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Summary Literature (1)
MIM:300261 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010284 - lacrimal punctum

Disease Ontology (DO):
DOID:0050764 - Armfield syndrome