I was diagnosed with something that was called a syndrome at the time but now, under new criteria, I would be diagnosed with a “spectrum disorder”.
It used to be thought to be very rare but now some expert estimate it’s prevalence at 1-2%
It is hereditary but so far no genes for it have been definitively found, just some preliminary candidate genes. It is probably caused by many different genes.
It can effect people in very different ways, even within members of the same family.
It effects every single part of me and I cannot separate it from “me”.
Assuming all of the statements above are true, what am I describing?