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Summary Literature (0)
MIM:619244 - NEURODEVELOPMENTAL DISORDER WITH CEREBRAL ATROPHY AND VARIABLE FACIAL DYSMORPHISM; NEDCAFD

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030999 - neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism