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Summary Literature (0)
MIM:613776 - CHROMOSOME 17p13.1 DELETION SYNDROME

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013415 - chromosome 17p13.1 deletion syndrome

Disease Ontology (DO):
DOID:0060402 - chromosome 17p13.1 deletion syndrome