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Summary Literature (0)
OMIM:617802 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, SEIZURES, AND CORTICAL ATROPHY; NDMSCA


Xenbase Genes: vars1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0060621 - neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy