Global Variome shared LOVD

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Phenotype #0000027978 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)

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