Dystonia due to hereditary disease   1260396009

SNOMED CT code


SNOMED code1260396009
nameDystonia due to hereditary disease
statusactive
date introduced2023-01-31
fully specified name(s)Dystonia due to hereditary disease (disorder)
synonyms
  • Dystonia due to inherited disorder
  • Dystonia due to hereditary disease
attributes - group2
InterpretsMovement   255324009
attributes - group3
Due toHereditary disease   32895009
attributes - group1
Finding siteExtrapyramidal system structure   76375004
parents
children
  • Dystonia due to ataxia telangiectasia syndrome   1260334009
  • Dystonia due to atypical pantothenate kinase associated neurodegeneration   1260360005
  • Dystonia due to GM2 gangliosidosis   1260380006
  • Dystonia due to hereditary spastic paraplegia   1260397000
  • Dystonia due to Leigh syndrome   1187533007
  • Dystonia due to Lesch Nyhan syndrome   1260390003
  • Dystonia due to metachromatic leucodystrophy   1260391004
  • Dystonia due to Niemann-Pick disease type C   1260366004
  • Dystonia due to Pelizaeus-Merzbacher disease   1260363007
  • Dystonia due to Rett syndrome   1260362002
  • Dystonia due to Wilson disease   1263524000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of movement   298325004
      Movement disorder   60342002
        Extrapyramidal disease   76349003
          Dystonia   15802004
            Dystonia due to hereditary disease   1260396009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Central nervous system finding   246556002
      Disorder of the central nervous system   23853001
        Central nervous system complication   87536007
          Dystonia due to hereditary disease   1260396009

ancestors
sorted most to least specific
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