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Summary Literature (1)
OMIM:613454 - RETT SYNDROME, CONGENITAL VARIANT


Xenbase Genes: foxg1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013270 - Rett syndrome, congenital variant
MONDO:0017746 - atypical Rett syndrome

Disease Ontology (DO):
DOID:1206 - Rett syndrome