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Summary Literature (0)
MIM:611867 - CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012740 - chromosome 22q11.2 deletion syndrome, distal

Disease Ontology (DO):
DOID:0060413 - chromosome 22q11.2 deletion syndrome, distal