Search Ontology:
Human Disease
tuberous sclerosis 2
- Term ID
- DOID:0080325
- 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. (2)
- References
- Ontology
- Human Disease ( DOID:0080325 )
Other Pages
Genes Involved
Zebrafish Models