Coffin-Siris syndrome is a rare genetic condition that affects many parts of the body, especially the brain, face, fingers, toes, hair, and growth. Children ...

X-linked dominant Coffin-Lowry syndrome is a rare genetic condition that affects how the brain, bones, and other body systems grow and work. It is present from ...

Coffin-Lowry syndrome is a rare genetic condition that affects many parts of the body, especially the brain, face, bones, heart, and muscles. It usually causes ...

Coenzyme Q10 deficiency disease is a rare health problem where the body does not have enough coenzyme Q10 (also called CoQ10 or ubiquinone). CoQ10 is a natural ...

Coenzyme Q10 deficiency means the body does not have enough coenzyme Q10 (also called CoQ10 or ubiquinone). CoQ10 is a fat-like substance that sits inside tiny ...

Codas syndrome is a very rare genetic disease that affects many parts of the body, especially the brain, eyes, teeth, ears, and bones. Doctors use the short ...

Fetal encasement syndrome, also called cocoon syndrome, is a very rare and very severe problem that happens very early in pregnancy when the baby is still an ...

Cocoon syndrome usually means abdominal cocoon syndrome, also called sclerosing encapsulating peritonitis or encapsulating peritoneal sclerosis. In this ...

Cockayne syndrome type 3 is a very rare, inherited disease that affects many parts of the body, especially the brain, eyes, ears, skin, and growth. It belongs ...

Cockayne syndrome type 2 is a very rare, very severe genetic disease that starts at birth or even before birth. It affects many parts of the body, especially ...

Cockayne syndrome caused by mutation in ercc8 is a rare genetic disease that affects many parts of the body, especially the brain, eyes, ears, skin, and ...

Classical Cockayne syndrome type 1 is a rare inherited disease. It mainly affects how a child grows and how the brain, eyes, ears, skin, and other organs work ...

Cockayne syndrome type 1 is a very rare inherited disease that affects many parts of the body, especially the brain, eyes, ears, skin, and growth. It happens ...

Neill-Dingwall syndrome is another name for Cockayne syndrome, a very rare, serious genetic disease in children. It affects many parts of the body, especially ...

Cockayne syndrome is a very rare genetic disease that affects many organs in the body. Children with this condition are usually very small in height, have a ...

Cochleosaccular degeneration with progressive cataract is a very rare inherited disease that affects both hearing and vision. In this disease, parts of the ...

Cochleosaccular degeneration-cataract syndrome is a very rare genetic disease. It affects two main organs: the inner ear (the cochlea and the saccule) and the ...

San Joaquin Valley fever is another name for Valley fever, a lung infection caused by a fungus called Coccidioides. A fungus is a tiny living thing, like mold, ...

Primary extrapulmonary coccidioidomycosis is an infection caused by a fungus called Coccidioides that shows itself first outside the lungs, such as in the ...

Posadas-Wernicke disease is another name for coccidioidomycosis, also called valley fever. It is an infection caused by a fungus called Coccidioides that lives ...