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
- MedDRA:10040868 (Orphanet:79376/e)
- HP:0001010 (MONDO:otherHierarchy)
- GARD:19005 (Orphanet:79376)
- Orphanet:183469 (MONDO:mondoIsBroaderThanSource)
- MESH:D017496 (MONDO:equivalentTo)
- Orphanet:79376 (MONDO:equivalentTo)
Subsets
gard_rare, disease_grouping, rare, orphanet_rare, ordo_group_of_disorders