PTPN13
Familial Hepatocellular Carcinoma
PTEN
Cowden syndrome; Bannayan-Riley-Ruvalcaba syndrome
PTCH1
nevoid basal cell carcinoma syndrome
PRKAR1A
Carney complex
POLD1
Lynch syndrome
PMS2
hereditary non-polyposis colorectal cancer; Turcot syndrome
PMS1
hereditary non-polyposis colorectal cancer
PHOX2B
familial neuroblastoma
Congenital central hypoventilation syndrome
PDGFRA
familial gastrointestinal stromal tumour
PALB2
Fanconi anaemia N; breast cancer susceptibility
NTHL1
Familial adenomatous polyposis
NF2
neurofibromatosis type 2
NF1
neurofibromatosis type 1
NBN
Nijmegen breakage syndrome
MUTYH
adenomatous polyposis coli
MSH6
hereditary non-polyposis colorectal cancer
MSH2
hereditary non-polyposis colorectal cancer
MPL
familial essential thrombocythemia
Congenital amegakaryocytic thrombocytopenia
MLH1
hereditary non-polyposis colorectal cancer; Turcot syndrome
MET
familial papillary renal cancer
MEN1
multiple endocrine neoplasia type 1
LZTR1
Schwannomatosis-2
Noonan syndrome 10
KIT
familial gastrointestinal stromal tumour
Piebald trait
HRAS
Costello syndrome
HNF1A
familial hepatic adenoma
Maturity-onset diabetes of the young; TYPE III
