ORPHA:178469

Autosomal dominant non-syndromic intellectual disability

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Childhood, Infancy

Estimated prevalence

Not documented in Orphadata

Rarity class

Not documented in Orphadata

ORPHA:178469 is classified under "Neurological diseases" in the Orphanet nomenclature.