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Download Data for craniometaphyseal dysplasia, autosomal dominant
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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 UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0001581
MESH:C565145
OMIM:123000
UMLS:C1852502
MONDO:0007397
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