Disorders of vitamin D metabolism are conditions that affect the way the body processes and utilizes vitamin D, an essential nutrient for bone health...

Dissecting cellulitis of the scalp is a rare, long-term skin condition that mainly affects the scalp. It is characterized by painful nodules, pustules...

Disseminated chorioretinitis is an ocular condition characterized by inflammation involving widespread areas of the retina and choroid. Because detail...

Disseminated eosinophilic collagen disease is a condition that appears to affect connective tissue, potentially involving abnormal collagen deposition...

Disseminated intravascular coagulation is a serious condition in which the body’s blood clotting mechanisms become overactive, leading to widespread c...

Disseminated intravascular coagulation in newborn is a clotting condition in which the normal balance between blood clot formation and breakdown is di...

Disseminated peritoneal leiomyomatosis is a rare, benign condition that affects the peritoneal cavity. It is characterized by the formation of multipl...

Disseminated sporotrichosis is a form of infection characterized by the spread of the disease beyond a localized site, potentially affecting multiple...

Disseminated superficial actinic porokeratosis (DSAP) is a skin condition characterized by the development of several small, annular plaques with a di...

Disseminated visceral giant cell angiitis is a necrotizing vasculitis characterized by widespread inflammation of small blood vessels with the presenc...

Distal 10q deletion syndrome is a chromosomal anomaly caused by a terminal deletion of the long arm of chromosome 10, which leads to a distinctive set...

Distal 16p11.2 microdeletion syndrome is a rare chromosomal anomaly that results from a partial deletion on the short arm of chromosome 16. This condi...

Distal 17p13.1 microdeletion syndrome is a rare chromosomal anomaly that affects several aspects of development, particularly cognitive and physical g...

Distal 17p13.3 microdeletion syndrome is a rare condition resulting from a deletion on the short arm of chromosome 17. Individuals with this syndrome...

Distal 22q11.2 microduplication syndrome is a rare chromosomal condition caused by the duplication of a small part of the long arm of chromosome 22. T...

Distal 7q11.23 microdeletion syndrome is a rare chromosomal anomaly that affects brain development and neurological function. Individuals with the con...

Distal 7q11.23 microduplication syndrome is a rare chromosomal anomaly primarily affecting neuropsychiatric function and, in some cases, physical appe...

Distal arthrogryposis is a muscle tissue condition primarily characterized by congenital joint contractures of the hands and feet. It is evident from...

Distal arthrogryposis Moore weaver type, also known as Moore Weaver syndrome, is a condition primarily characterized by congenital contractures that a...

Distal arthrogryposis type 10 is a developmental condition that primarily affects the musculoskeletal system, with characteristic joint contractures i...