Global Variome shared LOVD

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Phenotype #0000143513 Individual ID 00181327 Associated disease LIS3 Phenotype details Agenesis of the corpus callosum (HP:0001274); Agyria (HP:0031882); Cerebellar vermis hypoplasia (HP:0001320); Hypoplasia of the pons (HP:0012110); Cerebellar hypoplasia (HP:0001321); Gray matter heterotopia (HP:0002281); Microcephaly (HP:0000252); Optic nerve hypoplasia (HP:0000609) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination - 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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