Search results for "hyperopia"

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

90 hits were found for 'hyperopia'

# Family MCID Name MIFTS Score
1
PLD002 Pilodental Dysplasia with Refractive Errors 13 2.915
2
P MYP006 Myopia 59 0.387
3
AST006 Astigmatism 44 0.383
4
RFR003 Refractive Error 42 0.205
5
EYD002 Eye Disease 63 0.197
6
AMB002 Amblyopia 46 0.182
7
EST005 Esotropia 41 0.182
8
ETH011 Ethylmalonic Encephalopathy 59 0.173
9
CHR008 Choroiditis 43 0.173
10
RTN023 Retinitis 49 0.145
11
GLB003 Globe Disease 35 0.145
12
PRS025 Presbyopia 35 0.145
13
P CTR002 Cataract 57 0.134
14
EXT022 Exotropia 39 0.134
15
CRN024 Corneal Disease 44 0.122
16
ACC003 Accommodative Esotropia 25 0.122
17
P STR020 Strabismus 53 0.109
18
HYP066 Hyperglycemia 60 0.095
19
ANK001 Ankylosis 52 0.095
20
c MCR211 Microphthalmia, Isolated 6 22 0.095
21
CRN136 Cornea Plana Congenita, Recessive 16 0.095
22
c NNP012 Nanophthalmos 4 15 0.095
23
P HMN010 Hemangioma 60 0.077
24
P RTN025 Retinoschisis 59 0.077
25
MCR013 Microphthalmia 59 0.077
26
CTS003 Coats Disease 57 0.077
27
INT075 Intracranial Hypertension 53 0.077
28
P KRT007 Keratoconus 51 0.077
29
P CNG010 Congenital Stationary Night Blindness 50 0.077
30
P NGH001 Night Blindness 49 0.077
31
END072 Endotheliitis 42 0.077
32
WBR001 Weber Syndrome 37 0.077
33
c LBR004 Leber Congenital Amaurosis 1 34 0.077
34
c LBR005 Leber Congenital Amaurosis 10 33 0.077
35
ANS004 Anisometropia 29 0.077
36
P XLN012 X-Linked Congenital Stationary Night Blindness 26 0.077
37
EYC003 Eye Accommodation Disease 26 0.077
38
c LBR008 Leber Congenital Amaurosis 13 24 0.077
39
STP005 Stapes Ankylosis with Broad Thumb and Toes 20 0.077
40
P RTN008 Retinitis Pigmentosa 79 0.055
41
KRT004 Keratitis 70 0.055
42
P ESP024 Esophagitis 62 0.055
43
P LBR001 Leber Congenital Amaurosis 60 0.055
44
P SHR029 Short Syndrome 60 0.055
45
P NRP001 Neuropathy 60 0.055
46
P EXN002 Exanthem 57 0.055
47
RTN018 Retinal Disease 56 0.055
48
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.055
49
P BRC006 Brachydactyly 52 0.055
50
ESP020 Esophageal Atresia 49 0.055
51
LPD004 Lipoid Nephrosis 48 0.055
52
c LBR014 Leber Congenital Amaurosis 4 47 0.055
53
ATN002 Autonomic Nervous System Disease 47 0.055
54
KRT008 Keratopathy 46 0.055
55
ISC002 Ischemic Optic Neuropathy 46 0.055
56
ALN001 Aland Island Eye Disease 45 0.055
57
P CRV039 Cervicitis 44 0.055
58
CNT060 Central Serous Chorioretinopathy 40 0.055
59
SPC003 Specific Developmental Disorder 40 0.055
60
PRM024 Primary Angle-Closure Glaucoma 39 0.055
61
LNS003 Lens Disease 38 0.055
62
c CHR579 Chiari Malformation Type Ii 38 0.055
63
PHT003 Phototoxic Dermatitis 38 0.055
64
P RTN022 Retinal Vein Occlusion 37 0.055
65
c ACH034 Achromatopsia-2 37 0.055
66
P OTS001 Otosclerosis 35 0.055
67
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 35 0.055
68
RTN175 Retinitis Pigmentosa 7 and Digenic 33 0.055
69
c CRN158 Craniosynostosis, Type 2 31 0.055
70
CYC001 Cycloplegia 31 0.055
71
c LBR012 Leber Congenital Amaurosis 2 31 0.055
72
CRN022 Corneal Degeneration 31 0.055
73
c LBR015 Leber Congenital Amaurosis 5 30 0.055
74
c LBR013 Leber Congenital Amaurosis 3 29 0.055
75
c LBR009 Leber Congenital Amaurosis 14 28 0.055
76
IRR001 Irregular Astigmatism 27 0.055
77
c LBR017 Leber Congenital Amaurosis 7 26 0.055
78
c LBR007 Leber Congenital Amaurosis 12 26 0.055
79
c LBR019 Leber Congenital Amaurosis 9 26 0.055
80
c LBR016 Leber Congenital Amaurosis 6 26 0.055
81
c LBR018 Leber Congenital Amaurosis 8 25 0.055
82
P ISL020 Isolated Microphthalmia 25 0.055
83
c LBR006 Leber Congenital Amaurosis 11 25 0.055
84
c LBR010 Leber Congenital Amaurosis 15 24 0.055
85
c LBR011 Leber Congenital Amaurosis 16 23 0.055
86
GRL004 Gorlin-Chaudhry-Moss Syndrome 22 0.055
87
c LBR029 Leber Congenital Amaurosis 17 21 0.055
88
P NNP011 Nanophthalmos 2 17 0.055
89
ACC002 Accommodative Spasm 15 0.055
90
TRN011 Transient Refractive Change 12 0.055