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Dowling-Degos disease 1
Disease Summary
Associated Targets (5)
Tbio
3
Tchem
2
Mondo Description Any Dowling-Degos disease in which the cause of the disease is a mutation in the KRT5 gene.
Uniprot Description An autosomal dominant genodermatosis. Affected individuals develop a postpubertal reticulate hyperpigmentation that is progressive and disfiguring, and small hyperkeratotic dark brown papules that affect mainly the flexures and great skin folds. Patients usually show no abnormalities of the hair or nails.
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.
OMIM:179850
UMLS:C3714534
MONDO:0024534
High level summary of knowledge for a disease, including descriptions and datasource references.