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Download Data for spondyloepiphyseal dysplasia tarda, X-linked
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0004985
OMIM:313400
MONDO:0010737
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 RIN2 syndrome
Description from UniProt.
MESH:C567770
OMIM:613075
Orphanet:217335
SCTID:723367005
UMLS:C2751321
MONDO:0013115