Anyone have any tips for memorizing if a disease is autosomal dominant, recessive, or whatever? It seems like we have hundred of diseases to memorize this for and it just mushes together for me after awhile.
Anyone have any tips for memorizing if a disease is autosomal dominant, recessive, or whatever? It seems like we have hundred of diseases to memorize this for and it just mushes together for me after awhile.
To expand on this, loss of function mutations tend to be recessive while gain of function tend to be dominant. It all kinda makes sense when you think about it: mutations which cause 1 copy to not work tend to be compensated by the other copy. But you can't really do anything about a protein that mutates in a way to lose its regulation and is always "on". These end up being dominant more often than not.
Anyone have any tips for memorizing if a disease is autosomal dominant, recessive, or whatever? It seems like we have hundred of diseases to memorize this for and it just mushes together for me after awhile.