Disease Directory

Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3 is a neurodevelopmental condition characterized by impaired coordination and...

Cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4 is a neurodevelopmental disorder characterized by significant involvement of...

CAPOS syndrome is a rare autosomal dominant neurological disorder that primarily affects the cerebellum, peripheral nerves, and sensory organs. It is...

Cerebellar ataxia-ectodermal dysplasia syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information...

Cerebellar ataxia-hypogonadism syndrome is a very rare neurodegenerative disorder that primarily affects the cerebellum and the hormonal axis, leading...

Cerebellar atrophy, visual impairment, and psychomotor retardation; is a condition that involves abnormalities in brain structure and function leading...

Cerebellar dysfunction with variable cognitive and behavioral abnormalities is a neurologic condition that primarily affects coordination and brain de...

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

cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome is a multisystem condition character...

Cerebellar hypoplasia-tapetoretinal degeneration syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical in...

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

Cerebellar pilocytic astrocytoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Cerebellar vermis medulloblastoma is a type of brain tumor that arises specifically from the vermis of the cerebellum. Currently, there are no identif...

Cerebellar-facial-dental syndrome is an extremely rare condition affecting multiple systems, particularly involving neurodevelopment and craniofacial...

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

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

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...