Search results for hyperopia

121 hits were found for hyperopia

# Family MCID Name MIFTS Score
1
PLD002 Pilodental Dysplasia with Refractive Errors 15 2.955
2
P MYP006 Myopia 59 0.365
3
AST006 Astigmatism 43 0.361
4
RFR003 Refractive Error 41 0.188
5
EYD002 Eye Disease 57 0.181
6
AMB002 Amblyopia 44 0.174
7
CHR008 Choroiditis 43 0.166
8
EST005 Esotropia 42 0.166
9
P CTR002 Cataract 57 0.133
10
RTN023 Retinitis 49 0.133
11
PRS025 Presbyopia 33 0.133
12
EXT022 Exotropia 39 0.123
13
ACC003 Accommodative Esotropia 24 0.112
14
P STR020 Strabismus 52 0.100
15
c MCR211 Microphthalmia, Isolated 6 23 0.100
16
c NNP012 Nanophthalmos 4 16 0.100
17
c CRN280 Cornea Plana 2, Autosomal Recessive 15 0.100
18
HYP066 Hyperglycemia 59 0.087
19
ANK001 Ankylosis 51 0.087
20
c ALB021 Albinism, Oculocutaneous, Type Ii 49 0.087
21
c CRN277 Craniosynostosis 2 33 0.087
22
GRL004 Gorlin-Chaudhry-Moss Syndrome 26 0.087
23
STP005 Stapes Ankylosis with Broad Thumb and Toes 21 0.087
24
MCR013 Microphthalmia 59 0.071
25
P HMN010 Hemangioma 59 0.071
26
P RTN025 Retinoschisis 57 0.071
27
P CNG010 Congenital Stationary Night Blindness 53 0.071
28
INT075 Intracranial Hypertension 48 0.071
29
P KRT007 Keratoconus 48 0.071
30
P NGH001 Night Blindness 47 0.071
31
c LBR004 Leber Congenital Amaurosis 1 46 0.071
32
END072 Endotheliitis 41 0.071
33
c LBR019 Leber Congenital Amaurosis 9 40 0.071
34
WBR001 Weber Syndrome 36 0.071
35
c LBR005 Leber Congenital Amaurosis 10 36 0.071
36
ANS004 Anisometropia 30 0.071
37
P XLN012 X-Linked Congenital Stationary Night Blindness 28 0.071
38
c LBR010 Leber Congenital Amaurosis 15 26 0.071
39
EYC003 Eye Accommodation Disease 25 0.071
40
c LBR008 Leber Congenital Amaurosis 13 24 0.071
41
MTP032 Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness 20 0.071
42
P RTN008 Retinitis Pigmentosa 80 0.050
43
KRT004 Keratitis 70 0.050
44
P PRD006 Prader-Willi Syndrome 65 0.050
45
P ANG001 Angelman Syndrome 62 0.050
46
P LBR001 Leber Congenital Amaurosis 62 0.050
47
P SHR029 Short Syndrome 61 0.050
48
P ESP024 Esophagitis 59 0.050
49
P NRP001 Neuropathy 57 0.050
50
P EXN002 Exanthem 57 0.050
51
ALS001 Alstrom Syndrome 55 0.050
52
P BRC006 Brachydactyly 55 0.050
53
ARS001 Aarskog-Scott Syndrome 54 0.050
54
P STS008 Sotos Syndrome 1 54 0.050
55
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 52 0.050
56
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 51 0.050
57
P PRX021 Proximal Symphalangism 50 0.050
58
ESP020 Esophageal Atresia 50 0.050
59
c LBR012 Leber Congenital Amaurosis 2 48 0.050
60
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 47 0.050
61
P CRV039 Cervicitis 45 0.050
62
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 0.050
63
FLT006 Floating-Harbor Syndrome 44 0.050
64
DBW001 Dubowitz Syndrome 44 0.050
65
ISC002 Ischemic Optic Neuropathy 44 0.050
66
c LBR014 Leber Congenital Amaurosis 4 44 0.050
67
c ACH020 Achromatopsia 2 44 0.050
68
CRN024 Corneal Disease 43 0.050
69
c CCK005 Cockayne Syndrome, Type a 42 0.050
70
CNT060 Central Serous Chorioretinopathy 42 0.050
71
c CCK006 Cockayne Syndrome, Type B 40 0.050
72
c CHR579 Chiari Malformation Type Ii 40 0.050
73
RTN175 Retinitis Pigmentosa 7 and Digenic 40 0.050
74
MYH012 Myhre Syndrome 39 0.050
75
KRT008 Keratopathy 39 0.050
76
CHR386 Chromosome 6pter-P24 Deletion Syndrome 39 0.050
77
MCL027 Macular Dystrophy, Dominant Cystoid 39 0.050
78
SPC003 Specific Developmental Disorder 38 0.050
79
c MLT127 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 38 0.050
80
c LBR007 Leber Congenital Amaurosis 12 38 0.050
81
c ALB009 Albinism, Oculocutaneous, Type Ia 37 0.050
82
P RTN022 Retinal Vein Occlusion 37 0.050
83
PHT003 Phototoxic Dermatitis 37 0.050
84
PRM024 Primary Angle-Closure Glaucoma 37 0.050
85
c LBR013 Leber Congenital Amaurosis 3 36 0.050
86
c LBR009 Leber Congenital Amaurosis 14 36 0.050
87
c LBR011 Leber Congenital Amaurosis 16 36 0.050
88
c LBR016 Leber Congenital Amaurosis 6 35 0.050
89
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 35 0.050
90
P OTS001 Otosclerosis 35 0.050
91
c LBR018 Leber Congenital Amaurosis 8 33 0.050
92
c MCR124 Microphthalmia, Isolated 1 32 0.050
93
c HRM011 Hermansky-Pudlak Syndrome 8 31 0.050
94
c LBR015 Leber Congenital Amaurosis 5 30 0.050
95
CRN022 Corneal Degeneration 30 0.050
96
c KNN007 Kenny-Caffey Syndrome, Type 2 29 0.050
97
P HYP534 Hypomagnesemia 3, Renal 29 0.050
98
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 28 0.050
99
CYC001 Cycloplegia 27 0.050
100
PGM007 Pigmented Paravenous Chorioretinal Atrophy 27 0.050
101
MLT153 Multiple Joint Dislocations, Short Stature, Craniofacial Dysmorphism, with or Without Congenital Heart Defects 26 0.050
102
CRN274 Corneal Dystrophy, Posterior Amorphous 26 0.050
103
c LBR017 Leber Congenital Amaurosis 7 26 0.050
104
IRR001 Irregular Astigmatism 26 0.050
105
c PNT030 Pontocerebellar Hypoplasia, Type 8 25 0.050
106
c BRC045 Brachyolmia Type 3 25 0.050
107
P ISL020 Isolated Microphthalmia 25 0.050
108
c LBR029 Leber Congenital Amaurosis 17 24 0.050
109
c MNT242 Mental Retardation, Autosomal Dominant 40 24 0.050
110
c JBR035 Joubert Syndrome 24 24 0.050
111
c LBR006 Leber Congenital Amaurosis 11 24 0.050
112
IMM140 Immunodeficiency 47 22 0.050
113
WHT019 White-Sutton Syndrome 21 0.050
114
CRB165 Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation 21 0.050
115
P NNP011 Nanophthalmos 2 18 0.050
116
c NGH024 Night Blindness, Congenital Stationary, Type 1h 18 0.050
117
RTN037 Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma 16 0.050
118
CRN269 Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 16 0.050
119
ACC002 Accommodative Spasm 15 0.050
120
c CRN279 Cornea Plana 1, Autosomal Dominant 12 0.050
121
TRN011 Transient Refractive Change 12 0.050
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