Search results for "vitreoretinopathy"

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

172 hits were found for 'vitreoretinopathy'

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 61 7.932
2
PRL011 Proliferative Vitreoretinopathy 43 6.306
3
WGN003 Wagner Syndrome 48 4.455
4
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 16 3.544
5
c FML042 Familial Exudative Vitreoretinopathy, Autosomal Dominant 20 3.498
6
c EXD004 Exudative Vitreoretinopathy 4 14 3.462
7
c EXD006 Exudative Vitreoretinopathy 5 12 3.442
8
VTR013 Vitreoretinopathy, Neovascular Inflammatory 17 3.420
9
VCN001 Vcan-Related Vitreoretinopathy 6 3.420
10
P LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 6 3.395
11
P EXD005 Exudative Vitreoretinopathy, X-Linked 14 2.849
12
VTR011 Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia 6 2.802
13
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 5 2.772
14
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 5 2.772
15
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 5 2.772
16
c EXD003 Exudative Vitreoretinopathy-3 8 1.960
17
RTN023 Retinitis 53 0.561
18
RTN017 Retinal Detachment 55 0.436
19
DBT011 Diabetic Retinopathy 70 0.217
20
NRR002 Norrie Disease 74 0.206
21
PRL007 Proliferative Diabetic Retinopathy 53 0.206
22
BLN003 Blindness 52 0.134
23
END072 Endotheliitis 50 0.134
24
SYN053 Syndromic Diarrhea 32 0.134
25
ACN002 Acanthosis Nigricans 69 0.116
26
c CTR002 Cataract 57 0.116
27
P ATX010 Ataxia Neuropathy Spectrum 41 0.116
28
P AMY001 Amyotrophic Lateral Sclerosis 98 0.106
29
AND002 Androgen Insensitivity Syndrome 80 0.106
30
ANK002 Ankylosing Spondylitis 74 0.106
31
P ANG001 Angelman Syndrome 70 0.106
32
c AXN002 Axenfeld-Rieger Syndrome 66 0.106
33
ART019 Aortic Valve Stenosis 64 0.106
34
MYC002 Mycobacterium Avium Complex Disease 58 0.106
35
THR013 Thoracic Outlet Syndrome 52 0.106
36
AND005 Androgen Insensitivity Syndrome, Mild 21 0.106
37
HPT023 Hepatocellular Carcinoma 79 0.095
38
CTS003 Coats Disease 61 0.095
39
P RTN012 Retinopathy of Prematurity 56 0.095
40
MCL003 Macular Holes 51 0.095
41
P OST002 Osteoporosis 75 0.082
42
P DGR001 Digeorge Syndrome 67 0.082
43
c UVT001 Uveitis 65 0.082
44
ISC004 Ischemia 63 0.082
45
EYD002 Eye Disease 60 0.082
46
P GLC007 Glaucoma 60 0.082
47
c OPN001 Open-Angle Glaucoma 57 0.082
48
OST024 Osteoporosis-Pseudoglioma Syndrome 57 0.082
49
CHR008 Choroiditis 55 0.082
50
RTN003 Retinal Ischemia 48 0.082
51
RTN018 Retinal Disease 48 0.082
52
NRN002 Neuronitis 43 0.082
53
c MYP006 Myopia 40 0.082
54
P BRS047 Breast Cancer 100 0.067
55
CYS001 Cystic Fibrosis 96 0.067
56
P ATX002 Ataxia Telangiectasia 86 0.067
57
VNH001 Von Hippel-Lindau Disease 80 0.067
58
c DBT009 Diabetes Mellitus 78 0.067
59
LSH001 Leishmaniasis 74 0.067
60
VSC003 Visceral Leishmaniasis 59 0.067
61
c PRM010 Primary Open Angle Glaucoma 55 0.067
62
ART001 Arterial Tortuosity Syndrome 54 0.067
63
AND003 Andersen-Tawil Syndrome 53 0.067
64
P ENC008 Encephalocele 52 0.067
65
PRS062 Persistent Hyperplastic Primary Vitreous 48 0.067
66
SCH016 Schimke Immunoosseous Dysplasia 46 0.067
67
P RTN016 Retinal Degeneration 43 0.067
68
AST006 Astigmatism 42 0.067
69
ENC017 Encephaloceles 42 0.067
70
TTR016 Tetra-Amelia Syndrome 41 0.067
71
VTR003 Vitreous Detachment 41 0.067
72
FND003 Fundus Flavimaculatus 36 0.067
73
KLD001 Keloids 34 0.067
74
ANS004 Anisometropia 27 0.067
75
c BNG076 Benign Exophthalmos Syndrome 22 0.067
76
P TYP019 Type Ii Collagenopathies 15 0.067
77
P HNT001 Huntington's Disease 85 0.047
78
P LBR001 Leber Congenital Amaurosis 81 0.047
79
P RTN008 Retinitis Pigmentosa 80 0.047
80
P HMC003 Hemochromatosis 78 0.047
81
P PHC003 Pheochromocytoma 78 0.047
82
P PRP003 Porphyria Cutanea Tarda 75 0.047
83
P FML018 Familial Mediterranean Fever 74 0.047
84
KWS002 Kawasaki Disease 73 0.047
85
c THL005 Thalassemia 72 0.047
86
c CWD001 Cowden Disease 71 0.047
87
P STR022 Stargardt Disease 71 0.047
88
ART016 Aortic Aneurysm 70 0.047
89
RLP001 Relapsing Polychondritis 70 0.047
90
VSC007 Vascular Disease 70 0.047
91
P MLG068 Malignant Glioma 68 0.047
92
PSD012 Pseudoachondroplasia 67 0.047
93
GST023 Gastric Ulcer 67 0.047
94
ART021 Arteriosclerosis 67 0.047
95
ERD001 Erdheim-Chester Disease 66 0.047
96
CHR072 Chordoma 66 0.047
97
P LRY019 Laryngitis 65 0.047
98
c SCL016 Scleroderma 64 0.047
99
P VLC001 Velocardiofacial Syndrome 63 0.047
100
SPN027 Spinal Stenosis 62 0.047
101
DFC004 Deficiency Anemia 62 0.047
102
BLR001 Biliary Atresia 62 0.047
103
NRM002 Normal Pressure Hydrocephalus 61 0.047
104
STT002 Status Asthmaticus 60 0.047
105
P SCL015 Scleritis 59 0.047
106
NTR001 Neutral Lipid Storage Disease 59 0.047
107
PPL002 Papillary Carcinoma 59 0.047
108
NPH018 Nephrogenic Systemic Fibrosis 58 0.047
109
P PLC011 Pilocytic Astrocytoma 57 0.047
110
NNS002 Nonspecific Interstitial Pneumonia 57 0.047
111
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.047
112
IRN001 Iron Deficiency Anemia 57 0.047
113
SDR002 Siderosis 56 0.047
114
DFF003 Diffuse Scleroderma 56 0.047
115
P MYM002 Moyamoya Disease 56 0.047
116
CNG048 Congenital Hepatic Fibrosis 56 0.047
117
MSN001 Mesangial Proliferative Glomerulonephritis 55 0.047
118
RST001 Restless Legs Syndrome 55 0.047
119
c OST028 Osteochondroma 54 0.047
120
LYS001 Loeys-Dietz Syndrome 54 0.047
121
MBS002 Moebius Syndrome 53 0.047
122
CLN019 Colonic Disease 53 0.047
123
NPH010 Nephrosclerosis 53 0.047
124
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 53 0.047
125
CRN024 Corneal Disease 52 0.047
126
P SLV002 Salivary Gland Cancer 52 0.047
127
GNG012 Gingival Overgrowth 51 0.047
128
P STR020 Strabismus 51 0.047
129
USL001 Usual Interstitial Pneumonia 51 0.047
130
MNN014 Mononeuritis 51 0.047
131
P ART028 Aortic Aneurysm, Familial Thoracic 4 50 0.047
132
KRT008 Keratopathy 50 0.047
133
OCL020 Ocular Cicatricial Pemphigoid 49 0.047
134
ATX019 Ataxia with Vitamin E Deficiency 49 0.047
135
RDT013 Radiation Proctitis 49 0.047
136
HDN002 Head Injury 48 0.047
137
P FBR045 Fibromatosis, Gingival 47 0.047
138
ACR014 Acral Lentiginous Melanoma 47 0.047
139
OST032 Osteofibrous Dysplasia 47 0.047
140
LNG017 Lung Giant Cell Carcinoma 47 0.047
141
RNL077 Renal Fibrosis 46 0.047
142
EVN001 Evans' Syndrome 46 0.047
143
CNJ007 Conjunctivochalasis 46 0.047
144
QBC001 Quebec Platelet Disorder 45 0.047
145
HYP054 Hypochromic Anemia 45 0.047
146
DNR001 Duane Retraction Syndrome 45 0.047
147
BRN105 Burn Scar 45 0.047
148
URT031 Ureteral Disease 44 0.047
149
MCR001 Microcystic Meningioma 43 0.047
150
BLL004 Bullous Keratopathy 43 0.047
151
RTN020 Retinal Vascular Disease 41 0.047
152
P DNS004 Duane Syndrome Type 2 39 0.047
153
GST029 Gastric Cardia Adenocarcinoma 39 0.047
154
P LSS005 Lissencephaly 1 39 0.047
155
IPX001 Ipex Syndrome 37 0.047
156
VRL011 Viral Infectious Disease 36 0.047
157
ADS002 Adie Syndrome 35 0.047
158
FCT013 Factor V Leiden Thrombophilia 33 0.047
159
RHY001 Rhyns Syndrome 33 0.047
160
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.047
161
P MYP018 Myopia 6 30 0.047
162
TFT003 Tufting Enteropathy 28 0.047
163
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.047
164
HNM002 Hinman Syndrome 27 0.047
165
PL2001 Pla2g6-Associated Neurodegeneration 24 0.047
166
LKC002 Leukocoria 22 0.047
167
ADN025 Adenoameloblastoma 22 0.047
168
BLD053 Blood Platelet Disease 21 0.047
169
RTN002 Retinal Perforation 21 0.047
170
P CHR054 Chronic Closed-Angle Glaucoma 15 0.047
171
c CLL020 Collagenopathy Type 2 Alpha 1 14 0.047
172
MYP024 Myopia, X-Linked 7 0.047