MND MS MYAS Huntington's
Motor neurone disease, multiple sclerosis, myasthenia gravis, or Huntington’s disease.
Condition group | Dataset | Coding system | Code value | Code description |
---|---|---|---|---|
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | F022 | Dementia in Huntington disease |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G10 | Huntington disease |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G10X | Huntington disease |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G122 | Motor neuron disease |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G35 | Multiple sclerosis |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G35X | Multiple sclerosis |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G700 | Myasthenia gravis |
has_mnd_ms_myas_or_huntingtons | HES | ICD10 | G70 | Myasthenia gravis and other myoneural disorders |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230679002 | Abnormality of synaptic vesicles (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230671004 | Acetylcholine resynthesis deficiency (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 85505000 | Adult spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 86044005 | Amyotrophic lateral sclerosis (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230258005 | Amyotrophic lateral sclerosis with dementia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 85672005 | Anterior horn cell disease (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 864471000000106 | Anterior opercular syndrome (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230253001 | Bulbospinal neuronopathy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 193216006 | Congenital and developmental myasthenia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230673001 | Congenital end-plate acetylcholine receptor deficiency (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230677000 | Congenital end-plate acetylcholinesterase deficiency (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230672006 | Congenital myasthenia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230784003 | Congenital pseudobulbar palsy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230678005 | Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230247001 | Distal spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230249003 | Facioscapulohumeral spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230250003 | Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230686005 | Generalized myasthenia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230669004 | Genetically determined myasthenia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 58756001 | Huntington's chorea (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 193207007 | Juvenile or adult myasthenia gravis (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 54280009 | Kugelberg-Welander disease (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 37340000 | Motor neuron disease (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 91637004 | Myasthenia gravis (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230685009 | Myasthenia gravis associated with thymoma (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 305719002 | Neuromyotonia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230252006 | Oculopharyngeal spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230257000 | Paraneoplastic motor neurone disease (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 193206003 | Persistent neonatal myasthenia gravis (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 31097004 | Post poliomyelitis syndrome (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 81211007 | Primary lateral sclerosis (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 54304004 | Progressive bulbar palsy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230246005 | Progressive bulbar palsy of childhood (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 88923002 | Progressive muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 249892007 | Progressive pseudobulbar palsy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 7379000 | Pseudobulbar palsy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230674007 | Pseudomyopathic myasthenia (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230676009 | Putative defect in acetylcholine synthesis or packaging (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230251004 | Scapulohumeral spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 230248006 | Scapuloperoneal spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 5262007 | Spinal muscular atrophy (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 128212001 | Spinal muscular atrophy, type II (disorder) |
has_mnd_ms_myas_or_huntingtons | GP data | SNOMED | 64383006 | Werdnig-Hoffmann disease (disorder) |