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Hereditary sensory and autonomic neuropathy type 2d
Hereditary sensory and autonomic neuropathy type 2d
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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
HSAN2D, autosomal recessive
MONDO_0009459
SCN9A
Unknown
23596073
Open Targets
Taste transduction
Phase 0 - rapid depolarisation
HSAN2D, autosomal recessive, AR
MONDO_0009459
SCN9A
Unknown
23596073
25316021
17470132
28665811
15958509
24813307
24817410
14985375
16392115
28235406
16216943
17145499
1536168
17167479
17679678
Open Targets
Taste transduction
Phase 0 - rapid depolarisation
All
1
Causal
0
Unknown
1
Select all
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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1 shared gene
SCN9A
Related via 1 shared gene including SCN9A.
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1 shared gene
SCN9A
Related via 1 shared gene including SCN9A.
Erythermalgia, primary
1 shared gene
SCN9A
Related via 1 shared gene including SCN9A.
Small fiber neuropathy, ad
1 shared gene
SCN9A
Related via 1 shared gene including SCN9A.
Indifference to pain, congenital, autosomal recessive
1 shared gene
SCN9A
Related via 1 shared gene including SCN9A.
1
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