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xeroderma pigmentosum group B
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any xeroderma pigmentosum in which the cause of the disease is a mutation in the ERCC3 gene.
Uniprot Description An autosomal recessive pigmentary skin disorder characterized by solar hypersensitivity of the skin, high predisposition for developing cancers on areas exposed to sunlight and, in some cases, neurological abnormalities. The skin develops marked freckling and other pigmentation abnormalities. Some XP-B patients present features of Cockayne syndrome, including cachectic dwarfism, pigmentary retinopathy, ataxia, decreased nerve conduction velocities. The phenotype combining xeroderma pigmentosum and Cockayne syndrome traits is referred to as XP-CS complex.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110850
GARD:0005625
MESH:C562590
NCIT:C3966
OMIM:610651
SCTID:1073003
UMLS:C0268136
MONDO:0012531
High level summary of knowledge for a disease, including descriptions and datasource references.