ORPHA:190

Coats disease

Also called Congenital retinal telangiectasia, Leber miliary aneurysm

Body system

Neurological diseases

Inheritance pattern

Not applicable

Typical age of onset

Childhood

Estimated prevalence

<1 / 1 000 000 (United Kingdom)

Rarity class

<1 / 1 000 000

ORPHA:190 is classified under "Neurological diseases" in the Orphanet nomenclature.