Global Variome shared LOVD

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Phenotype #0000303058 Individual ID 00410968 Associated disease - Phenotype details low anterior hairline, development delay, severe intellectual disability, autism spectrum disorder, strabismus, global hypotonia, bifid uvula Diagnosis/Initial early-onset severe global development delay Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 10y (10 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Julia Lopez Date created 2022-05-31 18:45:49 +02:00 (CEST) Date last edited N/A

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