Hereditary cancer predisposition due to variation(s) in the CHEK2 gene. Pathogenic germline variation in CHEK2 confers an autosomal dominant predisposition to tumor formation at multiple primary sites, including breast cancer and prostate cancer.
Comprehensive, easy-to-understand information about this condition
Checking for content...
No external resources available.
mosaic variegated aneuploidy syndrome
MONDO:0000141
tuberous sclerosis
MONDO:0001734
hereditary breast ovarian cancer syndrome
MONDO:0003582
hereditary multiple osteochondromas
MONDO:0005508
nevoid basal cell carcinoma syndrome
MONDO:0007187
leukemia, chronic lymphocytic, susceptibility to, 2
MONDO:0007190