FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term xeroderma pigmentosum group C ID (Ontology) DOID:0110844 (Human Disease)
Definition A xeroderma pigmentosum characterized by increased propensity to develop malignant melanoma that has_material_basis_in mutation in the XPC gene on chromosome 3p25.
Also Known As "xeroderma pigmentosum III" ; "XP group C" ; "XP3" (for all, see Synonyms field below)
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 xeroderma pigmentosum group C       1
 for disease ribbon | xeroderma pigmentosum group C       1
 model of | xeroderma pigmentosum group C       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal recessive disease__
syndrome_____________________|
                             xeroderma pigmentosum
                              |__xeroderma pigmentosum group C  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a xeroderma pigmentosum
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "xeroderma pigmentosum III" EXACT
    "XP group C" EXACT
    "XP3" EXACT OMO:0003012
    "XPC" EXACT OMO:0003012
    "XPCC" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:Q82.1
MIM:278720