Disorder of amino-acid metabolism, NOS: Difference between revisions
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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=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}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||