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Xeroderma pigmentosum group F
Xeroderma pigmentosum group F
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Subtype of:
Xeroderma pigmentosum
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
xeroderma pigmentosum group F
MONDO_0010215
ERCC4
Unknown
10447254
17183314
22044607
23623386
23623389
28431612
29403087
29892709
3372781
8797827
9579555
9580660
ClinGen
,
Open Targets
Nucleotide excision repair
Fanconi anemia pathway
HDR through Single Strand Annealing (SSA)
Formation of Incision Complex in GG-NER
Dual Incision in GG-NER
Dual incision in TC-NER
Fanconi Anemia Pathway
+4 more
Xpf
MONDO_0010215
ERCC4
Unknown
8797827
Open Targets
Nucleotide excision repair
Fanconi anemia pathway
HDR through Single Strand Annealing (SSA)
Formation of Incision Complex in GG-NER
Dual Incision in GG-NER
Dual incision in TC-NER
Fanconi Anemia Pathway
+4 more
All
1
Causal
0
Unknown
1
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
1
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Xeroderma pigmentosum group F.
5
View disease cluster →
Xfe progeroid syndrome
1 shared gene
ERCC4
Related via 1 shared gene including ERCC4.
Xeroderma pigmentosum-cockayne syndrome
1 shared gene
ERCC4
Related via 1 shared gene including ERCC4.
Cockayne syndrome
1 shared gene
ERCC4
Related via 1 shared gene including ERCC4.
Testicular neoplasms
1 shared gene
ERCC4
Related via 1 shared gene including ERCC4.
Xeroderma
1 shared gene
ERCC4
Related via 1 shared gene including ERCC4.
1
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