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Summary Literature (0)
MIM:300055 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13; MRXS13

Xenbase Genes: mecp2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010235 - uvular muscle

Disease Ontology (DO):
DOID:0060827 - X-linked intellectual disability-psychosis-macroorchidism syndrome