ICD-10-CM Code E75.25
Metachromatic leukodystrophy
Billable Code
Billable codes are sufficient justification for admission to an acute care hospital when used a principal diagnosis.E75.25 is a billable ICD code used to specify a diagnosis of metachromatic leukodystrophy. A 'billable code' is detailed enough to be used to specify a medical diagnosis.
The ICD code E7525 is used to code Fabry disease
Fabry disease (/ˈfɑːbri/) (also known as Fabry's disease, Anderson-Fabry disease, angiokeratoma corporis diffusum, and alpha-galactosidase A deficiency) is a rare genetic lysosomal storage disease, inherited in an X-linked manner. Fabry disease can cause a wide range of systemic symptoms. It is a form of sphingolipidosis, as it involves dysfunctional metabolism of sphingolipids. The disease is named after one of its discoverers, Johannes Fabry (June 1, 1860 – June 29, 1930).
| Specialty: | Endocrinology |
| MeSH Code: | D000795 |
| ICD 9 Code: | 272.7 |
Alpha galactosidase - the deficient protein Fabry disease
MS-DRG Mapping
- DRG Group #056-057 - Degenerative nervous system disorders with MCC.
- DRG Group #056-057 - Degenerative nervous system disorders without MCC.
ICD-10-CM Alphabetical Index References for 'E75.25 - Metachromatic leukodystrophy'
The ICD-10-CM Alphabetical Index links the below-listed medical terms to the ICD code E75.25. 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 E75.25 and a single ICD9 code, 330.0 is an approximate match for comparison and conversion purposes.
Parent Code: E75.2 - Other sphingolipidosis