is a birth condition where one elbow is dislocated, limiting movement.

is a rare genetic disorder of intestinal cells causing diarrhea and malabsorption.

is a rare inherited disorder causing infant malabsorption, diarrhea, and poor growth.

is a rare birth condition causing poor intestinal lining formation and malabsorption.

is a virus passed before birth, causing newborn illness and complications.

is a rare Epstein-Barr virus infection present at birth.

is a rare, benign gum tumor in newborns, affecting feeding or breathing.

is a rare newborn skin disorder causing widespread blisters and erosions, scarring.

is a rare inherited porphyria causing severe photosensitivity and hemolytic anemia.

is a birth defect forming an esophageal pouch (diverticulum), affecting swallowing.

is a birth defect narrowing the esophagus and causing swallowing difficulties.

is present at birth; eyelids retract, exposing more eye surface.

is a rare inherited bleeding disorder causing easy bruising and bleeding.

is a rare lack of clotting protein (factor V) causing prolonged bleeding.

is an inherited bleeding disorder causing prolonged bleeding and easy bruising.

is a rare inherited bleeding disorder causing easy, prolonged, or severe bleeding.

is a rare inherited bleeding disorder causing variable bleeding, especially after surgery.

is a rare inherited clotting disorder causing prolonged tests, usually without bleeding.

is a rare inherited bleeding disorder causing unstable clots and prolonged bleeding.

is a genetic muscle disorder causing early hypotonia, weakness, and breathing difficulties.

is a rare inherited bleeding disorder from low fibrinogen, a clotting protein.

is a rare infant soft-tissue cancer, usually in limbs, often treatable.

is a rare birth condition causing limited eye movements and droopy eyelids.

is a genetic eye movement disorder causing droopy eyelids and limited gaze.