Search results for maculopathy

168 hits were found for maculopathy

# Family MCID Name MIFTS Score
1
c MCL042 Macular Degeneration, Age-Related, 1 79 5.446
2
P TXC009 Toxic Maculopathy 20 4.459
3
MCL018 Macular Dystrophy, Concentric Annular 22 3.709
4
c RTN116 Retinitis Pigmentosa 56 32 3.083
5
PRS110 Persistent Placoid Maculopathy 16 2.424
6
c SPN291 Spinocerebellar Ataxia 7 52 2.210
7
c TXC018 Toxic Maculopathy Due to Antimalarial Drugs 6 2.210
8
PRR004 Preretinal Fibrosis 37 2.141
9
c MCL043 Macular Degeneration, Age-Related, 2 20 2.141
10
MYP060 Myopic Macular Degeneration 13 2.141
11
AGN016 Aging 65 0.309
12
RTN023 Retinitis 52 0.235
13
CHR008 Choroiditis 47 0.188
14
RTN018 Retinal Disease 56 0.170
15
MCL006 Macular Retinal Edema 51 0.163
16
MLN008 Melanoma 72 0.133
17
P RTN016 Retinal Degeneration 56 0.133
18
P MYP006 Myopia 56 0.133
19
RTN209 Retinoschisis 1, X-Linked, Juvenile 56 0.124
20
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.124
21
RFR003 Refractive Error 45 0.124
22
P MCR115 Microvascular Complications of Diabetes 5 66 0.115
23
P MLN069 Melanoma, Uveal 63 0.115
24
VTR003 Vitreous Detachment 40 0.115
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.115
26
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.105
27
P RTN022 Retinal Vein Occlusion 53 0.094
28
P PNV001 Panuveitis 52 0.094
29
P ATS308 Autosomal Dominant Cerebellar Ataxia 47 0.094
30
ACT235 Acute Macular Neuroretinopathy 14 0.094
31
VNH007 Von Hippel-Lindau Syndrome 72 0.082
32
VSC011 Vasculitis 66 0.082
33
MTH009 Mouth Disease 64 0.082
34
RTN017 Retinal Detachment 59 0.082
35
TLN003 Telangiectasis 52 0.082
36
P HMC002 Homocystinuria 50 0.082
37
c CNT016 Central Retinal Vein Occlusion 50 0.082
38
c LBR014 Leber Congenital Amaurosis 4 48 0.082
39
P RTN014 Retinal Artery Occlusion 45 0.082
40
CNT060 Central Serous Chorioretinopathy 45 0.082
41
MCL003 Macular Holes 44 0.082
42
c MCL066 Macular Dystrophy, Vitelliform, 2 41 0.082
43
CHR078 Chorioretinitis 41 0.082
44
WHP002 Whiplash 39 0.082
45
RDN004 Radin Blood Group Antigen 23 0.082
46
MCL057 Macular Dystrophy with Central Cone Involvement 20 0.082
47
P RTN008 Retinitis Pigmentosa 81 0.067
48
VSC007 Vascular Disease 71 0.067
49
P LYM118 Lymphoma 71 0.067
50
ISC004 Ischemia 66 0.067
51
P NRP001 Neuropathy 63 0.067
52
SKN019 Skin Melanoma 63 0.067
53
P UVT001 Uveitis 61 0.067
54
c SPN294 Spinocerebellar Ataxia 1 58 0.067
55
P CNT005 Central Nervous System Lymphoma 57 0.067
56
NRT004 Neuritis 55 0.067
57
OPT009 Optic Neuritis 53 0.067
58
CLB010 Coloboma of Macula 52 0.067
59
CYT005 Cytomegalovirus Retinitis 51 0.067
60
HND002 Hand, Foot and Mouth Disease 50 0.067
61
DBT006 Diabetic Macular Edema 49 0.067
62
NRR001 Neuroretinitis 46 0.067
63
P VTL001 Vitelliform Macular Dystrophy 41 0.067
64
CRB009 Cerebritis 41 0.067
65
c PST022 Posterior Uveal Melanoma 39 0.067
66
c BLD140 Blood Group, I System 37 0.067
67
CHR079 Choroid Disease 37 0.067
68
RTN002 Retinal Perforation 36 0.067
69
DGN002 Degenerative Myopia 32 0.067
70
P INT080 Intraocular Melanoma 28 0.067
71
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 28 0.067
72
UVL003 Uveal Diseases 23 0.067
73
CNR012 Cone-Rod Dystrophy 11 19 0.067
74
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.047
75
P ATX030 Ataxia-Telangiectasia 80 0.047
76
P HRT032 Heart Disease 80 0.047
77
ALP046 Alport Syndrome, X-Linked 74 0.047
78
P DBT009 Diabetes Mellitus 72 0.047
79
c MNN043 Meningioma, Familial 69 0.047
80
LYM017 Lyme Disease 68 0.047
81
P PSD087 Pseudoxanthoma Elasticum 67 0.047
82
c DNG003 Dengue Disease 66 0.047
83
ACQ007 Acquired Immunodeficiency Syndrome 65 0.047
84
P DRM010 Dermatomyositis 65 0.047
85
P SLP006 Sleep Apnea 65 0.047
86
CNN005 Connective Tissue Disease 65 0.047
87
P WLF004 Wolfram Syndrome 61 0.047
88
P HMR003 Hemorrhagic Disease 61 0.047
89
ANR040 Aneurysm 61 0.047
90
P CTR002 Cataract 60 0.047
91
P STR022 Stargardt Disease 58 0.047
92
NRN004 Neuroendocrine Tumor 58 0.047
93
P SBS003 Substance Abuse 57 0.047
94
PRR016 Pierre Robin Syndrome 57 0.047
95
P DNG005 Dengue Virus 56 0.047
96
ALS001 Alstrom Syndrome 55 0.047
97
CHL028 Childhood Type Dermatomyositis 55 0.047
98
MCR004 Macroglobulinemia 54 0.047
99
P PRM002 Primary Hyperoxaluria 53 0.047
100
c ANT034 Anterior Uveitis 53 0.047
101
PRP016 Paraplegia 53 0.047
102
BRD025 Birdshot Chorioretinopathy 53 0.047
103
c STR084 Stargardt Disease 1 51 0.047
104
c GLC097 Glaucoma 3, Primary Congenital, a 51 0.047
105
P NGH001 Night Blindness 51 0.047
106
P MYT002 Myotonic Dystrophy 50 0.047
107
c PST005 Posterior Uveitis 50 0.047
108
PPL021 Papilledema 50 0.047
109
INT303 Intracranial Hypertension, Idiopathic 49 0.047
110
CTY001 Cat Eye Syndrome 49 0.047
111
SRS007 Sorsby Fundus Dystrophy 49 0.047
112
EWN002 Ewing's Family of Tumors 49 0.047
113
P HYP087 Hypotrichosis 48 0.047
114
CHN016 Cohen Syndrome 48 0.047
115
DNN001 Danon Disease 47 0.047
116
RTN001 Retinal Vasculitis 47 0.047
117
GLT007 Glutathione Synthetase Deficiency 47 0.047
118
LGH004 Light Chain Deposition Disease 47 0.047
119
ENH001 Enhanced S-Cone Syndrome 46 0.047
120
AMB002 Amblyopia 45 0.047
121
NRS003 Neurosyphilis 44 0.047
122
P PLL002 Pellagra 44 0.047
123
HRD026 Hereditary Ataxia 43 0.047
124
CNV002 Conversion Disorder 42 0.047
125
CND005 Cone Dystrophy 42 0.047
126
CTS003 Coats Disease 42 0.047
127
CLB003 Coloboma of Optic Nerve 42 0.047
128
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 0.047
129
SPS057 Spasticity 41 0.047
130
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.047
131
BST007 Best Vitelliform Macular Dystrophy 40 0.047
132
c CNT028 Central Retinal Artery Occlusion 40 0.047
133
c MCL060 Macular Dystrophy, Vitelliform, 3 39 0.047
134
P BLD051 Blood Coagulation Disease 38 0.047
135
c RTN069 Retinitis Pigmentosa 7 38 0.047
136
DBT007 Diabetic Cataract 38 0.047
137
RBS002 Rubeosis Iridis 37 0.047
138
VSC008 Vascular Hemostatic Disease 36 0.047
139
ANG037 Angiomatosis 36 0.047
140
c PRM032 Primary Congenital Glaucoma 36 0.047
141
SSC001 Susac Syndrome 36 0.047
142
ANG004 Angioid Streaks 35 0.047
143
PNG001 Pinguecula 35 0.047
144
BRN026 Branch Retinal Artery Occlusion 35 0.047
145
c LBR007 Leber Congenital Amaurosis 12 35 0.047
146
FCT008 Factitious Disorder 35 0.047
147
MLT035 Multifocal Choroiditis 35 0.047
148
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.047
149
DSS010 Dissociative Disorder 34 0.047
150
c GLC083 Glaucoma 3, Primary Infantile, B 33 0.047
151
DGN003 Degeneration of Macula and Posterior Pole 32 0.047
152
SCL014 Scleral Staphyloma 32 0.047
153
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.047
154
ALR002 Al-Raqad Syndrome 30 0.047
155
CVT001 Cavitary Optic Disc Anomalies 28 0.047
156
MXL008 Maxillary Sinus Cancer 27 0.047
157
RTN019 Retinal Telangiectasia 27 0.047
158
GLD003 Goldmann-Favre Syndrome 26 0.047
159
RTN032 Retinal Cone Dystrophy 1 25 0.047
160
c LBR010 Leber Congenital Amaurosis 15 22 0.047
161
c RTN195 Retinitis Pigmentosa 79 22 0.047
162
RTN145 Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis 22 0.047
163
P SNS011 Sinus Cancer 21 0.047
164
CNR016 Cone-Rod Dystrophy 7 20 0.047
165
RTN123 Retinochoroidal Coloboma 18 0.047
166
c MCL056 Macular Dystrophy, Vitelliform, 5 17 0.047
167
RTN212 Retinal Dystrophy with or Without Macular Staphyloma 17 0.047
168
ELS005 Elastoma 16 0.047
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