Use Cases
Submit Feedback
Download Data for autosomal recessive limb-girdle muscular dystrophy type 2D
data still loading...
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.
DOID:0110278
GARD:0000438
NCIT:C142081
OMIM:608099
Orphanet:62
SCTID:715340002
MONDO:0011968
High level summary of knowledge for a disease, including descriptions and datasource references.
click for section description and definitions
Opens the Target List with this set of targets