Search results for Methionine

939 hits were found for Methionine

#	Family	MCID	Name	MIFTS	Score
1		MTH074	Methionine Adenosyltransferase I/iii Deficiency	42	6.344

2		HYP003	Hypermethioninemia	40	6.097

3		HMC033	Homocystinuria-Megaloblastic Anemia, Cblg Complementation Type	36	4.279

4		MTH011	Methionine Adenosyltransferase Deficiency	18	3.071

5		MTH075	Methionine Malabsorption Syndrome	15	2.983

6		HMC042	Homocystinuria-Megaloblastic Anemia, Cble Complementation Type	32	2.200

7		GLY015	Glycine N-Methyltransferase Deficiency	39	2.168

8		MTH046	Methylmalonic Acidemia Without Homocystinuria	26	2.146

9		ALP077	Alpha-Methylacetoacetic Aciduria	55	2.119

10		MTH055	Methylmalonic Aciduria and Homocystinuria, Cbld Type	38	2.119

11		DSR079	Disorder of Methionine Cycle and Sulfur Amino Acid Metabolism	4	2.098

12		MTH021	Methylmalonic Acidemia with Homocystinuria	46	2.069

13		HMC014	Homocysteinemia	53	0.343

14	P	LVR013	Liver Disease	68	0.262

15		FTT001	Fatty Liver Disease	61	0.262

16		NNL006	Non-Alcoholic Steatohepatitis	54	0.257

17	P	HMC002	Homocystinuria	53	0.248

18		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.225

19		GLL048	Glial Tumor	45	0.194

20	P	GLM045	Glioma	63	0.193

21		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.188

22	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.187

23	P	HPT023	Hepatocellular Carcinoma	100	0.183

24	P	VSC007	Vascular Disease	63	0.182

25		NRL016	Neural Tube Defects	82	0.180

26		LVR012	Liver Cirrhosis	62	0.175

27		CHL068	Cholestasis	61	0.165

28		GLB015	Glioblastoma Multiforme	75	0.154

29	P	CLR023	Colorectal Cancer	99	0.152

30		DPR016	Depression	63	0.143

31		CHL045	Choline Deficiency Disease	39	0.140

32		ADN018	Adenoma	59	0.138

33	P	NRB001	Neuroblastoma	72	0.136

34		MNT002	Mental Depression	58	0.136

35		HLX001	Helix Syndrome	47	0.132

36		VSL002	Visual Epilepsy	59	0.125

37	P	SZR006	Seizure Disorder	56	0.125

38		VTM002	Vitamin B12 Deficiency	48	0.125

39	P	MJR001	Major Depressive Disorder	68	0.123

40	P	ALZ034	Alzheimer Disease	88	0.113

41		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	52	0.113

42		MGL001	Megaloblastic Anemia	51	0.113

43	P	AST007	Astrocytoma	51	0.113

44	P	HPT021	Hepatitis	67	0.110

45	P	BRS047	Breast Cancer	97	0.108

46		INS024	Insulin-Like Growth Factor I	79	0.108

47	P	ENC018	Encephalopathy	61	0.108

48		DSR002	Disorders of Intracellular Cobalamin Metabolism	31	0.105

49		ATH013	Atherosclerosis Susceptibility	65	0.102

50	P	HYP069	Hyperparathyroidism	63	0.102

51		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.099

52		DWN001	Down Syndrome	70	0.096

53	c	INH020	Inherited Metabolic Disorder	47	0.096

54	c	MNN043	Meningioma, Familial	74	0.093

55	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.093

56	P	PHC003	Pheochromocytoma	71	0.093

57		LPP008	Lipoprotein Quantitative Trait Locus	62	0.093

58		MNN042	Meningioma, Radiation-Induced	62	0.093

59		SPN021	Spinal Meningioma	50	0.093

60		ADR040	Adrenal Gland Pheochromocytoma	46	0.093

61		SCR001	Secretory Meningioma	41	0.093

62		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.093

63		MYL069	Myeloma, Multiple	85	0.090

64	c	MLG068	Malignant Glioma	46	0.090

65	c	PCH010	Pachyonychia Congenita 3	44	0.090

66		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.090

67	P	PRS040	Prostate Cancer	97	0.087

68	P	SCH015	Schizophrenia	74	0.087

69	P	AMY004	Amyloidosis	70	0.087

70	c	PRM005	Primary Hyperparathyroidism	58	0.087

71		ART140	Arteries, Anomalies of	52	0.087

72		48X005	48,xyyy	39	0.087

73		PPL052	Papillomatosis, Confluent and Reticulated	33	0.087

74	P	PNC035	Pancreatic Cancer	84	0.083

75	P	GST053	Gastric Cancer	83	0.083

76	P	CRN300	Coronary Heart Disease 1	63	0.083

77	P	PRN023	Prion Disease	57	0.083

78	P	MTH008	Methylmalonic Acidemia	50	0.083

79		HPT004	Hepatic Coma	45	0.083

80	P	MDL005	Medulloblastoma	77	0.080

81	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.080

82		DFC004	Deficiency Anemia	70	0.080

83	P	OLG002	Oligodendroglioma	67	0.080

84		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.080

85	P	HML002	Hemolytic Anemia	63	0.080

86	c	PRC016	Pre-Eclampsia	63	0.080

87		HPT019	Hepatic Encephalopathy	60	0.080

88	P	CTR002	Cataract	60	0.080

89		GRD007	Grade Iii Astrocytoma	59	0.080

90		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.080

91		AGN016	Aging	56	0.080

92		PYR009	Pyridoxine Deficiency Anemia	34	0.080

93		CYS001	Cystic Fibrosis	81	0.076

94	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.076

95		BRN028	Brain Cancer	74	0.076

96	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.076

97	P	LYM118	Lymphoma	68	0.076

98		SRC014	Sarcoma	65	0.076

99	P	ADN016	Adenocarcinoma	64	0.076

100	c	HPT001	Hepatitis C	62	0.076

101		NTR005	Nutritional Deficiency Disease	62	0.076

102	P	BCL017	B-Cell Lymphoma	58	0.076

103	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.076

104	P	CRD246	Cardiovascular System Disease	57	0.076

105		END040	Endogenous Depression	55	0.076

106		SPN035	Spindle Cell Sarcoma	53	0.076

107		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.076

108		HRN029	Hearing Loss, Noise-Induced	37	0.076

109		PRC051	Paracetamol Poisoning	30	0.076

110	P	OVR042	Ovarian Cancer	88	0.072

111	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.072

112	c	HPT073	Hepatitis C Virus	72	0.072

113		CRT072	Creutzfeldt-Jakob Disease	70	0.072

114		ALC007	Alcohol Dependence	66	0.072

115		LPD008	Lipid Metabolism Disorder	62	0.072

116	P	PRM006	Primary Biliary Cirrhosis	62	0.072

117		VSC002	Vascular Dementia	57	0.072

118	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.072

119	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.072

120		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.072

121	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.072

122	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.072

123	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.072

124	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.072

125	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.072

126	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.072

127	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.072

128	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.072

129	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.068

130	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.068

131	P	HRT032	Heart Disease	75	0.068

132	P	ATS364	Autism	70	0.068

133	P	DMN002	Dementia	66	0.068

134	c	ACT068	Acute Cystitis	63	0.068

135		ATM095	Autoimmune Disease	62	0.068

136		CRC021	Carcinosarcoma	62	0.068

137		ACQ007	Acquired Immunodeficiency Syndrome	60	0.068

138		ISC004	Ischemia	58	0.068

139	P	HDC001	Headache	57	0.068

140		HYP266	Hypoxia	57	0.068

141		NRT001	Neurotic Disorder	53	0.068

142	P	INT099	Intrahepatic Cholestasis of Pregnancy	51	0.068

143		PRT029	Parathyroid Adenoma	50	0.068

144		MTB004	Metabolic Acidosis	50	0.068

145		NWC001	Newcastle Disease	45	0.068

146		CHL065	Cholangiocarcinoma	68	0.064

147	P	LKM002	Leukemia	68	0.064

148		HYP056	Hypoglycemia	66	0.064

149		CLR108	Colorectal Adenoma	64	0.064

150	P	RHB003	Rhabdomyosarcoma	63	0.064

151		LSH001	Leishmaniasis	63	0.064

152		CYS013	Cystinuria	63	0.064

153		HYP066	Hyperglycemia	61	0.064

154	P	PNC044	Pancreatitis	61	0.064

155		LNG099	Lung Disease	60	0.064

156	P	ALC033	Alcohol Use Disorder	58	0.064

157	P	MYS005	Myositis	56	0.064

158	P	LTR001	Lateral Sclerosis	54	0.064

159	P	RCT021	Rectum Cancer	52	0.064

160		INT079	Intrahepatic Cholangiocarcinoma	51	0.064

161	P	HYP265	Hypotonia	43	0.064

162		CYT002	Cytokine Deficiency	42	0.064

163	P	KLZ004	Kala-Azar 1	41	0.064

164		HMC030	Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency	13	0.064

165	P	LNG032	Lung Cancer	98	0.059

166	c	HYP595	Hypertension, Essential	84	0.059

167		STR067	Stroke, Ischemic	81	0.059

168	P	BLD134	Bladder Cancer	79	0.059

169		OST012	Osteoarthritis	78	0.059

170	P	PRK057	Parkinson Disease, Late-Onset	78	0.059

171	P	KDN018	Kidney Disease	72	0.059

172	P	EPL164	Epilepsy	71	0.059

173	P	MYP004	Myopathy	70	0.059

174	P	MLN008	Melanoma	69	0.059

175	c	MGR028	Migraine with or Without Aura 1	67	0.059

176		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.059

177	P	MSC005	Muscular Dystrophy	66	0.059

178		CRN036	Craniopharyngioma	65	0.059

179	P	PLM036	Pulmonary Fibrosis	65	0.059

180	c	HPT003	Hepatitis a	62	0.059

181	c	BRN108	Branchiootic Syndrome 1	62	0.059

182		ALC006	Alcoholic Hepatitis	61	0.059

183	P	BNG030	Benign Ependymoma	60	0.059

184	c	HPT016	Hepatitis B	59	0.059

185		THR024	Thrombosis	57	0.059

186	P	BPL003	Bipolar Disorder	56	0.059

187		BRN004	Brain Edema	56	0.059

188	P	MLN007	Male Infertility	55	0.059

189		HYP060	Hyperinsulinism	54	0.059

190		CLL010	Cellular Ependymoma	54	0.059

191	P	ART021	Arteriosclerosis	54	0.059

192	P	CNT005	Central Nervous System Lymphoma	53	0.059

193		PNG002	Pain Agnosia	51	0.059

194		OCL069	Ocular Motor Apraxia	51	0.059

195		CCC002	Coccidiosis	51	0.059

196		END086	End Stage Renal Disease	51	0.059

197	P	TMP001	Temporal Lobe Epilepsy	50	0.059

198	P	OBS001	Obstructive Jaundice	50	0.059

199		HMC041	Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity	48	0.059

200	c	PRM226	Primary Central Nervous System Lymphoma	48	0.059

201	P	BNG032	Benign Mesothelioma	46	0.059

202		URL001	Urolithiasis	45	0.059

203	c	MJR024	Major Affective Disorder 9	41	0.059

204		ALL014	Allergic Encephalomyelitis	38	0.059

205	c	MJR022	Major Affective Disorder 8	38	0.059

206		HRW001	Hair Whorl	36	0.059

207		PYR016	Pyridoxine Deficiency	30	0.059

208	P	GLM040	Glioma Susceptibility 1	81	0.054

209	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.054

210		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.054

211	P	RTN024	Retinoblastoma	73	0.054

212		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.054

213		HMN044	Human Immunodeficiency Virus Type 1	71	0.054

214	P	SRC025	Sarcoidosis 1	70	0.054

215	P	MYC007	Myocardial Infarction	70	0.054

216		EWN003	Ewing Sarcoma	69	0.054

217		CRB039	Cerebrovascular Disease	67	0.054

218		OST159	Osteogenic Sarcoma	66	0.054

219		CLF027	Cleft Palate, Isolated	64	0.054

220		ANR007	Anorexia Nervosa	63	0.054

221		DRM006	Dermatitis	61	0.054

222		GST033	Gestational Diabetes	61	0.054

223	P	INF032	Infertility	57	0.054

224		IRN002	Iron Metabolism Disease	57	0.054

225		SFT003	Soft Tissue Sarcoma	56	0.054

226		MCS002	Mucositis	56	0.054

227	P	PLY019	Polyneuropathy	56	0.054

228	P	DRR001	Diarrhea	55	0.054

229	P	PTT006	Pituitary Adenoma	55	0.054

230		MTH054	Methylmalonic Aciduria and Homocystinuria, Cblc Type	54	0.054

231	P	TRM003	Tremor	54	0.054

232	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	53	0.054

233		PRN011	Pernicious Anemia	53	0.054

234	c	FML008	Familial Retinoblastoma	53	0.054

235		STM007	Stomatitis	50	0.054

236		47X002	47,xyy	49	0.054

237		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.054

238		CYS019	Cystathioninuria	45	0.054

239		HMP009	Haemophilus Influenzae	43	0.054

240		ANX004	Anoxia	40	0.054

241		SCR011	Scrapie	39	0.054

242	c	LKM005	Leukemia, T-Cell, Chronic	34	0.054

243		MLR004	Malaria	81	0.048

244		CRV035	Cervical Cancer	76	0.048

245		ULC004	Ulcerative Colitis	73	0.048

246	P	MLT020	Multiple Sclerosis	72	0.048

247	P	HNT016	Huntington Disease	72	0.048

248		WLS001	Wilson Disease	71	0.048

249		LYM133	Lymphoma, Hodgkin, Classic	69	0.048

250		BRN024	Bronchitis	68	0.048

251	P	TRN020	Turner Syndrome	67	0.048

252	c	RHB024	Rhabdomyosarcoma 2	67	0.048

253		PRT037	Pertussis	65	0.048

254	P	HRP006	Herpes Simplex	65	0.048

255		TBC004	Tobacco Addiction	64	0.048

256		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.048

257	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.048

258		TRN015	Transient Cerebral Ischemia	63	0.048

259	c	SVR001	Severe Acute Respiratory Syndrome	62	0.048

260	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.048

261	P	PRP029	Porphyria	62	0.048

262		THY029	Thyroid Carcinoma	59	0.048

263		CYS010	Cystinosis	59	0.048

264	P	TYR004	Tyrosinemia	58	0.048

265		FBR047	Fibromyalgia	58	0.048

266	P	GLM007	Glomerulonephritis	57	0.048

267	c	ACT134	Acute Liver Failure	56	0.048

268		DFF005	Diffuse Large B-Cell Lymphoma	55	0.048

269		HMS001	Hemosiderosis	54	0.048

270		PPL022	Papilloma	54	0.048

271		MST005	Mastitis	53	0.048

272	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.048

273		PTH003	Pathologic Nystagmus	52	0.048

274	c	INF145	Infantile Liver Failure Syndrome 1	50	0.048

275		VCC001	Vaccinia	49	0.048

276		ATS010	Autosomal Recessive Disease	48	0.048

277		MCR020	Microsporidiosis	48	0.048

278		LYM019	Lymphosarcoma	46	0.048

279		MXD026	Mixed Glioma	45	0.048

280		CYS009	Cystadenoma	44	0.048

281		KWS001	Kwashiorkor	44	0.048

282	c	MLG079	Malignant Pleural Mesothelioma	42	0.048

283		49X006	49, Xxxxy Syndrome	41	0.048

284	P	MLG074	Malignant Mesenchymoma	40	0.048

285		AMN002	Amino Acid Metabolic Disorder	39	0.048

286	P	VSC018	Visceral Steatosis	33	0.048

287	c	BLR024	Biliary Cirrhosis, Primary, 1	30	0.048

288		HYP814	Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency	29	0.048

289		ARG004	Argyria	27	0.048

290		ESP021	Esophageal Cancer	90	0.042

291	c	SYS001	Systemic Lupus Erythematosus	86	0.042

292	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.042

293		CNN003	Conn's Syndrome	79	0.042

294		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.042

295		KPS004	Kaposi Sarcoma	75	0.042

296		PHN003	Phenylketonuria	75	0.042

297		ADR007	Adrenoleukodystrophy	75	0.042

298	P	RSP003	Respiratory Failure	74	0.042

299		LPT014	Leptin Deficiency or Dysfunction	74	0.042

300	P	OST002	Osteoporosis	74	0.042

301	P	CNR004	Cone-Rod Dystrophy 2	73	0.042

302		ANX010	Anxiety	73	0.042

303		ACR007	Acromegaly	71	0.042

304		PRP027	Peripheral Vascular Disease	71	0.042

305	c	CHR684	Chronic Kidney Disease	70	0.042

306		ADL002	Adult Syndrome	70	0.042

307	P	HYP086	Hypothyroidism	69	0.042

308		ART016	Aortic Aneurysm	69	0.042

309	P	INF038	Influenza	68	0.042

310		PNC129	Pancreatic Adenocarcinoma	68	0.042

311	P	PLM037	Pulmonary Hypertension	67	0.042

312		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.042

313		TTN003	Tetanus	65	0.042

314	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.042

315		PRP001	Propionic Acidemia	65	0.042

316		BRR014	Barrett Esophagus	65	0.042

317	P	DBT009	Diabetes Mellitus	64	0.042

318	P	ANR048	Aniridia 1	63	0.042

319		SKN016	Skin Disease	63	0.042

320		CLT003	Colitis	62	0.042

321	P	HYP750	Hypertriglyceridemia, Familial	62	0.042

322	c	PNS012	Paine Syndrome	61	0.042

323		DPH001	Diphtheria	60	0.042

324	c	ACT027	Acute Pancreatitis	60	0.042

325		ACN002	Acanthosis Nigricans	60	0.042

326		SQM006	Squamous Cell Carcinoma	60	0.042

327		STT001	Status Epilepticus	60	0.042

328	P	THL005	Thalassemia	60	0.042

329	P	MCR010	Microcephaly	59	0.042

330		CHL014	Cholera	59	0.042

331	P	CYS018	Cystitis	59	0.042

332		ANR040	Aneurysm	59	0.042

333		PPT005	Peptic Ulcer Disease	59	0.042

334		INC002	Inclusion Body Myositis	58	0.042

335		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.042

336	P	PLV020	Pelvic Organ Prolapse	57	0.042

337	P	FBR017	Fibrosarcoma	56	0.042

338	P	NRP001	Neuropathy	56	0.042

339		BCT022	Bacterial Infectious Disease	56	0.042

340		SPN041	Spinal Cord Disease	56	0.042

341		HYP005	Hypokalemia	55	0.042

342	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.042

343		VSC003	Visceral Leishmaniasis	55	0.042

344	P	ACT010	Acth-Secreting Pituitary Adenoma	55	0.042

345		FCL014	Focal Epilepsy	54	0.042

346	P	INF037	Inflammatory Bowel Disease	54	0.042

347		PLM012	Pulmonary Sarcoidosis	53	0.042

348	P	PLM006	Pulmonary Alveolar Proteinosis	53	0.042

349		GST023	Gastric Ulcer	53	0.042

350	c	GLL024	Gallbladder Disease 1	53	0.042

351	c	VRL010	Viral Hepatitis	52	0.042

352		GLM004	Gliomatosis Cerebri	52	0.042

353		PLS009	Plasma Cell Neoplasm	51	0.042

354	P	THR015	Thrombophilia	51	0.042

355	P	CHL066	Cholangitis	51	0.042

356		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.042

357	P	OVR082	Overgrowth Syndrome	50	0.042

358	P	ECL001	Eclampsia	50	0.042

359		PLC008	Placenta Disease	50	0.042

360		FTL002	Fatal Familial Insomnia	49	0.042

361		ENT004	Enthesopathy	49	0.042

362	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.042

363		ANT018	Anthracosis	48	0.042

364		CNT033	Central Nervous System Cancer	47	0.042

365	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.042

366		GRW007	Growth Hormone Deficiency	46	0.042

367		SQM002	Squamous Cell Papilloma	46	0.042

368		KR002	Kuru	45	0.042

369		PTT037	Pituitary Tumors	44	0.042

370		MCR017	Macrocytic Anemia	44	0.042

371		MRG013	Mirage Syndrome	43	0.042

372	c	SRC023	Sarcoidosis 2	43	0.042

373	P	MJR007	Major Affective Disorder 1	43	0.042

374	P	CLS010	Cluster Headache	42	0.042

375	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.042

376	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.042

377		GRM004	Germinoma	40	0.042

378		CRV045	Cervical Intraepithelial Neoplasia	39	0.042

379		LWG005	Low-Grade Astrocytoma	38	0.042

380		ADR022	Adrenomyeloneuropathy	38	0.042

381		MTH056	Methylmalonic Aciduria and Homocystinuria, Cblf Type	38	0.042

382		DYS006	Dysembryoplastic Neuroepithelial Tumor	38	0.042

383		CRY036	Cryptogenic Cirrhosis	36	0.042

384		OLG006	Oligoastrocytoma	35	0.042

385		ATX010	Ataxia Neuropathy Spectrum	34	0.042

386		BRN034	Brain Meningioma	33	0.042

387		ACT064	Acute Necrotizing Encephalitis	33	0.042

388	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.042

389	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.042

390		PLY150	Polykaryocytosis Inducer	31	0.042

391		ISL099	Isolated Methylmalonic Acidemia	29	0.042

392		MTH051	Methylmalonic Aciduria and Homocystinuria, Cblj Type	28	0.042

393		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	26	0.042

394		PRS131	Prostate Cancer/brain Cancer Susceptibility	25	0.042

395		AMN012	Aminoacidopathies	21	0.042

396		BLD137	Blood Group--Ahonen	16	0.042

397		IMM167	Immune Deficiency Disease	78	0.034

398		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.034

399	P	LNG064	Lung Cancer Susceptibility 3	78	0.034

400		SVR004	Severe Combined Immunodeficiency	73	0.034

401		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.034

402		CNG034	Congestive Heart Failure	69	0.034

403	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.034

404	P	ART022	Arthritis	69	0.034

405		SKN019	Skin Melanoma	68	0.034

406	P	THR014	Thrombocytopenia	67	0.034

407	P	CRD119	Cardiac Arrest	67	0.034

408		FCT007	Factor Vii Deficiency	67	0.034

409		BRK010	Burkitt Lymphoma	67	0.034

410	P	FLL037	Follicular Lymphoma	67	0.034

411		THY111	Thyroid Carcinoma, Familial Medullary	67	0.034

412	P	CHR012	Chronic Granulomatous Disease	67	0.034

413		PSY004	Psychotic Disorder	67	0.034

414	P	PRP003	Porphyria Cutanea Tarda	67	0.034

415	c	ATS007	Autism Spectrum Disorder	67	0.034

416	c	TYR012	Tyrosinemia, Type I	66	0.034

417		ANG054	Angina Pectoris	66	0.034

418	c	FML021	Familial Hypercholesterolemia	66	0.034

419	P	ATR011	Atrial Fibrillation	66	0.034

420	P	DRM053	Dermatitis, Atopic	66	0.034

421	c	MCL013	Mucolipidosis Iv	66	0.034

422	c	FML001	Familial Atrial Fibrillation	65	0.034

423	P	VNW001	Von Willebrand's Disease	65	0.034

424		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.034

425		MND021	Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome	65	0.034

426	c	DBT099	Diabetes Mellitus, Type I	65	0.034

427		PTT048	Pituitary Adenoma, Prolactin-Secreting	65	0.034

428		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.034

429	P	PRD008	Periodontitis	64	0.034

430		PLM031	Poliomyelitis	64	0.034

431		HYP020	Hyperprolactinemia	64	0.034

432		OST017	Osteomyelitis	64	0.034

433		PLG002	Plague	63	0.034

434	c	MLG084	Malignant Fibrous Histiocytoma	63	0.034

435	P	PSR002	Psoriasis	62	0.034

436		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.034

437	P	ART023	Arthropathy	62	0.034

438	P	VSC011	Vasculitis	62	0.034

439		ALL026	Allergic Hypersensitivity Disease	62	0.034

440		GLY010	Glycine Encephalopathy	62	0.034

441	c	SCL052	Scleroderma, Familial Progressive	61	0.034

442	P	ENC004	Encephalitis	61	0.034

443		CHR066	Chronic Fatigue Syndrome	61	0.034

444	c	WLM018	Wilms Tumor 5	61	0.034

445		VRL011	Viral Infectious Disease	61	0.034

446	P	KDN017	Kidney Cancer	60	0.034

447	P	SNS001	Sensorineural Hearing Loss	60	0.034

448	c	ACT071	Acute Kidney Failure	60	0.034

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

450		PRT013	Portal Hypertension	59	0.034

451	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.034

452		CHL123	Chlamydia	59	0.034

453	P	PRD006	Prader-Willi Syndrome	59	0.034

454	P	BRS044	Breast Adenocarcinoma	59	0.034

455	P	DNG005	Dengue Virus	59	0.034

456		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.034

457	P	SYP003	Syphilis	58	0.034

458		CNS004	Constipation	58	0.034

459		GLS018	Glass Syndrome	57	0.034

460	c	ACT075	Acute Myocardial Infarction	57	0.034

461	c	MST023	Mesothelioma, Malignant	57	0.034

462		SCH014	Schistosomiasis	57	0.034

463	P	PLY011	Polycystic Ovary Syndrome	56	0.034

464		TRN018	Transitional Cell Carcinoma	56	0.034

465		PLS011	Plasmacytoma	56	0.034

466		ANN002	Anencephaly	56	0.034

467		HMG005	Hemoglobinopathy	56	0.034

468		SLC006	Silicosis	56	0.034

469	P	HYP076	Hyperthyroidism	55	0.034

470	P	DBT005	Diabetes Insipidus	55	0.034

471		PRP030	Purpura	54	0.034

472		HMN009	Hemangioblastoma	54	0.034

473		AMN003	Amnestic Disorder	54	0.034

474		GLC003	Glucose Intolerance	54	0.034

475		GNG004	Ganglioglioma	54	0.034

476	P	ALP008	Alopecia	54	0.034

477	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.034

478		THR013	Thoracic Outlet Syndrome	54	0.034

479		SLP001	Sleeping Sickness	54	0.034

480	c	HNT010	Huntington Disease-Like 1	53	0.034

481		CRH005	Crohn's Colitis	53	0.034

482	P	RTN016	Retinal Degeneration	53	0.034

483		FNG017	Fungal Infectious Disease	53	0.034

484		CLF001	Cleft Lip	53	0.034

485	P	RTN022	Retinal Vein Occlusion	53	0.034

486		ALC009	Alcoholic Liver Cirrhosis	53	0.034

487	P	SML001	Small Cell Carcinoma	52	0.034

488		PST011	Pustulosis of Palm and Sole	52	0.034

489	P	MSC003	Muscular Atrophy	52	0.034

490		MTH078	Methylmalonic Aciduria, Cblb Type	51	0.034

491		CLR109	Colorectal Adenocarcinoma	51	0.034

492		TRM010	Traumatic Brain Injury	51	0.034

493		FBR008	Fibrillary Astrocytoma	51	0.034

494	c	SCN007	Secondary Hyperparathyroidism	51	0.034

495		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.034

496		HYP781	Hypoascorbemia	51	0.034

497	c	HNT004	Huntington Disease-Like 2	50	0.034

498		FLT009	Folate Malabsorption, Hereditary	50	0.034

499		THY125	Thyroid Gland Medullary Carcinoma	50	0.034

500		TRY001	Trypanosomiasis	50	0.034

501		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	49	0.034

502	P	END046	Endometritis	49	0.034

503		CHL004	Cholelithiasis	49	0.034

504	c	BPL002	Bipolar I Disorder	49	0.034

505		URM002	Uremia	49	0.034

506		BCT004	Bacteriuria	49	0.034

507		BNR002	Bone Resorption Disease	48	0.034

508		BBS001	Babesiosis	48	0.034

509		PLC007	Placental Abruption	48	0.034

510		CLF056	Cleft Lip with or Without Cleft Palate	47	0.034

511		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.034

512		LPD004	Lipoid Nephrosis	46	0.034

513		CNT019	Central Neurocytoma	46	0.034

514	P	BRB001	Beriberi	46	0.034

515	P	MTH007	Methemoglobinemia	46	0.034

516		EPD015	Epidemic Typhus	45	0.034

517		CRB004	Cerebral Artery Occlusion	45	0.034

518	c	HYP793	Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1	45	0.034

519	P	CHR345	Chronic Pain	44	0.034

520		PPL001	Papillary Adenoma	44	0.034

521		ANP009	Anaplastic Oligodendroglioma	43	0.034

522		FNC007	Functioning Pituitary Adenoma	43	0.034

523		MDD018	Middle East Respiratory Syndrome	43	0.034

524		ATX019	Ataxia with Vitamin E Deficiency	42	0.034

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

526		MYF002	Myofascial Pain Syndrome	42	0.034

527		PLM020	Pleomorphic Xanthoastrocytoma	41	0.034

528		HPR006	Heparin Cofactor Ii Deficiency	40	0.034

529	c	PLM150	Pulmonary Alveolar Proteinosis, Acquired	40	0.034

530		CRB086	Cerebral Aneurysms	40	0.034

531		SCR015	Scarlet Fever	39	0.034

532		PTT003	Pituitary-Dependent Cushing's Disease	39	0.034

533		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.034

534	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.034

535		ANT019	Anterograde Amnesia	38	0.034

536		AMN006	Aminoaciduria	38	0.034

537		ATM052	Autoimmune Disease 1	37	0.034

538	P	CRB088	Cerebral Atrophy	37	0.034

539	c	PLZ002	Pelizaeus-Merzbacher-Like Disease	36	0.034

540	c	MJR008	Major Affective Disorder 2	35	0.034

541	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.034

542	c	MJR023	Major Affective Disorder 7	33	0.034

543		MCR025	Microhydranencephaly	33	0.034

544	c	MJR003	Major Affective Disorder 6	33	0.034

545	c	MJR006	Major Affective Disorder 5	33	0.034

546		HLT002	Halothane Hepatitis	32	0.034

547		WLD005	Wild Type Attr Amyloidosis	32	0.034

548		HGH041	High-Grade Astrocytoma	32	0.034

549		FNT004	Fainting	30	0.034

550		ANP008	Anaplastic Oligoastrocytoma	30	0.034

551		ACT228	Acute Radiation Syndrome	29	0.034

552	c	DFN116	Deafness, Autosomal Recessive 74	29	0.034

553		MYC088	Mycobacterium Avium Complex Infections	29	0.034

554	c	MJR004	Major Affective Disorder 4	28	0.034

555		MST020	Mast Cell Activation Syndrome	26	0.034

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

557		HRP008	Herpes Simiae	25	0.034

558		ADG002	Audiogenic Seizures	25	0.034

559		PRN071	Parenteral Nutrition-Associated Cholestasis	25	0.034

560		AND005	Androgen Insensitivity Syndrome, Mild	19	0.034

561	P	INB001	Inborn Amino Acid Metabolism Disorder	10	0.034

562	c	LKM061	Leukemia, Acute Myeloid	84	0.024

563	P	RHM011	Rheumatoid Arthritis	80	0.024

564	c	NRF023	Neurofibromatosis, Type Ii	80	0.024

565	c	DLT002	Dilated Cardiomyopathy	79	0.024

566	P	RTN008	Retinitis Pigmentosa	79	0.024

567	P	LYN001	Lynch Syndrome	77	0.024

568	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.024

569		END057	Endometrial Cancer	74	0.024

570		SCK003	Sickle Cell Anemia	74	0.024

571	c	BTT014	Beta-Thalassemia	74	0.024

572		CRH001	Crohn's Disease	74	0.024

573		MSC157	Muscular Dystrophy, Duchenne Type	72	0.024

574	P	FML011	Familial Adenomatous Polyposis	72	0.024

575		OTT002	Otitis Media	72	0.024

576		GST040	Gastric Adenocarcinoma	70	0.024

577		MYL009	Myelodysplastic Syndrome	70	0.024

578		LGH007	Leigh Syndrome	70	0.024

579	c	EPL184	Epileptic Encephalopathy, Early Infantile, 6	70	0.024

580		ADN011	Adenoid Cystic Carcinoma	70	0.024

581	P	TTR001	Tetralogy of Fallot	70	0.024

582	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	70	0.024

583	c	PNC108	Pancreatitis, Hereditary	70	0.024

584	c	PRG042	Progressive Familial Heart Block, Type Ia	69	0.024

585	P	MPL001	Maple Syrup Urine Disease	69	0.024

586	P	ANG001	Angelman Syndrome	69	0.024

587	P	SYS005	Systemic Scleroderma	68	0.024

588	P	MYC084	Mycobacterium Tuberculosis 1	68	0.024

589	P	MYS003	Myasthenia Gravis	68	0.024

590	P	HML033	Hemolytic Uremic Syndrome, Atypical 1	68	0.024

591		CNN005	Connective Tissue Disease	68	0.024

592		RCK004	Rickets	68	0.024

593		GST092	Gastroesophageal Reflux	67	0.024

594		OMN001	Omenn Syndrome	67	0.024

595		CRP001	Carpal Tunnel Syndrome	67	0.024

596		ALP100	Alpha-Thalassemia/mental Retardation Syndrome, X-Linked	66	0.024

597	P	NSP012	Nasopharyngeal Carcinoma	66	0.024

598	P	MCR115	Microvascular Complications of Diabetes 5	66	0.024

599	c	AMY087	Amyloidosis, Hereditary, Transthyretin-Related	66	0.024

600		AND002	Androgen Insensitivity Syndrome	66	0.024

601	P	MNN013	Meningitis	66	0.024

602		KHL003	Kohlschutter-Tonz Syndrome	65	0.024

603	P	AGM001	Agammaglobulinemia	65	0.024

604	P	DYS154	Dystonia	65	0.024

605		KRT019	Keratitis, Hereditary	65	0.024

606	P	MTR014	Motor Neuron Disease	65	0.024

607		IRR002	Irritable Bowel Syndrome	65	0.024

608		CHY002	Chylomicron Retention Disease	65	0.024

609	c	WLM013	Wilms Tumor 1	65	0.024

610	P	ADL010	Adult Respiratory Distress Syndrome	65	0.024

611	P	THY023	Thymoma	65	0.024

612	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.024

613	P	CHR071	Charcot-Marie-Tooth Disease	65	0.024

614		PTT046	Pituitary Hormone Deficiency, Combined, 2	64	0.024

615	P	GLC113	Galactosemia I	64	0.024

616		DGR001	Digeorge Syndrome	64	0.024

617	P	NTR004	Neutropenia	63	0.024

618		TYP007	Typhoid Fever	63	0.024

619		ACT119	Acute Promyelocytic Leukemia	63	0.024

620	c	OPT053	Optic Atrophy 1	63	0.024

621	c	ALP101	Alpha-Thalassemia	62	0.024

622	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.024

623	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.024

624	P	PLY014	Polycystic Kidney Disease	62	0.024

625	P	FCS012	Facioscapulohumeral Muscular Dystrophy 1	62	0.024

626	P	BCK002	Beckwith-Wiedemann Syndrome	62	0.024

627		LSC001	Lesch-Nyhan Syndrome	62	0.024

628	c	ANM038	Anemia, Autoimmune Hemolytic	62	0.024

629		HSH003	Hashimoto Thyroiditis	62	0.024

630		CTN007	Cutaneous Leishmaniasis	62	0.024

631		MDD011	Mood Disorder	62	0.024

632		TXC005	Toxic Shock Syndrome	62	0.024

633		MSL001	Measles	62	0.024

634	P	INT143	Interstitial Cystitis	61	0.024

635	P	SJG008	Sjogren Syndrome	61	0.024

636		ARG002	Argininosuccinic Aciduria	61	0.024

637	P	LPS004	Lupus Erythematosus	61	0.024

638		SPN186	Spinal Cord Injury	60	0.024

639		HRP004	Herpes Zoster	60	0.024

640	P	TST021	Testicular Germ Cell Tumor	60	0.024

641	P	VNT002	Ventricular Septal Defect	60	0.024

642		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.024

643	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.024

644		VRC005	Varicose Veins	60	0.024

645		CHC001	Chickenpox	60	0.024

646		INS001	Insulinoma	60	0.024

647		ETN001	Eating Disorder	60	0.024

648		ANT009	Antithrombin Iii Deficiency	59	0.024

649		SPP011	Suppression of Tumorigenicity 12	59	0.024

650	P	MYC008	Myocarditis	59	0.024

651	P	AXN002	Axenfeld-Rieger Syndrome	59	0.024

652	P	LKD001	Leukodystrophy	59	0.024

653	P	BRN022	Bronchiectasis	59	0.024

654	P	SLP005	Sleep Disorder	59	0.024

655		PLM033	Pulmonary Embolism	59	0.024

656		PRG009	Progressive Multifocal Leukoencephalopathy	59	0.024

657		AVN001	Avian Influenza	59	0.024

658		GST045	Gastroenteritis	59	0.024

659		GLB001	Gilbert Syndrome	58	0.024

660		ANT024	Anthrax Disease	58	0.024

661		PST028	Post-Traumatic Stress Disorder	58	0.024

662	P	INT070	Intestinal Obstruction	58	0.024

663		RBS001	Rabies	58	0.024

664		CMP010	Complex Regional Pain Syndrome	58	0.024

665	P	MMP001	Mumps	58	0.024

666		CHL028	Childhood Type Dermatomyositis	58	0.024

667		LYM027	Lymphopenia	58	0.024

668	P	CND004	Candidiasis	58	0.024

669	P	PRP019	Peripheral Nervous System Disease	58	0.024

670		LNG108	Langerhans Cell Histiocytosis	58	0.024

671	P	GLL018	Gallbladder Cancer	57	0.024

672	c	CHL119	Cholangitis, Primary Sclerosing	57	0.024

673		ARG007	Argininemia	57	0.024

674	P	FTL001	Fetal Alcohol Syndrome	57	0.024

675		BLR008	Bilirubin Metabolic Disorder	57	0.024

676	P	CTR177	Citrullinemia, Type Ii, Adult-Onset	57	0.024

677		CYT008	Cytomegalovirus Infection	57	0.024

678	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.024

679		PPL058	Papilloma of Choroid Plexus	56	0.024

680	P	PLY018	Polycythemia	56	0.024

681	P	ADL017	Adult T-Cell Leukemia	56	0.024

682	P	MLT074	Multiple Endocrine Neoplasia	56	0.024

683		ERY051	Erythroleukemia, Familial	56	0.024

684	P	MTC069	Mitochondrial Disorders	56	0.024

685	P	TMR010	Tumor Predisposition Syndrome	56	0.024

686		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.024

687	P	NRF002	Neurofibromatosis	56	0.024

688		GRS011	Gerstmann-Straussler Disease	56	0.024

689	P	PNM006	Pneumoconiosis	56	0.024

690	P	RST002	Restrictive Cardiomyopathy	56	0.024

691		AND020	Androgen Insensitivity, Partial	56	0.024

692	P	GST044	Gastritis	56	0.024

693		HPT022	Hepatoblastoma	56	0.024

694	c	CHR627	Charcot-Marie-Tooth Disease, Demyelinating, Type 1a	55	0.024

695	P	AGN002	Agnosia	55	0.024

696		ICH001	Ichthyosis Vulgaris	55	0.024

697		AMB001	Amebiasis	55	0.024

698	c	BCT007	Bacterial Meningitis	55	0.024

699	P	PLM034	Pulmonary Emphysema	55	0.024

700	P	GRV001	Graves' Disease	55	0.024

701		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.024

702		GNG005	Gangliocytoma	55	0.024

703		PRN001	Purine Nucleoside Phosphorylase Deficiency	55	0.024

704		HMZ003	Homozygous Familial Hypercholesterolemia	55	0.024

705	P	LRY044	Larynx Cancer	55	0.024

706		SYN007	Synovitis	54	0.024

707		TRD006	Tardive Dyskinesia	54	0.024

708		GLS001	Gliosarcoma	54	0.024

709	P	FML068	Familial Hypocalciuric Hypercalcemia	54	0.024

710		LYM040	Lymphoblastic Lymphoma	54	0.024

711		WST005	West Nile Virus	54	0.024

712		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.024

713		CLL003	Cellulitis	54	0.024

714	P	TCD001	Tic Disorder	53	0.024

715	c	CNT016	Central Retinal Vein Occlusion	53	0.024

716	P	CRB194	Cerebroretinal Microangiopathy with Calcifications and Cysts 1	53	0.024

717		ENC055	Encephalopathy, Ethylmalonic	53	0.024

718	P	HML001	Hemolytic-Uremic Syndrome	53	0.024

719	P	SHR001	Short Bowel Syndrome	53	0.024

720		GTR002	Goiter	53	0.024

721		GSG001	Gas Gangrene	53	0.024

722	P	INT068	Intestinal Disease	53	0.024

723		TRC008	Trachoma	53	0.024

724		OVR059	Ovary Adenocarcinoma	53	0.024

725	c	MCR113	Microvascular Complications of Diabetes 3	52	0.024

726		DMY004	Demyelinating Disease	52	0.024

727		PLM014	Pleomorphic Adenoma	52	0.024

728		CRB151	Cerebral Creatine Deficiency Syndrome 1	52	0.024

729		DYS015	Dysentery	52	0.024

730		THY030	Thyroid Gland Disease	52	0.024

731	P	CNG436	Congenital Disorder of Deglycosylation	52	0.024

732	c	THY107	Thymoma, Familial	52	0.024

733	P	THY032	Thyroiditis	52	0.024

734		FML037	Female Breast Cancer	52	0.024

735	P	TRT010	Teratoma	52	0.024

736		RYS001	Reye Syndrome	51	0.024

737	c	PNC106	Pancreatic Agenesis 1	51	0.024

738	P	LCT001	Lactic Acidosis	51	0.024

739		MYL020	Myelomeningocele	51	0.024

740		NRM004	Neuroma	51	0.024

741	c	PTT057	Pituitary Adenoma 4, Acth-Secreting	51	0.024

742		TLR001	Tularemia	51	0.024

743	P	HYP040	Hypospadias	51	0.024

744	c	MTC063	Mitochondrial Dna Depletion Syndrome 3	51	0.024

745		HYP081	Hypolipoproteinemia	51	0.024

746		RSP002	Respiratory Syncytial Virus Infectious Disease	51	0.024

747	P	MMB011	Membranous Nephropathy	50	0.024

748	P	HYP077	Hypertrichosis	50	0.024

749		PLR008	Pleurisy	50	0.024

750		MTH076	Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency	50	0.024

751		RTN003	Retinal Ischemia	50	0.024

752		ABN011	Abnormal Hair, Joint Laxity, and Developmental Delay	50	0.024

753		HPT014	Hepatorenal Syndrome	50	0.024

754		AZS001	Azoospermia	50	0.024

755		CRT013	Carotid Stenosis	50	0.024

756	c	THY112	Thyroid Hormone Resistance, Generalized, Autosomal Dominant	50	0.024

757		NTR046	Neutrophil Migration	50	0.024

758	c	LRG001	Large Cell Carcinoma	50	0.024

759	c	VNW010	Von Willebrand Disease, Type 2	50	0.024

760		NPH010	Nephrosclerosis	50	0.024

761		HYP017	Hypophosphatemia	50	0.024

762		RBF001	Riboflavin Deficiency	49	0.024

763		LFT001	Left Bundle Branch Hemiblock	49	0.024

764	c	L2H001	L-2-Hydroxyglutaric Aciduria	49	0.024

765		SPT005	Spotted Fever	49	0.024

766	P	CRV031	Cervical Adenocarcinoma	49	0.024

767		DYS009	Dysthymic Disorder	49	0.024

768		BRN071	Brain Injury	49	0.024

769		MTC005	Mitochondrial Metabolism Disease	49	0.024

770	P	CNG003	Congenital Dyserythropoietic Anemia	49	0.024

771	P	MGR001	Migraine Without Aura	49	0.024

772		HST010	Histiocytosis	48	0.024

773		HYP043	Hyperandrogenism	48	0.024

774		OLF005	Olfactory Neuroblastoma	48	0.024

775	P	SCL009	Sclerosing Cholangitis	48	0.024

776	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.024

777		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.024

778	P	RNV001	Renovascular Hypertension	48	0.024

779		PNC034	Pancreas Disease	48	0.024

780		SPL018	Splenomegaly	48	0.024

781		CHL147	Chlamydia Pneumonia	48	0.024

782		FBR009	Fibrous Dysplasia	48	0.024

783	P	TRT019	Torticollis	48	0.024

784		MLT006	Multidrug-Resistant Tuberculosis	48	0.024

785		ART004	Aortic Atherosclerosis	47	0.024

786		SXL003	Sexual Disorder	47	0.024

787		PHS004	Phosphoribosylpyrophosphate Synthetase Superactivity	47	0.024

788		PRC003	Proctitis	47	0.024

789		NDL007	Nodular Goiter	47	0.024

790		RNL077	Renal Fibrosis	47	0.024

791		ACT084	Acute Stress Disorder	47	0.024

792	c	MCR120	Microvascular Complications of Diabetes 7	47	0.024

793		KRT002	Keratomalacia	47	0.024

794		HYP082	Hypopharynx Cancer	47	0.024

795		RTN023	Retinitis	46	0.024

796		ATN005	Autonomic Dysfunction	46	0.024

797		TTH006	Tooth Disease	46	0.024

798		MYL013	Myeloperoxidase Deficiency	46	0.024

799	c	ALP104	Alport Syndrome 3, Autosomal Dominant	46	0.024

800		CRB196	Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome	46	0.024

801	P	PLL002	Pellagra	46	0.024

802		TRP008	Tropical Calcific Pancreatitis	46	0.024

803		MYX001	Myxopapillary Ependymoma	46	0.024

804		VGN019	Vaginal Discharge	46	0.024

805		CWP001	Cowpox	46	0.024

806	c	DRR009	Diarrhea 6	46	0.024

807		TRN022	Transcobalamin Ii Deficiency	45	0.024

808	c	HRD039	Hereditary Amyloidosis	45	0.024

809		URT010	Ureteral Obstruction	45	0.024

810		HMR023	Hemorrhagic Cystitis	45	0.024

811		LYD001	Leydig Cell Tumor	45	0.024

812		STS002	Situs Inversus	45	0.024

813		SWN001	Swine Influenza	45	0.024

814		BRN032	Brain Glioma	45	0.024

815		CRT015	Carotid Artery Occlusion	45	0.024

816		MLN073	Melanosis, Neurocutaneous	45	0.024

817		SPS057	Spasticity	45	0.024

818		DBT090	Diabetes and Deafness, Maternally Inherited	44	0.024

819	c	ATS204	Autosomal Recessive Non-Syndromic Intellectual Disability	44	0.024

820		DWR001	Dwarfism	44	0.024

821		LRY018	Laryngeal Squamous Cell Carcinoma	44	0.024

822	P	FBR003	Fibrous Histiocytoma	44	0.024

823	c	RNG023	Ring Chromosome 7	44	0.024

824		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.024

825		CLN003	Clonorchiasis	44	0.024

826	c	PRM038	Primary Agammaglobulinemia	44	0.024

827		CVD001	Covid-19	44	0.024

828		ADN022	Adenylosuccinase Deficiency	44	0.024

829		BNM001	Bone Marrow Cancer	43	0.024

830		GLL017	Gallbladder Adenocarcinoma	43	0.024

831		ENC005	Encephalomalacia	43	0.024

832		SDD008	Sudden Sensorineural Hearing Loss	43	0.024

833		LWC001	Low Compliance Bladder	43	0.024

834		RTC009	Reticulum Cell Sarcoma	43	0.024

835		PNM013	Pneumococcal Meningitis	42	0.024

836	P	CTR077	Citrullinemia, Type Ii, Neonatal-Onset	42	0.024

837	c	AGR019	Age-Related Hearing Loss	42	0.024

838		MRS001	Marasmus	42	0.024

839		SNL007	Senile Cataract	42	0.024

840	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.024

841		NRR001	Neuroretinitis	42	0.024

842		ANC002	Anca-Associated Vasculitis	41	0.024

843	c	MCR130	Microvascular Complications of Diabetes 6	41	0.024

844	c	MCR133	Microvascular Complications of Diabetes 4	41	0.024

845		TTT001	Tatton-Brown-Rahman Syndrome	41	0.024

846	P	RRH023	Rare Hereditary Hemochromatosis	41	0.024

847		MRP001	Morphine Dependence	41	0.024

848		RDN001	Reading Disorder	40	0.024

849	P	HRD086	Hereditary Hypophosphatemic Rickets	40	0.024

850		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.024

851		JWD001	Jawad Syndrome	40	0.024

852		CHN004	Chondroblastoma	40	0.024

853		PYR004	Pyuria	40	0.024

854		ALC005	Alcoholic Pancreatitis	40	0.024

855	P	PRG092	Pregnancy Loss, Recurrent 1	40	0.024

856		ENC038	Encephalopathy, Progressive, with or Without Lipodystrophy	40	0.024

857		PLY100	Polyploidy	40	0.024

858		SPN221	Spina Bifida Occulta	39	0.024

859		HNZ004	Heinz Body Anemias	39	0.024

860	c	ATR062	Atrial Septal Defect 1	39	0.024

861	c	PRG020	Paragangliomas 3	39	0.024

862		HYP141	Hyperphenylalaninemia	39	0.024

863		CRB001	Cerebral Lymphoma	39	0.024

864	c	RTN066	Retinitis Pigmentosa 4	39	0.024

865	P	PRC031	Preeclampsia/eclampsia 1	38	0.024

866		HYP264	Hypertonia	38	0.024

867		PRP005	Parapsoriasis	38	0.024

868		OVR094	Ovarian Epithelial Cancer	38	0.024

869		MNT310	Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type	38	0.024

870	c	HNT011	Huntington Disease-Like 3	38	0.024

871	c	SYS043	Systemic Lupus Erythematosus 1	38	0.024

872	c	2HY001	2-Hydroxyglutaric Aciduria	38	0.024

873		CTN011	Cutaneous Porphyria	38	0.024

874	P	FML187	Familial Hypertension	37	0.024

875		DFF039	Diffuse Midline Glioma, H3 K27m-Mutant	36	0.024

876		NRS005	Neurosarcoidosis	36	0.024

877		THR123	Thrombotic Microangiopathy	36	0.024

878		BRN018	Borna Disease	36	0.024

879		AMN007	Aminoacylase 1 Deficiency	36	0.024

880		PRS011	Persian Gulf Syndrome	36	0.024

881		PLC002	Plica Syndrome	36	0.024

882		ALC001	Alcohol-Related Birth Defect	36	0.024

883	c	ATM045	Autoimmune Glomerulonephritis	36	0.024

884	c	AMY088	Amyotrophic Lateral Sclerosis 3	36	0.024

885		CHR028	Chronic Wasting Disease	35	0.024

886	c	MCR312	Microphthalmia, Syndromic 10	35	0.024

887		CHR178	Chromosomal Triplication	35	0.024

888		PRM329	Premature Aging	35	0.024

889		ACT149	Acetaminophen Metabolism	35	0.024

890	c	NNS007	Nonsyndromic Deafness	35	0.024

891		KSH001	Keshan Disease	34	0.024

892		MYT011	Myotonia	34	0.024

893		MTH047	Methanol Poisoning	34	0.024

894		NND010	Nondisjunction	34	0.024

895		SPR006	Sparganosis	34	0.024

896		VSL003	Visual Agnosia	34	0.024

897		EXT054	Extra-Adrenal Pheochromocytoma	34	0.024

898		ALR002	Al-Raqad Syndrome	33	0.024

899		HND015	Hand Skill, Relative	33	0.024

900		HYP241	Hypermethioninemia Due to Adenosine Kinase Deficiency	32	0.024

901		TRG019	Trigonocephaly with Short Stature and Developmental Delay	32	0.024

902		ATS252	Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb	32	0.024

903	P	SPN042	Spinal Cord Ependymoma	31	0.024

904	P	ALB003	Albinism-Deafness Syndrome	31	0.024

905	c	FML324	Familial Porphyria Cutanea Tarda	31	0.024

906		NNS045	Non-Specific Syndromic Intellectual Disability	31	0.024

907		EXN003	Exencephaly	31	0.024

908		PLR005	Pleuropneumonia	31	0.024

909		GST029	Gastric Cardia Adenocarcinoma	31	0.024

910		EXT064	Extraoral Halitosis Due to Methanethiol Oxidase Deficiency	30	0.024

911		BRN049	Brain Tumor, Childhood	29	0.024

912		DSR074	Disorder of Purine Metabolism	29	0.024

913		PST092	Posttransplant Acute Limbic Encephalitis	29	0.024

914		RHM013	Rheumatoid Nodulosis	28	0.024

915	P	CRB210	Cerebrofacial Arteriovenous Metameric Syndrome	28	0.024

916	c	ATS006	Autosomal Recessive Nonsyndromic Deafness	27	0.024

917		CYT018	Cytochrome P450 2d6 Variant	27	0.024

918		CLR011	Clear Cell Ependymoma	27	0.024

919	c	RNG015	Ring Chromosome 2	26	0.024

920		ACT094	Acute Articular Rheumatism	26	0.024

921		THY006	Thymus Lymphoma	26	0.024

922		MTH040	Methylmalonyl-Coa Epimerase Deficiency	26	0.024

923		SHR097	Short Tarsus with Absence of Lower Eyelashes	26	0.024

924		NRM022	Neurometabolic Disease	25	0.024

925		BLD163	Blood Group, Dombrock System	24	0.024

926	c	ERY064	Erythrocytosis, Familial, 6	23	0.024

927		LRY027	Laryngeal Papillomatosis	23	0.024

928		CHR158	Charles Bonnet Syndrome	23	0.024

929	c	MTC129	Mitochondrial Dna Depletion Syndrome 15	22	0.024

930		DRG025	Drug-Induced Hearing Loss	22	0.024

931		LYM053	Lymphomatous Thyroiditis	22	0.024

932	P	SPN237	Spina Bifida Aperta	20	0.024

933		DSS012	Disseminated Infection with Mycobacterium Avium Complex	20	0.024

934		PRL045	Proline-Negative Auxotroph of Hamster, Complementation of	18	0.024

935		LTH004	Lathyrism	16	0.024

936	P	PLT029	Platelet Groups--Ko System	16	0.024

937	c	ART151	Aortic Aneurysm, Familial Abdominal, 2	14	0.024

938		MTH081	Mthfr Gene Variant	14	0.024

939		SLN002	Selenium Poisoning	11	0.024