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Summary Literature (0)
OMIM:612474 - CHROMOSOME 1q21.1 DELETION SYNDROME, 1.35-MB


Xenbase Genes: gja5, gja8

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012914 - chromosome 1q21.1 deletion syndrome

Disease Ontology (DO):
DOID:0060411 - chromosome 1q21.1 deletion syndrome