Phenotype #0000267706

Individual ID 00372391
Associated disease ?
Diagnosis/Initial Aicardi syndrome
Diagnosis/Definite -
Phenotype details see paper; ..., normal corpus callosum, retinal lacunae, 3.5m-infantile seizures; cerebellar cyst, periventricular
heterotopias
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2021-05-07 09:40:30 +02:00 (CEST)
Date last edited N/A

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