Phenotype #0000027978

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Individual ID	00034573
Associated disease	AD
Phenotype details	memory decline and biparietal posterior variant of AD; sporadic case (censoring effect, father)
Diagnosis/Initial	-
Inheritance	Isolated (sporadic)
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	53y
Phenotype/Onset	-
Protein	-
Owner name	Gael Nicolas
Database submission license	No license selected
Created by	Gael Nicolas
Date created	2015-04-01 08:24:50 +02:00 (CEST)
Date last edited	2015-04-03 16:10:48 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.