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Download Data for dyschromatosis symmetrica 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 UniProt.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0060257
EFO:0008878
GARD:0000334
MESH:C535729
NCIT:C118435
OMIM:127400
Orphanet:41
SCTID:239085000
UMLS:C0406775
MONDO:0007483
High level summary of knowledge for a disease, including descriptions and datasource references.
click for section description and definitions
Opens the Target List with this set of targets