Oncogenetics

hereditary cancerFor Oncogenetics we offer exome sequencing diagnostics, multiple gene diagnostics and single gene diagnostics.

Below you can find all the hereditary cancer disorders we currently offer. Please click on a disorder for more information about the price and to place your order. You can also visit our ordering site directly.


Exome sequencing diagnostics:
 

Multiple gene diagnostics:
 


Single gene diagnostics:

  Updated 29th of March 2018

 

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

 

A

ACTH-independent macronodular adrenal hyperplasia

B

Baller-Gerold syndrome
Bannayan-Riley-Ruvalcaba syndrome
BAP1-tumor predisposition syndrome
Bloom syndrome
Breast and Ovary cancer, hereditary

C

Cowden syndrome

D

Desmoplastic medulloblastoma, hereditary
DICER1 syndrome
Dyskeratosis congenita

G

Gastric cancer

H

Hereditary cancer (WES)

L

Leiomymatosis + kidney cancer
Leukemia
Li-Fraumeni syndrome
Lynch syndrome (HNPCC)

M

Mast cell disease
Mismatch repair cancer syndrome
Multiple endocrine neoplasia type 1 (MEN1)
Multiple endocrine neoplasia type 2 (MEN2)

N

Neurofibromatosis
Nijmegen breakage syndrome (NBS)

P

Paraganglioma and pheochromocytoma, Hereditary
Peutz-Jeghers syndrome
Platelet dysfunction, familial (with AML)
Polyposis
Predictive testing (cancer hotspot panel)
PTEN Hamartoma Tumor syndrome

R

Renal cancer, hereditary
Renal cell carcinoma
Rhabdoid tumor predisposition syndrome
Rothmund-Thomson syndrome

S

Schwannomatosis

T

Tylosis with esophageal cancer

U

Uveal melanoma, hereditary

V

Von Hippel-Lindau syndrome

W

Werner syndrome