Lynch Syndrome (HNPCC)

Lynch Syndrome(来自ICD-11)

别称:

Hereditary Nonpolyposis Colorectal Cancer

Hereditary Nonpolyposis Colon Cancer

Hereditary Nonpolyposis Colorectal Carcinoma

Hereditary Nonpolyposis Colorectal Neoplasms

Familial Nonpolyposis Colon Cancer

Hnpcc

Familial Nonpolyposis Colorectal Cancer

Hereditary Non-Polyposis Colorectal Cancer Syndrome

Colorectal Cancer, Hereditary Nonpolyposis, Type 1

Hereditary Nonpolyposis Colorectal Cancer Syndrome

Hereditary Non-Polyposis Colon Cancer Syndrome

Hereditary Defective Mismatch Repair Syndrome

Hereditary Nonpolyposis Colon Cancer Syndrome

Colorectal Neoplasms, Hereditary Nonpolyposis

Hnpcc - Hereditary Nonpolyposis Colon Cancer

Cancer, Colorectal, Nonpolyposis, Hereditary

Hereditary Nonpolyposis Colorectal Neoplasm

Hereditary Non-Polyposis Colorectal Cancer

Hereditary Non-Polyposis Colon Cancer

Colon Cancer, Familial Nonpolyposis

Cancer Family Syndrome

Coca 1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Lynch Syndrome, also known as hereditary nonpolyposis colorectal cancer, is related to lynch syndrome 1 and lynch syndrome 5. An important gene associated with Lynch Syndrome is MLH1 (MutL Homolog 1), and among its related pathways/superpathways are Infectious disease and Prolactin Signaling. The drugs Fluorouracil and Oxaliplatin have been mentioned in the context of this disorder. Affiliated tissues include colon and small intestine, and related phenotypes are constipation and malabsorption

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