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 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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