ValueSet-2.16.840.1.113762.1.4.1219.44

Sourceus.nlm.vsac#0.11.0:null (v4.0.1)
resourceTypeValueSet
id2.16.840.1.113762.1.4.1219.44
canonicalhttp://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1219.44
version20220315
statusactive
publisherCMS DRLS Steward
nameMotorNeuronDiseaseOrSpinalMuscularAtrophyDisorder
titleMotor Neuron Disease or Spinal Muscular Atrophy Disorder
date2022-03-15T01:04:14-04:00
experimentalfalse
Usages(none)

This value set contains 97 concepts

Code System Display
   1172588008 http://snomed.info/sct Early-onset progressive encephalopathy, spastic ataxia, distal spinal muscular atrophy syndrome (disorder)
   1172689007 http://snomed.info/sct Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder)
   1197523001 http://snomed.info/sct Autosomal dominant amyotrophic lateral sclerosis type 1 (disorder)
   1197524007 http://snomed.info/sct Autosomal recessive amyotrophic lateral sclerosis type 1 (disorder)
   1201863001 http://snomed.info/sct Amyotrophic lateral sclerosis type 1 (disorder)
   1201947005 http://snomed.info/sct Juvenile amyotrophic lateral sclerosis type 2 (disorder)
   1201950008 http://snomed.info/sct Amyotrophic lateral sclerosis type 3 (disorder)
   1201961000 http://snomed.info/sct Juvenile amyotrophic lateral sclerosis type 5 (disorder)
   1204334005 http://snomed.info/sct Amyotrophic lateral sclerosis type 6 (disorder)
   1204349002 http://snomed.info/sct Amyotrophic lateral sclerosis type 7 (disorder)
   1204350002 http://snomed.info/sct Amyotrophic lateral sclerosis type 8 (disorder)
   1204351003 http://snomed.info/sct Amyotrophic lateral sclerosis type 9 (disorder)
   1208412003 http://snomed.info/sct Amyotrophic lateral sclerosis type 10 (disorder)
   1208615009 http://snomed.info/sct Neurogenic scapuloperoneal syndrome Kaeser type (disorder)
   12239621000119103 http://snomed.info/sct Bells palsy of left side of face (disorder)
   12239661000119108 http://snomed.info/sct Bells palsy of right side of face (disorder)
   1259121008 http://snomed.info/sct Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea (disorder)
   1259122001 http://snomed.info/sct Amyotrophic lateral sclerosis with parkinsonism (disorder)
   1259123006 http://snomed.info/sct Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula (disorder)
   1259124000 http://snomed.info/sct Amyotrophic lateral sclerosis with frontotemporal dementia (disorder)
   1259125004 http://snomed.info/sct Amyotrophic lateral sclerosis with multiple system atrophy (disorder)
   1259126003 http://snomed.info/sct Amyotrophic lateral sclerosis with autonomic dysfunction (disorder)
   1259127007 http://snomed.info/sct Amyotrophic lateral sclerosis with cerebellar dysfunction (disorder)
   1259129005 http://snomed.info/sct Amyotrophic lateral sclerosis with spinocerebellar ataxia (disorder)
   128212001 http://snomed.info/sct Spinal muscular atrophy, type II (disorder)
   193093009 http://snomed.info/sct Bell's palsy (disorder)
   230246005 http://snomed.info/sct Progressive bulbar palsy of childhood (disorder)
   230247001 http://snomed.info/sct Distal spinal muscular atrophy (disorder)
   230248006 http://snomed.info/sct Scapuloperoneal spinal muscular atrophy (disorder)
   230249003 http://snomed.info/sct Facioscapulohumeral spinal muscular atrophy (disorder)
   230250003 http://snomed.info/sct Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder)
   230251004 http://snomed.info/sct Scapulohumeral spinal muscular atrophy (disorder)
   230252006 http://snomed.info/sct Oculopharyngeal spinal muscular atrophy (disorder)
   230253001 http://snomed.info/sct Bulbospinal neuronopathy (disorder)
   230254007 http://snomed.info/sct Western Pacific motor neurone disease (disorder)
   230255008 http://snomed.info/sct Madras-type motor neurone disease (disorder)
   230257000 http://snomed.info/sct Paraneoplastic motor neurone disease (disorder)
   230258005 http://snomed.info/sct Amyotrophic lateral sclerosis with dementia (disorder)
   230264003 http://snomed.info/sct Troyer syndrome (disorder)
   230274000 http://snomed.info/sct Frontal lobe degeneration with motor neurone disease (disorder)
   230784003 http://snomed.info/sct Congenital pseudobulbar palsy (disorder)
   249892007 http://snomed.info/sct Progressive pseudobulbar palsy (disorder)
   305719002 http://snomed.info/sct Neuromyotonia (disorder)
   31097004 http://snomed.info/sct Post poliomyelitis syndrome (disorder)
   37340000 http://snomed.info/sct Motor neuron disease (disorder)
   398432008 http://snomed.info/sct Bulbar weakness (disorder)
   44395000 http://snomed.info/sct Spastic tetraplegia with rigidity syndrome (disorder)
   46251005 http://snomed.info/sct Corticospinal motor disease (disorder)
   49793008 http://snomed.info/sct Hereditary motor neuron disease (disorder)
   5262007 http://snomed.info/sct Spinal muscular atrophy (disorder)
   54280009 http://snomed.info/sct Kugelberg-Welander disease (disorder)
   54304004 http://snomed.info/sct Progressive bulbar palsy (disorder)
   64383006 http://snomed.info/sct Werdnig-Hoffmann disease (disorder)
   699866005 http://snomed.info/sct Progressive bulbar palsy with sensorineural deafness (disorder)
   703524005 http://snomed.info/sct Spinal muscular atrophy with progressive myoclonic epilepsy (disorder)
   711406009 http://snomed.info/sct Autosomal recessive axonal neuropathy with neuromyotonia (disorder)
   715565004 http://snomed.info/sct Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)
   717964007 http://snomed.info/sct Juvenile primary lateral sclerosis (disorder)
   718555006 http://snomed.info/sct Juvenile amyotrophic lateral sclerosis (disorder)
   719836007 http://snomed.info/sct X-linked distal arthrogryposis multiplex congenita (disorder)
   722987009 http://snomed.info/sct Amyotrophic lateral sclerosis plus syndrome (disorder)
   723612001 http://snomed.info/sct Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)
   7379000 http://snomed.info/sct Pseudobulbar palsy (disorder)
   763067000 http://snomed.info/sct Autosomal dominant congenital benign spinal muscular atrophy (disorder)
   766764008 http://snomed.info/sct X-linked distal spinal muscular atrophy type 3 (disorder)
   770630005 http://snomed.info/sct Distal hereditary motor neuropathy type 1 (disorder)
   770727008 http://snomed.info/sct Spinal muscular atrophy with respiratory distress type 2 (disorder)
   771081007 http://snomed.info/sct Distal hereditary motor neuropathy type 7 (disorder)
   771238004 http://snomed.info/sct Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder)
   771302009 http://snomed.info/sct Autosomal recessive lower motor neuron disease with childhood onset (disorder)
   772129007 http://snomed.info/sct Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder)
   783257005 http://snomed.info/sct Familial recurrent peripheral facial palsy (disorder)
   783618006 http://snomed.info/sct Lower motor neuron syndrome with late-adult onset (disorder)
   784341001 http://snomed.info/sct Amyotrophic lateral sclerosis type 4 (disorder)
   784391002 http://snomed.info/sct Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder)
   785809005 http://snomed.info/sct Mills syndrome (disorder)
   81211007 http://snomed.info/sct Primary lateral sclerosis (disorder)
   838276009 http://snomed.info/sct Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)
   84590007 http://snomed.info/sct Lower motor neuron disease (disorder)
   85505000 http://snomed.info/sct Adult spinal muscular atrophy (disorder)
   85672005 http://snomed.info/sct Anterior horn cell disease (disorder)
   86044005 http://snomed.info/sct Amyotrophic lateral sclerosis (disorder)
   866051002 http://snomed.info/sct Motor neuron disease due to lead intoxication (disorder)
   88923002 http://snomed.info/sct Progressive muscular atrophy (disorder)
   95647008 http://snomed.info/sct Upper motor neuron disease (disorder)
   G12.0 http://hl7.org/fhir/sid/icd-10-cm Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]
   G12.1 http://hl7.org/fhir/sid/icd-10-cm Other inherited spinal muscular atrophy
   G12.2 http://hl7.org/fhir/sid/icd-10-cm Motor neuron disease
   G12.20 http://hl7.org/fhir/sid/icd-10-cm Motor neuron disease, unspecified
   G12.21 http://hl7.org/fhir/sid/icd-10-cm Amyotrophic lateral sclerosis
   G12.22 http://hl7.org/fhir/sid/icd-10-cm Progressive bulbar palsy
   G12.23 http://hl7.org/fhir/sid/icd-10-cm Primary lateral sclerosis
   G12.24 http://hl7.org/fhir/sid/icd-10-cm Familial motor neuron disease
   G12.25 http://hl7.org/fhir/sid/icd-10-cm Progressive spinal muscle atrophy
   G12.29 http://hl7.org/fhir/sid/icd-10-cm Other motor neuron disease
   G12.8 http://hl7.org/fhir/sid/icd-10-cm Other spinal muscular atrophies and related syndromes
   G12.9 http://hl7.org/fhir/sid/icd-10-cm Spinal muscular atrophy, unspecified

Produced 08 Sep 2023