FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term rhabdoid tumor predisposition syndrome ID (Ontology) DOID:0070617 (Human Disease)
Definition A syndrome characterized by a markedly increased risk for the development of rhabdoid tumors, rare and highly aggressive malignant tumors occurring in almost any anatomical location predominantly in infants and young children.
Also Known As "familial posterior fossa brain tumor syndrome of infancy" ; "rhabdoid predisposition syndrome" ; "RTPS"
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                rhabdoid tumor predisposition syndrome  2 rec.
                                 |__rhabdoid tumor predisposition syndrome 1 1 rec.
                                 |__rhabdoid tumor predisposition syndrome 2 1 rec.
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Is a autosomal dominant disease
syndrome
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Synonyms
  • "familial posterior fossa brain tumor syndrome of infancy" EXACT
    "rhabdoid predisposition syndrome" EXACT
    "RTPS" EXACT OMO:0003012
Secondary IDs
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MIM:PS609322
NCI:C93268
ORDO:231108
UMLS_CUI:C2985524