Global Variome shared LOVD

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Phenotype #0000239730 Individual ID 00315985 Associated disease ? Diagnosis/Initial neurodevelopmental delay Diagnosis/Definite - Phenotype details see paper; ..., no failure to thrive; no globe defect; no coloboma; no visual impairment; Retinopathy of prematurity; motor delay; speech delay; autistic features; hypotonia; no cardiac defect; kidney anomaly; Microcephaly; bilateral epicanthal folds Inheritance Isolated (sporadic) Age/Examination 00y05m (5 months) 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 International Created by Johan den Dunnen Date created 2020-11-01 10:06:29 +01:00 (CET) Date last edited 2022-11-30 19:51:23 +01:00 (CET)

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