FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term rhabdoid tumor predisposition syndrome 2 ID (Ontology) DOID:0060997 (Human Disease)
Definition A rhabdoid tumor predisposition syndrome that has_material_basis_in heterozygous germline mutation in the SMARCA4 gene on chromosome 19p13.
Also Known As "RTPS2"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 rhabdoid tumor predisposition syndrome 2       1
 for disease ribbon | rhabdoid tumor predisposition syndrome 2       1
 model of | rhabdoid tumor predisposition syndrome 2       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal dominant disease__
syndrome____________________|
                            rhabdoid tumor predisposition syndrome
                             |__rhabdoid tumor predisposition syndrome 2  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a rhabdoid tumor predisposition syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "RTPS2" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
MIM:613325