Phenotype #0000303348

Individual ID 00411273
Associated disease EEOC
Phenotype details Global severe neurodevelopmental delay.
Hypotonia severe, cortical visual impairment, opisthotonus.
Mild diffuse volume loss by MRI.
Diagnosis/Initial -
Inheritance -
Diagnosis/Definite -
Age/Examination 00y10m (10 months)
Age/Diagnosis -
Age/Onset 00y10m
Phenotype/Onset -
Protein -
Owner name Aguan Daniel Wei
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Aguan Daniel Wei
Date created 2022-06-09 22:56:48 +02:00 (CEST)
Date last edited 2022-11-14 15:52:49 +01:00 (CET)

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