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Summary Literature (2)
OMIM:312750 - RETT SYNDROME; RTT


Xenbase Genes: mecp2, cdkl5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010726 - Rett syndrome
MONDO:0017746 - atypical Rett syndrome

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