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Download Data for congenital hypothyroidism
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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 Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0050328
GARD:0001487
MESH:D003409
NCIT:C26734
Orphanet:442
SCTID:190268003
SCTID:217710005
UMLS:C0010308
MONDO:0018612
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