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Summary Literature (0)
MIM:500003 - STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010080 - familial infantile bilateral striatal necrosis
MONDO:0010774 - striatonigral degeneration, infantile, mitochondrial
MONDO:0015518 - infantile bilateral striatal necrosis

Disease Ontology (DO):
DOID:4751 - striatonigral degeneration