Phenotype #0000331118

Individual ID 00441693
Associated disease NDD
Diagnosis/Initial neurodevelopmental delay
Diagnosis/Definite -
Phenotype details see paper; ..., microcephaly; global developmental delay; 2y-sit; 3y-walk; language severely delayed; moderate intellectual disability; generalised tonic clonic seizures;
Inheritance Familial, autosomal recessive
Age/Examination 13y (13 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
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 2023-11-09 12:18:41 +01:00 (CET)
Date last edited N/A

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