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. [ https://pubmed.ncbi.nlm.nih.gov/27745641 ]

Synonyms: genetic photosensitivity genetic skin photosensitivity

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C5679594 (MONDO:equivalentTo)
  • Orphanet:183490 (MONDO:equivalentTo)
  • GARD:20277 (MONDO:GARD)
  • MEDGEN:1842494 (MONDO:equivalentTo)
Subsets

gard_rare, mondo_rare, otar, disease_grouping, rare, ordo_group_of_disorders

exactMatch

http://identifiers.org/medgen/1842494

http://www.orpha.net/ORDO/Orphanet_183490

http://linkedlifedata.com/resource/umls/id/C5679594

has broad synonym

photogénodermatose

photogenodermatosis

id

MONDO:0015951

Term relations