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Download Data for hereditary spastic paraplegia 11
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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:0110764
GARD:0004919
NCIT:C148317
OMIM:604360
Orphanet:2822
SCTID:715491000
MONDO:0011445
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