Search results for "maculopathy"

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

98 hits were found for 'maculopathy'

# Family MCID Name MIFTS Score
1
c MCL042 Macular Degeneration, Age-Related, 1 72 4.994
2
P TXC009 Toxic Maculopathy 13 4.659
3
PRS110 Persistent Placoid Maculopathy 8 3.401
4
c TXC018 Toxic Maculopathy Due to Antimalarial Drugs 6 3.193
5
c SPN291 Spinocerebellar Ataxia 7 42 2.233
6
PRR004 Preretinal Fibrosis 11 2.233
7
P MCL018 Macular Dystrophy, Concentric Annular 6 2.233
8
MYP060 Myopic Macular Degeneration 7 2.233
9
CHR008 Choroiditis 45 0.215
10
RTN023 Retinitis 44 0.200
11
P ATX004 Ataxia 50 0.124
12
P RTN025 Retinoschisis 50 0.124
13
P SPN049 Spinocerebellar Ataxia 53 0.111
14
MLN008 Melanoma 55 0.096
15
EYD002 Eye Disease 54 0.096
16
P HMC002 Homocystinuria 52 0.096
17
c PST005 Posterior Uveitis 50 0.096
18
RTN018 Retinal Disease 41 0.096
19
WHP002 Whiplash 36 0.096
20
P RTN008 Retinitis Pigmentosa 72 0.078
21
P UVL004 Uveal Melanoma 53 0.078
22
P NRP001 Neuropathy 52 0.078
23
P SPR013 Spiradenoma 47 0.078
24
P CNT005 Central Nervous System Lymphoma 45 0.078
25
THR013 Thoracic Outlet Syndrome 45 0.078
26
MTH009 Mouth Disease 43 0.078
27
OPT009 Optic Neuritis 42 0.078
28
TLN003 Telangiectasis 41 0.078
29
NRT004 Neuritis 40 0.078
30
HND002 Hand, Foot and Mouth Disease 39 0.078
31
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.078
32
VTR003 Vitreous Detachment 34 0.078
33
NRR001 Neuroretinitis 25 0.078
34
HPT023 Hepatocellular Carcinoma 95 0.055
35
AND015 Androgen Insensitivity 69 0.055
36
P ANG001 Angelman Syndrome 66 0.055
37
P WLF004 Wolfram Syndrome 61 0.055
38
P MYT002 Myotonic Dystrophy 57 0.055
39
VSC011 Vasculitis 57 0.055
40
LYM017 Lyme Disease 56 0.055
41
ATH003 Atherosclerosis 56 0.055
42
CLB001 Coloboma 54 0.055
43
DNN001 Danon Disease 52 0.055
44
P CTR002 Cataract 50 0.055
45
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.055
46
CYT005 Cytomegalovirus Retinitis 48 0.055
47
MCR004 Macroglobulinemia 48 0.055
48
c SPN225 Spondyloarthropathy 1 48 0.055
49
RTN017 Retinal Detachment 48 0.055
50
GLT007 Glutathione Synthetase Deficiency 47 0.055
51
PSD002 Pseudotumor Cerebri 47 0.055
52
P BLN003 Blindness 47 0.055
53
c PST022 Posterior Uveal Melanoma 46 0.055
54
PPL021 Papilledema 46 0.055
55
ACQ007 Acquired Immunodeficiency Syndrome 46 0.055
56
P PLL002 Pellagra 45 0.055
57
P STR022 Stargardt Disease 45 0.055
58
PNV001 Panuveitis 45 0.055
59
DBT006 Diabetic Macular Edema 45 0.055
60
c HRD026 Hereditary Ataxia 44 0.055
61
CTY001 Cat Eye Syndrome 43 0.055
62
MCL003 Macular Holes 43 0.055
63
CND005 Cone Dystrophy 43 0.055
64
c STR084 Stargardt Disease 1 43 0.055
65
P VTL001 Vitelliform Macular Dystrophy 42 0.055
66
RTN001 Retinal Vasculitis 42 0.055
67
P NGH001 Night Blindness 42 0.055
68
SBS003 Substance Abuse 41 0.055
69
c JVN042 Juvenile Retinoschisis 42 0.055
70
P MYP006 Myopia 41 0.055
71
RFR003 Refractive Error 40 0.055
72
PRP016 Paraplegia 40 0.055
73
AMB002 Amblyopia 39 0.055
74
P TRC086 Trichohepatoenteric Syndrome 1 39 0.055
75
P RTN016 Retinal Degeneration 38 0.055
76
ANR040 Aneurysm 35 0.055
77
DBT007 Diabetic Cataract 35 0.055
78
P HYP087 Hypotrichosis 35 0.055
79
c MCL060 Macular Dystrophy, Vitelliform, 3 35 0.055
80
CNT060 Central Serous Chorioretinopathy 34 0.055
81
SPS057 Spasticity 32 0.055
82
c ART101 Aortic Valve Disease 2 32 0.055
83
ENH001 Enhanced S-Cone Syndrome 31 0.055
84
INT080 Intraocular Melanoma 29 0.055
85
CLB003 Coloboma of Optic Nerve 29 0.055
86
TFT003 Tufting Enteropathy 26 0.055
87
PNG001 Pinguecula 25 0.055
88
GLD003 Goldmann-Favre Syndrome 24 0.055
89
NRS003 Neurosyphilis 25 0.055
90
ANG004 Angioid Streaks 23 0.055
91
SPN151 Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy 23 0.055
92
CNR016 Cone-Rod Dystrophy 7 20 0.055
93
MXL008 Maxillary Sinus Cancer 19 0.055
94
P SNS011 Sinus Cancer 15 0.055
95
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 15 0.055
96
DGN003 Degeneration of Macula and Posterior Pole 12 0.055
97
MCL017 Macular Dystrophy, Atypical Vitelliform 8 0.055
98
CVT001 Cavitary Optic Disc Anomalies 7 0.055