Global Variome shared LOVD

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Phenotype #0000351411 Individual ID 00466026 Associated disease microcephaly Diagnosis/Initial microcephaly Diagnosis/Definite - Phenotype details see paper; ..., birth microcephaly (SD−4.9); simplified gyration; pontocerebellar hypoplasia; seizures Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2025-07-07 15:39:31 +02:00 (CEST) Date last edited N/A

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