ICD-10-CM Code E71.440
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
E71.440 is a billable ICD code used to specify a diagnosis of ruvalcaba-Myhre-Smith syndrome. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E71 is used to code Congenital disorders of amino acid metabolism
Inborn errors of amino acid metabolism are metabolic disorders which impair the synthesis and degradation of amino acids.
|ICD 9 Code:||270|
The general structure of an α-amino acid, with the amino group on the left and the carboxyl group on the right.
- DRG Group #642 - Inborn and other disorders of metabolism.
ICD-10-CM Alphabetical Index References for 'E71.440 - Ruvalcaba-Myhre-Smith syndrome'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E71.440. Click on any term below to browse the alphabetical index.
Equivalent ICD-9 Code GENERAL EQUIVALENCE MAPPINGS (GEM)
This is the official approximate match mapping between ICD9 and ICD10, as provided by the General Equivalency mapping crosswalk. This means that while there is no exact mapping between this ICD10 code E71.440 and a single ICD9 code, 277.84 is an approximate match for comparison and conversion purposes.