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Summary Literature (0)
MIM:614563 - CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 13; CDCBM13

Xenbase Genes: dync1h1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013805 - intellectual disability, autosomal dominant 13
MONDO:0100172 - intellectual disability, autosomal dominant

Disease Ontology (DO):
DOID:0070043 - autosomal dominant intellectual developmental disorder 13