is a genetic bone disorder mainly affecting limb development and body shape.

is a genetic bone disorder causing short fingers and abnormal bone development.

is a rare genetic condition affecting bone development and other body systems.

is a genetic bone disorder causing short fingers and toes only.

is a rare genetic disorder affecting bone development and limb formation.

is a rare genetic disorder affecting bone development in limbs and face.

is a rare genetic disorder affecting bone development and the limbs.

is a rare genetic disorder mainly affecting skull and facial bone development.

is a rare genetic bone disorder mainly affecting the spine and ribs.

is a rare inherited bone disorder affecting skeletal growth and development.

is trouble swallowing caused by an abnormal artery pressing on the esophagus.

is a rare childhood bone overgrowth affecting one side of a joint.

is a rare childhood hip condition affecting development of the femoral head.

is a rare inherited disorder causing painful bone swelling in infancy.

is a rare genetic bone disorder causing abnormal bone thickening.

is a very rare genetic bone disorder affecting skull and limb growth.

is an inherited tendency to develop many unusual-looking moles and melanoma.

is a fatty tissue growth attached to the spinal cord before birth.

is a rare birth defect connecting the spinal cord to skin.

is a rare congenital syndrome causing spinal dysraphism, orofacial clefts, limb abnormalities.

is a rare genetic bone growth disorder causing severe short stature.

is a rare, severe skeletal disorder causing short stature and bone abnormalities.

is a rare bone disorder causing abnormal spine growth and cartilage tumors.

is a long-lasting depression causing persistent low mood and reduced enjoyment.