NTHL1-Related Tumor Syndrome

specific

A syndrome inherited in an autosomal recessive manner and caused by germline bi-allelic mutations in NTHL1 gene. It is characterized by the presence of multiple colorectal adenomatous polyps and an increased risk of developing colorectal cancer, breast cancer, endometrial cancer, and less often cancers in other anatomic sites.

Top Centers for NTHL1-Related Tumor Syndrome

Ranked by research excellence score (trials · grants · publications). Methodology →

No centers currently specializing in this cancer type.

Research tier badges reflect trial volume, NIH grant funding, and publication impact — not clinical outcomes or patient satisfaction. Learn about our methodology →