ICD-10-CM Code E75.21
Fabry (-Anderson) disease
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.E75.21 is a billable ICD code used to specify a diagnosis of fabry (-Anderson) disease. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E752 is used to code Multiple sulfatase deficiency
Multiple sulfatase deficiency (also known as "Austin disease," and "Mucosulfatidosis") is a very rare autosomal recessive:561 lysosomal storage disease caused by a deficiency in multiple sulfatase enzymes, or in formylglycine-generating enzyme, which activates sulfatases.:502 It is similar to mucopolysaccharidosis.
| Specialty: | Endocrinology |
| MeSH Codes: | D052517, D055577, D009542, D017825, D020371, D052556, D009542, D007965 |
| ICD 9 Codes: | , 272.8, 272.7, 330.0, 330.0, 272.7, 272.7, 330.0 |
MS-DRG Mapping
- DRG Group #642 - Inborn and other disorders of metabolism.
Related Concepts SNOMET-CT
- Fabry's disease (disorder)
ICD-10-CM Alphabetical Index References for 'E75.21 - Fabry (-Anderson) disease'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E75.21. 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 E75.21 and a single ICD9 code, 272.7 is an approximate match for comparison and conversion purposes.
Parent Code: E75.2 - Other sphingolipidosis