Disorder of amino-acid metabolism, NOS: Difference between revisions
No edit summary |
|||
| Line 12: | Line 12: | ||
== Additional Info == | == Additional Info == | ||
Includes | '''Includes''' | ||
* cystinosis | * cystinosis | ||
* L-Carnitine deficiency | * L-Carnitine deficiency | ||
* glutaric acidemia type 1 (GA1) combine with [[Malformation/disorder NOS, congenital]] | * glutaric acidemia type 1 (GA1) combine with [[Malformation/disorder NOS, congenital]] | ||
https://en.wikipedia.org/wiki/Congenital_disorders_of_amino_acid_metabolism | 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 == | ||