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Wilson-turner syndrome
Wilson-turner syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
WILSON-TURNER SYNDROME
3459
MONDO:0010665
HDAC8
Unknown
—
CTD
,
Orphanet
Cell cycle
Neutrophil extracellular trap formation
Alcoholism
Viral carcinogenesis
Separation of Sister Chromatids
Resolution of Sister Chromatid Cohesion
Constitutive Signaling by NOTCH1 PEST Domain Mutants
Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants
HDACs deacetylate histones
Notch-HLH transcription pathway
+7 more
WILSON-TURNER X-LINKED MENTAL RETARDATION SYNDROME
MESH:C536708
LAS1L
Unknown
26358559
25644381
CTD
Major pathway of rRNA processing in the nucleolus and cytosol
All
2
Causal
1
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
1
Disgenet
0
CTD
2
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Wilson-turner syndrome.
5
View disease cluster →
De lange syndrome
1 shared gene
HDAC8
Related via 1 shared gene including HDAC8.
X-linked syndromic intellectual disability
1 shared gene
LAS1L
Related via 1 shared gene including LAS1L.
Cornelia de lange syndrome
1 shared gene
HDAC8
Related via 1 shared gene including HDAC8.
Partington syndrome
1 shared gene
LAS1L
Related via 1 shared gene including LAS1L.
Clinodactyly
1 shared gene
HDAC8
Related via 1 shared gene including HDAC8.
1
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