Global Variome shared LOVD

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Phenotype #0000171765 Individual ID 00226653 Associated disease THMD Diagnosis/Initial biotin responsive basal ganglia disease Diagnosis/Definite THMD-2 Phenotype details developmental arrest, spasticity, dysarthria, dysphagia; neuroimaging abnormalities: caudate, putamen, cerebral atrophy, cerebellar atrophy; outcome: paroxysmal ataxia, spasticity, intellectual disability Inheritance Familial, autosomal recessive Age/Examination 4y (4 years) Age/Diagnosis - Age/Onset 23m Phenotype/Onset viral infection Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International 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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