Chronic nervous system disorder 128283000 SNOMED CT code SNOMED code 128283000 name Chronic nervous system disorder status active date introduced 2002-01-31 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 course Chronic 90734009 attributes - group1 Finding site Nervous 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 sorted most to least specific
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