Phenotype #0000147264

Individual ID 00188621
Associated disease CRC
Inheritance Unknown
Diagnosis/Initial -
Age/Examination -
Diagnosis/Definite -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details CRC patients found to have variant on imputation - MMR IHC/hm studies reported and number of patients in parenthesis: Normal (17), MLH1-hm (1), PMS2 fs (1)
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Eye/Retina -
Neoplasm -
Cysts -
Owner name Sigurdis Haraldsdottir
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by InSiGHT - John-Paul Plazzer
Date created 2016-12-21 00:00:00 +01:00 (CET)
Date last edited N/A

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