ORPHA:1799

Familial developmental dysphasia

Also called Billard-Toutain-Maheut syndrome, FOXP2-associated dysphasia

Body system

Neurological diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Childhood

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:1799 is classified under "Neurological diseases" in the Orphanet nomenclature.