ERCC5
xeroderma pigmentosum (G)
EXT1
multiple exostoses type 1
EXT2
multiple exostoses type 2
FANCA
Fanconi anaemia A
FANCC
Fanconi anaemia C
FANCD2
Fanconi anaemia D2
FANCE
Fanconi anaemia E
FANCF
Fanconi anaemia F
FANCG
Fanconi anaemia G
FH
hereditary leiomyomatosis and renal cell cancer
FLCN
Birt-Hogg-Dube syndrome
GPC3
Simpson-Golabi-Behmel syndrome
HNF1A
familial hepatic adenoma
Maturity-onset diabetes of the young; TYPE III
HRAS
Costello syndrome
KIT
familial gastrointestinal stromal tumour
Piebald trait
LZTR1
Schwannomatosis-2
Noonan syndrome 10
MEN1
multiple endocrine neoplasia type 1
MET
familial papillary renal cancer
MLH1
hereditary non-polyposis colorectal cancer; Turcot syndrome
MPL
familial essential thrombocythemia
Congenital amegakaryocytic thrombocytopenia
MSH2
hereditary non-polyposis colorectal cancer
MSH6
hereditary non-polyposis colorectal cancer
MUTYH
adenomatous polyposis coli
NBN
Nijmegen breakage syndrome
NF1
neurofibromatosis type 1
