All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

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