G11.6 Leukodystrophy with vanishing white matter disease
Billable / valid for submission ICD10CM Release FY2026
Version history
| Release | Valid from | Valid to | Description | Billable |
|---|---|---|---|---|
| FY2026 | 2025-10-01 | current | Leukodystrophy with vanishing white matter disease | yes |
Related codes in G11
- G11 Hereditary ataxia
- G11.0 Congenital nonprogressive ataxia
- G11.1 Early-onset cerebellar ataxia
- G11.10 Early-onset cerebellar ataxia, unspecified
- G11.11 Friedreich ataxia
- G11.19 Other early-onset cerebellar ataxia
- G11.2 Late-onset cerebellar ataxia
- G11.3 Cerebellar ataxia with defective DNA repair
- G11.4 Hereditary spastic paraplegia
- G11.5 Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.8 Other hereditary ataxias
- G11.9 Hereditary ataxia, unspecified