Answer:
Hunter syndrome is a very rare, inherited genetic disorder caused by a missing or malfunctioning enzyme. In Hunter syndrome, the body doesn't have enough of the enzyme iduronate 2-sulfatase.
One of the challenges that scientists face when classifying a new fossil is that any tiny detail is all that separates one species from another. Further exploration is required to identify another set of characteristics that may help in deciding which organism belongs or create a new class.
That would be the Thymus Gland.
According to this principal, if a recessive gene for tallness is paired with another recessive gene for tallness, the organism is categorized as a homozygous recessive in terms of its genotype.
Your "Digestive System" breaks down food into molecules that are then absorbed into your body.
