Global Variome shared LOVD

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Phenotype #0000339014 Individual ID 00449868 Associated disease SCZD Phenotype details Neonatal hypotonia, Delayed speech and language development, Scoliosis, Schizophrenia, Unilateral renal agenesis Diagnosis/Initial Syndromic Schizophrenia Inheritance Isolated (sporadic) Diagnosis/Definite Xia-Gibbs syndrome Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Camille Verebi Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Camille Verebi Date created 2024-05-21 15:33:59 +02:00 (CEST) Date last edited 2024-05-22 09:43:18 +02:00 (CEST)

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