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Download Data for atypical Werner syndrome
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0011910
Orphanet:79474
SCTID:715633008
UMLS:C4275075
UMLS:CN205977
MONDO:0019321
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