Double uterus-hemivagina-renal agenesis syndrome is a rare congenital anomaly affecting the urogenital system, characterized by the presence of a dupl...

Dowling-Degos disease is a skin condition marked by a net-like (reticulate) pattern of dark pigmentation, most notably in the folds and creases of the...

Dowling-Degos disease 1 is a rare genetic skin condition caused by a mutation in the KRT5 gene. This mutation leads to changes in the skin, and it is...

Dowling-Degos disease 2 is a rare skin condition that occurs due to a mutation in the POFUT1 gene. This gene mutation affects the normal functioning o...

Dowling-Degos disease 3 is a disorder primarily affecting the skin, with characteristic alterations in pigmentation. Individuals typically show a dist...

Dowling-Degos disease 4 is a rare condition where a mutation in the POGLUT1 gene causes changes typically seen in the skin. This condition is one of s...

Down syndrome is a chromosomal abnormality resulting from an extra copy of the genetic material on chromosome 21, and it is characterized by a spectru...

Doxorubicin induced cardiomyopathy is a condition characterized by damage to the heart muscle that develops following treatment with the chemotherapy...

Doyne honeycomb retinal dystrophy (DHRD) is a condition that affects the eyes and leads to vision loss. It is characterized by the presence of small,...

DPAGT1-congenital disorder of glycosylation (DPAGT1-CDG) is a rare genetic condition that affects a process called N-linked glycosylation, which is im...

DPM3-congenital disorder of glycosylation (DPM3-CDG) is an extremely rare type of congenital disorder of glycosylation. This group of conditions affec...

Drachtman Weinblatt Sitarz syndrome is a rare genetic disorder. It is characterized by an under-development of the bone marrow along with significant...

Dracunculiasis, also known as Guinea worm disease, is a parasitic infection that primarily affects the skin and soft tissues. The condition develops a...

Dravet syndrome is a severe form of epilepsy that typically begins in the first year of life, most often around 4 to 5 months of age. Affected childre...

Drug-induced autoimmune hemolytic anemia is a form of autoimmune hemolytic anemia that occurs as an adverse reaction to certain therapeutic drugs. Thi...

Drug-induced localized lipodystrophy is an acquired skin condition characterized by localized loss of fat at injection sites, leading to depressed, we...

Drug-induced lupus erythematosus is an autoimmune condition that mimics many features of systemic lupus erythematosus but is triggered by exposure to...

Drug-induced methemoglobinemia is an acquired condition characterized by an abnormal increase in methemoglobin in the blood following exposure to cert...

Drug-induced osteoporosis is a condition in which the bones lose density and strength as a result of exposure to certain medications. Unlike primary o...

Drug-induced vasculitis is a skin hypersensitivity reaction triggered by exposure to a pharmacologic substance. It is characterized by raised purpuric...