Disease Index

type of neurofibromatosis disease

human disease

congenital joint contracture in two or more areas of the body

Human disease

human disease

human disease

Neurogenic thoracic outlet syndrome (NTOS) is a form of thoracic outlet syndrome (TOS; see this term) that presents with pain, paresthesias and weakness in an upper extremity and is divided into true NTOS and disputed NTOS

nervous system disease that is characterized by hyperthermia, muscular rigidity, autonomic dysfunction and altered consciousness and is associated with administration of antipsychotic and other central dopaminergic blockers

disease of an anatomical entity located in the central or peripheral nervous system

human disease

neuropathy that affect the nerves that control the voluntary muscles

human disease

neuromuscular disease that is characterized by the disfunction of conduction through the neuromuscular junction

inflammatory demyelinating diseases of the central nervous system characterized mainly by attacks of uni- or bilateral optic neuritis and acute myelitis

Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune inflammatory disorder of the central nervous system primarily affecting the optic nerves and spinal cord. Approximately 80% of patients have aquaporin-4 antibodies (AQP4-IgG). Clinical features include severe optic neuritis, longitudinally extensive transverse myelitis, and area postrema syndrome. Prevalence varies by ethnicity, ranging from 0.5 to 10 per 100,000, with higher rates in Asian and African populations.

immune-mediated peripheral motor neuron disorder characterized by continuous muscle fiber activity at rest

Human disease

human disease

human disease

neuronal ceroid lipofuscinosis that has material basis in homozygous or compound heterozygous mutation in the CTSD gene on chromosome 11p15

human disease

human disease

condition associated with mutation(s) in the TPP1 gene, encoding tripeptidyl-peptidase- 1. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments

condition associated with mutation(s) in the CLN3 gene, encoding battenin. The condition is one of a group of genetically heterogeneous neurodegenerative disorders, characterized by accumulation of intracellular lipopigments

human disease

human disease

human disease

human disease

human disease

human disease