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X-linked syndromic complex neurodevelopmental disorder
X-linked syndromic complex neurodevelopmental disorder
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
X-linked syndromic complex neurodevelopmental disorder
AP1S2
Unknown
—
ClinGen
Lysosome
Human immunodeficiency virus 1 infection
Nef mediated downregulation of MHC class I complex cell surface expression
MHC class II antigen presentation
Lysosome Vesicle Biogenesis
Golgi Associated Vesicle Biogenesis
+3 more
TFE3
Unknown
—
ClinGen
Mitophagy - animal
Transcriptional misregulation in cancer
Renal cell carcinoma
ZFX
Unknown
—
ClinGen
—
All
3
Causal
0
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
3
Related Diseases
Diseases that share the most curated genes with X-linked syndromic complex neurodevelopmental disorder.
5
View disease cluster →
X-linked complex neurodevelopmental disorder
3 shared genes
AP1S2, TFE3, ZFX
Related via 3 shared genes including AP1S2, TFE3, ZFX.
Partington syndrome
1 shared gene
AP1S2
Related via 1 shared gene including AP1S2.
Intellectual developmental disorder, x-linked
3 shared genes
AP1S2, TFE3, ZFX
Related via 3 shared genes including AP1S2, TFE3, ZFX.
X-linked intellectual disability
1 shared gene
AP1S2
Related via 1 shared gene including AP1S2.
Renal cell carcinoma
1 shared gene
TFE3
Related via 1 shared gene including TFE3.
1
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