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Summary Literature (0)
MIM:300676 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 14; MRXS14

Xenbase Genes: upf3b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010398 - syndromic X-linked intellectual disability 14

Disease Ontology (DO):
DOID:0060821 - syndromic X-linked intellectual disability 14