Kemonomimi Genetic Immunodeficiency Disorder

Kemonomimi Genetic Immunodeficiency Disorder (K.G.I.D.) is a genetic disorder for Kemonomimi, that is a spectrum of conditions caused by infections, viruses and bacteria due to the failure of the Kemonomimi immunity system brought on by age. The Kemonomimi body, (Primary within the Borean Kemonomimi but not limited to the Borean variety) due to the genetic disorder stops or incredibly slows down the process of replicating antibodies such as the B-cells and T-cells. KGID commonly triggers around the 60 years of life for a Kemonomimi, with some cases triggering in earlier years.

Transmission and Pathophysiology

K.G.I.D. is transmitted through childbirth, while the child/children are still being developed during the pregnancy stage. The disease forms at the start in the first trimester in the fetus, there is on-going research about how KGID is transmitted during this stage. It is still unknown why the disease waits until the later in life despite great efforts from the medical community. The chromosome that hosts the disorder was claimed to be identified in 1986 by Dr. Matthieu Lachance and Gilbertine Lachance, however there has been debate about the validity of the claim by the wider medical community. Being fully discredited in 1992 by Dr. Laure Hardy.

The disease attacks the immune system, though it's activity in childhood and adulthood is usually nonexistence with few exceptional cases recorded within the modern era. Only triggering within 60 years of life with a few exceptions happening within 50 years of life, though rarely trigger that early.