Parent term(s)
Term with siblings
spondylometaphyseal dysplasia +

acheiropody
achondrogenesis +
achondroplasia
acrocapitofemoral dysplasia
acromesomelic dysplasia +
acromicric dysplasia
atelosteogenesis
Blount's disease
Boomerang dysplasia
brachyolmia
calvarial doughnut lesions with bone fragility
campomelic dysplasia
chondrodysplasia Blomstrand type
chondrodysplasia with joint dislocations gPAPP type
cleidocranial dysplasia
Desbuquois dysplasia
diaphyseal medullary stenosis with malignant fibrous histiocytoma
diastrophic dysplasia
fibrochondrogenesis +
gnathodiaphyseal dysplasia
hypertrichotic osteochondrodysplasia Cantu type
hypochondrogenesis
hypochondroplasia
Kenny-Caffey syndrome +
Kniest dysplasia
Leri-Weill dyschondrosteosis
metachondromatosis
metaphyseal dysplasia +
metaphyseal dysplasia-maxillary hypoplasia-brachydactyly syndrome
microcephalic osteodysplastic primordial dwarfism type I
microcephalic osteodysplastic primordial dwarfism type II
microcephaly, short stature, and limb abnormalities
midface dysplasia
multiple epiphyseal dysplasia +
omodysplasia +
osteogenesis imperfecta +
osteoglophonic dysplasia
otospondylomegaepiphyseal dysplasia, autosomal dominant
otospondylomegaepiphyseal dysplasia, autosomal recessive
parastremmatic dwarfism
progressive pseudorheumatoid arthropathy of childhood
pseudoachondroplasia
pycnodysostosis
schneckenbecken dysplasia
Silverman-Handmaker type dyssegmental dysplasia
spondyloepimetaphyseal dysplasia +
spondyloepiphyseal dysplasia +
spondyloperipheral dysplasia
thanatophoric dysplasia
Torrance type platyspondylic dysplasia
Weissenbacher-Zweymuller syndrome
Child term(s)

is-a denotes an 'is-a' relationship