autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis GARD:0009481 MESH:C536328 MONDO:0010856 OMIM:600273 Orphanet:88924 PKDTS Polycystic kidney disease with tuberous sclerosis (PKD-TSC) is characterised by early-onset and severe polycystic kidney disease with various manifestations of tuberous sclerosis (multiple angiomyolipomas, lymphangioleiomyomatosis and periventricular calcifications of the central nervous system). SCTID:765331004 UMLS:C1838327 chromosome 16P13.3 deletion syndrome, distal polycystic kidney disease, infantile severe, with tuberous sclerosis polycystic kidneys, severe infantile with tuberous sclerosis tuberous sclerosis polycystic kidney disease contiguous gene syndrome tuberous sclerosis/polycystic kidney disease contiguous gene syndrome partial deletion of the short arm of chromosome 16 familial cystic renal disease