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familial progressive hyperpigmentation
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Familial progressive hyperpigmentation is a rare, genetic, skin pigmentation anomaly disorder characterized by irregular patches of hyperpigmented skin which present at birth or in early infancy and increase in size, number and confluence with age. Affected areas of the body include the face, neck, trunk and limbs, as well as the palms, soles, oral mucosa and conjuctiva. No hypogmentation macules are observed and no systemic diseases are associated.
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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.
OMIM:614233
Orphanet:79146
SCTID:715630006
UMLS:C1840392
UMLS:CN205811
MONDO:0013648
High level summary of knowledge for a disease, including descriptions and datasource references.