Phenotype #0000340669

Individual ID 00452065
Associated disease EA2
Phenotype details Gait disturbance, Vertigo, Iron deficiency anemia, Ataxia, episodic, family history (father and brother)
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination 25y (25 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 2024-07-08 16:10:09 +02:00 (CEST)
Date last edited 2024-07-10 09:39:55 +02:00 (CEST)

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