Phenotype #0000016186

Individual ID 00017832
Associated disease ID
Diagnosis/Initial neurodevelopmental delay
Diagnosis/Definite -
Inheritance Isolated (sporadic)
Phenotype details see paper; no microcephaly, mild mental retardation, no seizures, no EEG anomalies, behavioral anomalies (short attention span, aggressiveness, stereotypies, friendliness), no MRI scan anomalies, no facial dysmorphism, no eye anomalies, no other abnormalities; 20m-walk; 18m-first words
Age/Examination 14y06m (14 years, 6 months)
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 2014-07-01 22:20:09 +02:00 (CEST)
Date last edited 2023-02-03 12:24:00 +01:00 (CET)

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