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Download Data for hyperargininemia
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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:9278
GARD:0005840
MESH:D020162
NCIT:C84568
OMIM:207800
Orphanet:90
SCTID:23501004
UMLS:C0268548
MONDO:0008814
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
Download Data for hereditary spastic paraplegia 3A
DOID:0110791
GARD:0005041
MESH:C536864
NCIT:C142893
OMIM:182600
Orphanet:100984
UMLS:C2931355
MONDO:0008437