Search results for corneal clouding, autosomal recessive

50 hits were found for corneal clouding, autosomal recessive

# Family MCID Name MIFTS Score
1
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 37 4.924
2
P CTR002 Cataract 60 0.257
3
P ANR048 Aniridia 1 68 0.224
4
RTN023 Retinitis 52 0.199
5
KRT019 Keratitis, Hereditary 62 0.186
6
CRN237 Corneal Dystrophy, Avellino Type 36 0.144
7
P CRN276 Corneal Endothelial Dystrophy 45 0.140
8
ALP046 Alport Syndrome, X-Linked 74 0.130
9
CRN045 Corneal Dystrophy and Perceptive Deafness 27 0.123
10
NRN002 Neuronitis 43 0.107
11
P AMY004 Amyloidosis 69 0.106
12
P MCP040 Mucopolysaccharidosis-Plus Syndrome 61 0.104
13
PTR032 Peters-Plus Syndrome 60 0.102
14
SCH036 Scheie Syndrome 68 0.101
15
FSH001 Fish-Eye Disease 45 0.095
16
P RTN016 Retinal Degeneration 56 0.089
17
HRL003 Hurler Syndrome 55 0.088
18
c MCP024 Mucopolysaccharidosis Type Vi 61 0.086
19
DBR002 De Barsy Syndrome 38 0.078
20
FBR012 Fabry Disease 72 0.077
21
P NRV007 Nervous System Disease 75 0.074
22
c MCP047 Mucopolysaccharidosis, Type Iva 44 0.074
23
c MCP048 Mucopolysaccharidosis, Type Ivb 32 0.074
24
P MCL013 Mucolipidosis Iv 67 0.073
25
c MCL046 Mucolipidosis Iii Alpha/beta 50 0.072
26
AMB002 Amblyopia 45 0.072
27
P SCL047 Sclerocornea 28 0.069
28
DWR001 Dwarfism 48 0.068
29
c MCP049 Mucopolysaccharidosis, Type Vii 64 0.067
30
MLT135 Multiple Sulfatase Deficiency 54 0.061
31
AST005 Asthma 83 0.061
32
DRM006 Dermatitis 67 0.060
33
LTH002 Lathosterolosis 34 0.060
34
GLC012 Galactosialidosis 53 0.059
35
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 53 0.058
36
c PSD106 Pseudo-Torch Syndrome 1 46 0.058
37
VSC007 Vascular Disease 71 0.057
38
RBR001 Roberts Syndrome 55 0.057
39
HRL004 Hurler-Scheie Syndrome 40 0.057
40
c MRQ002 Morquio Syndrome C 12 0.056
41
c PRX059 Peroxisome Biogenesis Disorder 1a 41 0.056
42
c GM1006 Gm1-Gangliosidosis, Type Iii 30 0.056
43
P ADN016 Adenocarcinoma 71 0.055
44
c MSC034 Muscular Dystrophy-Dystroglycanopathy , Type a, 5 26 0.055
45
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 60 0.051
46
SBR011 Subaortic Stenosis--Short Stature Syndrome 20 0.051
47
LTH046 Lethal Short-Limb Skeletal Dysplasia, Al Gazali Type 16 0.051
48
P FNC004 Fanconi Syndrome 54 0.050
49
c EXD008 Exudative Vitreoretinopathy 1 65 0.049
50
SLP005 Sleep Disorder 59 0.047
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