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}} | |||
{{EndPlaceHolder}} | |||
Latest revision as of 07:24, 29 January 2024
| ICD10 Diagnosis | |
| Dx: | Nervous system NOS, congenital malformation |
| ICD10 code: | Q07 |
| Pre-ICD10 counterpart: | Spina Bifida |
| Charlson/ALERT Scale: | none |
| APACHE Como Component: | none |
| APACHE Acute Component: | none |
| Start Date: | |
| Stop Date: | |
| Data Dependencies(Reports/Indicators/Data Elements): | No results |
| External ICD10 Documentation | |
This diagnosis is a part of ICD10 collection.
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
Candidate Combined ICD10 codes
Related CCI Codes
Data Integrity Checks (automatic list)
none found
Related Articles
Show all ICD10 Subcategories