Global Variome shared LOVD

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Phenotype #0000143487 Individual ID 00181301 Associated disease LIS3 Phenotype details Partial agenesis of the corpus callosum, Hypoplasia of the corpus callosum (HP:0001338, HP:0002079); Polymicrogyria (HP:0002126); Cerebellar vermis hypoplasia (HP:0001320); Dilated fourth ventricle (HP:0002198); Congenital microcephaly (HP:0011451); Focal seizures (HP:0007359); Nystagmus (HP:0000639) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 00y05m (5 months) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Moritz Hebebrand Database submission license Creative Commons Attribution 4.0 International Created by Moritz Hebebrand Date created 2018-10-04 18:03:58 +02:00 (CEST) Date last edited N/A

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