Global Variome shared LOVD

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Phenotype #0000143478 Individual ID 00181292 Associated disease LIS3 Phenotype details Partial agenesis of the corpus callosum (HP:0001338); Cortical gyral simplification (HP:0009879); no Abnormal cerebellum morphology (-HP:0001317); Gray matter heterotopia (HP:0002281); Microcephaly (HP:0000252) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 04y00m (4 years) 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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