Additional Disease Briefs

sudden infant death-dysgenesis of the testes syndrome

Also known as: SIDDT, sudden infant death - dysgenesis of the testes, sudden infant death with dysgenesis of the testes syndrome

sudden sensorineural hearing loss

Also known as: acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma, deafness, sudden, sudden deafness, sudden hearing loss, sudden sensorineural hearing loss

sulfhemoglobinemia

Also known as: Sulfemoglobinemia

sulfhemoglobinemia, congenital

Also known as: sulfhemoglobinemia, congenital

sulfite oxidase deficiency due to molybdenum cofactor deficiency type A

Also known as: MOCOD type A, MOCODA, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A, molybdenum cofactor deficiency A, molybdenum cofactor deficiency complementation group A, molybdenum cofactor deficiency type A, molybdenum cofactor deficiency, complementation group A, molybdenum cofactor deficiency, complementation group type a, sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, combined deficiency of

sulfite oxidase deficiency due to molybdenum cofactor deficiency type B

Also known as: MOCOD type B, MOCODB, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B, molybdenum cofactor deficiency B, molybdenum cofactor deficiency complementation group B, molybdenum cofactor deficiency type B, molybdenum cofactor deficiency, complementation group B, molybdenum cofactor deficiency, complementation group type B, sulfite oxidase deficiency due to molybdenum cofactor deficiency type B

sulfite oxidase deficiency due to molybdenum cofactor deficiency type C

Also known as: MOCOD type C, MOCODC, combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C, molybdenum cofactor deficiency C, molybdenum cofactor deficiency complementation group C, molybdenum cofactor deficiency type C, molybdenum cofactor deficiency, complementation group C, molybdenum cofactor deficiency, complementation group type C

SUNCT syndrome