Disease_May_Have_Associated_Disease CTRP Terminology CTRP Disease Terminology GDC Terminology Comorbidity Cellosaurus Disease Terminology ACC/AHA Pediatric and Congenital Cardiology EHR Terminology Risk Factor Retinal Astrocytoma Childhood Cancer Predisposition Study Terminology CCPS Disease Terminology GDC Value Terminology TSC1 Gene TSC2 Gene Tuberous Sclerosis GDC Cellosaurus CCPS C0041341 Tuberous Sclerosis C3424 Disease or Syndrome Tuberous Sclerosis Tuberous sclerosis 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. NICHD Bourneville's Disease Hereditary disease characterized by seizures, intracerebral tumors, cardiac tumors, developmental delay, and skin and ocular lesions. TSC Tuberous Sclerosis ACC/AHA Tuberous Sclerosis Complex tuberous sclerosis Tuberous_Sclerosis Tuberous Sclerosis Syndrome CTRP A genetic disorder in which benign (not cancer) tumors form in the kidneys, brain, eyes, heart, lungs, and skin. This disease can cause seizures, mental disabilities, and different types of skin lesions. Tuberous Sclerosis Small Intestinal Hamartoma Subependymal Giant Cell Astrocytoma PEComa Central Nervous System Hamartoma Colorectal Polyp Cardiac Rhabdomyoma Phakomatosis NICHD Terminology Neonatal Research Network Terminology