Xeroderma pigmentosum group D

Log in to bookmark this disease

Bookmark This Disease

Subtype of: Xeroderma pigmentosum
Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
xeroderma pigmentosum group D
MONDO_0010212
ERCC2 Unknown
10447254 11156600 11443545 11709541 15220921 15494306 17466626 26884178 28376890 7585650 7825573 7849702 7920640 8571952 9012405 9101292 9195225 9758621
ClinGen, Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Xeroderma pigmentosum group D.
5 View disease cluster →
Cerebro-oculo-facio-skeletal syndrome 2 1 shared geneERCC2 Related via 1 shared gene including ERCC2. Trichothiodystrophy 1, photosensitive 1 shared geneERCC2 Related via 1 shared gene including ERCC2. Xeroderma pigmentosum-cockayne syndrome 1 shared geneERCC2 Related via 1 shared gene including ERCC2. Cerebrooculofacioskeletal syndrome 1 shared geneERCC2 Related via 1 shared gene including ERCC2. Congenital skin anomaly 1 shared geneERCC2 Related via 1 shared gene including ERCC2.