Search results for Brimonidine

174 hits were found for Brimonidine

# Family MCID Name MIFTS Score
1
OCL006 Ocular Hypertension 53 0.757
2
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.713
3
P OPN001 Open-Angle Glaucoma 49 0.697
4
c HYP595 Hypertension, Essential 84 0.503
5
c GLC092 Glaucoma, Primary Open Angle 62 0.490
7
RSC001 Rosacea 54 0.363
8
P OPT006 Optic Nerve Disease 60 0.280
9
P CNJ013 Conjunctivitis 65 0.226
10
KRT013 Keratolytic Winter Erythema 46 0.226
11
P NRP001 Neuropathy 56 0.198
13
P UVT001 Uveitis 57 0.177
14
ALL009 Allergic Conjunctivitis 50 0.177
15
P CTR002 Cataract 60 0.172
16
c GLC078 Glaucoma 1, Open Angle, F 35 0.160
17
P MCR115 Microvascular Complications of Diabetes 5 66 0.154
18
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.154
19
IRD001 Iridocyclitis 53 0.154
20
DWN001 Down Syndrome 70 0.147
21
ADL002 Adult Syndrome 70 0.147
22
EYD002 Eye Disease 58 0.147
23
GLC084 Glaucoma, Normal Tension 46 0.147
24
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.140
25
MCL006 Macular Retinal Edema 55 0.140
26
TLN003 Telangiectasis 52 0.140
27
DRM006 Dermatitis 61 0.133
28
P SJG008 Sjogren Syndrome 61 0.133
29
CNT047 Contact Dermatitis 58 0.133
30
AYM001 Ayme-Gripp Syndrome 57 0.133
31
RTN020 Retinal Vascular Disease 46 0.133
32
c FNC043 Fanconi Anemia, Complementation Group E 62 0.125
33
ISC004 Ischemia 58 0.125
34
ALL010 Allergic Contact Dermatitis 56 0.125
35
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.117
36
KRT006 Keratoconjunctivitis 53 0.117
37
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.117
38
P GRF003 Graft-Versus-Host Disease 72 0.109
39
EXF001 Exfoliation Syndrome 56 0.109
40
RTN003 Retinal Ischemia 50 0.109
41
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.109
42
KRT001 Keratoconjunctivitis Sicca 49 0.109
43
DRY001 Dry Eye Syndrome 47 0.109
44
ACT011 Acute Contagious Conjunctivitis 40 0.109
45
HML018 Homologous Wasting Disease 22 0.109
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.099
47
P RTN008 Retinitis Pigmentosa 79 0.099
48
P CNR004 Cone-Rod Dystrophy 2 73 0.099
49
c LTN004 Late-Onset Retinal Degeneration 59 0.099
50
P LBR014 Leber Congenital Amaurosis 4 56 0.099
51
P MYP006 Myopia 55 0.099
52
DBT006 Diabetic Macular Edema 48 0.099
53
RTN023 Retinitis 46 0.099
54
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.099
55
P CRN026 Corneal Edema 43 0.099
56
NRR001 Neuroretinitis 42 0.099
57
PRM024 Primary Angle-Closure Glaucoma 40 0.099
58
c NRF023 Neurofibromatosis, Type Ii 80 0.089
59
RTN017 Retinal Detachment 61 0.089
60
P PTS002 Ptosis 53 0.089
61
P RTN018 Retinal Disease 53 0.089
62
47X002 47,xyy 49 0.089
63
c CHR086 Chronic Conjunctivitis 45 0.089
64
RFR003 Refractive Error 43 0.089
65
TRP009 Triple X Syndrome 42 0.089
66
PRS025 Presbyopia 38 0.089
67
c CHR054 Chronic Closed-Angle Glaucoma 32 0.089
68
OCL004 Ocular Hyperemia 26 0.089
69
CHR158 Charles Bonnet Syndrome 23 0.089
70
P PRS040 Prostate Cancer 97 0.077
71
STR067 Stroke, Ischemic 81 0.077
72
CRB039 Cerebrovascular Disease 67 0.077
73
P TRN020 Turner Syndrome 67 0.077
74
c RHB024 Rhabdomyosarcoma 2 67 0.077
75
c MCR129 Microvascular Complications of Diabetes 1 66 0.077
76
ALL026 Allergic Hypersensitivity Disease 62 0.077
77
P HMN010 Hemangioma 61 0.077
78
CHL014 Cholera 59 0.077
79
P STR020 Strabismus 55 0.077
80
ACR041 Acromelic Frontonasal Dysostosis 52 0.077
81
BLP005 Blepharitis 50 0.077
82
c CPL013 Capillary Malformations, Congenital 50 0.077
83
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.077
84
KHN001 Kuhnt-Junius Degeneration 47 0.077
85
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.077
86
P RTN014 Retinal Artery Occlusion 47 0.077
87
c NLD009 Nail Disorder, Nonsyndromic Congenital, 1 45 0.077
88
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.077
89
c PRM038 Primary Agammaglobulinemia 44 0.077
90
P CRN024 Corneal Disease 44 0.077
91
ATX019 Ataxia with Vitamin E Deficiency 42 0.077
92
MCH006 Mechanical Strabismus 42 0.077
93
RDN001 Reading Disorder 40 0.077
94
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.077
95
BRN026 Branch Retinal Artery Occlusion 40 0.077
96
c CHR682 Chronic Bilirubin Encephalopathy 39 0.077
97
c PRS136 Prostate Cancer, Hereditary, 6 33 0.077
98
c PRS130 Prostate Cancer, Hereditary, 8 32 0.077
99
P MLT020 Multiple Sclerosis 72 0.063
100
KRT019 Keratitis, Hereditary 65 0.063
101
P DBT009 Diabetes Mellitus 64 0.063
102
P DRM010 Dermatomyositis 61 0.063
103
HYP066 Hyperglycemia 61 0.063
104
c DWL002 Dowling-Degos Disease 1 58 0.063
105
P EXN002 Exanthem 57 0.063
106
HYP266 Hypoxia 57 0.063
107
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.063
108
P LCH002 Lichen Planus 53 0.063
109
P RTN016 Retinal Degeneration 53 0.063
110
P RTN022 Retinal Vein Occlusion 53 0.063
111
NRT004 Neuritis 52 0.063
112
P PLN008 Peeling Skin Syndrome 43 0.063
113
49X006 49, Xxxxy Syndrome 41 0.063
114
MCL003 Macular Holes 40 0.063
115
OCL010 Ocular Hypotension 39 0.063
116
P HRD217 Hereditary Optic Neuropathy 36 0.063
117
PST092 Posttransplant Acute Limbic Encephalitis 29 0.063
118
ANS021 Anisocoria 27 0.063
119
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.063
120
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.044
121
P KDN018 Kidney Disease 72 0.044
122
c EXD008 Exudative Vitreoretinopathy 1 71 0.044
123
c HMP029 Hemophilia a 67 0.044
124
PRT037 Pertussis 65 0.044
125
SKN016 Skin Disease 63 0.044
126
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.044
127
NTH001 Netherton Syndrome 60 0.044
128
SQM006 Squamous Cell Carcinoma 60 0.044
129
LBR030 Leber Optic Atrophy 60 0.044
130
P SNS001 Sensorineural Hearing Loss 60 0.044
131
HYD002 Hydronephrosis 60 0.044
132
c ACT071 Acute Kidney Failure 60 0.044
133
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.044
134
P OPT009 Optic Neuritis 57 0.044
135
P RHN004 Rhinitis 57 0.044
136
ORP003 Oropharynx Cancer 55 0.044
137
PPL022 Papilloma 54 0.044
138
NVS001 Neovascular Glaucoma 53 0.044
139
INT075 Intracranial Hypertension 53 0.044
140
P HMP007 Hemophilia 51 0.044
141
OCL069 Ocular Motor Apraxia 51 0.044
142
FCT001 Factor Viii Deficiency 51 0.044
143
P PRC012 Pericardial Effusion 51 0.044
144
TNG007 Tongue Carcinoma 51 0.044
145
LNT004 Lentigines 50 0.044
146
NTR046 Neutrophil Migration 50 0.044
147
HMP001 Hemopericardium 48 0.044
148
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.044
149
VRN004 Vernal Keratoconjunctivitis 47 0.044
150
KRT008 Keratopathy 47 0.044
151
CRN027 Corneal Neovascularization 47 0.044
152
AST006 Astigmatism 47 0.044
153
P VTR007 Vitreoretinopathy 46 0.044
154
BCK003 Background Diabetic Retinopathy 46 0.044
155
SQM002 Squamous Cell Papilloma 46 0.044
156
P HRN001 Horner's Syndrome 45 0.044
157
HMR002 Hemarthrosis 45 0.044
158
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.044
159
c JVN003 Juvenile Xanthogranuloma 44 0.044
160
TNS004 Tonsil Cancer 44 0.044
161
IRT001 Iritis 44 0.044
162
P HYP265 Hypotonia 43 0.044
163
P ECT005 Ectropion 42 0.044
164
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 41 0.044
165
c MCR112 Microvascular Complications of Diabetes 2 41 0.044
166
48X005 48,xyyy 39 0.044
167
ALL014 Allergic Encephalomyelitis 38 0.044
168
HYP264 Hypertonia 38 0.044
169
PPL019 Papillary Conjunctivitis 37 0.044
171
ART110 Arteritic Anterior Ischemic Optic Neuropathy 33 0.044
172
BLP006 Blepharoconjunctivitis 31 0.044
173
FNT004 Fainting 30 0.044
174
CCT001 Cicatricial Ectropion 25 0.044
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