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Congenital pain insensitivity
Congenital pain insensitivity
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
CONGENITAL PAIN INSENSITIVITY
C0002768
NGF
Unknown
—
Disgenet
MAPK signaling pathway
Ras signaling pathway
Rap1 signaling pathway
Calcium signaling pathway
Cytokine-cytokine receptor interaction
PI3K-Akt signaling pathway
Apoptosis
Neurotrophin signaling pathway
Inflammatory mediator regulation of TRP channels
NGF processing
Frs2-mediated activation
ARMS-mediated activation
Retrograde neurotrophin signalling
TRKA activation by NGF
PI3K/AKT activation
NFG and proNGF binds to p75NTR
NADE modulates death signalling
NRIF signals cell death from the nucleus
p75NTR recruits signalling complexes
NF-kB is activated and signals survival
Axonal growth stimulation
+18 more
PRDM12
Unknown
—
Disgenet
—
SCN11A
Unknown
—
Disgenet
Phase 0 - rapid depolarisation
SCN9A
Unknown
—
Disgenet
Taste transduction
Phase 0 - rapid depolarisation
All
4
Causal
0
Unknown
4
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
4
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Congenital pain insensitivity.
5
View disease cluster →
Congenital insensitivity to pain
3 shared genes
SCN11A, SCN9A, PRDM12
Related via 3 shared genes including SCN11A, SCN9A, PRDM12.
Erythromelalgia
2 shared genes
SCN11A, SCN9A
Related via 2 shared genes including SCN11A, SCN9A.
Paroxysmal extreme pain disorder
2 shared genes
SCN11A, SCN9A
Related via 2 shared genes including SCN11A, SCN9A.
Congenital sensory neuropathy
1 shared gene
NGF
Related via 1 shared gene including NGF.
Hereditary sensory and autonomic neuropathy
4 shared genes
NGF, SCN11A, SCN9A, PRDM12
Related via 4 shared genes including NGF, SCN11A, SCN9A.
1
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