involves abnormalities in muscle fiber proteins that affect muscle structure and function.

cause a rare inherited muscle disorder with severe weakness and breathing problems.

is a genetic muscle disorder caused by changes affecting nebulin protein.

is a rare genetic disorder affecting perlecan, causing muscle and bone problems.

is a genetic disorder affecting skin, muscles, and sometimes other tissues.

is a rare genetic disorder affecting how certain proteins are modified.

is a group of genetic muscle disorders caused by faulty alpha-dystroglycan glycosylation.

is a rare inherited disorder affecting muscle, brain, and eye development.

is a genetic disorder affecting muscle, brain, and eye development.

is a rare genetic disorder affecting muscle, brain, and eye development.

causes muscle stiffness and delayed relaxation after exercise from faulty calcium handling.

causes inherited muscle weakness and sometimes heart problems.

is a genetic muscle disease caused by missing or abnormal sarcoglycan proteins.

is a genetic muscle condition causing weakness, breathing problems, and delayed milestones.

is a rare inherited muscle disorder that causes progressive weakness and wasting.

involves inherited changes causing too little, too much, or abnormal titin.

causes rare inherited muscle, nerve, or heart problems that vary widely.

is a rare genetic disorder caused by changes in the TRIM32 gene.

involves inherited problems with tropomyosin, affecting muscle function or development.

can disrupt muscle protein function, often affecting the heart's pumping ability.

involves abnormal muscle or nerve proteins that impair movement and strength.

is a bleeding disorder where platelets do not work properly.

is a rare inherited immune disorder affecting white blood cell function.

is a rare inherited bleeding disorder causing easy or delayed bleeding.