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Deafness, autosomal recessive 12
Deafness, autosomal recessive 12
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Subtype of:
Deafness
·
Deafness, autosomal recessive
Include the contents of this disease's 1 subtype
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Show the subtype
Deafness, autosomal recessive 12, modifier of
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Deafness autosomal recessive type 12
MONDO_0019588
CDH23
Unknown
15537665
17850630
11138009
21228398
11090341
15829536
12075507
Open Targets
—
Deafness, autosomal recessive 12
MONDO_0019588
CDH23
Unknown
17850630
21228398
11138008
15358736
12522556
17805295
21940737
11090341
12407180
19270079
12075507
12485990
15537665
11857743
11138009
20399731
2706105
23135401
15829536
12910270
20639393
Open Targets
—
All
1
Causal
0
Unknown
1
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Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
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Diseases that share the most curated genes with Deafness, autosomal recessive 12.
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No strongly related diseases found yet for Deafness, autosomal recessive 12.
1
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