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Summary Literature (0)
MIM:271930 - STRIATONIGRAL DEGENERATION, INFANTILE; SNDI

Xenbase Genes: nup62

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010080 - familial infantile bilateral striatal necrosis
MONDO:0015518 - infantile bilateral striatal necrosis

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