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tuberous sclerosis
Disease Summary
Associated Targets (9)
Tchem
4
Tbio
3
Tclin
2
Mondo Description Hereditary disease characterized by seizures, mental retardation, developmental delay, and skin and ocular lesions. First signs usually occur during infancy or childhood but in rare cases may not occur until 2nd or 3rd decade.
Disease Ontology Description An autosomal dominant disease that is characterized by the growth of numerous noncancerous tumors in many parts of the body.
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 Disease Ontology
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:13515
ICD9:759.5
MESH:D014402
NCIT:C3424
OMIMPS:191100
SCTID:7199000
MONDO:0001734
High level summary of knowledge for a disease, including descriptions and datasource references.