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Summary Literature (0)
MIM:617672 - NEURODEGENERATION, CHILDHOOD-ONSET, WITH BRAIN ATROPHY; CONDBA

Xenbase Genes: ubtf, ubtf.2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0044701 - childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder

Disease Ontology (DO):
DOID:0070474 - childhood-onset neurodegeneration with brain atrophy