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Download Data for Amelogenesis imperfecta 1F
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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.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
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
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This disease has been annotated by GARD as a rare disease.
Description from Mondo Disease Ontology.
Description from Disease Ontology
COHD:438476
DOID:12387
GARD:0007178
ICD10:N25.1
ICD9:588.1
MESH:D018500
NCIT:C84919
Orphanet:223
SCTID:111395007
UMLS:C0162283
MONDO:0016383