E31.0
BillableAutoimmune polyglandular failure
Autoimmune polyglandular failure
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Schmidt's syndrome
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Also Known As / Clinical Terms
SNOMED CT
- APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy11244009
- Autoimmune polyendocrinopathy, candidosis AND ectodermal dystrophy11244009
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy11244009
- Candidiasis-endocrinopathy syndrome11244009
- HAM syndrome11244009
- Hypoadrenocorticism, hypoparathyroidism and superficial moniliasis11244009
- Hypoparathyroidism, Addison's disease AND moniliasis11244009
- Juvenile familial endocrinopathy11244009
- Polyglandular autoimmune syndrome - type 111244009
- Polyglandular autoimmune syndrome, type 111244009
- Polyglandular deficiency associated with mucocutaneous candidiasis11244009
- Type 1 polyendocrine autoimmunity syndrome11244009
- Whitaker syndrome11244009
- APS - autoimmune polyglandular syndrome41864002
- Autoimmune polyendocrinopathy41864002
- Autoimmune polyglandular failure41864002
- Autoimmune polyglandular syndrome41864002
- Lloyd's syndrome41864002
- Polyendocrine autoimmunity syndrome41864002
- Polyglandular autoimmune syndrome41864002
- A. Schmidt syndrome56120004
- A. Schmidt's syndrome56120004
- Vagoaccessory syndrome56120004
- Autoimmune hypoparathyroidism75316000
- Multiple cranial nerve palsy78152008
- APS type 283728000
- Addison's disease with struma lymphomatosa83728000
- Diabetes mellitus, Addison's disease and myxedema83728000
- Diabetes mellitus, Addison's disease and myxoedema83728000
- PGA - Polyglandular autoimmune syndrome - type II83728000
- Polyglandular autoimmune syndrome - type II83728000
- Polyglandular autoimmune syndrome, type 283728000
- Primary hypothyroidism AND adrenocortical insufficiency83728000
- Schmidt syndrome83728000
- Schmidt's syndrome83728000
- Type 2 polyendocrine autoimmunity syndrome83728000
- Autoimmune enteropathy235728001
- Addison disease363732003
- Addison's disease363732003
- Autoimmune polyendocrine syndrome type 4449730005
- Autoimmune polyendocrine syndrome type 3449731009
- Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome722288007
UMLS
- APS - autoimmune polyglandular syndromeC0085409
- Autoimmune PolyendocrinopathyC0085409
- Autoimmune Polyendocrinopathy SyndromeC0085409
- Autoimmune polyendocrinopathyC0085409
- Autoimmune polyendocrinopathy (disorder)C0085409
- Autoimmune polyglandular failureC0085409
- Autoimmune polyglandular syndromeC0085409
- Lloyd's syndromeC0085409
- Polyendocrine autoimmunity syndromeC0085409
- Polyendocrinopathies, AutoimmuneC0085409
- Polyendocrinopathy, AutoimmuneC0085409
- Polyglandular autoimmune syndromeC0085409
- apsC0085409
- autoimmune polyendocrinopathyC0085409
- lloyd's syndromeC0085409
- pgaC0085409
- APS IIC0085860
- APS type 2C0085860
- APS2C0085860
- AUTOIMMUNE POLYENDOCRINE SYNDROME, TYPE IIC0085860
- Addison's disease with struma lymphomatosaC0085860
- Autoimmune Polyendocrine Syndrome, Type 2C0085860
- Autoimmune Polyendocrine Syndrome, Type IIC0085860
- Autoimmune Polyglandular Syndrome Type 2C0085860
- Autoimmune Polyglandular Syndrome Type IIC0085860
- Autoimmune Syndrome Type II, PolyglandularC0085860
- Autoimmune polyendocrine syndrome type IIC0085860
- DIABETES MELLITUS, ADDISON DISEASE, MYXEDEMAC0085860
- Diabetes Mellitus, Addison Disease, MyxedemaC0085860
- Diabetes Mellitus, Addison's Disease, MyxedemaC0085860
- Diabetes mellitus, Addison's disease and myxedemaC0085860
- Diabetes mellitus, Addison's disease and myxoedemaC0085860
- Multiple Endocrine Deficiency Syndrome, Type 2C0085860
- PGA - Polyglandular autoimmune syndrome - type IIC0085860
- PGA IIC0085860
- POLYENDOCRINE AUTOIMMUNE SYNDROME, TYPE IIC0085860
- POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE IIC0085860
- Polyendocrine Autoimmune Syndrome, Type IIC0085860
- Polyglandular Autoimmune Syndrome, Type 2C0085860
- Polyglandular Deficiency Syndrome, Type 2C0085860
- Polyglandular Type II Autoimmune SyndromeC0085860
- Polyglandular autoimmune syndrome - type IIC0085860
- Polyglandular autoimmune syndrome type IIC0085860
- Polyglandular autoimmune syndrome, type 2C0085860
- Polyglandular autoimmune syndrome, type 2 (disorder)C0085860
- Primary hypothyroidism AND adrenocortical insufficiencyC0085860
- SCHMIDT SYNDROMEC0085860
- Schmidt SyndromeC0085860
- Schmidt syndromeC0085860
- Schmidt's SyndromeC0085860
- Schmidt's syndromeC0085860
- Syndrome, SchmidtC0085860
- Syndrome, Schmidt'sC0085860
- Type 2 polyendocrine autoimmunity syndromeC0085860
- schmidt syndromeC0085860
- schmidt's syndromeC0085860
- schmidts syndromeC0085860
- syndrome schmidtC0085860
Frequently Asked Questions
What is ICD-10 code E31.0?
ICD-10-CM code E31.0 represents "Autoimmune polyglandular failure". It is a billable/specific code that can be used on a claim.
Is E31.0 a billable code?
Yes, E31.0 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E31.0 in?
E31.0 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E31.0?
E31.0 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 3 more.
What SNOMED CT codes does E31.0 map to?
E31.0 maps to 11 SNOMED CT concepts: 56120004, 11244009, 41864002, 83728000, 363732003, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E31.0?
E31.0 is linked to 2 UMLS Concept Unique Identifiers: C0085409, C0085860. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.