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Cancer Institute NSW sites
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Home
Cancer genetics
Paediatric
Risk management
26 results
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AIP - risk management
ALK or PHOX2B – risk management
APC (Familial adenomatous polyposis) – risk management
Beckwith-Wiedemann syndrome – risk management
CDC73 (Hyperparathyroidism-jaw tumour syndrome) – risk management
CMMRD – risk management
DICER1 – risk management (child)
GATA2 deficiency syndrome – risk management
Juvenile polyposis of infancy (contiguous PTEN and BMPR1A deletion) – risk management
MEN1 or CDKN1B – risk management
NF1 (Neurofibromatosis type 1) – risk management
NF2 (Neurofibromatosis type 2) – risk management
PTCH1 or SUFU (Gorlin) – risk management
PTEN (PTEN hamartoma/Cowden) – risk management
RB1 (non-retinoblastoma cancer risk) – risk management
RET (MEN2) – risk management
RUNX1 – risk management
SDHA, SDHB or SDHC-related familial paraganglioma-phaeochromocytoma – risk management
SDHD or SDHAF2-related familial paraganglioma-phaeochromocytoma – risk management
SMAD4 or BMPR1A (Juvenile polyposis) – risk management
SMARCA4-associated rhabdoid tumour predisposition syndrome – risk management
SMARCB1-associated rhabdoid tumour predisposition syndrome – risk management
STK11 (Peutz-Jeghers) – risk management
TP53 (Li-Fraumeni) – risk management (child)
VHL (von Hippel-Lindau disease) – risk management
Wilms tumour – risk management
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