Autoimmune polyglandular failure
- E31.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2025 edition of ICD-10-CM E31.0 became effective on October 1, 2024.
- This is the American ICD-10-CM version of E31.0 – other international versions of ICD-10 E31.0 may differ.
Applicable To
- Schmidt’s syndrome
The following code(s) above E31.0 contain annotation back-references
that may be applicable to E31.0:
- E00-E89 Endocrine, nutritional and metabolic diseases
- E20-E35 Disorders of other endocrine glands
- E31 Polyglandular dysfunction
Approximate Synonyms
- Autoimmune polyendocrinopathy
- Lloyd syndrome
- Polyglandular autoimmune syndrome, type 2
- Schmidts syndrome
Clinical Information
- A rare genetic syndrome characterized by autoantibodies production against more than one endocrine organ. The range of endocrinopathies includes hypoparathyroidism, adrenal insufficiency, hypogonadism, type 1 diabetes mellitus and hypothyroidism.
- An autoimmune diseases affecting multiple endocrine organs
- Autoimmune diseases affecting multiple endocrine organs. Type i is characterized by childhood onset and chronic mucocutaneous candidiasis (candidiasis, chronic mucocutaneous), while type ii exhibits any combination of adrenal insufficiency (addison’s disease), lymphocytic thyroiditis (thyroiditis, autoimmune;), hypoparathyroidism; and gonadal failure. In both types organ-specific antibodies against a variety of endocrine glands have been detected. The type ii syndrome differs from type i in that it is associated with hla-a1 and b8 haplotypes, onset is usually in adulthood, and candidiasis is not present.
ICD-10-CM E31.0 is grouped within Diagnostic Related Group(s) (MS-DRG v42.0):
- 643 Endocrine disorders with mcc
- 644 Endocrine disorders with cc
- 645 Endocrine disorders without cc/mcc
Convert E31.0 to ICD-9-CMCode History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- 2024 (effective 10/1/2023): No change
- 2025 (effective 10/1/2024): No change
Code annotations containing back-references to E31.0:
- Code First: E20.812, E20.812
Diagnosis Index entries containing back-references to E31.0:
- Atrophy, atrophic (of)
- pluriglandularE31.8
- autoimmune E31.0
- pluriglandularE31.8
- Deficiency, deficient
- polyglandularE31.8
- autoimmune E31.0
- polyglandularE31.8
- Failure, failed
- polyglandular, autoimmune E31.0
- Insufficiency, insufficient
- progressive pluriglandular E31.0
- Polyglandular
- deficiency E31.0
- Schmidt’s syndrome E31.0 (polyglandular, autoimmune)
- Syndrome – see also Disease
- pluriglandular (compensatory) E31.8
- autoimmune E31.0
- polyglandularE31.8
- autoimmune E31.0
- autoimmune polyglandular E31.0
- thyroid-adrenocortical insufficiency E31.0
- pluriglandular (compensatory) E31.8