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Summary Literature (0)
MIM:617282 - DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES; DYTOABG

Xenbase Genes: mecr

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0015003 - dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities

Disease Ontology (DO):
DOID:0081419 - childhood-onset dystonia with optic atrophy and basal ganglia abnormalities