Phenotype #0000222543

Individual ID 00288838
Associated disease ?
Diagnosis/Initial dystonia, hypermanganesemia
Diagnosis/Definite HMNDYT2
Phenotype details see paper; ..., dystonia, hypermanganesemia
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
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 2020-02-22 14:25:02 +01:00 (CET)
Date last edited 2020-02-22 14:28:14 +01:00 (CET)

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