ICD-10-CM diagnosis code
G11.5 Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- Billable
- Yes, a complete code (FY2026)
- Category
- G11 Hereditary ataxia
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Other codes in G11
11 complete codes in this category.
- G11.0Congenital nonprogressive ataxia
- G11.10Early-onset cerebellar ataxia, unspecified
- G11.11Friedreich ataxia
- G11.19Other early-onset cerebellar ataxia
- G11.2Late-onset cerebellar ataxia
- G11.3Cerebellar ataxia with defective DNA repair
- G11.4Hereditary spastic paraplegia
- G11.5Hypomyelination - hypogonadotropic hypogonadism - hypodontia
- G11.6Leukodystrophy with vanishing white matter disease
- G11.8Other hereditary ataxias
- G11.9Hereditary ataxia, unspecified
Documentation tips
- Make sure the note supports every element of the title, “Hypomyelination - hypogonadotropic hypogonadism - hypodontia”: each detail in it should be traceable to the history, examination or assessment.
- Code to the highest specificity the documentation supports. If a detail is missing from the note, add it to the note rather than choosing a less specific code by default.
- Check the Tabular List and official guidelines for instructional notes (“code first”, “use additional code”, Excludes1/Excludes2) that apply to G11.
The international WHO ICD-10 also has G11, with its inclusion and exclusion notes; titles and detail can differ from ICD-10-CM.
ICD-10-CM is developed by the National Center for Health Statistics (NCHS), Centers for Disease Control and Prevention, U.S. Department of Health and Human Services, and is based on the WHO ICD-10. Codes and titles are reproduced unchanged from the FY2026 code list (effective 1 October 2025). Their use here does not imply endorsement by CDC, HHS or the U.S. Government. Changes effective on or after 1 October 2026 may not be reflected yet; check the current release at cdc.gov or cms.gov before submitting claims.
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