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Download Data for Ehlers-Danlos syndrome, arthrochalasis 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:0002084
MESH:C562625
NCIT:C125701
OMIM:130060
Orphanet:1899
SCTID:4170004
UMLS:CN200649
MONDO:0007525
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