Diseases

Hereditary Breast and Ovarian Cancer Syndrome

Autosomal dominant HEREDITARY CANCER SYNDROME in which a mutation most often in either BRCA1 or BRCA2 is associated with a significantly increased risk for breast and ovarian cancers.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

Autosomal dominant HEREDITARY CANCER SYNDROME in which a mutation most often in either BRCA1 or BRCA2 is associated with a significantly increased risk for breast and ovarian cancers.

MeSH Record

Classification

Related Concepts

Knowledge Graph

Loading graph…

Drag nodes to rearrange; hover to trace links; click a node to open its page.

MeSH Record

See Also

MeSH Record

Synonyms

4 entry terms
  • HBOC Syndrome
  • HBOC Syndromes
  • Syndrome, HBOC
  • Syndromes, HBOC

MeSH Record

Aspects Covered

35 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

Indexing Annotation

coordinate IM with histological type of neoplasm (IM) if pertinent

MeSH Record

History Note

2012

MeSH Record

Previous Indexing

  • Breast Neoplasms (1984-2011)
  • Ovarian Neoplasms (1989-2011)

MeSH Hierarchy

Tree Numbers

AMA Style

References

  1. National Library of Medicine. Hereditary Breast and Ovarian Cancer Syndrome. Medical Subject Headings (MeSH). 2026. Unique ID D061325. http://id.nlm.nih.gov/mesh/2026/D061325
  2. Hereditary Breast and Ovarian Cancer Syndrome. In: Wikipedia. https://en.wikipedia.org/wiki/Hereditary_breast%E2%80%93ovarian_cancer_syndrome
  3. Hereditary Breast and Ovarian Cancer Syndrome. In: Wikidata. https://www.wikidata.org/wiki/Q19000660