Disease Directory

Dilated cardiomyopathy 1JJ is a form of familial isolated dilated cardiomyopathy that primarily affects the heart by weakening its ability to pump blo...

Dilated cardiomyopathy 1K is a heart muscle disorder characterized by dilation and impaired contraction of the heart that may lead to congestive heart...

Dilated cardiomyopathy 1KK is a form of heart muscle disease characterized by an enlarged and weakened left ventricle, which impairs the heart’s abili...

Dilated cardiomyopathy 1L is a form of familial isolated cardiomyopathy that primarily affects the heart's ability to pump blood effectively. It is ca...

Dilated cardiomyopathy 1M is a familial heart condition characterized by an enlarged and weakened left ventricle, which impairs the heart's ability to...

Dilated cardiomyopathy 1NN is a familial form of isolated dilated cardiomyopathy caused by a mutation in the RAF1 gene. This condition primarily affec...

Dilated cardiomyopathy 1O is a form of familial isolated cardiomyopathy that primarily affects the heart, leading to impaired pumping function and abn...

Dilated cardiomyopathy 1P is a familial heart condition characterized by an enlarged and weakened heart, which can lead to diminished cardiac function...

Dilated cardiomyopathy 1Q is a cardiac condition characterized by enlargement and impaired contraction of the heart’s ventricles. It is defined by a v...

Dilated cardiomyopathy 1R is a familial heart condition that primarily affects the heart muscle, resulting in impaired contraction and cardiac dysfunc...

Dilated cardiomyopathy 1S is a familial form of isolated dilated cardiomyopathy caused by a mutation in the MYH7 gene. This condition primarily affect...

Dilated cardiomyopathy 1U is a familial cardiac condition that primarily affects the heart’s ability to pump blood effectively. It is caused by a muta...

Dilated cardiomyopathy 1V is a familial heart condition primarily affecting the structure and function of the heart, where the heart chambers become e...

Dilated cardiomyopathy 1W is a familial heart condition characterized by an enlarged and weakened left ventricle. It is caused by mutations in the VCL...

Dilated cardiomyopathy 1X is a familial heart condition characterized by enlargement and impaired contraction of the heart’s left ventricle. It is cau...

Dilated cardiomyopathy 1Y is a form of familial isolated cardiomyopathy that primarily affects the heart and is caused by mutations in the TPM1 gene....

Dilated cardiomyopathy 1Z is a familial form of heart muscle disease that primarily affects the cardiac system. It is caused by mutations in the TNNC1...

Dilated cardiomyopathy 2A is a heart muscle disorder that primarily affects the heart’s structure and function. It is characterized by features such a...

Dilated cardiomyopathy 2B is a form of familial isolated cardiomyopathy that primarily affects the heart, leading to reduced pumping function and hear...

Dilated cardiomyopathy 3B (CMD3B) is a genetic heart muscle disorder in which the left ventricle becomes enlarged and weakened. The condition results...