ICD-10-CM Code E76.3
Billable CodeBillable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.
E76.3 is a billable ICD code used to specify a diagnosis of mucopolysaccharidosis, unspecified. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E76 is used to code Lysosomal storage disease
Lysosomal storage diseases (LSDs; /ˌlaɪsəˈsoʊməl/) are a group of approximately 50 rare inherited metabolic disorders that result from defects in lysosomal function. Lysosomes are sacs of enzymes within cells that digest large molecules and pass the fragments on to other parts of the cell for recycling. This process requires several critical enzymes. If one of these enzymes is defective, because of a mutation, the large molecules accumulate within the cell, eventually killing it.
Micrograph of Gaucher disease, with cells that have the characteristic crumpled tissue paper-like cytoplasm. H&E stain.
- DRG Group #642 - Inborn and other disorders of metabolism.
Related Concepts SNOMET-CT
- Mucopolysaccharidosis cardiomyopathy (disorder)
ICD-10-CM Alphabetical Index References for 'E76.3 - Mucopolysaccharidosis, unspecified'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E76.3. 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 E76.3 and a single ICD9 code, 277.5 is an approximate match for comparison and conversion purposes.