Answer:
The digestive system excretes a solid waste, and the excretory system excretes liquid waste.
Explanation:
The digestive system is the system of the body that breaks down food substances to enhance so that they can absorb them. But it also excretes solid indigestible substances. For excreating, they use the defecation process.
Excretory system, on the other hand, is a system in the body that removes homeostatic wastes from the body by using a process which is called excretion. Excretory includes organs such as liver, sweat glands, lungs. Among this, the liver plays a critical role in the secretion of homeostatic wastes in the form of fluids.
The excretory system collects and then filters excess water which is present in the body and then excretes it as a liquid waste either from the liver, kidneys, or sweat glands on the skin through sweating.
Tay-Sachs disease is caused by mutations in the HEXA gene and inheritance is autosomal recessive . The HEXA gene gives the body instructions to make part of the beta-hexosaminidase A enzyme, which is needed to break down a substance called GM2 ganglioside.
i hope this helped! please mark me as brainliest and 5 stars >:)
There are 3 sources of energy, which are also known as macronutrients ,carbohydrates, protein, and fat.
Of these three, carbohydrates are the body’s preferred source of energy. Carbohydrates break down into glucose, which is an immediate source of energy especially for the brain and muscles. The macronutrient proportions recommended for general, healthy diet are: 45-65% of energy (or calories) from carbohydrates, 10-20% of energy (or calories) from protein and 20-35% of energy (or calories) from fat.
Answer:
Human males much more likely than human females to inherit the recessive condition hemophilia because it follows X-linked recessive pattern.
Explanation:
Actually hemophilia is an X-linked recessive disorder i-e the defective genes are located on the X chromosome (sex chromosome) and are transmitted through it. As males have only one X chromosome (inherited from mother), one altered copy of the gene in every cell cause this disease.On the other hand females have 2 X chromosomes thus this disease is rare in females.