Phenotype #0000143478

Individual ID 00181292
Associated disease LIS3
Phenotype details Partial agenesis of the corpus callosum (HP:0001338); Cortical gyral simplification (HP:0009879); no Abnormal cerebellum morphology (-HP:0001317); Gray matter heterotopia (HP:0002281); Microcephaly (HP:0000252)
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 04y00m (4 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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