GeDiPNet
☰
Home
Browse
Genes
Diseases
Proteins
SNPs / Variants
Pathways ►
Reactome
KEGG
Analysis
Statistics
Resources
Blogs
Login
Contact Us
Search
Home
/
Diseases
/
Amyloid neuropathy
Amyloid neuropathy
Log in to bookmark this disease
Bookmark This Disease
Title
Project / Tag (optional)
Note (optional)
Cancel
Save
Download ▾
Download as CSV
Download as PDF
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
AMYLOID NEUROPATHIES
C0206247
MESH:D017772
APP
Unknown
27567873
CTD
,
Disgenet
Serotonergic synapse
Alzheimer disease
Pathways of neurodegeneration - multiple diseases
Platelet degranulation
ECM proteoglycans
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
G alpha (q) signalling events
G alpha (i) signalling events
Lysosome Vesicle Biogenesis
Formyl peptide receptors bind formyl peptides and many other ligands
TAK1 activates NFkB by phosphorylation and activation of IKKs complex
The NLRP3 inflammasome
Advanced glycosylation endproduct receptor signaling
Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models
Post-translational protein phosphorylation
TRAF6 mediated NF-kB activation
Insertion of tail-anchored proteins into the endoplasmic reticulum membrane
Purinergic signaling in leishmaniasis infection
Amyloid fiber formation
+16 more
PSEN1
Unknown
27567873
CTD
,
Disgenet
Wnt signaling pathway
Notch signaling pathway
Neurotrophin signaling pathway
Alzheimer disease
Pathways of neurodegeneration - multiple diseases
Human papillomavirus infection
Nuclear signaling by ERBB4
Regulated proteolysis of p75NTR
NRIF signals cell death from the nucleus
Constitutive Signaling by NOTCH1 PEST Domain Mutants
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
EPH-ephrin mediated repulsion of cells
Neutrophil degranulation
NOTCH3 Activation and Transmission of Signal to the Nucleus
Noncanonical activation of NOTCH3
+12 more
AMYLOID NEUROPATHIES, FAMILIAL
C0206245
MESH:D028227
TTR
Unknown
10529370
12707074
15469931
20030258
CTD
,
Disgenet
Thyroid hormone synthesis
Retinoid cycle disease events
The canonical retinoid cycle in rods (twilight vision)
Non-integrin membrane-ECM interactions
Neutrophil degranulation
Retinoid metabolism and transport
Amyloid fiber formation
+4 more
All
3
Causal
0
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
3
CTD
3
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Amyloid neuropathy.
5
View disease cluster →
Abeta amyloidosis
1 shared gene
APP
Related via 1 shared gene including APP.
Amyloid angiopathy
1 shared gene
APP
Related via 1 shared gene including APP.
Partial epilepsy with variable foci
1 shared gene
APP
Related via 1 shared gene including APP.
Eye manifestations
1 shared gene
APP
Related via 1 shared gene including APP.
cerebral amyloid angiopathy, app-related
1 shared gene
APP
Related via 1 shared gene including APP.
1
GeDiPNet AI Assistant
Online