is a rare genetic condition affecting facial, limb, and speech development.

is a rare inherited condition affecting facial, limb, and growth development.

is when chronic lymphocytic leukemia changes into a fast-growing lymphoma.

is a rare, life-threatening poisoning caused by exposure to ricin toxin.

is a condition that softens and weakens bones in children.

is a tick-borne bacterial infection causing fever, rash, and a scab.

is a bacterial infection spread by ticks, fleas, mites, or lice.

is a rare bacterial infection spread by mites, causing fever and rash.

is a rare genetic disorder affecting DNA repair and immune function.

is a rare thyroid disease causing hard swelling and pressure symptoms.

is a rare eye condition affecting the iris and front of the eye.

is a mosquito-borne viral infection that can also spread from animals.

is a birth difference where the aorta arches to the right.

is a heart conduction delay on ECG, often harmless and symptom-free.

is a rare heart vein defect causing low blood oxygen levels.

is a rare birth condition where the heart and organs develop abnormally.

is a rare heart vessel abnormality causing oxygen-poor blood to bypass lungs.

is a rare muscle disorder causing stiff spine, weakness, and breathing problems.

is a rare inherited nerve disorder affecting autonomic and sensory function.

is a rare genetic condition causing macrocephaly, alopecia, cutis laxa, scoliosis.

is a rare genetic condition caused by a ring-shaped chromosome.

is a rare genetic condition caused by an abnormal chromosome 1 ring.

is a rare genetic condition that can affect growth and development.

is a rare genetic condition caused by a ring-shaped chromosome 11.