Search results for Glutathione

1357 hits were found for Glutathione

#	Family	MCID	Name	MIFTS	Score
1		GLT007	Glutathione Synthetase Deficiency	47	8.109

2		GLT036	Glutathione Synthetase Deficiency of Erythrocytes, Hemolytic Anemia Due to	18	6.845

3		GLT039	Glutathione Peroxidase Deficiency	34	5.233

4		HML010	Hemolytic Anemia Due to Glutathione Reductase Deficiency	19	5.130

5		HYD063	Hydroxyacyl Glutathione Hydrolase Deficiency	12	3.924

6		GLT034	Glutathione Transferase Activity Toward Trans-Stilbene Oxide	4	3.222

7	c	HML057	Hemolytic Anemia Due to Hexose Monophosphate Shunt and Glutathione Metabolism Anomalies	5	2.298

8	P	CTR002	Cataract	60	0.236

9	P	CLR023	Colorectal Cancer	99	0.222

10	P	LNG032	Lung Cancer	98	0.222

11	P	BLD134	Bladder Cancer	79	0.212

12	P	OVR042	Ovarian Cancer	88	0.210

13	P	LVR013	Liver Disease	68	0.203

14	P	BRS047	Breast Cancer	97	0.201

15	P	NRB001	Neuroblastoma	72	0.187

16		SQM006	Squamous Cell Carcinoma	60	0.177

17	P	HPT023	Hepatocellular Carcinoma	100	0.175

18	P	HML002	Hemolytic Anemia	63	0.175

19	P	ADN016	Adenocarcinoma	64	0.173

20	P	GLM045	Glioma	63	0.173

21		LNG099	Lung Disease	60	0.170

22		GLL048	Glial Tumor	45	0.170

23		LVR012	Liver Cirrhosis	62	0.168

24		SCH014	Schistosomiasis	57	0.164

25		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.163

26		CYS001	Cystic Fibrosis	81	0.161

27	P	GST053	Gastric Cancer	83	0.159

28		48X005	48,xyyy	39	0.157

29	P	PRS040	Prostate Cancer	97	0.151

30		DFC004	Deficiency Anemia	70	0.151

31		HYP066	Hyperglycemia	61	0.150

32	c	PRC016	Pre-Eclampsia	63	0.148

33	P	MYL006	Myeloid Leukemia	60	0.148

34		HYP266	Hypoxia	57	0.148

35		ISC004	Ischemia	58	0.145

36	P	KDN018	Kidney Disease	72	0.144

37	P	LKM002	Leukemia	68	0.144

38		HLX001	Helix Syndrome	47	0.144

39	P	PRK057	Parkinson Disease, Late-Onset	78	0.141

40		47X002	47,xyy	49	0.138

41		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.137

42	P	INF032	Infertility	57	0.135

43	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.129

44	P	ALZ034	Alzheimer Disease	88	0.129

45		GLB015	Glioblastoma Multiforme	75	0.129

46		ORL011	Oral Cancer	60	0.129

47	P	LTR001	Lateral Sclerosis	54	0.129

48		PPL052	Papillomatosis, Confluent and Reticulated	33	0.129

49		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.128

50		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.128

51		CHL068	Cholestasis	61	0.126

52		FTT001	Fatty Liver Disease	61	0.125

53	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.123

54		ADN018	Adenoma	59	0.123

55		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.123

56		AST005	Asthma	76	0.122

57	P	VSC007	Vascular Disease	63	0.122

58	c	SML038	Small Cell Cancer of the Lung	65	0.120

59	P	MLN007	Male Infertility	55	0.120

60	c	LKM061	Leukemia, Acute Myeloid	84	0.117

61		AGN016	Aging	56	0.117

62		RBF001	Riboflavin Deficiency	49	0.117

63		ESP021	Esophageal Cancer	90	0.113

64	P	LNG064	Lung Cancer Susceptibility 3	78	0.113

65	P	ALC033	Alcohol Use Disorder	58	0.113

66	c	CHR684	Chronic Kidney Disease	70	0.112

67		ANX004	Anoxia	40	0.112

68	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.110

69	P	END044	Endometriosis	63	0.108

70		CRV035	Cervical Cancer	76	0.106

71	P	ATS364	Autism	70	0.106

72	P	BPL003	Bipolar Disorder	56	0.106

73		TRN018	Transitional Cell Carcinoma	56	0.106

74	c	MJR024	Major Affective Disorder 9	41	0.106

75		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.106

76	c	MJR022	Major Affective Disorder 8	38	0.106

77	P	MSC005	Muscular Dystrophy	66	0.104

78	P	NRP001	Neuropathy	56	0.104

79	P	INF037	Inflammatory Bowel Disease	54	0.104

80	c	MCR130	Microvascular Complications of Diabetes 6	41	0.104

81	c	MCR113	Microvascular Complications of Diabetes 3	52	0.102

82	P	AST007	Astrocytoma	51	0.102

83	c	MCR120	Microvascular Complications of Diabetes 7	47	0.102

84	c	MCR133	Microvascular Complications of Diabetes 4	41	0.102

85		OVR094	Ovarian Epithelial Cancer	38	0.102

86	P	SCH015	Schizophrenia	74	0.101

87	P	MLN008	Melanoma	69	0.101

88		OST159	Osteogenic Sarcoma	66	0.101

89	P	SKN015	Skin Carcinoma	66	0.101

90		IRN002	Iron Metabolism Disease	57	0.101

91		MTB004	Metabolic Acidosis	50	0.101

92		ORL015	Oral Squamous Cell Carcinoma	43	0.101

93		CHR178	Chromosomal Triplication	35	0.101

94	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.099

95		DWN001	Down Syndrome	70	0.099

96	P	LRY044	Larynx Cancer	55	0.099

97		MLR004	Malaria	81	0.097

98		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.097

99		VLV047	Volvulus of Midgut	49	0.097

100		CYT002	Cytokine Deficiency	42	0.097

101	P	PHC003	Pheochromocytoma	71	0.095

102		CLN015	Colon Adenocarcinoma	65	0.095

103	P	PSR002	Psoriasis	62	0.095

104	P	PNC044	Pancreatitis	61	0.095

105	c	ACT027	Acute Pancreatitis	60	0.095

106		ERY051	Erythroleukemia, Familial	56	0.095

107		PST011	Pustulosis of Palm and Sole	52	0.095

108		ADR040	Adrenal Gland Pheochromocytoma	46	0.095

109		SNL007	Senile Cataract	42	0.095

110	c	LNG109	Lung Cancer Susceptibility 1	27	0.095

111	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.092

112	P	HNT016	Huntington Disease	72	0.092

113		ATH013	Atherosclerosis Susceptibility	65	0.092

114		LPP008	Lipoprotein Quantitative Trait Locus	62	0.092

115	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.092

116		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.092

117	c	VTL009	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6	42	0.092

118	P	HYP086	Hypothyroidism	69	0.090

119	P	CRN300	Coronary Heart Disease 1	63	0.090

120		ATM095	Autoimmune Disease	62	0.090

121		NNL005	Non-Alcoholic Fatty Liver Disease	61	0.090

122	P	THL005	Thalassemia	60	0.090

123		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	58	0.090

124		HMS001	Hemosiderosis	54	0.090

125		ART140	Arteries, Anomalies of	52	0.090

126	P	RRH023	Rare Hereditary Hemochromatosis	41	0.090

127		MYL009	Myelodysplastic Syndrome	70	0.088

128		CLT003	Colitis	62	0.088

129		DRM006	Dermatitis	61	0.088

130	P	BCL017	B-Cell Lymphoma	58	0.088

131		BLR008	Bilirubin Metabolic Disorder	57	0.088

132	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.086

133		SCK003	Sickle Cell Anemia	74	0.086

134		HMN044	Human Immunodeficiency Virus Type 1	71	0.086

135	c	BSL007	Basal Cell Carcinoma	68	0.086

136	P	PLM036	Pulmonary Fibrosis	65	0.086

137	P	DBT009	Diabetes Mellitus	64	0.086

138	P	PRD008	Periodontitis	64	0.086

139		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.086

140	c	ACT071	Acute Kidney Failure	60	0.086

141	P	ECL001	Eclampsia	50	0.086

142	c	PCH010	Pachyonychia Congenita 3	44	0.086

143	P	RHM011	Rheumatoid Arthritis	80	0.084

144		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.084

145	c	LKM063	Leukemia, Chronic Myeloid	72	0.084

146		ALC007	Alcohol Dependence	66	0.084

147		HYP056	Hypoglycemia	66	0.084

148		BRR014	Barrett Esophagus	65	0.084

149		ACT119	Acute Promyelocytic Leukemia	63	0.084

150		ALL026	Allergic Hypersensitivity Disease	62	0.084

151	P	OPN001	Open-Angle Glaucoma	49	0.084

152		IMM167	Immune Deficiency Disease	78	0.081

153	P	MLT020	Multiple Sclerosis	72	0.081

154		DPR016	Depression	63	0.081

155	P	BRS044	Breast Adenocarcinoma	59	0.081

156	P	FBR017	Fibrosarcoma	56	0.081

157	P	HYP076	Hyperthyroidism	55	0.081

158	c	VRL010	Viral Hepatitis	52	0.081

159		KRT002	Keratomalacia	47	0.081

160		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.081

161		MYL069	Myeloma, Multiple	85	0.079

162		END057	Endometrial Cancer	74	0.079

163	c	HPT073	Hepatitis C Virus	72	0.079

164	P	HPT021	Hepatitis	67	0.079

165		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.079

166	P	NTR004	Neutropenia	63	0.079

167		HLC007	Helicobacter Pylori Infection	59	0.079

168	c	ACT075	Acute Myocardial Infarction	57	0.079

169	P	SZR006	Seizure Disorder	56	0.079

170		HYP276	Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant	54	0.079

171		ANM045	Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency	49	0.079

172		HVY002	Heavy Metal Poisoning	22	0.079

173	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.076

174	c	HYP595	Hypertension, Essential	84	0.076

175	P	PNC035	Pancreatic Cancer	84	0.076

176	c	BTT014	Beta-Thalassemia	74	0.076

177	c	MNN043	Meningioma, Familial	74	0.076

178		ULC004	Ulcerative Colitis	73	0.076

179	c	ATM011	Autoimmune Hepatitis	63	0.076

180	c	GLC092	Glaucoma, Primary Open Angle	62	0.076

181		MNN042	Meningioma, Radiation-Induced	62	0.076

182		ALL006	Allergic Asthma	56	0.076

183		PPL022	Papilloma	54	0.076

184		HMC014	Homocysteinemia	53	0.076

185	P	SPP010	Suppressor of Tumorigenicity 3	51	0.076

186		END086	End Stage Renal Disease	51	0.076

187		SPN021	Spinal Meningioma	50	0.076

188		SQM002	Squamous Cell Papilloma	46	0.076

189		CRB004	Cerebral Artery Occlusion	45	0.076

190		SCR001	Secretory Meningioma	41	0.076

191		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.076

192	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.074

193		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.074

194	P	APL001	Aplastic Anemia	74	0.074

195	P	MYC007	Myocardial Infarction	70	0.074

196		GST040	Gastric Adenocarcinoma	70	0.074

197	P	LYM118	Lymphoma	68	0.074

198		CHL065	Cholangiocarcinoma	68	0.074

199		TXC005	Toxic Shock Syndrome	62	0.074

200	P	KDN017	Kidney Cancer	60	0.074

201		ACQ007	Acquired Immunodeficiency Syndrome	60	0.074

202		THY029	Thyroid Carcinoma	59	0.074

203		VSL002	Visual Epilepsy	59	0.074

204		MNT002	Mental Depression	58	0.074

205	P	PRP019	Peripheral Nervous System Disease	58	0.074

206		BRN056	Bronchopulmonary Dysplasia	57	0.074

207	P	TRM003	Tremor	54	0.074

208		NNL006	Non-Alcoholic Steatohepatitis	54	0.074

209	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.074

210		INT079	Intrahepatic Cholangiocarcinoma	51	0.074

211	P	SCK005	Sickle Cell Disease	50	0.074

212		URM002	Uremia	49	0.074

213	c	MLG068	Malignant Glioma	46	0.074

214	P	NSP012	Nasopharyngeal Carcinoma	66	0.071

215	P	MCR115	Microvascular Complications of Diabetes 5	66	0.071

216		CLR108	Colorectal Adenoma	64	0.071

217		LSH001	Leishmaniasis	63	0.071

218	c	HPT001	Hepatitis C	62	0.071

219	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	60	0.071

220	c	ACT073	Acute Leukemia	58	0.071

221		HPT046	Hepatic Veno-Occlusive Disease	56	0.071

222		FLR002	Filariasis	55	0.071

223	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.071

224	P	LCT001	Lactic Acidosis	51	0.071

225		ATS010	Autosomal Recessive Disease	48	0.071

226	P	MRC003	Mercury Poisoning	48	0.071

227		HMP009	Haemophilus Influenzae	43	0.071

228	P	KLZ004	Kala-Azar 1	41	0.071

229		LKP003	Leukoplakia	39	0.071

230		5XP001	5-Oxoprolinase Deficiency	31	0.071

231		PST092	Posttransplant Acute Limbic Encephalitis	29	0.071

232	c	SYS001	Systemic Lupus Erythematosus	86	0.068

233		CRH001	Crohn's Disease	74	0.068

234		SVR004	Severe Combined Immunodeficiency	73	0.068

235		SKN016	Skin Disease	63	0.068

236	P	ENC018	Encephalopathy	61	0.068

237		IGR001	Ige Responsiveness, Atopic	59	0.068

238		PLM010	Pulmonary Edema	54	0.068

239		DBT010	Diabetic Neuropathy	54	0.068

240		PRS045	Prostatic Hypertrophy	53	0.068

241	P	SML001	Small Cell Carcinoma	52	0.068

242	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.068

243		FSC002	Fascioliasis	42	0.068

244	c	DNT047	Dentinogenesis Imperfecta Type 2	31	0.068

245		STR067	Stroke, Ischemic	81	0.065

246	P	HRT032	Heart Disease	75	0.065

247		PHN003	Phenylketonuria	75	0.065

248		LPD008	Lipid Metabolism Disorder	62	0.065

249	P	PRM006	Primary Biliary Cirrhosis	62	0.065

250		ALC006	Alcoholic Hepatitis	61	0.065

251		PPT005	Peptic Ulcer Disease	59	0.065

252		CNT047	Contact Dermatitis	58	0.065

253	c	ACT134	Acute Liver Failure	56	0.065

254		HPT022	Hepatoblastoma	56	0.065

255	P	ART021	Arteriosclerosis	54	0.065

256	c	PRD040	Periodontitis, Chronic	53	0.065

257		PRS021	Prostatic Adenoma	51	0.065

258		KSH001	Keshan Disease	34	0.065

259	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.062

260		LYM133	Lymphoma, Hodgkin, Classic	69	0.062

261	P	PNM007	Pneumonia	68	0.062

262	P	MJR001	Major Depressive Disorder	68	0.062

263		GST092	Gastroesophageal Reflux	67	0.062

264		SRC014	Sarcoma	65	0.062

265	P	PRP029	Porphyria	62	0.062

266		NTR005	Nutritional Deficiency Disease	62	0.062

267		IRN001	Iron Deficiency Anemia	59	0.062

268		CYS010	Cystinosis	59	0.062

269		DSS008	Disease of Mental Health	58	0.062

270		BCT022	Bacterial Infectious Disease	56	0.062

271	P	GST044	Gastritis	56	0.062

272	P	INS002	in Situ Carcinoma	53	0.062

273		TRM010	Traumatic Brain Injury	51	0.062

274		VRC001	Varicocele	49	0.062

275	P	BNG032	Benign Mesothelioma	46	0.062

276		ORL012	Oral Leukoplakia	39	0.062

277		GLT014	Glutathionuria	39	0.062

278		HRN029	Hearing Loss, Noise-Induced	37	0.062

279	P	MDL005	Medulloblastoma	77	0.059

280		BRN028	Brain Cancer	74	0.059

281		MSC157	Muscular Dystrophy, Duchenne Type	72	0.059

282		PSY004	Psychotic Disorder	67	0.059

283	c	ATS007	Autism Spectrum Disorder	67	0.059

284		CHG001	Chagas Disease	66	0.059

285	P	DRM053	Dermatitis, Atopic	66	0.059

286	c	DWL002	Dowling-Degos Disease 1	58	0.059

287	P	GLM007	Glomerulonephritis	57	0.059

288		BRN004	Brain Edema	56	0.059

289		DFF005	Diffuse Large B-Cell Lymphoma	55	0.059

290		HYP060	Hyperinsulinism	54	0.059

291		SPN035	Spindle Cell Sarcoma	53	0.059

292		ALC009	Alcoholic Liver Cirrhosis	53	0.059

293	P	DDN001	Duodenal Ulcer	52	0.059

294		PRS129	Prostatic Hyperplasia, Benign	49	0.059

295		BRN071	Brain Injury	49	0.059

296		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.059

297		LRY018	Laryngeal Squamous Cell Carcinoma	44	0.059

298	c	LKM005	Leukemia, T-Cell, Chronic	34	0.059

299	P	ATX030	Ataxia-Telangiectasia	82	0.056

300	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.056

301		CNG034	Congestive Heart Failure	69	0.056

302		ANG054	Angina Pectoris	66	0.056

303	P	MTR014	Motor Neuron Disease	65	0.056

304		TBC004	Tobacco Addiction	64	0.056

305	P	RHB003	Rhabdomyosarcoma	63	0.056

306	c	HPT003	Hepatitis a	62	0.056

307		MDD011	Mood Disorder	62	0.056

308		BLD131	Bladder Urothelial Carcinoma	62	0.056

309		SPN186	Spinal Cord Injury	60	0.056

310		INS001	Insulinoma	60	0.056

311	c	HPT016	Hepatitis B	59	0.056

312	P	CYS018	Cystitis	59	0.056

313	P	TYR004	Tyrosinemia	58	0.056

314	P	CND004	Candidiasis	58	0.056

315	P	RHN004	Rhinitis	57	0.056

316		ALL010	Allergic Contact Dermatitis	56	0.056

317		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.056

318		EMB004	Embryonal Carcinoma	56	0.056

319		FLR001	Filarial Elephantiasis	55	0.056

320		PRT038	Protein-Energy Malnutrition	54	0.056

321	P	RCT021	Rectum Cancer	52	0.056

322		TLN003	Telangiectasis	52	0.056

323	P	TRT010	Teratoma	52	0.056

324		CLR109	Colorectal Adenocarcinoma	51	0.056

325	P	HRD144	Hereditary Mixed Polyposis Syndrome	51	0.056

326		HYP781	Hypoascorbemia	51	0.056

327		AZS001	Azoospermia	50	0.056

328	P	KRT007	Keratoconus	50	0.056

329		INT017	Intestinal Schistosomiasis	48	0.056

330		SPL018	Splenomegaly	48	0.056

331	c	CRV002	Cervix Uteri Carcinoma in Situ	46	0.056

332		KWS001	Kwashiorkor	44	0.056

333		CRV045	Cervical Intraepithelial Neoplasia	39	0.056

334		GMM011	Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to	25	0.056

335		NRL016	Neural Tube Defects	82	0.052

336	c	DLT002	Dilated Cardiomyopathy	79	0.052

337		OST012	Osteoarthritis	78	0.052

338	c	ATR087	Atrial Standstill 1	75	0.052

339	P	GRF003	Graft-Versus-Host Disease	72	0.052

340		PLM001	Pulmonary Tuberculosis	69	0.052

341		BRN024	Bronchitis	68	0.052

342		ALL003	Allergic Rhinitis	67	0.052

343	P	CHR012	Chronic Granulomatous Disease	67	0.052

344	c	DBT099	Diabetes Mellitus, Type I	65	0.052

345		GT001	Gout	64	0.052

346		TRN015	Transient Cerebral Ischemia	63	0.052

347	P	TRC086	Trichohepatoenteric Syndrome 1	62	0.052

348	P	LPS004	Lupus Erythematosus	61	0.052

349	P	NPH012	Nephrotic Syndrome	60	0.052

350	P	MYC008	Myocarditis	59	0.052

351		PRN019	Perinatal Necrotizing Enterocolitis	59	0.052

352	P	ADL017	Adult T-Cell Leukemia	56	0.052

353		CYS005	Cysticercosis	53	0.052

354		GST023	Gastric Ulcer	53	0.052

355	P	MSC003	Muscular Atrophy	52	0.052

356		ONC002	Onchocerciasis	52	0.052

357		ENT011	Enterocolitis	51	0.052

358		BLR001	Biliary Atresia	50	0.052

359	c	INH020	Inherited Metabolic Disorder	47	0.052

360		ILC002	Ileocolitis	43	0.052

361		DBT007	Diabetic Cataract	38	0.052

362		ALL014	Allergic Encephalomyelitis	38	0.052

363		HRW001	Hair Whorl	36	0.052

364	c	ECT041	Ectodermal Dysplasia-Syndactyly Syndrome 2	35	0.052

365	P	GLM040	Glioma Susceptibility 1	81	0.048

366		ANX010	Anxiety	73	0.048

367	P	MPL001	Maple Syrup Urine Disease	69	0.048

368	P	MYC084	Mycobacterium Tuberculosis 1	68	0.048

369	P	CRD119	Cardiac Arrest	67	0.048

370	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.048

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

372		ANR007	Anorexia Nervosa	63	0.048

373	c	SCL052	Scleroderma, Familial Progressive	61	0.048

374		CHR066	Chronic Fatigue Syndrome	61	0.048

375		GRD007	Grade Iii Astrocytoma	59	0.048

376		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.048

377	P	GLL018	Gallbladder Cancer	57	0.048

378	P	MTC069	Mitochondrial Disorders	56	0.048

379		HMG005	Hemoglobinopathy	56	0.048

380		MCS002	Mucositis	56	0.048

381		INT007	Intermediate Coronary Syndrome	55	0.048

382		TRD006	Tardive Dyskinesia	54	0.048

383		GLC003	Glucose Intolerance	54	0.048

384		HLL004	Hellp Syndrome	54	0.048

385		TRC023	Trichinosis	53	0.048

386		MST005	Mastitis	53	0.048

387	P	INT068	Intestinal Disease	53	0.048

388	P	RTN018	Retinal Disease	53	0.048

389		SRS001	Serous Cystadenocarcinoma	52	0.048

390	P	INT099	Intrahepatic Cholestasis of Pregnancy	51	0.048

391		SCH012	Schizoaffective Disorder	50	0.048

392		TRY001	Trypanosomiasis	50	0.048

393		HMG002	Hemoglobinuria	50	0.048

394	c	CNG027	Congenital Hemolytic Anemia	50	0.048

395		ASB001	Asbestosis	47	0.048

396		TST014	Testicular Cancer	46	0.048

397		CRT015	Carotid Artery Occlusion	45	0.048

398		MST004	Mast Cell Neoplasm	42	0.048

399		EXT007	Extracutaneous Mastocytoma	38	0.048

400		CNG017	Congenital Nonspherocytic Hemolytic Anemia	35	0.048

401		ARG004	Argyria	27	0.048

402		ASB003	Asbestos Intoxication	26	0.048

403	c	NRF023	Neurofibromatosis, Type Ii	80	0.044

404	P	RTN008	Retinitis Pigmentosa	79	0.044

405	P	RSP003	Respiratory Failure	74	0.044

406		OTT002	Otitis Media	72	0.044

407	c	EXD008	Exudative Vitreoretinopathy 1	71	0.044

408		WLS001	Wilson Disease	71	0.044

409	P	MYP004	Myopathy	70	0.044

410	P	ART022	Arthritis	69	0.044

411	P	LPR021	Leprosy 3	69	0.044

412	P	SYS005	Systemic Scleroderma	68	0.044

413		PNC129	Pancreatic Adenocarcinoma	68	0.044

414		CRB039	Cerebrovascular Disease	67	0.044

415	P	HYP098	Hypereosinophilic Syndrome	67	0.044

416	c	RHB024	Rhabdomyosarcoma 2	67	0.044

417	P	CLC063	Celiac Disease 1	66	0.044

418		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.044

419	P	DMN002	Dementia	66	0.044

420	P	MNN013	Meningitis	66	0.044

421		LNG039	Lung Squamous Cell Carcinoma	66	0.044

422		KRT019	Keratitis, Hereditary	65	0.044

423		PRT037	Pertussis	65	0.044

424	P	HRP006	Herpes Simplex	65	0.044

425	c	WLM013	Wilms Tumor 1	65	0.044

426	P	ADL010	Adult Respiratory Distress Syndrome	65	0.044

427	P	CHR071	Charcot-Marie-Tooth Disease	65	0.044

428	P	FRD001	Friedreich Ataxia	64	0.044

429		LYM017	Lyme Disease	64	0.044

430	P	VSC011	Vasculitis	62	0.044

431		YLL002	Yellow Fever	61	0.044

432		HPT019	Hepatic Encephalopathy	60	0.044

433	P	SNS001	Sensorineural Hearing Loss	60	0.044

434		STT001	Status Epilepticus	60	0.044

435	P	OPT006	Optic Nerve Disease	60	0.044

436		SPP011	Suppression of Tumorigenicity 12	59	0.044

437		CHL014	Cholera	59	0.044

438		EYD002	Eye Disease	58	0.044

439	P	CRD246	Cardiovascular System Disease	57	0.044

440	P	PLY018	Polycythemia	56	0.044

441	P	PLY011	Polycystic Ovary Syndrome	56	0.044

442		GST050	Gastrointestinal System Disease	56	0.044

443	P	PNM006	Pneumoconiosis	56	0.044

444		ORP003	Oropharynx Cancer	55	0.044

445	P	DRR001	Diarrhea	55	0.044

446	P	DRM007	Dermatitis Herpetiformis	55	0.044

447	P	ALP008	Alopecia	54	0.044

448		THR013	Thoracic Outlet Syndrome	54	0.044

449		SLP001	Sleeping Sickness	54	0.044

450		CLR030	Clear Cell Renal Cell Carcinoma	53	0.044

451	P	HMC002	Homocystinuria	53	0.044

452		NNT012	Neonatal Jaundice	53	0.044

453		TXC002	Toxic Encephalopathy	53	0.044

454		OVR059	Ovary Adenocarcinoma	53	0.044

455		PLS007	Plasmodium Falciparum Malaria	52	0.044

456		KRT009	Keratosis	51	0.044

457		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.044

458	P	CHL066	Cholangitis	51	0.044

459	c	SVR005	Severe Pre-Eclampsia	50	0.044

460		VTM002	Vitamin B12 Deficiency	48	0.044

461		ANT018	Anthracosis	48	0.044

462		LYM019	Lymphosarcoma	46	0.044

463	P	MTH007	Methemoglobinemia	46	0.044

464		HPT004	Hepatic Coma	45	0.044

465	c	SPR009	Sporadic Breast Cancer	45	0.044

466	c	SPR086	Spermatogenic Failure 3	44	0.044

467		OPS001	Opisthorchiasis	41	0.044

468	c	DRM040	Dermatitis Herpetiformis, Familial	35	0.044

469		ACT149	Acetaminophen Metabolism	35	0.044

470		HNS001	Hansen's Disease	34	0.044

471		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.044

472		PRS131	Prostate Cancer/brain Cancer Susceptibility	25	0.044

473		XRD010	Xeroderma Pigmentosum, Variant Type	73	0.039

474	P	RTN024	Retinoblastoma	73	0.039

475		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.039

476	P	FML011	Familial Adenomatous Polyposis	72	0.039

477	P	EPL164	Epilepsy	71	0.039

478		MLT157	Multiple System Atrophy 1	70	0.039

479	c	PNC108	Pancreatitis, Hereditary	70	0.039

480	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.039

481		ABT001	Abetalipoproteinemia	69	0.039

482	P	SPR120	Supranuclear Palsy, Progressive, 1	68	0.039

483		MLD001	Melioidosis	68	0.039

484	P	PLM037	Pulmonary Hypertension	67	0.039

485	c	MCR129	Microvascular Complications of Diabetes 1	66	0.039

486		TTN003	Tetanus	65	0.039

487	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.039

488		PRT036	Peritonitis	64	0.039

489	P	PLY014	Polycystic Kidney Disease	62	0.039

490	P	HYP750	Hypertriglyceridemia, Familial	62	0.039

491	P	ESP024	Esophagitis	62	0.039

492		BLL006	Bullous Pemphigoid	62	0.039

493		GNG013	Gingivitis	59	0.039

494		CHL067	Cholecystitis	57	0.039

495	P	EXN002	Exanthem	57	0.039

496	P	PRN023	Prion Disease	57	0.039

497	c	MST023	Mesothelioma, Malignant	57	0.039

498		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.039

499		TNS005	Tonsillitis	57	0.039

500		VSC002	Vascular Dementia	57	0.039

501	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.039

502		HYP005	Hypokalemia	55	0.039

503		ORL004	Oral Submucous Fibrosis	55	0.039

504	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	55	0.039

505		FND002	Fundus Dystrophy	55	0.039

506		VSC003	Visceral Leishmaniasis	55	0.039

507	c	BCT007	Bacterial Meningitis	55	0.039

508	P	RNL017	Renal Oncocytoma	53	0.039

509	P	ACT008	Actinic Keratosis	53	0.039

510	P	PNC025	Panic Disorder	53	0.039

511	c	FML008	Familial Retinoblastoma	53	0.039

512	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.039

513		IMP005	Impotence	52	0.039

514	P	THY032	Thyroiditis	52	0.039

515		PPT001	Peptic Esophagitis	52	0.039

516	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.039

517	c	INH030	Inherited Retinal Disorder	51	0.039

518		OCL069	Ocular Motor Apraxia	51	0.039

519		CYS014	Cystadenocarcinoma	51	0.039

520		LNG031	Lung Benign Neoplasm	51	0.039

521		SCB001	Scabies	50	0.039

522	P	FNC004	Fanconi Syndrome	50	0.039

523	P	OBS001	Obstructive Jaundice	50	0.039

524		IRR003	Irritant Dermatitis	49	0.039

525	P	BRS053	Breast Fibroadenoma	49	0.039

526		BNR002	Bone Resorption Disease	48	0.039

527	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.039

528	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.039

529		RTN023	Retinitis	46	0.039

530		TTH006	Tooth Disease	46	0.039

531	c	GLC111	Galactosemia Ii	46	0.039

532	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.039

533	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.039

534	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.039

535		URT010	Ureteral Obstruction	45	0.039

536		HMR023	Hemorrhagic Cystitis	45	0.039

537	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.039

538	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.039

539	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.039

540		SMN007	Seminoma	43	0.039

541		SDD008	Sudden Sensorineural Hearing Loss	43	0.039

542	c	AGR019	Age-Related Hearing Loss	42	0.039

543		ATX019	Ataxia with Vitamin E Deficiency	42	0.039

544		NRR001	Neuroretinitis	42	0.039

545	P	RRT020	Rare Tumor	41	0.039

546	c	MCR112	Microvascular Complications of Diabetes 2	41	0.039

547	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.039

548	c	PRG020	Paragangliomas 3	39	0.039

549		BRR002	Barrett's Adenocarcinoma	36	0.039

550		MTG002	Mutagen Sensitivity	35	0.039

551		PRM329	Premature Aging	35	0.039

552	P	CMP072	Camptodactyly Syndrome, Guadalajara, Type I	34	0.039

553		MNG007	Manganese Poisoning	29	0.039

554	c	MGR022	Migraine with or Without Aura 3	17	0.039

555		INS024	Insulin-Like Growth Factor I	79	0.034

556	c	SPN225	Spondyloarthropathy 1	73	0.034

557	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.034

558	P	SRC025	Sarcoidosis 1	70	0.034

559		MYL005	Myelofibrosis	70	0.034

560		LGH007	Leigh Syndrome	70	0.034

561		WRN001	Werner Syndrome	69	0.034

562		PLY001	Polycythemia Vera	69	0.034

563	P	SLP006	Sleep Apnea	69	0.034

564		ART016	Aortic Aneurysm	69	0.034

565	P	ANG001	Angelman Syndrome	69	0.034

566		OBS002	Obsessive-Compulsive Disorder	68	0.034

567	P	OLG002	Oligodendroglioma	67	0.034

568		BRK010	Burkitt Lymphoma	67	0.034

569	P	TRN020	Turner Syndrome	67	0.034

570	P	MLG056	Malignant Hyperthermia	67	0.034

571	c	TYR012	Tyrosinemia, Type I	66	0.034

572		GLN010	Glanzmann Thrombasthenia	66	0.034

573	P	NRV007	Nervous System Disease	66	0.034

574	P	THY023	Thymoma	65	0.034

575		NRM005	Neuromuscular Disease	64	0.034

576		CLF027	Cleft Palate, Isolated	64	0.034

577	P	GLC113	Galactosemia I	64	0.034

578	P	GCH001	Gaucher's Disease	63	0.034

579	P	ANR048	Aniridia 1	63	0.034

580	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.034

581		BRS099	Breast Ductal Carcinoma	62	0.034

582	P	TXP001	Toxoplasmosis	60	0.034

583	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.034

584		INT066	Interstitial Lung Disease	60	0.034

585		ACN002	Acanthosis Nigricans	60	0.034

586		PRT013	Portal Hypertension	59	0.034

587	P	DNG005	Dengue Virus	59	0.034

588		BRS051	Breast Disease	58	0.034

589		CNS004	Constipation	58	0.034

590		LYM027	Lymphopenia	58	0.034

591		PYR041	Pyruvate Kinase Deficiency of Red Cells	57	0.034

592	P	UVT001	Uveitis	57	0.034

593	c	CHL119	Cholangitis, Primary Sclerosing	57	0.034

594	P	HDC001	Headache	57	0.034

595		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.034

596		CMM005	Common Cold	57	0.034

597	P	FTL001	Fetal Alcohol Syndrome	57	0.034

598		CYT008	Cytomegalovirus Infection	57	0.034

599	P	PLY019	Polyneuropathy	56	0.034

600		MCL006	Macular Retinal Edema	55	0.034

601		NPH009	Nephrolithiasis	55	0.034

602		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.034

603		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.034

604	P	SBS003	Substance Abuse	55	0.034

605		MYM001	Myoma	54	0.034

606		PNC001	Pancytopenia	54	0.034

607	P	RTN016	Retinal Degeneration	53	0.034

608		CLF001	Cleft Lip	53	0.034

609		DNT012	Dental Caries	53	0.034

610	P	HMG032	Hemoglobin H Disease	52	0.034

611		THY030	Thyroid Gland Disease	52	0.034

612	c	THY107	Thymoma, Familial	52	0.034

613		CRV040	Cervix Carcinoma	51	0.034

614		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.034

615		ACT017	Acute Chest Syndrome	51	0.034

616		CRN030	Coronary Stenosis	50	0.034

617		NTR046	Neutrophil Migration	50	0.034

618	c	LRG001	Large Cell Carcinoma	50	0.034

619		LPR001	Lepromatous Leprosy	50	0.034

620	P	ATR005	Atrophic Gastritis	50	0.034

621		CHL004	Cholelithiasis	49	0.034

622	P	SCL009	Sclerosing Cholangitis	48	0.034

623		IGG001	Iga Glomerulonephritis	48	0.034

624		DRG003	Drug Dependence	47	0.034

625		PPL002	Papillary Carcinoma	47	0.034

626		THY128	Thyroid Tumor	47	0.034

627	P	BLR006	Biliary Tract Disease	47	0.034

628		RNL077	Renal Fibrosis	47	0.034

629		GST071	Gastrointestinal Carcinoma	47	0.034

630		CHR074	Choriocarcinoma	47	0.034

631		RTN020	Retinal Vascular Disease	46	0.034

632		ALB002	Albinism	46	0.034

633	c	GRN049	Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I	46	0.034

634		OLG001	Oligospermia	45	0.034

635		ATN004	Autonomic Neuropathy	45	0.034

636		TBR006	Tuberculoid Leprosy	44	0.034

637		GRN017	Granulocytopenia	44	0.034

638		CLN003	Clonorchiasis	44	0.034

639		DMP001	Dumping Syndrome	44	0.034

640		CVD001	Covid-19	44	0.034

641	P	CRN024	Corneal Disease	44	0.034

642		CLN044	Colon Adenoma	44	0.034

643		PLY068	Polysubstance Abuse	43	0.034

644		DRG002	Drug-Induced Hepatitis	43	0.034

645		MRS001	Marasmus	42	0.034

646	c	CHR576	Chronic Beryllium Disease	42	0.034

647		IDP091	Idiopathic Nephrotic Syndrome	42	0.034

648		THR035	Thrombasthenia	40	0.034

649		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.034

650		ALC005	Alcoholic Pancreatitis	40	0.034

651		PRM020	Premenstrual Tension	40	0.034

652	P	BRY005	Beryllium Disease	40	0.034

653		EXT006	Extrahepatic Cholestasis	39	0.034

654		CHL045	Choline Deficiency Disease	39	0.034

655	c	OVR114	Ovarian Cancer 1	38	0.034

656		SMT002	Smooth Muscle Tumor	38	0.034

657		SYS071	Systemic Autoimmune Disease	37	0.034

658		ATX010	Ataxia Neuropathy Spectrum	34	0.034

659		DXR001	Doxorubicin Induced Cardiomyopathy	33	0.034

660		ACT064	Acute Necrotizing Encephalitis	33	0.034

661		CND006	Candida Glabrata	32	0.034

662		XLN206	X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome	32	0.034

663		PRC051	Paracetamol Poisoning	30	0.034

664		TCK004	Tick Infestation	28	0.034

665		BRD005	Borderline Leprosy	27	0.034

666		BLD137	Blood Group--Ahonen	16	0.034

667	P	RTT002	Rett Syndrome	80	0.028

668	c	TBR025	Tuberous Sclerosis 1	77	0.028

669		KPS004	Kaposi Sarcoma	75	0.028

670	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.028

671		ADR007	Adrenoleukodystrophy	75	0.028

672		LPT014	Leptin Deficiency or Dysfunction	74	0.028

673	c	HMC039	Hemochromatosis, Type 1	74	0.028

674	P	CNR004	Cone-Rod Dystrophy 2	73	0.028

675	P	FML018	Familial Mediterranean Fever	73	0.028

676	P	AMY004	Amyloidosis	70	0.028

677	c	GCH015	Gaucher Disease, Type I	70	0.028

678	P	TTR001	Tetralogy of Fallot	70	0.028

679		ADL002	Adult Syndrome	70	0.028

680	P	TBR001	Tuberous Sclerosis	70	0.028

681	P	DMN001	Diamond-Blackfan Anemia	69	0.028

682	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.028

683		CRB037	Cerebral Palsy	69	0.028

684		MNT001	Mantle Cell Lymphoma	69	0.028

685		SKN019	Skin Melanoma	68	0.028

686	P	INF038	Influenza	68	0.028

687	P	FLL037	Follicular Lymphoma	67	0.028

688	P	PRP003	Porphyria Cutanea Tarda	67	0.028

689		FLL027	Fallopian Tube Carcinoma	67	0.028

690	P	BLD062	Bile Duct Cancer	67	0.028

691	c	MGR028	Migraine with or Without Aura 1	67	0.028

692		MYC006	Mycosis Fungoides	66	0.028

693		ART001	Arterial Tortuosity Syndrome	66	0.028

694	P	CNJ013	Conjunctivitis	65	0.028

695		PRP001	Propionic Acidemia	65	0.028

696		AND019	Andersen Cardiodysrhythmic Periodic Paralysis	65	0.028

697	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.028

698		ALC028	Alacrima, Achalasia, and Mental Retardation Syndrome	64	0.028

699	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.028

700	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.028

701		BRC012	Brucellosis	64	0.028

702		PLM031	Poliomyelitis	64	0.028

703	P	LMY004	Leiomyosarcoma	63	0.028

704	c	OPT053	Optic Atrophy 1	63	0.028

705	c	ALP101	Alpha-Thalassemia	62	0.028

706	P	ART023	Arthropathy	62	0.028

707		LSC001	Lesch-Nyhan Syndrome	62	0.028

708		CRC021	Carcinosarcoma	62	0.028

709		MSL001	Measles	62	0.028

710		INT002	Intermittent Claudication	61	0.028

711	P	ENC004	Encephalitis	61	0.028

712	c	WLM018	Wilms Tumor 5	61	0.028

713		GST033	Gestational Diabetes	61	0.028

714		VRL011	Viral Infectious Disease	61	0.028

715		DPH001	Diphtheria	60	0.028

716	P	ATR010	Atrial Heart Septal Defect	60	0.028

717		RHM001	Rheumatic Fever	60	0.028

718	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	60	0.028

719		ETN001	Eating Disorder	60	0.028

720	P	HRD011	Hereditary Spherocytosis	60	0.028

721	c	PRK089	Parkinson Disease 2, Autosomal Recessive Juvenile	59	0.028

722	P	BRN022	Bronchiectasis	59	0.028

723		CHL123	Chlamydia	59	0.028

724	P	LYM033	Lymphoproliferative Syndrome	59	0.028

725		DBN001	Dubin-Johnson Syndrome	59	0.028

726		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.028

727		GST045	Gastroenteritis	59	0.028

728		ANR040	Aneurysm	59	0.028

729	P	SYP003	Syphilis	58	0.028

730	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.028

731		GLB001	Gilbert Syndrome	58	0.028

732	c	SPN301	Spinocerebellar Ataxia 2	58	0.028

733		CRV038	Cervical Squamous Cell Carcinoma	58	0.028

734	P	PLY041	Polymyositis	57	0.028

735		THY122	Thyroid Gland Cancer	57	0.028

736		THR024	Thrombosis	57	0.028

737		CHR177	Chromophobe Renal Cell Carcinoma	57	0.028

738		JPN002	Japanese Encephalitis	57	0.028

739	P	PYL005	Pyelonephritis	56	0.028

740		PLS011	Plasmacytoma	56	0.028

741		ADN027	Adenomyosis	56	0.028

742		GNR004	Generalized Anxiety Disorder	56	0.028

743		GRS011	Gerstmann-Straussler Disease	56	0.028

744	c	THY109	Thyroid Cancer, Nonmedullary, 1	56	0.028

745	P	PLM034	Pulmonary Emphysema	55	0.028

746	P	ANT006	Antiphospholipid Syndrome	55	0.028

747	P	MYP006	Myopia	55	0.028

748	P	ALP106	Alport Syndrome 1, X-Linked	55	0.028

749		END040	Endogenous Depression	55	0.028

750		HRY003	Hairy Cell Leukemia	55	0.028

751		BRN015	Bronchiolo-Alveolar Adenocarcinoma	54	0.028

752	P	PMP001	Pemphigus	54	0.028

753	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.028

754		SNS003	Sensory Peripheral Neuropathy	54	0.028

755		PRC002	Paracoccidioidomycosis	54	0.028

756		CRH005	Crohn's Colitis	53	0.028

757		ECH003	Echinococcosis	53	0.028

758		GTR002	Goiter	53	0.028

759	c	HPT007	Hepatitis E	53	0.028

760		FML037	Female Breast Cancer	52	0.028

761		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	52	0.028

762		PRV004	Periventricular Leukomalacia	52	0.028

763		LMY002	Leiomyoma	52	0.028

764		PNG002	Pain Agnosia	51	0.028

765	c	SCN036	Secondary Progressive Multiple Sclerosis	51	0.028

766		PLS006	Plasmodium Vivax Malaria	51	0.028

767		ASP003	Aseptic Meningitis	51	0.028

768	P	HRD012	Hereditary Elliptocytosis	51	0.028

769	c	ACT078	Acute Porphyria	51	0.028

770		LNT004	Lentigines	50	0.028

771		PLR008	Pleurisy	50	0.028

772	c	HNT004	Huntington Disease-Like 2	50	0.028

773		RTN003	Retinal Ischemia	50	0.028

774		HPT014	Hepatorenal Syndrome	50	0.028

775		CHL122	Cholesteatoma of Middle Ear	50	0.028

776	c	INF145	Infantile Liver Failure Syndrome 1	50	0.028

777	P	TMP001	Temporal Lobe Epilepsy	50	0.028

778		PLC008	Placenta Disease	50	0.028

779		PRN009	Paranoid Schizophrenia	50	0.028

780	P	MTH008	Methylmalonic Acidemia	50	0.028

781		ILT001	Ileitis	50	0.028

782		HRT011	Heart Septal Defect	50	0.028

783		ONC007	Oncocytoma	49	0.028

784		ENT004	Enthesopathy	49	0.028

785		DRR003	Diarrhea 5, with Tufting Enteropathy, Congenital	49	0.028

786	c	BPL002	Bipolar I Disorder	49	0.028

787		VCC001	Vaccinia	49	0.028

788		CHL061	Childhood Leukemia	48	0.028

789		CCN001	Cocaine Dependence	48	0.028

790		END062	Endometrial Hyperplasia	48	0.028

791		GLC106	Glucocorticoid Resistance, Generalized	48	0.028

792		MCR018	Microcytic Anemia	47	0.028

793		CLF056	Cleft Lip with or Without Cleft Palate	47	0.028

794		NRN001	Neuroendocrine Carcinoma	47	0.028

795		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.028

796	c	HMN021	Human T-Cell Leukemia Virus Type 1	47	0.028

797	P	OVR046	Ovarian Cyst	47	0.028

798		ASP004	Asphyxia Neonatorum	46	0.028

799		MYC005	Myocardial Stunning	46	0.028

800	P	BRB001	Beriberi	46	0.028

801		CHD004	Chudley-Mccullough Syndrome	46	0.028

802	P	MYC033	Myoclonus	46	0.028

803		JNT004	Joint Laxity, Short Stature, and Myopia	45	0.028

804		AGR002	Agoraphobia	45	0.028

805	P	SBR004	Seborrheic Dermatitis	45	0.028

806	c	CHR517	Charcot-Marie-Tooth Disease, Type 4a	45	0.028

807		ATN011	Autoinflammation with Infantile Enterocolitis	44	0.028

808	P	CHR345	Chronic Pain	44	0.028

809	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.028

810	P	MTC004	Mitochondrial Encephalomyopathy	44	0.028

811	P	SDR002	Siderosis	44	0.028

812	P	END039	Endodermal Sinus Tumor	44	0.028

813	P	PRL003	Proliferative Glomerulonephritis	44	0.028

814		PRT035	Peritoneum Cancer	44	0.028

815	c	PRM038	Primary Agammaglobulinemia	44	0.028

816		MTR010	Mature Teratoma	44	0.028

817		ADR041	Adrenal Cortical Adenoma	43	0.028

818	P	PHR004	Pharynx Cancer	43	0.028

819		RDC006	Red Cell Aplasia	43	0.028

820	P	CND005	Cone Dystrophy	43	0.028

821	P	CRN026	Corneal Edema	43	0.028

822		STL007	Steel Syndrome	43	0.028

823		EPT021	Epithelial Recurrent Erosion Dystrophy	42	0.028

824		EXC002	Exocrine Pancreatic Insufficiency	42	0.028

825	c	MLG079	Malignant Pleural Mesothelioma	42	0.028

826	c	HMG001	Hemoglobin C Disease	40	0.028

827		MLT001	Multiple Chemical Sensitivity	40	0.028

828		HNZ004	Heinz Body Anemias	39	0.028

829		SKN020	Skin Papilloma	39	0.028

830		FRM003	Farmer's Lung	39	0.028

831		HYP141	Hyperphenylalaninemia	39	0.028

832		SCR011	Scrapie	39	0.028

833		ADR022	Adrenomyeloneuropathy	38	0.028

834		OVR047	Ovarian Cystadenocarcinoma	38	0.028

835		KSH004	Kashin-Beck Disease	38	0.028

836		PRP075	Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss	37	0.028

837	c	CHR020	Chronic Interstitial Cystitis	37	0.028

838		NRW001	Norwegian Scabies	37	0.028

839	P	HRD217	Hereditary Optic Neuropathy	36	0.028

840		PRS011	Persian Gulf Syndrome	36	0.028

841		ALC001	Alcohol-Related Birth Defect	36	0.028

842		OLG022	Oligoasthenoteratozoospermia	36	0.028

843		SPR020	Superficial Mycosis	35	0.028

844		OLG006	Oligoastrocytoma	35	0.028

845		INT040	Intrinsic Asthma	34	0.028

846		CLC008	Colchicine Resistance	34	0.028

847	c	PK3005	Pik3ca-Related Overgrowth Syndrome	34	0.028

848		CRB132	Cerebral Sinovenous Thrombosis	33	0.028

849		BWN006	Bowen's Disease	32	0.028

850		HRD218	Hereditary Stomatocytosis	32	0.028

851	c	BLD140	Blood Group, I System	32	0.028

852		WHT017	Wheat Allergy	32	0.028

853		BLD047	Bladder Squamous Cell Carcinoma	31	0.028

854		PLY150	Polykaryocytosis Inducer	31	0.028

855	c	ALC016	Alcohol Sensitivity, Acute	31	0.028

856		FNT004	Fainting	30	0.028

857		MTY003	Mutyh Polyposis	30	0.028

858		PYR016	Pyridoxine Deficiency	30	0.028

859		MYC088	Mycobacterium Avium Complex Infections	29	0.028

860		FTL007	Fetal Hydantoin Syndrome	29	0.028

861		ISL099	Isolated Methylmalonic Acidemia	29	0.028

862		GLT040	Glutamate-Cysteine Ligase Deficiency	29	0.028

863		MTR001	Mature Cataract	28	0.028

864		MYL080	Myalgic Encephalomyelitis/chronic Fatigue Syndrome	27	0.028

865		TRN002	Transitional Meningioma	25	0.028

866		ANT078	Antipyrine Metabolism	24	0.028

867		ACT133	Acetylation, Slow	23	0.028

868		HML018	Homologous Wasting Disease	22	0.028

869		AND005	Androgen Insensitivity Syndrome, Mild	19	0.028

870		PHC015	Phacoanaphylactic Uveitis	19	0.028

871	c	PGT006	Paget Disease of Bone 4	17	0.028

872		PRX092	Peroxidase, Salivary	9	0.028

873		CNN003	Conn's Syndrome	79	0.020

874		MRF001	Marfan Syndrome	77	0.020

875	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.020

876		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.020

877		BSL036	Basal Cell Nevus Syndrome	73	0.020

878		PRP027	Peripheral Vascular Disease	71	0.020

879		ADN011	Adenoid Cystic Carcinoma	70	0.020

880		PTZ001	Peutz-Jeghers Syndrome	70	0.020

881	P	HYP061	Hypertrophic Cardiomyopathy	70	0.020

882	P	ASP006	Aspergillosis	69	0.020

883		SVR097	Severe Cutaneous Adverse Reaction	69	0.020

884		EWN003	Ewing Sarcoma	69	0.020

885		MST024	Mastocytosis, Cutaneous	69	0.020

886		CMM004	Common Variable Immunodeficiency	68	0.020

887	P	MYS003	Myasthenia Gravis	68	0.020

888		RCK004	Rickets	68	0.020

889	P	THR014	Thrombocytopenia	67	0.020

890	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.020

891		GLL008	Gilles De La Tourette Syndrome	66	0.020

892		CHD001	Chediak-Higashi Syndrome	66	0.020

893	c	FML021	Familial Hypercholesterolemia	66	0.020

894	P	HYD006	Hydrocephalus	66	0.020

895		KHL003	Kohlschutter-Tonz Syndrome	65	0.020

896		GTL001	Gitelman Syndrome	65	0.020

897		LWC002	Lowe Oculocerebrorenal Syndrome	65	0.020

898		MSM014	Mismatch Repair Cancer Syndrome	65	0.020

899	c	ART101	Aortic Valve Disease 2	65	0.020

900	P	PRS038	Personality Disorder	65	0.020

901		MNK001	Menkes Disease	64	0.020

902		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.020

903	P	HRM001	Hermansky-Pudlak Syndrome	64	0.020

904		NRF007	Neurofibroma	64	0.020

905	P	PLY170	Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease	64	0.020

906		ALP103	Alpha-1-Antitrypsin Deficiency	64	0.020

907	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.020

908	c	CNG006	Congenital Hypothyroidism	64	0.020

909		MSC007	Muscle Hypertrophy	64	0.020

910		CYS013	Cystinuria	63	0.020

911	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.020

912		TYP007	Typhoid Fever	63	0.020

913		PLG002	Plague	63	0.020

914	c	MLG084	Malignant Fibrous Histiocytoma	63	0.020

915		END041	Endometrial Adenocarcinoma	63	0.020

916		HMT002	Hematologic Cancer	62	0.020

917		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.020

918	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.020

919	c	BRN108	Branchiootic Syndrome 1	62	0.020

920	c	SVR001	Severe Acute Respiratory Syndrome	62	0.020

921		HYD038	Hydrops Fetalis, Nonimmune	62	0.020

922		GLY010	Glycine Encephalopathy	62	0.020

923		ESP020	Esophageal Atresia	62	0.020

924		PSR001	Psoriatic Arthritis	61	0.020

925	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	61	0.020

926		OST003	Osteonecrosis	61	0.020

927		RCT015	Reactive Arthritis	61	0.020

928		SDD001	Sudden Infant Death Syndrome	61	0.020

929		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.020

930		SZR001	Sezary's Disease	60	0.020

931		HST017	Histiocytosis-Lymphadenopathy Plus Syndrome	60	0.020

932	P	TST021	Testicular Germ Cell Tumor	60	0.020

933	P	BNG030	Benign Ependymoma	60	0.020

934	P	VNT002	Ventricular Septal Defect	60	0.020

935		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.020

936		CRD223	Cardiac Arrhythmia	60	0.020

937	P	ALP009	Alopecia Areata	60	0.020

938	c	WLF013	Wolfram Syndrome 1	60	0.020

939	P	WLF004	Wolfram Syndrome	60	0.020

940		LBR030	Leber Optic Atrophy	60	0.020

941	c	HYP731	Hyperaldosteronism, Familial, Type I	60	0.020

942	P	PTN014	Patent Ductus Arteriosus 1	60	0.020

943	P	EMR001	Emery-Dreifuss Muscular Dystrophy	60	0.020

944	P	OCL002	Oculocutaneous Albinism	60	0.020

945	c	CRD186	Ceroid Lipofuscinosis, Neuronal, 3	60	0.020

946	P	GLY013	Glycogen Storage Disease	60	0.020

947	P	RBL001	Rubella	59	0.020

948	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.020

949	P	BND020	Bone Disease	59	0.020

950	P	SLP005	Sleep Disorder	59	0.020

951		SRC027	Sarcoma, Synovial	58	0.020

952		CRY005	Cryptococcosis	58	0.020

953		ALK013	Alkaptonuria	58	0.020

954		CRZ002	Crouzon Syndrome with Acanthosis Nigricans	58	0.020

955		PST028	Post-Traumatic Stress Disorder	58	0.020

956	c	XRD022	Xeroderma Pigmentosum, Complementation Group D	58	0.020

957		FBR047	Fibromyalgia	58	0.020

958		CMP010	Complex Regional Pain Syndrome	58	0.020

959	c	BNG091	Benign Chronic Pemphigus	58	0.020

960		CCC001	Coccidioidomycosis	58	0.020

961		ERY003	Erythema Multiforme	58	0.020

962		NWB001	Newborn Respiratory Distress Syndrome	58	0.020

963		EXT034	Extrinsic Allergic Alveolitis	58	0.020

964		LNG108	Langerhans Cell Histiocytosis	58	0.020

965		PMP006	Pemphigus Vulgaris, Familial	57	0.020

966	P	PLV020	Pelvic Organ Prolapse	57	0.020

967	c	CHR417	Chronic Graft Versus Host Disease	57	0.020

968		BLM002	Bulimia Nervosa	57	0.020

969		MCR013	Microphthalmia	57	0.020

970	c	ANM036	Anemia, Sideroblastic, 1	57	0.020

971		MNR012	Meniere Disease	57	0.020

972		CHK001	Chikungunya	57	0.020

973		DSS009	Disseminated Intravascular Coagulation	57	0.020

974		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.020

975		APH001	Aphthous Stomatitis	57	0.020

976	P	END033	Endocarditis	57	0.020

977	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.020

978	P	MYS005	Myositis	56	0.020

979		TCK001	Tick-Borne Encephalitis	56	0.020

980		EXF001	Exfoliation Syndrome	56	0.020

981	c	ESS001	Essential Tremor	56	0.020

982		SFT003	Soft Tissue Sarcoma	56	0.020

983		SCH003	Schizophreniform Disorder	56	0.020

984		PRS047	Prostatitis	56	0.020

985		ANS011	Anus Cancer	56	0.020

986		OVR012	Ovarian Serous Cystadenocarcinoma	56	0.020

987		MTH009	Mouth Disease	56	0.020

988	P	NRF002	Neurofibromatosis	56	0.020

989		SLC006	Silicosis	56	0.020

990	c	ERY071	Erythrocytosis, Familial, 2, Autosomal Recessive	55	0.020

991		MCN007	Meconium Aspiration Syndrome	55	0.020

992		LMB062	Limb Ischemia	55	0.020

993	P	GRV001	Graves' Disease	55	0.020

994	P	PTT006	Pituitary Adenoma	55	0.020

995		CHR100	Chronic Ulcer of Skin	55	0.020

996	P	VNS003	Venous Insufficiency	55	0.020

997	c	ATM024	Autoimmune Pancreatitis	55	0.020

998	P	GNR002	Generalized Epilepsy with Febrile Seizures Plus	55	0.020

999		HMP005	Hemiplegia	55	0.020

1000		PRP030	Purpura	54	0.020

1001		RSC001	Rosacea	54	0.020

1002		BRN014	Bronchopneumonia	54	0.020

1003		CLL010	Cellular Ependymoma	54	0.020

1004		WST005	West Nile Virus	54	0.020

1005		GST009	Gastroschisis	53	0.020

1006		MMM001	Mammary Paget's Disease	53	0.020

1007	P	EPD016	Epidermolysis Bullosa	53	0.020

1008		RHM028	Rheumatic Heart Disease	53	0.020

1009	c	CNR007	Cone-Rod Dystrophy 6	53	0.020

1010	P	MNC007	Monocytic Leukemia	53	0.020

1011		PRP036	Peripheral T-Cell Lymphoma	53	0.020

1012		ENC055	Encephalopathy, Ethylmalonic	53	0.020

1013	P	ORL007	Oral Cavity Cancer	53	0.020

1014	P	SHR001	Short Bowel Syndrome	53	0.020

1015	P	GRS003	Griscelli Syndrome	53	0.020

1016	P	CTN003	Cutaneous Lupus Erythematosus	53	0.020

1017		NRT001	Neurotic Disorder	53	0.020

1018		END002	Endometrioid Ovary Carcinoma	53	0.020

1019		PRN011	Pernicious Anemia	53	0.020

1020	P	LMB006	Limb-Girdle Muscular Dystrophy	53	0.020

1021		PRP080	Peripheral Artery Disease	53	0.020

1022	c	GLL024	Gallbladder Disease 1	53	0.020

1023	c	CNT035	Central Nervous System Disease	52	0.020

1024		CHR073	Choreatic Disease	52	0.020

1025		OST011	Osteomalacia	52	0.020

1026	P	PRG013	Paraganglioma	52	0.020

1027		ESP023	Esophageal Disease	52	0.020

1028		PLM014	Pleomorphic Adenoma	52	0.020

1029		PRP016	Paraplegia	52	0.020

1030	P	D2H002	D-2-Hydroxyglutaric Aciduria 1	52	0.020

1031		MRG003	Marginal Zone B-Cell Lymphoma	52	0.020

1032		DYS015	Dysentery	52	0.020

1033	P	ACT105	Acute Mountain Sickness	52	0.020

1034	P	PRV002	Periventricular Nodular Heterotopia	52	0.020

1035		DFF036	Differentiated Thyroid Carcinoma	52	0.020

1036	P	MGR003	Migraine with Aura	52	0.020

1037	c	ACT135	Acute Graft Versus Host Disease	52	0.020

1038		THR004	Thrombocytosis	51	0.020

1039		TRC010	Trichotillomania	51	0.020

1040		UNV001	Unverricht-Lundborg Syndrome	51	0.020

1041		FDL002	Food Allergy	51	0.020

1042		PLS009	Plasma Cell Neoplasm	51	0.020

1043	c	PNC106	Pancreatic Agenesis 1	51	0.020

1044		MGL001	Megaloblastic Anemia	51	0.020

1045		CYS036	Cystinosis, Nephropathic	51	0.020

1046		CCC002	Coccidiosis	51	0.020

1047		NRM004	Neuroma	51	0.020

1048		ACH005	Achalasia	51	0.020

1049		HND002	Hand, Foot and Mouth Disease	51	0.020

1050	P	RNL007	Renal Tubular Acidosis	51	0.020

1051		TLR001	Tularemia	51	0.020

1052		HYP081	Hypolipoproteinemia	51	0.020

1053	P	MMB011	Membranous Nephropathy	50	0.020

1054	P	OVR082	Overgrowth Syndrome	50	0.020

1055	P	PRS049	Persistent Mullerian Duct Syndrome	50	0.020

1056		STM007	Stomatitis	50	0.020

1057		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.020

1058		MCP006	Mucoepidermoid Carcinoma	50	0.020

1059		MLL001	Molluscum Contagiosum	50	0.020

1060	P	AGG001	Aggressive Periodontitis	50	0.020

1061		TRP002	Tropical Spastic Paraparesis	50	0.020

1062		CLR003	Clear Cell Adenocarcinoma	50	0.020

1063		OCL022	Ocular Melanoma	50	0.020

1064		DYS073	Dysphagia	50	0.020

1065		RNL078	Renal Dysplasia	50	0.020

1066	c	INF023	Inflammatory Breast Carcinoma	50	0.020

1067		HYP080	Hypogonadism	50	0.020

1068		DBT004	Diabetic Polyneuropathy	49	0.020

1069	c	CHR418	Chronic Leukemia	49	0.020

1070		VRR004	Verrucous Carcinoma	49	0.020

1071	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	0.020

1072		MCN001	Mucinous Adenocarcinoma	49	0.020

1073		PLY024	Polymicrogyria	49	0.020

1074		AMB002	Amblyopia	49	0.020

1075	P	END046	Endometritis	49	0.020

1076		SPN028	Spondyloepimetaphyseal Dysplasia, Strudwick Type	49	0.020

1077		GST049	Gastrointestinal System Cancer	49	0.020

1078	P	CRV031	Cervical Adenocarcinoma	49	0.020

1079		MTC005	Mitochondrial Metabolism Disease