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Summary Literature (0)
MIM:617788 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 51; MRD51


Xenbase Genes: kmt5b

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030917 - intellectual disability, autosomal dominant 51

Disease Ontology (DO):
DOID:0080232 - autosomal dominant mental retardation 51