Search results for "vitreoretinopathy"

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

186 hits were found for 'vitreoretinopathy'

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 57 7.605
2
PRL011 Proliferative Vitreoretinopathy 43 6.240
3
WGN003 Wagner Syndrome 51 5.185
4
VTR013 Vitreoretinopathy, Neovascular Inflammatory 20 3.894
5
VCN001 Vcan-Related Vitreoretinopathy 6 3.894
6
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 16 3.500
7
c FML042 Familial Exudative Vitreoretinopathy, Autosomal Dominant 22 3.455
8
c EXD008 Exudative Vitreoretinopathy 1 27 3.438
9
c EXD006 Exudative Vitreoretinopathy 5 15 3.420
10
c EXD004 Exudative Vitreoretinopathy 4 16 3.400
11
VTR011 Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia 6 3.378
12
c EXD007 Exudative Vitreoretinopathy 3 8 3.354
13
P EXD009 Exudative Vitreoretinopathy 2, X-Linked 14 2.767
14
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 7 2.738
15
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 7 2.738
16
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 2.738
17
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 7 2.738
18
RTN023 Retinitis 53 0.567
19
RTN017 Retinal Detachment 56 0.438
20
DBT011 Diabetic Retinopathy 70 0.216
21
NRR002 Norrie Disease 74 0.206
22
PRL007 Proliferative Diabetic Retinopathy 53 0.206
23
END072 Endotheliitis 50 0.146
24
BLN003 Blindness 52 0.138
25
SYN053 Syndromic Diarrhea 34 0.138
26
ACN002 Acanthosis Nigricans 64 0.122
27
c CTR002 Cataract 57 0.122
28
P ATX010 Ataxia Neuropathy Spectrum 47 0.122
29
ANK002 Ankylosing Spondylitis 76 0.113
30
P ANG001 Angelman Syndrome 71 0.113
31
ART019 Aortic Valve Stenosis 63 0.113
32
THR013 Thoracic Outlet Syndrome 52 0.113
33
AND002 Androgen Insensitivity Syndrome 80 0.103
34
c AXN002 Axenfeld-Rieger Syndrome 69 0.103
35
c AMY001 Amyotrophic Lateral Sclerosis 66 0.103
36
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.103
37
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.103
38
MYC002 Mycobacterium Avium Complex Disease 58 0.103
39
AND005 Androgen Insensitivity Syndrome, Mild 21 0.103
40
P LVR011 Liver Cancer 90 0.092
41
CTS003 Coats Disease 63 0.092
42
P RTN012 Retinopathy of Prematurity 56 0.092
43
MCL003 Macular Holes 51 0.092
44
P OST002 Osteoporosis 76 0.080
45
P DGR001 Digeorge Syndrome 67 0.080
46
c UVT001 Uveitis 65 0.080
47
ISC004 Ischemia 62 0.080
48
OST024 Osteoporosis-Pseudoglioma Syndrome 59 0.080
49
c OPN001 Open-Angle Glaucoma 59 0.080
50
EYD002 Eye Disease 58 0.080
51
P SPR013 Spiradenoma 55 0.080
52
CHR008 Choroiditis 53 0.080
53
RTN003 Retinal Ischemia 48 0.080
54
RTN018 Retinal Disease 48 0.080
55
NRN002 Neuronitis 43 0.080
56
c MYP006 Myopia 41 0.080
57
CYS001 Cystic Fibrosis 96 0.065
58
P ATX002 Ataxia Telangiectasia 87 0.065
59
P BRS047 Breast Cancer 85 0.065
60
VNH001 Von Hippel-Lindau Disease 81 0.065
61
LSH001 Leishmaniasis 73 0.065
62
c DBT009 Diabetes Mellitus 73 0.065
63
VSC003 Visceral Leishmaniasis 60 0.065
64
c MCR010 Microcephaly 56 0.065
65
ART001 Arterial Tortuosity Syndrome 55 0.065
66
c PRM010 Primary Open Angle Glaucoma 54 0.065
67
AND003 Andersen-Tawil Syndrome 53 0.065
68
P ENC008 Encephalocele 53 0.065
69
c LYM025 Lymphedema 52 0.065
70
SCH016 Schimke Immunoosseous Dysplasia 48 0.065
71
CTS011 Cutis Marmorata Telangiectatica Congenita 45 0.065
72
c RTN016 Retinal Degeneration 44 0.065
73
CHR078 Chorioretinitis 44 0.065
74
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.065
75
TTR016 Tetra-Amelia Syndrome 43 0.065
76
AST006 Astigmatism 42 0.065
77
VTR003 Vitreous Detachment 41 0.065
78
FND003 Fundus Flavimaculatus 37 0.065
79
KLD001 Keloids 36 0.065
80
c PRS062 Persistent Hyperplastic Primary Vitreous 34 0.065
81
ANS004 Anisometropia 27 0.065
82
c BNG076 Benign Exophthalmos Syndrome 22 0.065
83
P TYP019 Type Ii Collagenopathies 15 0.065
84
P HNT001 Huntington's Disease 87 0.046
85
P RTN008 Retinitis Pigmentosa 86 0.046
86
P HMC003 Hemochromatosis 85 0.046
87
P PHC003 Pheochromocytoma 82 0.046
88
P PRP003 Porphyria Cutanea Tarda 75 0.046
89
KWS002 Kawasaki Disease 75 0.046
90
P FML018 Familial Mediterranean Fever 75 0.046
91
RLP001 Relapsing Polychondritis 72 0.046
92
c CWD001 Cowden Disease 71 0.046
93
P STR022 Stargardt Disease 71 0.046
94
c THL005 Thalassemia 71 0.046
95
ART016 Aortic Aneurysm 70 0.046
96
VSC007 Vascular Disease 69 0.046
97
PSD012 Pseudoachondroplasia 69 0.046
98
KLP002 Klippel-Trenaunay Syndrome 69 0.046
99
P MLG068 Malignant Glioma 68 0.046
100
ART021 Arteriosclerosis 67 0.046
101
ERD001 Erdheim-Chester Disease 67 0.046
102
GST023 Gastric Ulcer 66 0.046
103
P VLC001 Velocardiofacial Syndrome 66 0.046
104
CHR072 Chordoma 65 0.046
105
BLR001 Biliary Atresia 65 0.046
106
NRM002 Normal Pressure Hydrocephalus 65 0.046
107
P UVL004 Uveal Melanoma 64 0.046
108
c SCL016 Scleroderma 64 0.046
109
P LRY019 Laryngitis 64 0.046
110
STT002 Status Asthmaticus 63 0.046
111
SPN027 Spinal Stenosis 62 0.046
112
DFC004 Deficiency Anemia 62 0.046
113
P SCL015 Scleritis 60 0.046
114
RST001 Restless Legs Syndrome 60 0.046
115
NTR001 Neutral Lipid Storage Disease 59 0.046
116
P GLB002 Glioblastoma 58 0.046
117
PPL002 Papillary Carcinoma 58 0.046
118
NNS002 Nonspecific Interstitial Pneumonia 57 0.046
119
P MYM002 Moyamoya Disease 57 0.046
120
P SDR002 Siderosis 57 0.046
121
DFF003 Diffuse Scleroderma 57 0.046
122
NPH018 Nephrogenic Systemic Fibrosis 57 0.046
123
LYS001 Loeys-Dietz Syndrome 57 0.046
124
IRN001 Iron Deficiency Anemia 56 0.046
125
P RPD001 Rapidly Progressive Glomerulonephritis 56 0.046
126
P PLC011 Pilocytic Astrocytoma 56 0.046
127
CNG048 Congenital Hepatic Fibrosis 56 0.046
128
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 55 0.046
129
MSN001 Mesangial Proliferative Glomerulonephritis 55 0.046
130
c OST028 Osteochondroma 54 0.046
131
MBS002 Moebius Syndrome 53 0.046
132
RHY001 Rhyns Syndrome 53 0.046
133
CRN024 Corneal Disease 53 0.046
134
P SLV002 Salivary Gland Cancer 53 0.046
135
P ART028 Aortic Aneurysm, Familial Thoracic 4 53 0.046
136
CLN019 Colonic Disease 52 0.046
137
USL001 Usual Interstitial Pneumonia 51 0.046
138
GNG012 Gingival Overgrowth 51 0.046
139
P STR020 Strabismus 51 0.046
140
NPH010 Nephrosclerosis 51 0.046
141
MNN014 Mononeuritis 51 0.046
142
ATX019 Ataxia with Vitamin E Deficiency 50 0.046
143
KRT008 Keratopathy 50 0.046
144
OCL020 Ocular Cicatricial Pemphigoid 50 0.046
145
TLN003 Telangiectasis 49 0.046
146
RDT013 Radiation Proctitis 48 0.046
147
RNL077 Renal Fibrosis 48 0.046
148
HDN002 Head Injury 48 0.046
149
ACR014 Acral Lentiginous Melanoma 48 0.046
150
P FBR045 Fibromatosis, Gingival 48 0.046
151
QBC001 Quebec Platelet Disorder 47 0.046
152
OST032 Osteofibrous Dysplasia 46 0.046
153
HYP054 Hypochromic Anemia 46 0.046
154
LNG017 Lung Giant Cell Carcinoma 46 0.046
155
CNJ007 Conjunctivochalasis 46 0.046
156
BRN105 Burn Scar 46 0.046
157
EVN001 Evans' Syndrome 45 0.046
158
DNR001 Duane Retraction Syndrome 45 0.046
159
SLV021 Salivary Gland Tumor 45 0.046
160
URT031 Ureteral Disease 44 0.046
161
MCR001 Microcystic Meningioma 43 0.046
162
BLL004 Bullous Keratopathy 42 0.046
163
P LSS005 Lissencephaly 1 42 0.046
164
RTN020 Retinal Vascular Disease 41 0.046
165
P DNS004 Duane Syndrome Type 2 40 0.046
166
CHR413 Chronic Myocardial Ischemia 40 0.046
167
GST029 Gastric Cardia Adenocarcinoma 39 0.046
168
P PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 39 0.046
169
VRL011 Viral Infectious Disease 38 0.046
170
IPX001 Ipex Syndrome 36 0.046
171
P MYP018 Myopia 6 36 0.046
172
ADS002 Adie Syndrome 35 0.046
173
FCT013 Factor V Leiden Thrombophilia 34 0.046
174
P INF069 Infantile Neuroaxonal Dystrophy 1 33 0.046
175
c STC012 Stickler Syndrome, Type Iv 31 0.046
176
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.046
177
HNM002 Hinman Syndrome 28 0.046
178
TFT003 Tufting Enteropathy 28 0.046
179
PL2001 Pla2g6-Associated Neurodegeneration 24 0.046
180
LKC002 Leukocoria 22 0.046
181
RTN002 Retinal Perforation 21 0.046
182
BLD053 Blood Platelet Disease 21 0.046
183
ADN025 Adenoameloblastoma 18 0.046
184
c LTH016 Lethal Congenital Contractural Syndrome 2 18 0.046
185
P CHR054 Chronic Closed-Angle Glaucoma 14 0.046
186
c CLL020 Collagenopathy Type 2 Alpha 1 14 0.046