Phenotype #0000138612

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00173758
Associated disease	HNPCC8
Phenotype details	see paper; …
Diagnosis/Initial	Lynch syndrome
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	HNPCC-8
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Diagnosis/Criteria	-
Tumor/MSI	-
Owner name	Mamata Sivagnanam
Database submission license	No license selected
Created by	Mamata Sivagnanam
Date created	2018-08-02 09:27:57 +02:00 (CEST)
Date last edited	N/A

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