Disease Directory

Cystic malformation of the posterior fossa is a congenital condition that affects the region at the back of the brain where the cerebellum and brainst...

Cystic partially differentiated nephroblastoma is a rare kidney tumor variant that presents with cystic spaces separated by septa containing immature...

Cystic renal cell carcinoma is a malignant neoplasm of the kidney that arises from the renal tubular epithelium and presents as a fluid-filled mass. A...

Cystic teratoma is a condition marked by the formation of a cystic mass that may contain a variety of tissue types. Although specific details regardin...

Cysticercosis is caused by the larvae of the Taenia solium tapeworm, leading to cyst formation in various tissues, particularly the brain, muscles, an...

Cystinosis is a rare metabolic disease caused by an abnormal buildup of cystine inside cell compartments called lysosomes. This buildup can damage var...

Cystinuria is a renal tubular amino acid transport disorder that results in the recurrent formation of cystine kidney stones. It is linked to changes...

Cystinuria type A is a condition recognized in medical practice, although detailed aspects of its presentation and underlying causes have not been ful...

Cystinuria type B is a condition that has been recognized in clinical settings, although detailed information on its definition is not available in th...

Cystoid macular edema is an inherited eye condition primarily affecting the central retina, leading to macular atrophy and visual impairment. It is ch...

Cysts and fistulae of the face and oral cavity is an otorhinolaryngologic condition characterized by the abnormal formation of cysts and passages in t...

Cytomegalovirus retinitis is an infection of the retina primarily seen in individuals with advanced immunosuppression, in patients with AIDS. It is ch...

Cytophagic histiocytic panniculitis (CHP), also known as Winkelmann cytophagic panniculitis, is a very rare inflammatory condition affecting the subcu...

Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder is an extremely rare condition that affects platelet function. It is linked t...

d-2-hydroxyglutaric aciduria 2 is a metabolic condition caused by mutations in the IDH2 gene and is characterized by the persistent presence of D-2-hy...

d-bifunctional protein deficiency is a severe metabolic disorder that impairs the ability to break down dietary fats. This condition arises from mutat...

Dacryocystitis-osteopoikilosis syndrome is an exceedingly rare condition that affects both the lacrimal system and the skeletal system. It is characte...

Dappled diaphyseal dysplasia is a skeletal condition primarily affecting the long bones. Although its precise biological cause is not yet defined, cur...

Dartoic leiomyoma is a benign cutaneous tumor that arises from the smooth muscle tissue of the dartos muscle in the scrotum or labia majora. It is typ...

de Barsy syndrome is a rare genetic disorder described as having an autosomal recessive pattern, primarily affecting multiple systems including the sk...