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Tuberous sclerosis 2
rareAn autosomal dominant syndrome caused by pathogenic variants in the TSC2 gene, characterized by the growth of hamartomas in multiple organs, including the brain, skin, kidneys, heart, and lungs. Other clinical features include seizures, intellectual disability, and skin lesions.
- Identifiers
- MONDO:0013199 OMIM:613254
- Part of
- Tuberous sclerosis
- Also known as
- TSC2 · TSC2-related tuberous sclerosis · tuberous sclerosis type 2 · tuberous sclerosis, type 2 · tuberous sclerosis-2
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