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Summary Literature (1)
MIM:613970 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6

Xenbase Genes: grin2b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013509 - lumbar vertebra cartilage element
MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):
DOID:0070036 - autosomal dominant intellectual developmental disorder 6