ICD-10-CM › H00-H59 › H30-H36 › H31.2 Hereditary choroidal dystrophy › H31.22
H31.22
Choroidal dystrophy (central areolar) (generalized) (peripapillary)
ValidICD-10-CM diagnosis code.
Valid for claims with a date of service in the current code year.
What has happened to this code
Every change the publisher made, from 2007 to now. Entries marked draft are from the pre-implementation releases: ICD-10 took effect on 1 October 2015, so nothing before FY2016 was ever valid on a claim.
- FY2007 Added to the draft code set draft Choroidal dystrophy (central areolar) (generalized) (peripapillary)
How CDC's index refers to this code
Wording from the official alphabetic index. Much of it appears nowhere in the code description, which is why a search for the everyday phrase so often finds nothing.
- Choroidopathy
- Behr's disease
- Stargardt's disease
- Macula > degeneration
- Retinitis > disciformis
- Kuhnt-Junius degeneration
- Heredodegeneration, macular
- Disorder > retina > dystrophy
- Disorder > choroid > dystrophy
- Sclerosis, sclerotic > choroid
- Disorder > retina > retinopathy
- Disorder > retina > degeneration
- Disorder > choroid > degeneration
- Macula > degeneration > hereditary
- Retinopathy > pigmentary, congenital
- Detachment > retina > pigment epithelium
- Disorder > retina > macular degeneration
- Degeneration, degenerative > eye, macular
- Degeneration, degenerative > Kuhnt-Junius
- Degeneration, degenerative > chorioretinal
- Degeneration, degenerative > tapetoretinal
- Degeneration, degenerative > retina > macula
- Degeneration, degenerative > Bruch's membrane
- Degeneration, degenerative > retina > hereditary
- Degeneration, degenerative > retina > pigmentary
- Degeneration, degenerative > choroid > hereditary
- Degeneration, degenerative > retina > Kuhnt-Junius
- Degeneration, degenerative > retina > posterior pole
- Degeneration, degenerative > eye, macular > congenital or hereditary
- Degeneration, degenerative > macula, macular > congenital or hereditary
- Dystrophy, dystrophia > choroid > central areolar
Codes in the same group
| Code | Description | Status |
|---|---|---|
| H31.20 | Hereditary choroidal dystrophy, unspecified | Valid |
| H31.21 | Choroideremia | Valid |
| H31.23 | Gyrate atrophy, choroid | Valid |
| H31.29 | Other hereditary choroidal dystrophy | Valid |