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MIM:618090 - NEURODEVELOPMENTAL DISORDER WITH EPILEPSY AND HYPOPLASIA OF THE CORPUS CALLOSUM; NEDEHCC
Xenbase Genes: lnpk
Human Disease Resource: MIM
MONDO:0060761 - neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum |
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MONDO:0060761 - neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum |