Search results for "corneal clouding, autosomal recessive"

The MalaCard for "corneal clouding, autosomal recessive" has been retired.
Searching MalaCards for entries containing "corneal clouding, autosomal recessive"

35 hits were found for 'corneal clouding, autosomal recessive'

# Family MCID Name MIFTS Score
1
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 34 3.317
2
P CTR002 Cataract 57 0.263
3
RTN023 Retinitis 49 0.219
4
EYD002 Eye Disease 62 0.186
5
ETH011 Ethylmalonic Encephalopathy 57 0.180
6
CRN237 Corneal Dystrophy, Avellino Type 31 0.120
7
NRN002 Neuronitis 40 0.111
8
P MCP010 Mucopolysaccharidosis 58 0.106
9
P ALP004 Alport Syndrome 68 0.105
10
P RTN016 Retinal Degeneration 50 0.102
11
ANR002 Aniridia 62 0.100
12
PTR006 Peters Anomaly 64 0.097
13
DBR002 De Barsy Syndrome 26 0.089
14
CRN142 Corneal Endothelial Dystrophy and Perceptive Deafness 23 0.087
15
c MCP024 Mucopolysaccharidosis Type Vi 61 0.081
16
c MCP037 Mucopolysaccharidosis is 65 0.078
17
P SCL047 Sclerocornea 27 0.077
18
P GNG009 Gangliosidosis 58 0.077
19
FSH001 Fish-Eye Disease 44 0.077
20
P NRV007 Nervous System Disease 71 0.077
21
DWR001 Dwarfism 42 0.076
22
c MCP023 Mucopolysaccharidosis Type Ivb 28 0.074
23
c MCP038 Mucopolysaccharidosis Iva 45 0.074
24
c MCP012 Mucopolysaccharidosis Ih 41 0.074
25
CTS003 Coats Disease 57 0.068
26
RSP006 Respiratory System Disease 61 0.067
27
c MCP004 Mucopolysaccharidosis Iv 60 0.062
28
c MCL046 Mucolipidosis Iii Alpha/beta 37 0.062
29
CNT047 Contact Dermatitis 62 0.061
30
DRM006 Dermatitis 58 0.060
31
FCH002 Fuchs' Heterochromic Uveitis 41 0.060
32
P MRN003 Marinesco-Sjogren Syndrome 37 0.059
33
P ADN016 Adenocarcinoma 69 0.058
34
P ISL078 Isolated Ectopia Lentis 32 0.056
35
c ALD008 Aldh18a1-Related Cutis Laxa 16 0.051