Search results for Danazol

219 hits were found for Danazol

# Family MCID Name MIFTS Score
1
P END044 Endometriosis 66 0.191
2
P ANG015 Angioedema 52 0.169
3
c HRD002 Hereditary Angioedema 55 0.155
4
P APL001 Aplastic Anemia 75 0.113
5
P THR014 Thrombocytopenia 64 0.098
6
PRP030 Purpura 58 0.098
7
THR024 Thrombosis 57 0.098
8
P INF032 Infertility 59 0.089
9
ADN027 Adenomyosis 46 0.089
10
MYL009 Myelodysplastic Syndrome 73 0.080
11
P PLM036 Pulmonary Fibrosis 71 0.080
12
DFC004 Deficiency Anemia 64 0.080
13
P DYS007 Dyskeratosis Congenita 63 0.080
14
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.080
15
HMG002 Hemoglobinuria 48 0.080
16
BLD053 Blood Platelet Disease 46 0.080
17
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 0.080
18
P BLD051 Blood Coagulation Disease 42 0.080
19
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 0.080
20
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.080
21
c PRM225 Primary Thrombocytopenia 39 0.080
22
CPL005 Capillary Disease 36 0.080
23
c THR037 Thrombocytopenia 2 35 0.080
24
VSC008 Vascular Hemostatic Disease 30 0.080
25
MRG013 Mirage Syndrome 29 0.080
26
END057 Endometrial Cancer 75 0.069
27
P MYL005 Myelofibrosis 67 0.069
28
SKN016 Skin Disease 66 0.069
29
P LPS004 Lupus Erythematosus 64 0.069
30
HMT002 Hematologic Cancer 64 0.069
31
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.069
32
ADN018 Adenoma 58 0.069
33
BNC003 Bone Cancer 58 0.069
34
URT039 Urticaria 57 0.069
35
P HMR003 Hemorrhagic Disease 57 0.069
36
TRP002 Tropical Spastic Paraparesis 55 0.069
37
THR100 Thrombocytopenic Purpura, Autoimmune 54 0.069
38
PRT014 Protein S Deficiency 53 0.069
39
BNM001 Bone Marrow Cancer 51 0.069
40
FML038 Female Reproductive Organ Cancer 50 0.069
41
FML039 Female Reproductive System Disease 48 0.069
42
PHY002 Physical Disorder 43 0.069
43
SPS057 Spasticity 42 0.069
44
HPT067 Hepatocellular Adenoma 42 0.069
45
SPS019 Spastic Paraparesis 41 0.069
46
PSD009 Pseudohermaphroditism 40 0.069
47
c ACQ012 Acquired Angioedema 39 0.069
48
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.069
49
P OCY001 Oocyte Maturation Defect 38 0.069
50
MCR019 Microglandular Adenosis 37 0.069
51
BNS002 Bone Structure Disease 37 0.069
52
ATM012 Autoimmune Disease of Blood 35 0.069
53
PRM243 Primary Bone Cancer 29 0.069
54
c THR048 Thrombocytopenia 4 26 0.069
55
ATM053 Autoimmune Disease 2 16 0.069
56
ATM055 Autoimmune Disease 4 15 0.069
57
P BRS047 Breast Cancer 100 0.056
58
c SYS001 Systemic Lupus Erythematosus 86 0.056
59
CYS001 Cystic Fibrosis 83 0.056
60
P OVR042 Ovarian Cancer 76 0.056
61
c MCL042 Macular Degeneration, Age-Related, 1 73 0.056
62
c FNC027 Fanconi Anemia, Complementation Group a 71 0.056
63
P ESS003 Essential Thrombocythemia 70 0.056
64
DRM006 Dermatitis 66 0.056
65
P KDN017 Kidney Cancer 65 0.056
66
LNG099 Lung Disease 64 0.056
67
PLY125 Polycythemia Vera, Somatic 63 0.056
68
VSC011 Vasculitis 62 0.056
69
FCT003 Factor X Deficiency 61 0.056
70
BRS051 Breast Disease 61 0.056
71
EYD002 Eye Disease 61 0.056
72
c ACT073 Acute Leukemia 60 0.056
73
OCL009 Ocular Cancer 59 0.056
74
P THR015 Thrombophilia 59 0.056
75
WLL006 Wells Syndrome 59 0.056
76
MYL031 Myeloproliferative Neoplasm 58 0.056
77
P PLY018 Polycythemia 58 0.056
78
PNC034 Pancreas Disease 58 0.056
79
CHL071 Child Syndrome 58 0.056
80
c MCR115 Microvascular Complications of Diabetes 5 57 0.056
81
ETH011 Ethylmalonic Encephalopathy 56 0.056
82
PLY023 Polycystic Liver Disease 56 0.056
83
P OVR049 Ovarian Disease 56 0.056
84
THR004 Thrombocytosis 55 0.056
85
MLN007 Male Infertility 55 0.056
86
P RTN016 Retinal Degeneration 54 0.056
87
c PND001 Pain Disorder 54 0.056
88
KDS001 Kid Syndrome 53 0.056
89
PNM008 Pneumothorax 53 0.056
90
RTN018 Retinal Disease 53 0.056
91
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.056
92
P PNC001 Pancytopenia 52 0.056
93
PRT011 Protein C Deficiency 52 0.056
94
P APL006 Aplasia Cutis Congenita 52 0.056
95
c PRM012 Primary Polycythemia 52 0.056
96
P OVR046 Ovarian Cyst 51 0.056
97
P RNL028 Renal Tubular Dysgenesis 51 0.056
98
UTR033 Uterine Corpus Cancer 49 0.056
99
c INH020 Inherited Metabolic Disorder 49 0.056
100
P FNC004 Fanconi Syndrome 49 0.056
101
CNG028 Congenital Hypoplastic Anemia 48 0.056
102
DBT006 Diabetic Macular Edema 47 0.056
103
ADR038 Adermatoglyphia 46 0.056
104
INC022 Inclusion-Cell Disease 46 0.056
105
EST007 Estrogen Resistance 46 0.056
106
ALN001 Aland Island Eye Disease 45 0.056
107
GDS001 Good Syndrome 44 0.056
108
DYS164 Dyskeratosis Congenita, X-Linked 44 0.056
109
SKN023 Skin Tag 44 0.056
110
c HMG003 Hemoglobin E Disease 44 0.056
111
PRM020 Premenstrual Tension 44 0.056
112
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.056
113
MLR006 Male Reproductive Organ Cancer 43 0.056
114
ACT058 Active Peptic Ulcer Disease 43 0.056
115
c ACR061 Aicardi-Goutieres Syndrome 1, Dominant and Recessive 43 0.056
116
RNL025 Renal Hypoplasia 42 0.056
117
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.056
118
RPR002 Reproductive System Disease 41 0.056
119
CYS036 Cystinosis, Nephropathic 41 0.056
120
P SDR003 Sideroblastic Anemia 40 0.056
121
GND003 Gonadal Disease 39 0.056
122
MCL006 Macular Retinal Edema 38 0.056
123
P UTR038 Uterine Disease 37 0.056
124
BLD054 Blood Protein Disease 37 0.056
125
c PNC106 Pancreatic Agenesis 1 37 0.056
126
FXF002 Fox-Fordyce Disease 36 0.056
127
MCL027 Macular Dystrophy, Dominant Cystoid 36 0.056
128
MLR007 Male Reproductive System Disease 34 0.056
129
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.056
130
P XLN007 X-Linked Disease 34 0.056
131
c MCL040 Macular Degeneration, Age-Related, 3 33 0.056
132
GGN002 Gigantism 32 0.056
133
RNL021 Renal Tubular Transport Disease 32 0.056
134
P CHR084 Chromosomal Disease 32 0.056
135
c MCL043 Macular Degeneration, Age-Related, 2 32 0.056
136
P ACT080 Acute Pulmonary Heart Disease 31 0.056
137
c THR090 Thrombocythemia 1 30 0.056
138
EYD001 Eye Degenerative Disease 30 0.056
139
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 29 0.056
140
CHL035 Cholinergic Urticaria 29 0.056
141
BNM010 Bone Marrow Failure Syndrome 1 29 0.056
142
PHY001 Physiological Polycythemia 28 0.056
143
INH011 Inherited Bone Marrow Failure Syndromes 27 0.056
144
END080 Endometrial Disease 27 0.056
145
P MCL035 Macular Dystrophy, Retinal, 2 25 0.056
146
c ATM007 Autoimmune Disease of Central Nervous System 25 0.056
147
BNM011 Bone Marrow Failure Syndrome 2 25 0.056
148
ATM052 Autoimmune Disease 1 25 0.056
149
c PRM200 Primary Fanconi Syndrome 24 0.056
150
ATM059 Autoimmune Disease 6 22 0.056
151
P CRN178 Coronary Heart Disease 6 21 0.056
152
c THR110 Thrombocytopenia 6 20 0.056
153
CTM001 Catamenial Pneumothorax 16 0.056
154
c MCL026 Macular Dystrophy, Retinal, 3 16 0.056
155
ATM054 Autoimmune Disease 3 15 0.056
156
MLG118 Malignancy Diagnosed During Pregnancy 15 0.056
157
RNL109 Renal Hypoplasia, Bilateral 14 0.056
158
CLL008 Cellular Phase Chronic Idiopathic Myelofibrosis 13 0.056
159
P LNG032 Lung Cancer 95 0.040
160
P HPT023 Hepatocellular Carcinoma 92 0.040
161
P NRV007 Nervous System Disease 71 0.040
162
P HPT021 Hepatitis 69 0.040
163
PCK002 Pick Disease 68 0.040
164
ATH003 Atherosclerosis 65 0.040
165
CNN005 Connective Tissue Disease 62 0.040
166
MXD005 Mixed Connective Tissue Disease 62 0.040
167
MTH009 Mouth Disease 61 0.040
168
P PNC044 Pancreatitis 61 0.040
169
P DRR001 Diarrhea 60 0.040
170
P ORL007 Oral Cavity Cancer 59 0.040
171
P UVT001 Uveitis 58 0.040
172
ORL011 Oral Cancer 56 0.040
173
HDC001 Headache 54 0.040
174
P HYP620 Hypoprothrombinemia 54 0.040
175
LMY002 Leiomyoma 54 0.040
176
P SPS003 Spastic Diplegia 52 0.040
177
MYM001 Myoma 52 0.040
178
P PRC019 Precocious Puberty 51 0.040
179
DSS009 Disseminated Intravascular Coagulation 51 0.040
180
MGL001 Megaloblastic Anemia 50 0.040
181
RTN020 Retinal Vascular Disease 48 0.040
182
GYN001 Gynecomastia 48 0.040
183
PRR002 Pure Red-Cell Aplasia 47 0.040
184
SPL012 Splenic Disease 46 0.040
185
PRP007 Priapism 46 0.040
186
DSC009 Discoid Lupus Erythematosus 45 0.040
187
ACD009 Acid-Labile Subunit, Deficiency of 45 0.040
188
SPL018 Splenomegaly 44 0.040
189
VGN023 Vaginitis 42 0.040
190
LYM052 Lymphomatoid Papulosis 41 0.040
191
CRT004 Carotid Artery Thrombosis 40 0.040
192
CRB009 Cerebritis 39 0.040
193
C1N001 C1 Inhibitor Deficiency 38 0.040
194
LPD014 Lipodermatosclerosis 37 0.040
195
CYC007 Cyclic Thrombocytopenia 37 0.040
196
c INH004 Inherited Blood Coagulation Disease 36 0.040
197
SPL011 Spleen Cancer 36 0.040
198
CLD011 Cold Urticaria 33 0.040
199
LNS003 Lens Disease 33 0.040
200
GLB003 Globe Disease 32 0.040
201
LVD002 Livedoid Vasculopathy 32 0.040
202
END045 Endometriosis of Uterus 32 0.040
203
PLS002 Peliosis Hepatis 31 0.040
204
CVT001 Cavitary Optic Disc Anomalies 31 0.040
205
CHR463 Chronic Actinic Dermatitis 31 0.040
206
c THR102 Thrombocytopenia 5 27 0.040
207
HYP029 Hyperthyroxinemia 26 0.040
208
PRX008 Paroxysmal Cold Hemoglobinuria 26 0.040
209
c THR086 Thrombocythemia 3 25 0.040
210
HRY002 Hairy Tongue 24 0.040
211
c MCL065 Macular Degeneration, Age-Related, 15 23 0.040
212
DBT018 Diabetic Mastopathy 22 0.040
213
ACQ031 Acquired Idiopathic Sideroblastic Anemia 21 0.040
214
BLC017 Black Hairy Tongue 18 0.040
215
c END071 Endometriosis 1 17 0.040
216
ATM026 Autoimmune Progesterone Dermatitis 17 0.040
217
P DYS070 Dysalbuminemic Hyperthyroxinemia 16 0.040
218
c ACQ015 Acquired Hypoprothrombinemia 14 0.040
219
HRD064 Hereditary Vascular Retinopathy 13 0.040
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