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Summary Literature (0)
DOID:0080325 - tuberous sclerosis 2

Disease Ontology 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.

Synonyms:

Xenbase Genes : ifng, tsc2



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): tuberous sclerosis (is_a)