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tuberous sclerosis

Disease Summary
Associated Targets (5)
Tbio

3

Tclin

2


Explore Associated Targets
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.
Mondo Term and Equivalent IDs
MONDO:0001734:  tuberous sclerosis
ICD9:759.5: 
MESH:D014402: 
NCIT:C3424: 
OMIMPS:191100: 
SCTID:7199000: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)