Global Variome shared LOVD

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Phenotype #0000002863 Individual ID 00004069 Associated disease MDDGA7 Phenotype details Walker-Warburg syndrome (WWS); massive hydrocephalus, cerebellar hypoplasia, cobblestone lissencephaly; bilateral optic nerve hypoplasia, loss of macular pigment Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - CK-level 3300 Protein DAG1 IIH6 negative Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2012-05-20 10:48:47 +02:00 (CEST) Date last edited N/A

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