Global Variome shared LOVD

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Phenotype #0000143460 Individual ID 00181274 Associated disease LIS3 Phenotype details Hypoplasia of the corpus callosum (HP:0002079); Perisylvian polymicrogyria (HP:0012650); no Abnormality of brainstem morphology (-HP:0002363); no Abnormal cerebellum morphology (-HP:0001317); no Microcephaly (-HP:0000252); Other neurological symptoms (NA); Focal seizures (HP:0007359) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 07y06m (7 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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