Global Variome shared LOVD

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Phenotype #0000325293 Individual ID 00435056 Associated disease NDD Diagnosis/Initial NDD Diagnosis/Definite - Phenotype details see paper; ..., global developmental delay; intellectual disability; language delay; impaired motor development; progressive supratentorial and infratentorial atrophy, leukoencephalopathy; hypotonia; seizures; microcephaly; optic atrophy; prenatal HELLP syndrome; prominent glabella, receding forehead Inheritance Familial, autosomal recessive Age/Examination 2y (2 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-05-05 15:10:52 +02:00 (CEST) Date last edited N/A

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