eDiPNet
☰
Home
Browse
Genes
Diseases
Proteins
SNPs / Variants
Pathways ►
Reactome
KEGG
Analysis
Statistics
Resources
Blogs
Login
Contact Us
Search
Home
/
Diseases
/
Radioulnar synostosis
Radioulnar synostosis
Log in to bookmark this disease
Bookmark This Disease
Title
Project / Tag (optional)
Note (optional)
Cancel
Save
Include the contents of this disease's 3 subtypes
in the table below
Show the subtypes
Congenital radioulnar synostosis
Radioulnar synostosis with amegakaryocytic thrombocytopenia 1
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
Download ▾
Download as CSV
Download as PDF
Pathways column key:
KEGG
Reactome
Disease terms
Disease ID
Gene Symbol
Classification
References
Source
Pathways
radioulnar synostosis
MONDO_0017985
MECOM
Causal
37407873
Open Targets
Lysine degradation
Metabolic pathways
MAPK signaling pathway
Pathways in cancer
Chronic myeloid leukemia
PKMTs methylate histone lysines
Regulation of PTEN gene transcription
+4 more
radioulnar synostosis
MONDO_0017985
OSR2
Unknown
41424369
Open Targets
—
radioulnar synostosis
MONDO_0017985
SMAD6
Causal
31138930
Open Targets
TGF-beta signaling pathway
Signaling by BMP
RUNX2 regulates bone development
All
3
Causal
2
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
3
Related Diseases
Diseases that share the most curated genes with Radioulnar synostosis.
5
View disease cluster →
MECOM-associated syndrome
1 shared gene
MECOM
Related via 1 shared gene including MECOM.
Hypocellular bone marrow
1 shared gene
MECOM
Related via 1 shared gene including MECOM.
Digit abnormalities
1 shared gene
MECOM
Related via 1 shared gene including MECOM.
B-cell lymphopenia
1 shared gene
MECOM
Related via 1 shared gene including MECOM.
Radioulnar synostosis with amegakaryocytic thrombocytopenia 2
1 shared gene
MECOM
Related via 1 shared gene including MECOM.
1
GeDiPNet AI Assistant
Online