Global Variome shared LOVD

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Phenotype #0000300861 Individual ID 00408742 Associated disease ID Diagnosis/Initial intellectual disability Diagnosis/Definite - Inheritance Isolated (sporadic) Phenotype details see paper; ..., mild developmental delay/intellectual disability; autistic behaviour; no hypotonia; no aspiration; clinically one episode of possible seizure activity, EEG no epileptiform activity identified; dysmorphism; no dry skin; no cardiac malformation; no cardiac arrhythmia; no ocular abnormalities; no renal malformation Age/Examination 12y (12 years) 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 2022-04-27 00:00:11 +02:00 (CEST) Date last edited N/A

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