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Deafness, autosomal recessive, 63
Deafness, autosomal recessive, 63
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Subtype of:
Deafness
·
Deafness, autosomal recessive
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Pathways column key:
KEGG
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Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Deafness, autosomal recessive 63
MONDO_0012670
LRTOMT
Unknown
18953341
18794526
17211611
17066295
17166180
28281779
Open Targets
Steroid hormone biosynthesis
Tyrosine metabolism
Metabolic pathways
Dopaminergic synapse
Enzymatic degradation of dopamine by COMT
+2 more
TOMT
Unknown
18953341
18794526
28281779
Open Targets
—
All
2
Causal
0
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
2
Related Diseases
Diseases that share the most curated genes with Deafness, autosomal recessive, 63.
0
View disease cluster →
No strongly related diseases found yet for Deafness, autosomal recessive, 63.
1
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