Search results for "vitreoretinopathy"

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

149 hits were found for 'vitreoretinopathy'

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 46 8.139
2
VTR013 Vitreoretinopathy, Neovascular Inflammatory 50 7.451
3
c EXD008 Exudative Vitreoretinopathy 1 60 5.722
4
c EXD004 Exudative Vitreoretinopathy 4 24 4.527
5
P EXD009 Exudative Vitreoretinopathy 2, X-Linked 24 4.514
6
c EXD006 Exudative Vitreoretinopathy 5 21 4.500
7
c WGN005 Wagner Syndrome 1 29 4.046
8
c EXD010 Exudative Vitreoretinopathy 6 18 4.031
9
P WGN003 Wagner Syndrome 37 3.940
10
c EXD007 Exudative Vitreoretinopathy 3 13 3.482
11
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 14 2.999
12
VCN001 Vcan-Related Vitreoretinopathy 6 2.850
13
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 2.030
14
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.030
15
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.030
16
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.030
17
RTN023 Retinitis 49 0.642
18
RTN017 Retinal Detachment 57 0.506
19
NRR002 Norrie Disease 61 0.204
20
END072 Endotheliitis 42 0.148
21
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.140
22
P CTR002 Cataract 57 0.131
23
RTN018 Retinal Disease 56 0.131
24
CHR008 Choroiditis 43 0.131
25
ALR002 Al-Raqad Syndrome 36 0.131
26
EYD002 Eye Disease 63 0.121
27
ETH011 Ethylmalonic Encephalopathy 59 0.121
28
AND005 Androgen Insensitivity Syndrome, Mild 16 0.121
29
HYP266 Hypoxia 55 0.110
30
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.110
31
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.110
32
PRR004 Preretinal Fibrosis 36 0.110
33
P OST002 Osteoporosis 64 0.099
34
ISC004 Ischemia 59 0.099
35
CTS003 Coats Disease 57 0.099
36
RTN003 Retinal Ischemia 48 0.099
37
MCL003 Macular Holes 41 0.099
38
GLB003 Globe Disease 35 0.099
39
P MYP006 Myopia 59 0.086
40
P UVT001 Uveitis 59 0.086
41
OST024 Osteoporosis-Pseudoglioma Syndrome 54 0.086
42
P DGR001 Digeorge Syndrome 52 0.086
43
CYS001 Cystic Fibrosis 86 0.070
44
P DYS007 Dyskeratosis Congenita 63 0.070
45
P SPN046 Spinal Muscular Atrophy 63 0.070
46
P LYM025 Lymphedema 61 0.070
47
P GT001 Gout 58 0.070
48
P MCR010 Microcephaly 58 0.070
49
P RTN016 Retinal Degeneration 54 0.070
50
P MSC003 Muscular Atrophy 51 0.070
51
RTN020 Retinal Vascular Disease 50 0.070
52
P OPN001 Open-Angle Glaucoma 48 0.070
53
P ENC008 Encephalocele 47 0.070
54
VTR005 Vitreous Disease 47 0.070
55
AYM001 Ayme-Gripp Syndrome 45 0.070
56
AST006 Astigmatism 44 0.070
57
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.070
58
CHR078 Chorioretinitis 41 0.070
59
c CHR054 Chronic Closed-Angle Glaucoma 38 0.070
60
CND005 Cone Dystrophy 38 0.070
61
P PRS062 Persistent Hyperplastic Primary Vitreous 37 0.070
62
VTR003 Vitreous Detachment 34 0.070
63
CTS011 Cutis Marmorata Telangiectatica Congenita 30 0.070
64
ANS004 Anisometropia 29 0.070
65
P BRS047 Breast Cancer 100 0.049
66
P RTN008 Retinitis Pigmentosa 79 0.049
67
P PLM036 Pulmonary Fibrosis 68 0.049
68
P MYL005 Myelofibrosis 67 0.049
69
VSC007 Vascular Disease 67 0.049
70
LVR012 Liver Cirrhosis 67 0.049
71
LSH001 Leishmaniasis 62 0.049
72
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.049
73
P MYM002 Moyamoya Disease 60 0.049
74
MTR014 Motor Neuron Disease 59 0.049
75
INT066 Interstitial Lung Disease 58 0.049
76
NRM005 Neuromuscular Disease 57 0.049
77
ABL002 Ablepharon-Macrostomia Syndrome 57 0.049
78
P MCR129 Microvascular Complications of Diabetes 1 57 0.049
79
IDP011 Idiopathic Interstitial Pneumonia 57 0.049
80
URN010 Urinary Tract Obstruction 56 0.049
81
VSC003 Visceral Leishmaniasis 55 0.049
82
MVM001 Movement Disease 54 0.049
83
STF002 Stiff Skin Syndrome 53 0.049
84
GNG012 Gingival Overgrowth 52 0.049
85
VND001 Vein Disease 52 0.049
86
BLR001 Biliary Atresia 51 0.049
87
GNG011 Gingival Disease 51 0.049
88
NPH018 Nephrogenic Systemic Fibrosis 51 0.049
89
P DWL002 Dowling-Degos Disease 1 51 0.049
90
KLD001 Keloids 51 0.049
91
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.049
92
LMB062 Limb Ischemia 48 0.049
93
NRM004 Neuroma 48 0.049
94
c SPN315 Spinal Muscular Atrophy-1 48 0.049
95
URT031 Ureteral Disease 47 0.049
96
RNL077 Renal Fibrosis 47 0.049
97
c GLC062 Glaucoma 1, Open Angle, E 46 0.049
98
c SPN317 Spinal Muscular Atrophy-3 46 0.049
99
ACR041 Acromelic Frontonasal Dysostosis 46 0.049
100
ALN001 Aland Island Eye Disease 45 0.049
101
VSC047 Vascular Malformation 45 0.049
102
c PST005 Posterior Uveitis 45 0.049
103
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.049
104
BRT030 Birth Defects 43 0.049
105
NPH010 Nephrosclerosis 42 0.049
106
P EPN001 Ependymoblastoma 42 0.049
107
OCL010 Ocular Hypotension 42 0.049
108
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.049
109
NRN002 Neuronitis 42 0.049
110
c SPN316 Spinal Muscular Atrophy-2 42 0.049
111
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.049
112
SPN369 Spinal Disease 41 0.049
113
c PRG001 Progressive Muscular Atrophy 40 0.049
114
CHR413 Chronic Myocardial Ischemia 40 0.049
115
GLC011 Galactose Epimerase Deficiency 40 0.049
116
P DPY001 Dupuytren Contracture 39 0.049
117
OCL011 Ocular Motility Disease 38 0.049
118
MCL027 Macular Dystrophy, Dominant Cystoid 38 0.049
119
LNS003 Lens Disease 38 0.049
120
LRG003 Large Cell Medulloblastoma 38 0.049
121
OST032 Osteofibrous Dysplasia 38 0.049
122
PRP024 Peripheral Osteosarcoma 37 0.049
123
CNJ007 Conjunctivochalasis 37 0.049
124
CRN021 Cornea Cancer 37 0.049
125
CHL013 Cholecystolithiasis 37 0.049
126
BNS002 Bone Structure Disease 36 0.049
127
PRX014 Proximal Spinal Muscular Atrophy 36 0.049
128
MSC004 Muscle Tissue Disease 36 0.049
129
TTR016 Tetra-Amelia Syndrome 36 0.049
130
ADH001 Adhesions of Uterus 36 0.049
131
P LTH016 Lethal Congenital Contractural Syndrome 2 36 0.049
132
c SPN318 Spinal Muscular Atrophy-4 35 0.049
133
MCR001 Microcystic Meningioma 33 0.049
134
KDN013 Kidney Hypertrophy 33 0.049
135
RTN002 Retinal Perforation 32 0.049
136
CVT001 Cavitary Optic Disc Anomalies 32 0.049
137
ANG009 Angiomatous Meningioma 30 0.049
138
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 29 0.049
139
ANT007 Anterior Horn Cell Disease 28 0.049
140
SRV001 Survival Motor Neuron Spinal Muscular Atrophy 25 0.049
141
c STC012 Stickler Syndrome, Type Iv 25 0.049
142
PPL023 Pupil Disease 23 0.049
143
MTR031 Motor Neuro-Ophthalmic Disorders 23 0.049
144
STX003 Setx 19 0.049
145
CMB069 Combined Hamartoma of the Retina and Retinal Pigment Epithelium 16 0.049
146
HRD064 Hereditary Vascular Retinopathy 15 0.049
147
c TYP019 Type Ii Collagenopathies 12 0.049
148
PRM009 Primary Eye Hypotony 11 0.049
149
NDP002 Ndp-Related Retinopathy of Prematurity 9 0.049