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Download Data for spondyloepimetaphyseal dysplasia, aggrecan type
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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.
GARD:0010513
MESH:C567558
OMIM:612813
Orphanet:171866
SCTID:719165004
UMLS:C2748544
MONDO:0013014
High level summary of knowledge for a disease, including descriptions and datasource references. Click the "?" for more details.
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Opens the Target List with this set of targets