ORPHA:101685

Rare non-syndromic intellectual disability

Also called Rare NSID

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Typical age of onset

Childhood, Infancy

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:101685 is classified under "Neurological diseases" in the Orphanet nomenclature.