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MIM:612621 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5
Xenbase Genes: syngap1
Human Disease Resource: MIM
MONDO:0012960 - intellectual disability, autosomal dominant 5 |
MONDO:0100172 - intellectual disability, autosomal dominant |
DOID:0070035 - autosomal dominant intellectual developmental disorder 5 |