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Download Data for ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
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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:0050754
GARD:0009283
MESH:C538013
OMIM:208920
Orphanet:1168
UMLS:C1859598
MONDO:0008842
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