Global Variome shared LOVD

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Phenotype #0000143464 Individual ID 00181278 Associated disease LIS3 Phenotype details Hypoplasia of the corpus callosum (HP:0002079); Pachygyria (HP:0001302); Cerebellar vermis hypoplasia (HP:0001320); Brainstem dysplasia (HP:0002508); Dysgenesis of the hippocampus (HP:0025101); Gray matter heterotopia (HP:0002281); Abnormality of the internal capsule (HP:0012502); Congenital microcephaly (HP:0011451); Other neurological symptoms (NA); Infantile spasms (HP:0012469) Diagnosis/Initial - Inheritance Isolated (sporadic) Diagnosis/Definite - Age/Examination 05y00m (5 years) 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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