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Download Data for autosomal recessive limb-girdle muscular dystrophy type 2H
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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.
DOID:0110282
GARD:0003844
MESH:C535897
OMIM:254110
Orphanet:1878
SCTID:43226001
UMLS:C0270968
MONDO:0009683
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