Global Variome shared LOVD

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Phenotype #0000125565 Individual ID 00152636 Associated disease LIS Diagnosis/Initial lissencephaly, type II Diagnosis/Definite - Phenotype details 22w pregnancy termination because of reoccurrence severe quadriventricular hydrocephalus/cerebellar hypoplasia (like fetus F1); fetus dysmorphic features, horizontal narrow palpebral slit, bulging eyes, hypertrichosis cheeks/shoulders Inheritance Isolated (sporadic) Age/Examination - Age/Onset <0d Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-04-22 00:16:26 +02:00 (CEST) Date last edited N/A

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