Search results for Desflurane

292 hits were found for Desflurane

#	Family	MCID	Name	MIFTS	Score
1		PNG002	Pain Agnosia	51	0.236

2		SBC016	Subacute Delirium	44	0.233

3		ISC004	Ischemia	58	0.208

4	P	MLG056	Malignant Hyperthermia	67	0.156

5	P	KDN018	Kidney Disease	72	0.138

6	P	STR020	Strabismus	55	0.133

7		MCH006	Mechanical Strabismus	42	0.133

8	c	HYP595	Hypertension, Essential	84	0.122

9		STR067	Stroke, Ischemic	81	0.122

10	P	SCL018	Scoliosis	60	0.122

11		CRB039	Cerebrovascular Disease	67	0.116

12		END086	End Stage Renal Disease	51	0.116

13	P	BDY004	Body Mass Index Quantitative Trait Locus 11	76	0.110

14	P	HRT032	Heart Disease	75	0.110

15	c	NRD033	Neurodegeneration with Brain Iron Accumulation 2a	69	0.110

16	P	ART062	Arthrogryposis, Renal Dysfunction, and Cholestasis 1	65	0.110

17		LPP008	Lipoprotein Quantitative Trait Locus	62	0.110

18		LVR012	Liver Cirrhosis	62	0.110

19		AMN003	Amnestic Disorder	54	0.110

20	c	BDY021	Body Mass Index Quantitative Trait Locus 20	52	0.110

21	c	BDY020	Body Mass Index Quantitative Trait Locus 19	52	0.110

22	c	BDY005	Body Mass Index Quantitative Trait Locus 9	48	0.110

23	c	BDY019	Body Mass Index Quantitative Trait Locus 18	47	0.110

24	c	BDY010	Body Mass Index Quantitative Trait Locus 4	46	0.110

25	c	BDY015	Body Mass Index Quantitative Trait Locus 12	46	0.110

26	c	BDY017	Body Mass Index Quantitative Trait Locus 14	45	0.110

27	c	BDY011	Body Mass Index Quantitative Trait Locus 10	45	0.110

28	c	BDY006	Body Mass Index Quantitative Trait Locus 8	44	0.110

29	c	BDY012	Body Mass Index Quantitative Trait Locus 7	44	0.110

30	c	BDY007	Body Mass Index Quantitative Trait Locus 1	42	0.110

31		48X005	48,xyyy	39	0.110

32	P	CLR023	Colorectal Cancer	99	0.104

33	P	MYC007	Myocardial Infarction	70	0.104

34	P	CRD119	Cardiac Arrest	67	0.104

35	P	OPT006	Optic Nerve Disease	60	0.104

36	P	HYP724	Hyperlipoproteinemia, Type Iii	73	0.097

37	P	LVR013	Liver Disease	68	0.097

38	P	BLD124	Bleeding Disorder, Platelet-Type, 11	63	0.097

39	P	VSC007	Vascular Disease	63	0.097

40	c	FNC043	Fanconi Anemia, Complementation Group E	62	0.097

41		ANR040	Aneurysm	59	0.097

42		ART140	Arteries, Anomalies of	52	0.097

43		CYT002	Cytokine Deficiency	42	0.097

44	P	ALZ034	Alzheimer Disease	88	0.090

45		LPT014	Leptin Deficiency or Dysfunction	74	0.090

46	c	CHR684	Chronic Kidney Disease	70	0.090

47	P	CRN300	Coronary Heart Disease 1	63	0.090

48	P	CRD246	Cardiovascular System Disease	57	0.090

49		HYP266	Hypoxia	57	0.090

50		ANG049	Angioedema Induced by Ace Inhibitors	40	0.090

51	P	PNC035	Pancreatic Cancer	84	0.082

52	P	PRT133	Proteasome-Associated Autoinflammatory Syndrome 1	81	0.082

53		ANX010	Anxiety	73	0.082

54		ADL002	Adult Syndrome	70	0.082

55		CNG034	Congestive Heart Failure	69	0.082

56	P	SLP006	Sleep Apnea	69	0.082

57		CHL065	Cholangiocarcinoma	68	0.082

58		DPR016	Depression	63	0.082

59	c	PNS012	Paine Syndrome	61	0.082

60	c	ACT071	Acute Kidney Failure	60	0.082

61	P	NRP001	Neuropathy	56	0.082

62		INT079	Intrahepatic Cholangiocarcinoma	51	0.082

63		PRM127	Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type	38	0.082

64	P	LNG032	Lung Cancer	98	0.074

65	P	PRS040	Prostate Cancer	97	0.074

66	P	ART022	Arthritis	69	0.074

67	P	TRN020	Turner Syndrome	67	0.074

68	P	DMN002	Dementia	66	0.074

69		KHL003	Kohlschutter-Tonz Syndrome	65	0.074

70	P	ADN016	Adenocarcinoma	64	0.074

71		TXC005	Toxic Shock Syndrome	62	0.074

72		CHL068	Cholestasis	61	0.074

73		NNR004	Nonarteritic Anterior Ischemic Optic Neuropathy	57	0.074

74	c	ACT075	Acute Myocardial Infarction	57	0.074

75		INT030	Intracranial Aneurysm	56	0.074

76	P	TCD001	Tic Disorder	53	0.074

77		BRN038	Bronchial Disease	53	0.074

78		MTN003	Motion Sickness	53	0.074

79		CRT013	Carotid Stenosis	50	0.074

80		PTT037	Pituitary Tumors	44	0.074

81	c	EPS039	Episodic Pain Syndrome, Familial, 1	42	0.074

82		IDP070	Idiopathic Scoliosis	42	0.074

83		ANX004	Anoxia	40	0.074

84	P	HMF004	Hemifacial Spasm	38	0.074

85	P	ENT005	Entropion	34	0.074

86	c	HMF011	Hemifacial Spasm, Familial	33	0.074

87	c	PRS136	Prostate Cancer, Hereditary, 6	33	0.074

88	c	PRS130	Prostate Cancer, Hereditary, 8	32	0.074

89		CHL079	Children's Interstitial Lung Disease	26	0.074

90	P	BLD134	Bladder Cancer	79	0.064

91	P	SCH015	Schizophrenia	74	0.064

92		PLM129	Pulmonary Disease, Chronic Obstructive	73	0.064

93		CNT097	Central Hypoventilation Syndrome, Congenital	71	0.064

94		DFC004	Deficiency Anemia	70	0.064

95		ART016	Aortic Aneurysm	69	0.064

96	P	PNM007	Pneumonia	68	0.064

97	P	THR014	Thrombocytopenia	67	0.064

98	P	BLD062	Bile Duct Cancer	67	0.064

99		ANM044	Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities	67	0.064

100		ANG054	Angina Pectoris	66	0.064

101	P	ATR011	Atrial Fibrillation	66	0.064

102		TTN003	Tetanus	65	0.064

103	c	FML001	Familial Atrial Fibrillation	65	0.064

104	P	ATT013	Attention Deficit-Hyperactivity Disorder	65	0.064

105		PRP001	Propionic Acidemia	65	0.064

106	c	ART101	Aortic Valve Disease 2	65	0.064

107		TRN015	Transient Cerebral Ischemia	63	0.064

108		HYP066	Hyperglycemia	61	0.064

109	P	PNC044	Pancreatitis	61	0.064

110	c	ACT027	Acute Pancreatitis	60	0.064

111		LNG099	Lung Disease	60	0.064

112	P	CTR002	Cataract	60	0.064

113		ING001	Inguinal Hernia	60	0.064

114		ADN018	Adenoma	59	0.064

115		HYD058	Hydrops, Lactic Acidosis, and Sideroblastic Anemia	59	0.064

116	P	ALC033	Alcohol Use Disorder	58	0.064

117		EYD002	Eye Disease	58	0.064

118		CNS004	Constipation	58	0.064

119		BRD001	Brody Myopathy	57	0.064

120	P	URF003	Urofacial Syndrome 1	57	0.064

121	P	LKD017	Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism	57	0.064

122		PHR003	Pharyngitis	57	0.064

123	P	SZR006	Seizure Disorder	56	0.064

124		AGN016	Aging	56	0.064

125		HYP005	Hypokalemia	55	0.064

126	P	PTT006	Pituitary Adenoma	55	0.064

127		URN010	Urinary Tract Obstruction	55	0.064

128		INT007	Intermediate Coronary Syndrome	55	0.064

129		PTT009	Pituitary Gland Disease	54	0.064

130		PNC001	Pancytopenia	54	0.064

131		HRT012	Heart Valve Disease	53	0.064

132		INT075	Intracranial Hypertension	53	0.064

133		OCL069	Ocular Motor Apraxia	51	0.064

134		TRM010	Traumatic Brain Injury	51	0.064

135		BHR001	Behr Syndrome	51	0.064

136		BLR001	Biliary Atresia	50	0.064

137		VGN020	Vaginal Disease	49	0.064

138		PCT003	Pectus Excavatum	49	0.064

139		BRN071	Brain Injury	49	0.064

140		STP011	Stapes Ankylosis with Broad Thumbs and Toes	49	0.064

141		URN009	Urinary System Disease	48	0.064

142	P	OVR046	Ovarian Cyst	47	0.064

143	c	GZP005	Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1	44	0.064

144		PPL001	Papillary Adenoma	44	0.064

145	P	ATX039	Ataxia-Pancytopenia Syndrome	43	0.064

146		ATX019	Ataxia with Vitamin E Deficiency	42	0.064

147		49X006	49, Xxxxy Syndrome	41	0.064

148		LWR018	Lower Urinary Tract Obstruction, Congenital	40	0.064

149		URG005	Uruguay Faciocardiomusculoskeletal Syndrome	40	0.064

150		HYP540	Hypertension, Diastolic	40	0.064

151	P	INT260	Intracranial Berry Aneurysm	39	0.064

152		BLR028	Biliary Atresia, Extrahepatic	37	0.064

153		PRK076	Porokeratosis 2, Palmar, Plantar, and Disseminated Type	28	0.064

154		PPL061	Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome	25	0.064

155	P	HPT023	Hepatocellular Carcinoma	100	0.052

156	P	BRS047	Breast Cancer	97	0.052

157		OST012	Osteoarthritis	78	0.052

158	c	ATR087	Atrial Standstill 1	75	0.052

159	c	THR092	Thrombophilia Due to Thrombin Defect	73	0.052

160	P	CNR004	Cone-Rod Dystrophy 2	73	0.052

161	P	MLT020	Multiple Sclerosis	72	0.052

162	P	PHC003	Pheochromocytoma	71	0.052

163		DWN001	Down Syndrome	70	0.052

164	P	MYS003	Myasthenia Gravis	68	0.052

165		PNC129	Pancreatic Adenocarcinoma	68	0.052

166	c	MCL062	Mucolipidosis Ii Alpha/beta	68	0.052

167		GST092	Gastroesophageal Reflux	67	0.052

168	c	VNT034	Ventricular Fibrillation, Paroxysmal Familial, 1	67	0.052

169	c	MCL013	Mucolipidosis Iv	66	0.052

170	P	ADL010	Adult Respiratory Distress Syndrome	65	0.052

171		APN008	Apnea, Obstructive Sleep	64	0.052

172	P	THR117	Three M Syndrome 1	63	0.052

173		INT323	Intraocular Pressure Quantitative Trait Locus	62	0.052

174	c	CRD177	Ceroid Lipofuscinosis, Neuronal, 1	62	0.052

175	P	PLY169	Polycystic Liver Disease 1 with or Without Kidney Cysts	60	0.052

176		STT001	Status Epilepticus	60	0.052

177		NWB001	Newborn Respiratory Distress Syndrome	58	0.052

178		MNT002	Mental Depression	58	0.052

179	P	GLL018	Gallbladder Cancer	57	0.052

180		CHL067	Cholecystitis	57	0.052

181	P	HDC001	Headache	57	0.052

182		THY122	Thyroid Gland Cancer	57	0.052

183		OPT066	Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy	56	0.052

184		ISL014	Isolated Growth Hormone Deficiency, Type Ia	55	0.052

185	P	TRM003	Tremor	54	0.052

186	c	GLL024	Gallbladder Disease 1	53	0.052

187		LMY002	Leiomyoma	52	0.052

188	P	SPP010	Suppressor of Tumorigenicity 3	51	0.052

189		LNG031	Lung Benign Neoplasm	51	0.052

190		MTB004	Metabolic Acidosis	50	0.052

191		47X002	47,xyy	49	0.052

192		LPT006	Leptin Receptor Deficiency	48	0.052

193		HRN026	Hernia, Hiatus	47	0.052

194		THY128	Thyroid Tumor	47	0.052

195		OST062	Osteoarthritis with Mild Chondrodysplasia	47	0.052

196		ADR040	Adrenal Gland Pheochromocytoma	46	0.052

197		3MC003	3mc Syndrome	46	0.052

198		CRB004	Cerebral Artery Occlusion	45	0.052

199		MYF001	Myofibroma	45	0.052

200		DWR001	Dwarfism	44	0.052

201		GST020	Gastric Antral Vascular Ectasia	41	0.052

202		NRN005	Neuronal Ceroid-Lipofuscinoses	41	0.052

203		ENT001	Enterocele	39	0.052

204		3MC001	3mc Syndrome 2	37	0.052

205		FST001	Foster-Kennedy Syndrome	36	0.052

206		IDP022	Idiopathic Spinal Cord Herniation	17	0.052

207	P	GST053	Gastric Cancer	83	0.037

208		GLB015	Glioblastoma Multiforme	75	0.037

209	P	RSP003	Respiratory Failure	74	0.037

210		ULC004	Ulcerative Colitis	73	0.037

211		OTT002	Otitis Media	72	0.037

212	c	EXD008	Exudative Vitreoretinopathy 1	71	0.037

213	P	HYP061	Hypertrophic Cardiomyopathy	70	0.037

214		CRB037	Cerebral Palsy	69	0.037

215	P	HPT021	Hepatitis	67	0.037

216	P	PLM037	Pulmonary Hypertension	67	0.037

217		WLF001	Wolff-Parkinson-White Syndrome	66	0.037

218	P	MSC005	Muscular Dystrophy	66	0.037

219	c	HRD010	Hereditary Spastic Paraplegia	66	0.037

220		NRM005	Neuromuscular Disease	64	0.037

221		PRP083	Porphyria, Acute Intermittent	64	0.037

222		MSC007	Muscle Hypertrophy	64	0.037

223		CLT003	Colitis	62	0.037

224		ATM095	Autoimmune Disease	62	0.037

225	P	PRP029	Porphyria	62	0.037

226	P	ENC018	Encephalopathy	61	0.037

227	P	HMN010	Hemangioma	61	0.037

228		HPT019	Hepatic Encephalopathy	60	0.037

229		CRD223	Cardiac Arrhythmia	60	0.037

230		RHM001	Rheumatic Fever	60	0.037

231		PRT013	Portal Hypertension	59	0.037

232	c	ART138	Aortic Aneurysm, Familial Abdominal, 1	59	0.037

233		PLM033	Pulmonary Embolism	59	0.037

234	P	BCL017	B-Cell Lymphoma	58	0.037

235		INT324	Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies	58	0.037

236	P	INF032	Infertility	57	0.037

237	P	GLL020	Gallbladder Disease	57	0.037

238		MBS002	Moebius Syndrome	57	0.037

239		THR024	Thrombosis	57	0.037

240		CMM005	Common Cold	57	0.037

241	c	ACT134	Acute Liver Failure	56	0.037

242		ACS001	Acoustic Neuroma	56	0.037

243		INS023	Insensitivity to Pain, Congenital, with Anhidrosis	56	0.037

244		CRT017	Cartilage Disease	54	0.037

245		NNL006	Non-Alcoholic Steatohepatitis	54	0.037

246		TXC002	Toxic Encephalopathy	53	0.037

247		DMY004	Demyelinating Disease	52	0.037

248		PRP016	Paraplegia	52	0.037

249		ACR041	Acromelic Frontonasal Dysostosis	52	0.037

250	P	NRC002	Narcolepsy	52	0.037

251		ILS001	Ileus	51	0.037

252	P	LCT001	Lactic Acidosis	51	0.037

253		MYL020	Myelomeningocele	51	0.037

254		NRM004	Neuroma	51	0.037

255	P	HYP040	Hypospadias	51	0.037

256		ALP041	Alopecia, Neurologic Defects, and Endocrinopathy Syndrome	51	0.037

257		RTN003	Retinal Ischemia	50	0.037

258		CRN030	Coronary Stenosis	50	0.037

259		CHL122	Cholesteatoma of Middle Ear	50	0.037

260	P	PRS049	Persistent Mullerian Duct Syndrome	50	0.037

261	c	INF145	Infantile Liver Failure Syndrome 1	50	0.037

262		PRT018	Portal Vein Thrombosis	50	0.037

263	P	OBS001	Obstructive Jaundice	50	0.037

264	P	MYT002	Myotonic Dystrophy	49	0.037

265		CVR006	Cavernous Hemangioma	49	0.037

266	P	CMP008	Compartment Syndrome	49	0.037

267		SBP001	Subependymal Giant Cell Astrocytoma	49	0.037

268		ASP007	Aspiration Pneumonia	48	0.037

269		ANH002	Anhidrosis	47	0.037

270		SHR059	Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis	47	0.037

271		MYC005	Myocardial Stunning	46	0.037

272		HPT004	Hepatic Coma	45	0.037

273		PRL008	Paralytic Ileus	45	0.037

274		ATN004	Autonomic Neuropathy	45	0.037

275		ASP008	Aspiration Pneumonitis	45	0.037

276		PRT035	Peritoneum Cancer	44	0.037

277		CRB090	Cerebral Hypoxia	44	0.037

278		MDD018	Middle East Respiratory Syndrome	43	0.037

279		BCK006	Back Pain	42	0.037

280		RDN001	Reading Disorder	40	0.037

281		MLG086	Malignant Hyperthermia Susceptibility	39	0.037

282		CMP080	Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy	38	0.037

283		MYT011	Myotonia	34	0.037

284		EXT054	Extra-Adrenal Pheochromocytoma	34	0.037

285		ACT032	Acute Hemorrhagic Leukoencephalitis	34	0.037

286		PRS064	Persistent Vegetative State	33	0.037

287		HLT002	Halothane Hepatitis	32	0.037

288		VSD001	Vas Deferens, Congenital Bilateral Aplasia of, X-Linked	28	0.037

289		CHR159	Charlie M Syndrome	24	0.037

290		PNS018	Pain Sensitivity Quantitative Trait Locus 1	23	0.037

291		CD4008	Cd4/cd8 T-Cell Ratio	20	0.037

292		ATR089	Atrioventricular Dissociation	20	0.037