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Cortical dysplasia
Cortical dysplasia
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
CORTICAL DYSPLASIA
C0431380
FAM20C
Causal
—
Disgenet
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Post-translational protein phosphorylation
TSC1
Causal
—
Disgenet
Phospholipase D signaling pathway
Autophagy - animal
mTOR signaling pathway
PI3K-Akt signaling pathway
AMPK signaling pathway
Longevity regulating pathway
Cellular senescence
Thermogenesis
Insulin signaling pathway
Human cytomegalovirus infection
Human papillomavirus infection
Herpes simplex virus 1 infection
Choline metabolism in cancer
Macroautophagy
Inhibition of TSC complex formation by PKB
Energy dependent regulation of mTOR by LKB1-AMPK
TP53 Regulates Metabolic Genes
TBC/RABGAPs
+15 more
KIF5C
Unknown
—
Disgenet
Endocytosis
Dopaminergic synapse
Motor proteins
Alzheimer disease
Parkinson disease
Amyotrophic lateral sclerosis
Huntington disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Salmonella infection
Non-small cell lung cancer
+8 more
TBR1
Unknown
—
Disgenet
—
All
4
Causal
2
Unknown
2
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 Cortical dysplasia.
5
View disease cluster →
lethal osteosclerotic bone dysplasia
1 shared gene
FAM20C
Related via 1 shared gene including FAM20C.
Focal cortical dysplasia
2 shared genes
TBR1, TSC1
Related via 2 shared genes including TBR1, TSC1.
Cortical occipital malformations
1 shared gene
TBR1
Related via 1 shared gene including TBR1.
Developmental delay with language impairment and movement disorder
1 shared gene
TBR1
Related via 1 shared gene including TBR1.
Intellectual developmental disorder autism speech
1 shared gene
TBR1
Related via 1 shared gene including TBR1.
1
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