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Summary Literature (0)
MIM:300705 - CHROMOSOME Xp11.22 DUPLICATION SYNDROME

Xenbase Genes: hsd17b10

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010406 - chromosome Xp11.22 duplication syndrome
MONDO:0019181 - non-syndromic X-linked intellectual disability

Disease Ontology (DO):
DOID:0112037 - chromosome Xp11.22 duplication syndrome