Phenylketonuria: Difference between revisions
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Ttenbergen (talk | contribs) m Text replacement - "Heredary/congenital" to "Hereditary/congenital" |
Ttenbergen (talk | contribs) m adding {{Data Integrity Check List}} |
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{{ICD10 transition status | {{ICD10 transition status | ||
| OldDxArticle =| CurrentStatus = | | OldDxArticle = | ||
| CurrentStatus = reconciled | |||
| InitialEditorAssigned = Gail Hall | | InitialEditorAssigned = Gail Hall | ||
}} | }} | ||
{{ICD10 dx | {{ICD10 dx | ||
| MinimumCombinedCodes = | |||
| ICD10 Code=E70 | | ICD10 Code=E70 | ||
| BugRequired= | | BugRequired= | ||
}} | }} | ||
{{ICD10 category|Skin}}{{ICD10 category|Metabolic/nutrition}}{{ICD10 category|Hereditary/congenital}} | |||
== Additional Info == | == Additional Info == | ||
https://en.wikipedia.org/wiki/Phenylketonuria | |||
== Alternate ICD10s to consider coding instead or in addition == | == Alternate ICD10s to consider coding instead or in addition == | ||
*[[Disorder of amino-acid metabolism, NOS]] | |||
*[[Metabolic disorder, NOS]] | |||
== Candidate [[Combined ICD10 codes]] == | |||
== | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} |
Latest revision as of 00:37, 2018 November 18
ICD10 Diagnosis | |
Dx: | Phenylketonuria |
ICD10 code: | E70 |
Pre-ICD10 counterpart: | none assigned |
Charlson/ALERT Scale: | none |
APACHE Como Component: | none |
APACHE Acute Component: | 2019-0: Renal/Metabolic NOS, 2019-0: Metabolic/Renal NOS |
Start Date: | |
Stop Date: | |
External ICD10 Documentation |
This diagnosis is a part of ICD10 collection.
Additional Info
https://en.wikipedia.org/wiki/Phenylketonuria
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