Search results for corneal clouding, autosomal recessive

52 hits were found for corneal clouding, autosomal recessive

# Family MCID Name MIFTS Score
1
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 32 3.220
2
P CTR002 Cataract 57 0.250
3
EYD002 Eye Disease 57 0.215
4
KRT004 Keratitis 70 0.199
5
RTN023 Retinitis 49 0.198
6
P ANR002 Aniridia 66 0.119
7
CRN142 Corneal Endothelial Dystrophy and Perceptive Deafness 23 0.118
8
P CRN231 Corneal Dystrophy, Posterior Polymorphous, 1 40 0.115
9
CRN237 Corneal Dystrophy, Avellino Type 32 0.111
10
P AMY004 Amyloidosis 64 0.103
11
P CRN282 Corneal Endothelial Dystrophy, Autosomal Recessive 31 0.102
12
NRN002 Neuronitis 39 0.099
13
P ALP004 Alport Syndrome 70 0.098
14
FSH001 Fish-Eye Disease 43 0.094
15
c MCP037 Mucopolysaccharidosis is 65 0.092
16
P RTN016 Retinal Degeneration 53 0.091
17
PTR032 Peters-Plus Syndrome 59 0.088
18
c MCP024 Mucopolysaccharidosis Type Vi 61 0.088
19
FBR012 Fabry Disease 71 0.076
20
P NRV007 Nervous System Disease 70 0.075
21
c MCP038 Mucopolysaccharidosis Iva 48 0.074
22
P MCP012 Mucopolysaccharidosis Ih 44 0.073
23
c MCL046 Mucolipidosis Iii Alpha/beta 46 0.073
24
DBR002 De Barsy Syndrome 31 0.072
25
AMB002 Amblyopia 44 0.072
26
c MCP023 Mucopolysaccharidosis Type Ivb 30 0.072
27
P MCL013 Mucolipidosis Iv 64 0.071
28
P USH001 Usher Syndrome 54 0.070
29
P SCL047 Sclerocornea 27 0.069
30
DWR001 Dwarfism 45 0.067
31
CTS003 Coats Disease 58 0.064
32
MLT135 Multiple Sulfatase Deficiency 54 0.063
33
DRM006 Dermatitis 63 0.062
34
P AST005 Asthma 81 0.062
35
ETH011 Ethylmalonic Encephalopathy 51 0.060
36
c PRX059 Peroxisome Biogenesis Disorder 1a 36 0.060
37
LTH002 Lathosterolosis 33 0.060
38
c PSD106 Pseudo-Torch Syndrome 1 42 0.060
39
GLC012 Galactosialidosis 49 0.059
40
RBR001 Roberts Syndrome 61 0.058
41
c USH006 Usher Syndrome, Type 1b 53 0.058
42
VSC007 Vascular Disease 65 0.057
43
c MCP036 Mucopolysaccharidosis Ih/s 34 0.057
44
RSP006 Respiratory System Disease 60 0.056
45
c MSC047 Muscular Dystrophy-Dystroglycanopathy , Type a, 1 42 0.056
46
c GM1006 Gm1-Gangliosidosis, Type Iii 34 0.056
47
c MSC034 Muscular Dystrophy-Dystroglycanopathy , Type a, 5 29 0.055
48
P ADN016 Adenocarcinoma 69 0.052
49
SBR011 Subaortic Stenosis--Short Stature Syndrome 18 0.051
50
CNT047 Contact Dermatitis 59 0.050
51
P NMN002 Niemann-Pick Disease 66 0.045
52
c ALD008 Aldh18a1-Related Cutis Laxa 15 0.045
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