Phenotype #0000342223

Individual ID 00453565
Associated disease NDD
Diagnosis/Initial neurodevelopmental disorder
Diagnosis/Definite -
Phenotype details see paper; ..., macrocephaly, ventriculomegaly; motor delay; hypotonia; paroxysmal movements
Inheritance Isolated (sporadic)
Age/Examination 1y5m (1 year, 5 months)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2024-09-10 17:46:49 +02:00 (CEST)
Date last edited N/A

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