Search results for hyperopia

92 hits were found for hyperopia

# Family MCID Name MIFTS Score
1
PLD002 Pilodental Dysplasia with Refractive Errors 12 2.919
2
P MYP006 Myopia 56 0.393
3
AST006 Astigmatism 45 0.382
4
RFR003 Refractive Error 43 0.204
5
EYD002 Eye Disease 61 0.197
6
AMB002 Amblyopia 46 0.189
7
CHR008 Choroiditis 44 0.181
8
EST005 Esotropia 41 0.181
9
ETH011 Ethylmalonic Encephalopathy 56 0.173
10
P CTR002 Cataract 58 0.144
11
RTN023 Retinitis 50 0.144
12
PRS025 Presbyopia 35 0.144
13
GLB003 Globe Disease 32 0.144
14
EXT022 Exotropia 39 0.134
15
CRN024 Corneal Disease 44 0.122
16
ACC003 Accommodative Esotropia 26 0.122
17
P STR020 Strabismus 51 0.109
18
HYP066 Hyperglycemia 61 0.095
19
ANK001 Ankylosis 51 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 14 0.095
23
MCR013 Microphthalmia 60 0.077
24
P HMN010 Hemangioma 59 0.077
25
P RTN025 Retinoschisis 58 0.077
26
CTS003 Coats Disease 57 0.077
27
P CNG010 Congenital Stationary Night Blindness 53 0.077
28
INT075 Intracranial Hypertension 50 0.077
29
P KRT007 Keratoconus 48 0.077
30
P NGH001 Night Blindness 48 0.077
31
c LBR004 Leber Congenital Amaurosis 1 44 0.077
32
END072 Endotheliitis 42 0.077
33
WBR001 Weber Syndrome 41 0.077
34
c LBR005 Leber Congenital Amaurosis 10 35 0.077
35
ANS004 Anisometropia 29 0.077
36
P XLN012 X-Linked Congenital Stationary Night Blindness 29 0.077
37
c LBR008 Leber Congenital Amaurosis 13 24 0.077
38
EYC003 Eye Accommodation Disease 24 0.077
39
STP005 Stapes Ankylosis with Broad Thumb and Toes 20 0.077
40
P RTN008 Retinitis Pigmentosa 80 0.055
41
KRT004 Keratitis 71 0.055
42
P ESP024 Esophagitis 61 0.055
43
P LBR001 Leber Congenital Amaurosis 61 0.055
44
P NRP001 Neuropathy 59 0.055
45
P SHR029 Short Syndrome 58 0.055
46
P EXN002 Exanthem 57 0.055
47
P BRC006 Brachydactyly 54 0.055
48
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.055
49
RTN018 Retinal Disease 53 0.055
50
P SYN001 Syndactyly 53 0.055
51
ESP020 Esophageal Atresia 50 0.055
52
P PRX021 Proximal Symphalangism 50 0.055
53
LPD004 Lipoid Nephrosis 48 0.055
54
ATN002 Autonomic Nervous System Disease 48 0.055
55
c LBR012 Leber Congenital Amaurosis 2 47 0.055
56
P CRV039 Cervicitis 45 0.055
57
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 0.055
58
ALN001 Aland Island Eye Disease 45 0.055
59
c LBR014 Leber Congenital Amaurosis 4 44 0.055
60
KRT008 Keratopathy 44 0.055
61
CNT060 Central Serous Chorioretinopathy 41 0.055
62
c LBR019 Leber Congenital Amaurosis 9 40 0.055
63
PRM024 Primary Angle-Closure Glaucoma 39 0.055
64
c ACH034 Achromatopsia-2 39 0.055
65
SPC003 Specific Developmental Disorder 38 0.055
66
P RTN022 Retinal Vein Occlusion 38 0.055
67
RTN175 Retinitis Pigmentosa 7 and Digenic 38 0.055
68
c CHR579 Chiari Malformation Type Ii 37 0.055
69
ISC002 Ischemic Optic Neuropathy 37 0.055
70
c LBR013 Leber Congenital Amaurosis 3 37 0.055
71
c LBR011 Leber Congenital Amaurosis 16 35 0.055
72
c LBR007 Leber Congenital Amaurosis 12 35 0.055
73
c LBR016 Leber Congenital Amaurosis 6 35 0.055
74
P OTS001 Otosclerosis 35 0.055
75
PHT003 Phototoxic Dermatitis 35 0.055
76
c LBR018 Leber Congenital Amaurosis 8 34 0.055
77
LNS003 Lens Disease 33 0.055
78
c LBR015 Leber Congenital Amaurosis 5 31 0.055
79
c CRN158 Craniosynostosis, Type 2 31 0.055
80
c LBR009 Leber Congenital Amaurosis 14 28 0.055
81
CRN022 Corneal Degeneration 28 0.055
82
IRR001 Irregular Astigmatism 27 0.055
83
CYC001 Cycloplegia 27 0.055
84
c LBR017 Leber Congenital Amaurosis 7 26 0.055
85
c LBR010 Leber Congenital Amaurosis 15 25 0.055
86
P ISL020 Isolated Microphthalmia 25 0.055
87
c LBR029 Leber Congenital Amaurosis 17 25 0.055
88
c LBR006 Leber Congenital Amaurosis 11 25 0.055
89
GRL004 Gorlin-Chaudhry-Moss Syndrome 23 0.055
90
P NNP011 Nanophthalmos 2 17 0.055
91
ACC002 Accommodative Spasm 15 0.055
92
TRN011 Transient Refractive Change 12 0.055
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