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Summary Literature (0)
MIM: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 - obsolete intellectual disability-expressive aphasia-facial dysmorphism syndrome

Disease Ontology (DO):
DOID:0070059 - autosomal dominant intellectual developmental disorder 29