ORPHA:93347

Anauxetic dysplasia

Also called Spondyloepimetaphyseal dysplasia, Menger type, Spondyloepimetaphyseal dysplasia, anauxetic type

Body system

Bone diseases

Inheritance pattern

Autosomal recessive

Typical age of onset

Antenatal, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:93347 is classified under "Bone diseases" in the Orphanet nomenclature.