(718555006) Juvenile amyotrophic lateral sclerosis (disorder) (304831001) Chronic intracranial subdural hematoma (784391002) Autosomal dominant adult-onset proximal spinal muscular atrophy (21664006) Chronic meningitis (88923002) Progressive muscular atrophy (846660004) Chronic infectious disease of central nervous system (724357007) Hereditary cerebral hemorrhage with amyloidosis (disorder) (1169360001) Chronic relapsing inflammatory optic neuropathy (disorder) (230648001) Abdominal cutaneous nerve entrapment syndrome (95657009) Chronic mixed headache syndrome (771144005) Hereditary motor and sensory neuropathy with acrodystrophy (724783000) Demyelination of central nervous system co-occurrent and due to Behcet disease (disorder) (2691000124105) Recurrent optic neuritis (disorder) (193184006) Chronic painful diabetic neuropathy (128209004) Chronic inflammatory demyelinating polyradiculoneuropathy (1208339007) Neuhauser Eichner Opitz syndrome (disorder) (1204351003) Amyotrophic lateral sclerosis type 9 (disorder) (782752005) Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (312923002) Chronic central serous chorioretinopathy (80328002) Progressive cone-rod dystrophy (719205008) Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder) (1172585006) Membrane metalloendopeptidase related autosomal dominant Charcot Marie Tooth disease type 2 (disorder) (773393001) Autosomal dominant Charcot-Marie-Tooth disease type 2Q (46252003) Progressive external ophthalmoplegia (762595001) Chronic painful polyneuropathy following chemotherapy (785809005) Mills syndrome (disorder) (1201863001) Amyotrophic lateral sclerosis type 1 (1172684002) Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation (719102004) Congenital cataract with ataxia and deafness syndrome (disorder) (1217379007) NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) (78689005) Chronic brain syndrome (1230343006) Distal hereditary motor neuropathy type 2 (disorder) (816984002) Progressive multiple sclerosis (1208621008) Multiple mitochondrial dysfunctions syndrome type 4 (1231256006) Intermittent horizontal conjugate gaze deviation (disorder) (773492007) Childhood-onset spasticity with hyperglycinemia (disorder) (791000124107) 2-methyl-3-hydroxybutyric aciduria (disorder) (1228871002) PCNA-related progressive neurodegenerative photosensitivity syndrome (782826009) Charcot-Marie-Tooth disease type 2P (disorder) (1204349002) Amyotrophic lateral sclerosis type 7 (disorder) (111505001) Muscle-eye-brain disease, congenital muscular dystrophy (609382000) Chronic non-traumatic intracranial subdural hemorrhage (disorder) (698754002) Chronic paralysis due to lesion of spinal cord (763739002) Idiopathic recurrent stupor (785723001) Persistent idiopathic facial pain (1187043002) Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder) (784341001) Amyotrophic lateral sclerosis type 4 (1230273004) Megaconial congenital muscular dystrophy (771081007) Distal hereditary motor neuropathy type 7 (771514002) Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder) (128200000) Complex regional pain syndrome (1222704008) Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy (disorder) (95651005) Chronic progressive paraparesis (703526007) Neuronal ceroid lipofuscinosis 8 (1204334005) Amyotrophic lateral sclerosis type 6 (782829002) Autosomal dominant Charcot-Marie-Tooth disease type 2O (1217665005) Chronic fourth nerve palsy (disorder) (7794004) Chronic motor tic disorder (770630005) Distal hereditary motor neuropathy type 1 (disorder) (52702003) Chronic fatigue syndrome (81854007) Alexander's disease (771302009) Autosomal recessive lower motor neuron disease with childhood onset (84438001) Pure autonomic failure (434371000124108) Chronic myelopathy (disorder) (1208412003) Amyotrophic lateral sclerosis type 10 (disorder) (771307003) Charcot-Marie-Tooth disease type 2B5 (771143004) Hereditary motor and sensory neuropathy type 5 (disorder) (698292000) Chronic paraplegia (disorder) (193206003) Persistent neonatal myasthenia gravis (773414009) Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (disorder) (1231257002) Intermittent upward gaze deviation (disorder) (783618006) Lower motor neuron syndrome with late-adult onset (disorder) (230256009) Benign monomelic amyotrophy (1230017000) Non-recovering brachial plexus injury due to birth trauma (disorder) (719156006) X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder) (771475006) Young adult-onset distal hereditary motor neuropathy (773555005) Severe neurodegenerative syndrome with lipodystrophy (1204350002) Amyotrophic lateral sclerosis type 8 (1201950008) Amyotrophic lateral sclerosis type 3 (230372003) Acute relapsing multiple sclerosis (81981006) Benign multirecurrent endothelioleukocytal meningitis

(27624003) Chronic disease (118940003) Disorder of nervous system (disorder)