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Download Data for neuronopathy, distal hereditary motor, type 2C
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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.
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:0111209
OMIM:613376
UMLS:C3150619
MONDO:0013243
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 craniometaphyseal dysplasia, autosomal dominant
This disease has been annotated by GARD as a rare disease.
GARD:0001581
MESH:C565145
OMIM:123000
UMLS:C1852502
MONDO:0007397