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Download Data for progressive myoclonus epilepsy
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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:891
GARD:0007140
MESH:D020191
NCIT:C7636
OMIMPS:254800
Orphanet:98261
SCTID:267581004
UMLS:C0751778
MONDO:0020074
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