Search results for Pseudoephedrine

366 hits were found for Pseudoephedrine

# Family MCID Name MIFTS Score
1
P RHN004 Rhinitis 59 0.388
2
ALL003 Allergic Rhinitis 69 0.354
3
CMM005 Common Cold 57 0.260
4
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.211
5
ALL026 Allergic Hypersensitivity Disease 65 0.168
6
ADL002 Adult Syndrome 62 0.168
7
P HDC001 Headache 59 0.113
8
FXD003 Fixed Drug Eruption 36 0.113
9
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.108
10
P TRN020 Turner Syndrome 66 0.108
11
48X005 48,xyyy 37 0.108
12
CLT003 Colitis 63 0.103
13
RSP021 Respiratory Allergy 45 0.090
14
STR067 Stroke, Ischemic 82 0.084
15
AST005 Asthma 80 0.084
16
OTT002 Otitis Media 71 0.084
17
CRB039 Cerebrovascular Disease 71 0.084
18
PRT058 Pure Autonomic Failure 60 0.084
19
P TRM003 Tremor 55 0.084
20
P MYC007 Myocardial Infarction 74 0.076
21
MLT157 Multiple System Atrophy 1 71 0.076
22
DWN001 Down Syndrome 70 0.076
23
c RHB024 Rhabdomyosarcoma 2 64 0.076
24
PHR003 Pharyngitis 56 0.076
25
GLS018 Glass Syndrome 51 0.076
26
ATN005 Autonomic Dysfunction 48 0.076
27
ATX019 Ataxia with Vitamin E Deficiency 46 0.076
28
ISC015 Ischemic Colitis 43 0.076
29
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.076
30
P KDN018 Kidney Disease 73 0.068
31
DPR016 Depression 64 0.068
32
DRM006 Dermatitis 63 0.068
33
ISC004 Ischemia 62 0.068
34
P URT039 Urticaria 61 0.068
35
P SZR006 Seizure Disorder 59 0.068
36
c ACT075 Acute Myocardial Infarction 59 0.068
37
VSL002 Visual Epilepsy 58 0.068
38
CRN019 Coronary Artery Vasospasm 48 0.068
39
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.068
40
VSM001 Vasomotor Rhinitis 36 0.068
41
c HYP595 Hypertension, Essential 87 0.059
42
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.059
43
P ENC018 Encephalopathy 64 0.059
44
VRL011 Viral Infectious Disease 62 0.059
45
c PNS012 Paine Syndrome 61 0.059
46
IGR001 Ige Responsiveness, Atopic 61 0.059
47
HYP005 Hypokalemia 55 0.059
48
PLL012 Pollen Allergy 46 0.059
49
MDD010 Middle Ear Disease 46 0.059
50
BCK006 Back Pain 44 0.059
51
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.059
52
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.059
53
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.059
54
IMM167 Immune Deficiency Disease 79 0.048
55
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.048
56
c ATR087 Atrial Standstill 1 76 0.048
57
HMN044 Human Immunodeficiency Virus Type 1 73 0.048
58
P SLP006 Sleep Apnea 71 0.048
59
c MGR028 Migraine with or Without Aura 1 70 0.048
60
BRN024 Bronchitis 70 0.048
61
CNG034 Congestive Heart Failure 69 0.048
62
P CNJ013 Conjunctivitis 67 0.048
63
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.048
64
P VSC007 Vascular Disease 65 0.048
65
P VSC011 Vasculitis 64 0.048
66
APN008 Apnea, Obstructive Sleep 64 0.048
67
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.048
68
TXC005 Toxic Shock Syndrome 63 0.048
69
SPN186 Spinal Cord Injury 63 0.048
70
MDD011 Mood Disorder 62 0.048
71
ACQ007 Acquired Immunodeficiency Syndrome 61 0.048
72
c ACT071 Acute Kidney Failure 60 0.048
73
CNS004 Constipation 59 0.048
74
CNT047 Contact Dermatitis 58 0.048
75
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.048
76
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.048
77
PLM010 Pulmonary Edema 56 0.048
78
P DRR001 Diarrhea 55 0.048
79
c GRV008 Graves Disease 1 55 0.048
80
GST009 Gastroschisis 52 0.048
81
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.048
82
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.048
83
SXL003 Sexual Disorder 49 0.048
84
ADT003 Auditory System Disease 49 0.048
85
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.048
86
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.048
87
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.048
88
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.048
89
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.048
90
PRP007 Priapism 47 0.048
91
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.048
92
LWC001 Low Compliance Bladder 45 0.048
93
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.048
94
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.048
95
DRG024 Drug Allergy 43 0.048
96
RST023 Resting Heart Rate, Variation in 43 0.048
97
c ORT011 Orthostatic Hypotension 1 42 0.048
98
SCR015 Scarlet Fever 41 0.048
99
ABD010 Abdominal Wall Defect 37 0.048
100
OCL004 Ocular Hyperemia 33 0.048
101
c ORT012 Orthostatic Hypotension 2 27 0.048
102
ANS021 Anisocoria 25 0.048
103
P CLR023 Colorectal Cancer 100 0.034
104
P BRS047 Breast Cancer 99 0.034
105
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.034
107
P PNC035 Pancreatic Cancer 86 0.034
108
P RHM011 Rheumatoid Arthritis 82 0.034
109
OST012 Osteoarthritis 80 0.034
110
P HRT032 Heart Disease 78 0.034
111
DFC004 Deficiency Anemia 77 0.034
112
P SCH015 Schizophrenia 76 0.034
113
BRN028 Brain Cancer 75 0.034
114
ANX010 Anxiety 75 0.034
115
c THR092 Thrombophilia Due to Thrombin Defect 74 0.034
116
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.034
117
SCK003 Sickle Cell Anemia 74 0.034
118
P MLT020 Multiple Sclerosis 73 0.034
119
PHN003 Phenylketonuria 73 0.034
120
PRP027 Peripheral Vascular Disease 72 0.034
121
P CNR004 Cone-Rod Dystrophy 2 72 0.034
122
LPT014 Leptin Deficiency or Dysfunction 72 0.034
123
P PHC003 Pheochromocytoma 71 0.034
124
P ART022 Arthritis 71 0.034
125
P PNM007 Pneumonia 71 0.034
126
P CRD119 Cardiac Arrest 71 0.034
127
P HYP086 Hypothyroidism 70 0.034
128
c EXD008 Exudative Vitreoretinopathy 1 69 0.034
129
P MYC084 Mycobacterium Tuberculosis 1 69 0.034
130
P INF038 Influenza 69 0.034
131
KRT019 Keratitis, Hereditary 69 0.034
132
OBS002 Obsessive-Compulsive Disorder 69 0.034
133
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.034
134
c CHR684 Chronic Kidney Disease 68 0.034
135
P DMN002 Dementia 68 0.034
136
P ORT004 Orthostatic Intolerance 68 0.034
137
P NRV007 Nervous System Disease 68 0.034
138
c FML001 Familial Atrial Fibrillation 67 0.034
139
P MCR115 Microvascular Complications of Diabetes 5 67 0.034
140
P CRN018 Coronary Artery Anomaly 67 0.034
141
P ATR011 Atrial Fibrillation 67 0.034
142
P HYP098 Hypereosinophilic Syndrome 67 0.034
143
P DBT009 Diabetes Mellitus 66 0.034
144
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.034
145
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.034
146
P PRS038 Personality Disorder 66 0.034
147
P PRD008 Periodontitis 66 0.034
148
DSS008 Disease of Mental Health 66 0.034
149
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.034
150
ANG054 Angina Pectoris 66 0.034
151
ALP100 Alpha-Thalassemia/mental Retardation Syndrome, X-Linked 65 0.034
152
P OCL013 Oculodentodigital Dysplasia 65 0.034
153
MSC007 Muscle Hypertrophy 65 0.034
154
TBC004 Tobacco Addiction 65 0.034
155
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.034
156
P ENC004 Encephalitis 64 0.034
157
KHL003 Kohlschutter-Tonz Syndrome 63 0.034
158
P PSR002 Psoriasis 63 0.034
159
P ART005 Arteriovenous Malformation 63 0.034
160
ART002 Arts Syndrome 63 0.034
161
P CNG001 Congenital Myasthenic Syndrome 63 0.034
162
c PRC016 Pre-Eclampsia 63 0.034
163
c GLC092 Glaucoma, Primary Open Angle 63 0.034
164
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.034
165
P RHB003 Rhabdomyosarcoma 62 0.034
166
c PRG042 Progressive Familial Heart Block, Type Ia 62 0.034
167
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.034
168
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.034
169
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.034
170
P CTR002 Cataract 62 0.034
171
CRD223 Cardiac Arrhythmia 61 0.034
172
TYP007 Typhoid Fever 61 0.034
173
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.034
174
STT001 Status Epilepticus 61 0.034
175
MLT163 Multiple Pterygium Syndrome, Escobar Variant 61 0.034
176
P ART023 Arthropathy 61 0.034
177
CHR066 Chronic Fatigue Syndrome 61 0.034
178
NTR005 Nutritional Deficiency Disease 61 0.034
179
P ADL010 Adult Respiratory Distress Syndrome 61 0.034
180
P SCL018 Scoliosis 61 0.034
181
P VNT002 Ventricular Septal Defect 61 0.034
182
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.034
183
CHL067 Cholecystitis 60 0.034
184
ANR040 Aneurysm 60 0.034
185
CHL123 Chlamydia 60 0.034
186
MNT002 Mental Depression 60 0.034
187
PLM033 Pulmonary Embolism 60 0.034
188
ART140 Arteries, Anomalies of 60 0.034
189
BRN002 Bronchiolitis 60 0.034
190
c MCL013 Mucolipidosis Iv 60 0.034
191
END030 End Stage Renal Failure 60 0.034
192
P GLL020 Gallbladder Disease 60 0.034
193
PST028 Post-Traumatic Stress Disorder 60 0.034
194
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 60 0.034
195
P INF032 Infertility 60 0.034
196
P CRN300 Coronary Heart Disease 1 59 0.034
197
EYD002 Eye Disease 59 0.034
198
P OPT006 Optic Nerve Disease 59 0.034
199
P BPL003 Bipolar Disorder 59 0.034
200
c ACT210 Acute Respiratory Distress Syndrome 59 0.034
201
NWB001 Newborn Respiratory Distress Syndrome 58 0.034
202
HYP266 Hypoxia 58 0.034
203
P EXN002 Exanthem 58 0.034
204
THR024 Thrombosis 58 0.034
205
AGN016 Aging 58 0.034
206
P SLP005 Sleep Disorder 58 0.034
207
P SJG008 Sjogren Syndrome 57 0.034
208
P NRP001 Neuropathy 57 0.034
209
BCT022 Bacterial Infectious Disease 57 0.034
210
GST050 Gastrointestinal System Disease 57 0.034
211
LMY014 Leiomyoma, Uterine 57 0.034
212
CHN016 Cohen Syndrome 57 0.034
213
P GRV001 Graves' Disease 57 0.034
214
INT030 Intracranial Aneurysm 57 0.034
215
CMP010 Complex Regional Pain Syndrome 57 0.034
216
RSP006 Respiratory System Disease 57 0.034
217
BRN004 Brain Edema 57 0.034
218
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.034
219
EXF001 Exfoliation Syndrome 56 0.034
220
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.034
221
MCS002 Mucositis 56 0.034
222
JPN002 Japanese Encephalitis 56 0.034
223
c FML035 Familial Hyperlipidemia 56 0.034
224
END040 Endogenous Depression 55 0.034
225
LMB002 Lambert-Eaton Myasthenic Syndrome 55 0.034
226
P HYP076 Hyperthyroidism 55 0.034
227
c PSR017 Psoriasis 2 55 0.034
228
ACT058 Active Peptic Ulcer Disease 55 0.034
229
RSC001 Rosacea 55 0.034
230
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 55 0.034
231
TRM010 Traumatic Brain Injury 54 0.034
232
P ANG015 Angioedema 54 0.034
233
TXC002 Toxic Encephalopathy 54 0.034
234
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.034
235
CRT017 Cartilage Disease 54 0.034
236
PTH003 Pathologic Nystagmus 53 0.034
237
P PTS002 Ptosis 53 0.034
238
IMP005 Impotence 53 0.034
239
P RTN018 Retinal Disease 53 0.034
240
KRT006 Keratoconjunctivitis 53 0.034
241
STT041 Stuttering 53 0.034
242
c GLL024 Gallbladder Disease 1 53 0.034
243
KRT001 Keratoconjunctivitis Sicca 53 0.034
244
c ACT134 Acute Liver Failure 53 0.034
245
NRT001 Neurotic Disorder 53 0.034
246
P ATN002 Autonomic Nervous System Disease 52 0.034
247
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.034
248
LMY002 Leiomyoma 52 0.034
249
DNT012 Dental Caries 52 0.034
250
PNG002 Pain Agnosia 52 0.034
251
MCL006 Macular Retinal Edema 52 0.034
252
P CHR345 Chronic Pain 52 0.034
253
P MSC003 Muscular Atrophy 52 0.034
254
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.034
255
AZS001 Azoospermia 51 0.034
256
STM007 Stomatitis 51 0.034
257
OVR082 Overgrowth Syndrome 51 0.034
258
HMF006 Hemifacial Microsomia 51 0.034
259
BRN071 Brain Injury 51 0.034
260
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.034
261
ADR040 Adrenal Gland Pheochromocytoma 51 0.034
262
PST011 Pustulosis of Palm and Sole 51 0.034
263
c SVR005 Severe Pre-Eclampsia 50 0.034
264
ALL001 Allan-Herndon-Dudley Syndrome 50 0.034
265
CHL004 Cholelithiasis 50 0.034
266
P PST095 Post-Thrombotic Syndrome 50 0.034
267
RFL001 Reflex Sympathetic Dystrophy 50 0.034
268
c PSR023 Psoriasis 1 50 0.034
269
SGW002 Segawa Syndrome, Autosomal Recessive 50 0.034
270
CRT013 Carotid Stenosis 50 0.034
271
P OVR046 Ovarian Cyst 50 0.034
272
RYN005 Raynaud Phenomenon 50 0.034
273
P OPN001 Open-Angle Glaucoma 50 0.034
274
PRS030 Persistent Fetal Circulation Syndrome 50 0.034
275
ALL009 Allergic Conjunctivitis 50 0.034
276
DRY001 Dry Eye Syndrome 50 0.034
277
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.034
278
RTN020 Retinal Vascular Disease 49 0.034
279
c PRG126 Progressive Familial Heart Block 49 0.034
280
47X002 47,xyy 49 0.034
281
PST048 Postural Orthostatic Tachycardia Syndrome 49 0.034
282
P RNL007 Renal Tubular Acidosis 49 0.034
283
P PLN008 Peeling Skin Syndrome 48 0.034
284
P TCL004 T-Cell Leukemia 48 0.034
285
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 48 0.034
286
P BLD051 Blood Coagulation Disease 48 0.034
287
CLS016 Clostridium Difficile Colitis 48 0.034
288
RYN001 Raynaud Disease 48 0.034
289
MCR141 Mucormycosis 48 0.034
290
PLC007 Placental Abruption 47 0.034
291
BHR001 Behr Syndrome 47 0.034
292
c MYS051 Myasthenic Syndrome, Congenital, 5 47 0.034
293
P HMR005 Hemorrhoid 47 0.034
294
LFT001 Left Bundle Branch Hemiblock 47 0.034
295
LPT006 Leptin Receptor Deficiency 47 0.034
296
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.034
297
CYT002 Cytokine Deficiency 46 0.034
298
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.034
299
P HRN001 Horner's Syndrome 46 0.034
300
EXS001 Exostosis 46 0.034
301
SYN036 Syncope 46 0.034
302
KRT013 Keratolytic Winter Erythema 45 0.034
303
TND005 Tendinitis 45 0.034
304
LRY022 Laryngoonychocutaneous Syndrome 45 0.034
305
c PRM038 Primary Agammaglobulinemia 45 0.034
306
MYC005 Myocardial Stunning 45 0.034
307
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 45 0.034
308
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.034
309
P CRN026 Corneal Edema 44 0.034
310
RFR003 Refractive Error 44 0.034
311
TND004 Tendinopathy 44 0.034
312
ENT001 Enterocele 44 0.034
313
PRP017 Periapical Periodontitis 43 0.034
314
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.034
315
P HYP265 Hypotonia 43 0.034
316
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 43 0.034
317
SBC016 Subacute Delirium 43 0.034
318
P ATS366 Autism X-Linked 2 43 0.034
319
ACT084 Acute Stress Disorder 42 0.034
320
c MJR024 Major Affective Disorder 9 42 0.034
321
GST020 Gastric Antral Vascular Ectasia 42 0.034
322
c CHR048 Chronic Rhinitis 42 0.034
323
OBS003 Obsessive-Compulsive Personality Disorder 42 0.034
324
TRP009 Triple X Syndrome 42 0.034
325
ANG049 Angioedema Induced by Ace Inhibitors 41 0.034
326
SKN005 Skin Atrophy 41 0.034
327
SNL007 Senile Cataract 41 0.034
328
INT060 Intestinal Atresia 41 0.034
329
LCR013 Lacrimal Duct Defect 41 0.034
330
MYF001 Myofibroma 40 0.034
331
c RTN047 Retinitis Pigmentosa 18 40 0.034
332
c PSR028 Psoriasis 7 40 0.034
333
c PSR018 Psoriasis 13 40 0.034
334
c PSR032 Psoriasis 11 40 0.034
335
c MJR022 Major Affective Disorder 8 39 0.034
336
HYP030 Hypoactive Sexual Desire Disorder 39 0.034
337
ACT056 Acute Cor Pulmonale 38 0.034
338
SPS057 Spasticity 38 0.034
339
ALG001 Algoneurodystrophy 38 0.034
340
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.034
341
BLP006 Blepharoconjunctivitis 38 0.034
342
CHL013 Cholecystolithiasis 37 0.034
343
P MXL015 Maxillary Sinusitis 37 0.034
344
ADN067 Adenoid Hypertrophy 37 0.034
345
PRS011 Persian Gulf Syndrome 37 0.034
346
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.034
347
BRK012 Broken Heart Syndrome 36 0.034
348
ACL001 Acalculous Cholecystitis 35 0.034
349
PLC009 Placenta Praevia 35 0.034
350
c LKM005 Leukemia, T-Cell, Chronic 35 0.034
351
EXC003 Excessive Tearing 35 0.034
352
c CTR174 Cataract 40 35 0.034
353
INF013 Inferior Myocardial Infarction 35 0.034
354
ACT011 Acute Contagious Conjunctivitis 35 0.034
355
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.034
356
LCR001 Lacrimal Duct Obstruction 34 0.034
357
CGH001 Cough Variant Asthma 34 0.034
358
PST103 Postpartum Psychosis 33 0.034
359
RRS014 Rare Surgical Neurologic Disease 33 0.034
360
FLM001 Filamentary Keratitis 30 0.034
361
HYP193 Hypocomplementemic Urticarial Vasculitis 30 0.034
362
CYC001 Cycloplegia 29 0.034
363
SPN031 Supine Hypotensive Syndrome 25 0.034
364
MCT002 Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency 22 0.034
365
PGM028 Pigmented Purpuric Dermatosis 22 0.034
366
ORG003 Organic Mood Syndrome 14 0.034
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