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Download Data for creatine transporter 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:0050800
GARD:0001608
MESH:C535598
NCIT:C125665
OMIM:300352
Orphanet:52503
SCTID:698290008
MONDO:0010305
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