ICD-10-CM › E00-E89 › E20-E35 › E31 Polyglandular dysfunction › E31.8
Other polyglandular dysfunction
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 Other polyglandular dysfunction
Official coding rules
Published by CDC for FY2027. A rule attached to a category binds every code beneath it, so the rules inherited from this code's ancestors are shown with the code they come from.
Inherited from E31 Polyglandular dysfunction
Excludes1 - never coded here
- ataxia telangiectasia [Louis-Bar] (G11.3)
- dystrophia myotonica [Steinert] (G71.11)
- pseudohypoparathyroidism (E20.1)
Inherited from the E20-E35 section Disorders of other endocrine glands (E20-E35)
Excludes1 - never coded here
- galactorrhea (N64.3)
- gynecomastia (N62)
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.
- Deficit
- Malfunction
- Avitaminosis
- Behr's disease
- Hypovitaminosis
- Vitamin deficiency
- Leukoencephalopathy
- Stargardt's disease
- Macula > degeneration
- Deprivation > vitamins
- Retinitis > disciformis
- Kuhnt-Junius degeneration
- Heredodegeneration, macular
- Disorder > retina > dystrophy
- Deficiency, deficient > factor
- Sclerosis, sclerotic > choroid
- Defect, defective > coagulation
- Disorder > retina > retinopathy
- Deficiency, deficient > clotting
- Disorder > retina > degeneration
- Disorder > choroid > degeneration
- Disturbance > absorption > vitamin
- Macula > degeneration > hereditary
- Retinopathy > pigmentary, congenital
- Encephalopathy > in > lack of vitamin
- Detachment > retina > pigment epithelium
- Disorder > retina > macular degeneration
- Degeneration, degenerative > eye, macular
- Degeneration, degenerative > Kuhnt-Junius
- Degeneration, degenerative > chorioretinal
- Degeneration, degenerative > tapetoretinal
- Deficiency, deficient > clotting factor NEC
- 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
- Deficiency, deficient > coagulation NOS > clotting factor NEC
Showing 40 of 52 index phrases.
Codes in the same group
| Code | Description | Status |
|---|---|---|
| E31.0 | Autoimmune polyglandular failure | Valid |
| E31.1 | Polyglandular hyperfunction | Valid |
| E31.2 | Multiple endocrine neoplasia [MEN] syndromes | Not billable |
| E31.9 | Polyglandular dysfunction, unspecified | Valid |