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"

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

# Family MCID Name MIFTS Score
1
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 35 3.279
2
P CTR002 Cataract 57 0.256
3
RTN023 Retinitis 49 0.215
4
EYD002 Eye Disease 63 0.204
5
ETH011 Ethylmalonic Encephalopathy 59 0.200
6
PTR006 Peters Anomaly 64 0.113
7
CRN237 Corneal Dystrophy, Avellino Type 30 0.110
8
NRN002 Neuronitis 42 0.107
9
P ALP004 Alport Syndrome 68 0.102
10
P MCP010 Mucopolysaccharidosis 58 0.101
11
ANR002 Aniridia 60 0.100
12
P RTN016 Retinal Degeneration 54 0.100
13
c MCP038 Mucopolysaccharidosis Iva 49 0.089
14
CRN142 Corneal Endothelial Dystrophy and Perceptive Deafness 24 0.086
15
DBR002 De Barsy Syndrome 24 0.082
16
c MCP024 Mucopolysaccharidosis Type Vi 61 0.080
17
c MCP037 Mucopolysaccharidosis is 66 0.078
18
FSH001 Fish-Eye Disease 43 0.077
19
c MCP012 Mucopolysaccharidosis Ih 42 0.077
20
P SCL047 Sclerocornea 26 0.074
21
P NRV007 Nervous System Disease 71 0.074
22
c MCP023 Mucopolysaccharidosis Type Ivb 27 0.074
23
DWR001 Dwarfism 46 0.073
24
CTS003 Coats Disease 57 0.067
25
DRM006 Dermatitis 61 0.062
26
c MCL046 Mucolipidosis Iii Alpha/beta 44 0.060
27
RSP006 Respiratory System Disease 62 0.059
28
P ADN016 Adenocarcinoma 69 0.059
29
VSC007 Vascular Disease 67 0.058
30
CHN055 Chanarin-Dorfman Syndrome 49 0.055
31
P MRN003 Marinesco-Sjogren Syndrome 35 0.055
32
CNT047 Contact Dermatitis 62 0.053
33
c ALD008 Aldh18a1-Related Cutis Laxa 15 0.051
34
OCL069 Ocular Motor Apraxia 44 0.050