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Summary Literature (0)
OMIM:617601 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 46; MRD46


Xenbase Genes: kcnq5

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0030911 - intellectual disability, autosomal dominant 46

Disease Ontology (DO):
DOID:0080237 - autosomal dominant mental retardation 46