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)
Related Codes(4)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(169)
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
Clinical Terms
- Polyglandular Autoimmune Syndrome, Type 2
- Polyglandular autoimmune syndrome
- Polyglandular autoimmune syndrome, type 2 (disorder)
- Type 1 polyendocrine autoimmunity syndrome
- PGA II
- Autoimmune enteropathy
- Autoimmune polyendocrinopathy (disorder)
- APS - autoimmune polyglandular syndrome
- syndrome schmidt
- Autoimmune polyendocrinopathy
- Autoimmune Polyglandular Syndrome Type 2
- Multiple Endocrine Deficiency Syndrome, Type 2
- Diabetes mellitus, Addison's disease and myxoedema
- Juvenile familial endocrinopathy
- Autoimmune Polyendocrinopathy Syndrome
- DIABETES MELLITUS, ADDISON DISEASE, MYXEDEMA
- A. Schmidt syndrome
- Polyglandular autoimmune syndrome - type II
- Schmidt Syndrome
- Multiple cranial nerve palsy
- Addison disease
- Autoimmune polyendocrinopathy, candidosis AND ectodermal dystrophy
- Polyendocrinopathy, Autoimmune
- Polyglandular autoimmune syndrome - type 1
- Addison's disease with struma lymphomatosa
- POLYENDOCRINE AUTOIMMUNE SYNDROME, TYPE II
- A. Schmidt's syndrome
- Autoimmune Polyendocrine Syndrome, Type II
- Polyendocrine autoimmunity syndrome
- Autoimmune polyendocrine syndrome type 4
- Whitaker syndrome
- Autoimmune polyendocrine syndrome type 3
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
- Autoimmune polyendocrine syndrome type II
- Polyglandular deficiency associated with mucocutaneous candidiasis
- Schmidt's syndrome
- PGA - Polyglandular autoimmune syndrome - type II
- Autoimmune Polyglandular Syndrome Type II
- Polyglandular Type II Autoimmune Syndrome
- APS type 2
- Hypoadrenocorticism, hypoparathyroidism and superficial moniliasis
- aps
- Lloyd's syndrome
- Type 2 polyendocrine autoimmunity syndrome
- Autoimmune polyglandular syndrome
- APS II
- APS2
- Diabetes mellitus, Addison's disease and myxedema
- Primary hypothyroidism AND adrenocortical insufficiency
- Addison's disease
- pga
- Syndrome, Schmidt's
- Polyglandular autoimmune syndrome type II
- Vagoaccessory syndrome
- Autoimmune Syndrome Type II, Polyglandular
- Autoimmune hypoparathyroidism
- schmidts syndrome
- APECED - Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy
- POLYGLANDULAR AUTOIMMUNE SYNDROME, TYPE II
- Hypoparathyroidism, Addison's disease AND moniliasis
- Syndrome, Schmidt
- Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome
- Autoimmune Polyendocrine Syndrome, Type 2
- Diabetes Mellitus, Addison's Disease, Myxedema
- Candidiasis-endocrinopathy syndrome
- Polyglandular autoimmune syndrome, type 1
- HAM syndrome
- Polyglandular Deficiency Syndrome, Type 2
- Polyendocrinopathies, Autoimmune
Frequently Asked Questions
What is the ICD-10 code for autoimmune polyglandular failure?
The ICD-10-CM code for autoimmune polyglandular failure is E31.0. The full clinical description is "Autoimmune polyglandular failure". E31.0 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E31.0 mean?
ICD-10-CM code E31.0 represents “Autoimmune polyglandular failure”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and 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.
How does E31.0 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like autoimmune polyglandular failure affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E31.0?
E31.0 maps to the ICD-11 code: 5B00 (Autoimmune polyendocrinopathy).
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.