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Summary Literature (0)
MIM:617393 - NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM

Xenbase Genes: nacc1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0044306 - neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination