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Summary Literature (0)
MIM:615761 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23


Xenbase Genes: setd5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014336 - intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency

Disease Ontology (DO):
DOID:0070053 - autosomal dominant intellectual developmental disorder 23