Nervous system NOS, congenital malformation: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =| CurrentStatus = | | OldDxArticle = Spina Bifida | ||
| InitialEditorAssigned = | | CurrentStatus = reconciled | ||
| InitialEditorAssigned = not assigned | |||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | |||
| ICD10 Code=Q07 | | ICD10 Code=Q07 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Neuro}}{{ICD10 category|Hereditary/congenital}} | |||
== 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 == | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Brain, congenital malformation]] | |||
*[[Spinal cord, congenital malformation NOS]] | |||
*[[Spina bifida]] | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related CCI Codes == | |||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | |||
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