Phenotype #0000201848

Individual ID 00263990
Associated disease HNPCC (Lynch)
Diagnosis/Initial 33y
Diagnosis/Definite -
Phenotype details CRC at age 33y, MSI-H, loss MSH2/(MSH6, positive famliy history
Inheritance Familial, autosomal dominant
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein loss MSH2/MSH6
Tumor/MSI MSI-H
Diagnosis/Criteria -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2019-09-05 11:56:03 +02:00 (CEST)
Date last edited 2019-09-09 08:35:57 +02:00 (CEST)

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