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Download Data for ornithine aminotransferase 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:1415
GARD:0006556
GARD:0007272
MESH:C538071
MESH:D015799
NCIT:C84744
OMIM:258870
Orphanet:414
UMLS:C0018425
MONDO:0009796
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