Term Name:	tuberous sclerosis 2
Synonyms:
Definition:	A tuberous sclerosis that is characterized by hamartomas in multiple organ systems and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the TSC2 gene, which encodes tuberin, on chromosome 16p13.
Ontology:	Human Disease [DOID:0080325]   ( DOID:0080325 )