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Download Data for spinal muscular atrophy-progressive myoclonic epilepsy 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.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0111527
GARD:0003044
GARD:0003875
MESH:C537563
OMIM:159950
Orphanet:2590
SCTID:703524005
UMLS:C1834569
MONDO:0008045
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