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Summary Literature (0)
MIM:300968 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F

Xenbase Genes: usp9x

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010502 - intellectual disability, X-linked 99, syndromic, female-restricted

Disease Ontology (DO):
DOID:0112025 - female-restricted syndromic X-linked intellectual disability 99