Nervous system NOS, congenital malformation: Difference between revisions
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== 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 | ||
| Line 20: | Line 20: | ||
* Peroneal muscular atrophy (axonal type) (hypertrophic type) | * Peroneal muscular atrophy (axonal type) (hypertrophic type) | ||
* Roussy-Levy syndrome | * 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 == | ||
Latest revision as of 08:24, 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: | |
| 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
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