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Download Data for dyschromatosis universalis hereditaria
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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.
This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0060304
GARD:0001996
MESH:C535730
OMIMPS:127500
Orphanet:241
SCTID:239082002
UMLS:C1306229
UMLS:C2930995
MONDO:0000736
High level summary of knowledge for a disease, including descriptions and datasource references.
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Opens the Target List with this set of targets