Search results for "vitreoretinopathy"

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

184 hits were found for 'vitreoretinopathy'

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 58 7.610
2
PRL011 Proliferative Vitreoretinopathy 43 6.248
3
WGN003 Wagner Syndrome 49 5.186
4
VTR013 Vitreoretinopathy, Neovascular Inflammatory 18 3.895
5
VCN001 Vcan-Related Vitreoretinopathy 6 3.895
6
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 17 3.501
7
P FML042 Familial Exudative Vitreoretinopathy, Autosomal Dominant 20 3.456
8
c EXD008 Exudative Vitreoretinopathy 1 23 3.439
9
c EXD004 Exudative Vitreoretinopathy 4 13 3.401
10
c EXD006 Exudative Vitreoretinopathy 5 12 3.401
11
VTR011 Vitreoretinopathy with Phalangeal Epiphyseal Dysplasia 6 3.379
12
c EXD007 Exudative Vitreoretinopathy 3 8 3.354
13
P EXD009 Exudative Vitreoretinopathy 2, X-Linked 11 2.768
14
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 5 2.739
15
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 5 2.739
16
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 5 2.739
17
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 5 2.739
18
RTN023 Retinitis 54 0.569
19
RTN017 Retinal Detachment 56 0.440
20
DBT011 Diabetic Retinopathy 71 0.217
21
NRR002 Norrie Disease 74 0.207
22
PRL007 Proliferative Diabetic Retinopathy 54 0.207
23
END072 Endotheliitis 51 0.147
24
BLN003 Blindness 53 0.139
25
SYN053 Syndromic Diarrhea 34 0.139
26
ACN002 Acanthosis Nigricans 63 0.123
27
c CTR002 Cataract 57 0.123
28
P ATX010 Ataxia Neuropathy Spectrum 43 0.123
29
ANK002 Ankylosing Spondylitis 77 0.113
30
P ANG001 Angelman Syndrome 70 0.113
31
ART019 Aortic Valve Stenosis 64 0.113
32
THR013 Thoracic Outlet Syndrome 52 0.113
33
AND002 Androgen Insensitivity Syndrome 80 0.104
34
c AXN002 Axenfeld-Rieger Syndrome 67 0.104
35
c AMY001 Amyotrophic Lateral Sclerosis 67 0.104
36
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.104
37
MYC002 Mycobacterium Avium Complex Disease 59 0.104
38
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.104
39
AND005 Androgen Insensitivity Syndrome, Mild 21 0.104
40
P LVR011 Liver Cancer 91 0.093
41
CTS003 Coats Disease 62 0.093
42
P RTN012 Retinopathy of Prematurity 57 0.093
43
MCL003 Macular Holes 52 0.093
44
P OST002 Osteoporosis 76 0.080
45
P DGR001 Digeorge Syndrome 67 0.080
46
c UVT001 Uveitis 66 0.080
47
ISC004 Ischemia 63 0.080
48
c OPN001 Open-Angle Glaucoma 60 0.080
49
EYD002 Eye Disease 59 0.080
50
OST024 Osteoporosis-Pseudoglioma Syndrome 58 0.080
51
P SPR013 Spiradenoma 56 0.080
52
CHR008 Choroiditis 54 0.080
53
RTN003 Retinal Ischemia 49 0.080
54
RTN018 Retinal Disease 49 0.080
55
NRN002 Neuronitis 44 0.080
56
c MYP006 Myopia 41 0.080
57
CYS001 Cystic Fibrosis 97 0.066
58
P ATX002 Ataxia Telangiectasia 87 0.066
59
P BRS047 Breast Cancer 86 0.066
60
VNH001 Von Hippel-Lindau Disease 81 0.066
61
LSH001 Leishmaniasis 74 0.066
62
c DBT009 Diabetes Mellitus 74 0.066
63
VSC003 Visceral Leishmaniasis 61 0.066
64
c PRM010 Primary Open Angle Glaucoma 55 0.066
65
ART001 Arterial Tortuosity Syndrome 55 0.066
66
AND003 Andersen-Tawil Syndrome 54 0.066
67
P ENC008 Encephalocele 54 0.066
68
MCR010 Microcephaly 53 0.066
69
c LYM025 Lymphedema 53 0.066
70
SCH016 Schimke Immunoosseous Dysplasia 47 0.066
71
CTS011 Cutis Marmorata Telangiectatica Congenita 45 0.066
72
CHR078 Chorioretinitis 44 0.066
73
P RTN016 Retinal Degeneration 44 0.066
74
AST006 Astigmatism 42 0.066
75
TTR016 Tetra-Amelia Syndrome 42 0.066
76
VTR003 Vitreous Detachment 42 0.066
77
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.066
78
FND003 Fundus Flavimaculatus 38 0.066
79
KLD001 Keloids 34 0.066
80
PRS062 Persistent Hyperplastic Primary Vitreous 32 0.066
81
ANS004 Anisometropia 28 0.066
82
c BNG076 Benign Exophthalmos Syndrome 22 0.066
83
P TYP019 Type Ii Collagenopathies 16 0.066
84
P HNT001 Huntington's Disease 87 0.046
85
P RTN008 Retinitis Pigmentosa 86 0.046
86
P HMC003 Hemochromatosis 83 0.046
87
P PHC003 Pheochromocytoma 80 0.046
88
P FML018 Familial Mediterranean Fever 76 0.046
89
KWS002 Kawasaki Disease 76 0.046
90
P PRP003 Porphyria Cutanea Tarda 75 0.046
91
c CWD001 Cowden Disease 72 0.046
92
c THL005 Thalassemia 72 0.046
93
RLP001 Relapsing Polychondritis 72 0.046
94
ART016 Aortic Aneurysm 71 0.046
95
P STR022 Stargardt Disease 71 0.046
96
VSC007 Vascular Disease 70 0.046
97
KLP002 Klippel-Trenaunay Syndrome 69 0.046
98
P MLG068 Malignant Glioma 69 0.046
99
ART021 Arteriosclerosis 68 0.046
100
PSD012 Pseudoachondroplasia 68 0.046
101
GST023 Gastric Ulcer 67 0.046
102
ERD001 Erdheim-Chester Disease 67 0.046
103
CHR072 Chordoma 66 0.046
104
c SCL016 Scleroderma 65 0.046
105
P LRY019 Laryngitis 65 0.046
106
P VLC001 Velocardiofacial Syndrome 64 0.046
107
STT002 Status Asthmaticus 64 0.046
108
P UVL004 Uveal Melanoma 64 0.046
109
SPN027 Spinal Stenosis 63 0.046
110
DFC004 Deficiency Anemia 63 0.046
111
BLR001 Biliary Atresia 63 0.046
112
NRM002 Normal Pressure Hydrocephalus 62 0.046
113
P SCL015 Scleritis 61 0.046
114
RST001 Restless Legs Syndrome 61 0.046
115
PPL002 Papillary Carcinoma 59 0.046
116
P GLB002 Glioblastoma 58 0.046
117
NNS002 Nonspecific Interstitial Pneumonia 58 0.046
118
P MYM002 Moyamoya Disease 58 0.046
119
P SDR002 Siderosis 58 0.046
120
NPH018 Nephrogenic Systemic Fibrosis 58 0.046
121
LYS001 Loeys-Dietz Syndrome 57 0.046
122
IRN001 Iron Deficiency Anemia 57 0.046
123
P RPD001 Rapidly Progressive Glomerulonephritis 57 0.046
124
P PLC011 Pilocytic Astrocytoma 57 0.046
125
DFF003 Diffuse Scleroderma 57 0.046
126
CNG048 Congenital Hepatic Fibrosis 57 0.046
127
MSN001 Mesangial Proliferative Glomerulonephritis 56 0.046
128
NTR001 Neutral Lipid Storage Disease 55 0.046
129
c OST028 Osteochondroma 54 0.046
130
CRN024 Corneal Disease 54 0.046
131
P SLV002 Salivary Gland Cancer 54 0.046
132
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 53 0.046
133
CLN019 Colonic Disease 53 0.046
134
MBS002 Moebius Syndrome 53 0.046
135
USL001 Usual Interstitial Pneumonia 52 0.046
136
GNG012 Gingival Overgrowth 52 0.046
137
P STR020 Strabismus 52 0.046
138
NPH010 Nephrosclerosis 52 0.046
139
RHY001 Rhyns Syndrome 51 0.046
140
MNN014 Mononeuritis 51 0.046
141
P ART028 Aortic Aneurysm, Familial Thoracic 4 51 0.046
142
KRT008 Keratopathy 51 0.046
143
OCL020 Ocular Cicatricial Pemphigoid 51 0.046
144
ATX019 Ataxia with Vitamin E Deficiency 50 0.046
145
TLN003 Telangiectasis 49 0.046
146
RDT013 Radiation Proctitis 49 0.046
147
RNL077 Renal Fibrosis 49 0.046
148
HDN002 Head Injury 49 0.046
149
ACR014 Acral Lentiginous Melanoma 49 0.046
150
P FBR045 Fibromatosis, Gingival 48 0.046
151
OST032 Osteofibrous Dysplasia 47 0.046
152
HYP054 Hypochromic Anemia 47 0.046
153
LNG017 Lung Giant Cell Carcinoma 47 0.046
154
CNJ007 Conjunctivochalasis 47 0.046
155
BRN105 Burn Scar 46 0.046
156
EVN001 Evans' Syndrome 46 0.046
157
QBC001 Quebec Platelet Disorder 46 0.046
158
DNR001 Duane Retraction Syndrome 45 0.046
159
URT031 Ureteral Disease 45 0.046
160
SLV021 Salivary Gland Tumor 44 0.046
161
MCR001 Microcystic Meningioma 44 0.046
162
BLL004 Bullous Keratopathy 43 0.046
163
RTN020 Retinal Vascular Disease 41 0.046
164
P LSS005 Lissencephaly 1 40 0.046
165
GST029 Gastric Cardia Adenocarcinoma 40 0.046
166
CHR413 Chronic Myocardial Ischemia 39 0.046
167
P DNS004 Duane Syndrome Type 2 39 0.046
168
VRL011 Viral Infectious Disease 39 0.046
169
IPX001 Ipex Syndrome 37 0.046
170
P MYP018 Myopia 6 36 0.046
171
ADS002 Adie Syndrome 35 0.046
172
PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 35 0.046
173
FCT013 Factor V Leiden Thrombophilia 34 0.046
174
P INF069 Infantile Neuroaxonal Dystrophy 1 31 0.046
175
TFT003 Tufting Enteropathy 28 0.046
176
HNM002 Hinman Syndrome 28 0.046
177
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.046
178
PL2001 Pla2g6-Associated Neurodegeneration 25 0.046
179
LKC002 Leukocoria 23 0.046
180
RTN002 Retinal Perforation 22 0.046
181
BLD053 Blood Platelet Disease 21 0.046
182
ADN025 Adenoameloblastoma 19 0.046
183
P CHR054 Chronic Closed-Angle Glaucoma 15 0.046
184
c CLL020 Collagenopathy Type 2 Alpha 1 14 0.046