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DOID:0070617 - rhabdoid tumor predisposition syndrome
Disease Ontology 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.
Synonyms: familial posterior fossa brain tumor syndrome of infancy, rhabdoid predisposition syndrome, RTPS
Xenbase Genes

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)