Table B.

OMIM Entries for MECP2 Disorders (View All in OMIM)

300005METHYL-CpG-BINDING PROTEIN 2; MECP2
300055INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 13; MRXS13
300496AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3
300673ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
312750RETT SYNDROME; RTT

From: MECP2 Disorders

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