ICD-10-CM Code E79.2
Myoadenylate deaminase deficiency
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.E79.2 is a billable ICD code used to specify a diagnosis of myoadenylate deaminase deficiency. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E79 is used to code Adenine phosphoribosyltransferase deficiency
Adenine phosphoribosyltransferase deficiency (also called APRT deficiency or 2,8 dihydroxyadenine urolithiasis) is an autosomal recessive metabolic disorder associated with a mutation in the enzyme adenine phosphoribosyltransferase.
| Specialty: | Endocrinology |
| ICD 9 Code: | 277.2 |
Dihydroxyadenine, an insoluble purine
MS-DRG Mapping
- DRG Group #642 - Inborn and other disorders of metabolism.
ICD-10-CM Alphabetical Index References for 'E79.2 - Myoadenylate deaminase deficiency'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E79.2. 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 E79.2 and a single ICD9 code, 277.2 is an approximate match for comparison and conversion purposes.
Parent Code: E79 - Disorders of purine and pyrimidine metabolism