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Witteveen-kolk syndrome
Witteveen-kolk syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
WITTEVEEN KOLK SYNDROME
C4310804
SIN3A
Unknown
11598004
36756855
Disgenet
TGF-beta signaling pathway
Thyroid hormone signaling pathway
Huntington disease
Epstein-Barr virus infection
Transcriptional misregulation in cancer
SUMOylation of transcription cofactors
Regulation of lipid metabolism by PPARalpha
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
Loss of MECP2 binding ability to 5mC-DNA
Regulation of MECP2 expression and activity
+7 more
SIN3B
Unknown
22231303
Disgenet
Regulation of lipid metabolism by PPARalpha
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
WITTEVEEN-KOLK SYNDROME
613406
OMIM:613406
SIN3A
Unknown
17086554
17141616
22231303
27742395
28903942
37055165
9405671
CTD
,
HPO
TGF-beta signaling pathway
Thyroid hormone signaling pathway
Huntington disease
Epstein-Barr virus infection
Transcriptional misregulation in cancer
SUMOylation of transcription cofactors
Regulation of lipid metabolism by PPARalpha
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
Loss of MECP2 binding ability to 5mC-DNA
Regulation of MECP2 expression and activity
+7 more
All
2
Causal
0
Unknown
2
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
2
CTD
1
HPO
1
GWAS catalog
0
GenCC
0
ClinGen
0
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Chromosome 15q24 deletion syndrome
1 shared gene
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Related via 1 shared gene including SIN3A.
SIN3A-related intellectual disability syndrome
1 shared gene
SIN3A
Related via 1 shared gene including SIN3A.
15q24 microdeletion
1 shared gene
SIN3A
Related via 1 shared gene including SIN3A.
Dwarfism
1 shared gene
SIN3A
Related via 1 shared gene including SIN3A.
Congenital diaphragmatic hernia
1 shared gene
SIN3A
Related via 1 shared gene including SIN3A.
1
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