ORPHA:163662

Spondyloepiphyseal dysplasia, Reardon type

Body system

Bone diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:163662 is classified under "Bone diseases" in the Orphanet nomenclature.