Disorder of amino-acid metabolism, NOS: Difference between revisions
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{{ICD10 transition status | {{ICD10 transition status | ||
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== Additional Info == | == Additional Info == | ||
'''Includes''' | |||
* cystinosis | |||
https://en.wikipedia.org/wiki/ | * 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 == | ||
*[[Phenylketonuria]] | *[[Phenylketonuria]] | ||
*[[Albinism (albino)]] | *[[Albinism (albino)]] | ||
*[[Metabolic disorder, NOS]] | |||
== Candidate [[Combined ICD10 codes]] == | == Candidate [[Combined ICD10 codes]] == | ||
== Related | == Related CCI Codes == | ||
{{Data Integrity Check List}} | |||
== Related Articles == | == Related Articles == | ||
{{Related Articles}} | {{Related Articles}} | ||
{{ICD10 footer}} | {{ICD10 footer}} | ||
{{EndPlaceHolder}} | {{EndPlaceHolder}} | ||