Chronic nervous system disorder

Code	`128283000`
Semantic tag	disorder
Module	international
Definition	defined
Effective time	20020131

7910001241072-methyl-3-hydroxybutyric aciduria disorder

230648001Abdominal cutaneous nerve entrapment syndrome disorder

81854007Alexander disease disorder

1201863001Amyotrophic lateral sclerosis type 1 disorder

1208412003Amyotrophic lateral sclerosis type 10 disorder

1201950008Amyotrophic lateral sclerosis type 3 disorder

784341001Amyotrophic lateral sclerosis type 4 disorder

1204334005Amyotrophic lateral sclerosis type 6 disorder

1204349002Amyotrophic lateral sclerosis type 7 disorder

1204350002Amyotrophic lateral sclerosis type 8 disorder

1204351003Amyotrophic lateral sclerosis type 9 disorder

782829002Autosomal dominant Charcot-Marie-Tooth disease type 2O disorder

773393001Autosomal dominant Charcot-Marie-Tooth disease type 2Q disorder

770901001Autosomal recessive intellectual disability, motor dysfunction, multiple joint contracture syndrome disorder

773414009Autosomal recessive intermediate Charcot-Marie-Tooth disease type C disorder

230256009Benign monomelic amyotrophy disorder

1340172003CLCN6-related childhood-onset progressive neurodegeneration, peripheral neuropathy syndrome disorder

1332382002COMMAD syndrome disorder

771307003Charcot-Marie-Tooth disease type 2B5 disorder

782826009Charcot-Marie-Tooth disease type 2P disorder

773492007Childhood-onset spasticity with hyperglycinaemia disorder

1119327001Chronic axonal neuropathy disorder

78689005Chronic brain syndrome disorder

39171000087109Chronic central neuropathic pain due to brain injury disorder

39181000087106Chronic central neuropathic pain due to multiple sclerosis disorder

39191000087108Chronic central neuropathic pain due to spinal cord injury disorder

312923002Chronic central serous chorioretinopathy disorder

846660004Chronic infectious disease of central nervous system disorder

128209004Chronic inflammatory demyelinating polyradiculoneuropathy disorder

304831001Chronic intracranial subdural haematoma disorder

21664006Chronic meningitis disorder

95657009Chronic mixed headache syndrome disorder

7794004Chronic motor tic disorder disorder

434371000124108Chronic myelopathy disorder

609382000Chronic nontraumatic intracranial subdural haemorrhage disorder

193184006Chronic painful neuropathy due to diabetes mellitus disorder

39231000087102Chronic painful polyneuropathy disorder

39241000087108Chronic painful radiculopathy disorder

698754002Chronic paralysis due to lesion of spinal cord disorder

698292000Chronic paraplegia disorder

39211000087107Chronic peripheral neuropathic pain following peripheral nerve injury disorder

95651005Chronic progressive paraparesis disorder

307177001Chronic sciatica disorder

1217665005Chronic trochlear nerve palsy disorder

128200000Complex regional pain syndrome disorder

719102004Congenital cataract with ataxia and deafness syndrome disorder

1230343006Distal hereditary motor neuropathy type 2 disorder

771514002Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome disorder

1348304006Fibrosis, neurodegeneration, cerebral angiomatosis syndrome disorder

724357007Hereditary cerebral haemorrhage with amyloidosis disorder

771143004Hereditary motor and sensory neuropathy type 5 disorder

771144005Hereditary motor and sensory neuropathy with acrodystrophy disorder

702381007Horizontal gaze palsy with progressive scoliosis disorder

1303585005Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome disorder

718555006Juvenile amyotrophic lateral sclerosis disorder

1234819007Limb girdle muscular dystrophy due to POMK deficiency disorder

52702003ME/CFS - myalgic encephalomyelitis/chronic fatigue syndrome disorder

1230273004Megaconial congenital muscular dystrophy disorder

785809005Mills syndrome disorder

1208621008Multiple mitochondrial dysfunctions syndrome type 4 disorder

1279890001Multiple mitochondrial dysfunctions syndrome type 5 disorder

24700007Multiple sclerosis disorder

444197004Multiple system atrophy, Parkinson's variant disorder

111505001Muscle-eye-brain disease, congenital muscular dystrophy disorder

237984008NARP syndrome disorder

1217379007NKX6-2-related autosomal recessive hypomyelinating leucodystrophy disorder

1230017000Non-recovering brachial plexus injury due to birth trauma disorder

1299151005O'Sullivan McLeod syndrome disorder

1228871002PCNA-related progressive neurodegenerative photosensitivity syndrome disorder

782752005Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome disorder

785723001Persistent idiopathic facial pain disorder

193206003Persistent neonatal myasthenia gravis disorder

80328002Progressive cone-rod dystrophy disorder

1260130005Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behaviour syndrome disorder

46252003Progressive external ophthalmoplegia disorder

88923002Progressive muscular atrophy disorder

1119329003Progressive peripheral neuropathy disorder

1187043002Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome disorder

84438001Pure autonomic failure disorder

773555005Severe neurodegenerative syndrome with lipodystrophy disorder

1255323007Spastic ataxia, dysarthria due to glutaminase deficiency disorder

5262007Spinal muscular atrophy disorder

719205008Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome disorder

719156006X-linked intellectual disability with hypogammaglobulinaemia and progressive neurological deterioration syndrome disorder

771475006Young adult-onset distal hereditary motor neuropathy disorder

Synonyms

Parents (2)

Children (85)