A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections. [ MESH:D017496 ]

Synonyms: hypopigmentation of the skin hypopigmentation of the skin (disease)

This is just here as a test because I lose it

Term information

database cross reference
  • UMLS:C0162835 (MONDO:equivalentTo)
  • MEDGEN:102477 (MONDO:equivalentTo)
  • Orphanet:79376 (MONDO:equivalentTo)
  • HP:0001010 (MONDO:otherHierarchy)
  • MedDRA:10040868 (Orphanet:79376/e)
  • MESH:D017496 (MONDO:equivalentTo)
Subsets

otar, disease_grouping, ordo_group_of_disorders

IAO 0000589

hypopigmentation of the skin (disease)

closeMatch

http://identifiers.org/meddra/10040868

exactMatch

http://linkedlifedata.com/resource/umls/id/C0162835

http://identifiers.org/mesh/D017496

http://identifiers.org/medgen/102477

http://www.orpha.net/ORDO/Orphanet_79376

has related synonym

hypomelanosis

hypomelanoses

id

MONDO:0019290

Term relations