ICD-10-CM Code E76.1
Mucopolysaccharidosis, type II
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.E76.1 is a billable ICD code used to specify a diagnosis of mucopolysaccharidosis, type II. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E761 is used to code Hunter syndrome
Hunter syndrome, or mucopolysaccharidosis II (MPS II), is a lysosomal storage disease caused by a deficient (or absent) enzyme, iduronate-2-sulfatase (I2S). The accumulated substrates in Hunter syndrome are heparan sulfate and dermatan sulfate. The syndrome has X-linked recessive inheritance.
| Specialty: | Endocrinology |
| MeSH Code: | D016532 |
| ICD 9 Code: | 277.5 |
Coding Notes for E76.1 Info for medical coders on how to properly use this ICD-10 code
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Inclusion Terms:
Inclusion Terms
Inclusion Terms are a list of concepts for which a specific code is used. The list of Inclusion Terms is useful for determining the correct code in some cases, but the list is not necessarily exhaustive. - Hunter's syndrome
MS-DRG Mapping
- DRG Group #642 - Inborn and other disorders of metabolism.
ICD-10-CM Alphabetical Index References for 'E76.1 - Mucopolysaccharidosis, type II'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E76.1. 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 E76.1 and a single ICD9 code, 277.5 is an approximate match for comparison and conversion purposes.
Parent Code: E76 - Disorders of glycosaminoglycan metabolism