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Summary Literature (0)
MIM:617862 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND BRAIN ATROPHY; NEDMEBA

Xenbase Genes: trappc6b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060640 - neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy