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Download Data for neuroferritinopathy
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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.
Description from Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110737
GARD:0010686
MESH:C548080
OMIM:606159
Orphanet:157846
SCTID:699299001
UMLS:C1853578
MONDO:0011638
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