Disease_Mapped_To_Gene CTRP Terminology CTRP Disease Terminology Cellosaurus Disease Terminology Syndrome Mucopolysaccharidosis Hunter Syndrome Hunter_Syndrome Hunter Syndrome An X-linked, inherited lysosomal storage disease caused by the deficiency of the enzyme iduronate sulfatase that is responsible for the degradation of mucopolysaccharides. It nearly always affects males and is characterized by the accumulation of mucopolysaccharides in various organs, resulting in mental dysfunction, enlarged abdomen, hearing loss, obstructive airway disease, heart disease, and hepatosplenomegaly. Cellosaurus C0026705 Hunter Syndrome Disease or Syndrome Hunter Syndrome C61260 Mucopolysaccharidosis Type II CTRP IDS Gene X-Linked Inherited Disorder