Phenotype #0000346291

Individual ID 00457843
Associated disease ALXDRD
Phenotype details see paper; ..., OFC SD+1; 1m-delayed psychomotor development; MRI abnormalities suggestive of Alexander disease
Diagnosis/Initial infantile disease Alexander disease
Inheritance Unknown
Diagnosis/Definite ALXDRD
Age/Examination 3.5y
Age/Diagnosis -
Age/Onset 1m
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 2024-11-20 12:59:57 +01:00 (CET)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.