Phenotype #0000322862

Individual ID 00432294
Associated disease CPPB2
Phenotype details Generalized non-motor (absence) seizure, Neurodevelopmental delay, Precocious puberty
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination 10y (10 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2023-02-21 09:33:02 +01:00 (CET)
Date last edited 2023-02-21 16:06:55 +01:00 (CET)

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