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Search results for Brinzolamide

124 hits were found for Brinzolamide

# Family MCID Name MIFTS Score
1
INT323 Intraocular Pressure Quantitative Trait Locus 64 29.618
2
P OPN001 Open-Angle Glaucoma 55 29.088
3
OCL006 Ocular Hypertension 53 28.023
4
c GLC092 Glaucoma, Primary Open Angle 62 18.574
5
c HYP595 Hypertension, Essential 85 9.054
7
P CTR002 Cataract 60 5.825
8
PTH003 Pathologic Nystagmus 52 5.410
9
CMP034 Complete Androgen Insensitivity Syndrome 55 5.277
10
P ANR048 Aniridia 1 64 4.988
11
GLC084 Glaucoma, Normal Tension 45 4.843
12
OCL004 Ocular Hyperemia 23 4.661
13
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 4.427
14
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.117
15
P OPT006 Optic Nerve Disease 58 3.766
16
P CNJ013 Conjunctivitis 66 3.691
17
P EYD002 Eye Disease 57 3.571
18
XLN247 X-Linked Congenital Retinoschisis 20 3.535
19
P JVN042 Juvenile Retinoschisis 39 3.535
20
NRR001 Neuroretinitis 42 3.501
21
RTN023 Retinitis 46 3.501
22
MCL006 Macular Retinal Edema 57 3.044
23
EXF001 Exfoliation Syndrome 56 2.969
24
KRT008 Keratopathy 46 2.948
25
MTB004 Metabolic Acidosis 48 2.847
26
P HDC001 Headache 57 2.559
27
KRT019 Keratitis, Hereditary 66 2.373
28
P MYP006 Myopia 56 2.347
29
P RTN008 Retinitis Pigmentosa 80 2.339
30
c PRM032 Primary Congenital Glaucoma 41 2.339
31
RHB024 Rhabdomyosarcoma 2 67 2.306
32
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 2.306
33
P CRN026 Corneal Edema 42 2.227
34
47X002 47,xyy 48 2.217
35
SNL007 Senile Cataract 40 2.217
36
DWN001 Down Syndrome 70 2.042
37
P TRN020 Turner Syndrome 67 2.042
38
LBR036 Leber Plus Disease 66 1.938
39
END072 Endotheliitis 36 1.799
40
AYM001 Ayme-Gripp Syndrome 56 1.799
41
c GLC114 Glaucoma, Primary Closed-Angle 36 1.799
42
ANT039 Antisynthetase Syndrome 55 1.799
43
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 1.799
44
c CHR054 Chronic Closed-Angle Glaucoma 33 1.799
45
PRM024 Primary Angle-Closure Glaucoma 39 1.799
46
SPN033 Spontaneous Ocular Nystagmus 25 1.799
47
CNT060 Central Serous Chorioretinopathy 38 1.799
48
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.772
49
c DWL002 Dowling-Degos Disease 1 58 1.772
50
SPR019 Superficial Keratitis 22 1.772
51
MCR013 Microphthalmia 60 1.772
52
P CNG024 Congenital Nystagmus 36 1.772
53
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 1.772
54
HYP742 Hyperpigmentation of Eyelids 11 1.574
55
ATS010 Autosomal Recessive Disease 42 1.317
56
SVR097 Severe Cutaneous Adverse Reaction 69 1.317
57
GYR004 Gyrate Atrophy of Choroid and Retina 58 1.317
58
ERY066 Erythema Multiforme Major 29 1.317
59
P NGH001 Night Blindness 52 1.317
60
ERY003 Erythema Multiforme 56 1.317
61
P OCL002 Oculocutaneous Albinism 59 1.241
63
ALB002 Albinism 47 1.241
64
P PLN008 Peeling Skin Syndrome 43 1.213
65
c INH030 Inherited Retinal Disorder 28 1.196
66
FND002 Fundus Dystrophy 55 1.196
67
ADL002 Adult Syndrome 70 1.162
68
c PST005 Posterior Uveitis 54 1.162
69
AMD002 Amed Syndrome, Digenic 37 1.162
70
CHR008 Choroiditis 48 1.162
71
AND005 Androgen Insensitivity Syndrome, Mild 21 1.162
72
RTN003 Retinal Ischemia 49 1.075
73
OPT001 Optic Disk Drusen 34 1.075
74
RTN017 Retinal Detachment 60 0.878
75
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.878
76
P EXN002 Exanthem 58 0.878
77
c MCR115 Microvascular Complications of Diabetes 5 65 0.878
78
EXP004 Exophthalmos 51 0.878
79
BLP005 Blepharitis 50 0.878
80
P TRM003 Tremor 48 0.878
81
P CRN024 Corneal Disease 44 0.878
82
P UVT001 Uveitis 57 0.878
83
ISC004 Ischemia 61 0.878
84
ALL010 Allergic Contact Dermatitis 56 0.697
85
CNT047 Contact Dermatitis 57 0.697
86
DRM006 Dermatitis 62 0.697
87
ANG004 Angioid Streaks 40 0.621
88
P CNR004 Cone-Rod Dystrophy 2 74 0.621
89
ANS021 Anisocoria 25 0.621
90
MLR004 Malaria 80 0.621
91
P NNP021 Nanophthalmos 39 0.621
92
c CNR016 Cone-Rod Dystrophy 7 37 0.621
93
P MCR129 Microvascular Complications of Diabetes 1 68 0.621
94
ORB019 Orbital Margin, Hypoplasia of 20 0.621
95
MLD001 Melioidosis 67 0.621
96
CRD137 Cardiogenic Shock 56 0.621
97
PHC001 Phacolytic Glaucoma 22 0.621
98
P NRB001 Neuroblastoma 66 0.621
99
IRD001 Iridocyclitis 53 0.621
100
P SBR004 Seborrheic Dermatitis 44 0.621
101
P HML002 Hemolytic Anemia 62 0.621
102
DBT010 Diabetic Neuropathy 54 0.621
103
CLL003 Cellulitis 53 0.621
104
P GST044 Gastritis 55 0.621
105
NRM005 Neuromuscular Disease 63 0.621
106
P KRT007 Keratoconus 50 0.621
107
c MCR112 Microvascular Complications of Diabetes 2 42 0.621
108
CNJ004 Conjunctival Pigmentation 19 0.621
109
CRT013 Carotid Stenosis 51 0.621
110
RTN020 Retinal Vascular Disease 46 0.621
111
CNT016 Central Retinal Vein Occlusion 54 0.621
112
BLL004 Bullous Keratopathy 48 0.621
113
CHR077 Chorioretinal Scar 28 0.621
114
CYS010 Cystinosis 62 0.621
115
P BLP003 Blepharospasm 46 0.621
116
LNS001 Lens Subluxation 39 0.621
117
P SCL015 Scleritis 48 0.621
118
P AXN002 Axenfeld-Rieger Syndrome 63 0.621
119
NVS001 Neovascular Glaucoma 52 0.621
120
P RTN022 Retinal Vein Occlusion 54 0.621
121
CLR033 Color Vision Deficiency 40 0.621
122
P HYP265 Hypotonia 42 0.621
123
P FNG006 Feingold Syndrome 1 62 0.576
124
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 0.576
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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