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Download Data for encephalopathy due to prosaposin deficiency
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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:0111330
GARD:0012505
MESH:C567125
OMIM:611721
Orphanet:139406
SCTID:720864008
UMLS:C2673635
UMLS:C4303785
MONDO:0012719
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