Nervous system NOS, congenital malformation: Difference between revisions
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== Additional Info == | == Additional Info == | ||
'''Includes''' | |||
* Chiari malformation | * Chiari malformation | ||
* 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 | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == |
Revision as of 08:13, 29 June 2023
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 malformation
- 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
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