disease has feature autosomal dominant disease tuberous sclerosis Bourneville Phacomatosis Bourneville disease Bourneville phakomatosis Bourneville pringle disease Bourneville pringle's disease Bourneville syndrome Bourneville's disease Bourneville's syndrome Bourneville-Pringles disease Bourneville-pringle disease Bourneville-pringle's disease DOID:13515 Editor note: TODO check MONDO:0019341; consider placement under neoplastic syndrome Epiloia 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. ICD10:Q85.1 ICD9:759.5 MESH:D014402 MONDO:0001734 NCIT:C3424 OMIMPS:191100 Phacomatosis, Bourneville SCTID:7199000 TSC adenoma sebaceum adenoma sebaceum syndrome bourneville's disease cerebral Scleroses cerebral sclerosis disease, Bourneville-pringle disease, Bourneville-pringle's phakomatosis, Bourneville sclerosis Tuberosa sclerosis, cerebral sclerosis, tuberose sclerosis, tuberous syndrome, Bourneville syndrome, Bourneville's ts - tuberous sclerosis tuberose sclerosis tuberous sclerosis tuberous sclerosis Complex tuberous sclerosis syndrome hamartoma (disease) hereditary neoplastic syndrome inherited neurodegenerative disorder neurocutaneous syndrome