disease has feature autosomal dominant disease tuberous sclerosis https://github.com/monarch-initiative/mondo/issues/1489 https://github.com/monarch-initiative/mondo/issues/6025 https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/tuberous_sclerosis https://www.malacards.org/card/tuberous_sclerosis_1_2 TSC tuberous sclerosis syndrome NANDO:1200607 MedDRA:10045138 NCIT:C3424 adenoma sebaceum syndrome tuberous sclerosis complex adenoma sebaceum MEDGEN:22518 ICD10CM:Q85.1 NANDO:2200826 icd11.foundation:1903085809 SCTID:7199000 Bourneville disease Bourneville's syndrome Hereditary disease characterized by seizures, intellectual disability, 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. Orphanet:805 UMLS:C0041341 epiloia MESH:D014402 OMIMPS:191100 NORD:1802 Bourneville syndrome ICD9:759.5 MONDO:0001734 GARD:0007830 tuberous sclerosis Bourneville's disease DOID:13515 hamartoma hereditary neoplastic syndrome obsolete inherited nervous system cancer-predisposing syndrome obsolete inherited renal cancer-predisposing syndrome inherited neurodegenerative disorder neurocutaneous syndrome hereditary neurological disease