Global Variome shared LOVD

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Phenotype #0000087500 Individual ID 00111414 Associated disease LIS3 Phenotype details Severe ID, severe epilepsy, developmental regression, scoliosis, hypotonia, MRI: agenesis of corpus callosum, Dandy-Walker malformation, opticus hypoplasia, delayed bone age Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Bernt Popp Database submission license No license selected Created by Bernt Popp Date created 2017-08-03 07:49:32 +02:00 (CEST) Date last edited 2017-08-04 09:29:30 +02:00 (CEST)

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