ORPHA:168443

Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome

Body system

Bone diseases

Inheritance pattern

Not documented in Orphadata

Typical age of onset

Infancy, Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:168443 is classified under "Bone diseases" in the Orphanet nomenclature.