Global Variome shared LOVD

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Phenotype #0000143456 Individual ID 00181270 Associated disease LIS3 Phenotype details Agenesis of the corpus callosum (HP:0001274); Polymicrogyria (HP:0002126); no Abnormality of brainstem morphology (-HP:0002363); Cerebellar hypoplasia (HP:0001321); Dilation of lateral ventricles (HP:0006956); no Congenital microcephaly (-HP:0011451); Microcephaly (HP:0000252); no Seizures (-HP:0001250); Optic nerve hypoplasia (HP:0000609) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 14d 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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