In de Nestor registratie worden data verzameld van o.a. de volgende genetische tumor risico syndromen: 

Schwannomatose

Neurofibromatose

• neurofibromatose type 1 (NF1)
• neurofibromatose type 2 (NF2)

Lynch syndroom en polyposis

• Lynch syndrome
• FAP
• Attenuated FAP
• AXIN2-associated polyposis
• MUTYH-associated polyposis
• Polymerase proofreading associated polyposis
• NTHL1-associated polyposis
• MSH3-associated polyposis
• Peutz-Jeghers syndrome
• Juvenile polyposis syndrome
• Hereditary mixed polyposis syndrome
• Hereditary Gastric carcinoma proximal polyposis of the stomach

Erfelijk Borst- en Eierstokkanker Syndroom

• BRCA1
• BRCA2

Overige Syndromen

• Ataxia teleangiectasia
• BAP1- related tumour predisposition syndrome
• Birt-Hogg Dube syndrome 
• Bloom syndrome
• Carney Complex
• CMMRD (Constitutional Mismatch repair deficiency)
• DICER1
• Familial malignant melanomaNevoid basal cell carcinoma syndrome / Gorlin syndrome
• Fanconie syndrome
• Hereditary pheochromocytoma-paragangliomahereditary renal cell cancer
• Hereditary retinoblastoma
• Li-Fraumeni syndrome
• PHTS (Cowden syndrome)
• rhabdoid Tumor predisposition syndromevon
• Hippel-Lindau disease
• Xeroderma pigmentosum