Search results for Ranibizumab

340 hits were found for Ranibizumab

# Family MCID Name MIFTS Score
2
MCL006 Macular Retinal Edema 55 1.023
3
KHN001 Kuhnt-Junius Degeneration 47 0.930
4
DBT006 Diabetic Macular Edema 48 0.779
5
P MCR115 Microvascular Complications of Diabetes 5 66 0.761
6
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.679
7
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.662
8
P RTN022 Retinal Vein Occlusion 53 0.646
9
c CNT016 Central Retinal Vein Occlusion 53 0.439
10
P RTN018 Retinal Disease 53 0.418
11
RTN017 Retinal Detachment 61 0.399
12
c MCR129 Microvascular Complications of Diabetes 1 66 0.391
13
c MCR112 Microvascular Complications of Diabetes 2 41 0.388
14
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.359
15
P END047 Endophthalmitis 53 0.351
16
P MYP006 Myopia 55 0.344
17
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.340
18
c EXD008 Exudative Vitreoretinopathy 1 71 0.316
19
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.307
20
c PRM038 Primary Agammaglobulinemia 44 0.297
21
c MCR120 Microvascular Complications of Diabetes 7 47 0.282
22
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.262
23
EYD002 Eye Disease 58 0.260
24
P UVT001 Uveitis 57 0.255
25
NVS001 Neovascular Glaucoma 53 0.248
26
P CTR002 Cataract 60 0.241
27
RTN020 Retinal Vascular Disease 46 0.241
28
48X005 48,xyyy 39 0.228
29
TLN003 Telangiectasis 52 0.220
30
DGN002 Degenerative Myopia 32 0.214
31
P VSC007 Vascular Disease 63 0.211
32
ALN001 Aland Island Eye Disease 50 0.205
33
ANG004 Angioid Streaks 39 0.205
34
c RHB024 Rhabdomyosarcoma 2 67 0.199
35
AYM001 Ayme-Gripp Syndrome 57 0.199
36
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.187
37
ISC004 Ischemia 58 0.187
38
RDN001 Reading Disorder 40 0.187
39
CYT002 Cytokine Deficiency 42 0.184
40
CNT060 Central Serous Chorioretinopathy 38 0.174
41
MCL003 Macular Holes 40 0.167
42
P MLN069 Melanoma, Uveal 59 0.163
43
CTS003 Coats Disease 53 0.159
44
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.159
45
CRN027 Corneal Neovascularization 47 0.155
46
RFR003 Refractive Error 43 0.155
47
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.151
48
P MLN008 Melanoma 69 0.147
49
P DBT009 Diabetes Mellitus 64 0.147
50
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.147
51
P OPT006 Optic Nerve Disease 60 0.143
52
CHR008 Choroiditis 46 0.143
53
SKN019 Skin Melanoma 68 0.139
54
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.139
55
GLS018 Glass Syndrome 57 0.139
56
P RTN016 Retinal Degeneration 53 0.139
57
RTN003 Retinal Ischemia 50 0.139
58
SCT002 Scotoma 44 0.134
59
DSS010 Dissociative Disorder 39 0.134
60
VTR003 Vitreous Detachment 39 0.130
61
P PSD087 Pseudoxanthoma Elasticum 65 0.125
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.125
63
HST011 Histoplasmosis 55 0.125
64
OCL006 Ocular Hypertension 53 0.125
65
MCL079 Macular Telangiectasia Type 2 27 0.125
66
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.120
67
RTN023 Retinitis 46 0.120
68
NRR001 Neuroretinitis 42 0.120
69
STR067 Stroke, Ischemic 81 0.115
70
P TRN020 Turner Syndrome 67 0.115
71
CRB039 Cerebrovascular Disease 67 0.110
72
c DBT099 Diabetes Mellitus, Type I 65 0.110
73
BCK003 Background Diabetic Retinopathy 46 0.110
74
ATX019 Ataxia with Vitamin E Deficiency 42 0.110
75
RBS002 Rubeosis Iridis 33 0.110
76
PNC059 Punctate Inner Choroidopathy 32 0.110
77
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.110
78
P RTN008 Retinitis Pigmentosa 79 0.104
79
VNH007 Von Hippel-Lindau Syndrome 73 0.104
80
P CNR004 Cone-Rod Dystrophy 2 73 0.104
81
PPL021 Papilledema 49 0.104
82
P VTR007 Vitreoretinopathy 46 0.104
83
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.104
84
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.098
85
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.098
86
HYP266 Hypoxia 57 0.098
87
P NRP001 Neuropathy 56 0.098
88
IRD001 Iridocyclitis 53 0.098
89
MLT035 Multifocal Choroiditis 32 0.098
91
KRT019 Keratitis, Hereditary 65 0.092
92
TRN015 Transient Cerebral Ischemia 63 0.092
93
P VSC011 Vasculitis 62 0.092
94
ALL026 Allergic Hypersensitivity Disease 62 0.092
95
P HMN010 Hemangioma 61 0.092
96
AGN016 Aging 56 0.092
97
c PST005 Posterior Uveitis 54 0.092
98
P OPN001 Open-Angle Glaucoma 49 0.092
99
OPT010 Optic Papillitis 38 0.092
100
DWN001 Down Syndrome 70 0.085
101
c LTN004 Late-Onset Retinal Degeneration 59 0.085
102
P CPL006 Capillary Hemangioma 51 0.085
103
RTN001 Retinal Vasculitis 47 0.085
104
NSP002 Nasopharyngitis 43 0.085
105
P VTL001 Vitelliform Macular Dystrophy 42 0.085
106
SVR002 Severe Nonproliferative Diabetic Retinopathy 37 0.085
107
BLN008 Blind Hypotensive Eye 18 0.085
108
P MYC007 Myocardial Infarction 70 0.078
109
ADL002 Adult Syndrome 70 0.078
110
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.078
111
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.078
112
P CNJ013 Conjunctivitis 65 0.078
113
P TXP001 Toxoplasmosis 60 0.078
114
P HDC001 Headache 57 0.078
115
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.078
116
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.078
117
P LBR014 Leber Congenital Amaurosis 4 56 0.078
118
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.078
119
OCL022 Ocular Melanoma 50 0.078
120
47X002 47,xyy 49 0.078
121
P SCL015 Scleritis 48 0.078
122
c CHR682 Chronic Bilirubin Encephalopathy 39 0.078
123
RTN004 Retinal Microaneurysm 33 0.078
124
c THR092 Thrombophilia Due to Thrombin Defect 73 0.069
125
ANX010 Anxiety 73 0.069
126
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.069
127
DPR016 Depression 63 0.069
128
ATM095 Autoimmune Disease 62 0.069
129
MNT002 Mental Depression 58 0.069
130
FND002 Fundus Dystrophy 55 0.069
131
PRS012 Pars Planitis 48 0.069
132
ELS001 Eales Disease 45 0.069
133
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.069
134
LRY022 Laryngoonychocutaneous Syndrome 44 0.069
135
RTN179 Retinal Arteries, Tortuosity of 44 0.069
136
ACT011 Acute Contagious Conjunctivitis 40 0.069
137
ATM052 Autoimmune Disease 1 37 0.069
138
PRR004 Preretinal Fibrosis 37 0.069
140
c ACT047 Acute Endophthalmitis 29 0.069
141
c MYP144 Myopia 12, Autosomal Dominant 18 0.069
142
P CLR023 Colorectal Cancer 99 0.060
143
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.060
144
P ALZ034 Alzheimer Disease 88 0.060
145
c HYP595 Hypertension, Essential 84 0.060
146
c NRF024 Neurofibromatosis, Type I 77 0.060
147
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.060
148
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.060
149
P KDN018 Kidney Disease 72 0.060
150
P SLP006 Sleep Apnea 69 0.060
151
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.060
152
HYL004 Hyaline Fibromatosis Syndrome 67 0.060
153
P NRV007 Nervous System Disease 66 0.060
154
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.060
155
ATH013 Atherosclerosis Susceptibility 65 0.060
156
NRF007 Neurofibroma 64 0.060
157
P CRN300 Coronary Heart Disease 1 63 0.060
158
c FNC043 Fanconi Anemia, Complementation Group E 62 0.060
159
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.060
160
LPP008 Lipoprotein Quantitative Trait Locus 62 0.060
161
NTR005 Nutritional Deficiency Disease 62 0.060
162
HYP066 Hyperglycemia 61 0.060
163
c PNS012 Paine Syndrome 61 0.060
164
c LPM012 Lipomatosis, Multiple 60 0.060
165
P CRD246 Cardiovascular System Disease 57 0.060
166
P NRF002 Neurofibromatosis 56 0.060
167
HYP005 Hypokalemia 55 0.060
168
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.060
169
P ART021 Arteriosclerosis 54 0.060
170
P RCT021 Rectum Cancer 52 0.060
171
ART140 Arteries, Anomalies of 52 0.060
172
c INH030 Inherited Retinal Disorder 51 0.060
173
VSC006 Vascular Cancer 51 0.060
174
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.060
176
DBT008 Diabetic Angiopathy 44 0.060
177
P CRN026 Corneal Edema 43 0.060
178
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.060
179
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.060
180
CLD014 Cole Disease 40 0.060
181
OCL025 Ocular Toxoplasmosis 39 0.060
182
RTN002 Retinal Perforation 38 0.060
183
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.060
184
FST001 Foster-Kennedy Syndrome 36 0.060
185
BST007 Best Vitelliform Macular Dystrophy 34 0.060
186
CNJ009 Conjunctival Cancer 32 0.060
187
PTT063 Pattern Dystrophy 29 0.060
188
PST092 Posttransplant Acute Limbic Encephalitis 29 0.060
189
DLT018 Dilution, Pigmentary 28 0.060
190
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.060
192
SRP002 Serpiginous Choroiditis 24 0.060
193
HYP213 Hypomelanotic Disorder 23 0.060
194
EXT062 Extracranial Carotid Artery Aneurysm 21 0.060
195
SCK003 Sickle Cell Anemia 74 0.049
196
P RTN024 Retinoblastoma 73 0.049
197
DFC004 Deficiency Anemia 70 0.049
198
P CRD119 Cardiac Arrest 67 0.049
199
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.049
200
ANG054 Angina Pectoris 66 0.049
201
INC021 Incontinentia Pigmenti 63 0.049
202
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.049
203
c GLC092 Glaucoma, Primary Open Angle 62 0.049
204
P PSR002 Psoriasis 62 0.049
205
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.049
206
BLL006 Bullous Pemphigoid 62 0.049
207
SQM006 Squamous Cell Carcinoma 60 0.049
208
ANR040 Aneurysm 59 0.049
209
THR024 Thrombosis 57 0.049
210
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.049
211
HMG005 Hemoglobinopathy 56 0.049
212
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.049
213
HMN009 Hemangioblastoma 54 0.049
214
P HMR003 Hemorrhagic Disease 53 0.049
215
INT075 Intracranial Hypertension 53 0.049
216
c FML008 Familial Retinoblastoma 53 0.049
217
c PSR017 Psoriasis 2 53 0.049
218
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.049
219
PST011 Pustulosis of Palm and Sole 52 0.049
220
c PSR023 Psoriasis 1 52 0.049
221
P SCK005 Sickle Cell Disease 50 0.049
222
P PNV001 Panuveitis 50 0.049
223
c CPL013 Capillary Malformations, Congenital 50 0.049
224
P NGH001 Night Blindness 48 0.049
225
c ANT086 Anterior Segment Dysgenesis 2 48 0.049
226
AST006 Astigmatism 47 0.049
227
c PSR032 Psoriasis 11 47 0.049
228
KRT002 Keratomalacia 47 0.049
229
TXC011 Toxocariasis 46 0.049
230
MLT073 Multisystemic Smooth Muscle Dysfunction Syndrome 44 0.049
231
RTN021 Retinal Vascular Occlusion 44 0.049
232
c PSR028 Psoriasis 7 42 0.049
233
GST020 Gastric Antral Vascular Ectasia 41 0.049
234
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.049
235
c PSR018 Psoriasis 13 41 0.049
236
SPR126 Superior Semicircular Canal Dehiscence 40 0.049
237
c HMG029 Hemoglobin Se Disease 39 0.049
238
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.049
240
THR123 Thrombotic Microangiopathy 36 0.049
242
OPT001 Optic Disk Drusen 34 0.049
243
RTN019 Retinal Telangiectasia 31 0.049
244
CHL079 Children's Interstitial Lung Disease 26 0.049
245
MYP060 Myopic Macular Degeneration 21 0.049
246
c MNN043 Meningioma, Familial 74 0.035
247
c HYP836 Hypercholesterolemia, Familial, 1 73 0.035
248
P SRC025 Sarcoidosis 1 70 0.035
249
P AMY004 Amyloidosis 70 0.035
250
c CHR684 Chronic Kidney Disease 70 0.035
251
P SYS005 Systemic Scleroderma 68 0.035
252
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.035
253
P MSC005 Muscular Dystrophy 66 0.035
254
P NSP012 Nasopharyngeal Carcinoma 66 0.035
255
HYP056 Hypoglycemia 66 0.035
256
c HRD010 Hereditary Spastic Paraplegia 66 0.035
257
OVR029 Ovarian Hyperstimulation Syndrome 64 0.035
258
OST017 Osteomyelitis 64 0.035
259
P MVM001 Movement Disease 63 0.035
260
P END044 Endometriosis 63 0.035
261
LPD008 Lipid Metabolism Disorder 62 0.035
262
MNN042 Meningioma, Radiation-Induced 62 0.035
263
CHL068 Cholestasis 61 0.035
264
P LPS004 Lupus Erythematosus 61 0.035
265
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.035
266
c ACT071 Acute Kidney Failure 60 0.035
267
P STR022 Stargardt Disease 58 0.035
268
PMP006 Pemphigus Vulgaris, Familial 57 0.035
269
GYR004 Gyrate Atrophy of Choroid and Retina 57 0.035
270
P GLM007 Glomerulonephritis 57 0.035
271
c ACT075 Acute Myocardial Infarction 57 0.035
272
ENH001 Enhanced S-Cone Syndrome 57 0.035
273
P PLY019 Polyneuropathy 56 0.035
274
MMB001 Membranoproliferative Glomerulonephritis 55 0.035
275
P STR020 Strabismus 55 0.035
276
c INT064 Intermediate Uveitis 55 0.035
277
P PMP001 Pemphigus 54 0.035
278
P TRM003 Tremor 54 0.035
279
CLL003 Cellulitis 54 0.035
280
MMM001 Mammary Paget's Disease 53 0.035
281
KRT006 Keratoconjunctivitis 53 0.035
282
P CTN003 Cutaneous Lupus Erythematosus 53 0.035
283
c MCR113 Microvascular Complications of Diabetes 3 52 0.035
284
EXP004 Exophthalmos 52 0.035
285
CLB010 Coloboma of Macula 52 0.035
286
PRP016 Paraplegia 52 0.035
287
SRS007 Sorsby Fundus Dystrophy 51 0.035
288
VTR010 Vitreoretinochoroidopathy 51 0.035
289
SPN021 Spinal Meningioma 50 0.035
290
BLP005 Blepharitis 50 0.035
291
CRT013 Carotid Stenosis 50 0.035
292
CHR078 Chorioretinitis 50 0.035
293
CYT005 Cytomegalovirus Retinitis 50 0.035
294
AMB002 Amblyopia 49 0.035
295
P KRT005 Keratoacanthoma 48 0.035
296
P RTN014 Retinal Artery Occlusion 47 0.035
297
c HRD039 Hereditary Amyloidosis 45 0.035
298
SPS057 Spasticity 45 0.035
299
IRT001 Iritis 44 0.035
300
c CNT028 Central Retinal Artery Occlusion 43 0.035
301
SNL007 Senile Cataract 42 0.035
302
MCH006 Mechanical Strabismus 42 0.035
303
CTS002 Cat-Scratch Disease 41 0.035
304
c MCL060 Macular Dystrophy, Vitelliform, 3 41 0.035
305
c MCR130 Microvascular Complications of Diabetes 6 41 0.035
306
c MCR133 Microvascular Complications of Diabetes 4 41 0.035
307
SCR001 Secretory Meningioma 41 0.035
308
BRN026 Branch Retinal Artery Occlusion 40 0.035
309
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 39 0.035
310
SPP007 Suppression Amblyopia 39 0.035
311
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.035
312
ABD002 Abducens Nerve Disease 37 0.035
313
GLM044 Glomerular Disease 37 0.035
314
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.035
315
CRB159 Cerebral Visual Impairment 35 0.035
316
END072 Endotheliitis 35 0.035
317
c MCL059 Macular Dystrophy, Patterned, 1 32 0.035
319
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.035
320
FML292 Familial Drusen 32 0.035
321
MYC014 Mycobacterium Chelonae 31 0.035
322
OCL051 Ocular Tuberculosis 31 0.035
323
WYB002 Wyburn-Mason Syndrome 30 0.035
324
DGN003 Degeneration of Macula and Posterior Pole 29 0.035
325
ARG004 Argyria 27 0.035
326
c NNS043 Nonsyndromic Retinitis Pigmentosa 27 0.035
327
c RNG015 Ring Chromosome 2 26 0.035
328
ABD009 Abducens Palsy 24 0.035
329
SCL014 Scleral Staphyloma 24 0.035
330
BTT011 Butterfly-Shaped Pigment Dystrophy 24 0.035
331
CHR158 Charles Bonnet Syndrome 23 0.035
332
c RNG019 Ring Chromosome 3 22 0.035
333
RTN123 Retinochoroidal Coloboma 20 0.035
334
ACT235 Acute Macular Neuroretinopathy 19 0.035
336
PRS110 Persistent Placoid Maculopathy 16 0.035
337
c MYP143 Myopia 11, Autosomal Dominant 15 0.035
338
c MYP134 Myopia 13, X-Linked 14 0.035
339
c IDP065 Idiopathic Macular Telangiectasia Type 1 12 0.035
340
FND005 Fundus Pulverulentus 9 0.035
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