Nervous system NOS, congenital malformation: Difference between revisions
Jump to navigation
Jump to search
| Line 13: | Line 13: | ||
== Additional Info == | == Additional Info == | ||
'''Includes''' | '''Includes''' | ||
* Chiari malformation | * Chiari type 1 or Chiari type 2 malformation, also known as Arnold-Chiari disease | ||
* Charcot-Marie-Tooth disease | * Charcot-Marie-Tooth disease | ||
* Déjérine-Sottas disease | * Déjérine-Sottas disease | ||
Latest revision as of 08:24, 29 January 2024
| ICD10 Diagnosis | |
| Dx: | Nervous system NOS, congenital malformation |
| ICD10 code: | Q07 |
| Pre-ICD10 counterpart: | none assigned |
| 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
| Related articles: |
Show all ICD10 Subcategories
|
ICD10 Categories: |