Search results for Dorzolamide

111 hits were found for Dorzolamide

# Family MCID Name MIFTS Score
1
P OPN001 Open-Angle Glaucoma 49 0.821
2
OCL006 Ocular Hypertension 53 0.691
3
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.634
4
c GLC092 Glaucoma, Primary Open Angle 62 0.606
5
c HYP595 Hypertension, Essential 84 0.352
7
MCL006 Macular Retinal Edema 55 0.272
8
P OPT006 Optic Nerve Disease 60 0.212
9
P MCR115 Microvascular Complications of Diabetes 5 66 0.185
10
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.185
11
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.178
12
P RTN008 Retinitis Pigmentosa 79 0.170
13
RTN023 Retinitis 46 0.170
14
NRR001 Neuroretinitis 42 0.170
15
c GLC078 Glaucoma 1, Open Angle, F 35 0.170
16
P CTR002 Cataract 60 0.163
18
ISC004 Ischemia 58 0.145
19
DBT006 Diabetic Macular Edema 48 0.145
20
CMP034 Complete Androgen Insensitivity Syndrome 46 0.145
21
DRM006 Dermatitis 61 0.136
22
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.136
23
EXF001 Exfoliation Syndrome 56 0.136
24
P RTN022 Retinal Vein Occlusion 53 0.136
25
KHN001 Kuhnt-Junius Degeneration 47 0.136
26
GLC084 Glaucoma, Normal Tension 46 0.136
27
P CNJ013 Conjunctivitis 65 0.126
28
CNT047 Contact Dermatitis 58 0.126
29
P NRP001 Neuropathy 56 0.126
30
DWN001 Down Syndrome 70 0.115
31
EYD002 Eye Disease 58 0.115
32
ENH001 Enhanced S-Cone Syndrome 57 0.115
33
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.115
34
MTB004 Metabolic Acidosis 50 0.115
35
OCL004 Ocular Hyperemia 26 0.115
36
ALL010 Allergic Contact Dermatitis 56 0.103
37
47X002 47,xyy 49 0.103
38
RTN020 Retinal Vascular Disease 46 0.103
39
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.089
40
P TRN020 Turner Syndrome 67 0.089
41
c MGR028 Migraine with or Without Aura 1 67 0.089
42
ALL026 Allergic Hypersensitivity Disease 62 0.089
43
RTN017 Retinal Detachment 61 0.089
44
c CNT016 Central Retinal Vein Occlusion 53 0.089
45
P RTN018 Retinal Disease 53 0.089
46
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.089
47
P CRN026 Corneal Edema 43 0.089
48
TRP009 Triple X Syndrome 42 0.089
49
49X006 49, Xxxxy Syndrome 41 0.089
50
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.089
51
RDN001 Reading Disorder 40 0.089
52
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.089
53
ADL002 Adult Syndrome 70 0.073
54
SVR097 Severe Cutaneous Adverse Reaction 69 0.073
55
P NSP012 Nasopharyngeal Carcinoma 66 0.073
56
KRT019 Keratitis, Hereditary 65 0.073
57
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.073
58
P USH001 Usher Syndrome 60 0.073
59
ERY003 Erythema Multiforme 58 0.073
60
c DWL002 Dowling-Degos Disease 1 58 0.073
61
P EXN002 Exanthem 57 0.073
62
P RTN016 Retinal Degeneration 53 0.073
63
KRT008 Keratopathy 47 0.073
64
P VTR007 Vitreoretinopathy 46 0.073
65
P PLN008 Peeling Skin Syndrome 43 0.073
66
MCL003 Macular Holes 40 0.073
67
48X005 48,xyyy 39 0.073
68
RTN002 Retinal Perforation 38 0.073
69
P NNP021 Nanophthalmos 36 0.073
70
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.073
71
BLP006 Blepharoconjunctivitis 31 0.073
72
ERY066 Erythema Multiforme Major 30 0.073
73
P BRS047 Breast Cancer 97 0.051
74
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.051
75
P KDN018 Kidney Disease 72 0.051
76
c CHR684 Chronic Kidney Disease 70 0.051
77
P THR014 Thrombocytopenia 67 0.051
78
P DMN002 Dementia 66 0.051
79
DPR016 Depression 63 0.051
80
P PSR002 Psoriasis 62 0.051
81
HYP066 Hyperglycemia 61 0.051
82
CHR081 Choroideremia 57 0.051
83
P UVT001 Uveitis 57 0.051
84
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.051
85
AYM001 Ayme-Gripp Syndrome 57 0.051
86
FND002 Fundus Dystrophy 55 0.051
87
NPH009 Nephrolithiasis 55 0.051
88
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.051
89
NVS001 Neovascular Glaucoma 53 0.051
90
PST011 Pustulosis of Palm and Sole 52 0.051
91
c INH030 Inherited Retinal Disorder 51 0.051
92
P HYP077 Hypertrichosis 50 0.051
93
ALL009 Allergic Conjunctivitis 50 0.051
94
RTN003 Retinal Ischemia 50 0.051
95
P NGH001 Night Blindness 48 0.051
96
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.051
97
P JVN008 Juvenile Glaucoma 47 0.051
98
FCH001 Fuchs' Endothelial Dystrophy 44 0.051
99
P CRN024 Corneal Disease 44 0.051
100
RFR003 Refractive Error 43 0.051
101
RTN187 Retinitis Pigmentosa-Deafness Syndrome 42 0.051
102
ATX019 Ataxia with Vitamin E Deficiency 42 0.051
103
c PRM032 Primary Congenital Glaucoma 41 0.051
104
PRM024 Primary Angle-Closure Glaucoma 40 0.051
105
OPT001 Optic Disk Drusen 34 0.051
107
P VTR008 Vitreoretinal Degeneration 29 0.051
108
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 0.051
109
SPR019 Superficial Keratitis 21 0.051
110
HYP742 Hyperpigmentation of Eyelids 13 0.051
111
CNT011 Contact Blepharoconjunctivitis 11 0.051
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