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Search results for Alprostadil

233 hits were found for Alprostadil

# Family MCID Name MIFTS Score
1
IMP005 Impotence 52 0.440
2
PRP007 Priapism 47 0.183
3
ISC004 Ischemia 58 0.165
4
SXL003 Sexual Disorder 47 0.139
5
P KDN018 Kidney Disease 72 0.120
6
PRP027 Peripheral Vascular Disease 71 0.120
7
ADL002 Adult Syndrome 70 0.120
8
P ART021 Arteriosclerosis 54 0.120
9
ATH013 Atherosclerosis Susceptibility 65 0.113
10
P VSC007 Vascular Disease 63 0.113
11
INT002 Intermittent Claudication 61 0.113
12
LMB062 Limb Ischemia 55 0.113
13
P HRT032 Heart Disease 75 0.106
14
ART008 Arteriosclerosis Obliterans 40 0.106
15
c CHR684 Chronic Kidney Disease 70 0.098
16
c ACT071 Acute Kidney Failure 60 0.098
17
RYN005 Raynaud Phenomenon 47 0.098
18
CNG034 Congestive Heart Failure 69 0.089
19
P DBT009 Diabetes Mellitus 64 0.089
20
c SCL052 Scleroderma, Familial Progressive 61 0.089
21
PRP080 Peripheral Artery Disease 53 0.089
22
c MCR113 Microvascular Complications of Diabetes 3 52 0.089
23
c MCR120 Microvascular Complications of Diabetes 7 47 0.089
24
c MCR130 Microvascular Complications of Diabetes 6 41 0.089
25
c MCR133 Microvascular Complications of Diabetes 4 41 0.089
26
P MYC007 Myocardial Infarction 70 0.080
27
P SYS005 Systemic Scleroderma 68 0.080
28
P TRN020 Turner Syndrome 67 0.080
29
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.080
30
HYP030 Hypoactive Sexual Desire Disorder 40 0.080
31
P PRS040 Prostate Cancer 97 0.069
32
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.069
34
STR067 Stroke, Ischemic 81 0.069
35
ADR007 Adrenoleukodystrophy 75 0.069
36
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.069
37
DWN001 Down Syndrome 70 0.069
38
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.069
39
CRB039 Cerebrovascular Disease 67 0.069
40
P PLM037 Pulmonary Hypertension 67 0.069
41
P ADL010 Adult Respiratory Distress Syndrome 65 0.069
42
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.069
43
SPN186 Spinal Cord Injury 60 0.069
44
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.069
45
NWB001 Newborn Respiratory Distress Syndrome 58 0.069
46
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.069
47
P CRD246 Cardiovascular System Disease 57 0.069
48
P NRP001 Neuropathy 56 0.069
49
ART140 Arteries, Anomalies of 52 0.069
50
RYN001 Raynaud Disease 48 0.069
51
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.069
52
SYN036 Syncope 45 0.069
53
DFF003 Diffuse Scleroderma 41 0.069
54
c PRS136 Prostate Cancer, Hereditary, 6 33 0.069
55
c PRS130 Prostate Cancer, Hereditary, 8 32 0.069
56
SNG003 Single Ventricular Heart 30 0.069
57
RSP007 Respiratory Distress Syndrome, Infant 30 0.069
58
CHL079 Children's Interstitial Lung Disease 26 0.069
59
c HYP595 Hypertension, Essential 84 0.057
60
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.057
61
c THR092 Thrombophilia Due to Thrombin Defect 73 0.057
62
P THR014 Thrombocytopenia 67 0.057
63
c RHB024 Rhabdomyosarcoma 2 67 0.057
64
P MCR115 Microvascular Complications of Diabetes 5 66 0.057
65
P ADN016 Adenocarcinoma 64 0.057
66
P CRN300 Coronary Heart Disease 1 63 0.057
67
c ACT068 Acute Cystitis 63 0.057
68
c BRN108 Branchiootic Syndrome 1 62 0.057
69
P VSC011 Vasculitis 62 0.057
70
P ENC018 Encephalopathy 61 0.057
71
HPT019 Hepatic Encephalopathy 60 0.057
72
P OPT006 Optic Nerve Disease 60 0.057
73
c HPT016 Hepatitis B 59 0.057
74
PLM033 Pulmonary Embolism 59 0.057
75
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.057
76
P INF032 Infertility 57 0.057
77
P HDC001 Headache 57 0.057
78
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.057
79
HYP266 Hypoxia 57 0.057
80
PLM010 Pulmonary Edema 54 0.057
81
DBT010 Diabetic Neuropathy 54 0.057
82
HPT004 Hepatic Coma 45 0.057
83
GST020 Gastric Antral Vascular Ectasia 41 0.057
84
48X005 48,xyyy 39 0.057
85
FST001 Foster-Kennedy Syndrome 36 0.057
86
PTN004 Patent Ductus Venosus 28 0.057
87
P HPT023 Hepatocellular Carcinoma 100 0.040
88
P ALZ034 Alzheimer Disease 88 0.040
89
c NRF023 Neurofibromatosis, Type Ii 80 0.040
90
OST012 Osteoarthritis 78 0.040
91
P PRK057 Parkinson Disease, Late-Onset 78 0.040
92
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.040
93
P CNR004 Cone-Rod Dystrophy 2 73 0.040
94
ANX010 Anxiety 73 0.040
95
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.040
96
DFC004 Deficiency Anemia 70 0.040
97
P ART022 Arthritis 69 0.040
98
P LVR013 Liver Disease 68 0.040
99
CNN005 Connective Tissue Disease 68 0.040
100
GST092 Gastroesophageal Reflux 67 0.040
101
P HPT021 Hepatitis 67 0.040
102
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.040
103
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.040
104
P DMN002 Dementia 66 0.040
105
c MCR129 Microvascular Complications of Diabetes 1 66 0.040
106
P ATR011 Atrial Fibrillation 66 0.040
107
c MCL013 Mucolipidosis Iv 66 0.040
108
KHL003 Kohlschutter-Tonz Syndrome 65 0.040
109
c FML001 Familial Atrial Fibrillation 65 0.040
110
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.040
111
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.040
112
c PRC016 Pre-Eclampsia 63 0.040
113
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.040
114
P HYP055 Hypoplastic Left Heart Syndrome 63 0.040
115
DPR016 Depression 63 0.040
116
P PSR002 Psoriasis 62 0.040
117
TKY002 Takayasu Arteritis 62 0.040
118
LPP008 Lipoprotein Quantitative Trait Locus 62 0.040
119
P ESP024 Esophagitis 62 0.040
120
ALL026 Allergic Hypersensitivity Disease 62 0.040
121
TXC005 Toxic Shock Syndrome 62 0.040
122
c LPM012 Lipomatosis, Multiple 60 0.040
123
P VNT002 Ventricular Septal Defect 60 0.040
124
c ACT027 Acute Pancreatitis 60 0.040
125
P ATR010 Atrial Heart Septal Defect 60 0.040
126
P PTN014 Patent Ductus Arteriosus 1 60 0.040
127
PRT013 Portal Hypertension 59 0.040
128
SPN027 Spinal Stenosis 59 0.040
129
PRT058 Pure Autonomic Failure 59 0.040
130
IRN001 Iron Deficiency Anemia 59 0.040
131
P PLY017 Polyarteritis Nodosa 58 0.040
132
PST028 Post-Traumatic Stress Disorder 58 0.040
133
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.040
134
DSS008 Disease of Mental Health 58 0.040
135
MNT002 Mental Depression 58 0.040
136
P PRP019 Peripheral Nervous System Disease 58 0.040
137
P GLM007 Glomerulonephritis 57 0.040
138
IRN002 Iron Metabolism Disease 57 0.040
139
PLM070 Pulmonic Stenosis 57 0.040
140
THR024 Thrombosis 57 0.040
141
HPT046 Hepatic Veno-Occlusive Disease 56 0.040
142
c ACT134 Acute Liver Failure 56 0.040
143
P PNL012 Penile Cancer 56 0.040
144
P PNM006 Pneumoconiosis 56 0.040
145
P ATR001 Atrioventricular Septal Defect 55 0.040
146
P DRR001 Diarrhea 55 0.040
147
INT007 Intermediate Coronary Syndrome 55 0.040
148
PRP030 Purpura 54 0.040
149
RSC001 Rosacea 54 0.040
150
MYM001 Myoma 54 0.040
151
P TRM003 Tremor 54 0.040
152
P HMR003 Hemorrhagic Disease 53 0.040
153
GSG001 Gas Gangrene 53 0.040
154
P ACT008 Actinic Keratosis 53 0.040
155
GST023 Gastric Ulcer 53 0.040
156
c PSR017 Psoriasis 2 53 0.040
157
PRP016 Paraplegia 52 0.040
158
c VRL010 Viral Hepatitis 52 0.040
159
ACR041 Acromelic Frontonasal Dysostosis 52 0.040
160
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.040
161
PST011 Pustulosis of Palm and Sole 52 0.040
162
P DDN001 Duodenal Ulcer 52 0.040
163
c PSR023 Psoriasis 1 52 0.040
164
PPT001 Peptic Esophagitis 52 0.040
165
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.040
166
NTR018 Neutrophilia, Hereditary 52 0.040
167
LMY002 Leiomyoma 52 0.040
168
PNG002 Pain Agnosia 51 0.040
169
KRT009 Keratosis 51 0.040
170
CLC001 Calciphylaxis 51 0.040
171
THR016 Thrombophlebitis 51 0.040
172
TRM010 Traumatic Brain Injury 51 0.040
173
CHR005 Chorioamnionitis 51 0.040
174
P ECL001 Eclampsia 50 0.040
175
HPT014 Hepatorenal Syndrome 50 0.040
176
c INF145 Infantile Liver Failure Syndrome 1 50 0.040
177
ECT026 Ectopic Pregnancy 50 0.040
178
HRT011 Heart Septal Defect 50 0.040
179
HYP080 Hypogonadism 50 0.040
180
P END046 Endometritis 49 0.040
181
PLM041 Pulmonary Valve Stenosis 49 0.040
182
BRN071 Brain Injury 49 0.040
183
PLC007 Placental Abruption 48 0.040
184
SND002 Sneddon Syndrome 48 0.040
185
ANT018 Anthracosis 48 0.040
186
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.040
187
P UTR058 Uterine Anomalies 47 0.040
188
c PSR032 Psoriasis 11 47 0.040
189
ACT084 Acute Stress Disorder 47 0.040
190
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.040
191
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.040
192
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.040
193
TST044 Testicular Torsion 47 0.040
194
ASP004 Asphyxia Neonatorum 46 0.040
195
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.040
196
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.040
197
VGN019 Vaginal Discharge 46 0.040
198
PLC001 Placenta Accreta 46 0.040
199
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.040
200
URT010 Ureteral Obstruction 45 0.040
201
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.040
202
MYF001 Myofibroma 45 0.040
203
SBC016 Subacute Delirium 44 0.040
204
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.040
205
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.040
206
CRB090 Cerebral Hypoxia 44 0.040
207
URT037 Urethral Stricture 43 0.040
208
DRG002 Drug-Induced Hepatitis 43 0.040
209
CYT002 Cytokine Deficiency 42 0.040
210
c PSR028 Psoriasis 7 42 0.040
211
ATX019 Ataxia with Vitamin E Deficiency 42 0.040
212
LCN001 Lice Infestation 42 0.040
213
LCH016 Lichen Sclerosus Et Atrophicus 41 0.040
214
c PSR018 Psoriasis 13 41 0.040
215
c MCR112 Microvascular Complications of Diabetes 2 41 0.040
216
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.040
217
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.040
218
PLC009 Placenta Praevia 39 0.040
219
P PRC031 Preeclampsia/eclampsia 1 38 0.040
220
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.040
221
P CRB088 Cerebral Atrophy 37 0.040
223
HRW001 Hair Whorl 36 0.040
224
LVD003 Livedoid Vasculitis 36 0.040
225
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 36 0.040
227
MLG163 Malignant Tumor of Penis 29 0.040
228
BLT003 Blue Toe Syndrome 29 0.040
229
SBM005 Submucous Uterine Fibroid 29 0.040
230
ART030 Aortic Arch Interruption 29 0.040
231
VSC004 Vasculogenic Impotence 28 0.040
232
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.040
233
MMM002 Mammary-Digital-Nail Syndrome 23 0.040
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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