Global Variome shared LOVD

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Phenotype #0000143581 Individual ID 00181395 Associated disease LIS3 Phenotype details Hypoplasia of the corpus callosum (HP:0002079); Polymicrogyria (HP:0002126); Brainstem dysplasia (HP:0002508); Cerebellar hypoplasia (HP:0001321); Abnormality of the internal capsule (HP:0012502); no Microcephaly (-HP:0000252); Muscular hypotonia (HP:0001252); Generalized tonic-clonic seizures (HP:0002069); Strabismus (HP:0000486) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 00y10m (10 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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