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tuberous sclerosis 1

Disease Summary
Associated Targets (3)




Explore Associated Targets
Mondo Description Tuberous sclerosis mapped to chromosome 9q34 (TSC1 gene).
Uniprot Description An autosomal dominant multi-system disorder that affects especially the brain, kidneys, heart, and skin. It is characterized by hamartomas (benign overgrowths predominantly of a cell or tissue type that occurs normally in the organ) and hamartias (developmental abnormalities of tissue combination). Clinical manifestations include epilepsy, learning difficulties, behavioral problems, and skin lesions. Seizures can be intractable and premature death can occur from a variety of disease-associated causes.
Mondo Term and Equivalent IDs
MONDO:0008612:  tuberous sclerosis 1
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found