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Summary Literature (0)
MIM:618569 - NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY; NEDAHM

Xenbase Genes: svbp

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0032816 - neurodevelopmental disorder with ataxia, hypotonia, and microcephaly