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Up to: Intellectual disability, autosomal dominant · KIF1A related neurological disorder
Intellectual disability, autosomal dominant 9
An autosomal dominant condition caused by mutation(s) in the KIF1A gene, encoding kinesin-like protein KIF1A. It is characterized by microcephaly, intellectual disability, and delayed psychomotor development. The condition is progressive, occurs in early infancy, and is of variable severity.
This condition has no sub-types.