ICD-10-CM Codes
E00-E89
E20-E35
Polyglandular dysfunction E31

Polyglandular dysfunction E31-

Type 1 Excludes

Type 1 Excludes Help

A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as E31. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.

ataxia telangiectasia [Louis-Bar] (
ICD-10-CM Diagnosis Code G11.3
Cerebellar ataxia with defective DNA repair
Applicable To
- Ataxia telangiectasia [Louis-Bar]
Type 2 Excludes
- Cockayne's syndrome (Q87.19)
- other disorders of purine and pyrimidine metabolism (E79.-)
- xeroderma pigmentosum (Q82.1)
G11.3
)
dystrophia myotonica [Steinert] (
ICD-10-CM Diagnosis Code G71.11
Myotonic muscular dystrophy
Applicable To
- Dystrophia myotonica [Steinert]
- Myotonia atrophica
- Myotonic dystrophy
- Proximal myotonic myopathy (PROMM)
- Steinert disease
G71.11
)
pseudohypoparathyroidism (
ICD-10-CM Diagnosis Code E20.1
Pseudohypoparathyroidism
E20.1
)

Codes

E31 Polyglandular dysfunction
- E31.0 Autoimmune polyglandular failure
- E31.1 Polyglandular hyperfunction
- E31.2 Multiple endocrine neoplasia [MEN] syndromes
  - E31.20 Multiple endocrine neoplasia [MEN] syndrome, unspecified
  - E31.21 Multiple endocrine neoplasia [MEN] type I
  - E31.22 Multiple endocrine neoplasia [MEN] type IIA
  - E31.23 Multiple endocrine neoplasia [MEN] type IIB
- E31.8 Other polyglandular dysfunction
- E31.9 Polyglandular dysfunction, unspecified

Polyglandular dysfunction E31-

Cerebellar ataxia with defective DNA repair

Myotonic muscular dystrophy

Pseudohypoparathyroidism