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Summary Literature (0)
MIM:612621 - INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5


Xenbase Genes: syngap1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012960 - intellectual disability, autosomal dominant 5
MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):
DOID:0070035 - autosomal dominant intellectual developmental disorder 5