Neuromyelitis optica spectrum disorder (NMOSD) without anti-MOG and anti-AQP4 antibodies is a rare neurological condition characterized by inflammatio...

Neuronal ceroid lipofuscinosis is a group of inherited progressive degenerative brain diseases that primarily affect neurological function and vision....

Neuronal ceroid lipofuscinosis 1 is a neurodegenerative disorder that primarily affects the nervous system and is one of several conditions characteri...

Neuronal ceroid lipofuscinosis 10 is a rare condition that primarily affects the nervous system. It is caused by changes in the CTSD gene, which impai...

Neuronal ceroid lipofuscinosis 11 is a neurodegenerative condition affecting the central nervous system, characterized by progressive neurological dec...

Neuronal ceroid lipofuscinosis 13 is an inherited neurodegenerative condition that primarily affects the brain, leading to progressive impairment in c...

Neuronal ceroid lipofuscinosis 2 is a neurodegenerative condition that primarily affects the nervous system, marked by the accumulation of lipopigment...

Neuronal ceroid lipofuscinosis 3 is a neurodegenerative condition that primarily affects the nervous system and the eyes. It is caused by mutations in...

Neuronal ceroid lipofuscinosis 5 is a rare neurodegenerative condition that primarily affects the nervous system. It is caused by mutations in the CLN...

Neuronal ceroid lipofuscinosis 7 is a rare neurological condition that primarily affects children, with signs typically appearing around the age of fi...

Neuronal ceroid lipofuscinosis 8 is a progressive disorder that primarily affects the nervous system and vision. It is caused by mutations in the CLN8...

Neuronal ceroid lipofuscinosis 8 northern epilepsy variant is a form of neuronal ceroid lipofuscinosis that primarily affects the central nervous syst...

Neuronal ceroid lipofuscinosis 9 (CLN9-NCL) is a rare condition that affects the nervous system and typically begins in early childhood, around the ag...

Neuronal intestinal dysplasia, type B is a condition that affects the enteric nervous system, leading to disturbances in intestinal function. Although...

Neuronal intranuclear inclusion disease (NIID) is a very rare multisystem neurodegenerative disorder characterized by the presence of eosinophilic int...

Neuronopathy, distal hereditary motor, autosomal dominant is a form of distal hereditary motor neuropathy that primarily affects the motor neurons con...