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Summary Literature (0)
MIM:610543 - CHROMOSOME 16p13.3 DELETION SYNDROME, PROXIMAL

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012519 - Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
MONDO:0019188 - Rubinstein-Taybi syndrome

Disease Ontology (DO):
DOID:1933 - Rubinstein-Taybi syndrome