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MIM:617519 - NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEUROPATHY, AND DEAFNESS; NEDHND
Xenbase Genes: sptbn4
Human Disease Resource: MIM
MONDO:0060496 - neurodevelopmental disorder with hypotonia, neuropathy, and deafness |
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MONDO:0060496 - neurodevelopmental disorder with hypotonia, neuropathy, and deafness |