Search results for hyperopia

142 hits were found for hyperopia

# Family MCID Name MIFTS Score
1
PLD002 Pilodental Dysplasia with Refractive Errors 16 3.437
2
STP011 Stapes Ankylosis with Broad Thumbs and Toes 20 2.507
3
HYP773 Hyperopia, High 8 2.507
4
c NNP017 Nanophthalmos 1 17 2.480
5
MCR336 Microphthalmia with Hyperopia, Retinal Degeneration, Macrophakia, and Dental Anomalies 8 2.480
6
P MYP006 Myopia 56 0.360
7
AST006 Astigmatism 48 0.357
8
RFR003 Refractive Error 45 0.190
9
AMB002 Amblyopia 45 0.170
10
EST005 Esotropia 43 0.170
11
CHR008 Choroiditis 47 0.162
12
RTN023 Retinitis 52 0.139
13
AGN016 Aging 65 0.130
14
P CTR002 Cataract 60 0.130
15
PRS025 Presbyopia 37 0.130
16
EXT022 Exotropia 41 0.120
17
ACC003 Accommodative Esotropia 27 0.110
18
STR020 Strabismus 55 0.098
19
c MCR211 Microphthalmia, Isolated 6 22 0.098
20
c CRN280 Cornea Plana 2, Autosomal Recessive 18 0.098
21
c NNP012 Nanophthalmos 4 17 0.098
22
HYP066 Hyperglycemia 64 0.085
23
MCR013 Microphthalmia 61 0.085
24
ANK001 Ankylosis 56 0.085
25
c CRN277 Craniosynostosis 2 35 0.085
26
GRL004 Gorlin-Chaudhry-Moss Syndrome 31 0.085
27
CYC001 Cycloplegia 29 0.085
28
HRN028 Horns in Sheep 15 0.085
29
P HMN010 Hemangioma 61 0.069
30
STR039 Sturge-Weber Syndrome 59 0.069
31
P CNG010 Congenital Stationary Night Blindness 56 0.069
32
RTN209 Retinoschisis 1, X-Linked, Juvenile 56 0.069
33
INT075 Intracranial Hypertension 53 0.069
34
P NGH001 Night Blindness 51 0.069
35
P KRT007 Keratoconus 49 0.069
36
c LBR014 Leber Congenital Amaurosis 4 48 0.069
37
CRN024 Corneal Disease 47 0.069
38
END072 Endotheliitis 46 0.069
39
OCL052 Ocular Dominance 44 0.069
40
c LBR019 Leber Congenital Amaurosis 9 41 0.069
41
c LBR004 Leber Congenital Amaurosis 1 41 0.069
42
WBR001 Weber Syndrome 40 0.069
43
GLS018 Glass Syndrome 38 0.069
44
ANS004 Anisometropia 32 0.069
45
c LBR005 Leber Congenital Amaurosis 10 31 0.069
46
XLN012 X-Linked Congenital Stationary Night Blindness 26 0.069
47
c LBR010 Leber Congenital Amaurosis 15 22 0.069
48
c LBR008 Leber Congenital Amaurosis 13 20 0.069
49
P RTN008 Retinitis Pigmentosa 81 0.049
50
c MCL042 Macular Degeneration, Age-Related, 1 79 0.049
51
P DBT009 Diabetes Mellitus 72 0.049
52
P PRD006 Prader-Willi Syndrome 66 0.049
53
P LBR001 Leber Congenital Amaurosis 65 0.049
54
P ESP024 Esophagitis 64 0.049
55
P NRP001 Neuropathy 63 0.049
56
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.049
57
KRT019 Keratitis, Hereditary 62 0.049
58
P EXN002 Exanthem 62 0.049
59
P ANG001 Angelman Syndrome 61 0.049
60
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.049
61
P BRC006 Brachydactyly 57 0.049
62
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 57 0.049
63
P STS008 Sotos Syndrome 1 56 0.049
64
P RTN016 Retinal Degeneration 56 0.049
65
ALS001 Alstrom Syndrome 55 0.049
66
ARS001 Aarskog-Scott Syndrome 55 0.049
67
P SHR029 Short Syndrome 54 0.049
68
ESP020 Esophageal Atresia 54 0.049
69
P RTN022 Retinal Vein Occlusion 53 0.049
70
P OTS001 Otosclerosis 53 0.049
71
c CCK007 Cockayne Syndrome B 52 0.049
72
P PRX021 Proximal Symphalangism 51 0.049
73
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 0.049
74
P CRV039 Cervicitis 49 0.049
75
c CCK008 Cockayne Syndrome a 48 0.049
76
ISC002 Ischemic Optic Neuropathy 48 0.049
77
c LBR012 Leber Congenital Amaurosis 2 47 0.049
78
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 47 0.049
79
c ALB021 Albinism, Oculocutaneous, Type Ii 47 0.049
80
CNT060 Central Serous Chorioretinopathy 45 0.049
81
MCL027 Macular Dystrophy, Dominant Cystoid 45 0.049
82
FLT006 Floating-Harbor Syndrome 45 0.049
83
DBW001 Dubowitz Syndrome 44 0.049
84
KRT008 Keratopathy 44 0.049
85
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 43 0.049
86
c CHR579 Chiari Malformation Type Ii 42 0.049
87
PRM024 Primary Angle-Closure Glaucoma 42 0.049
88
MYH012 Myhre Syndrome 41 0.049
89
c ALB009 Albinism, Oculocutaneous, Type Ia 41 0.049
90
c ACH020 Achromatopsia 2 40 0.049
91
CHR386 Chromosome 6pter-P24 Deletion Syndrome 40 0.049
92
c MLT127 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 3 40 0.049
93
PHT003 Phototoxic Dermatitis 39 0.049
94
c RTN069 Retinitis Pigmentosa 7 38 0.049
95
c BLD140 Blood Group, I System 37 0.049
96
c MCR124 Microphthalmia, Isolated 1 37 0.049
97
c HYP534 Hypomagnesemia 3, Renal 37 0.049
98
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 36 0.049
99
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 36 0.049
100
MLT162 Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects 36 0.049
101
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 35 0.049
102
c LBR007 Leber Congenital Amaurosis 12 35 0.049
103
c LBR011 Leber Congenital Amaurosis 16 35 0.049
104
CRN274 Corneal Dystrophy, Posterior Amorphous 33 0.049
105
c LBR009 Leber Congenital Amaurosis 14 33 0.049
106
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.049
107
c LBR016 Leber Congenital Amaurosis 6 30 0.049
108
c KNN007 Kenny-Caffey Syndrome, Type 2 30 0.049
109
c LBR013 Leber Congenital Amaurosis 3 30 0.049
110
c LBR015 Leber Congenital Amaurosis 5 30 0.049
111
c LBR018 Leber Congenital Amaurosis 8 29 0.049
112
FNT005 Fontaine Progeroid Syndrome 28 0.049
113
P STR035 Streptococcal Group a Invasive Disease 28 0.049
114
IRR001 Irregular Astigmatism 28 0.049
115
c HRM011 Hermansky-Pudlak Syndrome 8 28 0.049
116
CRN022 Corneal Degeneration 27 0.049
117
c BRC045 Brachyolmia Type 3 27 0.049
118
c MCR331 Microcephalic Osteodysplastic Primordial Dwarfism, Type Iii 26 0.049
119
PGM007 Pigmented Paravenous Chorioretinal Atrophy 25 0.049
120
c PNT030 Pontocerebellar Hypoplasia, Type 8 25 0.049
121
AMT001 Ametropic Amblyopia 24 0.049
122
WHT019 White-Sutton Syndrome 23 0.049
123
c JBR035 Joubert Syndrome 24 22 0.049
124
c PNT050 Pontocerebellar Hypoplasia, Type 11 22 0.049
125
c MNT242 Mental Retardation, Autosomal Dominant 40 22 0.049
126
CRB165 Cerebellar Atrophy, Visual Impairment, and Psychomotor Retardation 21 0.049
127
c LBR029 Leber Congenital Amaurosis 17 20 0.049
128
IMM140 Immunodeficiency 47 20 0.049
129
MTP032 Metaphyseal Dysostosis, Mental Retardation, and Conductive Deafness 20 0.049
130
c NGH024 Night Blindness, Congenital Stationary, Type 1h 19 0.049
131
ACC002 Accommodative Spasm 19 0.049
132
c LBR017 Leber Congenital Amaurosis 7 18 0.049
133
c LBR006 Leber Congenital Amaurosis 11 18 0.049
134
RTN037 Retinal Degeneration with Nanophthalmos, Cystic Macular Degeneration, and Angle Closure Glaucoma 18 0.049
135
CRN269 Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 17 0.049
136
RTN078 Retinoschisis of Fovea 17 0.049
137
DWR019 Dwarfism with Stiff Joints and Ocular Abnormalities 17 0.049
138
c RTN208 Retinopathy, Pericentral Pigmentary, Autosomal Recessive 15 0.049
139
c CRN279 Cornea Plana 1, Autosomal Dominant 14 0.049
140
P NNP011 Nanophthalmos 2 13 0.049
141
ASY006 Asymmetric Short Stature Syndrome 10 0.049
142
MTP027 Metaphyseal Dysostosis-Intellectual Disability-Conductive Deafness Syndrome 4 0.049
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