is a rare inherited condition causing stiffness and limited joint movement.

is an inherited condition causing joint stiffness in the hands and feet.

is an inherited condition causing joint contractures mainly in hands and feet.

is an inherited condition causing joint contractures mainly in hands and feet.

is a genetic condition causing joint stiffness and distinctive facial features.

is a genetic condition causing hand and foot contractures, distinctive facial features.

is an inherited condition causing joint contractures mainly in hands and feet.

is a rare genetic disorder causing joint stiffness in hands and feet.

is a rare genetic condition causing joint contractures and eye movement problems.

is a rare inherited disorder causing joint contractures and distinctive facial features.

is a rare cancer in the bile ducts near the small intestine.

is a rare genetic condition caused by missing material on chromosome 10p.

is a chromosome condition caused by missing DNA, with variable effects.

is a rare genetic condition caused by missing material on chromosome 12p.

is a rare chromosome disorder caused by missing genetic material on 12q.

is a rare chromosome disorder that can affect development and health.

is a rare chromosome disorder causing developmental delays and varied health issues.

is a rare chromosome disorder causing developmental delays and other variable symptoms.

is a rare chromosome disorder causing developmental delays and other health problems.

is a rare chromosome disorder that can affect development and health.

is a rare genetic condition caused by missing DNA on chromosome 1.

is a rare genetic condition caused by missing material on chromosome 3.

is a rare chromosome disorder causing developmental delays and birth differences.

is a rare chromosome disorder that can affect development and health.