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Summary Literature (0)
MIM:618056 - NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES; NEDCAS

Xenbase Genes: brat1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0020841 - neurodevelopmental disorder with cerebellar atrophy and with or without seizures