Search results for Busulfan

655 hits were found for Busulfan

#	Family	MCID	Name	MIFTS	Score
1	P	GRF003	Graft-Versus-Host Disease	72	0.590

2	P	LKM002	Leukemia	68	0.555

3	P	MYL006	Myeloid Leukemia	60	0.549

4	c	LKM061	Leukemia, Acute Myeloid	84	0.514

5		MYL009	Myelodysplastic Syndrome	70	0.474

6	P	LYM118	Lymphoma	68	0.421

7		LYM019	Lymphosarcoma	46	0.406

8	c	LKM063	Leukemia, Chronic Myeloid	72	0.404

9		ACT113	Acute Myeloblastic Leukemia with Maturation	46	0.376

10	c	ACT135	Acute Graft Versus Host Disease	52	0.375

11		HPT046	Hepatic Veno-Occlusive Disease	56	0.360

12		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.360

13	P	LKM062	Leukemia, Acute Lymphoblastic	69	0.350

14		MYL069	Myeloma, Multiple	85	0.349

15		LYM133	Lymphoma, Hodgkin, Classic	69	0.345

16	c	CHR064	Chronic Monocytic Leukemia	33	0.325

17	c	ACT073	Acute Leukemia	58	0.312

18		PLS009	Plasma Cell Neoplasm	51	0.310

19	c	CHR417	Chronic Graft Versus Host Disease	57	0.308

20		HMT002	Hematologic Cancer	62	0.305

21		LYM040	Lymphoblastic Lymphoma	54	0.287

22		HML018	Homologous Wasting Disease	22	0.287

23		DFC004	Deficiency Anemia	70	0.279

24		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.277

25		LYM143	Lymphoma, Non-Hodgkin, Familial	72	0.272

26	P	CNR004	Cone-Rod Dystrophy 2	73	0.270

27		MCS002	Mucositis	56	0.270

28	P	LKM071	Leukemia, Chronic Lymphocytic	79	0.255

29	P	BCL017	B-Cell Lymphoma	58	0.252

30		MYL031	Myeloproliferative Neoplasm	66	0.251

31		ADL002	Adult Syndrome	70	0.247

32		BNM001	Bone Marrow Cancer	43	0.238

33	P	CHR285	Chronic Myelomonocytic Leukemia	60	0.234

34		MYL005	Myelofibrosis	70	0.226

35		RFR010	Refractory Anemia	48	0.224

36		PDG002	Pdgfrb-Associated Chronic Eosinophilic Leukemia	27	0.223

37	P	FLL037	Follicular Lymphoma	67	0.215

38		MNT001	Mantle Cell Lymphoma	69	0.213

39	c	FLL041	Follicular Lymphoma 1	49	0.210

40		BRK010	Burkitt Lymphoma	67	0.203

41	c	LKM060	Leukemia, Acute Lymphoblastic 3	56	0.201

42	c	LKM056	Leukemia, Chronic Lymphocytic 2	48	0.200

43		PLS025	Plasmablastic Lymphoma	47	0.200

44		LYM048	Lymphoma, Large-Cell, Immunoblastic	29	0.200

45	P	TRN020	Turner Syndrome	67	0.196

46		CHL149	Childhood Acute Myeloid Leukemia	44	0.194

47		LYM129	Lymphoma, Mucosa-Associated Lymphoid Type	64	0.191

48	P	NRB001	Neuroblastoma	72	0.189

49		MYL075	Myelodysplastic/myeloproliferative Neoplasm	49	0.189

50		IMM167	Immune Deficiency Disease	78	0.187

51		MRG003	Marginal Zone B-Cell Lymphoma	52	0.181

52		MYL074	Myelodysplastic Syndrome with Excess Blasts	38	0.181

53		SPL004	Splenic Marginal Zone Lymphoma	51	0.173

54		NDL020	Nodal Marginal Zone B-Cell Lymphoma	34	0.173

55	c	JVN004	Juvenile Myelomonocytic Leukemia	67	0.171

56	P	PLY018	Polycythemia	56	0.169

57	P	APL001	Aplastic Anemia	74	0.167

58		PLY001	Polycythemia Vera	69	0.167

59		ATY042	Atypical Chronic Myeloid Leukemia	49	0.165

60		CHL152	Childhood Acute Lymphocytic Leukemia	44	0.165

61		RFR007	Refractory Anemia with Excess Blasts in Transformation	27	0.165

62	P	SZR006	Seizure Disorder	56	0.161

63		DFF005	Diffuse Large B-Cell Lymphoma	55	0.161

64		SVR004	Severe Combined Immunodeficiency	73	0.159

65	c	PRM038	Primary Agammaglobulinemia	44	0.159

66	P	PLM175	Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2	51	0.156

67	P	CYS018	Cystitis	59	0.154

68	P	THL005	Thalassemia	60	0.152

69	c	TCL024	T-Cell Non-Hodgkin Lymphoma	34	0.150

70	P	ESS003	Essential Thrombocythemia	68	0.147

71		HMR023	Hemorrhagic Cystitis	45	0.147

72		MGK001	Megakaryocytic Leukemia	64	0.145

73		48X005	48,xyyy	39	0.145

74	c	RHB024	Rhabdomyosarcoma 2	67	0.142

75		WLD007	Waldenstroem's Macroglobulinemia	61	0.142

76		ERY051	Erythroleukemia, Familial	56	0.142

77		ACT193	Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22)	54	0.142

78		MCR004	Macroglobulinemia	49	0.142

79		RTC005	Reticulosarcoma	47	0.142

80	P	NTR004	Neutropenia	63	0.137

81		VSL002	Visual Epilepsy	59	0.137

82		EWN003	Ewing Sarcoma	69	0.135

83	c	PRM012	Primary Polycythemia	50	0.135

84		CMB003	Combined T Cell and B Cell Immunodeficiency	49	0.135

85		CMB081	Combined Immunodeficiency, X-Linked	36	0.135

86	c	LKM070	Leukemia, Acute Monocytic	57	0.132

87		HMG005	Hemoglobinopathy	56	0.132

88		RTN193	Retinitis Pigmentosa and Erythrocytic Microcytosis	52	0.132

89		TCL028	T-Cell Lymphoblastic Leukemia/lymphoma	47	0.132

90	c	LKM005	Leukemia, T-Cell, Chronic	34	0.132

91	P	BRL012	Bare Lymphocyte Syndrome, Type Ii	66	0.130

92	P	LYM033	Lymphoproliferative Syndrome	59	0.130

93		TCL023	T-Cell Lymphoma, Subcutaneous Panniculitis-Like	50	0.130

94		LYM012	Lymphoplasmacytic Lymphoma	47	0.130

95		HDG002	Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance	42	0.130

96		SRC014	Sarcoma	65	0.127

97	P	ADL017	Adult T-Cell Leukemia	56	0.127

98	c	THR090	Thrombocythemia 1	49	0.127

99		LYM051	Lymphomatoid Granulomatosis	45	0.127

100	c	FNC027	Fanconi Anemia, Complementation Group a	81	0.124

101	P	SRC025	Sarcoidosis 1	70	0.124

102		SFT003	Soft Tissue Sarcoma	56	0.124

103	c	ATM082	Autoimmune Lymphoproliferative Syndrome, Type V	54	0.124

104		FNG017	Fungal Infectious Disease	53	0.124

105		SPN035	Spindle Cell Sarcoma	53	0.124

106	c	CHR418	Chronic Leukemia	49	0.124

107		CHR286	Chronic Neutrophilic Leukemia	42	0.124

108	P	MLG074	Malignant Mesenchymoma	40	0.124

109		SYS070	Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood	36	0.124

110		HDG004	Hodgkin's Granuloma	23	0.124

111		HDG006	Hodgkin's Paragranuloma	22	0.124

112	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.121

113		MYC006	Mycosis Fungoides	66	0.121

114		SZR001	Sezary's Disease	60	0.121

115		STM007	Stomatitis	50	0.121

116	P	SCK005	Sickle Cell Disease	50	0.121

117		CHR563	Chronic Eosinophilic Leukemia	48	0.121

118		ACT098	Acute Erythroid Leukemia	48	0.121

119	P	CHR012	Chronic Granulomatous Disease	67	0.118

120	P	CNT005	Central Nervous System Lymphoma	53	0.118

121	P	ATS406	Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2	45	0.118

122	P	MDL005	Medulloblastoma	77	0.115

123		SCK003	Sickle Cell Anemia	74	0.115

124	P	MNC007	Monocytic Leukemia	53	0.115

125		ACT200	Acute Monoblastic Leukemia	52	0.115

126	c	BTT014	Beta-Thalassemia	74	0.112

127	P	RHB003	Rhabdomyosarcoma	63	0.112

128	P	ANP001	Anaplastic Large Cell Lymphoma	58	0.112

129	c	PRM226	Primary Central Nervous System Lymphoma	48	0.112

130	c	CHR682	Chronic Bilirubin Encephalopathy	39	0.112

131		ACT114	Acute Myeloblastic Leukemia Without Maturation	33	0.112

132	c	ADL093	Adult Acute Monocytic Leukemia	20	0.112

133		PLS011	Plasmacytoma	56	0.109

134		MYL067	Myeloproliferative Disorder, Chronic, with Eosinophilia	37	0.109

135	P	THR014	Thrombocytopenia	67	0.106

136		PNC001	Pancytopenia	54	0.106

137		ANG046	Angioimmunoblastic T-Cell Lymphoma	52	0.106

138	P	FNC004	Fanconi Syndrome	50	0.106

139		LTH001	Lethal Midline Granuloma	44	0.106

140	P	CTN015	Cutaneous T Cell Lymphoma	49	0.102

141		ACT119	Acute Promyelocytic Leukemia	63	0.099

142	c	ALP101	Alpha-Thalassemia	62	0.099

143		VRL011	Viral Infectious Disease	61	0.099

144		AZS001	Azoospermia	50	0.099

145		PRL017	Prolymphocytic Leukemia	47	0.099

146		SPR126	Superior Semicircular Canal Dehiscence	40	0.099

147	c	HMG029	Hemoglobin Se Disease	39	0.099

148	P	PLM036	Pulmonary Fibrosis	65	0.095

149		HRY003	Hairy Cell Leukemia	55	0.095

150	P	DMN001	Diamond-Blackfan Anemia	69	0.092

151	P	MLN007	Male Infertility	55	0.092

152		CYS036	Cystinosis, Nephropathic	51	0.092

153		CNT033	Central Nervous System Cancer	47	0.092

154	P	FNC034	Fanconi Renotubular Syndrome 2	40	0.092

155		HMN044	Human Immunodeficiency Virus Type 1	71	0.088

156	P	HPT021	Hepatitis	67	0.088

157		FCT007	Factor Vii Deficiency	67	0.088

158		NTR005	Nutritional Deficiency Disease	62	0.088

159		ACQ007	Acquired Immunodeficiency Syndrome	60	0.088

160	P	EXN002	Exanthem	57	0.088

161		INT054	Intraocular Lymphoma	48	0.088

162	c	INH020	Inherited Metabolic Disorder	47	0.088

163	P	GLM040	Glioma Susceptibility 1	81	0.084

164		DWN001	Down Syndrome	70	0.084

165		SVR066	Severe Combined Immunodeficiency, X-Linked	66	0.084

166	P	CTR002	Cataract	60	0.084

167	c	FBR046	Fibrosis of Extraocular Muscles, Congenital, 1	57	0.084

168	P	HMP002	Hemophagocytic Lymphohistiocytosis	54	0.084

169	P	ALP008	Alopecia	54	0.084

170		PLS016	Plasma Cell Leukemia	53	0.084

171		PRP036	Peripheral T-Cell Lymphoma	53	0.084

172		HST010	Histiocytosis	48	0.084

173		SPL018	Splenomegaly	48	0.084

174		RFR002	Refractory Hairy Cell Leukemia	33	0.084

175		CLS052	Classic Hairy Cell Leukemia	27	0.084

176	P	LNG032	Lung Cancer	98	0.079

177	P	WSK001	Wiskott-Aldrich Syndrome	72	0.079

178	c	WLM013	Wilms Tumor 1	65	0.079

179	P	GLM045	Glioma	63	0.079

180	c	WLM018	Wilms Tumor 5	61	0.079

181	P	BNG030	Benign Ependymoma	60	0.079

182		LNG108	Langerhans Cell Histiocytosis	58	0.079

183		CLL010	Cellular Ependymoma	54	0.079

184		HMS001	Hemosiderosis	54	0.079

185	c	DMN023	Diamond-Blackfan Anemia 1	53	0.079

186		GLL048	Glial Tumor	45	0.079

187	P	RRH023	Rare Hereditary Hemochromatosis	41	0.079

188	c	WLM011	Wilms Tumor 6	37	0.079

189		RFR009	Refractory Cytopenia with Multilineage Dysplasia	31	0.079

190	P	BRS047	Breast Cancer	97	0.075

191		ADR007	Adrenoleukodystrophy	75	0.075

192	P	RSP003	Respiratory Failure	74	0.075

193	P	MCP040	Mucopolysaccharidosis-Plus Syndrome	69	0.075

194	P	LVR013	Liver Disease	68	0.075

195		3HY005	3-Hydroxyacyl-Coa Dehydrogenase Deficiency	62	0.075

196	P	INF032	Infertility	57	0.075

197	P	DRR001	Diarrhea	55	0.075

198	P	AST007	Astrocytoma	51	0.075

199		GRM005	Germ Cell Cancer	47	0.075

200	c	MLG068	Malignant Glioma	46	0.075

201		MXD026	Mixed Glioma	45	0.075

202	P	EPN001	Ependymoblastoma	44	0.075

203	P	ATX039	Ataxia-Pancytopenia Syndrome	43	0.075

204		MXD050	Mixed Phenotype Acute Leukemia	43	0.075

205		CYT002	Cytokine Deficiency	42	0.075

206		CHL079	Children's Interstitial Lung Disease	26	0.075

207		SCH036	Scheie Syndrome	72	0.070

208	P	KDN018	Kidney Disease	72	0.070

209	P	AMY004	Amyloidosis	70	0.070

210	P	OST001	Osteopetrosis	70	0.070

211		CMM004	Common Variable Immunodeficiency	68	0.070

212	P	HYP098	Hypereosinophilic Syndrome	67	0.070

213	P	MNN013	Meningitis	66	0.070

214		HRL003	Hurler Syndrome	65	0.070

215	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.070

216	c	HMP022	Hemophagocytic Lymphohistiocytosis, Familial, 1	63	0.070

217	P	LKD001	Leukodystrophy	59	0.070

218		IMM072	Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1	57	0.070

219		THR004	Thrombocytosis	51	0.070

220	c	ALM001	Al Amyloidosis	50	0.070

221		TCL002	T-Cell Large Granular Lymphocyte Leukemia	49	0.070

222		47X002	47,xyy	49	0.070

223		LYM138	Lymphoblastic Leukemia, Acute, with Lymphomatous Features	49	0.070

224	c	DRR009	Diarrhea 6	46	0.070

225		CMP090	Complement Component 3 Deficiency, Autosomal Recessive	45	0.070

226		IMM136	Immune System Disease	45	0.070

227	P	BCL004	B-Cell Non-Hodgkin Lymphoma	44	0.070

228		ATX019	Ataxia with Vitamin E Deficiency	42	0.070

229		ADR022	Adrenomyeloneuropathy	38	0.070

230		RNL114	Renal Cell Carcinoma, Nonpapillary	78	0.065

231	P	RTN024	Retinoblastoma	73	0.065

232	P	KRB001	Krabbe Disease	69	0.065

233		LKC009	Leukocyte Adhesion Deficiency, Type I	69	0.065

234	c	MCP052	Mucopolysaccharidosis, Type Vi	67	0.065

235		CHD001	Chediak-Higashi Syndrome	66	0.065

236	c	MNN047	Mannosidosis, Alpha B, Lysosomal	66	0.065

237		CHN016	Cohen Syndrome	63	0.065

238	c	SVR003	Severe Congenital Neutropenia	59	0.065

239		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.065

240		CMR002	Coumarin Resistance	56	0.065

241		HRL004	Hurler-Scheie Syndrome	55	0.065

242	c	FML008	Familial Retinoblastoma	53	0.065

243	c	INF023	Inflammatory Breast Carcinoma	50	0.065

244		ADN001	Adenosine Deaminase Deficiency	47	0.065

245		SPH010	Sphingolipidosis	47	0.065

246		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.065

247		SVR095	Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency	47	0.065

248		SPR008	Supratentorial Primitive Neuroectodermal Tumor	43	0.065

249		LRG008	Large Granular Lymphocyte Leukemia	41	0.065

250		GRM010	Germ Cells Tumors	34	0.065

251		BRN028	Brain Cancer	74	0.059

252	P	MTC003	Metachromatic Leukodystrophy	70	0.059

253		CNG034	Congestive Heart Failure	69	0.059

254	P	MLN008	Melanoma	69	0.059

255	P	PNM007	Pneumonia	68	0.059

256		SKN019	Skin Melanoma	68	0.059

257	P	OLG002	Oligodendroglioma	67	0.059

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

259	c	SML038	Small Cell Cancer of the Lung	65	0.059

260	P	HRP006	Herpes Simplex	65	0.059

261	P	PSR002	Psoriasis	62	0.059

262		FCS002	Fucosidosis	61	0.059

263		IRN002	Iron Metabolism Disease	57	0.059

264		MLT161	Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly	57	0.059

265		CYT008	Cytomegalovirus Infection	57	0.059

266		HPT022	Hepatoblastoma	56	0.059

267		HMN014	Human Immunodeficiency Virus Infectious Disease	55	0.059

268		AMN001	Amenorrhea	54	0.059

269	c	OST131	Osteopetrosis, Autosomal Dominant 2	53	0.059

270	c	MLN055	Melanoma, Cutaneous Malignant 10	52	0.059

271		PST011	Pustulosis of Palm and Sole	52	0.059

272	P	BRN035	Brain Stem Glioma	52	0.059

273	c	NTR049	Neutropenia, Severe Congenital, 3, Autosomal Recessive	51	0.059

274		TST014	Testicular Cancer	46	0.059

275		CRB026	Cerebellar Astrocytoma	37	0.059

276		ACT177	Acute Basophilic Leukemia	34	0.059

277		LTT002	Letterer-Siwe Disease	33	0.059

278		ENG004	Engraftment Syndrome	30	0.059

279		ACT118	Acute Non Lymphoblastic Leukemia	26	0.059

280	P	HPT023	Hepatocellular Carcinoma	100	0.053

281	P	OVR042	Ovarian Cancer	88	0.053

282	P	PNC035	Pancreatic Cancer	84	0.053

283		GLB015	Glioblastoma Multiforme	75	0.053

284		CRH001	Crohn's Disease	74	0.053

285		RNL065	Renal Cell Carcinoma, Papillary, 1	73	0.053

286	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.053

287	P	RHB008	Rhabdoid Tumor Predisposition Syndrome 1	65	0.053

288	c	MCP049	Mucopolysaccharidosis, Type Vii	63	0.053

289		RHB001	Rhabdoid Cancer	63	0.053

290		IMM174	Immunodeficiency with Hyper-Igm, Type 1	63	0.053

291	c	HPT001	Hepatitis C	62	0.053

292		ALL026	Allergic Hypersensitivity Disease	62	0.053

293		TXC005	Toxic Shock Syndrome	62	0.053

294		ASP002	Aspartylglucosaminuria	62	0.053

295		HYP066	Hyperglycemia	61	0.053

296	P	KDN017	Kidney Cancer	60	0.053

297	P	TST021	Testicular Germ Cell Tumor	60	0.053

298	P	PRX003	Paroxysmal Nocturnal Hemoglobinuria	60	0.053

299	c	HPT016	Hepatitis B	59	0.053

300		BRN002	Bronchiolitis	59	0.053

301		BLR008	Bilirubin Metabolic Disorder	57	0.053

302		PGM001	Pigmented Villonodular Synovitis	56	0.053

303		ISL001	Islet Cell Tumor	56	0.053

304	P	INF037	Inflammatory Bowel Disease	54	0.053

305	c	AMG001	Amegakaryocytic Thrombocytopenia, Congenital	54	0.053

306		HMG002	Hemoglobinuria	50	0.053

307	P	PNB001	Pineoblastoma	50	0.053

308		CHL018	Childhood Medulloblastoma	49	0.053

309		MNC006	Monoclonal Gammopathy of Uncertain Significance	48	0.053

310		GNG008	Ganglioneuroblastoma	48	0.053

311		PRC049	Precursor T-Cell Acute Lymphoblastic Leukemia	48	0.053

312	c	ADL052	Adult Acute Lymphocytic Leukemia	47	0.053

313		CD4003	Cd40 Ligand Deficiency	46	0.053

314		PRX001	Peroxisomal Disease	46	0.053

315		EXT010	Extramedullary Plasmacytoma	45	0.053

316	P	TST026	Testicular Germ Cell Cancer	43	0.053

317		GST020	Gastric Antral Vascular Ectasia	41	0.053

318		49X006	49, Xxxxy Syndrome	41	0.053

319	c	OVR114	Ovarian Cancer 1	38	0.053

320		MCP033	Mucopolysaccharidoses	38	0.053

321		CHL057	Childhood Brain Stem Glioma	32	0.053

322		PDT014	Pediatric Ependymoma	32	0.053

323		DFF031	Diffuse Alveolar Hemorrhage	30	0.053

324	c	TST046	Testicular Germ Cell Tumor 1	29	0.053

325		HMP028	Hemophagocytic Syndrome Associated with an Infection	24	0.053

326		PDT016	Pediatric Infratentorial Ependymoma	22	0.053

327		AML051	Aml with Myelodysplasia-Related Features	19	0.053

328	P	RFR014	Refractory Anemia with Excess Blasts Type 2	18	0.053

329	c	RFR015	Refractory Anemia with Excess Blasts Type 1	15	0.053

330		CHL009	Childhood Cerebral Astrocytoma	14	0.053

331	P	HRT032	Heart Disease	75	0.046

332	c	MNN043	Meningioma, Familial	74	0.046

333	c	MCP050	Mucopolysaccharidosis, Type Ii	72	0.046

334		MST024	Mastocytosis, Cutaneous	69	0.046

335	P	MYC084	Mycobacterium Tuberculosis 1	68	0.046

336		PCK003	Pick Disease of Brain	68	0.046

337	c	NMN015	Niemann-Pick Disease, Type C1	68	0.046

338	P	FRN006	Frontotemporal Dementia	68	0.046

339	P	PLM037	Pulmonary Hypertension	67	0.046

340		OST159	Osteogenic Sarcoma	66	0.046

341	P	SKN015	Skin Carcinoma	66	0.046

342	c	MCL013	Mucolipidosis Iv	66	0.046

343	P	ADL010	Adult Respiratory Distress Syndrome	65	0.046

344	P	THY023	Thymoma	65	0.046

345		LYS012	Lysosomal Acid Lipase Deficiency	65	0.046

346	P	ADN016	Adenocarcinoma	64	0.046

347		RBR001	Roberts Syndrome	64	0.046

348	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.046

349		SKN016	Skin Disease	63	0.046

350		ERL001	Early Myoclonic Encephalopathy	62	0.046

351		CLT003	Colitis	62	0.046

352	c	NMN013	Niemann-Pick Disease, Type a	62	0.046

353		ATM095	Autoimmune Disease	62	0.046

354		MNN042	Meningioma, Radiation-Induced	62	0.046

355		CHL068	Cholestasis	61	0.046

356	P	LYM113	Lymphoproliferative Syndrome, X-Linked, 1	61	0.046

357	P	THR005	Thrombotic Thrombocytopenic Purpura	61	0.046

358	P	ALP009	Alopecia Areata	60	0.046

359	P	NMN002	Niemann-Pick Disease	59	0.046

360		CRY035	Cryptorchidism, Unilateral or Bilateral	58	0.046

361	c	NMN016	Niemann-Pick Disease, Type B	58	0.046

362		CRD132	Cardiac Conduction Defect	58	0.046

363		MCS006	Macs Syndrome	58	0.046

364	c	DWL002	Dowling-Degos Disease 1	58	0.046

365		GLS018	Glass Syndrome	57	0.046

366		THY022	Thymic Carcinoma	57	0.046

367		AYM001	Ayme-Gripp Syndrome	57	0.046

368		BCT022	Bacterial Infectious Disease	56	0.046

369		BRN012	Bronchiolitis Obliterans	55	0.046

370		PRP030	Purpura	54	0.046

371	c	THR124	Thrombotic Thrombocytopenic Purpura, Hereditary	54	0.046

372		CLR030	Clear Cell Renal Cell Carcinoma	53	0.046

373	P	EPD016	Epidermolysis Bullosa	53	0.046

374		TXC002	Toxic Encephalopathy	53	0.046

375	c	PSR017	Psoriasis 2	53	0.046

376		LYS002	Lysosomal Storage Disease	52	0.046

377	c	VRL010	Viral Hepatitis	52	0.046

378	c	THY107	Thymoma, Familial	52	0.046

379	c	PSR023	Psoriasis 1	52	0.046

380	c	CNG208	Congenital Disorder of Glycosylation, Type Iic	51	0.046

381		TCL027	T-Cell Acute Lymphoblastic Leukemia	51	0.046

382		SPN021	Spinal Meningioma	50	0.046

383		MYL003	Myeloid Sarcoma	49	0.046

384		BLY001	B-Lymphoblastic Leukemia/lymphoma	48	0.046

385		MCR209	Microcephaly, Epilepsy, and Diabetes Syndrome	47	0.046

386	c	PSR032	Psoriasis 11	47	0.046

387	P	CHR573	Choroid Plexus Cancer	46	0.046

388		TCL003	T Cell Deficiency	46	0.046

389		OLG001	Oligospermia	45	0.046

390	c	EST002	Estrogen-Receptor Negative Breast Cancer	45	0.046

391		PNC056	Pineocytoma	45	0.046

392		LYM126	Lymphoma Aids Related	44	0.046

393		ANP009	Anaplastic Oligodendroglioma	43	0.046

394	c	PSR028	Psoriasis 7	42	0.046

395	P	PRT026	Parotitis	42	0.046

396		IMM078	Immunodeficiency 21	42	0.046

397		PNL014	Pineal Gland Cancer	41	0.046

398	c	PSR018	Psoriasis 13	41	0.046

399		SCR001	Secretory Meningioma	41	0.046

400	P	8P1002	8p11 Myeloproliferative Syndrome	39	0.046

401		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.046

402		THR123	Thrombotic Microangiopathy	36	0.046

403		LYM002	Lymphoplasmacyte-Rich Meningioma	36	0.046

404		CHR178	Chromosomal Triplication	35	0.046

405	P	INH011	Inherited Bone Marrow Failure Syndromes	34	0.046

406		VRS001	Virus Associated Hemophagocytic Syndrome	32	0.046

407		ACD003	Acid Sphingomyelinase Deficiency	32	0.046

408		CHL006	Childhood Oligodendroglioma	31	0.046

409		RFR004	Refractory Hematologic Cancer	30	0.046

410		MYC088	Mycobacterium Avium Complex Infections	29	0.046

411		CHR375	Chromosome 8p11 Myeloproliferative Syndrome	29	0.046

412		BRN049	Brain Tumor, Childhood	29	0.046

413	P	CNT036	Central Nervous System Germ Cell Tumor	28	0.046

414	P	SCK034	Sickle Beta Thalassemia	28	0.046

415		TST003	Testicular Leukemia	27	0.046

416		PGM030	Pigmentation Anomaly of the Skin	26	0.046

417		CHL015	Childhood Choroid Plexus Cancer	16	0.046

418	c	SYS001	Systemic Lupus Erythematosus	86	0.037

419	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.037

420		BRT054	Brittle Bone Disorder	72	0.037

421	c	HPT073	Hepatitis C Virus	72	0.037

422		AGM019	Agammaglobulinemia, X-Linked	71	0.037

423		PRP027	Peripheral Vascular Disease	71	0.037

424	c	GCH015	Gaucher Disease, Type I	70	0.037

425	P	TYS001	Tay-Sachs Disease	69	0.037

426	P	SYS005	Systemic Scleroderma	68	0.037

427		SND001	Sandhoff Disease	68	0.037

428		BRN024	Bronchitis	68	0.037

429		IMM106	Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked	68	0.037

430	P	SHW006	Shwachman-Diamond Syndrome 1	67	0.037

431	P	DMN002	Dementia	66	0.037

432	P	EPD009	Epidermolysis Bullosa Dystrophica	66	0.037

433	P	DRM053	Dermatitis, Atopic	66	0.037

434		KHL003	Kohlschutter-Tonz Syndrome	65	0.037

435	P	AGM001	Agammaglobulinemia	65	0.037

436		EPL118	Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation	65	0.037

437		LKN025	Leukoencephalopathy, Hereditary Diffuse, with Spheroids	65	0.037

438	P	NRN021	Neuronal Ceroid Lipofuscinosis	64	0.037

439	P	MST009	Mastocytosis	64	0.037

440		GST106	Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets	64	0.037

441	P	ABD014	Abdominal Obesity-Metabolic Syndrome 1	64	0.037

442		RFS006	Refsum Disease, Classic	64	0.037

443	P	GCH001	Gaucher's Disease	63	0.037

444	P	HML002	Hemolytic Anemia	63	0.037

445	P	VSC007	Vascular Disease	63	0.037

446	c	GM1007	Gm1 Gangliosidosis	62	0.037

447	c	BRN108	Branchiootic Syndrome 1	62	0.037

448		ATY005	Atypical Teratoid Rhabdoid Tumor	61	0.037

449	c	PRX045	Peroxisome Biogenesis Disorder 1b	61	0.037

450		DRM006	Dermatitis	61	0.037

451	c	SCL052	Scleroderma, Familial Progressive	61	0.037

452	P	ENC018	Encephalopathy	61	0.037

453	P	LPS004	Lupus Erythematosus	61	0.037

454		HRP004	Herpes Zoster	60	0.037

455		PNM010	Pneumothorax, Primary Spontaneous	60	0.037

456		LNG099	Lung Disease	60	0.037

457		SQM006	Squamous Cell Carcinoma	60	0.037

458	P	MCR010	Microcephaly	59	0.037

459		GRD007	Grade Iii Astrocytoma	59	0.037

460		CHR072	Chordoma	58	0.037

461		THY025	Thymus Cancer	58	0.037

462		LYM027	Lymphopenia	58	0.037

463		MCR013	Microphthalmia	57	0.037

464	P	ZLL001	Zellweger Syndrome	57	0.037

465		APH002	Aphasia	57	0.037

466		BCL010	B-Cell Expansion with Nfkb and T-Cell Anergy	57	0.037

467	c	GM1004	Gm1-Gangliosidosis, Type I	57	0.037

468		PNM008	Pneumothorax	56	0.037

469	P	FBR017	Fibrosarcoma	56	0.037

470	c	PRX059	Peroxisome Biogenesis Disorder 1a	56	0.037

471		SPN041	Spinal Cord Disease	56	0.037

472		EPT010	Epithelial-Myoepithelial Carcinoma	55	0.037

473		FRN051	Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related	55	0.037

474	P	DBT005	Diabetes Insipidus	55	0.037

475		GLS001	Gliosarcoma	54	0.037

476		PPL022	Papilloma	54	0.037

477		RCS002	Recessive Dystrophic Epidermolysis Bullosa	54	0.037

478		PST046	Post-Transplant Lymphoproliferative Disease	53	0.037

479	P	CRB194	Cerebroretinal Microangiopathy with Calcifications and Cysts 1	53	0.037

480	P	PLM006	Pulmonary Alveolar Proteinosis	53	0.037

481	c	EPD076	Epidermolysis Bullosa Dystrophica, Autosomal Recessive	52	0.037

482		ACR041	Acromelic Frontonasal Dysostosis	52	0.037

483	P	OVR049	Ovarian Disease	52	0.037

484		DSM007	Desmoplastic Small Round Cell Tumor	52	0.037

485		NTR018	Neutrophilia, Hereditary	52	0.037

486	P	TRT010	Teratoma	52	0.037

487		FCT001	Factor Viii Deficiency	51	0.037

488	c	MTC055	Mitochondrial Dna Depletion Syndrome 4b	51	0.037

489		GNT002	Giant Cell Glioblastoma	50	0.037

490	c	INF145	Infantile Liver Failure Syndrome 1	50	0.037

491		MLL001	Molluscum Contagiosum	50	0.037

492	c	THR071	Thrombocytopenia 1	50	0.037

493		CLR003	Clear Cell Adenocarcinoma	50	0.037

494		DYS073	Dysphagia	50	0.037

495	P	MST002	Mast-Cell Leukemia	49	0.037

496		GST049	Gastrointestinal System Cancer	49	0.037

497		SCT005	Scott Syndrome	49	0.037

498	c	TCL005	T-Cell Prolymphocytic Leukemia	49	0.037

499	P	SDR003	Sideroblastic Anemia	49	0.037

500		CHL061	Childhood Leukemia	48	0.037

501		WTH001	Withdrawal Disorder	48	0.037

502	P	PRR002	Pure Red-Cell Aplasia	47	0.037

503		TTR011	Tetraploidy	47	0.037

504		ALP012	Alpha-Methylacyl-Coa Racemase Deficiency	47	0.037

505		GST071	Gastrointestinal Carcinoma	47	0.037

506		NDL013	Nodular Regenerative Hyperplasia	47	0.037

507		SQM002	Squamous Cell Papilloma	46	0.037

508	P	PRD037	Periodontal Ehlers-Danlos Syndrome	45	0.037

509		GLY031	Glycoproteinosis	45	0.037

510	c	ZLL011	Zellweger Spectrum Disorder	45	0.037

511		OVR112	Ovarian Germ Cell Cancer	45	0.037

512		MCR225	Macrophage Activation Syndrome	44	0.037

513		CRD043	Ceroid Storage Disease	44	0.037

514		MTC111	Mitochondrial Neurogastrointestinal Encephalomyopathy	44	0.037

515	P	GNG009	Gangliosidosis	44	0.037

516		SPN040	Spinal Cancer	44	0.037

517		MRG013	Mirage Syndrome	43	0.037

518	c	MLG081	Malignant Teratoma	43	0.037

519		RDC006	Red Cell Aplasia	43	0.037

520		CRB138	Core Binding Factor Acute Myeloid Leukemia	43	0.037

521		TRP009	Triple X Syndrome	42	0.037

522	P	AVS003	Avascular Necrosis	42	0.037

523	c	HYP829	Hyper-Ige Recurrent Infection Syndrome 2, Autosomal Recessive	42	0.037

524		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.037

525		CMP009	Complement Deficiency	41	0.037

526		DFF003	Diffuse Scleroderma	41	0.037

527	P	CHL156	Childhood T-Cell Acute Lymphoblastic Leukemia	38	0.037

528		RPD005	Rapidly Involuting Congenital Hemangioma	38	0.037

529		KDN002	Kidney Rhabdoid Cancer	38	0.037

530		CHL010	Childhood Kidney Cell Carcinoma	38	0.037

531	c	SYS043	Systemic Lupus Erythematosus 1	38	0.037

532		MNT252	Mental Retardation, Skeletal Dysplasia, and Abducens Palsy	38	0.037

533		OPT032	Optic Pathway Glioma	35	0.037

534	c	ADL008	Adult Oligodendroglioma	34	0.037

535	c	SCN069	Secondary Hemophagocytic Lymphohistiocytosis	33	0.037

536		EXT025	Extragonadal Germ Cell Cancer	32	0.037

537		MDS019	Mediastinal Malignant Lymphoma	30	0.037

538		MCL022	Mucolipidoses	30	0.037

539		INT082	Intraocular Retinoblastoma	30	0.037

540		CYT018	Cytochrome P450 2d6 Variant	27	0.037

541		ACT162	Acute Sensory Ataxic Neuropathy	26	0.037

542		CRT084	Creatinine Clearance Quantitative Trait Locus	25	0.037

543		HRP008	Herpes Simiae	25	0.037

544		EXT029	Extraocular Retinoblastoma	24	0.037

545		PDT015	Pediatric Supratentorial Ependymoma	24	0.037

546		FRN030	Frontotemporal Dementia with Parkinsonism-17	24	0.037

547		CHR208	Chromosome 17p Deletion	23	0.037

548		DCK002	Dock8 Immunodeficiency Syndrome	19	0.037

549		NNN002	Noninvasive Malignant Thymoma	11	0.037

550		CRB054	Cerebellar Astrocytoma, Childhood	9	0.037

551	c	AMY091	Amyotrophic Lateral Sclerosis 1	89	0.026

552		STR067	Stroke, Ischemic	81	0.026

553	P	BLD134	Bladder Cancer	79	0.026

554		END057	Endometrial Cancer	74	0.026

555	P	MLT020	Multiple Sclerosis	72	0.026

556	P	EPL164	Epilepsy	71	0.026

557	P	HYP086	Hypothyroidism	69	0.026

558	P	MYS003	Myasthenia Gravis	68	0.026

559	P	DYS007	Dyskeratosis Congenita	67	0.026

560		CRB039	Cerebrovascular Disease	67	0.026

561	c	HMP029	Hemophilia a	67	0.026

562	P	PRP003	Porphyria Cutanea Tarda	67	0.026

563	c	PRM196	Premature Ovarian Failure 1	67	0.026

564		GLN010	Glanzmann Thrombasthenia	66	0.026

565	P	NRV007	Nervous System Disease	66	0.026

566		TTN003	Tetanus	65	0.026

567		END041	Endometrial Adenocarcinoma	63	0.026

568	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.026

569		CHR619	Chromosome 2q35 Duplication Syndrome	62	0.026

570	P	PRP029	Porphyria	62	0.026

571		OST003	Osteonecrosis	61	0.026

572		DPH001	Diphtheria	60	0.026

573		CRD223	Cardiac Arrhythmia	60	0.026

574	c	ACT071	Acute Kidney Failure	60	0.026

575		DYS164	Dyskeratosis Congenita, X-Linked	60	0.026

576	P	BRN019	Bernard-Soulier Syndrome	60	0.026

577	P	BND020	Bone Disease	59	0.026

578		PNM001	Pneumocystosis	59	0.026

579	P	SLP005	Sleep Disorder	59	0.026

580		PLM033	Pulmonary Embolism	59	0.026

581	P	BRS044	Breast Adenocarcinoma	59	0.026

582	P	PLY006	Polydactyly	59	0.026

583		GLB001	Gilbert Syndrome	58	0.026

584		ISC004	Ischemia	58	0.026

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

586		GRN051	Granulomatous Disease, Chronic, X-Linked	57	0.026

587		DSS009	Disseminated Intravascular Coagulation	57	0.026

588		TRN018	Transitional Cell Carcinoma	56	0.026

589		AGN016	Aging	56	0.026

590		PTS001	Patau Syndrome	55	0.026

591		ACT058	Active Peptic Ulcer Disease	55	0.026

592		BRN014	Bronchopneumonia	54	0.026

593		PLM010	Pulmonary Edema	54	0.026

594	P	LTR001	Lateral Sclerosis	54	0.026

595	P	INS002	in Situ Carcinoma	53	0.026

596	P	HYP083	Hypopituitarism	53	0.026

597	P	HML001	Hemolytic-Uremic Syndrome	53	0.026

598	c	CNT035	Central Nervous System Disease	52	0.026

599		HYP088	Hyper-Igd Syndrome	52	0.026

600	c	VRL005	Viral Pneumonia	52	0.026

601	P	HMP007	Hemophilia	51	0.026

602	c	CTS033	Cutis Laxa, Autosomal Recessive, Type Ic	51	0.026

603		LNG031	Lung Benign Neoplasm	51	0.026

604	P	RNL007	Renal Tubular Acidosis	51	0.026

605		END086	End Stage Renal Disease	51	0.026

606		ACT017	Acute Chest Syndrome	51	0.026

607	c	CNG027	Congenital Hemolytic Anemia	50	0.026

608		HYP080	Hypogonadism	50	0.026

609	c	ACQ017	Acquired Von Willebrand Syndrome	49	0.026

610		SLD003	Sialadenitis	49	0.026

611		EPD006	Epidermolysis Bullosa Acquisita	49	0.026

612		MLR002	Miliary Tuberculosis	49	0.026

613		BNR002	Bone Resorption Disease	48	0.026

614		ASP007	Aspiration Pneumonia	48	0.026

615		VSC058	Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome	48	0.026

616	P	ERY008	Erythromelalgia	47	0.026

617	c	PRM093	Premature Ovarian Failure 7	47	0.026

618		GST010	Gestational Trophoblastic Neoplasm	46	0.026

619	P	MYC033	Myoclonus	46	0.026

620		ASP008	Aspiration Pneumonitis	45	0.026

621		SPS057	Spasticity	45	0.026

622		ATX038	Ataxia and Polyneuropathy, Adult-Onset	45	0.026

623	P	HYP073	Hypersensitivity Reaction Type Iv Disease	44	0.026

624		BCT021	Bacterial Sepsis	44	0.026

625	c	TCL001	T-Cell Adult Acute Lymphocytic Leukemia	43	0.026

626		TST015	Testicular Disease	43	0.026

627		SNL007	Senile Cataract	42	0.026

628	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.026

629		ARC002	Arachnoiditis	42	0.026

630		FSR001	Fusariosis	42	0.026

631		THR035	Thrombasthenia	40	0.026

632		DND018	Dendritic Cell Tumor	40	0.026

633	c	HMG001	Hemoglobin C Disease	40	0.026

634	P	SPR119	Spermatogenic Failure, X-Linked, 1	39	0.026

635		CRB001	Cerebral Lymphoma	39	0.026

636		BLS007	Blastic Plasmacytoid Dendritic Cell	38	0.026

637		OVR094	Ovarian Epithelial Cancer	38	0.026

638		TRP005	Trophoblastic Neoplasm	38	0.026

639	c	SCN052	Secondary Adrenal Insufficiency	36	0.026

640		SPN354	Spinal Arachnoiditis	36	0.026

641	c	PRM340	Primary Adrenal Insufficiency	36	0.026

642	P	PLY188	Polyendocrinopathy	32	0.026

643		RLP008	Relapsed/refractory Diffuse Large B-Cell Lymphoma	31	0.026

644		TXC007	Toxic Pneumonitis	29	0.026

645	c	DRR018	Diarrhea 9	28	0.026

646		LPD001	Lipid Pneumonia	28	0.026

647		HYP855	Hyperpigmentation of the Skin	27	0.026

648	c	ATS210	Autosomal Recessive Sideroblastic Anemia	26	0.026

649		DFF010	Diffuse Alopecia Areata	26	0.026

650		MLG164	Malignant Epithelial Tumor of Ovary	26	0.026

651	c	LTB003	Ltbp4-Related Cutis Laxa	24	0.026

652		IND005	Indolent B Cell Lymphoma	20	0.026

653	c	CNT108	Central Polydactyly	15	0.026

654		TCL006	T Cell Immunodeficiency Primary	11	0.026

655		HMT020	Hematopoietic Stem Cell Kinetics, Control of	8	0.026