ORPHA:1540

Jackson-Weiss syndrome

Also called Craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome, JWS

Body system

Bone diseases

Inheritance pattern

Autosomal dominant

Typical age of onset

Neonatal

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:1540 is classified under "Bone diseases" in the Orphanet nomenclature.