HAN5:Volunteer Assignments and Opportunities

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WHO Classification of Head and Neck Tumours (5th Edition) Content

Disease	Page Type	Author	Date Assigned to Author	Target Completion Date	Author Content (Pending or Complete)	Date Completed by Author	Associate Editor	Date of Last Editor Review	Notes
Hereditary papillary renal carcinoma (MET)	Disease
Multiple endocrine neoplasia type 2 (RET)	Disease
Juvenile polyposis syndrome (BMPR1A, SMAD4)	Disease
Hereditary neuroblastoma (ALK, PHOX2B)	Disease
Encephalocraniocutaneous lipomatosis (FGFR1)	Disease
Glucagon cell hyperplasia and neoplasia (GCGR)	Disease
McCune-Albright syndrome (GNAS)	Disease
Sturge-Weber syndrome (GNAQ)	Disease
Neurofibromatosis type 1 (NF1)	Disease
NF2-related schwannomatosis (NF2)	Disease
Costello syndrome (HRAS)	Disease
Noonan syndrome (Various genes)	Disease
Schimmelpenning-Feuerstein-Mims (HRAS, KRAS)	Disease
Carney complex (PRKAR1A, PDE8B, PDE11A)	Disease
PROS syndrome (PIK3CA)	Disease
Familial adenomatous polyposis (APC)	Disease
Gastric Adenocarcinoma and Proximal Polyposis of Stomach - GAPPS (APC promoter)	Disease
AXIN2-associated polyposis (AXIN2)	Disease
Serrated polyposis (RNF43)	Disease
WT1 related tumour predisposition syndrome (WT1)	Disease
WAGR syndrome (WT1)	Disease
Multiple endocrine neoplasia type 1 (MEN1)	Disease
Peutz-Jeghers syndrome (STK11)	Disease
Hereditary gastric and breast cancer syndrome (CDH1, CTNNA1)	Disease
Hereditary mixed polyposis syndrome (GREM1)	Disease
Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161)	Disease
SMO-related Curry-Jones syndrome (SMO)	Disease
ELP1-related medulloblastoma predisposition syndrome(ELP1)	Disease
Osteochondromatosis (EXT1, EXT2)	Disease
Brooke-Spiegler syndrome (CYLD)	Disease
Tuberous sclerosis (TSC1, TSC1)	Disease
PTEN hamartoma tumour syndrome (PTEN)	Disease
Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD)	Disease
Multiple endocrine neoplasia type 5, MAX related tumours (MAX)	Disease
MAFA-related familial insulinomatosis (MAFA)	Disease
Birt-Hogg-Dube syndrome (FLCN)	Disease
Familial chordoma (TBXT)	Disease
Hyperparathyroidism jaw tumour syndrome (CDC73)	Disease
Von Hippel-Lindau syndrome (VHL)	Disease
SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2)	Disease
Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH)	Disease
Hereditary tyrosinaemia type 1 (FAH)	Disease
Li-Fraumeni syndrome (TP53)	Disease
Retinoblastoma syndrome (RB1)	Disease
Multiple endocrine neoplasia type 4 (CDKN1B)	Disease
CDKN2A-related tumour predisposition syndrome (CDKN2A)	Disease
CDK4-related melanoma predisposition syndrome (CDK4)	Disease
Autoimmune lymphoproliferative syndrome (FAS)	Disease
Lynch Syndrome (MLH1, PMS2, MSH2, MSH6)	Disease
Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6)	Disease
Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6)	Disease
BRCA-related cancer predisposition syndrome (BRCA1, BRCA2)	Disease
PALB2-related cancer predisposition syndrome (PALB2)	Disease
RAD51-related cancer predisposition syndrome (RAD51C, RAD51D)	Disease
Fanconi anaemia (FANC genes)	Disease
MUTYH-associated polyposis (MUTYH)	Disease
NTHL1-related tumour syndrome (NTHL1)	Disease
MBD4-associated neoplasia syndrome (MBD4)	Disease
Xeroderma Pigmentosum	Disease
Ataxia-telangiectasia syndrome (ATM)	Disease
CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2)	Disease
Nijmegen breakage syndrome (NBN)	Disease
Polymerase proofreading-associated polyposis (POLD1, POLE)	Disease
Bloom syndrome (BLM)	Disease
Werner syndrome (WRN)	Disease
Rothmund-Thomson syndrome (ANAPC1, RECQL4)	Disease
DDX41-related haematologic tumour predisposition syndrome (DDX41)	Disease
Mosaic variegated aneuploidy (BUB1B, CEP57, TRIP13, BUB1, BUB3)	Disease
Klinefelter syndrome	Disease
Turner syndrome	Disease
Down syndrome	Disease
Dyskeratosis congenita (DKC1, TERT, TERC, TINF2, Other IBMFS genes)	Disease
POT1 and Shelterin-related tumour predisposition syndrome (POT1, ACD, TERF2IP, TERT promoter)	Disease
Beckwith-Wiedemann spectrum (IGF2; CDKN1C)	Disease
Enchondromatosis (IDH1, IDH2)	Disease
Rhabdoid tumour predisposition syndrome (SMARCB1, SMARCA4)	Disease
Schwannomatosis (SMARCB1, LZTR1)	Disease
Clear cell meningioma predisposition syndrome (SMARCE1)	Disease
Weaver syndrome (EZH2)	Disease
DICER1-related tumour predisposition syndrome (DICER1)	Disease
MicroRNA processor tumour predisposition syndromes (DROSHA, DGCR8)	Disease
Goldenhar syndrome (MYT1, SF3B2)	Disease
BAP1-related tumour predisposition syndrome (BAP1)	Disease