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 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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