Phenotype #0000143489

Individual ID 00181303
Associated disease LIS3
Phenotype details Hypoplasia of the corpus callosum (HP:0002079); Perisylvian polymicrogyria (HP:0012650); Dysgenesis of the cerebellar vermis (HP:0002195); Congenital microcephaly (HP:0011451); Spasticity (HP:0001257); Strabismus (HP:0000486)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 22y00m (22 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Moritz Hebebrand
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Moritz Hebebrand
Date created 2018-10-04 18:03:58 +02:00 (CEST)
Date last edited N/A

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