Hereditary Breast and Ovarian Cancer Syndrome D061325

Related MeSH Hierarchy (11)

Diseases [C] » Neoplasms [C04] » Neoplastic Syndromes, Hereditary » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Neoplastic Syndromes, Hereditary » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Breast Diseases » Breast Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Endocrine System Diseases [C19] » Endocrine Gland Neoplasms » Ovarian Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Endocrine System Diseases [C19] » Gonadal Disorders » Ovarian Diseases » Ovarian Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Neoplasms [C04] » Neoplasms by Site » Breast Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Neoplasms [C04] » Neoplasms by Site » Endocrine Gland Neoplasms » Ovarian Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Urogenital Diseases [C12] » Genital Diseases » Genital Diseases, Female » Adnexal Diseases » Ovarian Diseases » Ovarian Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Diseases [C] » Urogenital Diseases [C12] » Urogenital Neoplasms » Genital Neoplasms, Female » Ovarian Neoplasms » Hereditary Breast and Ovarian Cancer Syndrome

Description

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

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Phase 2 Indicated Drugs (1)

Other Experimental Indicated Drugs (1)


Organization Involved with Phase 1 Indications (1)

Organization Involved with Other Experimental Indications (1)

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