Disorder of amino-acid metabolism, NOS: Difference between revisions
Jump to navigation
Jump to search
Ttenbergen (talk | contribs) m 1 revision imported |
No edit summary |
||
| (23 intermediate revisions by 5 users not shown) | |||
| Line 1: | Line 1: | ||
{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =| CurrentStatus = | | OldDxArticle = | ||
| CurrentStatus = reconciled | |||
| InitialEditorAssigned = Gail Hall | | InitialEditorAssigned = Gail Hall | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | |||
| ICD10 Code=E72.9 | | ICD10 Code=E72.9 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Metabolic/nutrition}} | |||
== Additional Info == | == Additional Info == | ||
'''Includes''' | |||
* cystinosis | |||
* L-Carnitine deficiency | |||
* glutaric acidemia type 1 (GA1) combine with [[Malformation/disorder NOS, congenital]] | |||
https://en.wikipedia.org/wiki/Congenital_disorders_of_amino_acid_metabolism | |||
* Maple syrup urine disease | |||
== Alternate ICD10s to consider coding instead == | == Alternate ICD10s to consider coding instead or in addition == | ||
( | *[[Phenylketonuria]] | ||
*[[Albinism (albino)]] | |||
*[[Metabolic disorder, NOS]] | |||
== 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 05:36, 2 September 2025
| ICD10 Diagnosis | |
| Dx: | Disorder of amino-acid metabolism, NOS |
| ICD10 code: | E72.9 |
| Pre-ICD10 counterpart: | none assigned |
| Charlson/ALERT Scale: | none |
| APACHE Como Component: | none |
| APACHE Acute Component: | 2019-0: Metabolic/Renal NOS, 2019-0: Renal/Metabolic NOS |
| 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
- cystinosis
- L-Carnitine deficiency
- glutaric acidemia type 1 (GA1) combine with Malformation/disorder NOS, congenital
https://en.wikipedia.org/wiki/Congenital_disorders_of_amino_acid_metabolism
- Maple syrup urine disease
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