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Potocki-shaffer syndrome
Potocki-shaffer syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
POTOCKI-SHAFFER SYNDROME
52022
MONDO:0011022
ALX4
Unknown
15852040
Orphanet
—
EXT2
Unknown
15852040
Orphanet
Glycosaminoglycan biosynthesis - heparan sulfate / heparin
Metabolic pathways
HS-GAG biosynthesis
Defective EXT2 causes exostoses 2
Defective EXT1 causes exostoses 1, TRPS2 and CHDS
+2 more
PHF21A
Unknown
22770980
36876344
36843358
GWAS catalog
,
Orphanet
HDACs deacetylate histones
Factors involved in megakaryocyte development and platelet production
All
3
Causal
0
Unknown
3
Select all
Clear
ClinVar
0
Orphanet
3
Disgenet
0
CTD
0
HPO
0
GWAS catalog
1
GenCC
0
ClinGen
0
Related Diseases
Diseases that share the most curated genes with Potocki-shaffer syndrome.
5
View disease cluster →
11p11.2 deletion syndrome
3 shared genes
ALX4, EXT2, PHF21A
Related via 3 shared genes including ALX4, EXT2, PHF21A.
Frontonasal dysplasia with alopecia and genital anomaly
1 shared gene
ALX4
Related via 1 shared gene including ALX4.
Seizures, scoliosis, and macrocephaly/microcephaly syndrome
1 shared gene
EXT2
Related via 1 shared gene including EXT2.
exostoses, multiple, type 2
1 shared gene
EXT2
Related via 1 shared gene including EXT2.
Intellectual developmental disorder behavioral dysmorphic
1 shared gene
PHF21A
Related via 1 shared gene including PHF21A.
1
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