Search results for corneal clouding

73 hits were found for corneal clouding

# Family MCID Name MIFTS Score
1
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 37 5.332
2
DBR002 De Barsy Syndrome 38 3.986
3
P CTR002 Cataract 60 0.268
4
KRT019 Keratitis, Hereditary 62 0.231
5
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 47 0.191
6
CRN237 Corneal Dystrophy, Avellino Type 36 0.179
7
SCH076 Schnyder Corneal Dystrophy 44 0.173
8
P CRN276 Corneal Endothelial Dystrophy 45 0.163
9
P ANR048 Aniridia 1 68 0.161
10
c CRN236 Corneal Dystrophy, Lattice Type I 33 0.149
11
CRN045 Corneal Dystrophy and Perceptive Deafness 27 0.148
12
CRN241 Corneal Dystrophy, Congenital Stromal 41 0.135
13
RTN023 Retinitis 52 0.127
14
SCH036 Scheie Syndrome 68 0.126
15
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.121
16
P AMY004 Amyloidosis 69 0.120
17
c CRN160 Corneal Dystrophy, Lattice Type Iiia 25 0.120
18
PTR032 Peters-Plus Syndrome 60 0.117
19
FSH001 Fish-Eye Disease 45 0.115
20
HRL003 Hurler Syndrome 55 0.105
21
CRN128 Corneal Dystrophy, Endothelial, X-Linked 26 0.103
22
c MCP024 Mucopolysaccharidosis Type Vi 61 0.100
23
ALP046 Alport Syndrome, X-Linked 74 0.094
24
c CTS041 Cutis Laxa, Autosomal Dominant 3 25 0.094
25
FBR012 Fabry Disease 72 0.091
26
AMB002 Amblyopia 45 0.087
27
NRN002 Neuronitis 43 0.085
28
P RTN016 Retinal Degeneration 56 0.082
29
c MCP047 Mucopolysaccharidosis, Type Iva 44 0.082
30
c MCP048 Mucopolysaccharidosis, Type Ivb 32 0.082
31
P SCL047 Sclerocornea 28 0.082
32
P MCL013 Mucolipidosis Iv 67 0.079
33
RSP006 Respiratory System Disease 63 0.078
34
c MCL046 Mucolipidosis Iii Alpha/beta 50 0.078
35
c MCP049 Mucopolysaccharidosis, Type Vii 64 0.074
36
MCP039 Mucoepithelial Dysplasia, Hereditary 30 0.072
37
AST005 Asthma 83 0.069
38
SPN391 Spondyloepiphyseal Dysplasia, Maroteaux Type 25 0.068
39
P NRV007 Nervous System Disease 75 0.066
40
VSC007 Vascular Disease 71 0.066
41
DRM006 Dermatitis 67 0.066
42
P SLP006 Sleep Apnea 65 0.066
43
MLT135 Multiple Sulfatase Deficiency 54 0.066
44
GLC012 Galactosialidosis 53 0.066
45
HRL004 Hurler-Scheie Syndrome 40 0.066
46
LTH002 Lathosterolosis 34 0.066
47
MND027 Mandibulofacial Dysostosis with Macroblepharon and Macrostomia 22 0.062
48
c MRQ002 Morquio Syndrome C 12 0.062
49
P ADN016 Adenocarcinoma 71 0.058
50
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 60 0.058
51
P FTL001 Fetal Alcohol Syndrome 59 0.058
52
RBR001 Roberts Syndrome 55 0.058
53
P FNC004 Fanconi Syndrome 54 0.058
54
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 53 0.058
55
DWR001 Dwarfism 48 0.058
56
c PSD106 Pseudo-Torch Syndrome 1 46 0.058
57
c PRX059 Peroxisome Biogenesis Disorder 1a 41 0.058
58
c OTP007 Otopalatodigital Syndrome, Type Ii 38 0.058
59
FCH002 Fuchs' Heterochromic Uveitis 32 0.058
60
c GM1006 Gm1-Gangliosidosis, Type Iii 30 0.058
61
c MSC034 Muscular Dystrophy-Dystroglycanopathy , Type a, 5 26 0.058
62
PLV015 Pelvis-Shoulder Dysplasia 21 0.058
63
SBR011 Subaortic Stenosis--Short Stature Syndrome 20 0.058
64
LTH046 Lethal Short-Limb Skeletal Dysplasia, Al Gazali Type 16 0.058
65
APN008 Apnea, Obstructive Sleep 67 0.052
66
c EXD008 Exudative Vitreoretinopathy 1 65 0.052
67
CNT047 Contact Dermatitis 64 0.052
68
SLP005 Sleep Disorder 59 0.052
69
P BRS044 Breast Adenocarcinoma 58 0.052
70
VCC001 Vaccinia 50 0.052
71
VTR003 Vitreous Detachment 40 0.052
72
SBV001 Subvalvular Aortic Stenosis 27 0.052
73
P OTP001 Otopalatodigital Syndrome 21 0.052
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