Phenotype #0000171758

Individual ID 00226646
Associated disease THMD
Diagnosis/Initial biotin responsive basal ganglia disease
Diagnosis/Definite THMD-2
Phenotype details encephalopathy, spasticity; neuroimaging abnormalities: caudate, putamen; outcome: dystonia
Inheritance Familial, autosomal recessive
Age/Examination 24y (24 years)
Age/Diagnosis -
Age/Onset 2y
Phenotype/Onset viral infection
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 2019-03-09 21:20:59 +01:00 (CET)
Date last edited N/A

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