GeDiPNet
☰
Home
Browse
Genes
Diseases
Proteins
SNPs / Variants
Pathways ►
Reactome
KEGG
Analysis
Statistics
Resources
Blogs
Login
Contact Us
Search
Home
/
Diseases
/
Chudley-mccullough syndrome
Chudley-mccullough syndrome
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
CHUDLEY-MCCULLOUGH SYNDROME
314597
604213
C1858695
MESH:C535459
MONDO:0011411
GPSM2
Causal
20602914
22578326
CTD
,
ClinGen
,
ClinVar
,
Disgenet
,
HPO
,
Orphanet
G alpha (i) signalling events
SPTB
Causal
—
Disgenet
NCAM signaling for neurite out-growth
Interaction between L1 and Ankyrins
RAF/MAP kinase cascade
COPI-mediated anterograde transport
+1 more
All
3
Causal
2
Unknown
1
Select all
Clear
ClinVar
1
Orphanet
1
Disgenet
2
CTD
1
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
1
Related Diseases
Diseases that share the most curated genes with Chudley-mccullough syndrome.
5
View disease cluster →
Neonatal anemia
1 shared gene
SPTB
Related via 1 shared gene including SPTB.
Perinatal hemolytic anemia
1 shared gene
SPTB
Related via 1 shared gene including SPTB.
Hereditary elliptocytosis
1 shared gene
SPTB
Related via 1 shared gene including SPTB.
Spherocytosis
1 shared gene
SPTB
Related via 1 shared gene including SPTB.
Chagas cardiomyopathy
1 shared gene
SPTB
Related via 1 shared gene including SPTB.
1
GeDiPNet AI Assistant
Online