All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02664 THMD2 thiamine metabolism dysfunction syndrome, type 2 (THMD-2, basal ganglia disease, biotin-responsive) 607483 AR 2 1 SLC19A3 - autosomal recessive
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