You are using an outdated browser. Please upgrade your browser to improve your experience.
hypopigmentation of the skin
Disease Summary
Associated Targets (46)
Tbio
38
Tclin
4
Tchem
2
Tdark
2
Mondo Description 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.
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.
MESH:D017496
Orphanet:79376
MONDO:0019290
High level summary of knowledge for a disease, including descriptions and datasource references.