Search results for vitreoretinopathy

222 hits were found for vitreoretinopathy

# Family MCID Name MIFTS Score
1
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 10.215
2
P EXD001 Exudative Vitreoretinopathy 51 8.405
3
c EXD008 Exudative Vitreoretinopathy 1 65 5.992
4
EXD009 Exudative Vitreoretinopathy 2, X-Linked 32 5.622
5
WGN007 Wagner Vitreoretinopathy 24 5.184
6
c EXD004 Exudative Vitreoretinopathy 4 25 4.751
7
c EXD006 Exudative Vitreoretinopathy 5 19 4.704
8
c EXD007 Exudative Vitreoretinopathy 3 20 3.707
9
c EXD010 Exudative Vitreoretinopathy 6 19 3.666
10
WGN003 Wagner Syndrome 27 3.615
11
c EXD012 Exudative Vitreoretinopathy 7 16 3.022
12
VCN001 Vcan-Related Vitreoretinopathy 4 2.168
13
RTN023 Retinitis 52 0.567
14
RTN017 Retinal Detachment 59 0.449
15
P MCR115 Microvascular Complications of Diabetes 5 66 0.196
16
c MCR129 Microvascular Complications of Diabetes 1 62 0.192
17
NRR002 Norrie Disease 61 0.182
18
c MCR112 Microvascular Complications of Diabetes 2 30 0.182
19
END072 Endotheliitis 46 0.142
20
P ANR048 Aniridia 1 68 0.135
21
RTN018 Retinal Disease 56 0.135
22
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 45 0.135
23
ALR002 Al-Raqad Syndrome 30 0.135
24
P STR035 Streptococcal Group a Invasive Disease 28 0.135
25
ANR038 Anorexia Nervosa 1 21 0.135
26
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.135
27
BLD137 Blood Group--Ahonen 17 0.135
28
P CTR002 Cataract 60 0.128
29
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.128
30
CHR008 Choroiditis 47 0.121
31
c BLD140 Blood Group, I System 37 0.121
32
MCL003 Macular Holes 44 0.113
33
HYP266 Hypoxia 61 0.105
34
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 51 0.105
35
CTS003 Coats Disease 42 0.105
36
P MYP006 Myopia 56 0.096
37
P OST002 Osteoporosis 75 0.086
38
ISC004 Ischemia 66 0.086
39
OST024 Osteoporosis-Pseudoglioma Syndrome 55 0.086
40
DGR001 Digeorge Syndrome 55 0.086
41
RTN003 Retinal Ischemia 50 0.086
42
VTR003 Vitreous Detachment 40 0.086
43
P RTN024 Retinoblastoma 76 0.074
44
ALP046 Alport Syndrome, X-Linked 74 0.074
45
P DYS007 Dyskeratosis Congenita 68 0.074
46
P MCR010 Microcephaly 57 0.074
47
AST006 Astigmatism 48 0.074
48
NRN002 Neuronitis 43 0.074
49
P PRS062 Persistent Hyperplastic Primary Vitreous 41 0.074
50
CHR078 Chorioretinitis 41 0.074
51
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.074
52
BNM029 Bone Mineral Density Quantitative Trait Locus 15 39 0.074
53
P BLD124 Bleeding Disorder, Platelet-Type, 11 38 0.074
54
PRR004 Preretinal Fibrosis 37 0.074
55
c PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 33 0.074
56
BNM022 Bone Mineral Density Quantitative Trait Locus 8 32 0.074
57
BLD163 Blood Group, Dombrock System 23 0.074
58
P BRS047 Breast Cancer 100 0.061
59
CYS001 Cystic Fibrosis 85 0.061
60
LSH001 Leishmaniasis 71 0.061
61
VSC007 Vascular Disease 71 0.061
62
AGN016 Aging 65 0.061
63
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.061
64
P SPN046 Spinal Muscular Atrophy 63 0.061
65
P LYM025 Lymphedema 63 0.061
66
P UVT001 Uveitis 61 0.061
67
GT001 Gout 60 0.061
68
VSC003 Visceral Leishmaniasis 59 0.061
69
P RTN016 Retinal Degeneration 56 0.061
70
P MSC003 Muscular Atrophy 55 0.061
71
STR020 Strabismus 55 0.061
72
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.061
73
HPT082 Hepatic Adenomas, Familial 52 0.061
74
P OPN001 Open-Angle Glaucoma 51 0.061
75
KLD001 Keloids 50 0.061
76
P ENC008 Encephalocele 48 0.061
77
RTN020 Retinal Vascular Disease 46 0.061
78
c LTH008 Lethal Congenital Contracture Syndrome 2 46 0.061
79
CND005 Cone Dystrophy 42 0.061
80
CHR413 Chronic Myocardial Ischemia 41 0.061
81
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 36 0.061
82
CTS011 Cutis Marmorata Telangiectatica Congenita 36 0.061
83
ANS004 Anisometropia 32 0.061
84
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 31 0.061
85
c CHR054 Chronic Closed-Angle Glaucoma 28 0.061
86
LKC002 Leukocoria 27 0.061
87
RTN019 Retinal Telangiectasia 27 0.061
88
CMB069 Combined Hamartoma of the Retina and Retinal Pigment Epithelium 21 0.061
89
INS024 Insulin-Like Growth Factor I 83 0.043
90
P RTN008 Retinitis Pigmentosa 81 0.043
91
P MYL005 Myelofibrosis 75 0.043
92
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.043
93
PSY004 Psychotic Disorder 72 0.043
94
VNH007 Von Hippel-Lindau Syndrome 72 0.043
95
P TTR001 Tetralogy of Fallot 70 0.043
96
LNG099 Lung Disease 67 0.043
97
P CNJ013 Conjunctivitis 67 0.043
98
P KDN017 Kidney Cancer 66 0.043
99
c PRC016 Pre-Eclampsia 65 0.043
100
P THR014 Thrombocytopenia 65 0.043
101
HYP066 Hyperglycemia 64 0.043
102
PMS001 Poems Syndrome 64 0.043
103
LRN002 Laron Syndrome 63 0.043
104
P HMN010 Hemangioma 61 0.043
105
c AFB002 Afibrinogenemia, Congenital 61 0.043
106
BRN056 Bronchopulmonary Dysplasia 61 0.043
107
IDP011 Idiopathic Interstitial Pneumonia 60 0.043
108
KLP010 Klippel-Trenaunay-Weber Syndrome 60 0.043
109
CLR108 Colorectal Adenoma 60 0.043
110
PLC005 Placental Insufficiency 59 0.043
111
c GLC092 Glaucoma, Primary Open Angle 58 0.043
112
P ACT105 Acute Mountain Sickness 58 0.043
113
P RNL003 Renal Clear Cell Carcinoma 58 0.043
114
P ECL001 Eclampsia 57 0.043
115
ANG020 Angiosarcoma 57 0.043
116
URN010 Urinary Tract Obstruction 57 0.043
117
P SLV001 Silver-Russell Syndrome 57 0.043
118
BRN106 Burns 57 0.043
119
P LRY019 Laryngitis 57 0.043
120
P CPL006 Capillary Hemangioma 56 0.043
121
BLR001 Biliary Atresia 56 0.043
122
CRT049 Critical Limb Ischemia 56 0.043
123
NPH018 Nephrogenic Systemic Fibrosis 56 0.043
124
c BRS049 Breast Carcinoma in Situ 55 0.043
125
CLR030 Clear Cell Renal Cell Carcinoma 55 0.043
126
KRT002 Keratomalacia 55 0.043
127
c OST164 Osteoporosis, Juvenile 54 0.043
128
c PYR010 Peyronie's Disease 54 0.043
129
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.043
130
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 53 0.043
131
STF002 Stiff Skin Syndrome 53 0.043
132
PRV004 Periventricular Leukomalacia 53 0.043
133
ENT011 Enterocolitis 52 0.043
134
LMB062 Limb Ischemia 52 0.043
135
CHR005 Chorioamnionitis 52 0.043
136
GNG012 Gingival Overgrowth 52 0.043
137
c STR084 Stargardt Disease 1 51 0.043
138
NRM004 Neuroma 51 0.043
139
CRN027 Corneal Neovascularization 51 0.043
140
OST032 Osteofibrous Dysplasia 51 0.043
141
AML029 Ameloblastoma 51 0.043
142
TWN001 Twin-to-Twin Transfusion Syndrome 51 0.043
143
P NGH001 Night Blindness 51 0.043
144
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 0.043
145
SHH001 Sheehan Syndrome 50 0.043
146
GNG011 Gingival Disease 50 0.043
147
P EPT020 Epithelioid Hemangioendothelioma 50 0.043
148
URT031 Ureteral Disease 50 0.043
149
c PST005 Posterior Uveitis 50 0.043
150
P GNG025 Gingival Fibromatosis 50 0.043
151
HYD002 Hydronephrosis 49 0.043
152
c FBR084 Fibromatosis, Gingival, 1 49 0.043
153
RNL077 Renal Fibrosis 49 0.043
154
c ERY048 Erythrocytosis, Familial, 2 48 0.043
155
HYP457 Hypertrophic Scars 48 0.043
156
PRT014 Protein S Deficiency 47 0.043
157
c LSS005 Lissencephaly 1 46 0.043
158
ACD008 Acid-Labile Subunit Deficiency 46 0.043
159
P EPN001 Ependymoblastoma 46 0.043
160
c PTT056 Pituitary Adenoma 1, Multiple Types 46 0.043
161
NPH010 Nephrosclerosis 46 0.043
162
PLC001 Placenta Accreta 46 0.043
163
LKM006 Leukomalacia 46 0.043
164
GLC011 Galactose Epimerase Deficiency 46 0.043
165
NTR005 Nutritional Deficiency Disease 46 0.043
166
PYG006 Pyogenic Granuloma 45 0.043
167
RFR003 Refractive Error 45 0.043
168
ISL015 Isolated Growth Hormone Deficiency, Type Ib 44 0.043
169
MCR225 Macrophage Activation Syndrome 44 0.043
170
P PLL002 Pellagra 44 0.043
171
VTR005 Vitreous Disease 43 0.043
172
ACT032 Acute Hemorrhagic Leukoencephalitis 43 0.043
173
VSC006 Vascular Cancer 43 0.043
174
MLR003 Melorheostosis 43 0.043
175
CNV002 Conversion Disorder 42 0.043
176
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.043
177
P OPT070 Optic Nerve Hypoplasia, Bilateral 42 0.043
178
LPD014 Lipodermatosclerosis 42 0.043
179
c SCN052 Secondary Adrenal Insufficiency 41 0.043
180
ADP007 Adie Pupil 41 0.043
181
P EPL116 Epileptic Encephalopathy, Childhood-Onset 41 0.043
182
CHP002 Chops Syndrome 40 0.043
183
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.043
184
FNS001 Funisitis 40 0.043
185
RVS001 Revesz Syndrome 39 0.043
186
END025 Endometrial Squamous Cell Carcinoma 39 0.043
187
OCL010 Ocular Hypotension 39 0.043
188
CHL013 Cholecystolithiasis 39 0.043
189
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.043
190
PRL008 Paralytic Ileus 38 0.043
191
ADN008 Adenosquamous Pancreas Carcinoma 38 0.043
192
BLT001 Bilateral Retinoblastoma 38 0.043
193
HMC038 Hemochromatosis, Neonatal 38 0.043
194
SLP010 Slipped Capital Femoral Epiphysis 37 0.043
195
c DFN120 Deafness, Autosomal Recessive 39 36 0.043
196
RTN002 Retinal Perforation 36 0.043
197
INT104 Intravascular Papillary Endothelial Hyperplasia 35 0.043
198
c DFN330 Deafness, Autosomal Recessive 97 35 0.043
199
NNT011 Neonatal Anemia 35 0.043
200
LRG003 Large Cell Medulloblastoma 34 0.043
201
DSS010 Dissociative Disorder 34 0.043
202
CRT012 Cortical Blindness 34 0.043
203
c FML008 Familial Retinoblastoma 33 0.043
204
ANG007 Angiokeratoma Circumscriptum 33 0.043
205
HRD016 Hereditary Retinal Dystrophy 32 0.043
206
ANG009 Angiomatous Meningioma 32 0.043
207
P KLZ004 Kala-Azar 1 31 0.043
208
P VTR008 Vitreoretinal Degeneration 30 0.043
209
CYC001 Cycloplegia 29 0.043
210
ATX010 Ataxia Neuropathy Spectrum 29 0.043
211
GLM001 Glomeruloid Hemangioma 29 0.043
212
CRN021 Cornea Cancer 27 0.043
213
ADM001 Adamantinous Craniopharyngioma 26 0.043
214
c STC012 Stickler Syndrome, Type Iv 23 0.043
215
NTR027 Neutrophil Actin Dysfunction 23 0.043
216
NDL006 Nodular Prostate 22 0.043
217
SHK001 Shaken Baby Syndrome 21 0.043
218
c MNT159 Mental Retardation, Autosomal Dominant 19 20 0.043
219
BLN008 Blind Hypotensive Eye 19 0.043
220
MSC148 Musical Perfect Pitch 19 0.043
221
ORB003 Orbital Tenonitis 17 0.043
222
AND005 Androgen Insensitivity Syndrome, Mild 16 0.043
Content
Loading form....