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Tritan color blindness
Tritan color blindness
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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
Tritan color blindness
MONDO_0008610
OPN1SW
Unknown
1386496
1531728
23022137
Open Targets
The retinoid cycle in cones (daylight vision)
Retinoid cycle disease events
G alpha (i) signalling events
Opsins
+1 more
Tritanopia
190900
88629
OMIM:190900
OPN1SW
Unknown
1386496
1531728
CTD
,
HPO
,
Orphanet
The retinoid cycle in cones (daylight vision)
Retinoid cycle disease events
G alpha (i) signalling events
Opsins
+1 more
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
1
Disgenet
0
CTD
1
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Tritan color blindness.
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Blue cone monochromatism
1 shared gene
OPN1SW
Related via 1 shared gene including OPN1SW.
Cardioembolic stroke
1 shared gene
OPN1SW
Related via 1 shared gene including OPN1SW.
Hypertrophic cardiomyopathy
1 shared gene
OPN1SW
Related via 1 shared gene including OPN1SW.
Retinitis pigmentosa
1 shared gene
OPN1SW
Related via 1 shared gene including OPN1SW.
Hodgkin lymphoma
1 shared gene
OPN1SW
Related via 1 shared gene including OPN1SW.
1
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