Phenotype #0000143495

Individual ID 00181309
Associated disease LIS3
Phenotype details Partial agenesis of the corpus callosum, Hypoplasia of the corpus callosum (HP:0001338, HP:0002079); Dysgenesis of the cerebellar vermis (HP:0002195); Brainstem dysplasia (HP:0002508); Dilated fourth ventricle (HP:0002198); Abnormality of the internal capsule (HP:0012502); Congenital microcephaly (HP:0011451); Muscular hypotonia (HP:0001252); no Seizures (-HP:0001250); Strabismus, Nystagmus (HP:0000486, HP:0000639)
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 01y08m (1 year, 8 months)
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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