Phenotype #0000298726

Individual ID 00406228
Associated disease NDD
Diagnosis/Initial neurodevelopmental delay
Diagnosis/Definite -
Phenotype details see paper; ..., global developmental delay, severe speech delay, autistic features, feeding difficulties; mother intellectual disability; affected brother developmental delay, mild intellectual disability, short stature
Inheritance Familial, autosomal dominant
Age/Examination 4y (4 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 2022-03-25 18:43:34 +01:00 (CET)
Date last edited N/A

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