Category
page 1Syndromes affecting bones
Legg–Calvé–Perthes disease
osteochondrosis that results in death and fracture located in hip joint
Werner syndrome
Lethal autosomal recessive disorder
nail-patella syndrome
Human disease
Blount's disease
osteochondrodysplasia that results in inward turning of lower leg, located in tibia, which fails to develop normally
rapadilino syndrome
Human disease
Marshall–Smith syndrome
syndrome that is characterized by advanced bone age, failure to thrive, respiratory problems, dysmorphic facial features, and variable mental retardation
Baller-Gerold syndrome
synostosis characterized by coronal craniosynostosis, short stature, and aplasia or hypoplasia of the radial bone

Mueller Weiss syndrome
osteonecrotic disease of the foot
Bruck syndrome
syndrome characterized by a combination of multiple joint contractures and osteogenesis imperfecta
Congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
rare genetic disorder
Okamoto syndrome
Autosomal dominant genetic condition