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Disease Ontology Browser
rhabdoid tumor predisposition syndrome (DOID:0070617)
Alliance: disease page
Synonyms: familial posterior fossa brain tumor syndrome of infancy; rhabdoid predisposition syndrome; RTPS
Alt IDs: NCI:C93268, OMIM:PS609322, ORDO:231108, UMLS_CUI:C2985524
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory