Nervous system NOS, congenital malformation: Difference between revisions
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== Additional Info == | == Additional Info == | ||
'''Includes''' | |||
* Chiari type 1 or Chiari type 2 malformation, also known as Arnold-Chiari disease | |||
* Charcot-Marie-Tooth disease | |||
* Déjérine-Sottas disease | |||
* Hereditary motor and sensory neuropathy, types I-IV | |||
* Hypertrophic neuropathy of infancy | |||
* Peroneal muscular atrophy (axonal type) (hypertrophic type) | |||
* Roussy-Levy syndrome | |||
* Encephalocele of congenital cause (link with [[Disorder of nervous system (any part), NOS]]) | |||
*Combine with [[Chromosomal abnormality, NOS]] if appropriate | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
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== Related CCI Codes == | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||