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Download Data for ornithine carbamoyltransferase 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.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:9271
EFO:0007409
GARD:0008391
MESH:D020163
NCIT:C84957
OMIM:311250
Orphanet:664
SCTID:80908008
UMLS:C0268542
MONDO:0010703
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