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hereditary photodermatosis
Disease Summary
Associated Targets (58)
Tbio
39
Tchem
15
Tclin
4
Mondo Description Hereditary photodermatoses are a spectrum of rare photosensitive disorders that are often caused by genetic deficiency or malfunction of various components of the DNA repair pathway. This results clinically in extreme photosensitivity, with many syndromes exhibiting an increased risk of cutaneous malignancies.
Mondo Term and Equivalent IDs
MONDO:0015951: hereditary photodermatosis
Orphanet:183490:
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
Orphanet:183490
MONDO:0015951
High level summary of knowledge for a disease, including descriptions and datasource references.