Chronic nervous system disorder   128283000

SNOMED CT code


SNOMED code128283000
nameChronic nervous system disorder
statusactive
date introduced2002-01-31
fully specified name(s)Chronic nervous system disorder (disorder)
synonyms
  • Chronic nervous system disease
  • Chronic disorder of nervous system
  • Chronic disease of nervous system
  • Chronic nervous system disorder
attributes - group2
Clinical courseChronic   90734009
attributes - group1
Finding siteNervous system structure   25087005
parents
children
  • 2-methyl-3-hydroxybutyric aciduria   791000124107
  • Abdominal cutaneous nerve entrapment syndrome   230648001
  • Acute relapsing multiple sclerosis   230372003
  • Alexander's disease   81854007
  • Amyotrophic lateral sclerosis type 1   1201863001
  • Amyotrophic lateral sclerosis type 10   1208412003
  • Amyotrophic lateral sclerosis type 3   1201950008
  • Amyotrophic lateral sclerosis type 4   784341001
  • Amyotrophic lateral sclerosis type 6   1204334005
  • Amyotrophic lateral sclerosis type 7   1204349002
  • Amyotrophic lateral sclerosis type 8   1204350002
  • Amyotrophic lateral sclerosis type 9   1204351003
  • Autosomal dominant adult-onset proximal spinal muscular atrophy   784391002
  • Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation   1172684002
  • Autosomal dominant Charcot-Marie-Tooth disease type 2O   782829002
  • Autosomal dominant Charcot-Marie-Tooth disease type 2Q   773393001
  • Autosomal recessive intermediate Charcot-Marie-Tooth disease type C   773414009
  • Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy   1222704008
  • Autosomal recessive lower motor neuron disease with childhood onset   771302009
  • Benign monomelic amyotrophy   230256009
  • Charcot-Marie-Tooth disease type 2B5   771307003
  • Charcot-Marie-Tooth disease type 2P   782826009
  • Childhood-onset spasticity with hyperglycinemia   773492007
  • Chronic brain syndrome   78689005
  • Chronic central neuropathic pain due to brain injury   39171000087109
  • Chronic central neuropathic pain due to multiple sclerosis   39181000087106
  • Chronic central neuropathic pain due to spinal cord injury   39191000087108
  • Chronic central serous chorioretinopathy   312923002
  • Chronic fatigue syndrome   52702003
  • Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra   698744001
  • Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra   698742002
  • Chronic infectious disease of central nervous system   846660004
  • Chronic inflammatory demyelinating polyneuropathy   444728005  removed: 2020-01-31
  • Chronic inflammatory demyelinating polyradiculoneuropathy   128209004
  • Chronic intracranial subdural hematoma   304831001
  • Chronic meningitis   21664006
  • Chronic mixed headache syndrome   95657009
  • Chronic motor tic disorder   7794004
  • Chronic myelopathy   434371000124108
  • Chronic non-traumatic intracranial subdural hemorrhage   609382000
  • Chronic painful neuropathy due to diabetes mellitus   193184006
  • Chronic painful polyneuropathy   39231000087102
  • Chronic painful radiculopathy   39241000087108
  • Chronic paraplegia   698292000
  • Chronic peripheral neuropathic pain following peripheral nerve injury   39211000087107
  • Chronic progressive paraparesis   95651005
  • Chronic relapsing inflammatory optic neuropathy   1169360001
  • Chronic sciatica   307177001
  • Chronic trochlear nerve palsy   1217665005
  • Complex regional pain syndrome   128200000
  • Congenital cataract with ataxia and deafness syndrome   719102004
  • Distal hereditary motor neuropathy type 1   770630005
  • Distal hereditary motor neuropathy type 2   1230343006
  • Distal hereditary motor neuropathy type 7   771081007
  • Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome   771514002
  • Hemifacial spasm   13753008
  • Hereditary cerebral hemorrhage with amyloidosis   724357007
  • Hereditary motor and sensory neuropathy type 5   771143004
  • Hereditary motor and sensory neuropathy with acrodystrophy   771144005
  • Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome   1260129000
  • Intermittent horizontal conjugate gaze deviation   1231256006
  • Intermittent upward gaze deviation   1231257002
  • Juvenile amyotrophic lateral sclerosis   718555006
  • Limb girdle muscular dystrophy due to POMK deficiency   1234819007
  • Lower motor neuron syndrome with late-adult onset   783618006
  • Megaconial congenital muscular dystrophy   1230273004
  • Mills syndrome   785809005
  • MME-related autosomal dominant Charcot Marie Tooth disease type 2   1172585006
  • Multiple mitochondrial dysfunctions syndrome type 4   1208621008
  • Multiple mitochondrial dysfunctions syndrome type 5   1279890001
  • Muscle-eye-brain disease, congenital muscular dystrophy   111505001
  • NARP syndrome   237984008
  • Neuronal ceroid lipofuscinosis 8   703526007
  • NKX6-2-related autosomal recessive hypomyelinating leukodystrophy   1217379007
  • Non-recovering brachial plexus injury due to birth trauma   1230017000
  • PCNA-related progressive neurodegenerative photosensitivity syndrome   1228871002
  • Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome   782752005
  • Persistent idiopathic facial pain   785723001
  • Persistent neonatal myasthenia gravis   193206003
  • Progressive cone-rod dystrophy   80328002
  • Progressive essential tremor, speech impairment, facial dysmorphism, intellectual disability, abnormal behavior syndrome   1260130005
  • Progressive external ophthalmoplegia   46252003
  • Progressive multiple sclerosis   816984002
  • Progressive muscular atrophy   88923002
  • Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome   1187043002
  • Pure autonomic failure   84438001
  • Severe neurodegenerative syndrome with lipodystrophy   773555005
  • Spastic ataxia, dysarthria due to glutaminase deficiency   1255323007
  • Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome   719205008
  • X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome   719156006
  • Young adult-onset distal hereditary motor neuropathy   771475006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Chronic nervous system disorder   128283000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Chronic disease   27624003
        Chronic nervous system disorder   128283000

ancestors
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