Phenotype #0000210222

Individual ID 00275611
Associated disease ?
Diagnosis/Initial intellectual disability
Diagnosis/Definite -
Phenotype details birth at term; moderate intellectual disability; global developmental delay; gross motor delay; fine motor delay; speech delay; no seizures; no other abnormal movements; hypotonia; no hypertonia; no ophthalmological findings
Inheritance Familial, autosomal recessive
Age/Examination 24y (24 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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 2020-01-11 14:20:58 +01:00 (CET)
Date last edited N/A

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