Q82.0
Hereditary lymphedema
Billable code
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Inherited from Q82Other congenital malformations of skin
Inherited from chapter 17Congenital malformations, deformations and chromosomal abnormalities
Excludes 2
inborn errors of metabolism (E70-E88)
Note
Codes from this chapter are not for use on maternal records
Official Guidelines for Q82.0
FY 2026 ›Sections that reference Q82.0
Sections whose FY 2026 text names Q82.0, its Q82 category, or a range containing it — the chapter guidance above is the authoritative source.
Find Q82.0 in the alphabetic index
19 index paths lead to this code
- Meige-Milroy disease
- Meige's syndrome
- Milroy's disease
- Nonne-Milroy syndrome
- Pseudoelephantiasis neuroarthritica
- Trophedema
- Tropholymphedema
- Disease, diseased › Meige's
- Disease, diseased › Milroy's
- Disease, diseased › Nonne-Milroy-Meige
- Edema, edematous › chronic hereditary
- Edema, edematous › familial, hereditary
- Edema, edematous › hereditary
- Edema, edematous › Milroy's
- Elephantiasis › congenital
- Lymphedema › congenital
- Lymphedema › hereditary
- Syndrome › Nonne-Milroy-Meige
- Edema, edematous › legs › hereditary