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

200 hits were found for 'vitreoretinopathy'

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 64 7.789
2
PRL011 Proliferative Vitreoretinopathy 44 6.144
3
WGN003 Wagner Syndrome 42 3.932
4
P LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 6 3.793
5
c FML042 Familial Exudative Vitreoretinopathy, Autosomal Dominant 21 3.555
6
c EXD004 Exudative Vitreoretinopathy 4 11 3.423
7
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 11 3.405
8
ATS090 Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy 14 3.365
9
c EXD006 Exudative Vitreoretinopathy 5 8 3.341
10
VCN001 Vcan-Related Vitreoretinopathy 4 3.341
11
P EXD005 Exudative Vitreoretinopathy, X-Linked 23 2.959
12
VTR013 Vitreoretinopathy, Neovascular Inflammatory 5 2.728
13
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 4 2.728
14
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 4 2.728
15
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 4 2.728
16
VTR011 Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia 4 2.728
17
c EXD003 Exudative Vitreoretinopathy-3 4 1.929
18
RTN023 Retinitis 61 0.528
19
RTN017 Retinal Detachment 60 0.411
20
c LRP002 Lrp5-Related Autosomal Dominant Osteopetrosis 7 0.297
21
END072 Endotheliitis 47 0.257
22
IDP042 Idiopathic Recurrent Stupor 15 0.237
23
DBT011 Diabetic Retinopathy 73 0.219
24
PRL007 Proliferative Diabetic Retinopathy 57 0.219
25
FCT013 Factor V Leiden Thrombophilia 35 0.155
26
P MYP018 Myopia 6 29 0.155
27
P UVT001 Uveitis 67 0.149
28
VTR003 Vitreous Detachment 39 0.149
29
ANK002 Ankylosing Spondylitis 75 0.142
30
THR035 Thrombasthenia 37 0.142
31
PRS062 Persistent Hyperplastic Primary Vitreous 36 0.142
32
CNR017 Cone-Rod Dystrophy 9 19 0.142
33
P STR035 Streptococcal Group a Invasive Disease 14 0.142
34
P HMP004 Hemophilia B 80 0.134
35
THR013 Thoracic Outlet Syndrome 54 0.134
36
NPH018 Nephrogenic Systemic Fibrosis 44 0.134
37
P MBS002 Moebius Syndrome 42 0.134
38
RDT013 Radiation Proctitis 33 0.134
39
P INF069 Infantile Neuroaxonal Dystrophy 1 32 0.134
40
P ATX002 Ataxia Telangiectasia 93 0.127
41
NRR002 Norrie Disease 67 0.127
42
c CTR002 Cataract 53 0.127
43
CTS003 Coats Disease 50 0.127
44
RHY001 Rhyns Syndrome 49 0.127
45
FML089 Familial Thoracic Aortic Aneurysm and Dissection 43 0.127
46
LKC002 Leukocoria 23 0.127
47
GST023 Gastric Ulcer 72 0.119
48
LNG017 Lung Giant Cell Carcinoma 47 0.119
49
ENT015 Enthesitis-Related Arthritis 48 0.110
50
CHL079 Children's Interstitial Lung Disease 46 0.110
51
ERL004 Early Yaws 33 0.110
52
RPD005 Rapidly Involuting Congenital Hemangioma 16 0.110
53
VNB003 Van Buchem Disease Type 2 16 0.110
54
P RTN012 Retinopathy of Prematurity 62 0.100
55
BRN105 Burn Scar 44 0.100
56
PRL042 Proliferating Trichilemmal Cyst 38 0.100
57
P XLN007 X-Linked Disease 36 0.100
58
TFT003 Tufting Enteropathy 21 0.100
59
HPT023 Hepatocellular Carcinoma 89 0.090
60
P OST002 Osteoporosis 77 0.090
61
BRN024 Bronchitis 76 0.090
62
ACN002 Acanthosis Nigricans 73 0.090
63
VSC007 Vascular Disease 72 0.090
64
RLP001 Relapsing Polychondritis 69 0.090
65
c LCL006 Localized Scleroderma 68 0.090
66
P DGR001 Digeorge Syndrome 67 0.090
67
c PRP029 Porphyria 64 0.090
68
WST001 West Syndrome 64 0.090
69
RTN018 Retinal Disease 58 0.090
70
MYC002 Mycobacterium Avium Complex Disease 57 0.090
71
P THR090 Thrombocythemia 1 54 0.090
72
CNR004 Cone-Rod Dystrophy 2 53 0.090
73
CNG048 Congenital Hepatic Fibrosis 53 0.090
74
P ALV004 Alveolar Rhabdomyosarcoma 51 0.090
75
MCL003 Macular Holes 50 0.090
76
SYN053 Syndromic Diarrhea 42 0.090
77
P DNS004 Duane Syndrome Type 2 41 0.090
78
NNS006 Non-Suppurative Otitis Media 26 0.090
79
HNM002 Hinman Syndrome 24 0.090
80
FND003 Fundus Flavimaculatus 17 0.090
81
AMY016 Amyopathic Dermatomyositis 17 0.090
82
CYS001 Cystic Fibrosis 103 0.078
83
VNH001 Von Hippel-Lindau Disease 89 0.078
84
LSH001 Leishmaniasis 74 0.078
85
c CWD001 Cowden Disease 69 0.078
86
BLR001 Biliary Atresia 67 0.078
87
NRN002 Neuronitis 64 0.078
88
P GLC007 Glaucoma 58 0.078
89
CHR008 Choroiditis 57 0.078
90
EVN001 Evans' Syndrome 54 0.078
91
BLL004 Bullous Keratopathy 51 0.078
92
MNN014 Mononeuritis 48 0.078
93
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 43 0.078
94
ENT001 Enterocele 42 0.078
95
c MYP006 Myopia 41 0.078
96
CNG116 Congenital Nephrotic Syndrome Finnish Type 39 0.078
97
c BLN003 Blindness 37 0.078
98
CTS011 Cutis Marmorata Telangiectatica Congenita 35 0.078
99
ANS004 Anisometropia 26 0.078
100
P PLM103 Pulmonary Capillary Hemangiomatosis 26 0.078
101
c HMP017 Hemophilia a, Congenital 21 0.078
102
HYP166 Hyperostosis Corticalis Generalisata 15 0.078
103
P BRS047 Breast Cancer 105 0.063
104
P AMY001 Amyotrophic Lateral Sclerosis 100 0.063
105
AND002 Androgen Insensitivity Syndrome 88 0.063
106
P HNT001 Huntington's Disease 87 0.063
107
P RFS001 Refsum Disease 83 0.063
108
AGR001 Age Related Macular Degeneration 83 0.063
109
c DBT009 Diabetes Mellitus 80 0.063
110
KWS002 Kawasaki Disease 74 0.063
111
P ANG001 Angelman Syndrome 70 0.063
112
ART019 Aortic Valve Stenosis 68 0.063
113
ISC004 Ischemia 64 0.063
114
ART001 Arterial Tortuosity Syndrome 62 0.063
115
VSC003 Visceral Leishmaniasis 61 0.063
116
c AXN002 Axenfeld-Rieger Syndrome 60 0.063
117
HYP003 Hypermethioninemia 60 0.063
118
CNR002 Cone-Rod Dystrophy 58 0.063
119
RTN003 Retinal Ischemia 56 0.063
120
c OPN001 Open-Angle Glaucoma 56 0.063
121
ATX019 Ataxia with Vitamin E Deficiency 55 0.063
122
P RPD001 Rapidly Progressive Glomerulonephritis 55 0.063
123
OST024 Osteoporosis-Pseudoglioma Syndrome 53 0.063
124
c PRM010 Primary Open Angle Glaucoma 51 0.063
125
SCH016 Schimke Immunoosseous Dysplasia 49 0.063
126
CHY002 Chylomicron Retention Disease 49 0.063
127
HYP457 Hypertrophic Scars 48 0.063
128
GST029 Gastric Cardia Adenocarcinoma 48 0.063
129
P RTN016 Retinal Degeneration 47 0.063
130
P LSS005 Lissencephaly 1 44 0.063
131
RCR001 Recurrent Corneal Erosion 44 0.063
132
P ATX010 Ataxia Neuropathy Spectrum 44 0.063
133
AND003 Andersen-Tawil Syndrome 43 0.063
134
TTR016 Tetra-Amelia Syndrome 43 0.063
135
KLD001 Keloids 42 0.063
136
ACR014 Acral Lentiginous Melanoma 42 0.063
137
DNR001 Duane Retraction Syndrome 41 0.063
138
AST006 Astigmatism 41 0.063
139
URT031 Ureteral Disease 40 0.063
140
IPX001 Ipex Syndrome 39 0.063
141
P FBR045 Fibromatosis, Gingival 38 0.063
142
OST032 Osteofibrous Dysplasia 37 0.063
143
STR039 Sturge-Weber Syndrome 37 0.063
144
P SLP004 Salpingo-Oophoritis 31 0.063
145
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.063
146
PL2001 Pla2g6-Associated Neurodegeneration 21 0.063
147
c BNG076 Benign Exophthalmos Syndrome 21 0.063
148
AND005 Androgen Insensitivity Syndrome, Mild 18 0.063
149
HLR003 Hole Retinal Cyst 17 0.063
150
ADN025 Adenoameloblastoma 13 0.063
151
MYP024 Myopia, X-Linked 6 0.063
152
P LFR001 Li-Fraumeni Syndrome 93 0.045
153
P LBR001 Leber Congenital Amaurosis 83 0.045
154
P RTN008 Retinitis Pigmentosa 81 0.045
155
GLN003 Glanzmann's Thrombasthenia 80 0.045
156
P ACT074 Acute Lymphocytic Leukemia 77 0.045
157
P FML018 Familial Mediterranean Fever 74 0.045
158
P STR022 Stargardt Disease 74 0.045
159
P VLC001 Velocardiofacial Syndrome 60 0.045
160
CRT049 Critical Limb Ischemia 60 0.045
161
NRM002 Normal Pressure Hydrocephalus 59 0.045
162
c SCL016 Scleroderma 59 0.045
163
NTR001 Neutral Lipid Storage Disease 59 0.045
164
GNG012 Gingival Overgrowth 57 0.045
165
DBT062 Diabetic Foot Ulcers 56 0.045
166
NPH010 Nephrosclerosis 56 0.045
167
P STR020 Strabismus 56 0.045
168
PYR010 Peyronie's Disease 56 0.045
169
P MYM002 Moyamoya Disease 56 0.045
170
NNS002 Nonspecific Interstitial Pneumonia 55 0.045
171
EMB003 Embryonal Cancer 55 0.045
172
CRN027 Corneal Neovascularization 55 0.045
173
DFF003 Diffuse Scleroderma 54 0.045
174
DBT008 Diabetic Angiopathy 54 0.045
175
c WRD001 Waardenburg's Syndrome 53 0.045
176
CRN029 Coronary Arteriosclerosis 53 0.045
177
KRT008 Keratopathy 52 0.045
178
CRN024 Corneal Disease 52 0.045
179
CNV002 Conversion Disorder 50 0.045
180
IRN002 Iron Metabolism Disease 50 0.045
181
P ART028 Aortic Aneurysm, Familial Thoracic 4 49 0.045
182
HYP054 Hypochromic Anemia 45 0.045
183
CHR415 Chronic Venous Leg Ulcers 45 0.045
184
NVS001 Neovascular Glaucoma 41 0.045
185
ESN011 Eisenmenger Syndrome 40 0.045
186
MCR001 Microcystic Meningioma 40 0.045
187
HYP030 Hypoactive Sexual Desire Disorder 39 0.045
188
QBC001 Quebec Platelet Disorder 39 0.045
189
RTN020 Retinal Vascular Disease 39 0.045
190
USL001 Usual Interstitial Pneumonia 38 0.045
191
VRL011 Viral Infectious Disease 37 0.045
192
ADS002 Adie Syndrome 33 0.045
193
PYR026 Peyronies Disease 32 0.045
194
c FRT001 Fourth Cranial Nerve Palsy 30 0.045
195
CHR084 Chromosomal Disease 28 0.045
196
BLD053 Blood Platelet Disease 27 0.045
197
RTN002 Retinal Perforation 24 0.045
198
P ISC010 Isochromosome Yp 14 0.045
199
c CLL020 Collagenopathy Type 2 Alpha 1 13 0.045
200
P CHR054 Chronic Closed-Angle Glaucoma 12 0.045