Phenotype #0000229911

Individual ID 00302829
Associated disease NBIA
Phenotype details see paper; ...
Diagnosis/Initial severe infantile male encephalopathy
Inheritance Isolated (sporadic)
Diagnosis/Definite NBIA5
Age/Examination 02y (2 years)
Age/Onset -
Phenotype/Onset 2m
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 2020-06-01 19:59:56 +02:00 (CEST)
Date last edited N/A

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