Search results for vitreoretinopathy

252 hits were found for vitreoretinopathy

# Family MCID Name MIFTS Score
1
P EXD001 Exudative Vitreoretinopathy 47 7.919
2
VTR013 Vitreoretinopathy, Neovascular Inflammatory 50 7.386
3
c EXD008 Exudative Vitreoretinopathy 1 59 5.658
4
c EXD004 Exudative Vitreoretinopathy 4 24 4.476
5
P EXD009 Exudative Vitreoretinopathy 2, X-Linked 24 4.465
6
c EXD006 Exudative Vitreoretinopathy 5 21 4.453
7
c WGN005 Wagner Syndrome 1 28 4.001
8
c EXD010 Exudative Vitreoretinopathy 6 18 3.988
9
P WGN003 Wagner Syndrome 36 3.912
10
c EXD007 Exudative Vitreoretinopathy 3 13 3.461
11
c XLN033 X-Linked Familial Exudative Vitreoretinopathy 14 2.944
12
VCN001 Vcan-Related Vitreoretinopathy 6 2.820
13
c LRP004 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Recessive 7 2.006
14
c FZD001 Fzd4-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.006
15
c LRP003 Lrp5-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.006
16
c TSP001 Tspan12-Related Familial Exudative Vitreoretinopathy, Autosomal Dominant 6 2.006
17
RTN023 Retinitis 50 0.537
18
RTN017 Retinal Detachment 56 0.422
19
NRR002 Norrie Disease 60 0.170
20
END072 Endotheliitis 42 0.123
21
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.116
22
P CTR002 Cataract 58 0.109
23
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.109
24
RTN018 Retinal Disease 53 0.109
25
CHR008 Choroiditis 44 0.109
26
ALR002 Al-Raqad Syndrome 36 0.109
27
EYD002 Eye Disease 61 0.101
28
ETH011 Ethylmalonic Encephalopathy 56 0.101
29
AND005 Androgen Insensitivity Syndrome, Mild 16 0.101
30
HYP266 Hypoxia 56 0.092
31
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 46 0.092
32
P OST002 Osteoporosis 64 0.082
33
ISC004 Ischemia 61 0.082
34
CTS003 Coats Disease 57 0.082
35
RTN003 Retinal Ischemia 48 0.082
36
GLB003 Globe Disease 32 0.082
37
P MYP006 Myopia 56 0.071
38
OST024 Osteoporosis-Pseudoglioma Syndrome 54 0.071
39
P DGR001 Digeorge Syndrome 53 0.071
40
MCL003 Macular Holes 41 0.071
41
PRR004 Preretinal Fibrosis 36 0.071
42
CYS001 Cystic Fibrosis 83 0.058
43
P SPN046 Spinal Muscular Atrophy 65 0.058
44
P DYS007 Dyskeratosis Congenita 63 0.058
45
P LYM025 Lymphedema 61 0.058
46
P GT001 Gout 58 0.058
47
P MCR010 Microcephaly 58 0.058
48
P UVT001 Uveitis 58 0.058
49
P RTN016 Retinal Degeneration 54 0.058
50
P MSC003 Muscular Atrophy 50 0.058
51
P OPN001 Open-Angle Glaucoma 49 0.058
52
P ENC008 Encephalocele 48 0.058
53
RTN020 Retinal Vascular Disease 48 0.058
54
AST006 Astigmatism 45 0.058
55
ALN001 Aland Island Eye Disease 45 0.058
56
P CPL003 Capillary Leak Syndrome 41 0.058
57
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.058
58
CHR078 Chorioretinitis 40 0.058
59
CND005 Cone Dystrophy 39 0.058
60
P PRS062 Persistent Hyperplastic Primary Vitreous 38 0.058
61
TTR016 Tetra-Amelia Syndrome 36 0.058
62
VTR003 Vitreous Detachment 34 0.058
63
CTS011 Cutis Marmorata Telangiectatica Congenita 30 0.058
64
ANS004 Anisometropia 29 0.058
65
CMB069 Combined Hamartoma of the Retina and Retinal Pigment Epithelium 17 0.058
66
P BRS047 Breast Cancer 100 0.041
67
P RTN008 Retinitis Pigmentosa 80 0.041
68
P ART022 Arthritis 75 0.041
69
P RTN024 Retinoblastoma 74 0.041
70
P LGH007 Leigh Syndrome 70 0.041
71
KPS004 Kaposi Sarcoma 67 0.041
72
VSC007 Vascular Disease 67 0.041
73
LSH001 Leishmaniasis 66 0.041
74
P ART023 Arthropathy 64 0.041
75
P HYP098 Hypereosinophilic Syndrome 63 0.041
76
P PRD008 Periodontitis 63 0.041
77
OST085 Osteosarcoma, Somatic 63 0.041
78
P OST001 Osteopetrosis 63 0.041
79
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.041
80
c SPN225 Spondyloarthropathy 1 62 0.041
81
TNG002 Tangier Disease 62 0.041
82
GNG013 Gingivitis 61 0.041
83
OST017 Osteomyelitis 61 0.041
84
PRD007 Periodontal Disease 60 0.041
85
DPH001 Diphtheria 59 0.041
86
CMM005 Common Cold 59 0.041
87
PGT001 Paget's Disease of Bone 59 0.041
88
RSP006 Respiratory System Disease 58 0.041
89
BRN012 Bronchiolitis Obliterans 58 0.041
90
SYN007 Synovitis 58 0.041
91
ING001 Inguinal Hernia 58 0.041
92
SCH014 Schistosomiasis 58 0.041
93
ABL002 Ablepharon-Macrostomia Syndrome 57 0.041
94
VSC003 Visceral Leishmaniasis 56 0.041
95
PLM034 Pulmonary Emphysema 55 0.041
96
LKC001 Leukocyte Adhesion Deficiency 55 0.041
97
P MCR129 Microvascular Complications of Diabetes 1 54 0.041
98
c ART101 Aortic Valve Disease 2 53 0.041
99
FDL002 Food Allergy 53 0.041
100
LBR030 Leber Optic Atrophy 53 0.041
101
BRN106 Burns 52 0.041
102
c OPT055 Optic Atrophy Plus Syndrome 52 0.041
103
ANK001 Ankylosis 51 0.041
104
P STR020 Strabismus 51 0.041
105
P ESN008 Eosinophilic Pneumonia 51 0.041
106
STR008 Strongyloidiasis 51 0.041
107
KLD001 Keloids 51 0.041
108
MTC097 Mitochondrial Complex Iv Deficiency 51 0.041
109
VRN004 Vernal Keratoconjunctivitis 51 0.041
110
ALL009 Allergic Conjunctivitis 51 0.041
111
c VRL012 Viral Meningitis 50 0.041
112
ESN005 Eosinophilic Gastroenteritis 50 0.041
113
P HYP614 Hyperlipidemia, Familial Combined 50 0.041
114
P AGG001 Aggressive Periodontitis 50 0.041
115
HPT074 Hepatic Adenoma, Somatic 50 0.041
116
ONC002 Onchocerciasis 49 0.041
117
P GNT008 Giant Cell Tumor 49 0.041
118
c TRC102 Trichothiodystrophy 1, Photosensitive 49 0.041
119
MVM001 Movement Disease 49 0.041
120
LPD004 Lipoid Nephrosis 48 0.041
121
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.041
122
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 48 0.041
123
PYC001 Pycnodysostosis 48 0.041
124
URN003 Urinary Schistosomiasis 48 0.041
125
P NGH001 Night Blindness 48 0.041
126
CHR005 Chorioamnionitis 48 0.041
127
FML039 Female Reproductive System Disease 48 0.041
128
P TRC086 Trichohepatoenteric Syndrome 1 48 0.041
129
VND001 Vein Disease 47 0.041
130
GST009 Gastroschisis 47 0.041
131
PLP001 Pulpitis 47 0.041
132
MLT016 Multicentric Reticulohistiocytosis 46 0.041
133
GNG011 Gingival Disease 46 0.041
134
RSP002 Respiratory Syncytial Virus Infectious Disease 46 0.041
135
c PST005 Posterior Uveitis 46 0.041
136
PRT082 Preterm Premature Rupture of the Membranes 46 0.041
137
CNR007 Cone-Rod Dystrophy 6 46 0.041
138
PLM035 Pulmonary Eosinophilia 46 0.041
139
INT017 Intestinal Schistosomiasis 45 0.041
140
c CHR086 Chronic Conjunctivitis 45 0.041
141
ACR041 Acromelic Frontonasal Dysostosis 45 0.041
142
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 45 0.041
143
VSC047 Vascular Malformation 45 0.041
144
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 0.041
145
CWP001 Cowpox 45 0.041
146
c GLC062 Glaucoma 1, Open Angle, E 44 0.041
147
PLL012 Pollen Allergy 44 0.041
148
CHR056 Chronic Tic Disorder 44 0.041
149
VTR005 Vitreous Disease 44 0.041
150
HYP299 Hyperostosis, Endosteal 43 0.041
151
BRT030 Birth Defects 43 0.041
152
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.041
153
LNG017 Lung Giant Cell Carcinoma 43 0.041
154
LKC003 Leukocyte Disease 43 0.041
155
PRD004 Prediabetes Syndrome 43 0.041
156
c ACT159 Acute Transverse Myelitis 42 0.041
157
BHR001 Behr Syndrome 42 0.041
158
PRN019 Perinatal Necrotizing Enterocolitis 42 0.041
159
PGT008 Paget Disease of Bone 5, Juvenile-Onset 42 0.041
160
c HYP011 Hyperlipoproteinemia Type Iii 42 0.041
161
RTR008 Root Resorption 42 0.041
162
TND004 Tendinopathy 42 0.041
163
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.041
164
VGN020 Vaginal Disease 41 0.041
165
c ACH036 Achromatopsia-3 41 0.041
166
c OST131 Osteopetrosis, Autosomal Dominant 2 41 0.041
167
CST005 Castleman Disease 41 0.041
168
GLC011 Galactose Epimerase Deficiency 41 0.041
169
NRN002 Neuronitis 41 0.041
170
P ESP035 Esophagitis, Eosinophilic, 1 40 0.041
171
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.041
172
ANG025 Angioimmunoblastic Lymphadenopathy with Dysproteinemia 40 0.041
173
STR077 Streptococcal Toxic-Shock Syndrome 40 0.041
174
TTH001 Tooth Ankylosis 40 0.041
175
PRG008 Paragonimiasis 40 0.041
176
c 3MT015 3-Methylglutaconic Aciduria, Type I 40 0.041
177
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.041
178
c INF087 Inflammatory Bowel Disease 4 40 0.041
179
CHR100 Chronic Ulcer of Skin 40 0.041
180
ANG002 Angiostrongyliasis 39 0.041
181
c FBR084 Fibromatosis, Gingival, 1 39 0.041
182
OST079 Osteolysis, Familial Expansile 39 0.041
183
P 3MT007 3-Methylglutaconic Aciduria 39 0.041
184
MRC001 Marchiafava Bignami Disease 39 0.041
185
DNT008 Denture Stomatitis 39 0.041
186
GNT006 Giant Papillary Conjunctivitis 38 0.041
187
PRS034 Parasitic Helminthiasis Infectious Disease 38 0.041
188
LTX001 Latex Allergy 38 0.041
189
OCL010 Ocular Hypotension 38 0.041
190
TTH008 Tooth Resorption 38 0.041
191
CHL050 Cholesterol Ester Storage Disease 38 0.041
192
c DFN092 Deafness, Autosomal Recessive 49 38 0.041
193
BNR001 Bone Remodeling Disease 37 0.041
194
NTL004 Nut Allergy 37 0.041
195
APP016 Apple Allergy 37 0.041
196
OCL011 Ocular Motility Disease 37 0.041
197
FNS001 Funisitis 37 0.041
198
BNS002 Bone Structure Disease 37 0.041
199
CPL005 Capillary Disease 36 0.041
200
CRV025 Cervical Incompetence 36 0.041
201
OPS001 Opisthorchiasis 36 0.041
202
c HRD015 Hereditary Night Blindness 36 0.041
203
ISC005 Ischemic Bone Disease 36 0.041
204
CNJ007 Conjunctivochalasis 36 0.041
205
c 3MT014 3-Methylglutaconic Aciduria, Type V 36 0.041
206
P LTH016 Lethal Congenital Contractural Syndrome 2 36 0.041
207
MCL027 Macular Dystrophy, Dominant Cystoid 36 0.041
208
MTC005 Mitochondrial Metabolism Disease 36 0.041
209
RDT001 Radiation Cystitis 36 0.041
210
RCR001 Recurrent Corneal Erosion 35 0.041
211
PPL019 Papillary Conjunctivitis 35 0.041
212
ARC001 Arcus Senilis 35 0.041
213
c ATS282 Autosomal Recessive Malignant Osteopetrosis 35 0.041
214
CRC001 Cercarial Dermatitis 34 0.041
215
ADP007 Adie Pupil 34 0.041
216
c OST129 Osteopetrosis, Autosomal Recessive 2 34 0.041
217
HMP018 Hemophilic Arthropathy 34 0.041
218
BGS001 Bagassosis 33 0.041
219
c SBR001 Seborrheic Infantile Dermatitis 33 0.041
220
c PRD030 Periodontitis 1, Juvenile 33 0.041
221
MND001 Mandibular Cancer 33 0.041
222
LKC002 Leukocoria 33 0.041
223
LNS003 Lens Disease 33 0.041
224
ESN006 Eosinophilic Meningitis 33 0.041
225
RTN002 Retinal Perforation 31 0.041
226
PRP002 Periapical Granuloma 31 0.041
227
CVT001 Cavitary Optic Disc Anomalies 31 0.041
228
3MT013 3-Methylglutaconic Aciduria with Deafness, Encephalopathy, and Leigh-Like Syndrome 31 0.041
229
c CNG208 Congenital Disorder of Glycosylation, Type Iic 31 0.041
230
CYT002 Cytokine Deficiency 30 0.041
231
P ATX010 Ataxia Neuropathy Spectrum 30 0.041
232
MTC014 Mitochondrial Dna Deletion Syndromes 30 0.041
233
c CHR013 Chronic Apical Periodontitis 30 0.041
234
c 3MT019 3-Methylglutaconic Aciduria, Type Iv 30 0.041
235
P XLN012 X-Linked Congenital Stationary Night Blindness 29 0.041
236
c TRC101 Trichothiodystrophy 4, Nonphotosensitive 28 0.041
237
c OST134 Osteopetrosis, Autosomal Recessive 6 28 0.041
238
c NGH018 Night Blindness, Congenital Stationary , 1e, Autosomal Recessive 27 0.041
239
MCR216 Microcephaly with or Without Chorioretinopathy, Lymphedema, or Mental Retardation 27 0.041
240
c STC012 Stickler Syndrome, Type Iv 26 0.041
241
c CHR054 Chronic Closed-Angle Glaucoma 25 0.041
242
HNM002 Hinman Syndrome 25 0.041
243
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 25 0.041
244
PGT010 Paget Disease of Bone 5, Juvenile 24 0.041
245
PPL023 Pupil Disease 23 0.041
246
c LGH008 Leigh-Like Syndrome 21 0.041
247
MTR031 Motor Neuro-Ophthalmic Disorders 19 0.041
248
P NNP004 Nonphotosensitive Trichothiodystrophy 15 0.041
249
HRD064 Hereditary Vascular Retinopathy 13 0.041
250
c TYP019 Type Ii Collagenopathies 12 0.041
251
PRM009 Primary Eye Hypotony 11 0.041
252
NDP002 Ndp-Related Retinopathy of Prematurity 6 0.041
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