Global Variome shared LOVD

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Phenotype #0000338833 Individual ID 00449659 Associated disease NDD Diagnosis/Initial neurodevelopmental syndrome Diagnosis/Definite - Phenotype details see paper; ..., cardiac anomalies; urogenital anomalies; ophthalmological anomalies; developmental delay; too young to make an autistic spectrum disorder diagnosis; no epilepsy; facial dysmorphisms; hand dysmorphisms; synophrys; hypotonia with ataxic cerebral palsy; no attention-deficit/hyperactivity disorder Inheritance Isolated (sporadic) Age/Examination 2y6m (2 years, 6 months) 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 2024-04-29 16:49:29 +02:00 (CEST) Date last edited N/A

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