Disease Directory

Corneal-cerebellar syndrome is a very rare genetic neurological disorder that primarily affects both the nervous system and the eyes. It is characteri...

Coronal synostosis, syndactyly and jejunal atresia is a complex condition that involves the premature fusion of the skull’s coronal sutures, abnormal...

Coronary arterial fistulas are congenital anomalies characterized by an abnormal connection between one or more coronary arteries and a heart chamber...

Coronary artery congenital malformation is a heart disorder present at birth that involves an abnormal origin, course, or structure of one or more cor...

Coronary artery intramyocardial course is a condition in which an artery normally located on the surface of the heart follows an atypical path by cour...

Coronary sinus atresia is a congenital cardiac anomaly affecting the heart’s venous drainage system. It involves an abnormal development of the struct...

Coronary sinus stenosis is a condition characterized by the narrowing of the coronary sinus, the large venous channel that drains blood from the heart...

Corpus callosum agenesis-abnormal genitalia syndrome is a congenital condition characterized by the absence of the corpus callosum along with a spectr...

Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome is a developmental anomalies condition that primarily impacts brain de...

Corpus callosum agenesis-macrocephaly-hypertelorism syndrome is a condition characterized by abnormalities in brain structure, including partial or co...

Corpus callosum oligodendroglioma is a type of brain tumor that specifically affects the corpus callosum, the structure that connects the left and rig...

Corpus callosum agenesis is a congenital condition characterized by the complete absence of the corpus callosum, the major structure connecting the tw...

Cortical blindness-intellectual disability-polydactyly syndrome is a condition characterized primarily by significant visual impairment due to cortica...

Cortical dysplasia-focal epilepsy syndrome is a neurodevelopmental disorder characterized by the onset of intractable seizures and cognitive challenge...

Cortical thymoma is a tumor arising from the epithelial cells of the thymus, most commonly located in the anterior mediastinum. It is characterized by...

Corticobasal syndrome (CBS) is a rare neurodegenerative disorder characterized by a combination of motor and cognitive dysfunctions. Patients may expe...

Corticosteroid-binding globulin deficiency is an endocrine metabolic condition that disrupts the normal transport of the stress hormone cortisol throu...

Corticosteroid-induced osteoporosis is a condition characterized by reduced bone density and increased fragility that develops as an adverse effect of...

Corticosteroid-sensitive aseptic abscess syndrome is a distinct autoinflammatory disorder characterized by the formation of non-infectious abscesses i...

Corticosterone methyloxidase type 1 deficiency is a congenital endocrine condition that results from alterations in a gene crucial for adrenal steroid...