Carcinoma of the liver and intrahepatic biliary tract encompasses cancers that arise from hepatocytes or the intrahepatic bile ducts. The main subtype...

Carcinoma of the ampulla of vater is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Carcinosarcoma of the corpus uteri is an aggressive malignant tumor that arises from the body of the uterus, exhibiting both carcinomatous (epithelial...

Cardiac anomalies - developmental delay - facial dysmorphism syndrome is a very rare genetic condition that primarily affects neurodevelopment and car...

Cardiac anomalies-heterotaxy syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited...

cardiac anomalies-short stature-joint hypermobility-facial dysmorphism syndrome due to TAB2 mutation is an extremely rare condition. Because few cases...

Cardiac arrhythmia, ankyrin-B-related, is associated with variants in the ANK2 gene, which plays a critical role in cardiac electrical activity. This...

Cardiac diverticulum is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cardiac germ cell tumor is a tumor that arises within the myocardium or cardiac chambers, with reported cases including teratomas and yolk sac tumors....

Cardiac granular cell neoplasm is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

cardiac lipidosis, familial is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cardiac sarcoidosis is a form of sarcoidosis that specifically affects the heart tissues. The exact genetic basis of this condition remains unidentifi...

cardiac tuberculosis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cardiac-urogenital syndrome is a complex, multisystem condition primarily affecting the heart, lungs, and urogenital tract. It is caused by alteration...

Cardiac valvular dysplasia, X-linked is a condition that primarily affects the structure and function of the heart valves. It is linked to changes in...

Pfeiffer-type cardiocranial syndrome is an extremely rare disorder characterized by congenital heart defects, sagittal craniosynostosis, and severe de...

Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 is a severe multisystem condition that primarily affects infants, u...

Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 is a severe, multi-system disorder characterized by early-onset hea...

Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3 is a severe disorder that affects both the heart and the brain in e...

Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4 is a severe disorder that primarily affects the heart and brain of...