tuberous sclerosis tuberous sclerosis 2 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/9178 https://www.malacards.org/card/tuberous_sclerosis_2 NCIT:C75331 tuberous sclerosis, type 2 TSC2 tuberous sclerosis-2 DOID:0080325 tuberous sclerosis type 2 An 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. UMLS:C1860707 MEDGEN:348170 OMIM:613254 TSC2-related tuberous sclerosis MESH:C566021 MONDO:0013199 GARD:0015640 tuberous sclerosis 2 obsolete tuberous sclerosis complex