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Usher syndrome type 2
Usher syndrome type 2
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Usher syndrome type 2
ADGRV1
Causal
—
ClinGen
—
USH2A
Causal
—
ClinGen
—
All
2
Causal
2
Unknown
0
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
2
Related Diseases
Diseases that share the most curated genes with Usher syndrome type 2.
5
View disease cluster →
Beta-mannosidosis
1 shared gene
ADGRV1
Related via 1 shared gene including ADGRV1.
Post-operative atrial fibrillation
1 shared gene
ADGRV1
Related via 1 shared gene including ADGRV1.
Congenital sensorineural hearing loss
1 shared gene
USH2A
Related via 1 shared gene including USH2A.
Congenital arteriovenous malformation
1 shared gene
ADGRV1
Related via 1 shared gene including ADGRV1.
Retinitis pigmentosa-deafness syndrome
1 shared gene
USH2A
Related via 1 shared gene including USH2A.
1
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