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...

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome is a very rare multisystem condition primarily affecting the heart and the reproductive...

Dimethylglycine dehydrogenase deficiency is an extremely rare metabolic disorder that affects glycine metabolism. It is caused by changes in the DMGDH...

Dipetalonemiasis is a parasitic infection caused by filarial worms of the genus Dipetalonema. The infection is characterized by the production of micr...

Diphallia is a congenital condition characterized by the duplication of the penis along with a spectrum of related anomalies that primarily affect the...

Diphtheria is a serious Gram-positive bacterial infection caused by Corynebacterium diphtheriae that primarily affects the upper respiratory tract, in...

Diphtheritic myocarditis is an inflammatory heart condition that develops as a severe complication of infection with Corynebacterium diphtheriae. It i...

Diphyllobothriasis is an intestinal parasitic infection caused by fish tapeworms that primarily affects the gastrointestinal system. Individuals with...

Diploid-triploid mosaicism is a chromosomal disorder in which some cells have the usual 46 chromosomes while others have 69 chromosomes, leading to a...

Diprosopus is a severe developmental defect characterized by the partial or complete duplication of facial structures on a single head, often accompan...