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 14 2.916
2
P MYP006 Myopia 58 0.387
3
AST006 Astigmatism 42 0.383
4
RFR003 Refractive Error 39 0.205
5
EST005 Esotropia 39 0.182
6
AMB002 Amblyopia 42 0.182
7
EYD002 Eye Disease 62 0.173
8
CHR008 Choroiditis 43 0.173
9
ETH011 Ethylmalonic Encephalopathy 57 0.145
10
PRS025 Presbyopia 33 0.145
11
RTN023 Retinitis 49 0.145
12
P CTR002 Cataract 57 0.134
13
EXT022 Exotropia 37 0.134
14
CRN024 Corneal Disease 45 0.122
15
GLB003 Globe Disease 34 0.122
16
ACC003 Accommodative Esotropia 25 0.122
17
P STR020 Strabismus 55 0.110
18
HYP066 Hyperglycemia 61 0.095
19
CRN136 Cornea Plana Congenita, Recessive 16 0.095
20
c NNP012 Nanophthalmos 4 13 0.095
21
ANK001 Ankylosis 52 0.095
22
MCR013 Microphthalmia 57 0.077
23
P HMN010 Hemangioma 62 0.077
24
c MCR211 Microphthalmia, Isolated 6 22 0.077
25
CTS003 Coats Disease 57 0.077
26
P KRT007 Keratoconus 48 0.077
27
STP005 Stapes Ankylosis with Broad Thumb and Toes 21 0.077
28
P NGH001 Night Blindness 49 0.077
29
P RTN025 Retinoschisis 51 0.077
30
INT075 Intracranial Hypertension 52 0.077
31
P CNG010 Congenital Stationary Night Blindness 46 0.077
32
P XLN012 X-Linked Congenital Stationary Night Blindness 25 0.077
33
ANS004 Anisometropia 27 0.077
34
EYC003 Eye Accommodation Disease 25 0.077
35
WBR001 Weber Syndrome 36 0.077
36
END072 Endotheliitis 41 0.077
37
KRT004 Keratitis 70 0.055
38
P RTN008 Retinitis Pigmentosa 78 0.055
39
P SHR029 Short Syndrome 60 0.055
40
P LBR001 Leber Congenital Amaurosis 61 0.055
41
c ACH034 Achromatopsia-2 28 0.055
42
c LBR009 Leber Congenital Amaurosis 14 28 0.055
43
RTN175 Retinitis Pigmentosa 7 and Digenic 33 0.055
44
c LBR014 Leber Congenital Amaurosis 4 41 0.055
45
c LBR004 Leber Congenital Amaurosis 1 31 0.055
46
c CHR579 Chiari Malformation Type Ii 38 0.055
47
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.055
48
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 25 0.055
49
c CRN158 Craniosynostosis, Type 2 32 0.055
50
c LBR008 Leber Congenital Amaurosis 13 24 0.055
51
P PRX021 Proximal Symphalangism 49 0.055
52
c LBR012 Leber Congenital Amaurosis 2 25 0.055
53
c LBR013 Leber Congenital Amaurosis 3 28 0.055
54
RTN018 Retinal Disease 55 0.055
55
P ESP024 Esophagitis 62 0.055
56
c LBR010 Leber Congenital Amaurosis 15 23 0.055
57
c LBR005 Leber Congenital Amaurosis 10 29 0.055
58
c LBR017 Leber Congenital Amaurosis 7 32 0.055
59
c LBR007 Leber Congenital Amaurosis 12 22 0.055
60
c LBR016 Leber Congenital Amaurosis 6 22 0.055
61
c LBR006 Leber Congenital Amaurosis 11 20 0.055
62
c LBR018 Leber Congenital Amaurosis 8 22 0.055
63
c LBR019 Leber Congenital Amaurosis 9 22 0.055
64
c LBR011 Leber Congenital Amaurosis 16 21 0.055
65
P NNP011 Nanophthalmos 2 16 0.055
66
c LBR015 Leber Congenital Amaurosis 5 25 0.055
67
GRL004 Gorlin-Chaudhry-Moss Syndrome 24 0.055
68
P SYN001 Syndactyly 49 0.055
69
c LBR029 Leber Congenital Amaurosis 17 26 0.055
70
LPD004 Lipoid Nephrosis 49 0.055
71
LNS003 Lens Disease 37 0.055
72
P OTS001 Otosclerosis 33 0.055
73
PRM024 Primary Angle-Closure Glaucoma 38 0.055
74
CYC001 Cycloplegia 30 0.055
75
ESP020 Esophageal Atresia 48 0.055
76
P BRC006 Brachydactyly 53 0.055
77
CNT060 Central Serous Chorioretinopathy 42 0.055
78
P NRP001 Neuropathy 57 0.055
79
CRN022 Corneal Degeneration 29 0.055
80
PHT003 Phototoxic Dermatitis 37 0.055
81
P EXN002 Exanthem 57 0.055
82
SPC003 Specific Developmental Disorder 39 0.055
83
KRT008 Keratopathy 49 0.055
84
P CRV039 Cervicitis 45 0.055
85
ACC002 Accommodative Spasm 16 0.055
86
P RTN022 Retinal Vein Occlusion 36 0.055
87
P ISL020 Isolated Microphthalmia 24 0.055
88
IRR001 Irregular Astigmatism 25 0.055
89
TRN011 Transient Refractive Change 10 0.055
90
ISC002 Ischemic Optic Neuropathy 45 0.055