ORPHA:168451

Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome

Also called SEMDAD

Body system

Bone diseases

Inheritance pattern

Not documented in Orphadata

Typical age of onset

Infancy

Estimated prevalence

<1 / 1 000 000 (Worldwide)

Rarity class

<1 / 1 000 000

ORPHA:168451 is classified under "Bone diseases" in the Orphanet nomenclature.