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

205 hits were found for 'vitreoretinopathy'

# ++ Fam MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 52 7.785
2
PRL011 Proliferative Vitreoretinopathy 42 6.131
3
WGN003 Wagner Syndrome 42 3.933
4
P LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 4 3.791
5
ATS090 Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy 13 3.750
6
FML042 Familial Exudative Vitreoretinopathy, Autosomal Dominant 17 3.544
7
c EXD004 Exudative Vitreoretinopathy 4 5 3.423
8
P XLN033 X-Linked Familial Exudative Vitreoretinopathy 10 3.406
9
VCN001 Vcan-Related Vitreoretinopathy 4 3.366
10
c EXD006 Exudative Vitreoretinopathy 5 4 3.342
11
c EXD005 Exudative Vitreoretinopathy, X-Linked 15 2.959
12
VTR013 Vitreoretinopathy, Neovascular Inflammatory 9 2.854
13
VTR011 Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia 3 2.729
14
FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 2 2.729
15
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 2 2.729
16
TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 2 2.729
17
c EXD003 Exudative Vitreoretinopathy-3 4 1.929
18
RTN017 Retinal Detachment 53 0.407
19
LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 3 0.295
20
END072 Endotheliitis 51 0.255
21
FML089 Familial Thoracic Aortic Aneurysm and Dissection 39 0.239
22
IDP042 Idiopathic Recurrent Stupor 15 0.235
23
DBT011 Diabetic Retinopathy 66 0.218
24
PRL007 Proliferative Diabetic Retinopathy 54 0.218
25
NRR002 Norrie Disease 64 0.213
26
P CRT049 Critical Limb Ischemia 58 0.183
27
THR013 Thoracic Outlet Syndrome 53 0.172
28
FCT013 Factor V Leiden Thrombophilia 31 0.154
29
P MYP018 Myopia 6 23 0.154
30
P UVT001 Uveitis 66 0.147
31
PRS062 Persistent Hyperplastic Primary Vitreous 41 0.147
32
VTR003 Vitreous Detachment 37 0.147
33
ANK002 Ankylosing Spondylitis 75 0.141
34
THR035 Thrombasthenia 49 0.141
35
CNR017 Cone-Rod Dystrophy 9 19 0.141
36
P STR035 Streptococcal Group a Invasive Disease 15 0.141
37
P HMP004 Hemophilia B 66 0.133
38
NPH018 Nephrogenic Systemic Fibrosis 50 0.133
39
P MBS002 Moebius Syndrome 45 0.133
40
RDT013 Radiation Proctitis 36 0.133
41
ATX002 Ataxia Telangiectasia 81 0.126
42
CTS003 Coats Disease 53 0.126
43
c CTR002 Cataract 48 0.126
44
RHY001 Rhyns Syndrome 45 0.126
45
LKC002 Leukocoria 23 0.126
46
GST023 Gastric Ulcer 67 0.118
47
LNG017 Lung Giant Cell Carcinoma 43 0.118
48
ENT015 Enthesitis-Related Arthritis 50 0.109
49
CHL079 Children's Interstitial Lung Disease 39 0.109
50
c ERL004 Early Yaws 29 0.109
51
RPD005 Rapidly Involuting Congenital Hemangioma 19 0.109
52
VNB003 Van Buchem Disease Type 2 11 0.109
53
c LCL006 Localized Scleroderma 64 0.099
54
BRN105 Burn Scar 41 0.099
55
PRL042 Proliferating Trichilemmal Cyst 40 0.099
56
HNM001 Hinman's Syndrome 28 0.099
57
TFT003 Tufting Enteropathy 26 0.099
58
P OST002 Osteoporosis 73 0.089
59
BRN024 Bronchitis 71 0.089
60
ACN002 Acanthosis Nigricans 70 0.089
61
VSC007 Vascular Disease 69 0.089
62
HPT023 Hepatocellular Carcinoma 69 0.089
63
RLP001 Relapsing Polychondritis 66 0.089
64
WST001 West Syndrome 64 0.089
65
P DGR001 Digeorge Syndrome 60 0.089
66
c PRP029 Porphyria 56 0.089
67
MYC002 Mycobacterium Avium Complex Disease 56 0.089
68
CNG048 Congenital Hepatic Fibrosis 52 0.089
69
P ALV004 Alveolar Rhabdomyosarcoma 51 0.089
70
RTN018 Retinal Disease 49 0.089
71
P THR090 Thrombocythemia 1 48 0.089
72
CNR004 Cone-Rod Dystrophy 2 47 0.089
73
CTS011 Cutis Marmorata Telangiectatica Congenita 37 0.089
74
P DNS004 Duane Syndrome Type 2 31 0.089
75
AMY016 Amyopathic Dermatomyositis 25 0.089
76
NNS006 Non-Suppurative Otitis Media 24 0.089
77
FND003 Fundus Flavimaculatus 24 0.089
78
HYP166 Hyperostosis Corticalis Generalisata 17 0.089
79
CYS001 Cystic Fibrosis 91 0.077
80
P LSH001 Leishmaniasis 65 0.077
81
c CWD001 Cowden Disease 63 0.077
82
P BLR001 Biliary Atresia 60 0.077
83
c BLN003 Blindness 54 0.077
84
RTN023 Retinitis 53 0.077
85
EVN001 Evans' Syndrome 50 0.077
86
P GLC007 Glaucoma 49 0.077
87
OST024 Osteoporosis-Pseudoglioma Syndrome 47 0.077
88
BLL004 Bullous Keratopathy 45 0.077
89
MNN014 Mononeuritis 40 0.077
90
ENT001 Enterocele 39 0.077
91
CNG116 Congenital Nephrotic Syndrome Finnish Type 39 0.077
92
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.077
93
c MYP006 Myopia 36 0.077
94
P PLM103 Pulmonary Capillary Hemangiomatosis 28 0.077
95
c HMP017 Hemophilia a, Congenital 26 0.077
96
ANS004 Anisometropia 24 0.077
97
P AMY001 Amyotrophic Lateral Sclerosis 87 0.063
98
P BRS047 Breast Cancer 85 0.063
99
P HNT001 Huntington's Disease 81 0.063
100
AND002 Androgen Insensitivity Syndrome 75 0.063
101
P RFS001 Refsum Disease 73 0.063
102
AGR001 Age Related Macular Degeneration 71 0.063
103
KWS002 Kawasaki Disease 69 0.063
104
c DBT009 Diabetes Mellitus 68 0.063
105
P ANG001 Angelman Syndrome 67 0.063
106
ART019 Aortic Valve Stenosis 64 0.063
107
VNH001 Von Hippel-Lindau Disease 63 0.063
108
c VSC003 Visceral Leishmaniasis 58 0.063
109
ISC004 Ischemia 57 0.063
110
c AXN002 Axenfeld-Rieger Syndrome 57 0.063
111
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.063
112
RTN003 Retinal Ischemia 52 0.063
113
HYP003 Hypermethioninemia 52 0.063
114
KLD001 Keloids 52 0.063
115
ART001 Arterial Tortuosity Syndrome 52 0.063
116
P RPD001 Rapidly Progressive Glomerulonephritis 51 0.063
117
c PRM010 Primary Open Angle Glaucoma 51 0.063
118
P OPN001 Open-Angle Glaucoma 51 0.063
119
STR039 Sturge-Weber Syndrome 47 0.063
120
c ENC008 Encephalocele 47 0.063
121
CNR002 Cone-Rod Dystrophy 46 0.063
122
CHY002 Chylomicron Retention Disease 46 0.063
123
HYP457 Hypertrophic Scars 46 0.063
124
MCL003 Macular Holes 45 0.063
125
GST029 Gastric Cardia Adenocarcinoma 44 0.063
126
RCR001 Recurrent Corneal Erosion 43 0.063
127
c FBR045 Fibromatosis, Gingival 43 0.063
128
P LSS005 Lissencephaly 1 42 0.063
129
c RTN016 Retinal Degeneration 41 0.063
130
DNR001 Duane Retraction Syndrome 41 0.063
131
RTN012 Retinopathy of Prematurity 40 0.063
132
ATX019 Ataxia with Vitamin E Deficiency 40 0.063
133
SCH016 Schimke Immunoosseous Dysplasia 40 0.063
134
OST032 Osteofibrous Dysplasia 39 0.063
135
AND003 Andersen-Tawil Syndrome 39 0.063
136
ACR014 Acral Lentiginous Melanoma 39 0.063
137
AST006 Astigmatism 38 0.063
138
TTR016 Tetra-Amelia Syndrome 36 0.063
139
ENC017 Encephaloceles 36 0.063
140
IPX001 Ipex Syndrome 35 0.063
141
EMN001 Emanuel Syndrome 34 0.063
142
c ATX010 Ataxia Neuropathy Spectrum 33 0.063
143
URT031 Ureteral Disease 32 0.063
144
P SLP004 Salpingo-Oophoritis 30 0.063
145
CCM003 Cecum Cancer 25 0.063
146
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.063
147
AND005 Androgen Insensitivity Syndrome, Mild 19 0.063
148
HLR003 Hole Retinal Cyst 18 0.063
149
c BNG076 Benign Exophthalmos Syndrome 17 0.063
150
ADN025 Adenoameloblastoma 16 0.063
151
PL2001 Pla2g6-Associated Neurodegeneration 14 0.063
152
c DGR004 Digeorge Syndrome 2 11 0.063
153
MYP024 Myopia, X-Linked 6 0.063
154
P RTN008 Retinitis Pigmentosa 76 0.044
155
P LFR001 Li-Fraumeni Syndrome 75 0.044
156
P LBR001 Leber Congenital Amaurosis 74 0.044
157
P FML018 Familial Mediterranean Fever 73 0.044
158
P TRN020 Turner Syndrome 71 0.044
159
ACT074 Acute Lymphocytic Leukemia 69 0.044
160
GLN003 Glanzmann's Thrombasthenia 68 0.044
161
P STR022 Stargardt Disease 61 0.044
162
P VLC001 Velocardiofacial Syndrome 57 0.044
163
NRM002 Normal Pressure Hydrocephalus 54 0.044
164
c WRD001 Waardenburg's Syndrome 54 0.044
165
P STR020 Strabismus 53 0.044
166
NPH010 Nephrosclerosis 53 0.044
167
c SCL016 Scleroderma 53 0.044
168
P MYM002 Moyamoya Disease 52 0.044
169
DBT062 Diabetic Foot Ulcers 52 0.044
170
CHR008 Choroiditis 51 0.044
171
PYR010 Peyronie's Disease 51 0.044
172
NNS002 Nonspecific Interstitial Pneumonia 50 0.044
173
GNG012 Gingival Overgrowth 50 0.044
174
P NTR001 Neutral Lipid Storage Disease 49 0.044
175
CRN024 Corneal Disease 48 0.044
176
CNV002 Conversion Disorder 48 0.044
177
CRN027 Corneal Neovascularization 48 0.044
178
KRT008 Keratopathy 47 0.044
179
NRN002 Neuronitis 47 0.044
180
DFF003 Diffuse Scleroderma 47 0.044
181
DBT008 Diabetic Angiopathy 47 0.044
182
CRN029 Coronary Arteriosclerosis 45 0.044
183
USL001 Usual Interstitial Pneumonia 45 0.044
184
HYP054 Hypochromic Anemia 44 0.044
185
ESN011 Eisenmenger Syndrome 44 0.044
186
EMB003 Embryonal Cancer 44 0.044
187
IRN002 Iron Metabolism Disease 44 0.044
188
P ART028 Aortic Aneurysm, Familial Thoracic 4 39 0.044
189
HYP030 Hypoactive Sexual Desire Disorder 39 0.044
190
NVS001 Neovascular Glaucoma 38 0.044
191
MCR001 Microcystic Meningioma 35 0.044
192
VRL011 Viral Infectious Disease 35 0.044
193
QBC001 Quebec Platelet Disorder 34 0.044
194
CTR027 Cataract-Glaucoma 34 0.044
195
RTN020 Retinal Vascular Disease 33 0.044
196
CHR415 Chronic Venous Leg Ulcers 33 0.044
197
ADS002 Adie Syndrome 32 0.044
198
PYR026 Peyronies Disease 26 0.044
199
c FRT001 Fourth Cranial Nerve Palsy 26 0.044
200
BLD053 Blood Platelet Disease 25 0.044
201
RTN002 Retinal Perforation 21 0.044
202
c CHR187 Chromosome 11q Deletion 15 0.044
203
P ISC010 Isochromosome Yp 14 0.044
204
P CHR054 Chronic Closed-Angle Glaucoma 11 0.044
205
c CLL020 Collagenopathy Type 2 Alpha 1 11 0.044