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Cancer Prevention: What You Need To Know

Hereditary Diseases and Cancer

Peer Review Status: Internally Reviewed by Cancer Center Staff
Creation Date: 1996
Last Revision Date: April 2001

* Definition of Terms

Cancer Site

Hereditary Risk Factors

Adrenal Gland Cancer Familial Adenomatous Polyposis (FAP)
Li-Fraumeni Syndrome
Multiple Endocrine Neoplasia I and II
Neurofibromatosis
von Hippel-Lindau Syndrome
Anal Cancer Fanconi Anemia
Bile Duct Cancer Familial Adenomatous Polyposis (FAP)
Lynch II Syndrome
Werner Syndrome
Bladder Cancer Lynch II Syndrome
Bone Cancer Familial Adenomatous Polyposis (FAP)
Li-Fraumeni Syndrome
Retinoblastoma Gene
Werner Syndrome
Brain Cancer Ataxia Telangiectasia
Basal Cell Nevus Syndrome (Childhood Medulloblastoma)
BRCA 1
possibly Fanconi Anemia
Li-Fraumeni Syndrome
Lynch II Syndrome
Neurofibromatosis
Retinoblastoma Gene
Tuberous Sclerosis (Childhood Brain Tumor)
Turcot Syndrome
von Hippel-Lindau Syndrome
Xeroderma Pigmentosum
Breast Cancer Ataxia Telangiectasia
Bloom Syndrome
BRCA1 Gene Mutations
BRCA2 Gene Mutations (Females and Males)
Cowden Syndrome
Li-Fraumeni Syndrome
Peutz-Jeghers Syndrome
Werner Syndrome
Central Nervous System Familial Adenomatous Polyposis (FAP)
Neurofibromatosis
Cervical Cancer Bloom Syndrome
Fanconi Anemia
Peutz-Jeghers Syndrome
Colorectal Cancer Agammaglobulinemia
Bloom Syndrome
BRCA 1
possibly BRCA 2
Familial Adenomatous Polyposis (FAP)
Familial Non-Medullary Thyroid Cancer (FNMTC)
Lynch I Syndrome
Lynch II Syndrome
Muir-Torre Syndrome
Peutz-Jeghers Syndrome
Turcot Syndrome
Esophagus Bloom Syndrome
Fanconi Anemia
Eye Cancer Neurofibromatosis
Retinoblastoma Gene
Xeroderma Pigmentosum
Head and neck Fanconi Anemia
Hypothalamus Neurofibromatosis
Gastric (Stomach) Cancer Ataxia Telangiectasia
Familial Adenomatous Polyposis (FAP)
possibly Li-Fraumeni Syndrome
Lynch II Syndrome
Turcot Syndrome
Werner Syndrome
Xeroderma Pigmentosum
Kidney Cancer Cowden Syndrome
Neurofibromatosis
Tuberous Sclerosis
von Hippel-Lindau Syndrome
Wilms Tumor Gene
Larynx Cancer Bloom Syndrome
possibly Li Fraumeni Syndrome
Muir-Torre Syndrome
Leukemia Ataxia-Telangiectasia
Bloom Syndrome
Fanconi Anemia
Li-Fraumeni Syndrome
Neurofibromatosis (childhood Leukemia)
Retinoblastoma Gene
Werner Syndrome
Xeroderma Pigmentosum
Liver Cancer Familial Adenomatous Polyposis (FAP)
Fanconi Anemia
Werner Syndrome
Lung Cancer Bloom Syndrome
BRCA 1
Li-Fraumeni Syndrome
Multiple Endocrine Neoplasia I (Bronchial Carcinoma and Carcinoid)
Wilms Tumor Gene (Mesothelioma: May also occur in abdomen)
Xeroderma Pigmentosum
Lymphoma Ataxia Telangiectasia
Bloom Syndrome
Li-Fraumeni Syndrome
Retinoblastoma Gene
Ovarian Cancer Basal Cell Nevus Syndrome
BRCA1
Lynch II Syndrome
Multiple Endocrine Neoplasia I
Peutz-Jeghers Syndrome
Ovarian Germ Cell Tumor Li-Fraumeni Syndrome
Pancreatic Cancer BRCA 1
BRCA 2
Familial Melanoma Syndrome
Li-Fraumeni Syndrome
Lynch II Syndrome
Multiple Endocrine Neoplasia I
Peutz-Jeghers Syndrome
von Hippel-Lindau Syndrome
Parathyroid Cancer Multiple Endocrine Neoplasia I & II
Neurofibromatosis
Pituitary Gland Multiple Endocrine Neoplasia I
Prostate Cancer BRCA1
Possibly BRCA 2
Hereditary Prostate Cancer 1 (HPC1)
Li-Fraumeni Syndrome
Skin Cancer  
  • Melanoma
BRCA 1
Familial Melanoma Syndrome
Li-Fraumeni Syndrome
Retinoblastoma Gene
Werner Syndrome
Xeroderma Pigmentosum
  • Non-melanoma skin cancer
Ataxia Telangiectasia
Basal Cell Nevus Syndrome
Bloom Syndrome
Lynch II Syndrome
Muir-Torre Syndrome
Turcot Syndrome (Scalp)
Xeroderma Pigmentosum
  • Merkel Cell Skin Cancer
Cowden Syndrome
Small Intestine Familial Adenomatous Polyposis (FAP) (Duodenum)
Lynch II Syndrome
Muir-Torre Syndrome (Duodenum)
Multiple Endocrine Neoplasia I (Duodenum)
Neurofibromatosis (Duodenum)
Peutz-Jeghers Syndrome (Duodenum)
Soft Tissue Sarcoma BRCA 1
Li-Fraumeni Syndrome
Multiple Endocrine Neoplasia I
Neurofibromatosis
Retinoblastoma Gene
Werner Syndrome
Spinal Cord Neurofibromatosis
von Hippel-Lindau Syndrome
Testicular Cancer Peutz-Jeghers Syndrome
Testes Germ Cell Tumors Li-Fraumeni Syndrome
Thymus Multiple Endocrine Neoplasia I
Thyroid Cowden Syndrome
Familial Adenomatous Polyposis (FAP)
Familial Non-Medullary Thyroid Cancer (FNMTC) (Papillary) Multiple Endocrine Neoplasia II (Medullary)
Werner Syndrome
Tongue Bloom Syndrome
Xeroderma Pigmentosum
Urologic Systems Cancer Lynch II Syndrome
Uterine Cancer Ataxia Telangiectasia
Lynch II Syndrome
Vulva Fanconi Anemia

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Last modification date: Tue Jan 9 11:59:14 2007
URL: http://www.uihealthcare.com /topics/medicaldepartments/cancercenter/prevention/hereditarydiseases.html