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frank-ter haar syndrome
frank-ter haar syndrome
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Frank-ter Haar syndrome
SH3PXD2B
Causal
15523657
20137777
7158646
ClinGen
—
All
1
Causal
1
Unknown
0
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
1
Related Diseases
Diseases that share the most curated genes with frank-ter haar syndrome.
5
View disease cluster →
Eye abnormalities
1 shared gene
SH3PXD2B
Related via 1 shared gene including SH3PXD2B.
Growth disorder
1 shared gene
SH3PXD2B
Related via 1 shared gene including SH3PXD2B.
Ocular hypertension
1 shared gene
SH3PXD2B
Related via 1 shared gene including SH3PXD2B.
Bone disease
1 shared gene
SH3PXD2B
Related via 1 shared gene including SH3PXD2B.
Preeclampsia
1 shared gene
SH3PXD2B
Related via 1 shared gene including SH3PXD2B.
1
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