Global Variome shared LOVD

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Phenotype #0000143497 Individual ID 00181311 Associated disease LIS3 Phenotype details Hypoplasia of the corpus callosum (HP:0002079); Perisylvian polymicrogyria (HP:0012650); no Abnormality of brainstem morphology (-HP:0002363); Abnormality of the internal capsule (HP:0012502); Congenital microcephaly (HP:0011451); Spasticity (HP:0001257); no Seizures (-HP:0001250) Diagnosis/Initial - Inheritance Unknown Diagnosis/Definite - Age/Examination 03y06m (3 years, 6 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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