All diseases

1 entry on 1 page. Showing entry 1.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05614 DYTOABG dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities (DYTOABG) 617282 - 0 0 MECR - autosomal recessive
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