Cerebral amyloid angiopathy (CAA) is a rare hereditary condition characterized by the deposition of amyloid proteins in the cerebral blood vessels. Th...

Cerebral amyloid angiopathy, APP-related is a condition that affects the blood vessels in the brain, leading to a predisposition for hemorrhagic event...

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (commonly called CADASIL) is a hereditary disorder that mai...

Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 is a condition that primarily affects the small b...

cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy 1 is an extremely rare condition. Because few cases have...

Cerebral arteriopathy with subcortical infarcts and leukoencephalopathy, also known as CADASIL, is associated with variants in the NOTCH3 and HTRA1 ge...

Cerebral arteritis is an inflammatory condition that involves a pathogenic inflammatory response in the cerebral artery. This condition affects the bl...

Cerebral astrocytoma is a type of brain tumor that arises in the cerebral hemispheres. It represents a form of astrocytoma that develops from star-sha...

Cerebral cavernous malformation 1 (CCM1) is associated with genetic variants in the KRIT1 gene, which is inherited in an autosomal dominant manner. Th...

Cerebral cavernous malformation 2 is a condition characterized by abnormal blood vessel formations in the brain that result from a mutation in the CCM...

Cerebral cavernous malformation 3 is an inherited condition that primarily affects the brain’s vascular system, leading to the development of abnormal...

Cerebral cavernous malformation 4 (CCM4) is associated with variants in the PIK3CA gene and follows an autosomal dominant inheritance pattern. While t...

Cerebral cavernous malformations 5 is associated with variants in the MAP3K3 gene, which is believed to play a role in vascular development and integr...

Cerebral convexity meningioma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cerebral cortical dysplasia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cerebral creatine deficiency syndrome (CCDS) is a group of metabolic disorders where the body has difficulty producing or transporting creatine. Creat...

Cerebral falx meningioma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cerebral folate deficiency is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cerebral gigantism-jaw cysts syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited...

Cerebral lipidosis with dementia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.