Search results for Danazol

144 hits were found for Danazol

# Family MCID Name MIFTS Score
1
P END044 Endometriosis 71 0.257
2
P ANG015 Angioedema 57 0.202
3
c HRD002 Hereditary Angioedema 59 0.185
4
APL001 Aplastic Anemia 74 0.153
5
P THR014 Thrombocytopenia 65 0.153
6
PRP030 Purpura 61 0.146
7
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.139
8
BLD053 Blood Platelet Disease 45 0.131
9
CPL005 Capillary Disease 38 0.131
10
P BLD051 Blood Coagulation Disease 38 0.131
11
THR024 Thrombosis 61 0.122
12
P INF032 Infertility 59 0.122
13
P PLM036 Pulmonary Fibrosis 68 0.113
14
ATM095 Autoimmune Disease 66 0.113
15
P HMR003 Hemorrhagic Disease 61 0.113
16
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.113
17
P MYL005 Myelofibrosis 75 0.103
18
MYL009 Myelodysplastic Syndrome 75 0.103
19
P DYS007 Dyskeratosis Congenita 68 0.103
20
BRS051 Breast Disease 67 0.103
21
ANT009 Antithrombin Iii Deficiency 58 0.103
22
ADN027 Adenomyosis 57 0.103
23
PNC001 Pancytopenia 50 0.103
24
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.103
25
c MCL042 Macular Degeneration, Age-Related, 1 79 0.092
26
END057 Endometrial Cancer 76 0.092
27
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.092
28
RTN018 Retinal Disease 56 0.092
29
P RTN016 Retinal Degeneration 56 0.092
30
HMG002 Hemoglobinuria 52 0.092
31
MCL006 Macular Retinal Edema 51 0.092
32
DBT006 Diabetic Macular Edema 49 0.092
33
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.092
34
CYS001 Cystic Fibrosis 85 0.080
35
P FNC027 Fanconi Anemia, Complementation Group a 78 0.080
36
P LVR013 Liver Disease 76 0.080
37
PLY001 Polycythemia Vera 75 0.080
38
P LKM002 Leukemia 75 0.080
39
P ESS003 Essential Thrombocythemia 71 0.080
40
P LPS004 Lupus Erythematosus 69 0.080
41
P KDN018 Kidney Disease 69 0.080
42
LNG099 Lung Disease 67 0.080
43
MYL031 Myeloproliferative Neoplasm 64 0.080
44
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.080
45
ADN018 Adenoma 63 0.080
46
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.080
47
c ACT073 Acute Leukemia 61 0.080
48
P PLY018 Polycythemia 60 0.080
49
URT039 Urticaria 59 0.080
50
PNC034 Pancreas Disease 59 0.080
51
P OVR049 Ovarian Disease 58 0.080
52
TRP002 Tropical Spastic Paraparesis 58 0.080
53
P THR015 Thrombophilia 58 0.080
54
URN009 Urinary System Disease 58 0.080
55
P UTR058 Uterine Anomalies 55 0.080
56
THR004 Thrombocytosis 55 0.080
57
SPS003 Spastic Diplegia 55 0.080
58
P FNC004 Fanconi Syndrome 54 0.080
59
c PRM012 Primary Polycythemia 53 0.080
60
P OVR046 Ovarian Cyst 52 0.080
61
HPT082 Hepatic Adenomas, Familial 52 0.080
62
UTR033 Uterine Corpus Cancer 51 0.080
63
PRT014 Protein S Deficiency 47 0.080
64
c ACQ012 Acquired Angioedema 45 0.080
65
HPT067 Hepatocellular Adenoma 43 0.080
66
PSD009 Pseudohermaphroditism 42 0.080
67
SPS057 Spasticity 41 0.080
68
FXF002 Fox-Fordyce Disease 40 0.080
69
MYL057 Myelopathy, Htlv-1-Associated 38 0.080
70
SPS019 Spastic Paraparesis 33 0.080
71
GND003 Gonadal Disease 32 0.080
72
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 29 0.080
73
INH011 Inherited Bone Marrow Failure Syndromes 28 0.080
74
c PRM200 Primary Fanconi Syndrome 27 0.080
75
RNL021 Renal Tubular Transport Disease 27 0.080
76
P BRS047 Breast Cancer 100 0.065
77
c SYS001 Systemic Lupus Erythematosus 86 0.065
78
P NRV007 Nervous System Disease 75 0.065
79
DRM006 Dermatitis 67 0.065
80
P MCR115 Microvascular Complications of Diabetes 5 66 0.065
81
VSC011 Vasculitis 66 0.065
82
SVR097 Severe Cutaneous Adverse Reaction 64 0.065
83
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.065
84
FCT003 Factor X Deficiency 58 0.065
85
PNM008 Pneumothorax 57 0.065
86
HDC001 Headache 55 0.065
87
INT303 Intracranial Hypertension, Idiopathic 49 0.065
88
PRM020 Premenstrual Tension 49 0.065
89
PRT011 Protein C Deficiency 48 0.065
90
P SDR003 Sideroblastic Anemia 43 0.065
91
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.065
92
C1N001 C1 Inhibitor Deficiency 40 0.065
93
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 39 0.065
94
GGN002 Gigantism 36 0.065
95
CHL035 Cholinergic Urticaria 29 0.065
96
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.065
97
CTM001 Catamenial Pneumothorax 18 0.065
98
P LNG032 Lung Cancer 99 0.046
99
P HPT023 Hepatocellular Carcinoma 94 0.046
100
P HPT021 Hepatitis 75 0.046
101
MXD005 Mixed Connective Tissue Disease 66 0.046
102
CNN005 Connective Tissue Disease 65 0.046
103
P PNC044 Pancreatitis 64 0.046
104
HMT002 Hematologic Cancer 64 0.046
105
P UVT001 Uveitis 61 0.046
106
c THR092 Thrombophilia Due to Thrombin Defect 61 0.046
107
P DRR001 Diarrhea 60 0.046
108
VGN023 Vaginitis 59 0.046
109
LMY002 Leiomyoma 58 0.046
110
MYM001 Myoma 56 0.046
111
DSS009 Disseminated Intravascular Coagulation 56 0.046
112
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.046
113
CRD223 Cardiac Arrhythmia 52 0.046
114
BNM001 Bone Marrow Cancer 52 0.046
115
P MGL001 Megaloblastic Anemia 52 0.046
116
PRR002 Pure Red-Cell Aplasia 52 0.046
117
P PRC019 Precocious Puberty 52 0.046
118
PRP007 Priapism 49 0.046
119
DSC009 Discoid Lupus Erythematosus 48 0.046
120
c ANG068 Angioedema, Hereditary, Type I 48 0.046
121
GYN001 Gynecomastia 47 0.046
122
LYM052 Lymphomatoid Papulosis 45 0.046
123
SPL018 Splenomegaly 45 0.046
124
LPD014 Lipodermatosclerosis 42 0.046
125
CRB009 Cerebritis 41 0.046
126
MCR019 Microglandular Adenosis 39 0.046
127
END045 Endometriosis of Uterus 38 0.046
128
CRT004 Carotid Artery Thrombosis 37 0.046
129
c BLD140 Blood Group, I System 37 0.046
130
CLD011 Cold Urticaria 36 0.046
131
LVD002 Livedoid Vasculopathy 36 0.046
132
PLS002 Peliosis Hepatis 36 0.046
133
MNG003 Mungan Syndrome 34 0.046
134
CHR463 Chronic Actinic Dermatitis 34 0.046
135
PRX008 Paroxysmal Cold Hemoglobinuria 30 0.046
136
HYP029 Hyperthyroxinemia 27 0.046
137
INF021 Infant Gynecomastia 25 0.046
138
HYP677 Hyperthyroxinemia, Familial Dysalbuminemic 25 0.046
139
ACQ031 Acquired Idiopathic Sideroblastic Anemia 24 0.046
140
HRY002 Hairy Tongue 22 0.046
141
THR116 Thrombocytopenia, Cyclic 22 0.046
142
ATM026 Autoimmune Progesterone Dermatitis 19 0.046
143
BLC017 Black Hairy Tongue 19 0.046
144
P ACQ015 Acquired Hypoprothrombinemia 14 0.046
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