Search results for Clotrimazole

1355 hits were found for Clotrimazole

#	Family	MCID	Name	MIFTS	Score
1	P	CND004	Candidiasis	58	0.250

2		ORL005	Oral Candidiasis	56	0.151

3		VLV011	Vulvovaginal Candidiasis	49	0.143

4		DRM011	Dermatophytosis	52	0.131

5		FNG017	Fungal Infectious Disease	53	0.114

6		VGN023	Vaginitis	54	0.113

7		TNP001	Tinea Pedis	46	0.085

8		DRM006	Dermatitis	61	0.077

9		OTM001	Otomycosis	27	0.077

10	P	ASP006	Aspergillosis	69	0.074

11		VGN019	Vaginal Discharge	46	0.074

12		PTY002	Pityriasis Versicolor	38	0.072

13		CNT047	Contact Dermatitis	58	0.069

14		ATX019	Ataxia with Vitamin E Deficiency	42	0.069

15		DRM009	Dermatomycosis	36	0.069

16	P	SCK005	Sickle Cell Disease	50	0.067

17		VLV010	Vulvovaginitis	41	0.067

18		TRC003	Trichomoniasis	53	0.064

19		SCK003	Sickle Cell Anemia	74	0.059

20		CTN033	Cutaneous Candidiasis	38	0.059

21		BCT002	Bacterial Vaginosis	53	0.053

22		STM007	Stomatitis	50	0.053

23		TNC003	Tinea Corporis	39	0.053

24		CND006	Candida Glabrata	32	0.053

25		CHR063	Chronic Mucocutaneous Candidiasis	63	0.049

26		ACQ007	Acquired Immunodeficiency Syndrome	60	0.049

27		ALL010	Allergic Contact Dermatitis	56	0.049

28	P	OTT001	Otitis Externa	39	0.049

29		TNC001	Tinea Cruris	36	0.049

30		DNT008	Denture Stomatitis	35	0.049

31		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.049

32		KRT019	Keratitis, Hereditary	65	0.045

33	P	EXN002	Exanthem	57	0.045

34	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.042

35	P	RHM011	Rheumatoid Arthritis	80	0.042

36	c	NRF023	Neurofibromatosis, Type Ii	80	0.042

37	P	ART022	Arthritis	69	0.042

38		SKN016	Skin Disease	63	0.042

39		CRY005	Cryptococcosis	58	0.042

40		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.042

41		SPR010	Sporotrichosis	46	0.042

42		ESP018	Esophageal Candidiasis	44	0.042

43		RTN135	Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome	40	0.042

44		SPR126	Superior Semicircular Canal Dehiscence	40	0.042

45		48X005	48,xyyy	39	0.042

46	c	HMG029	Hemoglobin Se Disease	39	0.042

47		IMM167	Immune Deficiency Disease	78	0.037

48		GLB015	Glioblastoma Multiforme	75	0.037

49		HMN044	Human Immunodeficiency Virus Type 1	71	0.037

50		DFC004	Deficiency Anemia	70	0.037

51	P	MLN008	Melanoma	69	0.037

52	P	TRN020	Turner Syndrome	67	0.037

53		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.037

54		YMN001	Yemenite Deaf-Blind Hypopigmentation Syndrome	65	0.037

55		CLT003	Colitis	62	0.037

56		NTR005	Nutritional Deficiency Disease	62	0.037

57	P	TXP001	Toxoplasmosis	60	0.037

58		ISC004	Ischemia	58	0.037

59		CCC001	Coccidioidomycosis	58	0.037

60	P	RHN004	Rhinitis	57	0.037

61		ERY051	Erythroleukemia, Familial	56	0.037

62		BCT022	Bacterial Infectious Disease	56	0.037

63		KRT009	Keratosis	51	0.037

64		VGN020	Vaginal Disease	49	0.037

65		CRY014	Cryptococcal Meningitis	48	0.037

66		FLL008	Folliculitis	46	0.037

67	P	SBR004	Seborrheic Dermatitis	45	0.037

68		FNG016	Fungal Keratitis	40	0.037

69		SPR020	Superficial Mycosis	35	0.037

70		MLR004	Malaria	81	0.032

71		ULC004	Ulcerative Colitis	73	0.032

72	P	KDN018	Kidney Disease	72	0.032

73		DWN001	Down Syndrome	70	0.032

74		SKN019	Skin Melanoma	68	0.032

75	c	INF071	Inflammatory Bowel Disease 1	67	0.032

76	P	MNN013	Meningitis	66	0.032

77	P	DRM053	Dermatitis, Atopic	66	0.032

78		CLN015	Colon Adenocarcinoma	65	0.032

79	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.032

80		LSH001	Leishmaniasis	63	0.032

81	P	END044	Endometriosis	63	0.032

82	P	ESP024	Esophagitis	62	0.032

83		CTN007	Cutaneous Leishmaniasis	62	0.032

84		SQM006	Squamous Cell Carcinoma	60	0.032

85	c	ACT073	Acute Leukemia	58	0.032

86		HST011	Histoplasmosis	55	0.032

87		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.032

88	P	INF037	Inflammatory Bowel Disease	54	0.032

89	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.032

90		ILT001	Ileitis	50	0.032

91	c	DRM054	Dermatitis, Atopic, 2	44	0.032

92		ORL015	Oral Squamous Cell Carcinoma	43	0.032

93	P	KLZ004	Kala-Azar 1	41	0.032

94		PCH007	Pouchitis	39	0.032

95		ERY010	Erythrasma	25	0.032

96	P	CLR023	Colorectal Cancer	99	0.026

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

98	c	LKM061	Leukemia, Acute Myeloid	84	0.026

99		END057	Endometrial Cancer	74	0.026

100	c	BTT014	Beta-Thalassemia	74	0.026

101		CRH001	Crohn's Disease	74	0.026

102	P	GRF003	Graft-Versus-Host Disease	72	0.026

103	c	CHR684	Chronic Kidney Disease	70	0.026

104	P	LKM002	Leukemia	68	0.026

105	c	RHB024	Rhabdomyosarcoma 2	67	0.026

106	P	MCR115	Microvascular Complications of Diabetes 5	66	0.026

107	c	MCR129	Microvascular Complications of Diabetes 1	66	0.026

108		CHG001	Chagas Disease	66	0.026

109	c	DBT099	Diabetes Mellitus, Type I	65	0.026

110	P	DBT009	Diabetes Mellitus	64	0.026

111	P	ADN016	Adenocarcinoma	64	0.026

112	P	PNC044	Pancreatitis	61	0.026

113	c	ACT027	Acute Pancreatitis	60	0.026

114		INS001	Insulinoma	60	0.026

115	P	THL005	Thalassemia	60	0.026

116		PNM001	Pneumocystosis	59	0.026

117	P	CYS018	Cystitis	59	0.026

118		BRN002	Bronchiolitis	59	0.026

119		EYD002	Eye Disease	58	0.026

120	c	DWL002	Dowling-Degos Disease 1	58	0.026

121	P	HDC001	Headache	57	0.026

122		CYT008	Cytomegalovirus Infection	57	0.026

123		PHR003	Pharyngitis	57	0.026

124		BRN012	Bronchiolitis Obliterans	55	0.026

125	P	DRR001	Diarrhea	55	0.026

126	P	NLD001	Nail Disease	54	0.026

127	P	ALP008	Alopecia	54	0.026

128	P	LCH002	Lichen Planus	53	0.026

129	c	MCR113	Microvascular Complications of Diabetes 3	52	0.026

130	P	OVR082	Overgrowth Syndrome	50	0.026

131	P	CRN028	Corneal Ulcer	47	0.026

132	c	MCR120	Microvascular Complications of Diabetes 7	47	0.026

133		KRT013	Keratolytic Winter Erythema	46	0.026

134		ORL013	Oral Lichen Planus	45	0.026

135		SPS204	Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity	45	0.026

136		MLN073	Melanosis, Neurocutaneous	45	0.026

137		HYP084	Hypopyon	43	0.026

138		PHH001	Phaeohyphomycosis	42	0.026

139	c	MCR130	Microvascular Complications of Diabetes 6	41	0.026

140	c	MCR133	Microvascular Complications of Diabetes 4	41	0.026

141		OPS001	Opisthorchiasis	41	0.026

142	c	MCR112	Microvascular Complications of Diabetes 2	41	0.026

143		PST029	Postmenopausal Atrophic Vaginitis	38	0.026

144		PMP010	Pompholyx	37	0.026

145		BLN010	Balanitis	37	0.026

146		CYT004	Cytomegalic Inclusion Disease	31	0.026

147		BLN009	Balanoposthitis	31	0.026

148		CYT018	Cytochrome P450 2d6 Variant	27	0.026

149		TRC121	Trichomonas Vaginalis Trichomoniasis	23	0.026

150	P	HPT023	Hepatocellular Carcinoma	100	0.019

151	P	BRS047	Breast Cancer	97	0.019

152	P	DBT026	Diabetes Mellitus, Noninsulin-Dependent	90	0.019

153	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.019

154	c	SYS001	Systemic Lupus Erythematosus	86	0.019

155		MYL069	Myeloma, Multiple	85	0.019

156	c	HYP595	Hypertension, Essential	84	0.019

157	P	PNC035	Pancreatic Cancer	84	0.019

158		NRL016	Neural Tube Defects	82	0.019

159	P	ATX030	Ataxia-Telangiectasia	82	0.019

160	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.019

161		CYS001	Cystic Fibrosis	81	0.019

162		STR067	Stroke, Ischemic	81	0.019

163	P	BLD134	Bladder Cancer	79	0.019

164	c	DLT002	Dilated Cardiomyopathy	79	0.019

165	P	RTN008	Retinitis Pigmentosa	79	0.019

166	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.019

167	c	CWD006	Cowden Syndrome 1	78	0.019

168		GST019	Gastrointestinal Stromal Tumor	78	0.019

169		OST012	Osteoarthritis	78	0.019

170	P	LNG064	Lung Cancer Susceptibility 3	78	0.019

171	P	PRK057	Parkinson Disease, Late-Onset	78	0.019

172	P	MDL005	Medulloblastoma	77	0.019

173		MRF001	Marfan Syndrome	77	0.019

174	c	TBR025	Tuberous Sclerosis 1	77	0.019

175		PLM134	Pulmonary Fibrosis, Idiopathic	77	0.019

176	c	NRF024	Neurofibromatosis, Type I	77	0.019

177		AST005	Asthma	76	0.019

178	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.019

179		CRV035	Cervical Cancer	76	0.019

180		KPS004	Kaposi Sarcoma	75	0.019

181	P	HRT032	Heart Disease	75	0.019

182	c	PLM164	Pulmonary Hypertension, Primary, 1	75	0.019

183	c	ATR087	Atrial Standstill 1	75	0.019

184		ADR007	Adrenoleukodystrophy	75	0.019

185		LPT014	Leptin Deficiency or Dysfunction	74	0.019

186	P	OST002	Osteoporosis	74	0.019

187	c	ATM006	Autoimmune Lymphoproliferative Syndrome	74	0.019

188	c	MNN043	Meningioma, Familial	74	0.019

189		VNH007	Von Hippel-Lindau Syndrome	73	0.019

190		SVR004	Severe Combined Immunodeficiency	73	0.019

191	c	HYP836	Hypercholesterolemia, Familial, 1	73	0.019

192		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.019

193	c	SPN225	Spondyloarthropathy 1	73	0.019

194	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.019

195		BSL036	Basal Cell Nevus Syndrome	73	0.019

196	P	CNR004	Cone-Rod Dystrophy 2	73	0.019

197	P	RTN024	Retinoblastoma	73	0.019

198		ANX010	Anxiety	73	0.019

199	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.019

200		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.019

201		SCH036	Scheie Syndrome	72	0.019

202		BRT054	Brittle Bone Disorder	72	0.019

203	c	MCP050	Mucopolysaccharidosis, Type Ii	72	0.019

204	c	TBR026	Tuberous Sclerosis 2	72	0.019

205	P	MLT020	Multiple Sclerosis	72	0.019

206	c	HPT073	Hepatitis C Virus	72	0.019

207	P	HNT016	Huntington Disease	72	0.019

208	P	NRB001	Neuroblastoma	72	0.019

209	P	FML011	Familial Adenomatous Polyposis	72	0.019

210		OTT002	Otitis Media	72	0.019

211	P	WSK001	Wiskott-Aldrich Syndrome	72	0.019

212		AGM019	Agammaglobulinemia, X-Linked	71	0.019

213	P	PHC003	Pheochromocytoma	71	0.019

214		PRP027	Peripheral Vascular Disease	71	0.019

215		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.019

216		BHC003	Behcet Syndrome	71	0.019

217	P	SRC025	Sarcoidosis 1	70	0.019

218	P	ATS364	Autism	70	0.019

219	P	MYC007	Myocardial Infarction	70	0.019

220	P	MTC003	Metachromatic Leukodystrophy	70	0.019

221	P	AMY004	Amyloidosis	70	0.019

222		MYL009	Myelodysplastic Syndrome	70	0.019

223		MLT157	Multiple System Atrophy 1	70	0.019

224	c	GLY008	Glycogen Storage Disease Ii	70	0.019

225		MYL005	Myelofibrosis	70	0.019

226		ADN011	Adenoid Cystic Carcinoma	70	0.019

227		PTZ001	Peutz-Jeghers Syndrome	70	0.019

228	P	OST001	Osteopetrosis	70	0.019

229	P	HYP061	Hypertrophic Cardiomyopathy	70	0.019

230	c	MLT160	Multiple Endocrine Neoplasia, Type Iia	70	0.019

231	P	MYP004	Myopathy	70	0.019

232	P	TBR001	Tuberous Sclerosis	70	0.019

233		CNG034	Congestive Heart Failure	69	0.019

234	P	DMN001	Diamond-Blackfan Anemia	69	0.019

235	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.019

236	P	KRB001	Krabbe Disease	69	0.019

237		PLY001	Polycythemia Vera	69	0.019

238		SVR097	Severe Cutaneous Adverse Reaction	69	0.019

239	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.019

240	P	SLP006	Sleep Apnea	69	0.019

241	P	TYS001	Tay-Sachs Disease	69	0.019

242		LYM133	Lymphoma, Hodgkin, Classic	69	0.019

243	P	OCL013	Oculodentodigital Dysplasia	69	0.019

244	P	HYP086	Hypothyroidism	69	0.019

245	P	LPR021	Leprosy 3	69	0.019

246		ART016	Aortic Aneurysm	69	0.019

247		LKC009	Leukocyte Adhesion Deficiency, Type I	69	0.019

248		EWN003	Ewing Sarcoma	69	0.019

249		LYM007	Lymphangioleiomyomatosis	69	0.019

250	P	HYP802	Hypocalcemia, Autosomal Dominant 1	69	0.019

251	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.019

252	P	LYM118	Lymphoma	68	0.019

253	P	CRN037	Craniosynostosis	68	0.019

254	P	TMP003	Temporal Arteritis	68	0.019

255	P	LVR013	Liver Disease	68	0.019

256	P	SYS005	Systemic Scleroderma	68	0.019

257	P	MYC084	Mycobacterium Tuberculosis 1	68	0.019

258		CHL065	Cholangiocarcinoma	68	0.019

259		SND001	Sandhoff Disease	68	0.019

260		CMM004	Common Variable Immunodeficiency	68	0.019

261	c	BSL007	Basal Cell Carcinoma	68	0.019

262	c	NMN015	Niemann-Pick Disease, Type C1	68	0.019

263	P	MYS003	Myasthenia Gravis	68	0.019

264	P	INF038	Influenza	68	0.019

265	c	CRD086	Cardiomyopathy, Familial Hypertrophic, 1	68	0.019

266	P	ESS003	Essential Thrombocythemia	68	0.019

267		BRN024	Bronchitis	68	0.019

268		CNN005	Connective Tissue Disease	68	0.019

269		RCK004	Rickets	68	0.019

270	P	MJR001	Major Depressive Disorder	68	0.019

271		PNC129	Pancreatic Adenocarcinoma	68	0.019

272	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.019

273		IMM106	Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked	68	0.019

274	c	MCP052	Mucopolysaccharidosis, Type Vi	67	0.019

275	P	THR014	Thrombocytopenia	67	0.019

276		HYL004	Hyaline Fibromatosis Syndrome	67	0.019

277	P	CWD010	Cowden Syndrome	67	0.019

278	P	3MT016	3-Methylglutaconic Aciduria, Type Iii	67	0.019

279		GST092	Gastroesophageal Reflux	67	0.019

280	P	HPT021	Hepatitis	67	0.019

281	P	DYS007	Dyskeratosis Congenita	67	0.019

282		FCT007	Factor Vii Deficiency	67	0.019

283	c	JVN004	Juvenile Myelomonocytic Leukemia	67	0.019

284		CRB039	Cerebrovascular Disease	67	0.019

285		ALL003	Allergic Rhinitis	67	0.019

286	c	HMP029	Hemophilia a	67	0.019

287	P	SHW006	Shwachman-Diamond Syndrome 1	67	0.019

288	P	CHR012	Chronic Granulomatous Disease	67	0.019

289		FLL027	Fallopian Tube Carcinoma	67	0.019

290	P	HYP098	Hypereosinophilic Syndrome	67	0.019

291	c	ATS007	Autism Spectrum Disorder	67	0.019

292	P	PLM037	Pulmonary Hypertension	67	0.019

293	c	MGR028	Migraine with or Without Aura 1	67	0.019

294		MYC006	Mycosis Fungoides	66	0.019

295	P	LNG028	Long Qt Syndrome	66	0.019

296	c	PLY168	Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease	66	0.019

297		ALP042	Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity	66	0.019

298		ALC007	Alcohol Dependence	66	0.019

299		OST159	Osteogenic Sarcoma	66	0.019

300		ANG054	Angina Pectoris	66	0.019

301		GLL008	Gilles De La Tourette Syndrome	66	0.019

302		CHD001	Chediak-Higashi Syndrome	66	0.019

303	P	DMN002	Dementia	66	0.019

304	c	FML021	Familial Hypercholesterolemia	66	0.019

305	P	SKN015	Skin Carcinoma	66	0.019

306	P	NSP012	Nasopharyngeal Carcinoma	66	0.019

307		MYX005	Myxoid Liposarcoma	66	0.019

308	c	FML346	Familial Adenomatous Polyposis 1	66	0.019

309	c	MNN047	Mannosidosis, Alpha B, Lysosomal	66	0.019

310		HYP056	Hypoglycemia	66	0.019

311		AND002	Androgen Insensitivity Syndrome	66	0.019

312	P	CCK001	Cockayne Syndrome	66	0.019

313		MYL031	Myeloproliferative Neoplasm	66	0.019

314	c	MCL013	Mucolipidosis Iv	66	0.019

315		SVR066	Severe Combined Immunodeficiency, X-Linked	66	0.019

316		KHL003	Kohlschutter-Tonz Syndrome	65	0.019

317		CRN036	Craniopharyngioma	65	0.019

318		HTC003	Hutchinson-Gilford Progeria Syndrome	65	0.019

319	P	ART005	Arteriovenous Malformation	65	0.019

320	P	AGM001	Agammaglobulinemia	65	0.019

321	P	CNJ013	Conjunctivitis	65	0.019

322		SRC014	Sarcoma	65	0.019

323		PPL049	Papillon-Lefevre Syndrome	65	0.019

324	P	LPS002	Liposarcoma	65	0.019

325		ATM096	Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia	65	0.019

326		AFB002	Afibrinogenemia, Congenital	65	0.019

327	P	MTR014	Motor Neuron Disease	65	0.019

328		ACH022	Achalasia-Addisonianism-Alacrima Syndrome	65	0.019

329		PRT037	Pertussis	65	0.019

330		HRL003	Hurler Syndrome	65	0.019

331		IRR002	Irritable Bowel Syndrome	65	0.019

332	P	HRP006	Herpes Simplex	65	0.019

333		GRN037	Granulomatosis with Polyangiitis	65	0.019

334		MRK001	Merkel Cell Carcinoma	65	0.019

335		ATH013	Atherosclerosis Susceptibility	65	0.019

336	c	WLM013	Wilms Tumor 1	65	0.019

337	P	PLR004	Pleuropulmonary Blastoma	65	0.019

338	P	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	65	0.019

339	P	ADL010	Adult Respiratory Distress Syndrome	65	0.019

340	P	THY023	Thymoma	65	0.019

341		LYS012	Lysosomal Acid Lipase Deficiency	65	0.019

342	c	MCP001	Mucopolysaccharidosis Iii	65	0.019

343	c	ATS347	Autosomal Dominant Polycystic Kidney Disease	65	0.019

344		PRT036	Peritonitis	64	0.019

345		APN008	Apnea, Obstructive Sleep	64	0.019

346		ANG020	Angiosarcoma	64	0.019

347		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.019

348		NRF007	Neurofibroma	64	0.019

349	P	MST009	Mastocytosis	64	0.019

350		TBC004	Tobacco Addiction	64	0.019

351		CTR172	Citrullinemia, Classic	64	0.019

352	c	JVN010	Juvenile Rheumatoid Arthritis	64	0.019

353		GT001	Gout	64	0.019

354		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.019

355		CNG510	Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi	64	0.019

356		DGR001	Digeorge Syndrome	64	0.019

357	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.019

358		MLT163	Multiple Pterygium Syndrome, Escobar Variant	64	0.019

359	P	PRD008	Periodontitis	64	0.019

360		MSC007	Muscle Hypertrophy	64	0.019

361		SPT006	Septooptic Dysplasia	64	0.019

362		DSM004	Desmoid Tumor	64	0.019

363		MGK001	Megakaryocytic Leukemia	64	0.019

364		RBR001	Roberts Syndrome	64	0.019

365	P	RHB003	Rhabdomyosarcoma	63	0.019

366	c	MCP049	Mucopolysaccharidosis, Type Vii	63	0.019

367		VNT035	Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy	63	0.019

368		BRT002	Birt-Hogg-Dube Syndrome	63	0.019

369	P	GLM045	Glioma	63	0.019

370	P	HML002	Hemolytic Anemia	63	0.019

371	c	PRC016	Pre-Eclampsia	63	0.019

372	P	NTR004	Neutropenia	63	0.019

373	P	ANR048	Aniridia 1	63	0.019

374	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.019

375		PLG002	Plague	63	0.019

376	c	MLG084	Malignant Fibrous Histiocytoma	63	0.019

377	P	CRN300	Coronary Heart Disease 1	63	0.019

378	P	DST002	Distal Arthrogryposis	63	0.019

379		ACT119	Acute Promyelocytic Leukemia	63	0.019

380		CHN016	Cohen Syndrome	63	0.019

381		END041	Endometrial Adenocarcinoma	63	0.019

382	P	MVM001	Movement Disease	63	0.019

383	c	ACT068	Acute Cystitis	63	0.019

384	P	LMY004	Leiomyosarcoma	63	0.019

385		TRN015	Transient Cerebral Ischemia	63	0.019

386	c	HMP022	Hemophagocytic Lymphohistiocytosis, Familial, 1	63	0.019

387		DPR016	Depression	63	0.019

388		RHB001	Rhabdoid Cancer	63	0.019

389	c	ATM011	Autoimmune Hepatitis	63	0.019

390		IMM174	Immunodeficiency with Hyper-Igm, Type 1	63	0.019

391	c	ALP101	Alpha-Thalassemia	62	0.019

392		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.019

393	c	MTR018	Maturity-Onset Diabetes of the Young, Type 1	62	0.019

394		LPD008	Lipid Metabolism Disorder	62	0.019

395	c	HPT001	Hepatitis C	62	0.019

396	P	PLY014	Polycystic Kidney Disease	62	0.019

397	P	PSR002	Psoriasis	62	0.019

398	c	GM1007	Gm1 Gangliosidosis	62	0.019

399	c	HPT003	Hepatitis a	62	0.019

400	c	BRN108	Branchiootic Syndrome 1	62	0.019

401		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.019

402		TKY002	Takayasu Arteritis	62	0.019

403	P	SPN046	Spinal Muscular Atrophy	62	0.019

404	c	SVR001	Severe Acute Respiratory Syndrome	62	0.019

405		LPP008	Lipoprotein Quantitative Trait Locus	62	0.019

406		PRM126	Primary Peritoneal Carcinoma	62	0.019

407	P	HYP750	Hypertriglyceridemia, Familial	62	0.019

408	P	ART023	Arthropathy	62	0.019

409	P	VSC011	Vasculitis	62	0.019

410	c	ANM038	Anemia, Autoimmune Hemolytic	62	0.019

411		ATM095	Autoimmune Disease	62	0.019

412		ALL026	Allergic Hypersensitivity Disease	62	0.019

413		MNN042	Meningioma, Radiation-Induced	62	0.019

414		CRC021	Carcinosarcoma	62	0.019

415		TXC005	Toxic Shock Syndrome	62	0.019

416	P	PRM006	Primary Biliary Cirrhosis	62	0.019

417		LVR012	Liver Cirrhosis	62	0.019

418		BLD131	Bladder Urothelial Carcinoma	62	0.019

419		ASP002	Aspartylglucosaminuria	62	0.019

420		MSL001	Measles	62	0.019

421	P	DRM010	Dermatomyositis	61	0.019

422		PSR001	Psoriatic Arthritis	61	0.019

423	c	MCP043	Mucopolysaccharidosis, Type Iiia	61	0.019

424	P	INT143	Interstitial Cystitis	61	0.019

425	P	KLL001	Kallmann Syndrome	61	0.019

426	P	LYM113	Lymphoproliferative Syndrome, X-Linked, 1	61	0.019

427		HYP066	Hyperglycemia	61	0.019

428		INT002	Intermittent Claudication	61	0.019

429		CHR001	Churg-Strauss Syndrome	61	0.019

430	c	PNS012	Paine Syndrome	61	0.019

431	c	SCL052	Scleroderma, Familial Progressive	61	0.019

432	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.019

433	P	ENC018	Encephalopathy	61	0.019

434	P	ENC004	Encephalitis	61	0.019

435		ALC006	Alcoholic Hepatitis	61	0.019

436		FCS002	Fucosidosis	61	0.019

437		WLD007	Waldenstroem's Macroglobulinemia	61	0.019

438		ALV005	Alveolar Soft Part Sarcoma	61	0.019

439	c	WLM018	Wilms Tumor 5	61	0.019

440	P	SJG008	Sjogren Syndrome	61	0.019

441		ARG002	Argininosuccinic Aciduria	61	0.019

442		RTN017	Retinal Detachment	61	0.019

443		VRL011	Viral Infectious Disease	61	0.019

444		APP008	Appendicitis	61	0.019

445	c	ART144	Arthrogryposis, Distal, Type 1a	61	0.019

446	P	HMN010	Hemangioma	61	0.019

447		DCB001	Decubitus Ulcer	61	0.019

448		PRG017	Paraganglioma and Gastric Stromal Sarcoma	61	0.019

449		BTN003	Biotinidase Deficiency	60	0.019

450	P	MYL006	Myeloid Leukemia	60	0.019

451		NPH091	Nephrolithiasis, Calcium Oxalate	60	0.019

452	P	KDN017	Kidney Cancer	60	0.019

453		SPN186	Spinal Cord Injury	60	0.019

454		HRP004	Herpes Zoster	60	0.019

455	P	NPH012	Nephrotic Syndrome	60	0.019

456		SZR001	Sezary's Disease	60	0.019

457		DBT084	Diabetes Mellitus, Ketosis-Prone	60	0.019

458	P	TST021	Testicular Germ Cell Tumor	60	0.019

459	c	LPM012	Lipomatosis, Multiple	60	0.019

460		TRG002	Trigeminal Neuralgia	60	0.019

461	c	JVN061	Juvenile Arthritis	60	0.019

462	P	BNG030	Benign Ependymoma	60	0.019

463		INT066	Interstitial Lung Disease	60	0.019

464		CNG410	Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly	60	0.019

465		HPT019	Hepatic Encephalopathy	60	0.019

466		THR100	Thrombocytopenic Purpura, Autoimmune	60	0.019

467		LNG099	Lung Disease	60	0.019

468	c	ORF037	Orofaciodigital Syndrome I	60	0.019

469	P	ALP009	Alopecia Areata	60	0.019

470		STR039	Sturge-Weber Syndrome	60	0.019

471		LBR030	Leber Optic Atrophy	60	0.019

472	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.019

473		CHC001	Chickenpox	60	0.019

474	P	CTR002	Cataract	60	0.019

475		ORL011	Oral Cancer	60	0.019

476	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	60	0.019

477		ETN001	Eating Disorder	60	0.019

478	P	GLY013	Glycogen Storage Disease	60	0.019

479	c	ACT071	Acute Kidney Failure	60	0.019

480	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.019

481		VGN017	Vaginal Cancer	60	0.019

482	P	VTL004	Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1	60	0.019

483		DYS164	Dyskeratosis Congenita, X-Linked	60	0.019

484	c	HRD002	Hereditary Angioedema	60	0.019

485	P	OPT006	Optic Nerve Disease	60	0.019

486		ORN008	Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to	59	0.019

487		SPP011	Suppression of Tumorigenicity 12	59	0.019

488	P	MYC008	Myocarditis	59	0.019

489		PRT013	Portal Hypertension	59	0.019

490		CHL014	Cholera	59	0.019

491	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.019

492	P	BND020	Bone Disease	59	0.019

493	c	HPT016	Hepatitis B	59	0.019

494	P	BRN022	Bronchiectasis	59	0.019

495	c	PCH015	Pachyonychia Congenita 1	59	0.019

496		THY029	Thyroid Carcinoma	59	0.019

497		IGR001	Ige Responsiveness, Atopic	59	0.019

498		CHL123	Chlamydia	59	0.019

499		PLM033	Pulmonary Embolism	59	0.019

500	P	LYM033	Lymphoproliferative Syndrome	59	0.019

501		VSL002	Visual Epilepsy	59	0.019

502		HYP257	Hypoparathyroidism, Sensorineural Deafness, and Renal Disease	59	0.019

503	c	LTN004	Late-Onset Retinal Degeneration	59	0.019

504	P	HYP535	Hypogonadotropic Hypogonadism 7 with or Without Anosmia	59	0.019

505	c	HRD031	Hereditary Paraganglioma-Pheochromocytoma Syndromes	59	0.019

506	c	MCP045	Mucopolysaccharidosis, Type Iiic	59	0.019

507	P	BRS044	Breast Adenocarcinoma	59	0.019

508		KLP010	Klippel-Trenaunay-Weber Syndrome	59	0.019

509	P	HMN036	Hemangiopericytoma, Malignant	59	0.019

510		GNG013	Gingivitis	59	0.019

511		ADN018	Adenoma	59	0.019

512		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.019

513		GST045	Gastroenteritis	59	0.019

514		ANR040	Aneurysm	59	0.019

515	c	SVR003	Severe Congenital Neutropenia	59	0.019

516		PPT005	Peptic Ulcer Disease	59	0.019

517		SRC027	Sarcoma, Synovial	58	0.019

518		INC002	Inclusion Body Myositis	58	0.019

519		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.019

520		KRT071	Keratosis, Seborrheic	58	0.019

521	P	PLY017	Polyarteritis Nodosa	58	0.019

522	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.019

523		PST028	Post-Traumatic Stress Disorder	58	0.019

524	P	INT070	Intestinal Obstruction	58	0.019

525		RBS001	Rabies	58	0.019

526	P	BCL017	B-Cell Lymphoma	58	0.019

527		CRD132	Cardiac Conduction Defect	58	0.019

528		CHR072	Chordoma	58	0.019

529		MCS006	Macs Syndrome	58	0.019

530		THY025	Thymus Cancer	58	0.019

531	c	PRG018	Paragangliomas 1	58	0.019

532		SPT004	Septic Arthritis	58	0.019

533	P	ALC033	Alcohol Use Disorder	58	0.019

534		HYP458	Hyper Ige Syndrome	58	0.019

535		RSP019	Respiratory Distress Syndrome in Premature Infants	58	0.019

536		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.019

537		ERY003	Erythema Multiforme	58	0.019

538	P	URT039	Urticaria	58	0.019

539		NWB001	Newborn Respiratory Distress Syndrome	58	0.019

540		DSS008	Disease of Mental Health	58	0.019

541	P	MMP001	Mumps	58	0.019

542		MNT002	Mental Depression	58	0.019

543	P	EPD003	Epidermolysis Bullosa Simplex	58	0.019

544		LYM027	Lymphopenia	58	0.019

545	P	PRP019	Peripheral Nervous System Disease	58	0.019

546		LNG108	Langerhans Cell Histiocytosis	58	0.019

547		MXD005	Mixed Connective Tissue Disease	58	0.019

548	P	INF032	Infertility	57	0.019

549	P	UVT001	Uveitis	57	0.019

550		PMP006	Pemphigus Vulgaris, Familial	57	0.019

551	P	ESP035	Esophagitis, Eosinophilic, 1	57	0.019

552		APL002	Aplasia of Lacrimal and Salivary Glands	57	0.019

553	P	GLM007	Glomerulonephritis	57	0.019

554		GLS018	Glass Syndrome	57	0.019

555		CST005	Castleman Disease	57	0.019

556	c	CHR417	Chronic Graft Versus Host Disease	57	0.019

557		IRN002	Iron Metabolism Disease	57	0.019

558		BRN056	Bronchopulmonary Dysplasia	57	0.019

559	P	PLY041	Polymyositis	57	0.019

560	c	PLY172	Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease	57	0.019

561		THY122	Thyroid Gland Cancer	57	0.019

562		IMM072	Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1	57	0.019

563	c	ACT075	Acute Myocardial Infarction	57	0.019

564		THR024	Thrombosis	57	0.019

565	c	MST023	Mesothelioma, Malignant	57	0.019

566		APH001	Aphthous Stomatitis	57	0.019

567		PLY023	Polycystic Liver Disease	57	0.019

568	P	END033	Endocarditis	57	0.019

569		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.019

570	P	FCL005	Focal Segmental Glomerulosclerosis	57	0.019

571		THY022	Thymic Carcinoma	57	0.019

572	P	PRV006	Pervasive Developmental Disorder	57	0.019

573		CRB197	Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to	57	0.019

574		BCL010	B-Cell Expansion with Nfkb and T-Cell Anergy	57	0.019

575		CMM005	Common Cold	57	0.019

576	c	ANG068	Angioedema, Hereditary, Type I	57	0.019

577	c	GM1004	Gm1-Gangliosidosis, Type I	57	0.019

578	c	LKM070	Leukemia, Acute Monocytic	57	0.019

579		HMR039	Hemorrhage, Intracerebral	57	0.019

580		SCH014	Schistosomiasis	57	0.019

581		SKN022	Skin Squamous Cell Carcinoma	57	0.019

582		HYP266	Hypoxia	57	0.019

583		AYM001	Ayme-Gripp Syndrome	57	0.019

584	P	ANG015	Angioedema	57	0.019

585		PGM001	Pigmented Villonodular Synovitis	56	0.019

586	P	PYL005	Pyelonephritis	56	0.019

587	c	BSL024	Basal Cell Carcinoma 1	56	0.019

588		PLM102	Palmoplantar Keratoderma, Epidermolytic	56	0.019

589	P	MYS005	Myositis	56	0.019

590	P	PLY018	Polycythemia	56	0.019

591	P	ADL017	Adult T-Cell Leukemia	56	0.019

592	P	CHN012	Chondrosarcoma	56	0.019

593		CMR002	Coumarin Resistance	56	0.019

594	P	FBR017	Fibrosarcoma	56	0.019

595	P	PLY011	Polycystic Ovary Syndrome	56	0.019

596		HPT046	Hepatic Veno-Occlusive Disease	56	0.019

597		TRN018	Transitional Cell Carcinoma	56	0.019

598		PLS011	Plasmacytoma	56	0.019

599		EXF001	Exfoliation Syndrome	56	0.019

600	c	ACT134	Acute Liver Failure	56	0.019

601		LMY014	Leiomyoma, Uterine	56	0.019

602	P	NRP001	Neuropathy	56	0.019

603		SPN041	Spinal Cord Disease	56	0.019

604		SFT003	Soft Tissue Sarcoma	56	0.019

605		ISL001	Islet Cell Tumor	56	0.019

606		RLP002	Relapsing-Remitting Multiple Sclerosis	56	0.019

607		HMG005	Hemoglobinopathy	56	0.019

608	P	NRF002	Neurofibromatosis	56	0.019

609		EMB004	Embryonal Carcinoma	56	0.019

610		GST050	Gastrointestinal System Disease	56	0.019

611	P	LBR014	Leber Congenital Amaurosis 4	56	0.019

612		MCR141	Mucormycosis	56	0.019

613		INT030	Intracranial Aneurysm	56	0.019

614		SCP002	Scapuloperoneal Spinal Muscular Atrophy	56	0.019

615	P	HYP024	Hypoparathyroidism	56	0.019

616		MCS002	Mucositis	56	0.019

617		BRN004	Brain Edema	56	0.019

618		AGN016	Aging	56	0.019

619	P	GST044	Gastritis	56	0.019

620		MRD002	Marden-Walker Syndrome	56	0.019

621		HPT022	Hepatoblastoma	56	0.019

622	c	FML035	Familial Hyperlipidemia	55	0.019

623		HYP005	Hypokalemia	55	0.019

624		NRN004	Neuroendocrine Tumor	55	0.019

625	c	CRD184	Ceroid Lipofuscinosis, Neuronal, 5	55	0.019

626		MCL006	Macular Retinal Edema	55	0.019

627		LMB062	Limb Ischemia	55	0.019

628		ZLL002	Zollinger-Ellison Syndrome	55	0.019

629		MMB001	Membranoproliferative Glomerulonephritis	55	0.019

630	P	MLN007	Male Infertility	55	0.019

631		VSC003	Visceral Leishmaniasis	55	0.019

632	c	BCT007	Bacterial Meningitis	55	0.019

633		DFF005	Diffuse Large B-Cell Lymphoma	55	0.019

634	c	CTS029	Cutis Laxa, Autosomal Recessive, Type Iiia	55	0.019

635	P	ANT006	Antiphospholipid Syndrome	55	0.019

636		ENC067	Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis	55	0.019

637		HRL004	Hurler-Scheie Syndrome	55	0.019

638		CRC006	Carcinoid Syndrome	55	0.019

639	c	INT064	Intermediate Uveitis	55	0.019

640		EPT010	Epithelial-Myoepithelial Carcinoma	55	0.019

641		JVN009	Juvenile Pilocytic Astrocytoma	55	0.019

642		ESN005	Eosinophilic Gastroenteritis	55	0.019

643		HNC001	Henoch-Schoenlein Purpura	55	0.019

644		END040	Endogenous Depression	55	0.019

645		INT007	Intermediate Coronary Syndrome	55	0.019

646		HRY003	Hairy Cell Leukemia	55	0.019

647		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.019

648		SYN007	Synovitis	54	0.019

649		PRP030	Purpura	54	0.019

650		RSC001	Rosacea	54	0.019

651	P	PMP001	Pemphigus	54	0.019

652		GLS001	Gliosarcoma	54	0.019

653		ACD008	Acid-Labile Subunit Deficiency	54	0.019

654		MNN032	Meningococcal Meningitis	54	0.019

655		GLC003	Glucose Intolerance	54	0.019

656	c	THR124	Thrombotic Thrombocytopenic Purpura, Hereditary	54	0.019

657	P	HMP002	Hemophagocytic Lymphohistiocytosis	54	0.019

658	P	CNT116	Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a	54	0.019

659		VLC001	Velocardiofacial Syndrome	54	0.019

660	P	CYS039	Cystic Kidney Disease	54	0.019

661		GST037	Gastroparesis	54	0.019

662		AMY027	Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1	54	0.019

663		CRY003	Cryptosporidiosis	54	0.019

664		PRT038	Protein-Energy Malnutrition	54	0.019

665	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.019

666		CLL010	Cellular Ependymoma	54	0.019

667	c	MLG077	Malignant Peripheral Nerve Sheath Tumor	54	0.019

668		ANL018	Analbuminemia	54	0.019

669	P	ART021	Arteriosclerosis	54	0.019

670		RVS001	Revesz Syndrome	54	0.019

671	P	LTR001	Lateral Sclerosis	54	0.019

672		HMS001	Hemosiderosis	54	0.019

673		LYM040	Lymphoblastic Lymphoma	54	0.019

674	c	PST005	Posterior Uveitis	54	0.019

675	c	AMG001	Amegakaryocytic Thrombocytopenia, Congenital	54	0.019

676		PPL022	Papilloma	54	0.019

677		SLP001	Sleeping Sickness	54	0.019

678		CLL003	Cellulitis	54	0.019

679		NNL006	Non-Alcoholic Steatohepatitis	54	0.019

680		PNC001	Pancytopenia	54	0.019

681		LYM022	Lymphangioma	54	0.019

682		CLR030	Clear Cell Renal Cell Carcinoma	53	0.019

683	c	THR001	Thrombocytopenia Due to Platelet Alloimmunization	53	0.019

684	P	END047	Endophthalmitis	53	0.019

685	P	TCD001	Tic Disorder	53	0.019

686		CRY001	Cryptogenic Organizing Pneumonia	53	0.019

687		PST046	Post-Transplant Lymphoproliferative Disease	53	0.019

688	P	EPD016	Epidermolysis Bullosa	53	0.019

689	c	DMN023	Diamond-Blackfan Anemia 1	53	0.019

690		PLM136	Palmoplantar Keratoderma, Nonepidermolytic	53	0.019

691		PLS016	Plasma Cell Leukemia	53	0.019

692		KRT006	Keratoconjunctivitis	53	0.019

693		IMM102	Immunodeficiency 14	53	0.019

694	P	MNC007	Monocytic Leukemia	53	0.019

695		PRP036	Peripheral T-Cell Lymphoma	53	0.019

696		CRH005	Crohn's Colitis	53	0.019

697		BRN038	Bronchial Disease	53	0.019

698	P	EMB005	Embryonal Rhabdomyosarcoma	53	0.019

699	P	RTN016	Retinal Degeneration	53	0.019

700	P	ALL008	Allergic Bronchopulmonary Aspergillosis	53	0.019

701	c	PRD040	Periodontitis, Chronic	53	0.019

702	c	PRM092	Primary Lateral Sclerosis, Adult, 1	53	0.019

703	P	CNT005	Central Nervous System Lymphoma	53	0.019

704		INF034	Infective Endocarditis	53	0.019

705	P	HMR003	Hemorrhagic Disease	53	0.019

706		HYP063	Hypersplenism	53	0.019

707		PLY118	Polyglucosan Body Myopathy 1 with or Without Immunodeficiency	53	0.019

708		INT075	Intracranial Hypertension	53	0.019

709		SPN035	Spindle Cell Sarcoma	53	0.019

710	P	ACT008	Actinic Keratosis	53	0.019

711		ERD001	Erdheim-Chester Disease	53	0.019

712		IRD001	Iridocyclitis	53	0.019

713		NRT001	Neurotic Disorder	53	0.019

714		GST023	Gastric Ulcer	53	0.019

715		TXC002	Toxic Encephalopathy	53	0.019

716		DNT012	Dental Caries	53	0.019

717		PRP080	Peripheral Artery Disease	53	0.019

718	c	FML008	Familial Retinoblastoma	53	0.019

719	c	PSR017	Psoriasis 2	53	0.019

720	P	INT068	Intestinal Disease	53	0.019

721	c	OST131	Osteopetrosis, Autosomal Dominant 2	53	0.019

722	P	RTN018	Retinal Disease	53	0.019

723		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.019

724		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.019

725	P	PRG013	Paraganglioma	52	0.019

726		ESP023	Esophageal Disease	52	0.019

727		MCN017	Meconium Ileus	52	0.019

728		LYS002	Lysosomal Storage Disease	52	0.019

729	c	VRL010	Viral Hepatitis	52	0.019

730		ACR041	Acromelic Frontonasal Dysostosis	52	0.019

731	P	SML001	Small Cell Carcinoma	52	0.019

732		SMT003	Somatostatinoma	52	0.019

733		GLM004	Gliomatosis Cerebri	52	0.019

734	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.019

735		PST011	Pustulosis of Palm and Sole	52	0.019

736	P	HYP730	Hypogonadotropic Hypogonadism	52	0.019

737	P	DDN001	Duodenal Ulcer	52	0.019

738	P	RCT021	Rectum Cancer	52	0.019

739		IMP005	Impotence	52	0.019

740		CRT016	Carotid Artery Disease	52	0.019

741		ART140	Arteries, Anomalies of	52	0.019

742		THY030	Thyroid Gland Disease	52	0.019

743	P	MSC003	Muscular Atrophy	52	0.019

744	c	THY107	Thymoma, Familial	52	0.019

745	c	PSR023	Psoriasis 1	52	0.019

746		HYP014	Hyperuricemia	52	0.019

747		ACT200	Acute Monoblastic Leukemia	52	0.019

748	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.019

749		TLN003	Telangiectasis	52	0.019

750	P	OVR049	Ovarian Disease	52	0.019

751		DSM007	Desmoplastic Small Round Cell Tumor	52	0.019

752		INV006	Inverted Papilloma	52	0.019

753	c	ACT135	Acute Graft Versus Host Disease	52	0.019

754	P	BRN035	Brain Stem Glioma	52	0.019

755		SRS001	Serous Cystadenocarcinoma	52	0.019

756	P	TRT010	Teratoma	52	0.019

757		LMY002	Leiomyoma	52	0.019

758		PNG002	Pain Agnosia	51	0.019

759		SPN051	Spondylitis	51	0.019

760	P	HMP007	Hemophilia	51	0.019

761		THR004	Thrombocytosis	51	0.019

762	c	CNG208	Congenital Disorder of Glycosylation, Type Iic	51	0.019

763		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.019

764	c	CTS033	Cutis Laxa, Autosomal Recessive, Type Ic	51	0.019

765	P	SPP010	Suppressor of Tumorigenicity 3	51	0.019

766		FCT001	Factor Viii Deficiency	51	0.019

767	c	NMN014	Niemann-Pick Disease, Type C2	51	0.019

768		FDL002	Food Allergy	51	0.019

769		ALK024	Alkuraya-Kucinskas Syndrome	51	0.019

770		PLS009	Plasma Cell Neoplasm	51	0.019

771		ILS001	Ileus	51	0.019

772	P	LCT001	Lactic Acidosis	51	0.019

773	P	CPL006	Capillary Hemangioma	51	0.019

774	c	NTR049	Neutropenia, Severe Congenital, 3, Autosomal Recessive	51	0.019

775		CYS014	Cystadenocarcinoma	51	0.019

776		INT079	Intrahepatic Cholangiocarcinoma	51	0.019

777		CYS036	Cystinosis, Nephropathic	51	0.019

778		VSC006	Vascular Cancer	51	0.019

779		CCC002	Coccidiosis	51	0.019

780		SPL004	Splenic Marginal Zone Lymphoma	51	0.019

781		BLL003	Bell's Palsy	51	0.019

782		FBR008	Fibrillary Astrocytoma	51	0.019

783		TNG007	Tongue Carcinoma	51	0.019

784		GNG012	Gingival Overgrowth	51	0.019

785	P	HYP040	Hypospadias	51	0.019

786		HYP074	Hypersensitivity Vasculitis	51	0.019

787		END086	End Stage Renal Disease	51	0.019

788		CRV040	Cervix Carcinoma	51	0.019

789		SKN013	Skin Benign Neoplasm	51	0.019

790		PNM005	Pneumonic Plague	51	0.019

791	P	CHL066	Cholangitis	51	0.019

792		URC002	Urea Cycle Disorder	51	0.019

793		ACT017	Acute Chest Syndrome	51	0.019

794		HYP081	Hypolipoproteinemia	51	0.019

795		RSP002	Respiratory Syncytial Virus Infectious Disease	51	0.019

796		CHR005	Chorioamnionitis	51	0.019

797	c	ALM001	Al Amyloidosis	50	0.019

798		GNT002	Giant Cell Glioblastoma	50	0.019

799		PTT041	Pituitary Stalk Interruption Syndrome	50	0.019

800	P	MMB011	Membranous Nephropathy	50	0.019

801	P	HYP077	Hypertrichosis	50	0.019

802		PLR007	Pleural Empyema	50	0.019

803	c	PRM012	Primary Polycythemia	50	0.019

804	P	FNC004	Fanconi Syndrome	50	0.019

805		BRX001	Bruxism	50	0.019

806		SPN021	Spinal Meningioma	50	0.019

807		ALL009	Allergic Conjunctivitis	50	0.019

808	P	ECL001	Eclampsia	50	0.019

809		RSP006	Respiratory System Disease	50	0.019

810		HPT014	Hepatorenal Syndrome	50	0.019

811		CRN030	Coronary Stenosis	50	0.019

812	c	HRD202	Hereditary Lymphedema I	50	0.019

813	c	INF145	Infantile Liver Failure Syndrome 1	50	0.019

814		MCL027	Macular Dystrophy, Dominant Cystoid	50	0.019

815		MCP006	Mucoepidermoid Carcinoma	50	0.019

816		PYD002	Pyoderma	50	0.019

817	P	PNV001	Panuveitis	50	0.019

818	c	CPL013	Capillary Malformations, Congenital	50	0.019

819		TRY001	Trypanosomiasis	50	0.019

820	P	KRT007	Keratoconus	50	0.019

821		HMG002	Hemoglobinuria	50	0.019

822		TRP002	Tropical Spastic Paraparesis	50	0.019

823		BLS002	Blastomycosis	50	0.019

824		CLR003	Clear Cell Adenocarcinoma	50	0.019

825	c	CNG027	Congenital Hemolytic Anemia	50	0.019

826		DYS073	Dysphagia	50	0.019

827	P	LNR013	Linear Skin Defects with Multiple Congenital Anomalies 1	50	0.019

828		TCL002	T-Cell Large Granular Lymphocyte Leukemia	49	0.019

829		ATY042	Atypical Chronic Myeloid Leukemia	49	0.019

830	c	CHR418	Chronic Leukemia	49	0.019

831	c	THR090	Thrombocythemia 1	49	0.019

832		VRR004	Verrucous Carcinoma	49	0.019

833		BLD053	Blood Platelet Disease	49	0.019

834	P	IGN003	Iga Nephropathy 1	49	0.019

835		KRT001	Keratoconjunctivitis Sicca	49	0.019

836	P	EST001	Estrogen-Receptor Positive Breast Cancer	49	0.019

837		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.019

838		MYC012	Mycetoma	49	0.019

839		PLP001	Pulpitis	49	0.019

840		PRN014	Paronychia	49	0.019

841	P	MST002	Mast-Cell Leukemia	49	0.019

842		47X002	47,xyy	49	0.019

843	P	OPN001	Open-Angle Glaucoma	49	0.019

844		MCR004	Macroglobulinemia	49	0.019

845		GST049	Gastrointestinal System Cancer	49	0.019

846		LYM138	Lymphoblastic Leukemia, Acute, with Lymphomatous Features	49	0.019

847	P	CRV031	Cervical Adenocarcinoma	49	0.019

848		MNN009	Meningoencephalitis	49	0.019

849		MYL003	Myeloid Sarcoma	49	0.019

850		ACT029	Acute Interstitial Pneumonia	49	0.019

851	P	CMP008	Compartment Syndrome	49	0.019

852		STP011	Stapes Ankylosis with Broad Thumbs and Toes	49	0.019

853	P	HYP828	Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant	49	0.019

854		SBP001	Subependymal Giant Cell Astrocytoma	49	0.019

855		HST010	Histiocytosis	48	0.019

856		RYN001	Raynaud Disease	48	0.019

857	c	BCT013	Bacterial Pneumonia	48	0.019

858		BNR002	Bone Resorption Disease	48	0.019

859		INT054	Intraocular Lymphoma	48	0.019

860		NRL018	Neural Tube Defects, Folate-Sensitive	48	0.019

861		ATS010	Autosomal Recessive Disease	48	0.019

862	P	CPL014	Capillary Malformation-Arteriovenous Malformation 1	48	0.019

863		EVN001	Evans' Syndrome	48	0.019

864		ASP007	Aspiration Pneumonia	48	0.019

865		CHR661	Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction	48	0.019

866		CHR563	Chronic Eosinophilic Leukemia	48	0.019

867		CRY004	Cryoglobulinemia	48	0.019

868		OLF005	Olfactory Neuroblastoma	48	0.019

869		RFR010	Refractory Anemia	48	0.019

870	c	HYP864	Hypoparathyroidism, Familial Isolated, 1	48	0.019

871		ACT098	Acute Erythroid Leukemia	48	0.019

872	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.019

873		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.019

874		CLS016	Clostridium Difficile Colitis	48	0.019

875	P	BNM029	Bone Mineral Density Quantitative Trait Locus 15	48	0.019

876		DBT006	Diabetic Macular Edema	48	0.019

877		GNG008	Ganglioneuroblastoma	48	0.019

878		SPL018	Splenomegaly	48	0.019

879	P	SCL015	Scleritis	48	0.019

880		IGG001	Iga Glomerulonephritis	48	0.019

881		PRS012	Pars Planitis	48	0.019

882	P	MCL001	Mucolipidosis	48	0.019

883		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.019

884		DSM003	Desmoid Disease, Hereditary	48	0.019

885		LPT006	Leptin Receptor Deficiency	48	0.019

886	c	PNT034	Pontocerebellar Hypoplasia, Type 2e	48	0.019

887		CHL056	Cheilitis	48	0.019

888		HYP025	Hyperphosphatemia	48	0.019

889		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.019

890	c	PRK071	Parkinson Disease 14, Autosomal Recessive	48	0.019

891		VSC058	Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome	48	0.019

892	c	PRM226	Primary Central Nervous System Lymphoma	48	0.019

893		RCT020	Rectum Adenocarcinoma	48	0.019

894	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.019

895		ADN009	Adenosquamous Carcinoma	47	0.019

896		GRM005	Germ Cell Cancer	47	0.019

897		PRL017	Prolymphocytic Leukemia	47	0.019

898		CRY008	Cryopyrin-Associated Periodic Syndrome	47	0.019

899		DRY001	Dry Eye Syndrome	47	0.019

900		CRC014	Carcinoid Tumors, Intestinal	47	0.019

901		MCC002	Mucocutaneous Leishmaniasis	47	0.019

902		ADN001	Adenosine Deaminase Deficiency	47	0.019

903	P	PRR002	Pure Red-Cell Aplasia	47	0.019

904		VRN004	Vernal Keratoconjunctivitis	47	0.019

905		MLT152	Multiple Self-Healing Squamous Epithelioma	47	0.019

906		SPH010	Sphingolipidosis	47	0.019

907		CRN017	Coronary Thrombosis	47	0.019

908	P	HMN032	Human Herpesvirus 8	47	0.019

909		KRT008	Keratopathy	47	0.019

910		NRN001	Neuroendocrine Carcinoma	47	0.019

911	c	PSR032	Psoriasis 11	47	0.019

912		RNL077	Renal Fibrosis	47	0.019

913		ACT055	Actinomycosis	47	0.019

914		ACT084	Acute Stress Disorder	47	0.019

915	c	OPT050	Opitz Gbbb Syndrome, Type Ii	47	0.019

916		KRT002	Keratomalacia	47	0.019

917		RTC005	Reticulosarcoma	47	0.019

918		KHN001	Kuhnt-Junius Degeneration	47	0.019

919		LYM012	Lymphoplasmacytic Lymphoma	47	0.019

920		RTN001	Retinal Vasculitis	47	0.019

921	c	INH020	Inherited Metabolic Disorder	47	0.019

922		STV007	Stevens-Johnson Syndrome/toxic Epidermal Necrolysis	47	0.019

923		SRT004	Serotonin Syndrome	47	0.019

924		STM006	Stomach Disease	47	0.019

925	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.019

926		SVR095	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency	47	0.019

927		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.019

928		MLT113	Multicentric Castleman Disease	47	0.019

929		GST071	Gastrointestinal Carcinoma	47	0.019

930		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.019

931		CNT033	Central Nervous System Cancer	47	0.019

932		NDL013	Nodular Regenerative Hyperplasia	47	0.019

933		STR103	Streptococcus Pneumonia	47	0.019

934		CRD137	Cardiogenic Shock	47	0.019

935		CHR074	Choriocarcinoma	47	0.019

936	P	OVR046	Ovarian Cyst	47	0.019

937	c	PRM093	Premature Ovarian Failure 7	47	0.019

938		NSS002	Neisseria Meningitidis Infection	47	0.019

939		RYN005	Raynaud Phenomenon	47	0.019

940	P	BLD051	Blood Coagulation Disease	46	0.019

941		LYM019	Lymphosarcoma	46	0.019

942		RTN023	Retinitis	46	0.019

943		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.019

944	P	ATM019	Autoimmune Polyendocrine Syndrome	46	0.019

945		CD4003	Cd40 Ligand Deficiency	46	0.019

946		TST014	Testicular Cancer	46	0.019

947		HYR002	Hoyeraal Hreidarsson Syndrome	46	0.019

948		PRP017	Periapical Periodontitis	46	0.019

949		MCS004	Mucosal Melanoma	46	0.019

950		MNN020	Meningococcal Infection	46	0.019

951	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.019

952	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.019

953		FCL012	Facial Paralysis	46	0.019

954		CLN045	Colonic Benign Neoplasm	46	0.019

955	P	BRB001	Beriberi	46	0.019

956	P	CHR573	Choroid Plexus Cancer	46	0.019

957	P	BNG032	Benign Mesothelioma	46	0.019

958		ANP006	Anaplastic Ependymoma	46	0.019

959		ADR040	Adrenal Gland Pheochromocytoma	46	0.019

960		SBP004	Subependymoma	46	0.019

961		MYX001	Myxopapillary Ependymoma	46	0.019

962		GST010	Gestational Trophoblastic Neoplasm	46	0.019

963		ANG018	Angiomyolipoma	46	0.019

964		SQM002	Squamous Cell Papilloma	46	0.019

965		SPR005	Superficial Basal Cell Carcinoma	46	0.019

966	c	FCL025	Focal Segmental Glomerulosclerosis 1	46	0.019

967	c	DRR009	Diarrhea 6	46	0.019

968		PRX001	Peroxisomal Disease	46	0.019

969	c	MLG068	Malignant Glioma	46	0.019

970		GLL048	Glial Tumor	45	0.019

971		BNS007	Bone Sarcoma	45	0.019

972		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	45	0.019

973		GST030	Gastrinoma	45	0.019

974		SYN036	Syncope	45	0.019

975		EXT010	Extramedullary Plasmacytoma	45	0.019

976		RTR008	Root Resorption	45	0.019

977		GLY031	Glycoproteinosis	45	0.019

978		MXD026	Mixed Glioma	45	0.019

979	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.019

980	c	NLD009	Nail Disorder, Nonsyndromic Congenital, 1	45	0.019

981		PPL018	Papillary Adenocarcinoma	45	0.019

982		INT253	Intestinal Benign Neoplasm	45	0.019

983		HMR023	Hemorrhagic Cystitis	45	0.019

984		TSY002	Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations	45	0.019

985	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.019

986		HPT004	Hepatic Coma	45	0.019

987		IMM136	Immune System Disease	45	0.019

988	P	ATS406	Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2	45	0.019

989		ESP027	Esophagus Squamous Cell Carcinoma	45	0.019

990		GLC098	Glaucoma-Related Pigment Dispersion Syndrome	45	0.019

991		ACT003	Acute Kidney Tubular Necrosis	45	0.019

992		LYM051	Lymphomatoid Granulomatosis	45	0.019

993		URT051	Ureter, Cancer of	45	0.019

994		SPP008	Suppurative Otitis Media	45	0.019

995		CLL014	Cll/sll	45	0.019

996		GLC036	Glucagonoma	45	0.019

997	c	HYP513	Hypogonadotropic Hypogonadism 1 with or Without Anosmia	45	0.019

998	c	ACQ014	Acquired Hemophilia	45	0.019

999		END035	Endocrine Gland Cancer	45	0.019

1000		MYF001	Myofibroma	45	0.019

1001		OVR112	Ovarian Germ Cell Cancer	45	0.019

1002		ASP008	Aspiration Pneumonitis	45	0.019

1003	c	CLR017	Clear Cell Sarcoma	45	0.019

1004		SPS057	Spasticity	45	0.019

1005	P	FTL033	Fetal Hemoglobin Quantitative Trait Locus 1	45	0.019

1006		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.019

1007		MXD023	Mixed Cell Type Cancer	44	0.019

1008		LYM126	Lymphoma Aids Related	44	0.019

1009	P	CHR345	Chronic Pain	44	0.019

1010	P	EPT012	Epithelioid Sarcoma	44	0.019

1011		SBC016	Subacute Delirium	44	0.019

1012		CYS009	Cystadenoma	44	0.019

1013	c	MYL058	Myeloproliferative Syndrome, Transient	44	0.019

1014		APP009	Appendix Adenocarcinoma	44	0.019

1015		GRN017	Granulocytopenia	44	0.019

1016		LTH001	Lethal Midline Granuloma	44	0.019

1017	P	SMK004	Smoking As a Quantitative Trait Locus 3	44	0.019

1018		CNN002	Cannabis Abuse	44	0.019

1019	P	END039	Endodermal Sinus Tumor	44	0.019

1020	P	GNG009	Gangliosidosis	44	0.019

1021	P	FBR003	Fibrous Histiocytoma	44	0.019

1022		PLX002	Plexiform Neurofibroma	44	0.019

1023		OVR063	Overnutrition	44	0.019

1024		ACN001	Acinar Cell Carcinoma	44	0.019

1025		PRT035	Peritoneum Cancer	44	0.019

1026		PPL001	Papillary Adenoma	44	0.019

1027	c	HYP272	Hypercholesterolemia, Familial, 3	44	0.019

1028		THR012	Thoracic Cancer	44	0.019

1029	P	BCT020	Bacteremia 2	44	0.019

1030	P	EPN001	Ependymoblastoma	44	0.019

1031	c	HRD173	Hereditary Late-Onset Parkinson Disease	44	0.019

1032	c	PRM038	Primary Agammaglobulinemia	44	0.019

1033		MTR010	Mature Teratoma	44	0.019

1034	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.019

1035	c	ADL023	Adult Medulloblastoma	44	0.019

1036		CVD001	Covid-19	44	0.019

1037	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.019

1038	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.019

1039	P	CRN024	Corneal Disease	44	0.019

1040		FBR054	Fibroma	44	0.019

1041		FNG004	Fungal Meningitis	44	0.019

1042		IDP033	Idiopathic Edema	44	0.019

1043		ANP009	Anaplastic Oligodendroglioma	43	0.019

1044	c	RHB023	Rhabdomyosarcoma, Embryonal, 1	43	0.019

1045		SMN007	Seminoma	43	0.019

1046	c	HYP847	Hyper Ige Recurrent Infection Syndrome 1	43	0.019

1047		SKN005	Skin Atrophy	43	0.019

1048	P	TST026	Testicular Germ Cell Cancer	43	0.019

1049		LMY003	Leiomyomatosis	43	0.019

1050		MRG013	Mirage Syndrome	43	0.019

1051	c	MLG081	Malignant Teratoma	43	0.019

1052	P	PHR004	Pharynx Cancer	43	0.019

1053		NRF003	Neurofibrosarcoma	43	0.019

1054	P	ATX039	Ataxia-Pancytopenia Syndrome	43	0.019

1055		SPC005	Speech Disorder	43	0.019

1056		RDC006	Red Cell Aplasia	43	0.019

1057		KPS002	Kaposiform Hemangioendothelioma	43	0.019

1058		AST052	Asthma, Nasal Polyps, and Aspirin Intolerance	43	0.019

1059		LWC001	Low Compliance Bladder	43	0.019

1060	c	PNT049	Pontocerebellar Hypoplasia, Type 2d	43	0.019

1061		SPR008	Supratentorial Primitive Neuroectodermal Tumor	43	0.019

1062		OPP002	Opportunistic Mycosis	43	0.019

1063		MXD050	Mixed Phenotype Acute Leukemia	43	0.019

1064	c	CHR056	Chronic Tic Disorder	43	0.019

1065		HYP457	Hypertrophic Scars	42	0.019

1066		TRP009	Triple X Syndrome	42	0.019

1067	P	AVS003	Avascular Necrosis	42	0.019

1068		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.019

1069		DNT014	Dental Pulp Disease	42	0.019

1070	c	PSR028	Psoriasis 7	42	0.019

1071	c	BNM022	Bone Mineral Density Quantitative Trait Locus 8	42	0.019

1072	P	PRT026	Parotitis	42	0.019

1073		CHR286	Chronic Neutrophilic Leukemia	42	0.019

1074