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Summary Literature (0)
OMIM:616078 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 29; MRD29


Xenbase Genes: setbp1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014482 - intellectual disability, autosomal dominant 29
MONDO:0018574 - intellectual disability-expressive aphasia-facial dysmorphism syndrome