Search results for Cysteine

1352 hits were found for Cysteine

#	Family	MCID	Name	MIFTS	Score
1		MRC009	Mercaptolactate-Cysteine Disulfiduria	22	5.022

2		CYS043	Cysteine Peptiduria	7	3.545

3		GMM011	Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to	26	3.537

4		AMP011	Ampola Syndrome	4	2.506

5		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.706

6		HLX001	Helix Syndrome	47	0.227

7		CHG001	Chagas Disease	66	0.160

8		LSH001	Leishmaniasis	63	0.158

9	P	KLZ004	Kala-Azar 1	41	0.158

10		TRD008	Triiodothyronine Receptor Auxiliary Protein	34	0.140

11	P	PRD008	Periodontitis	62	0.139

12	c	NRP064	Neuropathy, Congenital Hypomyelinating, 2	32	0.124

13	P	KDN018	Kidney Disease	70	0.120

14	P	NRB001	Neuroblastoma	71	0.119

15		BNR002	Bone Resorption Disease	48	0.119

16	P	CLR023	Colorectal Cancer	98	0.115

17		HMN044	Human Immunodeficiency Virus Type 1	71	0.114

18		HMC014	Homocysteinemia	53	0.114

19	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.110

20		BRT054	Brittle Bone Disorder	70	0.108

21		CYS001	Cystic Fibrosis	80	0.105

22		AMB001	Amebiasis	49	0.103

23	c	ACT071	Acute Kidney Failure	59	0.101

24	P	BRS047	Breast Cancer	96	0.099

25	P	LVR013	Liver Disease	68	0.099

26		VSC003	Visceral Leishmaniasis	55	0.099

27	P	PLY011	Polycystic Ovary Syndrome	56	0.097

28		TRY001	Trypanosomiasis	50	0.097

29		SLP001	Sleeping Sickness	48	0.097

30		CYT002	Cytokine Deficiency	44	0.097

31	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.095

32	P	MSC005	Muscular Dystrophy	66	0.095

33	P	ADN016	Adenocarcinoma	64	0.095

34	P	CTR002	Cataract	60	0.095

35	P	LTR001	Lateral Sclerosis	53	0.095

36		47X002	47,xyy	49	0.095

37		CYS013	Cystinuria	62	0.093

38		SQM006	Squamous Cell Carcinoma	60	0.093

39	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.093

40	P	HMC002	Homocystinuria	54	0.093

41		PRS131	Prostate Cancer/brain Cancer Susceptibility	25	0.093

42		GLB015	Glioblastoma Multiforme	75	0.091

43	P	LKM002	Leukemia	66	0.091

44		IDP011	Idiopathic Interstitial Pneumonia	63	0.091

45	P	PLM036	Pulmonary Fibrosis	61	0.091

46		ISC004	Ischemia	60	0.091

47		48X005	48,xyyy	39	0.091

48	P	PNC035	Pancreatic Cancer	84	0.089

49		SVR004	Severe Combined Immunodeficiency	73	0.089

50		BRN024	Bronchitis	68	0.089

51		ALL026	Allergic Hypersensitivity Disease	64	0.089

52		CHL123	Chlamydia	59	0.089

53	P	LNG032	Lung Cancer	97	0.086

54	P	PHC003	Pheochromocytoma	71	0.086

55		PRT037	Pertussis	65	0.086

56	P	GLM045	Glioma	63	0.086

57		LNG099	Lung Disease	61	0.086

58		ATM095	Autoimmune Disease	61	0.086

59	P	BPL003	Bipolar Disorder	56	0.086

60		ATX031	Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus	56	0.086

61		BCT022	Bacterial Infectious Disease	56	0.086

62		ADR040	Adrenal Gland Pheochromocytoma	46	0.086

63		GLL048	Glial Tumor	45	0.086

64	c	MJR024	Major Affective Disorder 9	41	0.086

65	c	MJR022	Major Affective Disorder 8	38	0.086

66	c	CRB175	Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1	69	0.084

67	P	VSC007	Vascular Disease	63	0.084

68		CTN007	Cutaneous Leishmaniasis	61	0.084

69		CYS010	Cystinosis	60	0.084

70		THY029	Thyroid Carcinoma	59	0.084

71	P	INF032	Infertility	57	0.084

72		TRC003	Trichomoniasis	52	0.084

73		BRN071	Brain Injury	49	0.084

74	P	OVR042	Ovarian Cancer	89	0.082

75		ATH013	Atherosclerosis Susceptibility	66	0.082

76		LVR012	Liver Cirrhosis	63	0.082

77		HYP066	Hyperglycemia	61	0.082

78		SCH014	Schistosomiasis	56	0.082

79		SCH060	Schistosoma Mansoni Infection, Susceptibility/	39	0.082

80	P	GST053	Gastric Cancer	83	0.079

81		IMM167	Immune Deficiency Disease	78	0.079

82	c	HYP836	Hypercholesterolemia, Familial, 1	72	0.079

83		MLN008	Melanoma	69	0.079

84	c	SVR001	Severe Acute Respiratory Syndrome	55	0.079

85		PRG008	Paragonimiasis	38	0.079

86		PPL052	Papillomatosis, Confluent and Reticulated	34	0.079

87	P	HPT023	Hepatocellular Carcinoma	100	0.077

88		OST012	Osteoarthritis	78	0.077

89	P	PRK057	Parkinson Disease, Late-Onset	76	0.077

90	c	CHR684	Chronic Kidney Disease	66	0.077

91		DPR016	Depression	63	0.077

92		TXC005	Toxic Shock Syndrome	61	0.077

93		TRM010	Traumatic Brain Injury	53	0.077

94		VCC001	Vaccinia	49	0.077

95	c	MCR120	Microvascular Complications of Diabetes 7	47	0.077

96	P	ALZ034	Alzheimer Disease	88	0.074

97		MLR004	Malaria	80	0.074

98		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.074

99		OST159	Osteogenic Sarcoma	66	0.074

100	P	ATS364	Autism	65	0.074

101	P	HRP006	Herpes Simplex	65	0.074

102		HYP266	Hypoxia	56	0.074

103		CLN003	Clonorchiasis	43	0.074

104		FSC002	Fascioliasis	41	0.074

105	P	RHM011	Rheumatoid Arthritis	80	0.071

106	P	AMY004	Amyloidosis	70	0.071

107		FTT001	Fatty Liver Disease	61	0.071

108	P	SZR006	Seizure Disorder	58	0.071

109		MNT002	Mental Depression	57	0.071

110	c	MCR113	Microvascular Complications of Diabetes 3	52	0.071

111		ATX038	Ataxia and Polyneuropathy, Adult-Onset	44	0.071

112	c	MCR130	Microvascular Complications of Diabetes 6	41	0.071

113	c	MCR133	Microvascular Complications of Diabetes 4	41	0.071

114	c	FML021	Familial Hypercholesterolemia	68	0.069

115	P	THR014	Thrombocytopenia	68	0.069

116		HYP056	Hypoglycemia	66	0.069

117	c	HPT003	Hepatitis a	63	0.069

118		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	63	0.069

119		ACQ007	Acquired Immunodeficiency Syndrome	60	0.069

120	P	ALC033	Alcohol Use Disorder	58	0.069

121	P	LYM031	Lymphocytic Leukemia	55	0.069

122		CYS005	Cysticercosis	54	0.069

123	P	AST007	Astrocytoma	50	0.069

124		INS024	Insulin-Like Growth Factor I	79	0.066

125	P	BLD134	Bladder Cancer	78	0.066

126		MRF001	Marfan Syndrome	75	0.066

127		PLM134	Pulmonary Fibrosis, Idiopathic	75	0.066

128	P	MYC007	Myocardial Infarction	70	0.066

129		THY111	Thyroid Carcinoma, Familial Medullary	67	0.066

130	c	SML038	Small Cell Cancer of the Lung	65	0.066

131	P	MYP004	Myopathy	64	0.066

132		NTR005	Nutritional Deficiency Disease	61	0.066

133	P	MLT074	Multiple Endocrine Neoplasia	55	0.066

134		THY125	Thyroid Gland Medullary Carcinoma	51	0.066

135	c	ACT134	Acute Liver Failure	51	0.066

136		OBS002	Obsessive-Compulsive Disorder	68	0.063

137	P	INF038	Influenza	68	0.063

138	c	RHB024	Rhabdomyosarcoma 2	65	0.063

139		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.063

140	c	WLM013	Wilms Tumor 1	65	0.063

141	c	ACT027	Acute Pancreatitis	59	0.063

142	P	BCL017	B-Cell Lymphoma	58	0.063

143		END030	End Stage Renal Failure	58	0.063

144	P	MLN007	Male Infertility	56	0.063

145	P	GST044	Gastritis	55	0.063

146	c	OST080	Osteogenesis Imperfecta, Type Ii	55	0.063

147	P	CHR345	Chronic Pain	50	0.063

148		FSC004	Fasciitis	50	0.063

149		NCR007	Necrotizing Fasciitis	49	0.063

150		CRB004	Cerebral Artery Occlusion	44	0.063

151	c	PLY105	Polycystic Ovary Syndrome 1	38	0.063

152		HRN029	Hearing Loss, Noise-Induced	37	0.063

153		SPR006	Sparganosis	32	0.063

154		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.063

155	c	SYS001	Systemic Lupus Erythematosus	86	0.059

156		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.059

157	P	SCH015	Schizophrenia	75	0.059

158		MSC157	Muscular Dystrophy, Duchenne Type	71	0.059

159	c	HPT073	Hepatitis C Virus	70	0.059

160	P	LKM062	Leukemia, Acute Lymphoblastic	68	0.059

161		ALC007	Alcohol Dependence	66	0.059

162	P	MCR115	Microvascular Complications of Diabetes 5	66	0.059

163	P	TRN020	Turner Syndrome	65	0.059

164	c	PRC016	Pre-Eclampsia	63	0.059

165	P	NRN021	Neuronal Ceroid Lipofuscinosis	63	0.059

166	P	CRN300	Coronary Heart Disease 1	63	0.059

167	P	ADL010	Adult Respiratory Distress Syndrome	63	0.059

168	c	PRT132	Protoporphyria, Erythropoietic, 1	61	0.059

169		HMS001	Hemosiderosis	54	0.059

170	c	PRD040	Periodontitis, Chronic	54	0.059

171	P	MSC003	Muscular Atrophy	52	0.059

172		PNC041	Pancreatic Ductal Adenocarcinoma	51	0.059

173		VLV047	Volvulus of Midgut	50	0.059

174		ANX004	Anoxia	42	0.059

175	P	RRH023	Rare Hereditary Hemochromatosis	41	0.059

176		PLY150	Polykaryocytosis Inducer	31	0.059

177	c	MCL042	Macular Degeneration, Age-Related, 1	85	0.056

178	c	LKM061	Leukemia, Acute Myeloid	83	0.056

179	P	RTN008	Retinitis Pigmentosa	77	0.056

180	P	HRT032	Heart Disease	75	0.056

181		ADR007	Adrenoleukodystrophy	74	0.056

182	P	OST002	Osteoporosis	73	0.056

183	P	HYP724	Hyperlipoproteinemia, Type Iii	72	0.056

184	P	HNT016	Huntington Disease	71	0.056

185		CNG034	Congestive Heart Failure	70	0.056

186	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	69	0.056

187	P	PLM037	Pulmonary Hypertension	68	0.056

188		PSY004	Psychotic Disorder	67	0.056

189	c	HPT001	Hepatitis C	63	0.056

190		NNL005	Non-Alcoholic Fatty Liver Disease	62	0.056

191	P	PNC044	Pancreatitis	61	0.056

192		SPN186	Spinal Cord Injury	60	0.056

193		VSL002	Visual Epilepsy	58	0.056

194		BRN056	Bronchopulmonary Dysplasia	57	0.056

195	P	NRP001	Neuropathy	56	0.056

196		AGN016	Aging	56	0.056

197	c	OST135	Osteogenesis Imperfecta, Type I	55	0.056

198		CHK001	Chikungunya	53	0.056

199		HMC040	Homocystinuria Due to Cystathionine Beta-Synthase Deficiency	51	0.056

200		NNL006	Non-Alcoholic Steatohepatitis	51	0.056

201		MTB004	Metabolic Acidosis	50	0.056

202		PTH002	Pathological Gambling	48	0.056

203		RTN023	Retinitis	46	0.056

204		NRR001	Neuroretinitis	43	0.056

205		ALL014	Allergic Encephalomyelitis	39	0.056

206		ADR022	Adrenomyeloneuropathy	38	0.056

207		PRC051	Paracetamol Poisoning	30	0.056

208		ESP021	Esophageal Cancer	90	0.052

209		SQM013	Squamous Cell Carcinoma, Head and Neck	80	0.052

210	P	LNG064	Lung Cancer Susceptibility 3	77	0.052

211		DFC004	Deficiency Anemia	75	0.052

212	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.052

213	P	RTN024	Retinoblastoma	72	0.052

214		ANX010	Anxiety	72	0.052

215	P	GRF003	Graft-Versus-Host Disease	71	0.052

216		PLM001	Pulmonary Tuberculosis	70	0.052

217	c	MGR028	Migraine with or Without Aura 1	69	0.052

218		CRB039	Cerebrovascular Disease	69	0.052

219	P	LYM118	Lymphoma	68	0.052

220	P	PNM007	Pneumonia	68	0.052

221		BRK010	Burkitt Lymphoma	67	0.052

222	P	HPT021	Hepatitis	67	0.052

223	P	VNW001	Von Willebrand's Disease	64	0.052

224		TBC004	Tobacco Addiction	64	0.052

225	P	END044	Endometriosis	62	0.052

226	P	PRP029	Porphyria	62	0.052

227		ALC006	Alcoholic Hepatitis	61	0.052

228	c	HPT016	Hepatitis B	59	0.052

229		ADN018	Adenoma	58	0.052

230		IRN002	Iron Metabolism Disease	57	0.052

231	P	FTT008	Fatty Liver Disease, Nonalcoholic 1	57	0.052

232		DSS008	Disease of Mental Health	57	0.052

233	P	TRM003	Tremor	53	0.052

234	c	FML008	Familial Retinoblastoma	53	0.052

235		TRC010	Trichotillomania	50	0.052

236		STM007	Stomatitis	49	0.052

237		MNN009	Meningoencephalitis	49	0.052

238		BBS001	Babesiosis	48	0.052

239		CYS019	Cystathioninuria	45	0.052

240		DWR001	Dwarfism	44	0.052

241	c	PCH010	Pachyonychia Congenita 3	43	0.052

242	P	MJR007	Major Affective Disorder 1	43	0.052

243		HMP009	Haemophilus Influenzae	42	0.052

244		STR077	Streptococcal Toxic-Shock Syndrome	37	0.052

245	c	MJR008	Major Affective Disorder 2	34	0.052

246	c	MJR003	Major Affective Disorder 6	33	0.052

247	c	MJR006	Major Affective Disorder 5	33	0.052

248	c	MJR023	Major Affective Disorder 7	33	0.052

249	c	MJR004	Major Affective Disorder 4	28	0.052

250	P	PRS040	Prostate Cancer	97	0.048

251	c	DLT002	Dilated Cardiomyopathy	79	0.048

252		AST005	Asthma	77	0.048

253	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.048

254		ULC004	Ulcerative Colitis	73	0.048

255		ADL002	Adult Syndrome	69	0.048

256	c	EXD008	Exudative Vitreoretinopathy 1	69	0.048

257	P	HYP086	Hypothyroidism	68	0.048

258	c	NMN015	Niemann-Pick Disease, Type C1	68	0.048

259	P	DBT085	Diabetes Mellitus, Insulin-Dependent	67	0.048

260	P	CRN018	Coronary Artery Anomaly	63	0.048

261	P	NTR004	Neutropenia	63	0.048

262	c	ACT068	Acute Cystitis	63	0.048

263		LPD008	Lipid Metabolism Disorder	62	0.048

264	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	62	0.048

265	P	HML002	Hemolytic Anemia	62	0.048

266	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.048

267	P	ENC018	Encephalopathy	61	0.048

268	P	LPS004	Lupus Erythematosus	61	0.048

269		MSL001	Measles	61	0.048

270	P	MYL006	Myeloid Leukemia	60	0.048

271	P	BND020	Bone Disease	59	0.048

272	P	BRS044	Breast Adenocarcinoma	59	0.048

273		ANR040	Aneurysm	58	0.048

274	c	ACT073	Acute Leukemia	58	0.048

275		NWB001	Newborn Respiratory Distress Syndrome	58	0.048

276	P	EXN002	Exanthem	57	0.048

277	P	DRR001	Diarrhea	57	0.048

278	P	FBR017	Fibrosarcoma	56	0.048

279	P	INF037	Inflammatory Bowel Disease	56	0.048

280		ALL006	Allergic Asthma	56	0.048

281		PRP030	Purpura	55	0.048

282		MCS002	Mucositis	55	0.048

283		PPL022	Papilloma	54	0.048

284	P	RTN016	Retinal Degeneration	53	0.048

285		ART140	Arteries, Anomalies of	53	0.048

286	c	HPT007	Hepatitis E	52	0.048

287		BCT002	Bacterial Vaginosis	52	0.048

288		GLC009	Glucosephosphate Dehydrogenase Deficiency	52	0.048

289		CYS036	Cystinosis, Nephropathic	51	0.048

290		HYP781	Hypoascorbemia	50	0.048

291	P	TMP001	Temporal Lobe Epilepsy	50	0.048

292		SPL018	Splenomegaly	48	0.048

293		ANV001	Anovulation	47	0.048

294		LYM019	Lymphosarcoma	47	0.048

295	c	INH020	Inherited Metabolic Disorder	46	0.048

296		CHL147	Chlamydia Pneumonia	45	0.048

297		ACT003	Acute Kidney Tubular Necrosis	45	0.048

298		NWC001	Newcastle Disease	44	0.048

299	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.048

300		SQM002	Squamous Cell Papilloma	42	0.048

301		THR035	Thrombasthenia	41	0.048

302	c	HYP595	Hypertension, Essential	84	0.044

303	c	ATR087	Atrial Standstill 1	74	0.044

304	P	EPL164	Epilepsy	71	0.044

305		PRP027	Peripheral Vascular Disease	71	0.044

306		OTT002	Otitis Media	71	0.044

307	P	FRN006	Frontotemporal Dementia	70	0.044

308	P	MJR001	Major Depressive Disorder	68	0.044

309	P	DMN002	Dementia	67	0.044

310	P	DRM053	Dermatitis, Atopic	66	0.044

311		ACH004	Achondroplasia	66	0.044

312		SPN209	Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations	66	0.044

313	c	MCR129	Microvascular Complications of Diabetes 1	66	0.044

314	P	DBT009	Diabetes Mellitus	64	0.044

315		PPL049	Papillon-Lefevre Syndrome	63	0.044

316		CLT003	Colitis	62	0.044

317	P	THN009	Thanatophoric Dysplasia, Type I	62	0.044

318		MDD011	Mood Disorder	62	0.044

319	c	PNS012	Paine Syndrome	61	0.044

320		DPH001	Diphtheria	60	0.044

321		INS001	Insulinoma	60	0.044

322		GNG013	Gingivitis	59	0.044

323		GST045	Gastroenteritis	59	0.044

324		BRN002	Bronchiolitis	59	0.044

325	P	PRV006	Pervasive Developmental Disorder	57	0.044

326	P	HDC001	Headache	57	0.044

327	P	PRP019	Peripheral Nervous System Disease	57	0.044

328		VSC002	Vascular Dementia	57	0.044

329		BRN004	Brain Edema	55	0.044

330		PRT038	Protein-Energy Malnutrition	54	0.044

331		END040	Endogenous Depression	54	0.044

332		HYP060	Hyperinsulinism	54	0.044

333		TRC008	Trachoma	53	0.044

334		NRT001	Neurotic Disorder	52	0.044

335		LYS002	Lysosomal Storage Disease	52	0.044

336	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.044

337		VNZ002	Venezuelan Equine Encephalitis	46	0.044

338		HDN002	Head Injury	45	0.044

339		GRD001	Giardiasis	45	0.044

340	P	SPR086	Spermatogenic Failure 3	44	0.044

341	P	PHT010	Photoparoxysmal Response 1	42	0.044

342	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.044

343	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	41	0.044

344	c	MCR112	Microvascular Complications of Diabetes 2	41	0.044

345	c	PLM150	Pulmonary Alveolar Proteinosis, Acquired	40	0.044

346		PRM004	Primary Amebic Meningoencephalitis	31	0.044

347		ARG004	Argyria	28	0.044

348	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	89	0.040

349	P	ATX030	Ataxia-Telangiectasia	83	0.040

350		NRL016	Neural Tube Defects	82	0.040

351	P	GLM040	Glioma Susceptibility 1	81	0.040

352		STR067	Stroke, Ischemic	80	0.040

353	P	NRF023	Neurofibromatosis, Type Ii	76	0.040

354		PHN003	Phenylketonuria	75	0.040

355	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.040

356	P	RSP003	Respiratory Failure	74	0.040

357		CRH001	Crohn's Disease	74	0.040

358	P	MLT020	Multiple Sclerosis	72	0.040

359	P	CNR004	Cone-Rod Dystrophy 2	71	0.040

360	P	SLP006	Sleep Apnea	69	0.040

361	P	CLC063	Celiac Disease 1	68	0.040

362	c	ATS007	Autism Spectrum Disorder	67	0.040

363		CHL065	Cholangiocarcinoma	67	0.040

364		ALL003	Allergic Rhinitis	67	0.040

365	P	NSP012	Nasopharyngeal Carcinoma	67	0.040

366	P	SKN015	Skin Carcinoma	67	0.040

367		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.040

368	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	66	0.040

369	c	HMP029	Hemophilia a	65	0.040

370	P	MNN013	Meningitis	65	0.040

371		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.040

372		KHL003	Kohlschutter-Tonz Syndrome	64	0.040

373	c	SCL052	Scleroderma, Familial Progressive	62	0.040

374		BRS099	Breast Ductal Carcinoma	62	0.040

375	c	NMN013	Niemann-Pick Disease, Type a	62	0.040

376	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.040

377		CHR066	Chronic Fatigue Syndrome	61	0.040

378	c	BRN108	Branchiootic Syndrome 1	61	0.040

379	P	SNS001	Sensorineural Hearing Loss	61	0.040

380		CRD223	Cardiac Arrhythmia	60	0.040

381	P	NMN002	Niemann-Pick Disease	60	0.040

382		ORL011	Oral Cancer	60	0.040

383		CHC001	Chickenpox	60	0.040

384	P	THL005	Thalassemia	60	0.040

385	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	60	0.040

386	P	BRN022	Bronchiectasis	59	0.040

387		HLC007	Helicobacter Pylori Infection	59	0.040

388		PPT005	Peptic Ulcer Disease	58	0.040

389		CMP010	Complex Regional Pain Syndrome	58	0.040

390		EYD002	Eye Disease	58	0.040

391	P	RHN004	Rhinitis	57	0.040

392		PLG002	Plague	57	0.040

393		RSP019	Respiratory Distress Syndrome in Premature Infants	57	0.040

394		APH002	Aphasia	57	0.040

395		SCH003	Schizophreniform Disorder	56	0.040

396		LMB062	Limb Ischemia	55	0.040

397		CHL014	Cholera	55	0.040

398		RLP002	Relapsing-Remitting Multiple Sclerosis	55	0.040

399		HMZ003	Homozygous Familial Hypercholesterolemia	55	0.040

400		FCT001	Factor Viii Deficiency	55	0.040

401		PRN019	Perinatal Necrotizing Enterocolitis	54	0.040

402		CLL003	Cellulitis	54	0.040

403	P	LRY044	Larynx Cancer	54	0.040

404		BRN038	Bronchial Disease	53	0.040

405		KRT009	Keratosis	53	0.040

406		GLS018	Glass Syndrome	53	0.040

407		SPN008	Spondyloepiphyseal Dysplasia Congenita	52	0.040

408		CMB003	Combined T Cell and B Cell Immunodeficiency	52	0.040

409	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.040

410	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.040

411	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.040

412	c	ACT135	Acute Graft Versus Host Disease	51	0.040

413		TLN003	Telangiectasis	51	0.040

414		DNT012	Dental Caries	51	0.040

415		GLC004	Galactokinase Deficiency	51	0.040

416	P	ATR005	Atrophic Gastritis	50	0.040

417		ENT011	Enterocolitis	50	0.040

418		CCC002	Coccidiosis	50	0.040

419		INT079	Intrahepatic Cholangiocarcinoma	50	0.040

420		VGN020	Vaginal Disease	50	0.040

421		CCN001	Cocaine Dependence	48	0.040

422		ATS010	Autosomal Recessive Disease	48	0.040

423	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.040

424	P	TCL004	T-Cell Leukemia	47	0.040

425	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.040

426	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.040

427	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.040

428		ANR004	Anuria	46	0.040

429	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.040

430	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.040

431		CWP001	Cowpox	45	0.040

432		ACT029	Acute Interstitial Pneumonia	44	0.040

433	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.040

434	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.040

435		SLF014	Sulfite Oxidase Deficiency, Isolated	40	0.040

436	c	EPS039	Episodic Pain Syndrome, Familial, 1	40	0.040

437		PRM329	Premature Aging	39	0.040

438		ACT228	Acute Radiation Syndrome	29	0.040

439		PLY028	Polycystic Bone Disease	17	0.040

440	P	MDL005	Medulloblastoma	77	0.034

441		CRV035	Cervical Cancer	76	0.034

442		END057	Endometrial Cancer	74	0.034

443	c	MNN043	Meningioma, Familial	74	0.034

444		BRN028	Brain Cancer	73	0.034

445	c	BTT014	Beta-Thalassemia	72	0.034

446	P	SRC025	Sarcoidosis 1	70	0.034

447		DWN001	Down Syndrome	70	0.034

448		ART016	Aortic Aneurysm	68	0.034

449	P	MYC084	Mycobacterium Tuberculosis 1	68	0.034

450		PCK003	Pick Disease of Brain	68	0.034

451		CNN005	Connective Tissue Disease	66	0.034

452		GLN010	Glanzmann Thrombasthenia	66	0.034

453		DBT091	Diabetes Insipidus, Nephrogenic, Autosomal	66	0.034

454		ANG054	Angina Pectoris	66	0.034

455		SRC014	Sarcoma	65	0.034

456		LNG039	Lung Squamous Cell Carcinoma	65	0.034

457	c	MSC165	Muscular Dystrophy, Congenital, Lmna-Related	65	0.034

458	P	LPS002	Liposarcoma	65	0.034

459	P	TRC102	Trichothiodystrophy 1, Photosensitive	65	0.034

460	P	THY023	Thymoma	65	0.034

461		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	64	0.034

462		TTN003	Tetanus	64	0.034

463	P	GCH001	Gaucher's Disease	64	0.034

464		CLN015	Colon Adenocarcinoma	63	0.034

465		LYM017	Lyme Disease	63	0.034

466		SKN016	Skin Disease	63	0.034

467	P	FRD001	Friedreich Ataxia	63	0.034

468		ACT119	Acute Promyelocytic Leukemia	63	0.034

469		ANR007	Anorexia Nervosa	63	0.034

470	P	RHB003	Rhabdomyosarcoma	62	0.034

471	c	CRB172	Cerebral Amyloid Angiopathy, Cst3-Related	62	0.034

472	c	WLM018	Wilms Tumor 5	62	0.034

473		MNN042	Meningioma, Radiation-Induced	62	0.034

474		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	61	0.034

475	P	PRM006	Primary Biliary Cirrhosis	61	0.034

476	P	KDN017	Kidney Cancer	61	0.034

477		CHL068	Cholestasis	60	0.034

478		ACN002	Acanthosis Nigricans	60	0.034

479		RTN017	Retinal Detachment	60	0.034

480		DNG002	Dengue Hemorrhagic Fever	60	0.034

481		ANT009	Antithrombin Iii Deficiency	59	0.034

482	P	CYS018	Cystitis	59	0.034

483		PLM033	Pulmonary Embolism	59	0.034

484	c	NMN016	Niemann-Pick Disease, Type B	58	0.034

485		CNS004	Constipation	57	0.034

486		DSS009	Disseminated Intravascular Coagulation	57	0.034

487	P	DNG005	Dengue Virus	57	0.034

488	P	EHL001	Ehlers-Danlos Syndrome	57	0.034

489	P	GLM007	Glomerulonephritis	57	0.034

490		THR024	Thrombosis	56	0.034

491	P	ISL078	Isolated Ectopia Lentis	56	0.034

492	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.034

493	P	CHN012	Chondrosarcoma	56	0.034

494	c	ACT075	Acute Myocardial Infarction	56	0.034

495	P	CRD246	Cardiovascular System Disease	56	0.034

496	P	PLY019	Polyneuropathy	56	0.034

497		SLC006	Silicosis	56	0.034

498		HPT022	Hepatoblastoma	56	0.034

499		MCL006	Macular Retinal Edema	55	0.034

500	c	SCN036	Secondary Progressive Multiple Sclerosis	55	0.034

501		PYC001	Pycnodysostosis	55	0.034

502	P	DBT005	Diabetes Insipidus	55	0.034

503		PLM010	Pulmonary Edema	55	0.034

504		AMN003	Amnestic Disorder	54	0.034

505		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	54	0.034

506	P	ART021	Arteriosclerosis	54	0.034

507		FCL014	Focal Epilepsy	54	0.034

508	c	THY107	Thymoma, Familial	54	0.034

509		PLM012	Pulmonary Sarcoidosis	53	0.034

510	c	CRD184	Ceroid Lipofuscinosis, Neuronal, 5	53	0.034

511		ECH003	Echinococcosis	53	0.034

512		NNT012	Neonatal Jaundice	53	0.034

513		PRP080	Peripheral Artery Disease	53	0.034

514		PLS007	Plasmodium Falciparum Malaria	52	0.034

515	c	LTN004	Late-Onset Retinal Degeneration	52	0.034

516	P	HMR003	Hemorrhagic Disease	52	0.034

517		DMY004	Demyelinating Disease	52	0.034

518		PRS045	Prostatic Hypertrophy	52	0.034

519	P	HMP007	Hemophilia	51	0.034

520	c	VRL010	Viral Hepatitis	51	0.034

521		PRS021	Prostatic Adenoma	51	0.034

522	P	ECL001	Eclampsia	51	0.034

523		PNG002	Pain Agnosia	51	0.034

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

525		SPN035	Spindle Cell Sarcoma	51	0.034

526		HPT014	Hepatorenal Syndrome	50	0.034

527		LNG031	Lung Benign Neoplasm	50	0.034

528		CLR109	Colorectal Adenocarcinoma	50	0.034

529	P	SCK005	Sickle Cell Disease	50	0.034

530	c	INF145	Infantile Liver Failure Syndrome 1	50	0.034

531	P	OVR082	Overgrowth Syndrome	50	0.034

532		IMP004	Impetigo	49	0.034

533		PRS129	Prostatic Hyperplasia, Benign	49	0.034

534		URM002	Uremia	49	0.034

535		DBT006	Diabetic Macular Edema	48	0.034

536		HYP043	Hyperandrogenism	48	0.034

537		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.034

538		CCN002	Cocaine Abuse	48	0.034

539	c	SCH079	Schizophrenia 1	48	0.034

540		SPN021	Spinal Meningioma	47	0.034

541	P	VTR007	Vitreoretinopathy	46	0.034

542		GLT007	Glutathione Synthetase Deficiency	46	0.034

543	P	OCY003	Oocyte Maturation Defect 1	45	0.034

544		CHR466	Chronic Thromboembolic Pulmonary Hypertension	45	0.034

545		IMP006	Impulse Control Disorder	45	0.034

546	P	GNT008	Giant Cell Tumor	44	0.034

547		HYP003	Hypermethioninemia	44	0.034

548		CNN002	Cannabis Abuse	44	0.034

549		LMY003	Leiomyomatosis	43	0.034

550		DNT014	Dental Pulp Disease	43	0.034

551		SNL007	Senile Cataract	42	0.034

552	c	ADL066	Adult Neuronal Ceroid Lipofuscinosis	42	0.034

553		DNT006	Dental Pulp Necrosis	40	0.034

554	c	GRN014	Grn-Related Frontotemporal Dementia	40	0.034

555		ANC001	Ancylostomiasis	39	0.034

556		CNN001	Cannabis Dependence	38	0.034

557		SCR001	Secretory Meningioma	37	0.034

558		PLM101	Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis	37	0.034

559		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.034

560		HRW001	Hair Whorl	36	0.034

561		INT020	Intravenous Leiomyomatosis	36	0.034

562	c	SCH073	Schizophrenia 9	33	0.034

563	c	SCH083	Schizophrenia 7	33	0.034

564	c	DNT047	Dentinogenesis Imperfecta Type 2	33	0.034

565		ACD003	Acid Sphingomyelinase Deficiency	32	0.034

566		CNJ001	Conjugate Gaze Palsy	30	0.034

567		RSP007	Respiratory Distress Syndrome, Infant	30	0.034

568		MYC021	Mycobacterium Xenopi	25	0.034

569		FRN030	Frontotemporal Dementia with Parkinsonism-17	24	0.034

570		CYN003	Cyanide Poisoning	24	0.034

571	P	STR035	Streptococcal Group a Invasive Disease	23	0.034

572	c	TRC125	Trichothiodystrophy 7, Nonphotosensitive	17	0.034

573	P	RTT002	Rett Syndrome	80	0.028

574	c	LKM071	Leukemia, Chronic Lymphocytic	79	0.028

575		PFF001	Pfeiffer Syndrome	79	0.028

576		GST019	Gastrointestinal Stromal Tumor	76	0.028

577		KPS004	Kaposi Sarcoma	75	0.028

578	c	SPN225	Spondyloarthropathy 1	73	0.028

579	c	GCH015	Gaucher Disease, Type I	70	0.028

580	P	ART022	Arthritis	70	0.028

581		GST040	Gastric Adenocarcinoma	70	0.028

582		RCK004	Rickets	69	0.028

583	c	PNC108	Pancreatitis, Hereditary	69	0.028

584	P	ALP004	Alport Syndrome	68	0.028

585		CRB037	Cerebral Palsy	68	0.028

586	c	HMP004	Hemophilia B	67	0.028

587	P	MLG056	Malignant Hyperthermia	67	0.028

588	P	CRD119	Cardiac Arrest	67	0.028

589		KRT019	Keratitis, Hereditary	67	0.028

590		PNC129	Pancreatic Adenocarcinoma	67	0.028

591	P	ATR011	Atrial Fibrillation	66	0.028

592	P	HYP098	Hypereosinophilic Syndrome	66	0.028

593	P	NRV007	Nervous System Disease	66	0.028

594	c	PRD013	Periodic Fever, Familial, Autosomal Dominant	65	0.028

595	P	LNG028	Long Qt Syndrome	65	0.028

596		GST092	Gastroesophageal Reflux	65	0.028

597		PRT036	Peritonitis	65	0.028

598	P	PRS038	Personality Disorder	65	0.028

599		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	64	0.028

600		CLF027	Cleft Palate, Isolated	64	0.028

601	P	MTR014	Motor Neuron Disease	64	0.028

602		GT001	Gout	63	0.028

603		LKN025	Leukoencephalopathy, Hereditary Diffuse, with Spheroids	63	0.028

604		MSC152	Muscular Dystrophy, Becker Type	63	0.028

605		OVR029	Ovarian Hyperstimulation Syndrome	63	0.028

606	P	HYP069	Hyperparathyroidism	62	0.028

607	P	LMY004	Leiomyosarcoma	62	0.028

608	P	ART023	Arthropathy	62	0.028

609		VTR013	Vitreoretinopathy, Neovascular Inflammatory	62	0.028

610		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.028

611		WLL001	Williams-Beuren Syndrome	62	0.028

612	c	ALP101	Alpha-Thalassemia	62	0.028

613		TRN015	Transient Cerebral Ischemia	62	0.028

614	P	PLZ001	Pelizaeus-Merzbacher Disease	62	0.028

615	P	BLD124	Bleeding Disorder, Platelet-Type, 11	61	0.028

616	P	MVM001	Movement Disease	61	0.028

617	P	ENC004	Encephalitis	61	0.028

618		BRC012	Brucellosis	61	0.028

619		SDD001	Sudden Infant Death Syndrome	61	0.028

620		VRL011	Viral Infectious Disease	61	0.028

621		ING001	Inguinal Hernia	60	0.028

622		HPT019	Hepatic Encephalopathy	60	0.028

623	P	TXP001	Toxoplasmosis	60	0.028

624	P	ATS308	Autosomal Dominant Cerebellar Ataxia	60	0.028

625		DCB001	Decubitus Ulcer	60	0.028

626	P	HRD011	Hereditary Spherocytosis	60	0.028

627		ETN001	Eating Disorder	59	0.028

628	P	SLP005	Sleep Disorder	59	0.028

629	P	MYC008	Myocarditis	59	0.028

630		STT001	Status Epilepticus	59	0.028

631	P	RBL001	Rubella	58	0.028

632		IRN001	Iron Deficiency Anemia	58	0.028

633		PRL032	Perlman Syndrome	58	0.028

634		CRV038	Cervical Squamous Cell Carcinoma	58	0.028

635	c	DWL002	Dowling-Degos Disease 1	58	0.028

636		CNT047	Contact Dermatitis	57	0.028

637		SPT004	Septic Arthritis	57	0.028

638	P	OST122	Osteogenesis Imperfecta, Type Iii	57	0.028

639		BLM002	Bulimia Nervosa	57	0.028

640		OBS525	Obsolete: Squamous Cell Carcinoma of Head and Neck	57	0.028

641	P	PRN023	Prion Disease	57	0.028

642		TNS005	Tonsillitis	57	0.028

643		ERY051	Erythroleukemia, Familial	56	0.028

644		PHR003	Pharyngitis	56	0.028

645		PLS011	Plasmacytoma	56	0.028

646		SFT003	Soft Tissue Sarcoma	56	0.028

647	P	ALP008	Alopecia	56	0.028

648		GLL018	Gallbladder Cancer	56	0.028

649	P	MTC069	Mitochondrial Disorders	56	0.028

650		MTH009	Mouth Disease	56	0.028

651		FNC009	Fanconi-Bickel Syndrome	56	0.028

652		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.028

653		HYP005	Hypokalemia	55	0.028

654	P	PLY018	Polycythemia	55	0.028

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

656	c	MYP132	Myopathy, Congenital	55	0.028

657		FLR002	Filariasis	55	0.028

658		INT007	Intermediate Coronary Syndrome	55	0.028

659	P	MYP006	Myopia	55	0.028

660		DBT010	Diabetic Neuropathy	55	0.028

661		VGN023	Vaginitis	55	0.028

662	P	ANG015	Angioedema	54	0.028

663		ANL018	Analbuminemia	54	0.028

664		ACR058	Acrofacial Dysostosis 1, Nager Type	54	0.028

665		GLC003	Glucose Intolerance	54	0.028

666		CRY003	Cryptosporidiosis	54	0.028

667	P	SPN052	Spondyloarthropathy	54	0.028

668		PRT082	Preterm Premature Rupture of the Membranes	54	0.028

669	c	CNT035	Central Nervous System Disease	54	0.028

670		CHR100	Chronic Ulcer of Skin	53	0.028

671		RFL001	Reflex Sympathetic Dystrophy	53	0.028

672		CCC001	Coccidioidomycosis	53	0.028

673	P	EPD016	Epidermolysis Bullosa	53	0.028

674	c	LBR014	Leber Congenital Amaurosis 4	53	0.028

675		HRT012	Heart Valve Disease	53	0.028

676	P	BRC006	Brachydactyly	53	0.028

677		MST005	Mastitis	53	0.028

678	c	CHL116	Cholestasis, Intrahepatic, of Pregnancy, 1	53	0.028

679	P	RTN018	Retinal Disease	52	0.028

680	c	HYP768	Hyperlipoproteinemia, Type I	52	0.028

681	P	SHR001	Short Bowel Syndrome	52	0.028

682		MCN007	Meconium Aspiration Syndrome	52	0.028

683		SPN051	Spondylitis	52	0.028

684		DYS165	Dysfibrinogenemia, Congenital	52	0.028

685		IMP005	Impotence	52	0.028

686		PRV004	Periventricular Leukomalacia	51	0.028

687		HYP014	Hyperuricemia	51	0.028

688		CHL122	Cholesteatoma of Middle Ear	51	0.028

689	c	VNW010	Von Willebrand Disease, Type 2	51	0.028

690		PRT129	Prothrombin Deficiency, Congenital	51	0.028

691		ONC002	Onchocerciasis	51	0.028

692		HYP081	Hypolipoproteinemia	50	0.028

693	P	PST095	Post-Thrombotic Syndrome	50	0.028

694		RTN003	Retinal Ischemia	50	0.028

695		LMY002	Leiomyoma	50	0.028

696		DYS015	Dysentery	50	0.028

697	c	AMY009	Amyloidosis Aa	50	0.028

698		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.028

699	P	ART153	Arthrochalasia Ehlers-Danlos Syndrome	50	0.028

700		NTR046	Neutrophil Migration	50	0.028

701		BLR001	Biliary Atresia	50	0.028

702	c	HYP843	Hypoalphalipoproteinemia, Primary, 2	50	0.028

703		PLC008	Placenta Disease	49	0.028

704	P	OPN001	Open-Angle Glaucoma	49	0.028

705	P	GND004	Gonadal Dysgenesis	49	0.028

706	c	LRG001	Large Cell Carcinoma	49	0.028

707		GYN001	Gynecomastia	49	0.028

708	c	SPN330	Spondylocostal Dysostosis 5	49	0.028

709		URT001	Urethritis	48	0.028

710		MTC005	Mitochondrial Metabolism Disease	48	0.028

711		KHN001	Kuhnt-Junius Degeneration	48	0.028

712	P	MRC003	Mercury Poisoning	48	0.028

713		BNG036	Bone Giant Cell Tumor	48	0.028

714		RTN020	Retinal Vascular Disease	48	0.028

715		ATX019	Ataxia with Vitamin E Deficiency	48	0.028

716		STM006	Stomach Disease	48	0.028

717	P	CRN028	Corneal Ulcer	47	0.028

718		RFT001	Rift Valley Fever	47	0.028

719		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.028

720		RNL077	Renal Fibrosis	47	0.028

721		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.028

722		CLS016	Clostridium Difficile Colitis	46	0.028

723		TST014	Testicular Cancer	46	0.028

724		ALB002	Albinism	46	0.028

725	c	SPN312	Spinocerebellar Ataxia 14	45	0.028

726		SYN036	Syncope	45	0.028

727	c	MLG068	Malignant Glioma	45	0.028

728	P	PSD003	Pseudohypoaldosteronism	45	0.028

729	P	BNG032	Benign Mesothelioma	45	0.028

730		KWS001	Kwashiorkor	45	0.028

731	P	END084	Endocrine System Disease	44	0.028

732		CRB025	Carbohydrate Metabolic Disorder	44	0.028

733		ATN011	Autoinflammation with Infantile Enterocolitis	43	0.028

734		BRN032	Brain Glioma	43	0.028

735		PNM013	Pneumococcal Meningitis	43	0.028

736		HPT004	Hepatic Coma	43	0.028

737		TST015	Testicular Disease	43	0.028

738	c	PRM038	Primary Agammaglobulinemia	43	0.028

739		BSL008	Basal Ganglia Disease	43	0.028

740	c	SRC023	Sarcoidosis 2	43	0.028

741	P	CLS010	Cluster Headache	43	0.028

742	c	CHR576	Chronic Beryllium Disease	42	0.028

743		CRD178	Cardiac Conduction Disease with or Without Dilated Cardiomyopathy	42	0.028

744		CTS005	Catastrophic Antiphospholipid Syndrome	42	0.028

745		GST020	Gastric Antral Vascular Ectasia	41	0.028

746		49X006	49, Xxxxy Syndrome	41	0.028

747		RDN001	Reading Disorder	40	0.028

748		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.028

749		TXC011	Toxocariasis	40	0.028

750	P	BRY005	Beryllium Disease	40	0.028

751		C1N001	C1 Inhibitor Deficiency	40	0.028

752		AGR019	Age-Related Hearing Loss	39	0.028

753		ANS003	Anisakiasis	39	0.028

754		ENT001	Enterocele	39	0.028

755	c	MLG074	Malignant Mesenchymoma	39	0.028

756		FLT009	Folate Malabsorption, Hereditary	39	0.028

757		AML001	Amelanotic Melanoma	39	0.028

758	c	CHR682	Chronic Bilirubin Encephalopathy	38	0.028

759		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	38	0.028

760		SCR011	Scrapie	38	0.028

761		ENC005	Encephalomalacia	38	0.028

762		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.028

763		OVR094	Ovarian Epithelial Cancer	38	0.028

764		BLR028	Biliary Atresia, Extrahepatic	37	0.028

765	c	CHR020	Chronic Interstitial Cystitis	37	0.028

766	c	WLM011	Wilms Tumor 6	37	0.028

767	P	MXL015	Maxillary Sinusitis	37	0.028

768		LYM011	Lymphogranuloma Venereum	36	0.028

769		PSD088	Pseudobulbar Affect	36	0.028

770		FXD003	Fixed Drug Eruption	35	0.028

771		ACT149	Acetaminophen Metabolism	35	0.028

772	c	ACR088	Aicardi-Goutieres Syndrome 3	35	0.028

773		HWK001	Hawkinsinuria	35	0.028

774		PYR009	Pyridoxine Deficiency Anemia	34	0.028

775	c	PLM127	Pulmonary Hypertension, Primary, 3	33	0.028

776	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.028

777	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.028

778		HPT085	Hepatitis, Fulminant Viral	32	0.028

779		MTC108	Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency	32	0.028

780		INF009	Inflammatory Spondylopathy	32	0.028

781	P	HRD084	Hereditary Cerebral Amyloid Angiopathy	31	0.028

782		INF021	Infant Gynecomastia	31	0.028

783		FNT004	Fainting	31	0.028

784		PYR016	Pyridoxine Deficiency	30	0.028

785		ATS251	Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna	30	0.028

786	P	SKL032	Skeletal Muscle Disease	29	0.028

787	c	ALC016	Alcohol Sensitivity, Acute	29	0.028

788		HYP346	Hypotrichosis and Recurrent Skin Vesicles	29	0.028

789		GRN004	Granulomatous Amebic Encephalitis	29	0.028

790		PST092	Posttransplant Acute Limbic Encephalitis	29	0.028

791		TBL029	Tubulin, Beta	28	0.028

792		TCK004	Tick Infestation	27	0.028

793	c	CRN110	Cranioectodermal Dysplasia 3	27	0.028

794		CHL079	Children's Interstitial Lung Disease	27	0.028

795		MST020	Mast Cell Activation Syndrome	27	0.028

796		PDT043	Pediatric Acute-Onset Neuropsychiatric Syndrome	26	0.028

797	c	HYP819	Hyperlipoproteinemia, Type Id	24	0.028

798		HVY002	Heavy Metal Poisoning	22	0.028

799		EXT009	Extratemporal Epilepsy	21	0.028

800		LTH004	Lathyrism	16	0.028

801		FCS014	Fucosidase Regulator	15	0.028

802		MYL069	Myeloma, Multiple	85	0.020

803	P	LYN001	Lynch Syndrome	77	0.020

804	c	TBR025	Tuberous Sclerosis 1	76	0.020

805	P	APL001	Aplastic Anemia	74	0.020

806	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.020

807	c	HMC039	Hemochromatosis, Type 1	74	0.020

808		ACR006	Aceruloplasminemia	73	0.020

809		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.020

810		LPT014	Leptin Deficiency or Dysfunction	73	0.020

811	P	ALG028	Alagille Syndrome 1	73	0.020

812		AGM019	Agammaglobulinemia, X-Linked	72	0.020

813	P	FML011	Familial Adenomatous Polyposis	72	0.020

814	c	LKM063	Leukemia, Chronic Myeloid	71	0.020

815		FBR012	Fabry Disease	71	0.020

816		MLT157	Multiple System Atrophy 1	70	0.020

817		WLS001	Wilson Disease	70	0.020

818	P	TBR001	Tuberous Sclerosis	70	0.020

819	P	MTC003	Metachromatic Leukodystrophy	70	0.020

820		MYL009	Myelodysplastic Syndrome	70	0.020

821	P	SYS005	Systemic Scleroderma	70	0.020

822	P	TTR001	Tetralogy of Fallot	69	0.020

823		CRT072	Creutzfeldt-Jakob Disease	69	0.020

824	P	OCL013	Oculodentodigital Dysplasia	69	0.020

825	c	BSL007	Basal Cell Carcinoma	68	0.020

826		NVS017	Nevus, Epidermal	68	0.020

827	P	HYP802	Hypocalcemia, Autosomal Dominant 1	68	0.020

828	P	CRN037	Craniosynostosis	68	0.020

829		CRZ001	Crouzon Syndrome	68	0.020

830		SKN019	Skin Melanoma	67	0.020

831	P	LBR001	Leber Congenital Amaurosis	67	0.020

832	P	PRP003	Porphyria Cutanea Tarda	67	0.020

833	P	LPR021	Leprosy 3	67	0.020

834	P	PSD087	Pseudoxanthoma Elasticum	67	0.020

835		MLD001	Melioidosis	67	0.020

836	P	ANG001	Angelman Syndrome	67	0.020

837	c	FML001	Familial Atrial Fibrillation	66	0.020

838	P	HYP061	Hypertrophic Cardiomyopathy	66	0.020

839		ADR054	Adrenocortical Carcinoma, Hereditary	66	0.020

840		AND002	Androgen Insensitivity Syndrome	66	0.020

841		LPT001	Leptospirosis	66	0.020

842	P	ASP006	Aspergillosis	66	0.020

843	P	LYS001	Loeys-Dietz Syndrome	66	0.020

844		NPH091	Nephrolithiasis, Calcium Oxalate	66	0.020

845	P	HYD006	Hydrocephalus	65	0.020

846		GLC006	Galactosemia	65	0.020

847	c	CNG006	Congenital Hypothyroidism	65	0.020

848	P	AGM001	Agammaglobulinemia	65	0.020

849	P	HRS035	Hirschsprung Disease 1	65	0.020

850		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.020

851		DMN031	Dementia, Lewy Body	65	0.020

852	P	DYS154	Dystonia	65	0.020

853		BRR014	Barrett Esophagus	64	0.020

854	c	HYP604	Hyperinsulinemic Hypoglycemia, Familial, 2	64	0.020

855		INC002	Inclusion Body Myositis	64	0.020

856		KWS002	Kawasaki Disease	64	0.020

857	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	64	0.020

858		CLR108	Colorectal Adenoma	64	0.020

859		MYC079	Myoclonic Epilepsy of Lafora	64	0.020

860	P	KLL001	Kallmann Syndrome	64	0.020

861	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.020

862		PRP083	Porphyria, Acute Intermittent	63	0.020

863		IRR002	Irritable Bowel Syndrome	63	0.020

864		MSC007	Muscle Hypertrophy	63	0.020

865		NRF026	Neurofibromatosis, Type Iv, of Riccardi	63	0.020

866		NRM005	Neuromuscular Disease	63	0.020

867		THY121	Thyroid Gland Anaplastic Carcinoma	63	0.020

868	P	ANR048	Aniridia 1	63	0.020

869	P	MCH002	Machado-Joseph Disease	63	0.020

870	P	PRM002	Primary Hyperoxaluria	62	0.020

871	c	GLC092	Glaucoma, Primary Open Angle	62	0.020

872	P	VSC011	Vasculitis	62	0.020

873	P	ESP024	Esophagitis	62	0.020

874		HMT002	Hematologic Cancer	62	0.020

875	c	ATM011	Autoimmune Hepatitis	62	0.020

876		HYD038	Hydrops Fetalis, Nonimmune	61	0.020

877	P	CRG003	Crigler-Najjar Syndrome, Type I	61	0.020

878		INT002	Intermittent Claudication	61	0.020

879		CRC021	Carcinosarcoma	61	0.020

880	P	HYP750	Hypertriglyceridemia, Familial	61	0.020

881		DRM006	Dermatitis	61	0.020

882	c	NRD017	Neurodegeneration with Brain Iron Accumulation 1	61	0.020

883	c	HRD002	Hereditary Angioedema	61	0.020

884	P	TST021	Testicular Germ Cell Tumor	61	0.020

885		OST003	Osteonecrosis	61	0.020

886		RHM001	Rheumatic Fever	61	0.020

887		HRD029	Hereditary Leiomyomatosis and Renal Cell Cancer	61	0.020

888	P	ACH003	Achromatopsia	60	0.020

889		PRT013	Portal Hypertension	60	0.020

890	P	BRN019	Bernard-Soulier Syndrome	60	0.020

891	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	60	0.020

892		RCT015	Reactive Arthritis	60	0.020

893	P	VNT002	Ventricular Septal Defect	60	0.020

894		STF001	Stiff-Person Syndrome	60	0.020

895	P	HYP035	Hypophosphatasia	60	0.020

896		HRP004	Herpes Zoster	60	0.020

897	P	SCL018	Scoliosis	60	0.020

898	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	60	0.020

899	P	CNT110	Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a	60	0.020

900		CHR072	Chordoma	59	0.020

901	P	GLL022	Guillain-Barre Syndrome	59	0.020

902	P	ECT006	Ectodermal Dysplasia	59	0.020

903		SPP011	Suppression of Tumorigenicity 12	59	0.020

904		CLS005	Clouston Syndrome	59	0.020

905	P	LKD001	Leukodystrophy	59	0.020

906	P	PLY014	Polycystic Kidney Disease	59	0.020

907	P	TRC086	Trichohepatoenteric Syndrome 1	59	0.020

908		GRD007	Grade Iii Astrocytoma	59	0.020

909	c	MLT159	Multiple Endocrine Neoplasia, Type Iib	59	0.020

910	P	SYP003	Syphilis	59	0.020

911		DCT002	Ductal Carcinoma in Situ	59	0.020

912		HYP042	Hypochondroplasia	59	0.020

913	c	BNG091	Benign Chronic Pemphigus	59	0.020

914	P	PLV020	Pelvic Organ Prolapse	59	0.020

915		CRD132	Cardiac Conduction Defect	59	0.020

916		CHL067	Cholecystitis	58	0.020

917		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.020

918		BRS051	Breast Disease	58	0.020

919	P	GLL020	Gallbladder Disease	58	0.020

920		RBS001	Rabies	58	0.020

921		ADL030	Adult-Onset Still's Disease	58	0.020

922		PLM070	Pulmonic Stenosis	57	0.020

923		ACR056	Acrodermatitis Enteropathica, Zinc-Deficiency Type	57	0.020

924	P	MMP001	Mumps	57	0.020

925		THY022	Thymic Carcinoma	57	0.020

926		LYM027	Lymphopenia	57	0.020

927	P	END033	Endocarditis	57	0.020

928	P	PLY041	Polymyositis	57	0.020

929		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	57	0.020

930	c	ADL017	Adult T-Cell Leukemia	57	0.020

931	P	STC001	Stickler Syndrome	57	0.020

932	P	EPD003	Epidermolysis Bullosa Simplex	56	0.020

933		PRS047	Prostatitis	56	0.020

934	c	ANG068	Angioedema, Hereditary, Type I	56	0.020

935		TRN018	Transitional Cell Carcinoma	56	0.020

936		EHL052	Ehlers-Danlos Syndrome, Vascular Type	56	0.020

937	P	EXD001	Exudative Vitreoretinopathy	56	0.020

938		LMY014	Leiomyoma, Uterine	56	0.020

939		AVN001	Avian Influenza	56	0.020

940		SKN022	Skin Squamous Cell Carcinoma	56	0.020

941		KRT071	Keratosis, Seborrheic	56	0.020

942		CMM005	Common Cold	56	0.020

943	P	MYS005	Myositis	56	0.020

944		RHM027	Rheumatic Disease	56	0.020

945		CHR177	Chromophobe Renal Cell Carcinoma	56	0.020

946		GST050	Gastrointestinal System Disease	56	0.020

947		BRN012	Bronchiolitis Obliterans	56	0.020

948		DFF005	Diffuse Large B-Cell Lymphoma	56	0.020

949	P	PLM034	Pulmonary Emphysema	56	0.020

950		HMG005	Hemoglobinopathy	55	0.020

951	P	PNM006	Pneumoconiosis	55	0.020

952		SYN007	Synovitis	55	0.020

953		GRN034	Grange Syndrome	55	0.020

954	c	FML035	Familial Hyperlipidemia	55	0.020

955	P	GRV001	Graves' Disease	55	0.020

956	c	BCT007	Bacterial Meningitis	55	0.020

957		ATR057	Atrioventricular Block	55	0.020

958		ALL010	Allergic Contact Dermatitis	55	0.020

959		PLV003	Pelvic Inflammatory Disease	55	0.020

960		ACT058	Active Peptic Ulcer Disease	55	0.020

961		GNG005	Gangliocytoma	55	0.020

962	P	HYP076	Hyperthyroidism	55	0.020

963		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	55	0.020

964		SHG001	Shigellosis	55	0.020

965		NRN004	Neuroendocrine Tumor	55	0.020

966		AND020	Androgen Insensitivity, Partial	55	0.020

967	c	THY109	Thyroid Cancer, Nonmedullary, 1	55	0.020

968	P	PMP001	Pemphigus	55	0.020

969		END002	Endometrioid Ovary Carcinoma	55	0.020

970	P	SBS003	Substance Abuse	54	0.020

971		CFF003	Caffey Disease	54	0.020

972		FCT004	Factor Xii Deficiency	54	0.020

973	P	PTT006	Pituitary Adenoma	54	0.020

974		HMP005	Hemiplegia	54	0.020

975	P	CNG010	Congenital Stationary Night Blindness	54	0.020

976	P	HYP050	Hyperinsulinemic Hypoglycemia	54	0.020

977		LYM040	Lymphoblastic Lymphoma	54	0.020

978	P	CLS054	Classic Ehlers-Danlos Syndrome	54	0.020

979	P	NLD001	Nail Disease	54	0.020

980	P	MNC007	Monocytic Leukemia	54	0.020

981	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.020

982		PRP016	Paraplegia	53	0.020

983		MLT135	Multiple Sulfatase Deficiency	53	0.020

984		MYM001	Myoma	53	0.020

985		RST011	Restrictive Dermopathy, Lethal	53	0.020

986		OCL006	Ocular Hypertension	53	0.020

987	c	BRS111	Breast-Ovarian Cancer, Familial 2	53	0.020

988	P	RCT021	Rectum Cancer	53	0.020

989		OST016	Osteochondrosis	53	0.020

990		PRP036	Peripheral T-Cell Lymphoma	53	0.020

991	P	ALL008	Allergic Bronchopulmonary Aspergillosis	53	0.020

992		GST023	Gastric Ulcer	53	0.020

993	P	HST010	Histiocytosis	53	0.020

994	P	THY032	Thyroiditis	53	0.020

995		GNG002	Ganglioneuroma	53	0.020

996		THR013	Thoracic Outlet Syndrome	53	0.020

997		PRG009	Progressive Multifocal Leukoencephalopathy	53	0.020

998	P	INT068	Intestinal Disease	52	0.020

999		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.020

1000		ACR041	Acromelic Frontonasal Dysostosis	52	0.020

1001	P	PTS002	Ptosis	52	0.020

1002		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	52	0.020

1003		ABL002	Ablepharon-Macrostomia Syndrome	52	0.020

1004		MCN017	Meconium Ileus	52	0.020

1005		DRM011	Dermatophytosis	52	0.020

1006	P	END047	Endophthalmitis	52	0.020

1007		GTR002	Goiter	52	0.020

1008	P	ACT105	Acute Mountain Sickness	52	0.020

1009	P	INS002	in Situ Carcinoma	52	0.020

1010	c	GLL024	Gallbladder Disease 1	52	0.020

1011		ESN005	Eosinophilic Gastroenteritis	52	0.020

1012		CHR073	Choreatic Disease	52	0.020

1013	P	RTN022	Retinal Vein Occlusion	52	0.020

1014	P	ACT008	Actinic Keratosis	52	0.020

1015		THY124	Thyroid Gland Papillary Carcinoma	52	0.020

1016		INF034	Infective Endocarditis	52	0.020

1017		OCL069	Ocular Motor Apraxia	51	0.020

1018	P	LRY019	Laryngitis	51	0.020

1019		CHR005	Chorioamnionitis	51	0.020

1020		MSC190	Muscular Disease	51	0.020

1021		THR016	Thrombophlebitis	51	0.020

1022		ILS001	Ileus	51	0.020

1023		SPP010	Suppressor of Tumorigenicity 3	51	0.020

1024		ADR049	Adrenal Hypoplasia, Congenital	51	0.020

1025		PLR008	Pleurisy	51	0.020

1026	c	EHL078	Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1	51	0.020

1027		SCB001	Scabies	51	0.020

1028		GSG001	Gas Gangrene	50	0.020

1029		SCH012	Schizoaffective Disorder	50	0.020

1030	c	SCN007	Secondary Hyperparathyroidism	50	0.020

1031		AZS001	Azoospermia	50	0.020

1032		HRT011	Heart Septal Defect	50	0.020

1033		MTP025	Metaphyseal Chondrodysplasia, Schmid Type	50	0.020

1034	P	FNC004	Fanconi Syndrome	50	0.020

1035	P	CHL066	Cholangitis	50	0.020

1036	P	AGG001	Aggressive Periodontitis	50	0.020

1037		FLR001	Filarial Elephantiasis	50	0.020

1038		CRT013	Carotid Stenosis	50	0.020

1039		ILT001	Ileitis	50	0.020

1040		MCR004	Macroglobulinemia	50	0.020

1041		CRV040	Cervix Carcinoma	50	0.020

1042		CRN030	Coronary Stenosis	50	0.020

1043	c	ALZ049	Alzheimer Disease 2	50	0.020

1044		PRS034	Parasitic Helminthiasis Infectious Disease	49	0.020

1045		TLR001	Tularemia	49	0.020

1046		SPN405	Spondyloepiphyseal Dysplasia Tarda, X-Linked	49	0.020

1047		VRC001	Varicocele	49	0.020

1048	c	CRD187	Cardiomyopathy, Dilated, 3b	49	0.020

1049		HYP017	Hypophosphatemia	49	0.020

1050		FDL002	Food Allergy	49	0.020

1051	P	MTC133	Mitochondrial Myopathy	49	0.020

1052		MLL001	Molluscum Contagiosum	49	0.020

1053	c	CNT016	Central Retinal Vein Occlusion	49	0.020

1054		BLP005	Blepharitis	49	0.020

1055		CHL004	Cholelithiasis	49	0.020

1056		LRN003	Learning Disability	49	0.020

1057		ART017	Aortic Disease	49	0.020

1058	c	OST121	Osteogenesis Imperfecta, Type Iv	49	0.020

1059		HMG002	Hemoglobinuria	49	0.020

1060		ECT026	Ectopic Pregnancy	49	0.020

1061		PLY024	Polymicrogyria	49	0.020

1062		ALN001	Aland Island Eye Disease	49	0.020

1063	c	VNW005	Von Willebrand Disease, Type 1	49	0.020

1064	c	HPT015	Hepatitis D	49	0.020

1065	P	CMP008	Compartment Syndrome	48	0.020

1066	c	OST119	Osteogenesis Imperfecta, Type Vii	48	0.020

1067		VTM033	Vitamin K Deficiency Bleeding	48	0.020

1068	c	OST132	Osteogenesis Imperfecta, Type Vi	48	0.020

1069		SBP001	Subependymal Giant Cell Astrocytoma	48	0.020

1070	P	ART106	Arterial Calcification, Generalized, of Infancy, 1	48	0.020

1071		STP011	Stapes Ankylosis with Broad Thumbs and Toes	48	0.020

1072	P	CLR019	Color Blindness	48	0.020

1073		CRD137	Cardiogenic Shock	48	0.020

1074		ASP007	Aspiration Pneumonia	48	0.020

1075		IGG001	Iga Glomerulonephritis	48	0.020

1076	P	MYF003	Myofibrillar Myopathy	48	0.020

1077		SXL003	Sexual Disorder	48	0.020

1078		ERY004	Erysipelas	48	0.020

1079