Search results for "vitreoretinopathy"

The MalaCard for "vitreoretinopathy" has been retired.
Searching MalaCards for entries containing "vitreoretinopathy"

286 hits were found for 'vitreoretinopathy'

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 47 7.275
2
VTR013 Vitreoretinopathy, Neovascular Inflammatory 43 6.853
3
c EXD008 Exudative Vitreoretinopathy 1 50 4.948
4
c EXD004 Exudative Vitreoretinopathy 4 28 4.474
5
c EXD006 Exudative Vitreoretinopathy 5 26 4.464
6
P WGN003 Wagner Syndrome 32 4.373
7
P EXD009 Exudative Vitreoretinopathy 2, X-Linked 25 4.011
8
c EXD007 Exudative Vitreoretinopathy 3 15 3.446
9
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 15 2.928
10
c WGN005 Wagner Syndrome 1 23 2.880
11
c EXD010 Exudative Vitreoretinopathy 6 19 2.866
12
VCN001 Vcan-Related Vitreoretinopathy 6 2.801
13
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 8 2.006
14
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 8 2.006
15
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 8 2.006
16
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 8 2.006
17
RTN023 Retinitis 43 0.499
18
RTN017 Retinal Detachment 44 0.396
19
NRR002 Norrie Disease 63 0.172
20
EYD002 Eye Disease 54 0.158
21
P SPR013 Spiradenoma 46 0.158
22
NRN002 Neuronitis 40 0.131
23
P CTR002 Cataract 48 0.125
24
END072 Endotheliitis 39 0.125
25
ANR002 Aniridia 72 0.118
26
ACN002 Acanthosis Nigricans 53 0.118
27
THR013 Thoracic Outlet Syndrome 47 0.118
28
RTN018 Retinal Disease 46 0.118
29
P TRC086 Trichohepatoenteric Syndrome 1 42 0.118
30
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.118
31
P ATX010 Ataxia Neuropathy Spectrum 31 0.118
32
NRR001 Neuroretinitis 38 0.112
33
c SPN225 Spondyloarthropathy 1 66 0.104
34
P ANG001 Angelman Syndrome 66 0.104
35
AND015 Androgen Insensitivity 65 0.104
36
P HRM001 Hermansky-Pudlak Syndrome 62 0.104
37
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.104
38
c PNC108 Pancreatitis, Hereditary 59 0.104
39
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.104
40
HNT002 Hantavirus Pulmonary Syndrome 52 0.104
41
c ART101 Aortic Valve Disease 2 46 0.104
42
ALR002 Al-Raqad Syndrome 23 0.104
43
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.097
44
MYC002 Mycobacterium Avium Complex Disease 46 0.097
45
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.097
46
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 43 0.097
47
c BNG076 Benign Exophthalmos Syndrome 21 0.097
48
AND005 Androgen Insensitivity Syndrome, Mild 19 0.097
49
OST024 Osteoporosis-Pseudoglioma Syndrome 55 0.088
50
CTS003 Coats Disease 44 0.088
51
FCT013 Factor V Leiden Thrombophilia 43 0.088
52
HYP266 Hypoxia 42 0.088
53
P RTN016 Retinal Degeneration 42 0.088
54
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 42 0.088
55
VTR003 Vitreous Detachment 28 0.088
56
P OST002 Osteoporosis 75 0.079
57
ISC004 Ischemia 47 0.079
58
P MYP006 Myopia 46 0.079
59
RTN003 Retinal Ischemia 40 0.079
60
RTN020 Retinal Vascular Disease 38 0.079
61
MCL003 Macular Holes 37 0.079
62
CHR008 Choroiditis 37 0.079
63
P ATX030 Ataxia-Telangiectasia 76 0.068
64
P RTN008 Retinitis Pigmentosa 75 0.068
65
ART001 Arterial Tortuosity Syndrome 59 0.068
66
P AND016 Andersen Syndrome 58 0.068
67
P DGR001 Digeorge Syndrome 51 0.068
68
SCH016 Schimke Immunoosseous Dysplasia 51 0.068
69
c RTN164 Retinitis Pigmentosa Autosomal Recessive 43 0.068
70
CHR078 Chorioretinitis 41 0.068
71
P PRS062 Persistent Hyperplastic Primary Vitreous 40 0.068
72
TTR016 Tetra-Amelia Syndrome 38 0.068
73
LKC002 Leukocoria 31 0.068
74
PRR004 Preretinal Fibrosis 22 0.068
75
GLB003 Globe Disease 22 0.068
76
CYS001 Cystic Fibrosis 90 0.056
77
P RFS001 Refsum Disease 65 0.056
78
c HPT001 Hepatitis C 64 0.056
79
P HPT021 Hepatitis 58 0.056
80
P SPN046 Spinal Muscular Atrophy 58 0.056
81
P GT001 Gout 51 0.056
82
P OPN001 Open-Angle Glaucoma 50 0.056
83
P MCR010 Microcephaly 49 0.056
84
P UVT001 Uveitis 49 0.056
85
P FNG005 Feingold Syndrome 48 0.056
86
P LYM025 Lymphedema 48 0.056
87
P MCR115 Microvascular Complications of Diabetes 5 47 0.056
88
CNR007 Cone-Rod Dystrophy 6 46 0.056
89
P ENC008 Encephalocele 46 0.056
90
P MSC003 Muscular Atrophy 45 0.056
91
c PND001 Pain Disorder 43 0.056
92
c MCR129 Microvascular Complications of Diabetes 1 41 0.056
93
PLV005 Pelviureteric Junction Obstruction 36 0.056
94
CND005 Cone Dystrophy 34 0.056
95
AST006 Astigmatism 34 0.056
96
VTR005 Vitreous Disease 33 0.056
97
CTS011 Cutis Marmorata Telangiectatica Congenita 32 0.056
98
c CHR054 Chronic Closed-Angle Glaucoma 31 0.056
99
CHR413 Chronic Myocardial Ischemia 29 0.056
100
ANG009 Angiomatous Meningioma 29 0.056
101
LNS003 Lens Disease 26 0.056
102
ANS004 Anisometropia 25 0.056
103
RTN019 Retinal Telangiectasia 25 0.056
104
PLL005 Pallister-Killian Mosaic Syndrome 18 0.056
105
P BRS047 Breast Cancer 100 0.039
106
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 0.039
107
CRH001 Crohn's Disease 80 0.039
108
c MCL042 Macular Degeneration, Age-Related, 1 74 0.039
109
P BRD002 Bardet-Biedl Syndrome 68 0.039
110
CRZ001 Crouzon Syndrome 67 0.039
111
P FML161 Familial Mediterranean Fever, Ar 67 0.039
112
CNR002 Cone-Rod Dystrophy 64 0.039
113
P VLC001 Velocardiofacial Syndrome 61 0.039
114
PLM001 Pulmonary Tuberculosis 60 0.039
115
c BRD010 Bardet-Biedl Syndrome 1 59 0.039
116
TYP007 Typhoid Fever 59 0.039
117
LVR012 Liver Cirrhosis 59 0.039
118
LRN004 Laron Dwarfism 59 0.039
119
P PLM036 Pulmonary Fibrosis 59 0.039
120
P SLV001 Silver-Russell Syndrome 58 0.039
121
LSH001 Leishmaniasis 58 0.039
122
P RSP003 Respiratory Failure 58 0.039
123
P USH001 Usher Syndrome 58 0.039
124
MBS002 Moebius Syndrome 57 0.039
125
LPR018 Leprechaunism 56 0.039
126
IMG001 Image Syndrome 56 0.039
127
P RCK004 Rickets 55 0.039
128
P MYM002 Moyamoya Disease 55 0.039
129
VSC007 Vascular Disease 55 0.039
130
SMT008 Smith-Magenis Syndrome 54 0.039
131
P HMN010 Hemangioma 54 0.039
132
PLM134 Pulmonary Fibrosis, Idiopathic 54 0.039
133
P ACR001 Aicardi-Goutieres Syndrome 53 0.039
134
RBS003 Rabson-Mendenhall Syndrome 53 0.039
135
MCR013 Microphthalmia 53 0.039
136
P CHN012 Chondrosarcoma 52 0.039
137
VSC003 Visceral Leishmaniasis 52 0.039
138
PMS001 Poems Syndrome 51 0.039
139
c PRC016 Pre-Eclampsia 51 0.039
140
P CND004 Candidiasis 50 0.039
141
P FBR017 Fibrosarcoma 50 0.039
142
VHW001 Vohwinkel Syndrome 50 0.039
143
P ABD003 Abdominal Aortic Aneurysm 50 0.039
144
CMP002 Campylobacteriosis 49 0.039
145
RTC002 Reticular Dysgenesis 49 0.039
146
KRT002 Keratomalacia 49 0.039
147
STF002 Stiff Skin Syndrome 48 0.039
148
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 47 0.039
149
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 47 0.039
150
P PRC031 Preeclampsia/eclampsia 1 47 0.039
151
P STR020 Strabismus 47 0.039
152
PTN002 Patent Ductus Arteriosus 46 0.039
153
c GLC062 Glaucoma 1, Open Angle, E 46 0.039
154
CHY002 Chylomicron Retention Disease 46 0.039
155
IDP011 Idiopathic Interstitial Pneumonia 46 0.039
156
P ACT105 Acute Mountain Sickness 46 0.039
157
P CPL006 Capillary Hemangioma 46 0.039
158
ANG020 Angiosarcoma 46 0.039
159
c LBR014 Leber Congenital Amaurosis 4 46 0.039
160
P PNM006 Pneumoconiosis 45 0.039
161
CHL068 Cholestasis 45 0.039
162
c RNL003 Renal Clear Cell Carcinoma 45 0.039
163
BLR001 Biliary Atresia 44 0.039
164
VGN023 Vaginitis 44 0.039
165
IDP002 Idiopathic Juvenile Osteoporosis 43 0.039
166
BRN056 Bronchopulmonary Dysplasia 43 0.039
167
c CNT075 Central Precocious Puberty 43 0.039
168
PLC005 Placental Insufficiency 43 0.039
169
MLR003 Melorheostosis 43 0.039
170
P SCL048 Sclerosteosis 43 0.039
171
NPH018 Nephrogenic Systemic Fibrosis 43 0.039
172
P CLR030 Clear Cell Renal Cell Carcinoma 43 0.039
173
GNG012 Gingival Overgrowth 43 0.039
174
TWN001 Twin-to-Twin Transfusion Syndrome 42 0.039
175
CRN027 Corneal Neovascularization 42 0.039
176
P CRV039 Cervicitis 42 0.039
177
PTH002 Pathological Gambling 42 0.039
178
c USH003 Usher Syndrome Type Ii 42 0.039
179
KLD001 Keloids 42 0.039
180
PRM024 Primary Angle-Closure Glaucoma 42 0.039
181
EPT020 Epithelioid Hemangioendothelioma 42 0.039
182
TLN003 Telangiectasis 41 0.039
183
NTR005 Nutritional Deficiency Disease 41 0.039
184
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 41 0.039
185
VSC006 Vascular Cancer 40 0.039
186
TFT001 Tufted Angioma 40 0.039
187
c USH032 Usher Syndrome, Type 2a 40 0.039
188
ANT011 Antisocial Personality Disorder 40 0.039
189
P CRT033 Corticobasal Degeneration 40 0.039
190
c CTR130 Cataract 9, Multiple Types 39 0.039
191
P RST011 Restrictive Dermopathy, Lethal 39 0.039
192
ACT032 Acute Hemorrhagic Leukoencephalitis 39 0.039
193
MNN014 Mononeuritis 39 0.039
194
P FBR084 Fibromatosis, Gingival, 1 39 0.039
195
DFF003 Diffuse Scleroderma 39 0.039
196
MCL027 Macular Dystrophy, Dominant Cystoid 39 0.039
197
GRW007 Growth Hormone Deficiency 38 0.039
198
LMB062 Limb Ischemia 38 0.039
199
NPH010 Nephrosclerosis 38 0.039
200
c PST005 Posterior Uveitis 37 0.039
201
GLC011 Galactose Epimerase Deficiency 37 0.039
202
PYG006 Pyogenic Granuloma 37 0.039
203
CRB149 Cerebroretinal Microangiopathy with Calcifications and Cysts 37 0.039
204
RNL077 Renal Fibrosis 37 0.039
205
PLC001 Placenta Accreta 36 0.039
206
LNG026 Long Bone Adamantinoma 36 0.039
207
IRN002 Iron Metabolism Disease 36 0.039
208
VSC047 Vascular Malformation 35 0.039
209
SHH001 Sheehan Syndrome 35 0.039
210
LKS001 Leukostasis 35 0.039
211
HMN016 Hemangioendothelioma 35 0.039
212
VND001 Vein Disease 34 0.039
213
MCL006 Macular Retinal Edema 34 0.039
214
ADS002 Adie Syndrome 34 0.039
215
URT031 Ureteral Disease 34 0.039
216
CNC014 Cancer-Associated Retinopathy 34 0.039
217
RHY001 Rhyns Syndrome 34 0.039
218
P EPN001 Ependymoblastoma 33 0.039
219
PTT052 Pituitary Gigantism 33 0.039
220
BLD053 Blood Platelet Disease 32 0.039
221
LPD014 Lipodermatosclerosis 32 0.039
222
OCL010 Ocular Hypotension 32 0.039
223
c CTR102 Cataract 2, Multiple Types 32 0.039
224
SNL007 Senile Cataract 32 0.039
225
INT104 Intravascular Papillary Endothelial Hyperplasia 32 0.039
226
c JVN006 Juvenile Spinal Muscular Atrophy 32 0.039
227
EXH001 Exhibitionism 31 0.039
228
c USH012 Usher Syndrome, Type 2c 31 0.039
229
MCR001 Microcystic Meningioma 31 0.039
230
MVM001 Movement Disease 31 0.039
231
SST001 Sost-Related Sclerosing Bone Dysplasia 31 0.039
232
HYP047 Hypertropia 31 0.039
233
CNJ007 Conjunctivochalasis 31 0.039
234
CTR014 Cataract Microcornea Syndrome 31 0.039
235
UND005 Undifferentiated Pleomorphic Sarcoma 31 0.039
236
HPT074 Hepatic Adenoma, Somatic 30 0.039
237
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 30 0.039
238
P PST016 Posterior Polar Cataract 30 0.039
239
SLP010 Slipped Capital Femoral Epiphysis 30 0.039
240
PRS025 Presbyopia 30 0.039
241
PTN008 Patent Arterial Duct 29 0.039
242
P NCL005 Nuclear Cataract 29 0.039
243
ENC005 Encephalomalacia 29 0.039
244
FNS001 Funisitis 29 0.039
245
c PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 29 0.039
246
DBT007 Diabetic Cataract 28 0.039
247
ANG007 Angiokeratoma Circumscriptum 28 0.039
248
CNG069 Congenital Cytomegalovirus 28 0.039
249
BCK003 Background Diabetic Retinopathy 28 0.039
250
c CTR025 Cataract, Total Congenital 28 0.039
251
c SCN052 Secondary Adrenal Insufficiency 28 0.039
252
HNM002 Hinman Syndrome 27 0.039
253
OCL004 Ocular Hyperemia 27 0.039
254
c STC012 Stickler Syndrome, Type Iv 27 0.039
255
CHR079 Choroid Disease 26 0.039
256
DPN001 Dependent Personality Disorder 26 0.039
257
KHN001 Kuhnt-Junius Degeneration 26 0.039
258
PRP024 Peripheral Osteosarcoma 26 0.039
259
PNG002 Pain Agnosia 26 0.039
260
CHL013 Cholecystolithiasis 26 0.039
261
KDN013 Kidney Hypertrophy 26 0.039
262
OCL011 Ocular Motility Disease 26 0.039
263
NNT011 Neonatal Anemia 25 0.039
264
CTR026 Cataract, Zonular 25 0.039
265
MTR001 Mature Cataract 25 0.039
266
LRG003 Large Cell Medulloblastoma 25 0.039
267
CRL001 Cerulean Cataract 25 0.039
268
ATY001 Atypical Depressive Disorder 24 0.039
269
CRB032 Cerebral Convexity Meningioma 24 0.039
270
BNS002 Bone Structure Disease 24 0.039
271
P LTH016 Lethal Congenital Contractural Syndrome 2 23 0.039
272
c MCR112 Microvascular Complications of Diabetes 2 22 0.039
273
NNS034 Non-Syndromic Congenital Cataract 20 0.039
274
MGK002 Megakaryocytic Tumor 20 0.039
275
CRB137 Cerebral Creatine Deficiency Syndrome 20 0.039
276
CHR075 Choriocarcinoma of Ovary 18 0.039
277
CTR143 Cataract with Y-Shaped Suture Opacities 17 0.039
278
P CRL005 Coralliform Cataract 17 0.039
279
APN006 Apnea of Prematurity 16 0.039
280
HRD064 Hereditary Vascular Retinopathy 15 0.039
281
P TYP019 Type Ii Collagenopathies 13 0.039
282
NDP002 Ndp-Related Retinopathy of Prematurity 10 0.039
283
PPL023 Pupil Disease 7 0.039
284
MTR031 Motor Neuro-Ophthalmic Disorders 6 0.039
285
PRM009 Primary Eye Hypotony 5 0.039
286
EXD011 Exudative Retinopathy, Familial 2 0.039