47	0.093

20	P	ANG015	Angioedema	57	0.089

21	P	HPT023	Hepatocellular Carcinoma	100	0.085

22	P	ADN016	Adenocarcinoma	64	0.085

23	P	BRS047	Breast Cancer	97	0.081

24		OST012	Osteoarthritis	78	0.077

25	P	KDN018	Kidney Disease	72	0.077

26	P	GLM045	Glioma	63	0.077

27	c	ACT068	Acute Cystitis	63	0.077

28	P	RHN004	Rhinitis	57	0.077

29		TRM010	Traumatic Brain Injury	51	0.077

30		BRN071	Brain Injury	49	0.077

31	P	PRS040	Prostate Cancer	97	0.073

32	P	BLD134	Bladder Cancer	79	0.073

33	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.073

34	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.073

35		CRB039	Cerebrovascular Disease	67	0.073

36	P	PLM037	Pulmonary Hypertension	67	0.073

37		ANG054	Angina Pectoris	66	0.073

38	P	THY023	Thymoma	65	0.073

39	P	VSC007	Vascular Disease	63	0.073

40	P	PSR002	Psoriasis	62	0.073

41		LPP008	Lipoprotein Quantitative Trait Locus	62	0.073

42		ADN018	Adenoma	59	0.073

43	P	INF037	Inflammatory Bowel Disease	54	0.073

44		PST011	Pustulosis of Palm and Sole	52	0.073

45		ART140	Arteries, Anomalies of	52	0.073

46	c	THY107	Thymoma, Familial	52	0.073

47	P	MNN013	Meningitis	66	0.068

48		TXC005	Toxic Shock Syndrome	62	0.068

49		HYP066	Hyperglycemia	61	0.068

50	P	THL005	Thalassemia	60	0.068

51		MTH009	Mouth Disease	56	0.068

52		END086	End Stage Renal Disease	51	0.068

53	P	ECL001	Eclampsia	50	0.068

54		GLL048	Glial Tumor	45	0.068

55		CRB004	Cerebral Artery Occlusion	45	0.068

56		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.068

57		CRV035	Cervical Cancer	76	0.063

58		CRH001	Crohn's Disease	74	0.063

59	P	MYC007	Myocardial Infarction	70	0.063

60		ALL003	Allergic Rhinitis	67	0.063

61	c	MGR028	Migraine with or Without Aura 1	67	0.063

62		ALL026	Allergic Hypersensitivity Disease	62	0.063

63	P	TMP001	Temporal Lobe Epilepsy	50	0.063

64		RNL077	Renal Fibrosis	47	0.063

65		48X005	48,xyyy	39	0.063

66	P	LNG032	Lung Cancer	98	0.058

67		STR067	Stroke, Ischemic	81	0.058

68		AST005	Asthma	76	0.058

69		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.058

70	P	NRB001	Neuroblastoma	72	0.058

71		CNG034	Congestive Heart Failure	69	0.058

72		ATH013	Atherosclerosis Susceptibility	65	0.058

73	P	CRN300	Coronary Heart Disease 1	63	0.058

74		SKN016	Skin Disease	63	0.058

75	P	NPH012	Nephrotic Syndrome	60	0.058

76	c	HRD002	Hereditary Angioedema	60	0.058

77	P	INF032	Infertility	57	0.058

78		THR024	Thrombosis	57	0.058

79	P	CRD246	Cardiovascular System Disease	57	0.058

80	P	NRP001	Neuropathy	56	0.058

81		EMB004	Embryonal Carcinoma	56	0.058

82		INT007	Intermediate Coronary Syndrome	55	0.058

83	P	ART021	Arteriosclerosis	54	0.058

84	P	RCT021	Rectum Cancer	52	0.058

85		CLR109	Colorectal Adenocarcinoma	51	0.058

86		ASP003	Aseptic Meningitis	51	0.058

87		MNN009	Meningoencephalitis	49	0.058

88		BNR002	Bone Resorption Disease	48	0.058

89		URT010	Ureteral Obstruction	45	0.058

90		CYT002	Cytokine Deficiency	42	0.058

91		ESP021	Esophageal Cancer	90	0.051

92	c	ATR087	Atrial Standstill 1	75	0.051

93	P	PHC003	Pheochromocytoma	71	0.051

94		DFC004	Deficiency Anemia	70	0.051

95	c	CHR684	Chronic Kidney Disease	70	0.051

96		ART016	Aortic Aneurysm	69	0.051

97	P	CLC063	Celiac Disease 1	66	0.051

98		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.051

99	P	HRP006	Herpes Simplex	65	0.051

100		PRT036	Peritonitis	64	0.051

101		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.051

102		CLR108	Colorectal Adenoma	64	0.051

103	P	RHB003	Rhabdomyosarcoma	63	0.051

104	P	NTR004	Neutropenia	63	0.051

105		ATM095	Autoimmune Disease	62	0.051

106		LVR012	Liver Cirrhosis	62	0.051

107		MSL001	Measles	62	0.051

108		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.051

109		FTT001	Fatty Liver Disease	61	0.051

110	P	ENC004	Encephalitis	61	0.051

111		SPN186	Spinal Cord Injury	60	0.051

112		CHL014	Cholera	59	0.051

113		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.051

114	c	ACT075	Acute Myocardial Infarction	57	0.051

115		ALL006	Allergic Asthma	56	0.051

116		BCT022	Bacterial Infectious Disease	56	0.051

117	P	DRR001	Diarrhea	55	0.051

118		HMC014	Homocysteinemia	53	0.051

119		OCL069	Ocular Motor Apraxia	51	0.051

120	P	LCT001	Lactic Acidosis	51	0.051

121		HND002	Hand, Foot and Mouth Disease	51	0.051

122		PLR008	Pleurisy	50	0.051

123		HPT014	Hepatorenal Syndrome	50	0.051

124		MTB004	Metabolic Acidosis	50	0.051

125		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.051

126		ADR040	Adrenal Gland Pheochromocytoma	46	0.051

127	c	LKM005	Leukemia, T-Cell, Chronic	34	0.051

128		NNT021	Neonatal Meningitis	25	0.051

129	P	ALZ034	Alzheimer Disease	88	0.045

130	c	SYS001	Systemic Lupus Erythematosus	86	0.045

131	c	DLT002	Dilated Cardiomyopathy	79	0.045

132		ULC004	Ulcerative Colitis	73	0.045

133		PRP027	Peripheral Vascular Disease	71	0.045

134	P	SLP006	Sleep Apnea	69	0.045

135	P	THR014	Thrombocytopenia	67	0.045

136	P	HPT021	Hepatitis	67	0.045

137	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.045

138	c	RHB024	Rhabdomyosarcoma 2	67	0.045

139		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.045

140		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.045

141		KRT019	Keratitis, Hereditary	65	0.045

142	P	DBT009	Diabetes Mellitus	64	0.045

143		DPR016	Depression	63	0.045

144	c	ALP101	Alpha-Thalassemia	62	0.045

145		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.045

146		NTR005	Nutritional Deficiency Disease	62	0.045

147		DRM006	Dermatitis	61	0.045

148	P	ENC018	Encephalopathy	61	0.045

149		ALC006	Alcoholic Hepatitis	61	0.045

150	P	PNC044	Pancreatitis	61	0.045

151	P	LPS004	Lupus Erythematosus	61	0.045

152		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.045

153		LNG099	Lung Disease	60	0.045

154	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.045

155	c	ACT071	Acute Kidney Failure	60	0.045

156	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.045

157	P	SLP005	Sleep Disorder	59	0.045

158		PLM033	Pulmonary Embolism	59	0.045

159	P	CYS018	Cystitis	59	0.045

160		IRN001	Iron Deficiency Anemia	59	0.045

161		IRN002	Iron Metabolism Disease	57	0.045

162	P	EXN002	Exanthem	57	0.045

163	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.045

164		HYP266	Hypoxia	57	0.045

165	P	PYL005	Pyelonephritis	56	0.045

166		HMG005	Hemoglobinopathy	56	0.045

167		FDB001	Foodborne Botulism	55	0.045

168		PRP030	Purpura	54	0.045

169		DBT010	Diabetic Neuropathy	54	0.045

170		IMP005	Impotence	52	0.045

171		STT002	Status Asthmaticus	50	0.045

172		47X002	47,xyy	49	0.045

173		INT078	Intracranial Thrombosis	49	0.045

174	P	RNV001	Renovascular Hypertension	48	0.045

175	c	ACT076	Acute Myocarditis	46	0.045

176		ACT003	Acute Kidney Tubular Necrosis	45	0.045

177	P	CHR345	Chronic Pain	44	0.045

178	c	PCH010	Pachyonychia Congenita 3	44	0.045

179	c	PRM038	Primary Agammaglobulinemia	44	0.045

180		C1N001	C1 Inhibitor Deficiency	39	0.045

181	c	BLD156	Bleeding Disorder, Platelet-Type, 14	32	0.045

182		PST092	Posttransplant Acute Limbic Encephalitis	29	0.045

183		CHL079	Children's Interstitial Lung Disease	26	0.045

184	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.036

185		NRL016	Neural Tube Defects	82	0.036

186	P	PRK057	Parkinson Disease, Late-Onset	78	0.036

187	c	TBR025	Tuberous Sclerosis 1	77	0.036

188	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.036

189	P	RSP003	Respiratory Failure	74	0.036

190		END057	Endometrial Cancer	74	0.036

191	c	BTT014	Beta-Thalassemia	74	0.036

192	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.036

193	P	RTN024	Retinoblastoma	73	0.036

194	c	HPT073	Hepatitis C Virus	72	0.036

195	c	MLT156	Multiple Endocrine Neoplasia, Type I	72	0.036

196		HMN044	Human Immunodeficiency Virus Type 1	71	0.036

197	P	SRC025	Sarcoidosis 1	70	0.036

198		DWN001	Down Syndrome	70	0.036

199	P	OST001	Osteopetrosis	70	0.036

200	P	MYP004	Myopathy	70	0.036

201	P	TBR001	Tuberous Sclerosis	70	0.036

202	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.036

203		PLM001	Pulmonary Tuberculosis	69	0.036

204	P	LYM118	Lymphoma	68	0.036

205	P	MYC084	Mycobacterium Tuberculosis 1	68	0.036

206	P	LKM002	Leukemia	68	0.036

207	P	ESS003	Essential Thrombocythemia	68	0.036

208		RCK004	Rickets	68	0.036

209		CRP001	Carpal Tunnel Syndrome	67	0.036

210		OST159	Osteogenic Sarcoma	66	0.036

211	c	FML021	Familial Hypercholesterolemia	66	0.036

212	P	MSC005	Muscular Dystrophy	66	0.036

213	P	SKN015	Skin Carcinoma	66	0.036

214	P	ATR011	Atrial Fibrillation	66	0.036

215		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.036

216	P	VNW001	Von Willebrand's Disease	65	0.036

217		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.036

218	c	DBT099	Diabetes Mellitus, Type I	65	0.036

219		CLN015	Colon Adenocarcinoma	65	0.036

220		APN008	Apnea, Obstructive Sleep	64	0.036

221		GT001	Gout	64	0.036

222		OST017	Osteomyelitis	64	0.036

223		LSH001	Leishmaniasis	63	0.036

224	P	END044	Endometriosis	63	0.036

225		LPD008	Lipid Metabolism Disorder	62	0.036

226	c	HPT001	Hepatitis C	62	0.036

227	P	HYP750	Hypertriglyceridemia, Familial	62	0.036

228		CHR619	Chromosome 2q35 Duplication Syndrome	62	0.036

229		BRS099	Breast Ductal Carcinoma	62	0.036

230		MTC114	Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes	61	0.036

231	c	PNS012	Paine Syndrome	61	0.036

232	P	MYL006	Myeloid Leukemia	60	0.036

233	c	ACT027	Acute Pancreatitis	60	0.036

234	P	CTR002	Cataract	60	0.036

235		STT001	Status Epilepticus	60	0.036

236	c	HPT016	Hepatitis B	59	0.036

237		VSL002	Visual Epilepsy	59	0.036

238		GNG013	Gingivitis	59	0.036

239		GST045	Gastroenteritis	59	0.036

240		HLC007	Helicobacter Pylori Infection	59	0.036

241		PPT005	Peptic Ulcer Disease	59	0.036

242		FBR047	Fibromyalgia	58	0.036

243		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.036

244	P	MTR012	Mitral Valve Disease	58	0.036

245		MNT002	Mental Depression	58	0.036

246	P	GLM007	Glomerulonephritis	57	0.036

247	P	ZLL001	Zellweger Syndrome	57	0.036

248	P	HDC001	Headache	57	0.036

249		DSS009	Disseminated Intravascular Coagulation	57	0.036

250		CPR004	Coproporphyria, Hereditary	57	0.036

251		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.036

252	P	PLY018	Polycythemia	56	0.036

253	P	ADL017	Adult T-Cell Leukemia	56	0.036

254	P	FBR017	Fibrosarcoma	56	0.036

255		LST001	Listeriosis	56	0.036

256	P	MLT074	Multiple Endocrine Neoplasia	56	0.036

257		ERY051	Erythroleukemia, Familial	56	0.036

258	P	SZR006	Seizure Disorder	56	0.036

259		CYS008	Cystic Echinococcosis	56	0.036

260		MCS002	Mucositis	56	0.036

261	P	PLY019	Polyneuropathy	56	0.036

262	P	GST044	Gastritis	56	0.036

263		LMB062	Limb Ischemia	55	0.036

264		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.036

265	P	MYP006	Myopia	55	0.036

266		SYN007	Synovitis	54	0.036

267	P	ALP008	Alopecia	54	0.036

268		PRC013	Pericarditis	54	0.036

269		PLM010	Pulmonary Edema	54	0.036

270		ECH003	Echinococcosis	53	0.036

271	P	HML001	Hemolytic-Uremic Syndrome	53	0.036

272		GTR002	Goiter	53	0.036

273		NNT012	Neonatal Jaundice	53	0.036

274	c	FML008	Familial Retinoblastoma	53	0.036

275	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.036

276	P	DDN001	Duodenal Ulcer	52	0.036

277	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.036

278	P	HMP007	Hemophilia	51	0.036

279		THR004	Thrombocytosis	51	0.036

280		ENT011	Enterocolitis	51	0.036

281	P	LSS002	Lissencephaly	51	0.036

282		STM007	Stomatitis	50	0.036

283		PLC008	Placenta Disease	50	0.036

284		NTR046	Neutrophil Migration	50	0.036

285		RNL078	Renal Dysplasia	50	0.036

286	P	MTC133	Mitochondrial Myopathy	49	0.036

287	c	MTR002	Mitral Valve Insufficiency	48	0.036

288	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.036

289		HPR003	Heparin-Induced Thrombocytopenia	48	0.036

290		CRN017	Coronary Thrombosis	47	0.036

291		KRT002	Keratomalacia	47	0.036

292	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.036

293		CRD137	Cardiogenic Shock	47	0.036

294	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.036

295	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.036

296		HDN002	Head Injury	46	0.036

297	c	MLG068	Malignant Glioma	46	0.036

298	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.036

299	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.036

300		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.036

301	P	MTC004	Mitochondrial Encephalomyopathy	44	0.036

302	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.036

303	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.036

304		RFR003	Refractive Error	43	0.036

305	P	CRN026	Corneal Edema	43	0.036

306		RNL025	Renal Hypoplasia	42	0.036

307	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.036

308	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.036

309		EPT021	Epithelial Recurrent Erosion Dystrophy	42	0.036

310	P	KLZ004	Kala-Azar 1	41	0.036

311		ASP030	Aspirin Resistance	39	0.036

312		ALL014	Allergic Encephalomyelitis	38	0.036

313		EPL199	Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure	36	0.036

314		PLC002	Plica Syndrome	36	0.036

315		PYR009	Pyridoxine Deficiency Anemia	34	0.036

316		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.036

317		CMP040	Complement Component 4, Partial Deficiency of	33	0.036

318	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.036

319	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.036

320		PYR016	Pyridoxine Deficiency	30	0.036

321	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.036

322		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.036

323		IMM165	Immunoglobulin Switch Sequences	15	0.036

324	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.026

325	P	OVR042	Ovarian Cancer	88	0.026

326	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.026

327	c	LKM061	Leukemia, Acute Myeloid	84	0.026

328	P	PNC035	Pancreatic Cancer	84	0.026

329	P	GST053	Gastric Cancer	83	0.026

330		MLR004	Malaria	81	0.026

331	P	RTT002	Rett Syndrome	80	0.026

332	P	RHM011	Rheumatoid Arthritis	80	0.026

333		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.026

334	c	NRF023	Neurofibromatosis, Type Ii	80	0.026

335		INS024	Insulin-Like Growth Factor I	79	0.026

336		IMM167	Immune Deficiency Disease	78	0.026

337		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.026

338		KPS004	Kaposi Sarcoma	75	0.026

339	P	HRT032	Heart Disease	75	0.026

340		PHN003	Phenylketonuria	75	0.026

341		GLB015	Glioblastoma Multiforme	75	0.026

342		BRN028	Brain Cancer	74	0.026

343	P	SCH015	Schizophrenia	74	0.026

344	P	OST002	Osteoporosis	74	0.026

345		SVR004	Severe Combined Immunodeficiency	73	0.026

346	c	SPN225	Spondyloarthropathy 1	73	0.026

347		ANX010	Anxiety	73	0.026

348		MSC157	Muscular Dystrophy, Duchenne Type	72	0.026

349	P	MLT020	Multiple Sclerosis	72	0.026

350	P	FML011	Familial Adenomatous Polyposis	72	0.026

351	P	AMY004	Amyloidosis	70	0.026

352		GST040	Gastric Adenocarcinoma	70	0.026

353		MLT157	Multiple System Atrophy 1	70	0.026

354		LGH007	Leigh Syndrome	70	0.026

355	P	HYP061	Hypertrophic Cardiomyopathy	70	0.026

356		PLY001	Polycythemia Vera	69	0.026

357	P	MLN008	Melanoma	69	0.026

358	P	ART022	Arthritis	69	0.026

359		SVR097	Severe Cutaneous Adverse Reaction	69	0.026

360		CRB037	Cerebral Palsy	69	0.026

361	P	OCL013	Oculodentodigital Dysplasia	69	0.026

362	P	HYP086	Hypothyroidism	69	0.026

363	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.026

364	P	TMP003	Temporal Arteritis	68	0.026

365	P	PNM007	Pneumonia	68	0.026

366	P	MYS003	Myasthenia Gravis	68	0.026

367		BRN024	Bronchitis	68	0.026

368		CNN005	Connective Tissue Disease	68	0.026

369	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.026

370	c	PRD013	Periodic Fever, Familial, Autosomal Dominant	67	0.026

371	c	INF071	Inflammatory Bowel Disease 1	67	0.026

372		BRK010	Burkitt Lymphoma	67	0.026

373	P	CHR012	Chronic Granulomatous Disease	67	0.026

374	P	TRN020	Turner Syndrome	67	0.026

375	P	HYP098	Hypereosinophilic Syndrome	67	0.026

376		LPT001	Leptospirosis	66	0.026

377		ALC007	Alcohol Dependence	66	0.026

378		GLN010	Glanzmann Thrombasthenia	66	0.026

379	P	NSP012	Nasopharyngeal Carcinoma	66	0.026

380	P	MCR115	Microvascular Complications of Diabetes 5	66	0.026

381	c	FML346	Familial Adenomatous Polyposis 1	66	0.026

382		HYP056	Hypoglycemia	66	0.026

383	P	HYD006	Hydrocephalus	66	0.026

384	P	DRM053	Dermatitis, Atopic	66	0.026

385		MYL031	Myeloproliferative Neoplasm	66	0.026

386	c	SML038	Small Cell Cancer of the Lung	65	0.026

387	P	PLM036	Pulmonary Fibrosis	65	0.026

388	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.026

389	P	ART005	Arteriovenous Malformation	65	0.026

390	P	CNJ013	Conjunctivitis	65	0.026

391		PPL049	Papillon-Lefevre Syndrome	65	0.026

392		PND002	Pendred Syndrome	65	0.026

393	P	PRS038	Personality Disorder	65	0.026

394	P	ADL010	Adult Respiratory Distress Syndrome	65	0.026

395	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.026

396		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.026

397	P	MST009	Mastocytosis	64	0.026

398	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.026

399	P	PRD008	Periodontitis	64	0.026

400		MSC007	Muscle Hypertrophy	64	0.026

401	c	DPH024	Diaphragmatic Hernia, Congenital	63	0.026

402		INC021	Incontinentia Pigmenti	63	0.026

403	P	HML002	Hemolytic Anemia	63	0.026

404	P	ANR048	Aniridia 1	63	0.026

405	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.026

406		TYP007	Typhoid Fever	63	0.026

407	P	HYP069	Hyperparathyroidism	63	0.026

408		ACT119	Acute Promyelocytic Leukemia	63	0.026

409		INT146	Intervertebral Disc Disease	63	0.026

410	c	SYS004	Systemic Mastocytosis	63	0.026

411		TRN015	Transient Cerebral Ischemia	63	0.026

412		ANR007	Anorexia Nervosa	63	0.026

413	c	GLC092	Glaucoma, Primary Open Angle	62	0.026

414	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.026

415		CLT003	Colitis	62	0.026

416	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.026

417	c	HPT003	Hepatitis a	62	0.026

418	c	BRN108	Branchiootic Syndrome 1	62	0.026

419		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.026

420	c	SVR001	Severe Acute Respiratory Syndrome	62	0.026

421	P	ESP024	Esophagitis	62	0.026

422	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.026

423		BLL006	Bullous Pemphigoid	62	0.026

424		CTN007	Cutaneous Leishmaniasis	62	0.026

425		MDD011	Mood Disorder	62	0.026

426		BLD131	Bladder Urothelial Carcinoma	62	0.026

427	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.026

428		OSS012	Osseous Heteroplasia, Progressive	61	0.026

429		ART141	Arteriovenous Malformations of the Brain	61	0.026

430	P	ART067	Aortic Aneurysm, Familial Thoracic 1	61	0.026

431		DRR016	Diarrhea 2, with Microvillus Atrophy	60	0.026

432		DPH001	Diphtheria	60	0.026

433	P	SCL018	Scoliosis	60	0.026

434	P	VNT002	Ventricular Septal Defect	60	0.026

435		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.026

436		ACN002	Acanthosis Nigricans	60	0.026

437		ACQ007	Acquired Immunodeficiency Syndrome	60	0.026

438		SQM006	Squamous Cell Carcinoma	60	0.026

439		DNG002	Dengue Hemorrhagic Fever	60	0.026

440		VRC005	Varicose Veins	60	0.026

441	P	PTN014	Patent Ductus Arteriosus 1	60	0.026

442		ORL011	Oral Cancer	60	0.026

443		INS001	Insulinoma	60	0.026

444		HYD002	Hydronephrosis	60	0.026

445	P	BRN019	Bernard-Soulier Syndrome	60	0.026

446	P	OPT006	Optic Nerve Disease	60	0.026

447		SPP011	Suppression of Tumorigenicity 12	59	0.026

448	P	RBL001	Rubella	59	0.026

449	P	BND020	Bone Disease	59	0.026

450	c	DNG003	Dengue Disease	59	0.026

451		PRN019	Perinatal Necrotizing Enterocolitis	59	0.026

452		DCT002	Ductal Carcinoma in Situ	59	0.026

453	P	BRS044	Breast Adenocarcinoma	59	0.026

454		AVN001	Avian Influenza	59	0.026

455		BRN002	Bronchiolitis	59	0.026

456		ANR040	Aneurysm	59	0.026

457		PST028	Post-Traumatic Stress Disorder	58	0.026

458	P	ALC033	Alcohol Use Disorder	58	0.026

459		CNT047	Contact Dermatitis	58	0.026

460		ERY003	Erythema Multiforme	58	0.026

461		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.026

462	P	EHL001	Ehlers-Danlos Syndrome	58	0.026

463		EYD002	Eye Disease	58	0.026

464		DSS008	Disease of Mental Health	58	0.026

465	P	MMP001	Mumps	58	0.026

466		CNS004	Constipation	58	0.026

467	c	DWL002	Dowling-Degos Disease 1	58	0.026

468	P	CND004	Candidiasis	58	0.026

469	P	PRP019	Peripheral Nervous System Disease	58	0.026

470		GLS018	Glass Syndrome	57	0.026

471	P	PLV020	Pelvic Organ Prolapse	57	0.026

472		CHL067	Cholecystitis	57	0.026

473	P	PLY041	Polymyositis	57	0.026

474	c	MST023	Mesothelioma, Malignant	57	0.026

475		APH001	Aphthous Stomatitis	57	0.026

476	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.026

477		CMM005	Common Cold	57	0.026

478		BLR008	Bilirubin Metabolic Disorder	57	0.026

479		SCH014	Schistosomiasis	57	0.026

480		SKN022	Skin Squamous Cell Carcinoma	57	0.026

481		PHR003	Pharyngitis	57	0.026

482	P	MYS005	Myositis	56	0.026

483		CMR002	Coumarin Resistance	56	0.026

484	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.026

485		TRN018	Transitional Cell Carcinoma	56	0.026

486	c	ACT134	Acute Liver Failure	56	0.026

487		LMY014	Leiomyoma, Uterine	56	0.026

488		PRS047	Prostatitis	56	0.026

489	c	BRC078	Brachydactyly, Type A1	56	0.026

490	P	NRF002	Neurofibromatosis	56	0.026

491		GST050	Gastrointestinal System Disease	56	0.026

492		ORL005	Oral Candidiasis	56	0.026

493		SLC006	Silicosis	56	0.026

494		ATR057	Atrioventricular Block	55	0.026

495	c	FML035	Familial Hyperlipidemia	55	0.026

496		HYP005	Hypokalemia	55	0.026

497		MCL006	Macular Retinal Edema	55	0.026

498	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.026

499	P	MLN007	Male Infertility	55	0.026

500	c	BCT007	Bacterial Meningitis	55	0.026

501		NPH009	Nephrolithiasis	55	0.026

502	c	CTS029	Cutis Laxa, Autosomal Recessive, Type Iiia	55	0.026

503	P	ANT006	Antiphospholipid Syndrome	55	0.026

504		DFN344	Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome	55	0.026

505	P	PTT006	Pituitary Adenoma	55	0.026

506		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.026

507		OCL020	Ocular Cicatricial Pemphigoid	55	0.026

508	P	SBS003	Substance Abuse	55	0.026

509		BRN045	Brunner Syndrome	55	0.026

510	P	HYP050	Hyperinsulinemic Hypoglycemia	55	0.026

511		URN010	Urinary Tract Obstruction	55	0.026

512		END040	Endogenous Depression	55	0.026

513	P	JNC001	Junctional Epidermolysis Bullosa	54	0.026

514		RSC001	Rosacea	54	0.026

515		ACD008	Acid-Labile Subunit Deficiency	54	0.026

516	P	ICH004	Ichthyosis	54	0.026

517		PRT038	Protein-Energy Malnutrition	54	0.026

518		RST011	Restrictive Dermopathy, Lethal	54	0.026

519	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.026

520		THR013	Thoracic Outlet Syndrome	54	0.026

521		AMN001	Amenorrhea	54	0.026

522		SLP001	Sleeping Sickness	54	0.026

523	P	TRM003	Tremor	54	0.026

524		CLL003	Cellulitis	54	0.026

525		NNL006	Non-Alcoholic Steatohepatitis	54	0.026

526	P	BRC006	Brachydactyly	53	0.026

527		PLM012	Pulmonary Sarcoidosis	53	0.026

528		ABL002	Ablepharon-Macrostomia Syndrome	53	0.026

529	P	END047	Endophthalmitis	53	0.026

530	P	EPD016	Epidermolysis Bullosa	53	0.026

531	P	INS002	in Situ Carcinoma	53	0.026

532		HRT012	Heart Valve Disease	53	0.026

533	P	HMC002	Homocystinuria	53	0.026

534		CRH005	Crohn's Colitis	53	0.026

535		ICH054	Ichthyosis, X-Linked	53	0.026

536	P	RTN016	Retinal Degeneration	53	0.026

537		MST005	Mastitis	53	0.026

538		CYS005	Cysticercosis	53	0.026

539		INT075	Intracranial Hypertension	53	0.026

540		GST023	Gastric Ulcer	53	0.026

541		DNT012	Dental Caries	53	0.026

542	P	RTN022	Retinal Vein Occlusion	53	0.026

543	c	HPT007	Hepatitis E	53	0.026

544		PRP080	Peripheral Artery Disease	53	0.026

545		ALC009	Alcoholic Liver Cirrhosis	53	0.026

546	c	PSR017	Psoriasis 2	53	0.026

547	P	INT068	Intestinal Disease	53	0.026

548	P	RTN018	Retinal Disease	53	0.026

549		CHR073	Choreatic Disease	52	0.026

550		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.026

551		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.026

552		LYS002	Lysosomal Storage Disease	52	0.026

553	c	VRL010	Viral Hepatitis	52	0.026

554		ACR041	Acromelic Frontonasal Dysostosis	52	0.026

555		DYS015	Dysentery	52	0.026

556	P	MSC003	Muscular Atrophy	52	0.026

557	P	NRC002	Narcolepsy	52	0.026

558		NRP045	Neuropathy, Ataxia, and Retinitis Pigmentosa	52	0.026

559	c	PSR023	Psoriasis 1	52	0.026

560		BWN001	Bowen-Conradi Syndrome	52	0.026

561		PTH003	Pathologic Nystagmus	52	0.026

562		HYP014	Hyperuricemia	52	0.026

563		ART074	Aortic Dissection	52	0.026

564		LMY002	Leiomyoma	52	0.026

565		SPN051	Spondylitis	51	0.026

566		SPS003	Spastic Diplegia	51	0.026

567	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.026

568		FDL002	Food Allergy	51	0.026

569		ILS001	Ileus	51	0.026

570		ANK001	Ankylosis	51	0.026

571	c	PRM108	Primary Progressive Multiple Sclerosis	51	0.026

572		CYS014	Cystadenocarcinoma	51	0.026

573		CCC002	Coccidiosis	51	0.026

574	P	PRC012	Pericardial Effusion	51	0.026

575	P	THR015	Thrombophilia	51	0.026

576	c	VRL007	Viral Encephalitis	51	0.026

577		CCT002	Cicatricial Pemphigoid	51	0.026

578	P	RNL007	Renal Tubular Acidosis	51	0.026

579	c	BRC051	Brachydactyly, Type B1	51	0.026

580	c	SCN007	Secondary Hyperparathyroidism	51	0.026

581		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.026

582	c	BRC079	Brachydactyly, Type A2	51	0.026

583	c	EHL078	Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1	51	0.026

584		HYP781	Hypoascorbemia	51	0.026

585	c	RBN018	Robinow Syndrome, Autosomal Dominant 1	51	0.026

586		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.026

587		HYP081	Hypolipoproteinemia	51	0.026

588	P	MMB011	Membranous Nephropathy	50	0.026

589		PRS034	Parasitic Helminthiasis Infectious Disease	50	0.026

590	P	OVR082	Overgrowth Syndrome	50	0.026

591	P	BRT029	Brittle Cornea Syndrome 2	50	0.026

592		PST021	Postpartum Depression	50	0.026

593	c	SVR005	Severe Pre-Eclampsia	50	0.026

594		TRY001	Trypanosomiasis	50	0.026

595	P	KRT007	Keratoconus	50	0.026

596		HRT011	Heart Septal Defect	50	0.026

597	c	INF023	Inflammatory Breast Carcinoma	50	0.026

598	P	ATR005	Atrophic Gastritis	50	0.026

599		DBT004	Diabetic Polyneuropathy	49	0.026

600		ADR038	Adermatoglyphia	49	0.026

601		KRT001	Keratoconjunctivitis Sicca	49	0.026

602		BLL004	Bullous Keratopathy	49	0.026

603		MCN001	Mucinous Adenocarcinoma	49	0.026

604		VLV047	Volvulus of Midgut	49	0.026

605		PLP001	Pulpitis	49	0.026

606		CCN002	Cocaine Abuse	49	0.026

607	P	OPN001	Open-Angle Glaucoma	49	0.026

608	P	RBN002	Robinow Syndrome	49	0.026

609		STP011	Stapes Ankylosis with Broad Thumbs and Toes	49	0.026

610		URM002	Uremia	49	0.026

611	c	DSB006	Desbuquois Dysplasia 1	48	0.026

612		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.026

613		CCN001	Cocaine Dependence	48	0.026

614		VTM033	Vitamin K Deficiency Bleeding	48	0.026

615		DPN005	Du Pan Syndrome	48	0.026

616	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.026

617		SPL018	Splenomegaly	48	0.026

618		HMP001	Hemopericardium	48	0.026

619		TBR011	Tuberculous Meningitis	48	0.026

620		RCT020	Rectum Adenocarcinoma	48	0.026

621		OPD006	Opioid Addiction	48	0.026

622	c	HYD064	Hydrocephalus, Congenital, 1	48	0.026

623		SXL003	Sexual Disorder	47	0.026

624		PRP007	Priapism	47	0.026

625		DRG003	Drug Dependence	47	0.026

626	P	CRN028	Corneal Ulcer	47	0.026

627		KRT008	Keratopathy	47	0.026

628		AST006	Astigmatism	47	0.026

629	c	PSR032	Psoriasis 11	47	0.026

630		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.026

631	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.026

632		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.026

633		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.026

634	P	CRC039	Coarctation of Aorta	47	0.026

635		CHR607	Chorea, Childhood-Onset, with Psychomotor Retardation	47	0.026

636		ASP004	Asphyxia Neonatorum	46	0.026

637		RTN020	Retinal Vascular Disease	46	0.026

638		CLN045	Colonic Benign Neoplasm	46	0.026

639	P	BRB001	Beriberi	46	0.026

640	P	PLL002	Pellagra	46	0.026

641	P	BNG032	Benign Mesothelioma	46	0.026

642	c	RBN017	Robinow Syndrome, Autosomal Dominant 2	46	0.026

643		CRN019	Coronary Artery Vasospasm	46	0.026

644	P	PRX021	Proximal Symphalangism	46	0.026

645		LKS001	Leukostasis	46	0.026

646	c	DRR009	Diarrhea 6	46	0.026

647		ANR004	Anuria	46	0.026

648		PLC001	Placenta Accreta	46	0.026

649		TRT001	Teratocarcinoma	45	0.026

650		NWC001	Newcastle Disease	45	0.026

651		SYN005	Synostosis	45	0.026

652	P	SBR004	Seborrheic Dermatitis	45	0.026

653		MYF001	Myofibroma	45	0.026

654		SBC016	Subacute Delirium	44	0.026

655		DBT008	Diabetic Angiopathy	44	0.026

656		APP009	Appendix Adenocarcinoma	44	0.026

657		GRN017	Granulocytopenia	44	0.026

658		IMM064	Immunodeficiency, Common Variable, 10	44	0.026

659		ORG002	Organic Acidemia	44	0.026

660		CNN002	Cannabis Abuse	44	0.026

661		LRY018	Laryngeal Squamous Cell Carcinoma	44	0.026

662		KWS001	Kwashiorkor	44	0.026

663	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.026

664		HPT082	Hepatic Adenomas, Familial	44	0.026

665	P	CRN024	Corneal Disease	44	0.026

666	P	HYP121	Hypoalphalipoproteinemia	43	0.026

667		SKN005	Skin Atrophy	43	0.026

668		ECC004	Eccrine Porocarcinoma	43	0.026

669	c	CHR096	Chronic Pulmonary Heart Disease	43	0.026

670		MGS001	Megaesophagus	43	0.026

671	c	SRC023	Sarcoidosis 2	43	0.026

672		PLY068	Polysubstance Abuse	43	0.026

673		PRS042	Prostate Disease	43	0.026

674	P	PRP034	Purpura Fulminans	43	0.026

675		TRP009	Triple X Syndrome	42	0.026

676		PNM013	Pneumococcal Meningitis	42	0.026

677	c	RTN047	Retinitis Pigmentosa 18	42	0.026

678		BRC004	Brachydactyly-Syndactyly Syndrome	42	0.026

679	c	PSR028	Psoriasis 7	42	0.026

680	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.026

681	P	DST107	Distal Renal Tubular Acidosis	42	0.026

682		TRS002	Tarsal-Carpal Coalition Syndrome	42	0.026

683		ATX019	Ataxia with Vitamin E Deficiency	42	0.026

684	c	MLG079	Malignant Pleural Mesothelioma	42	0.026

685		BNB002	Bainbridge-Ropers Syndrome	42	0.026

686		MYF002	Myofascial Pain Syndrome	42	0.026

687		FSC002	Fascioliasis	42	0.026

688	c	CTR132	Cataract 3, Multiple Types	41	0.026

689		EPC002	Epicondylitis	41	0.026

690	c	ATS082	Autosomal Dominant Robinow Syndrome	41	0.026

691		XRP001	Xerophthalmia	41	0.026

692		MMM006	Mammographic Density	41	0.026

693	c	PSR018	Psoriasis 13	41	0.026

694		PRS063	Paresthesia	41	0.026

695		VSL013	Visual Impairment and Progressive Phthisis Bulbi	41	0.026

696		DHY010	Dihydrolipoamide Dehydrogenase Deficiency	40	0.026

697		THR035	Thrombasthenia	40	0.026

698		ANX004	Anoxia	40	0.026

699		MCN008	Mucinous Cystadenocarcinoma	40	0.026

700		CNS002	Constrictive Pericarditis	40	0.026

701		HPR006	Heparin Cofactor Ii Deficiency	40	0.026

702		FNG016	Fungal Keratitis	40	0.026

703		HYP030	Hypoactive Sexual Desire Disorder	40	0.026

704	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.026

705		PLY100	Polyploidy	40	0.026

706		CNN001	Cannabis Dependence	40	0.026

707		ART008	Arteriosclerosis Obliterans	40	0.026

708		WND001	Wound Botulism	39	0.026

709	c	CTR130	Cataract 9, Multiple Types	39	0.026

710		PCH007	Pouchitis	39	0.026

711		ADP007	Adie Pupil	39	0.026

712	P	MLT072	Multiple Synostoses Syndrome	39	0.026

713	c	HYP555	Hypertriglyceridemia, Transient Infantile	39	0.026

714		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.026

715	c	SYS043	Systemic Lupus Erythematosus 1	38	0.026

716		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.026

717		HPT070	Hepatosplenic T-Cell Lymphoma	38	0.026

718		CRT004	Carotid Artery Thrombosis	38	0.026

719		CNT060	Central Serous Chorioretinopathy	38	0.026

720		FRS019	Farsightedness	38	0.026

721	c	BRC080	Brachydactyly, Type A1, B	38	0.026

722		SPS226	Spastic Paraplegia, Ataxia, and Mental Retardation	37	0.026

723	P	FML187	Familial Hypertension	37	0.026

724		ATM052	Autoimmune Disease 1	37	0.026

725		GLM044	Glomerular Disease	37	0.026

726		CRN022	Corneal Degeneration	36	0.026

727		GRN055	Granular Corneal Dystrophy	36	0.026

728		SYN086	Synostoses, Tarsal, Carpal, and Digital	35	0.026

729		BRK012	Broken Heart Syndrome	35	0.026

730		PRG080	Progressive Non-Infectious Anterior Vertebral Fusion	35	0.026

731		BCL014	B-Cell Growth Factor	35	0.026

732		ATX010	Ataxia Neuropathy Spectrum	34	0.026

733		MTC023	Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes	34	0.026

734		ACT064	Acute Necrotizing Encephalitis	33	0.026

735	P	VSC018	Visceral Steatosis	33	0.026

736	c	KRT029	Keratoconus 1	33	0.026

737		HND015	Hand Skill, Relative	33	0.026

738	c	BRC099	Brachydactyly, Type A4	32	0.026

739	c	BRC075	Brachydactyly, Type A1, C	32	0.026

740		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.026

741	P	SCL047	Sclerocornea	32	0.026

742		HYP806	Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy	32	0.026

743		INF009	Inflammatory Spondylopathy	31	0.026

744		DRF001	Dirofilariasis	31	0.026

745		GST007	Gastric Dilatation	31	0.026

746		SGR001	Sugarman Brachydactyly	30	0.026

747		ERY066	Erythema Multiforme Major	30	0.026

748		ERY069	Erythrokeratoderma ''en Cocardes''	30	0.026

749		IRR001	Irregular Astigmatism	30	0.026

750	P	AST056	Asthma-Related Traits 2	30	0.026

751		GNT019	Giant Cell Myocarditis	30	0.026

752		PRN008	Peroneal Nerve Paralysis	29	0.026

753		PRN035	Perniosis	28	0.026

754	c	AST034	Asthma-Related Traits 4	28	0.026

755		CRC001	Cercarial Dermatitis	28	0.026

756	c	FTL067	Fetal Hemoglobin Quantitative Trait Locus 6	28	0.026

757		CLN002	Colon Mucinous Adenocarcinoma	28	0.026

758		ARG004	Argyria	27	0.026

759		HNM002	Hinman Syndrome	27	0.026

760		HYP855	Hyperpigmentation of the Skin	27	0.026

761		URN022	Urinary Tract Infections, Recurrent	27	0.026

762		MLR020	Malaria, Mild	27	0.026

763		CTR014	Cataract Microcornea Syndrome	26	0.026

764		PRQ002	Paraquat Poisoning	26	0.026

765	c	CRD150	Cardiomyopathy, Familial Hypertrophic, 18	26	0.026

766		CNR001	Coenurosis	25	0.026

767		ADG002	Audiogenic Seizures	25	0.026

768		SYM024	Symphalangism, Distal	22	0.026

769		FNG003	Fungal Esophagitis	22	0.026

770		PLL009	Pellucid Marginal Degeneration	22	0.026

771	c	BLD123	Bleeding Disorder, Platelet-Type, 13	22	0.026

772	c	PLD003	Plod1-Related Kyphoscoliotic Ehlers-Danlos Syndrome	21	0.026

773	c	PST001	Posterior Myocardial Infarction	21	0.026

774		DSS012	Disseminated Infection with Mycobacterium Avium Complex	20	0.026

775	c	CHR688	Chronic Acquired Demyelinating Polyneuropathy	19	0.026

776	P	TLN014	Tl Antigen	19	0.026

777		PRL045	Proline-Negative Auxotroph of Hamster, Complementation of	18	0.026

778	P	RSS029	Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha	16	0.026

779		BLD137	Blood Group--Ahonen	16	0.026

780		MYC004	Mycotic Corneal Ulcer	14	0.026

781	P	EST010	Esterase B	14	0.026