Phenotype #0000351161

Individual ID 00465618
Associated disease ID
Diagnosis/Initial intellectual disability
Diagnosis/Definite MRXSHG
Inheritance Familial, X-linked recessive
Phenotype details see paper; ..., developmental delay; speech delay; mild-moderate intellectual disability; epilepsy/seizures; borderline microcephaly; attention deficit hyperactivity disorder
Age/Examination 05y (5 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2025-05-27 19:53:16 +02:00 (CEST)
Date last edited N/A

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