Disorder of amino-acid metabolism, NOS: Difference between revisions

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{{ICD10 transition status
{{ICD10 transition status
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| InitialEditorAssigned = Gail Hall
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== Additional Info ==
== Additional Info ==
{sc:phenylketonuria, albinism}
'''Includes'''
 
* cystinosis
https://en.wikipedia.org/wiki/Phenylketonuria
* 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 ==
== Alternate ICD10s to consider coding instead or in addition ==
(turn these into links to the actual diagnosis articles if possible. For some that might make no sense.)
{sc:phenylketonuria, albinism}
*[[Phenylketonuria]]
*[[Phenylketonuria]]
*[[Albinism (albino)]]
*[[Albinism (albino)]]
*[[Metabolic disorder, NOS]]


== Candidate [[Combined ICD10 codes]] ==
== Candidate [[Combined ICD10 codes]] ==
(put links to likely candidates coded with this one, eg. a cause for a trauma.)


== Related CCI Codes ==
== Related CCI Codes ==
 
{{Data Integrity Check List}}


== Related Articles ==
== Related Articles ==
{{Related Articles}}
{{Related Articles}}


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{{ICD10 footer}}
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