Phenotype #0000339018

Individual ID 00449871
Associated disease SCZD
Phenotype details Schizophrenia, Scoliosis, Aplasia/Hypoplasia of the cerebellar vermis, Neurodevelopmental delay
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite Neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Camille Verebi
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Camille Verebi
Date created 2024-05-21 16:57:29 +02:00 (CEST)
Date last edited 2024-05-22 09:36:38 +02:00 (CEST)

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