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...

Cystinosis is a metabolic disorder characterized by the abnormal accumulation of cystine within lysosomes, which leads to multi-organ damage, most in...

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 ocular condition that primarily affects the retina, manifesting with features such as macular atrophy, strabismu...

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...

Czeizel-Losonci syndrome (CLS) is an extremely rare congenital disorder noted for its severe malformations. It is characterized by limb abnormalities...

D-2-hydroxyglutaric aciduria (D-2-HGA) is a rare neurological condition that is part of a group of disorders known as 2-hydroxyglutaric acidurias. It...

D-2-hydroxyglutaric aciduria 1 is a condition caused by a mutation in the D2HGDH gene. This disorder is classified under D-2-hydroxyglutaric acidurias...

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...

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

Dahlberg-Borer-Newcomer syndrome is a very rare disorder that affects several parts of the body. People with this condition have been reported to expe...

Dandy-Walker malformation-postaxial polydactyly syndrome is a complex condition characterized by structural brain abnormalities, specifically a poster...

Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia is a rare disease. Detailed information about this condition is curren...

Dandy-Walker syndrome is a rare brain malformation that affects the cerebellum, a part of the brain important for balance and coordination, as well as...

Danon disease is a lysosomal glycogen storage disorder that primarily affects the heart and skeletal muscles, and it is frequently associated with cog...