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Summary Literature (0)
MIM:617519 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND


Xenbase Genes: sptbn4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060496 - neurodevelopmental disorder with hypotonia, neuropathy, and deafness